Difference between revisions of "Glycosides"

Latest revision as of 16:26, 28 August 2024

Glycosides are flavorless compounds often found in plants/fruits that are composed of a molecule (often a flavor active compound) bound to a sugar molecule. The glycosidic bond can be broken, releasing the sugar molecule and the potentially flavor active compound. These bonds can be broken with exposure to acid, as well as specific enzymes which can be added synthetically or produced naturally by some microorganisms, including some strains of Brettanomyces ^[1]. When the glycosidic bond is broken by an enzyme produced by a microorganism, it can be classified under the generic term as a "biotransformation" ^[2]. The release of flavor molecules from glycosides is thought to contribute to the flavor development of aging wines, as well as kriek (cherry) lambic ^[3]. It is speculated that flavor compounds from hops can also be released from glycosides ^[4].

Glycosides and Beta-Glucosidase Activity

Monoterpenes and Glycosides

Monoterpenes generally exist as aromatic and flavorful alcohols that tend to smell floral with low odor thresholds (100-400 ppb), and are present in plant material. These alcohols mostly consist of linalool (a major contributor to hop aroma ^[5]), geraniol, nerol, and linalool oxides, but also includes other monoterpenes such as citronellol, alpha-terpineol, hotrienol, nerol oxide, myrcenol, the ocimenols, and other oxides, aldehydes and hydrocarbons. In wine (and probably sour beer), these alcohols bind with acids to create aromatic monoterpene ethyl esters and acetate esters, and can also be transformed into other types of monoterpenes by yeast metabolism ^[6]^[3]. Monoterpenes can also be odorless polyols, some of which can break down easily to produce pleasant aromas. For example, diendiol can break down into hotrienol (tropical, floral, fennel, ginger aroma ^[7]) and nerol oxide (green, vegetative and floral with a minty undernote ^[8]). It is thought that some strains of Saccharomyces cerevisiae might be able to produce monoterpenes such as geraniol during fermentation in ways not related to beta-glucosidase activity ^[9].

Glycosides are a very diverse group of non-volatile and flavorless molecules that generally encompass any molecule that has a sugar bound to a non-sugar molecule (thus separating them from polysaccharides). The sugar (monosaccharide or oligosaccharide) component of the molecule is known as the "glycone", and the non-sugar component is known as the "aglycone". By breaking the glycosidic bond of a glycoside, the aglycone component is released. The aglycone component of glycosides are often polyphenols or the floral monoterpene alcohols described above. Glycosides can be categorized based on their glycone (glucose vs fructose), type of glycosidic bond (α-glycosides or β-glycosides), or by their aglycone (alcoholic, anthraquinone, coumarin, cyanogenic, flavonoid, phenolic, aponins, steroidal/cardiac, steviol, or thioglycosides). Glycosides play important roles in living organisms, especially many types of plants which store glycosides in their tissue and then break the bond between the sugar and non-sugar aglycone when the aglycone is needed for certain biological functions ^[10]. These include protecting cells from toxins in the plant and attracting insects via the fragrance of flowers ^[11].

Aglycones have been identified in many fruits and herbs such as grapes, apricots, peaches, yellow plums, quince, sour cherry, passion fruit, kiwi, papaya, pineapple, mango, lulo, raspberry, strawberry, and tea ^[12]^[11]. They have been found in different parts of plants, including the green leafy parts, fruit, roots, rhizomes, petals, and seeds. Aglycones in plants are highly complex structures and very diverse, and their percentages can vary from crop to crop. In plants, these include alcohol type aglycones such as terpenols, terpenes, linalool oxides, as well as other flavor precursors including various alcohols, norisoprenoids, phenolic acids and probably volatile phenols such as vanillin ^[12]. In fruits, there are mostly just 4 types of flavonol type aglycones: quercetin (found in nearly all fruits), kaempherol (found in 80% of fruit), and less commonly quercetin and isorhamnetin ^[13] (see this UC Davis PDF for amounts in different fruit and potential health benefits as antioxidants). In many cases of fruit, the amount of aromatic aglycones that are bound up in glycosides outnumber the amount that are free in a ratio of 2:1 to 8:1 ^[12]. Aglycones that are bound up in glycosides tend to be more water soluble and less reactive once unbound than the naturally free version. By providing enzymes that break the glycosidic bond, discarded parts of plants (peels, stems, skins, etc.) have been used to produce natural flavorings from the remaining and abundant glycosides ^[11].

Acidic Hydrolysis

Aglycones can be released from glycosides via a low pH. Generally, this occurs at lower pH's and Daenen et al. (2007) attributed most of the breakdown of glycosides to beta-glucosidase enzymes ^[3], but different types of glycosides are more readily broken down at different pH's. For example, ocimenols (lemon, lime ^[14]) are formed from glycoside breakdown at a pH of 1, but terpenes such as linalool, nerol, and geraniol (commonly found in hops and other plant material) are formed at a pH of 3, and alpha-terpineol was formed at both pH values. The acidic breakdown of these glycosides were found to contribute to the flavor of wine during aging ^[12]. Daenen et al. (2007) also found that acidic hydrolysis was responsible for the formation of alpha-ionol, beta-damascenone, linalool and alpha-terpineol and to a lesser extent benzyl alcohol ^[3].

In beer, it was found that the lower the pH of the beer the higher the amount of the ketone damascenone (floral, rose ^[15]) and dimethyl trisulfide (sulfury cooked onion ^[16]). In one study, at a pH of 3, beta-damascenone was reported to be ~27 ppb and dimethyl trisulfide was reported to be 650 ppt. At a pH of 4.2, they were 17 ppb and 300 ppt respectively. At a ph of 5, beta-damascenone was around 12 ppb and dimethyl trisulfide 50 ppt. This was believed to be due to the acidic hydrolysis of glycosides, and it was speculated that other glycosides could have a flavor impact on beers that contain fruit or herbs due to acidic hydrolysis of glycosides ^[17].

See also: Glycosides In Hops.

Beta-Glucosidase

Aglycones can also be released chemically from glycosides by enzymes called beta-glucosidases. Enzymatic breakdown of glycosides has been described as producing a more "natural" flavor in wines versus acidic breakdown. Some fruits have been observed (mostly wine grapes) to have limited beta-glucosidase activity within themselves, however it has been observed as being unstable and having low activity at the low pH of wine and sour beer ^[12].

Beta-glycosidase enzymes can be added artificially, however there has been much interest in the natural capability of microorganisms to produce beta-glucosidases, particularly 1,4-β-glucosidase ^[11]. Microorganisms that can break down glycosides by using beta-glucosidases can then access the resulting sugars for fermentation ^[18]. There are two major categories of glucosidase activity: endogenous and exogenous. Endogenous enzymatic activity takes place inside of the cell, and exogenous enzymatic activity takes place outside of the cell. Bacteria and fungi that show endogenous glucosidase activity have been shown not to be effective in alcoholic fermentation due to not tolerating low pH (optimum pH of 5), glucose, and/or ethanol. Generally, the flavorless glycosides remain unaffected by yeast fermentation, leaving them unused as a potential source for flavor and aroma ^[11].

Exogenous beta-glycosidase activity has been shown to be much more effective at releasing aglycones from glycosides in bacteria and fungi. For glycosides which contain a glucose, which is the majority, beta-glucosidase cleaves the sugar, thus releasing the aglycone. For glycosides that contain disaccharides, usually another enzyme must be present to first break down the disaccharide before the beta-glucosidase can release the aglycone (beta-xylosidase, alpha-arabinosidase, alpha-rhamnosidase, or beta-apiosidase) ^[11]. However, glycosides in tea leaves that contain disaccharide sugars (cellulose/cellobiose ^[19]) have been observed to be broken down without the use of these other enzymes; the beta-glucosidase cleaves the aglycone from the disaccharide on its own. Some species of yeast (Debaryomyces castelli, D. hansenii, D. polymorphus, Kloeckera apiculata, Hansenula anomala, and Brettanomyces spp), bacteria (Oenococcus oeni), and fungi (Aspergillus niger) have been found to have strain dependent beta-glucosidase activity, however several inhibitors for glucosidase activity vary for different strains of microbes. These inhibitors include the presence of glucose, pH, temperature, ethanol, and phenols ^[12]^[20]. For example, for some strains of O. oeni, as little as 10mg/L of glucose is enough to inhibit beta-glucosidase activity, or the presence of alcohol or typical wine pH (3.0 - 4.0) was enough to inhibit. Other strains of O. oeni are not inhibited by some or all of these inhibitors ^[21].

Different types of beta-glucosidase enzymes have different optimal pH and temperatures. For example, beta-glucosidase produced from A. niger is optimal at a pH of 4.5 and a temperature of 58°C (136°F), whereas the enzyme for Brettanomyces anomalus is optimal at a pH of 5.75 and a temperature of 37°C (98°F) (it was active to some extent between 15°-55°C). The beta-glucosidase enzyme ceases effectiveness below a pH of 4.5 for one strain of B anomalus studied ^[22].

Activity of Brettanomyces and Saccharomyces

Daenen et al. (2007) screened the beta-glucosidase activity of several strains of Saccharomyces cerevisiae, Saccharomyces pastorianus, and several Brettanomyces species. None of the lager brewing strains showed beta-glucosidase activity. Out of 32 strains of S. cerevisiae, only one strain (a wine strain called "U228") showed beta-glucosidase activity, however its activity was repressed in the presence of glucose. This indicates that most S. cerevisiae strains do not have the capability of producing beta-glucosidase, but it is possible that some very few strains can ^[4]. Additionally, beta-glucosidase activity for S. cerevisiae can be inhibited by the pH levels found in wine and sour beer (optimal at pH 5) ^[20]. All strains of S. cerevisiae did release another enzyme called beta-glucanase, which led to varying degrees of breaking down some smaller glycosides found in hops (hop extract was tested, not whole hops) containing the aglycones methyl salicylate, 1-octen-3-ol, and cis-3-hexen-1-ol, but not linalool. None of the B. bruxellensis strains showed this activity, but the researchers only tested strain of B. custersianus and both of the B. anomala strains tested did show cell-associated (intracellular) beta-glucosidase activity. In particular, the B. custersianus strain was tested against glycosides from hops, in which case high amounts of the aglycones linalool (citrus, orange, lemon, floral ^[23]), methyl salicylate (minty, wintergreen ^[24]), 1-octen-3-ol (mushroom, earthy ^[25]) and cis-3-hexen-1-ol (grassy, melon rind ^[26]) were released from hop extracts ^[4]. The beta-glucosidase activity was elevated when co-fermenting B. custersianus with S. cerevisiae. The authors also found dihydroedulan 1 and 2 (elderberry aroma) and theaspirane A and B (woody and campfire aromas), which are classified as norisoprenoids, were released from dry hopping ^[27]. B. custersianus has been isolated from the later stages of lambic fermentation, and it is thought that its ability to produce beta-glucosidase, which gives it the ability to ferment cellobiose and cellotriose, is a possible adaptation from living in oak barrels ^[4]. Recent studies on hops have linked an increase in fruity thiols from hops (3-mercaptohexan-1-ol and 4-mercapto-4-methylpentan-2-one) being produced during fermentation from the production of beta-lyase enzyme, and this could also explain anecdotal reports of increased fruity aromas from exposing hops to fermentation (see this article by Scott Janish on beta-lyase enzymes in GM and non-GM yeast strains). ^[28]^[29].

Palmeri et al. (2002) reported one wine strain out of 80 strains of S. cerevisiae found in Sicilian must that had high beta-glucosidase activity and is active during wine fermentation conditions ^[30]. Another study by Sharp et al. found that both ale and lager yeasts exhibit a wide range of beta-glucosidase activity, but the results should be repeated using a different substrate because the substrate that was used could have been broken down by beta-glucanase enzyme instead of beta-glucosidase ^[31]Additionally, Lallemand claims that three brewing strains that they offer produce beta-glucosidase enzymes that can promote hop biotransformation, but the details of this activity have not been published to our knowledge (BRY-97, New England, and Belle Saison) ^[32] (~8:50 min in).

The same strain of B. custersianus was screened for beta-glucosidase activity and aglycone byproducts during the refermentation of sour cherries in beer (a very small amount of the byproducts were manufactured by the yeast de novo, particularly linalool, alpha-terpineol, alpha-ionol, and a precursor that leads to beta-damascenone under low pH conditions). Different portions of the cherries were tested: whole cherries with stones (pits), cherry pulp without stones, cherry juice without stones or other solids from the fruit, and the stones alone. Benzaldehyde (almond, cherry stone flavor) was produced during fermentation in all cases, and reduced to benzyl alcohol (almond flavor) and benzyl acetate (fruity, jasmine flavor) by the end of fermentation. There were higher levels of these benzyl based compounds in the whole cherries and cherry stone alone samples, indicating that cherry stones make a big impact on the almond flavors found in cherry sour beers. Methyl salicylate, linalool, alpha-terpineol (pine), geraniol (rose, lime, floral) and alpha-ionol (floral, violet), eugenol (spicy, clove, medicinal) and isoeugenol (fine delicate clove) levels increased in all forms of cherries added except for stones alone, indicating that these aglycones are more present in the flesh and juice of the cherries ^[3]. Another study that performed whole genome sequencing on a strain of B. naardenensis found that it had two genes that could potentially allow this species to produce beta-glucosidase, but this was not confirmed in the study ^[33].

Many strains of B. bruxellensis have also been found to have varying degrees of intracellular (produced inside the cell only) or parietal (attached to the cell wall) beta-glucosidase activity. At least one mutant strain of B. bruxellensis found in wine (D. bruxellensis BCRC920084 from the Bioresource Collection and Research Center, Hsin-Chu, Taiwan) has been reported to have high extracellular (excreted out of the cell) production of beta-glucosidase that was very efficient at breaking down a glycoside called "piceid" that released resveratrol, which has been marketed as a dietary supplement ^[34]^[35]. Brettanomyces has more strains that can produce beta-glucosidase than other genera of yeast, and the strains generally also have a higher rate of beta-glucosidase activity than other genera of yeast ^[36]^[20]. Strains with higher beta-glucosidase activity have been isolated from lambic, suggesting that these strains may have an adapted ability to utilize sugar from glycosides ^[22]. Some Brettanomyces strains may only be capable of beta-glucosidase activity, and not the other enzymes which are needed to break down disaccharide type glycosides. Additionally, cell death and autolysis can result in an increase in beta-glucosidase activity in solution due to the cell contents being released into solution ^[20]. Strains that can metabolize cellobiose tend to also have higher beta-glucosidase activity because they possess an extra gene for beta-glucosidase enzyme production ^[37].

Sensory analysis of beers with cherries or hops have shown that there is a significantly detectable difference between cherry beers that have been exposed to beta-glucosidase from one strain of B. anomalus versus not exposed to the enzyme, but no significant difference was found in beers hopped with pellets. The cherry beers exposed to the enzyme contained more and above odor threshold eugenol (clove, honey aroma), benzyl alcohol (sweet, flower), benzaldehyde (almond, cherry) than cherry beers that were not exposed to the enzyme. The cherry beers exposed to the enzyme were not only identified in a blind tasting but were also preferred to the cherry beers without exposure to the enzyme, indicating that beta-glucosidase activity in cherry beers provides a significant flavor difference. Other types of beta-glucosidase enzymes released different levels of different flavor compounds, indicating that the source (bacteria or yeast) of the enzyme make a significant difference in the flavors that are produced ^[22].

The effects of beta-glucosidase on hops may be limited even in ideal conditions using pure beta-glucosidase that is highly efficient in beer where beta-glucosidase activity by yeast is limited. Sharp et al. (2017) determined that hops contain such a small amount of glycosides that their release doesn't contribute much to hop flavor and aroma. While previous studies focused on hop extracts, they studied glycosides in whole leaf hops for the first time and found non-significant levels of hop-derived monoterpenes from glycosides even when using pure beta-glucosidase extracted from almonds. For example, linalool was increased by 16.5 μg/L when using the highest hopping rate, but this amount has little impact on the overall aroma and flavor of the beer. Terpineol, citronellol, nerol, and geraniol were also not increased in significant amounts, however 1-octanol (waxy, green, citrus, orange, aldehydic, fruity ^[38]) was increased significantly ^[31].

In 2020, whole genome sequencing and glycosidic activity were tested for 84 strains of Brettanomyces by Colomer et al. They found that the capability of Brettanomyces to break down glycosides is determined by possessing two genes: BbBGL1 and BbBGL2. The genes called BbBGL2 have a major role in whether glycosides are broken down, while the role of BbBGL1 is minimal. About half of the strains had some level of glycosidic activity, although the majority was low with a couple of strains that had high levels of glycosidic activity, thus these genes alone do not account for the wide variation in glycosidic activity levels in Brettanomyces (see this figure from the study which maps beta-glucosidase activity for the 84 strains that were sequenced) ^[39]. The beta-glucidase levels were also measured for 5 strains (4 strains of B. bruxellensis and 1 strain of B. anomalus) that have the genetic make up to produce this enzyme; most of the enzyme was only produced within the cell (intracellular) for all of the strains tested, and only small amounts were produced outside of the cells except for one strain of B. anomalus. The enzyme therefore wouldn't act on glycosides outside of the cell unless the cell ruptured. There was also a small amount of beta-glucosidase activity within the cell wall of one of the strains of B. anomalus. They also fermented a dry hopped beer with these strains and found that the strains with the lowest beta-glucosidase activity had the lowest conversion of geraniol to β‐citronellol, and therefore there was no correlation between beta-glucosidase activity and hop biotransformation (although there was evidence of another unidentified type of biotransformation occurring with the hops (see Brettanomyces hop biotransformation) ^[40].

Wang et al. (2018) reported another type of glycosidic activity in one strain of B bruxellensis which is the conversion of the glycoside "mogroside V" into an artificial sweetener called siamenoside I. Other yeast and bacteria species were tested and did not find this particular glycosidic activity. Mogroside V is found naturally in some fruit, specifically, an Asian fruit called Lo Han Kuo (Siraitia grosvenorii). The artificial sweetener siamenoside is 563 times sweeter tasting than 5% sucrose. The specific enzyme responsible for this conversion that this strain of B. bruxellensis produced is called DbExg1 ^[41].

Activity of Other Yeasts

A strain of Candida glabrata was selected in a study for its high beta-glucosidase activity, its tolerance to ethanol, and its ability to utilize maltose, and was shown to produce novel flavor characteristics in beer fermentation, including a significant increase in geraniol ^[42]. Strains of Meyerozyma guilliermondii and Hanseniaspora uvarum that were isolated from a spontaneous wine fermentation have also been found to have positive results when co-fermented with S. cerevisiae in wine. Specifically, compared to the control wines, there were higher levels of the terpenes: isopulegol, citronellol, geranylacetone, geraniol, trans-nerolidol, and nerol. This was associated with the high beta-glucosidase activity of these yeast strains ^[43].

Activity of Lactic Acid Bacteria

(To do)

http://www.icfsnmalaysia2017.org/ICFSN2017%20proceedings%20-%20pp%2054-60.pdf

https://search.proquest.com/docview/752091646?pq-origsite=gscholar

https://www.researchgate.net/profile/Prafulla_Mahajan/publication/225362291_Production_of_Cell_Membrane-Bound_a-_and_b-Glucosidase_by_Lactobacillus_acidophilus/links/55fd56cd08aeba1d9f56bdbd.pdf

http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2672.2009.04461.x/full

https://ifst.onlinelibrary.wiley.com/doi/abs/10.1111/jfpp.16368

https://www.mdpi.com/2076-3921/11/2/305

https://www.sciencedirect.com/science/article/abs/pii/S2212429224014354

Cyanogenic Glycosides

All plants contain at least tiny amounts of hydrogen cyanide (HCN), however, some plants also release high amounts of HCN from a class of glycosides called "cyanogenic glycosides", also called "cyanoglycosides". Amygdalin and linamarin are common examples of cyanogenic glycosides ^[44]. Amygdalin is sometimes marketed as a cure for cancer by the health food industry, but this claim is not supported by clinical data, and digestion of too much amygdalin can be dangerous ^[45]^[46]^[47]^[48]. HCN is released from cyanogenic glycosides just like other types of glycosides: beta-glucosidase enzyme or exposure to low pH breaks the bond between a glucose molecule and an unstable compound called "cyanohydrin" (or "alpha-hydroxynnitrile"), which then disassociates into a ketone or benzaldehyde and an HCN molecule. In cyanogenic glycosides, this reaction is called "cyanogenesis". Cyanogenesis is stimulated by maceration, and by bacteria in the human gut ^[49]. Although the optimum pH of cyanogenesis (at least for amygdalin) is 5.0 - 5.8, cyongenesis can occur at a wide range of pH values, and can occur in the presence of acid ^[50]. If seeds containing cyanogenic glycosides are ground up, the coarseness to which they are ground effects how quickly cyanogenesis occurs. Finely ground seeds extract HCN within an hour, where as coarsely ground seeds extract within 24 hours ^[51]. HCN boils at a relatively low temperature (25.6°C / 78.1°F) ^[44]. In some cases, soaking, cooking, and/or sometimes fermenting foods with certain bacteria or yeast (this has not been fully documented with Saccharomyces or Brettanomyces) that contain cyanogenic glycosides allows the HCN to be released, and then subsequent cooking afterwards will boil off the cyanide ^[52]^[53].

After being released from cyanogenic glycosides, HCN is highly toxic to animals. The human body is used to breaking down trace amounts of cyanide into the less toxic substance thiocyanate with an enzyme called rhodanese, which then leaves the body via urination ^[44]. Although there are more than 3,000 plant species that are cyanogenic (a number of them cultivated by farmers perhaps because their cyanogenic properties deter animals from eating them), only a few parts of plants that are considered foods contain enough HCN from cyanogenic glycosides to be considered dangerous (generally, other forms of cyanide are considered more dangerous, such as from exposure to air or water that is polluted with cyanide) ^[54]. The location of the cyanogenic glycosides and the enzymes that release them are often each located in different (or all) parts of plants, and those locations are diverse across species. In some plants, the cyanogenic glycosides are concentrated in the stems or leaves of the plant and not the seeds (e.g. sorghum, barley, and lima beans). In fruits sometimes the seeds contain concentrated amounts (e.g. black cherry pits), and other times in the fruit itself (e.g. Passiflora edulis). In rosaceous stone fruits, cyanogenic glycosides are located in the seeds, but the beta-glucosidase enzyme that the plant uses to release HCN is located in the roots of the plant. The concentration of cyanogenic glycosides is generally higher in seedling plants compared to mature plants, however there are a few exceptions where this is the opposite (e.g. some Eucalyptus species, and lima beans). The HCN potential of plants varies highly depending on the species, strain, and climate/environmental conditions of the crop year ^[44].

Although rare, there have been a few reported deaths due to cyanide poisoning from foods containing cyanogenic glycosides. These reports include deaths from elderberry juice that was thought to contain stems and/or leaves (the stems and leaves contain much higher cyanogenic glycosides than the berries, and ripe berries by themselves are considered safe) ^[55], apricot kernels (pits), choke cherry pits, and improperly processed cassava (a staple food in parts of North Africa) ^[56]. A lethal dosage of cyanide in humans is estimated to be around 1.52 mg per kilogram of body weight, with 0.56 mg per kilogram of body weight being the lowest recorded (although this lowest figure was obtained from a historical case when the measurements taken may not have been accurate) ^[57]. High exposure can cause light-headedness, nausea, vomiting, stomach cramps, diarrhea, convulsions, harm to the brain and heart, comas, and death. Exposure to 0.05 mg of cyanide per kilogram of body weight per day for 15-364 days is considered to be the minimum accumulative cyanide exposure by the US CDC. Accumulative exposure can cause health risks, such as reproductive, respiratory, neurological, thyroid, and gastrointestinal issues ^[58]. In some foods, such as marzipan and persipan (made from bitter apricot seeds), the processing of this food destroys the natural beta-glucosidase enzyme (which denatures at 75°C), leaving the flora in the human gut to break down the cyanogenic glycosides. Even if an abnormally large portion of marzipan or persipan is ingested, the lack of beta-glucosidase along with the high calories in the food acts as a slow release of cyanide into the human body which the body can deal with ^[59].

Upon learning about cyanogenic glycosides, brewers often question the toxicity of ingredients such as cherry pits or apricot kernels in beer. Cherry pits have traditionally been used in lambic kriek beers in Belgium. However, the dilution of HCN from cherry pits in beer results in benign levels. Assuming full breakdown of these glycosides, and that none of the HCN boils off (25.6°C boiling temperature), levels of HCN introduced from cherry pits are too low to cause harm to adult humans. The EU regulates that alcoholic beverages cannot exceed 1 mg of HCN per ABV percentage (v/v%) per liter ^[60]. Luk Daenen, a glycoside researcher, calculated that for a 4% ABV alcohol beer, 4 mg of HCN per liter is allowed. With 200 grams of cherries per liter, and the pits being 10 - 14 grams of that weight, there is 22 - 30.8 mg amygdalin per liter of beer. Around 6% of the weight of amygdalin is converted into HCN. Assuming maximum extraction of HCN from the amygdalin glycoside, which is unlikely because the pits are not ground up when used in beer, this equates to 1.3 - 1.82 mg of HCN per liter of beer. This amount is less than the 4 mg of HCN per liter that the EU regulation states. Considering that ~42 mg of HCN is required to kill a person that weighs 70 kilograms (154 pounds), that person would need to drink around 23 liters of beer ^[61]. Considering that 350 mL of pure alcohol would kill a 70 kilogram adult ^[62], the amount of 4% ABV beer required to kill a 70 kg adult from alcohol poisoning is around 8.75 liters. Alcohol would kill such a person far before cyanide poisoning would become a concern. In general, the potential cyanide in most plants will become too dilute to have any health problems when added to beer in normal amounts, however there might still be plants that are extremely high in HCN content that should be avoided in beer (see the table below). If there is a concern that an ingredient containing potentially high levels of HCN could reach unhealthy levels in beer, the beer should be sent for lab analysis so that the HCN levels can be determined before being consumed.

Some cyanogenic foods can have their cyanogenic glycosides reduced by cooking them at 230°C for 15 minutes (flaxseed, for example) ^[53]^[63], however some amygdalin based cyanogenic plants may have their amygdalin content reduced to about 25% by cooking alone (apricot seeds, for example; only the cooking temperature of 100°C was tested ^[51]). Fermentation by certain species of microbes can have a greater effect on reducing amygdalin to HCN than cooking alone. Microbes that have been shown to break down amygdalin include some species of lactic acid bacteria including Lactobacillus plantarum, and fungi such as Endomyces fibuliger, Pichia etchellsii, and Hanseniaspora valbyensis. Some strains of Brettanomyces that have high beta-glucosidase activity might be able to break down amygdalin by around 64%, and some strains of S. cerevisiae might be able to break down up to around 10% of amygdalin, but this needs to be verified by science. Once the amygdalin is broken down into HCN, the HCN can then be volatilized off by cooking in a ventilated space ^[64]^[65]^[4]. In normal brewing procedures, however, the beer is not cooked nor ventilated, so any HCN that is produced by the breakdown of cyanogenic glycosides should be presumed to remain in the beer.

Determining HCN Potential

The The DIY picric acid test for HCN could help in measuring HCN content in beer. Make sure that this test is performed against the finished beer after any glycosides would be broken down. Toxicology labs, if available, should be able to offer services that measure HCN in beer. The following table also lists potential HCN content for various food items. For finding the HCN content based on amygdalin content, approximately 6% of amygdalin by weight is converted to HCN.

Plant	mg HCN/kg or mg/liter *	Prominent Glycoside
Cereal grains and their products	0.001-0.45 ^[56]
Soy protein products	0.07-0.3 ^[56]	Linmarin ^[66]
Soybean hulls	1.24 ^[56]	Linmarin ^[66]
Home-made cherry juice from pitted fruits	5.1 ^[56]	Amygdalin ^[44]
Home-made cherry juice containing 100% crushed pits	23 ^[56]	Amydalin ^[44]
Almonds (wild bitter)	1062-4690 ^[53]^[67]	Amygdalin ^[68]
Almonds (sweet domesticated)	25 ^[53]	Amygdalin ^[68]
Cherries with pit	6.5-9.1 ^[61]	Amygdalin ^[44]
Cherry pits only (black)	161 ^[69]	Amygdalin ^[69]
Cherry pits only (red)	233 ^[69]	Amygdalin ^[69]
Cherry pits only (morello)	3900 ^[70]	Amygdalin ^[70]
Apricot pits, wet weight	89-2170 (depends on region/variety) ^[53]^[56]	Amgydalin ^[44]
Sweet Apricots with kernel (14-24 fruits for 1 kg; single kernel avg weight is 6 grams ^[71])	4.2 - 7.2 (avg 0.3 mg per kernel ^[72])	Amygdalin ^[44]
Bitter Apricots with kernel (14-24 fruits for 1 kg; single kernel avg weight is 6 grams ^[71])	25.2 - 43.2 (avg 1.8 mg per kernel ^[72])	Amygdalin ^[44]
Elderflower (leaves/stems)	1600 ^[73]	Sambunigrin (or sometimes prunasin, holocalin, or zierin) ^[74]
Elderberries (fully ripe; under-ripe will contain more)	30 ^[73]	Sambunigrin (or sometimes prunasin, holocalin, or zierin) ^[74]
Peach seeds/kernels	54-2600 (variety dependent; mostly reported between 54-666) ^[70]^[69]^[75]	Amygdalin ^[69]
Nectarine seeds (summer fire)	7.2 ^[69]	Amygdalin ^[69]
Plum seeds (green)	1050 ^[69]	Amygdalin ^[69]
Plum seeds (black; firar black)	600 ^[69]	Amygdalin ^[69]
Plum seeds (purple; larry anne)	130 ^[69]	Amygdalin ^[69]
Plum seeds (yellow; son gold)	92 ^[69]	Amygdalin ^[69]
Plum seeds (red; laetitia)	26 ^[69]	Amygdalin ^[69]
Apple seeds (royal gala)	178 ^[69]	Amygdalin ^[69]
Pear (conference)	77 ^[69]	Amygdalin ^[69]
Non-Rosaceae fruit seeds (courgette, cucumber, marrow, honey dew melon, squash varieties)	0.6-12.6 ^[69]	Amygdalin ^[69]
Commercial fruit juices
Cherry	4.6 ^[56]	Amygdalin ^[44]
Apricot	2.2 ^[56]	Amygdalin ^[44]
Prune	1.9 ^[56]	Amygdalin ^[44]
Tropical foodstuffs
Cassava(bitter)/dried root cortex	2360-2450 ^[56]^[49]	Linamarin ^[44]
Cassava(bitter)/leaves	300-310 ^[56]^[49]	Linamarin ^[44]
Cassava(bitter)/whole tubers	380-395 ^[56]^[49]	Linamarin ^[44]
Cassava(sweet)/leaves	451-468 ^[56]^[49]	Linamarin ^[44]
Cassava(sweet)/whole tubers	445-462 ^[56]^[49]	Linamarin ^[44]
Gari flour (Nigeria)	10.6-22.1 ^[56]	Linamarin ^[44]
Sorghum/whole immature plant	2400-2500 ^[56]^[49]	Dhurrin ^[44]
Bamboo/immature shoot tip	7700-8000 ^[56]^[49]	Taxiphyllin ^[76]
Lima beans from Java (coloured)	3000-3120 ^[56]^[49]	Linmarin ^[66]
Lima beans from Puerto Rico (black)	2900-3000 ^[56]^[49]	Linmarin ^[66]
Lima beans from Burma (white)	2000-2100 ^[56]^[49]	Linmarin ^[66]
Flaxseed	910 ^[63]	Linamarin, linustatin and neolinustatin ^[63]

* Amounts are averages, or are single examples. Actual levels may vary greatly between strains and growth conditions.

References

[1] "Glycoside." Wikipedia. Retrieved 06/27/2016.

[2] Enzymes in Winemaking: Harnessing Natural Catalysts for Efficient Biotransformations - A Review. P. van Rensburg and I.S. Pretorius. 2000.

[Daenen2-3] 3.0 ^3.1 ^3.2 ^3.3 ^3.4 Evaluation of the glycoside hydrolase activity of aBrettanomyces strain on glycosides from sour cherry (Prunus cerasus L.) used in the production of special fruit beers. Luk Daenen, Femke Sterckx, Freddy R. Delvaux, Hubert Verachtert & Guy Derdelinckx. 2007.

[Daenen1-4] 4.0 ^4.1 ^4.2 ^4.3 ^4.4 Screening and evaluation of the glucoside hydrolase activity in Saccharomyces and Brettanomyces brewing yeasts. L. Daenen, D. Saison, F. Sterckx, F.R. Delvaux, H. Verachtert, G. Derdelinckx. 2007.

[5] Linalool in Hops. MBAA. Stefan Hanke, University Weihenstephan, Germany. 2009.

[6] Monoterpene alcohols release and bioconversion by Saccharomyces species and hybrids. A. Gamero, P. Manzanares, A. Querol, C. Belloch. 2011.

[7] "Hotrienol." The Good Scents Company. Retrieved 05/11/2016.

[8] "Nerol Oxide." The Good Scents Company. Retrieved 05/11/2016.

[9] De novo synthesis of monoterpenes by Saccharomyces cerevisiae wine yeasts. Francisco M. Carrau, Karina Medina, Eduardo Boido, Laura Farina, Carina Gaggero, Eduardo Dellacassa, Giuseppe Versini, Paul A. Henschke. 2005.

[10] "Glycoside." New World Encyclopedia. Retrieved 05/06/2016.

[Winterhalter-11] 11.0 ^11.1 ^11.2 ^11.3 ^11.4 ^11.5 "Glycoconjugated aroma compounds: Occurrence, role and biotechnological transformation." Peter Winterhalter, George K. Skouroumounis. 1997.

[Maicas-12] 12.0 ^12.1 ^12.2 ^12.3 ^12.4 ^12.5 "Hydrolysis of terpenyl glycosides in grape juice and other fruit juices: a review." Sergi Maicas, José Juan Mateo. May 2005.

[13] Fruit Phenolics. Jean-Jacques Macheix, Annie Fleuriet. CRC Press, Mar 20, 1990. Pgs 57-61.

[14] "Ocimenol". The Good Scents Company. Retrieved 06/26/2017.

[15] "Damascenone". Wikipedia. Retrieved 06/26/2017.

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[17] How Low pH Can Intensify ?-Damascenone and Dimethyl Trisulfide Production through Beer Aging. LAURENCE GIJS, FABIENNE CHEVANCE, VESNA JERKOVIC, AND SONIA COLLIN. 2002. DOI: 10.1021/jf020563p.

[Steensels-18] Brettanomyces yeasts — From spoilage organisms to valuable contributors to industrial fermentations. Jan Steensels, Luk Daenen, Philippe Malcorps, Guy Derdelinckx, Hubert Verachtert, Kevin J. Verstrepen. International Journal of Food Microbiology Volume 206, 3 August 2015, Pages 24–38.

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[21] A survey of glycosidase activities of commercial wine strains of Oenococcus oeni. Antonio Grimaldi, Eveline Bartowsky, Vladimir Jiranek. 2005.

[Vervoort-22] 22.0 ^22.1 ^22.2 Characterization of the recombinant Brettanomyces anomalus β-glucosidase and its potential for bioflavoring. Yannick Vervoort, Beatriz Herrera-Malaver, Stijn Mertens, Victor Guadalupe Medina, Jorge Duitama, Lotte Michiels, Guy Derdelinckx, Karin Voordeckers, and Kevin J. Verstrepen. 2016.

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[24] "Methyl salicylate." Chemistry World. Retrieved 05/12/2016.

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[Sharp_2017-31] 31.0 ^31.1 The effect of hopping regime, cultivar and β-glucosidase activity on monoterpene alcohol concentrations in wort and beer. Daniel C. Sharp, Jan Steensels, Thomas H. Shellhammer. 2017.

[32] Eric Abbot. Master Brewers Association podcast, episode 119. 02/04/2019.

[33] Assembly and Analysis of the Genome Sequence of the Yeast Brettanomyces naardenensis CBS 7540. Ievgeniia A. Tiukova, Huifeng Jiang, Jacques Dainat, Marc P. Hoeppner, Henrik Lantz, Jure Piskur, Mats Sandgren, Jens Nielsen, Zhenglong Gu, and Volkmar Passoth. 2019. DOI: https://doi.org/10.3390/microorganisms7110489.

[34] Characterization of an extracellular β-glucosidase from Dekkera bruxellensis for resveratrol production. Kuo HP, Wang R, Huang CY, Lai JT, Lo YC, Huang ST. 2018.

[35] Wikipedia. "Resveratrol" article. Retrieved 02/09/2018.

[36] Quantification of glycosidase activities in selected yeasts and lactic acid bacteria. H McMahon, B W Zoecklein, K Fugelsang, Y Jasinski. 1999.

[Crauwels1-37] Comparative phenomics and targeted use of genomics reveals variation in carbon and nitrogen assimilation among different Brettanomyces bruxellensis strains. S. Crauwels, A. Van Assche, R. de Jonge, A. R. Borneman, C. Verreth, P. Troels, G. De Samblanx, K. Marchal, Y. Van de Peer, K. A. Willems, K. J. Verstrepen, C. D. Curtin, B. Lievens. 2015

[38] Octanol. The Good Scents Company. Retrieved 03/31/2017.

[39] Assessing Population Diversity of Brettanomyces Yeast Species and Identification of Strains for Brewing Applications. Marc Serra Colomer, Anna Chailyan, Ross T. Fennessy, Kim Friis Olsson, Lea Johnsen, Natalia Solodovnikova and Jochen Forster. 2020. DOI: https://doi.org/10.3389/fmicb.2020.00637.

[40] Biotransformation of hop derived compounds by Brettanomyces yeast strains. Marc Serra Colomer, Birgitte Funch, Natalia Solodovnikova, Timothy John Hobley, Jochen Förster. 2020. DOI: https://doi.org/10.1002/jib.610.

[41] Dekkera bruxellensis, a beer yeast that specifically bioconverts mogroside extracts into the intense natural sweetener siamenoside I. Reuben Wang, Yi-Chieh Chen, Yun-Ju Lai, Ting-Jang Lu, Shyue-Tsong Huang, Yi-Chen Lo. 2018. DOI: https://doi.org/10.1016/j.foodchem.2018.09.163.

[42] Application of non-Saccharomyces yeasts with high β-glucosidase activity to enhance terpene-related floral flavor in craft beer. Xiaoyu Han, Qiuxing Qin, Chenyu Li, Xiaoxuan Zhao, Fangxu Song, Mengjiao An, Ying Chen, Xiuqin Wang, Weidong Huang, Jicheng Zhan, Yilin You. 2022.

[43] Indigenous Non-Saccharomyces Yeasts With β-Glucosidase Activity in Sequential Fermentation With Saccharomyces cerevisiae: A Strategy to Improve the Volatile Composition and Sensory Characteristics of Wines. Gao Pingping, Peng Shuai, Sam Faisal Eudes, Zhu Yatong, Liang Lihong, Li Min, Wang Jing. 2022.

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[45] Wilson, Benjamin. "The Rise and Fall of Laetrile". Quackwatch.org website. 01/07/2017. retrieved 03/30/2017.

[46] A Clinical Trial of Amygdalin (Laetrile) in the Treatment of Human Cancer. Charles G. Moertel, M.D., Thomas R. Fleming, Ph.D., Joseph Rubin, M.D., Larry K. Kvols, M.D., Gregory Sarna, M.D., Robert Koch, M.D., Violante E. Currie, M.D., Charles W. Young, M.D., Stephen E. Jones, M.D., and J. Paul Davignon, Ph.D. 1982. DOI: 10.1056/NEJM198201283060403.

[47] Laetrile for cancer: a systematic review of the clinical evidence. Stefania Milazzo, Stephane Lejeune, Edzard Ernst. 2007. DOI: 10.1007/s00520-006-0168-9.

[48] Amygdalin, quackery or cure? Roman A. Blahetaa, Karen Nelsonb, Axel Haferkampa, Eva Juengela. 2016.

[Speijers-49] 49.00 ^49.01 ^49.02 ^49.03 ^49.04 ^49.05 ^49.06 ^49.07 ^49.08 ^49.09 ^49.10 "Cyanogenic Glycosides", First Draft. Dr G. Speijers. National Institute of Public Health and Environmental Protection Laboratory for Toxicology, Bilthoven, The Netherlands. Retrieved 08/25/2016.

[50] Total cyanide determination of plants and foods using the picrate and acid hydrolysis methods. M Rezaul Haque, J Howard Bradbury. 2002.

[tuncel-51] 51.0 ^51.1 The effects of grinding, soaking and cooking on the degradation of amygdalin of bitter apricot seeds. G Tunçel, M.J.R Nout, L Brimer. 1995.

[52] International Journal of Food Microbiology. M.J.R. Nout, G. Tunçe, L. Brimer. 1995.

[Chaouali-53] 53.0 ^53.1 ^53.2 ^53.3 ^53.4 Potential Toxic Levels of Cyanide in Almonds (Prunus amygdalus), Apricot Kernels (Prunus armeniaca), and Almond Syrup. Nadia Chaouali, Ines Gana, Amira Dorra, Fathia Khelifi, Anouer Nouioui, Wafa Masri, Ines Belwaer, Hayet Ghorbel, and Abderazzek Hedhili. 2013.

[CDC1-54] Toxicology Profile for Cyanide. Agency for Toxic Substances & Disease Registry. July 2006. Retrieved 08/25/2016.

[55] Poisoning from Elderberry Juice -- California. CDC website. 1998. Retrieved 08/30/2016.

[who-56] 56.00 ^56.01 ^56.02 ^56.03 ^56.04 ^56.05 ^56.06 ^56.07 ^56.08 ^56.09 ^56.10 ^56.11 ^56.12 ^56.13 ^56.14 ^56.15 ^56.16 ^56.17 ^56.18 ^56.19 ^56.20 Concise International Chemical Assessment Document 61. HYDROGEN CYANIDE AND CYANIDES: HUMAN HEALTH ASPECTS. World Health Organization. 2004. Pg 13. Retrieved 08/29/2016.

[57] Toxicology Profile for Cyanide. Agency for Toxic Substances & Disease Registry. July 2006. Pg 42. Retrieved 08/25/2016.

[58] Toxicology Profile for Cyanide. Agency for Toxic Substances & Disease Registry. July 2006. Pg 21. Retrieved 08/25/2016.

[59] Bioavailability of cyanide after consumption of a single meal of foods containing high levels of cyanogenic glycosides: a crossover study in humans. Klaus Abraham, Thorsten Buhrke, Alfonso Lampen. 2015.

[60] COUNCIL DIRECTIVE of 22 June 1988 on the approximation of the laws of the Member States relating to flavourings for use in foodstuffs and to source materials for their production (88/388/EEC). The European Food Commission, Food Safety. Retrieved 08/26/2016.

[daenen-61] 61.0 ^61.1 "Use of beta-glucosidase activity for flavour enhancement in specialty beers," slideshow by Luk Daenen. 2012. Retrieved 08/26/2016.

[62] "Alcohol Poisoning". NZ Health Promotion Agency. Retrieved 08/26/2016.

[flax-63] 63.0 ^63.1 ^63.2 Cyanogenic Glycosides of Flaxseeds. Fereidoon Shahidi and P. K. J. P. D. Wanasundara. 1997.

[64] Simple screening procedure for microorganisms to degrade amygdalin. L. Brimer, G. Tunçel, M. J. R. Nout. 1993.

[65] Microbial degradation of amygdalin of bitter apricot seeds (Prunus armeniaca). Nout MJ, Tunçel G, Brimer L. 1995.

[soybean-66] 66.0 ^66.1 ^66.2 ^66.3 ^66.4 Determination of cyanide in soybeans and soybean products. David H. Honig, M. Elaine Hockridge, Robert M. Gould, Joseph J. Rackis. 1983.

[67] Cyanide poisoning after bitter almond ingestion. T A Shragg, T E Albertson, and C J Fisher, Jr. 1982.

[wikipedia_almond-68] 68.0 ^68.1 "Almond". Wikipedia. Retrieved 09/06/2016.

[Bolarinwa_2014-69] 69.00 ^69.01 ^69.02 ^69.03 ^69.04 ^69.05 ^69.06 ^69.07 ^69.08 ^69.09 ^69.10 ^69.11 ^69.12 ^69.13 ^69.14 ^69.15 ^69.16 ^69.17 ^69.18 ^69.19 ^69.20 ^69.21 ^69.22 ^69.23 Amygdalin content of seeds, kernels and food products commercially-available in the UK. Islamiyat F. Bolarinwa, Caroline Orfila, Michael R.A. Morgan. 2014. DOI: https://doi.org/10.1016/j.foodchem.2013.11.002.

[VOLD.C5.98ICH_1992-70] 70.0 ^70.1 ^70.2 Cyanogenesis in Canned Stone Fruits. VOLDŘICH, M., KYZLINK, V. 1992. DOI: 10.1111/j.1365-2621.1992.tb05446.x.

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[75] The cyanide content of laetrile preparations, apricot, peach and apple seeds. Holzbecher, M.D., Moss, M.A., Ellenberger, H.A 1984.

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@@ Line 1: / Line 1: @@
-Glycosides are flavorless compounds often found in plants/fruits that are composed of a molecule (often a flavor active compound) bound to a sugar molecule.  The glycosidic bond can be broken, releasing the sugar molecule and the potentially flavor active compound.  These bonds can be broken with exposure to acid, as well as specific enzymes which can be added synthetically or produced naturally by some microorganisms, including some strains of ''Brettanomyces'' <ref>[https://en.wikipedia.org/wiki/Glycoside "Glycoside."  Wikipedia.  Retrieved 06/27/2016.]</ref>.  The release of flavor molecules from glycosides is thought to contribute to the flavor development of aging wines, as well as kriek (cherry) lambic <ref name="Daenen2"></ref>.  It is speculated that flavor compounds from hops can also be released from glycosides <ref name="Daenen1"></ref>.
+Glycosides are flavorless compounds often found in plants/fruits that are composed of a molecule (often a flavor active compound) bound to a sugar molecule.  The glycosidic bond can be broken, releasing the sugar molecule and the potentially flavor active compound.  These bonds can be broken with exposure to acid, as well as specific enzymes which can be added synthetically or produced naturally by some microorganisms, including some strains of ''Brettanomyces'' <ref>[https://en.wikipedia.org/wiki/Glycoside "Glycoside."  Wikipedia.  Retrieved 06/27/2016.]</ref>.  When the glycosidic bond is broken by an enzyme produced by a microorganism, it can be classified under the generic term as a [https://en.wikipedia.org/wiki/Biotransformation "biotransformation"] <ref>[http://www.sawislibrary.co.za/dbtextimages/17163.pdf Enzymes in Winemaking: Harnessing Natural Catalysts for Efficient Biotransformations - A Review.  P. van Rensburg and I.S. Pretorius.  2000.] </ref>.  The release of flavor molecules from glycosides is thought to contribute to the flavor development of aging wines, as well as kriek (cherry) lambic <ref name="Daenen2"></ref>.  It is speculated that flavor compounds from hops can also be released from glycosides <ref name="Daenen1"></ref>.
 ==Glycosides and Beta-Glucosidase Activity==
@@ Line 8: / Line 8: @@
 Aglycones have been identified in many fruits and herbs such as grapes, apricots, peaches, yellow plums, quince, sour cherry, passion fruit, kiwi, papaya, pineapple, mango, lulo, raspberry, strawberry, and tea <ref name="Maicas">[http://www.ncbi.nlm.nih.gov/pubmed/15635463 "Hydrolysis of terpenyl glycosides in grape juice and other fruit juices: a review." Sergi Maicas, José Juan Mateo.  May 2005.]</ref><ref name="Winterhalter"></ref>.  They have been found in different parts of plants, including the green leafy parts, fruit, roots, rhizomes, petals, and seeds.  Aglycones in plants are highly complex structures and very diverse, and their percentages can vary from crop to crop.  In plants, these include alcohol type aglycones such as terpenols, terpenes, linalool oxides, as well as other flavor precursors including various alcohols, norisoprenoids, phenolic acids and probably volatile phenols such as vanillin <ref name="Maicas"></ref>.  In fruits, there are mostly just 4 types of flavonol type aglycones: [https://en.wikipedia.org/wiki/Quercetin quercetin] (found in nearly all fruits), [https://en.wikipedia.org/wiki/Kaempferol kaempherol] (found in 80% of fruit), and less commonly [https://en.wikipedia.org/wiki/Quercetin quercetin] and [https://en.wikipedia.org/wiki/Isorhamnetin isorhamnetin] <ref>[https://books.google.com/books?id=vHqke7F4lWYC&pg=PA59&lpg=PA59&dq=aglycones+in+fruit&source=bl&ots=7Gb10SPZk7&sig=6gaZlwpVaHuteoiVP68zvt6HcpE&hl=en&sa=X&ved=0ahUKEwjk0qW9wp3NAhUCKZQKHfUzDrQQ6AEIKTAC#v=onepage&q=aglycones%20in%20fruit&f=false Fruit Phenolics.  Jean-Jacques Macheix, Annie Fleuriet.  CRC Press, Mar 20, 1990.  Pgs 57-61.]</ref> (see [http://nutrition.ucdavis.edu/content/infosheets/fact-pro-flavonol.pdf this UC Davis PDF] for amounts in different fruit and potential health benefits as antioxidants).  In many cases of fruit, the amount of aromatic aglycones that are bound up in glycosides outnumber the amount that are free in a ratio of 2:1 to 8:1 <ref name="Maicas"></ref>.  Aglycones that are bound up in glycosides tend to be more water soluble and less reactive once unbound than the naturally free version.  By providing enzymes that break the glycosidic bond, discarded parts of plants (peels, stems, skins, etc.) have been used to produce natural flavorings from the remaining and abundant glycosides <ref name="Winterhalter">[http://link.springer.com/chapter/10.1007%2FBFb0102063 "Glycoconjugated aroma compounds: Occurrence, role and biotechnological transformation."   Peter Winterhalter, George K. Skouroumounis.  1997.]</ref>.
+===Acidic Hydrolysis===
+Aglycones can be released from glycosides via a low pH.  Generally, this occurs at lower pH's and Daenen et al. (2007) attributed most of the breakdown of glycosides to beta-glucosidase enzymes <ref name="Daenen2" />, but different types of glycosides are more readily broken down at different pH's.  For example, ocimenols (lemon, lime <ref>[http://www.thegoodscentscompany.com/data/rw1020581.html "Ocimenol".  The Good Scents Company.  Retrieved 06/26/2017.]</ref>)  are formed from glycoside breakdown at a pH of 1, but terpenes such as linalool, nerol, and geraniol (commonly found in hops and other plant material) are formed at a pH of 3, and alpha-terpineol was formed at both pH values.  The acidic breakdown of these glycosides were found to contribute to the flavor of wine during aging <ref name="Maicas"></ref>.  Daenen et al. (2007) also found that acidic hydrolysis was responsible for the formation of alpha-ionol, beta-damascenone, linalool and alpha-terpineol and to a lesser extent benzyl alcohol <ref name="Daenen2" />.
+In beer, it was found that the lower the pH of the beer the higher the amount of the ketone damascenone (floral, rose <ref>[https://en.wikipedia.org/wiki/Damascenone "Damascenone".  Wikipedia.  Retrieved 06/26/2017.]</ref>) and dimethyl trisulfide (sulfury cooked onion <ref>[http://www.thegoodscentscompany.com/data/rw1008101.html "Dimethyl trisulfide".  The Good Scents Company.  Retrieved 06/26/2017.]</ref>).  In one study, at a pH of 3, beta-damascenone was reported to be ~27 ppb and dimethyl trisulfide was reported to be 650 ppt.  At a pH of 4.2, they were 17 ppb and 300 ppt respectively.  At a ph of 5, beta-damascenone was around 12 ppb and dimethyl trisulfide 50 ppt.  This was believed to be due to the acidic hydrolysis of glycosides, and it was speculated that other glycosides could have a flavor impact on beers that contain fruit or herbs due to acidic hydrolysis of glycosides <ref>How Low pH Can Intensify ?-Damascenone and Dimethyl Trisulfide Production through Beer Aging.  LAURENCE GIJS, FABIENNE CHEVANCE, VESNA JERKOVIC, AND SONIA COLLIN.  2002.  DOI: 10.1021/jf020563p.</ref>.
+* See also: [[Hops#Glycosides|Glycosides In Hops]].
 ===Beta-Glucosidase===
-Aglycones can be released from glycosides by either exposure to acid (generally pH of 3 or lower, and different pH's giving different results on which glycosides are broken down; this breakdown of glycosides under low pH has been linked to the slow flavor development of aging wine <ref name="Maicas"></ref>), or by enzymes called beta-glucosidases.  Enzymatic breakdown of glycosides has been described as producing a more "natural" flavor in wines versus acidic breakdown.  Some fruits have been observed (mostly wine grapes) to have limited beta-glucosidase activity within themselves, however it has been observed as being unstable and having low activity at the low pH of wine and sour beer <ref name="Maicas"></ref>.
+Aglycones can also be released chemically from glycosides by enzymes called beta-glucosidases.  Enzymatic breakdown of glycosides has been described as producing a more "natural" flavor in wines versus acidic breakdown.  Some fruits have been observed (mostly wine grapes) to have limited beta-glucosidase activity within themselves, however it has been observed as being unstable and having low activity at the low pH of wine and sour beer <ref name="Maicas"></ref>.
 Beta-glycosidase enzymes can be added artificially, however there has been much interest in the natural capability of microorganisms to produce beta-glucosidases, particularly 1,4-β-glucosidase <ref name="Winterhalter"></ref>.  Microorganisms that can break down glycosides by using beta-glucosidases can then access the resulting sugars for fermentation <ref name="Steensels">[http://www.sciencedirect.com/science/article/pii/S0168160515001865 Brettanomyces yeasts — From spoilage organisms to valuable contributors to industrial fermentations.  Jan Steensels, Luk Daenen, Philippe Malcorps, Guy Derdelinckx, Hubert Verachtert, Kevin J. Verstrepen. International Journal of Food Microbiology Volume 206, 3 August 2015, Pages 24–38.]</ref>.  There are two major categories of glucosidase activity: endogenous and exogenous.  Endogenous enzymatic activity takes place inside of the cell, and exogenous enzymatic activity takes place outside of the cell.  Bacteria and fungi that show endogenous glucosidase activity have been shown not to be effective in alcoholic fermentation due to not tolerating low pH (optimum pH of 5), glucose, and/or ethanol.  Generally, the flavorless glycosides remain unaffected by yeast fermentation, leaving them unused as a potential source for flavor and aroma <ref name="Winterhalter"></ref>.
@@ Line 19: / Line 26: @@
 Different types of beta-glucosidase enzymes have different optimal pH and temperatures.  For example, beta-glucosidase produced from ''A. niger'' is optimal at a pH of 4.5 and a temperature of 58°C (136°F), whereas the enzyme for ''Brettanomyces anomalus'' is optimal at a pH of 5.75 and a temperature of 37°C (98°F) (it was active to some extent between 15°-55°C).  The beta-glucosidase enzyme ceases effectiveness below a pH of 4.5 for one strain of ''B anomalus'' studied <ref name="Vervoort"></ref>.
-===Activity of Brettanomyces and Saccharomyces===
+See also:
+* [http://www.cazy.org/Glycoside-Hydrolases.html Database of glycoside hydrolases.]
+===Activity of ''Brettanomyces'' and ''Saccharomyces''===
+[http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2672.2007.03566.x/full Daenen et al. (2007)] screened the beta-glucosidase activity of several strains of ''Saccharomyces cerevisiae'', ''Saccharomyces pastorianus'', and several ''Brettanomyces'' species.  None of the lager brewing strains showed beta-glucosidase activity.  Out of 32 strains of ''S. cerevisiae'', only one strain (a wine strain called "U228") showed beta-glucosidase activity, however its activity was repressed in the presence of glucose.  This indicates that most ''S. cerevisiae'' strains do not have the capability of producing beta-glucosidase, but it is possible that some very few strains can <ref name="Daenen1">[http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2672.2007.03566.x/full Screening and evaluation of the glucoside hydrolase activity in Saccharomyces and Brettanomyces brewing yeasts. L. Daenen, D. Saison, F. Sterckx, F.R. Delvaux, H. Verachtert, G. Derdelinckx.  2007.]</ref>.  Additionally, beta-glucosidase activity for ''S. cerevisiae'' can be inhibited by the pH levels found in wine and sour beer (optimal at pH 5) <ref name="Mansfield"></ref>.  All strains of ''S. cerevisiae'' did release another enzyme called beta-glucanase, which led to varying degrees of breaking down some smaller glycosides found in hops (hop extract was tested, not whole hops) containing the aglycones methyl salicylate, 1-octen-3-ol, and cis-3-hexen-1-ol, but not linalool. None of the ''B. bruxellensis'' strains showed this activity, but the researchers only tested strain of ''B. custersianus'' and both of the ''B. anomala'' strains tested did show cell-associated (intracellular) beta-glucosidase activity.  In particular, the ''B. custersianus'' strain was tested against glycosides from hops, in which case high amounts of the aglycones linalool (citrus, orange, lemon, floral <ref>[http://www.thegoodscentscompany.com/data/rw1007872.html "Linalool."  The Good Scents Company.  Retrieved 05/12/2016.]</ref>), methyl salicylate (minty, wintergreen <ref>[http://www.rsc.org/chemistryworld/2015/09/methyl-salicylate-oil-wintergreen-podcast "Methyl salicylate."  Chemistry World.  Retrieved 05/12/2016.]</ref>), 1-octen-3-ol (mushroom, earthy <ref>[http://www.thegoodscentscompany.com/data/rw1024051.html "1-octen-3-ol."  The Good Scents Company.  Retrieved 05/12/2016.]</ref>) and cis-3-hexen-1-ol (grassy, melon rind <ref>[http://www.thegoodscentscompany.com/data/rw1005932.html "(Z)-3-hexen-1-ol." The Good Scents Company.  Retrieved 05/12/2016.]</ref>) were released from hop extracts <ref name="Daenen1"></ref>.  The beta-glucosidase activity was elevated when co-fermenting ''B. custersianus'' with ''S. cerevisiae''.  The authors also found dihydroedulan 1 and 2 (elderberry aroma) and theaspirane A and B (woody and campfire aromas), which are classified as norisoprenoids, were released from dry hopping <ref>[http://www.asbcnet.org/events/archives/Documents/2008WBCprogbook.pdf World Brewing Congress, 2008.  Pg 80.  Retrieved 05/13/2016.]</ref>.  ''B. custersianus'' has been isolated from the later stages of lambic fermentation, and it is thought that its ability to produce beta-glucosidase, which gives it the ability to ferment cellobiose and cellotriose, is a possible adaptation from living in oak barrels <ref name="Daenen1"></ref>.  Recent studies on hops have linked an increase in fruity thiols from hops (3-mercaptohexan-1-ol and 4-mercapto-4-methylpentan-2-one) being produced during fermentation from the production of beta-lyase enzyme, and this could also explain anecdotal reports of increased fruity aromas from exposing hops to fermentation (see [http://scottjanish.com/genetically-modified-gm-yeast-strains-unlocking-bound-hop-thiols-and-engineering-targeted-fermentation-characteristics/ this article by Scott Janish] on beta-lyase enzymes in GM and non-GM yeast strains). <ref>Private correspondence with Richard Preiss by Dan Pixley.  05/16/2016.</ref><ref>[https://beerandbrewing.com/VuhJRCUAAHMUNfil/article/hops-oils--aroma-uncharted-waters "Hops Oils & Aroma: Uncharted Waters," by Stan Hieronymus.  Beer & Brewing.  03/16/2016.  Retrieved 05/16/2016.]</ref>.
+[https://www.academia.edu/23874347/Properties_of_endogenous_%CE%B2_glucosidase_of_a_Saccharomyces_cerevisiae_strain_isolated_from_Sicilian_musts_and_wines Palmeri et al. (2002)] reported one wine strain out of 80 strains of ''S. cerevisiae'' found in Sicilian must that had high beta-glucosidase activity and is active during wine fermentation conditions <ref>[https://www.academia.edu/23874347/Properties_of_endogenous_%CE%B2_glucosidase_of_a_Saccharomyces_cerevisiae_strain_isolated_from_Sicilian_musts_and_wines Spagna, G., Barbagallo, R. N., Palmeri, R., Restuccia, C., & Giudici, P. (2002). Properties of endogenous β-glucosidase of a Saccharomyces cerevisiae strain isolated from Sicilian musts and wines. Enzyme and Microbial Technology, 31(7), 1030–1035. https://doi.org/10.1016/S0141-0229(02)00233-8]</ref>. Another study by [http://onlinelibrary.wiley.com/doi/10.1002/jib.418/abstract Sharp et al.] found that both ale and lager yeasts exhibit a wide range of beta-glucosidase activity, but the results should be repeated using a different substrate because the substrate that was used could have been broken down by beta-glucanase enzyme instead of beta-glucosidase <ref name="Sharp_2017">[http://onlinelibrary.wiley.com/doi/10.1002/jib.418/abstract The effect of hopping regime, cultivar and β-glucosidase activity on monoterpene alcohol concentrations in wort and beer.  Daniel C. Sharp, Jan Steensels, Thomas H. Shellhammer.  2017.]</ref>Additionally, Lallemand claims that three brewing strains that they offer produce beta-glucosidase enzymes that can promote hop biotransformation, but the details of this activity have not been published to our knowledge (BRY-97, New England, and Belle Saison) <ref>[http://masterbrewerspodcast.com/119-biotransformation Eric Abbot.  Master Brewers Association podcast, episode 119.  02/04/2019.]</ref> (~8:50 min in).
-One study screened the beta-glucosidase activity of several strains of ''Saccharomyces cerevisiae'', ''Saccharomyces pastorianus'', and ''Brettanomyces'' spp <ref name="Daenen1">[http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2672.2007.03566.x/full Screening and evaluation of the glucoside hydrolase activity in Saccharomyces and Brettanomyces brewing yeasts. L. Daenen, D. Saison, F. Sterckx, F.R. Delvaux, H. Verachtert, G. Derdelinckx.  2007.]</ref>.  None of the lager brewing strains showed beta-glucosidase activity.  Out of 32 strains of ''S. cerevisiae'', only one strain (a wine strain called "U228") showed beta-glucosidase activity, however its activity was repressed in the presence of glucose.  This indicates that most ''S. cerevisiae'' strains do not have the capability of producing beta-glucosidase, but it is possible that some very few strains can <ref name="Daenen1"></ref>.  However, beta-glucosidase activity for ''S. cerevisiae'' is inhibited by pH levels of wine and sour beer (optimal at pH 5) <ref name="Mansfield"></ref>.  All strains of ''S. cerevisiae'' did release another enzyme called beta-glucanase, which led to varying degrees of breaking down some smaller glycosides found in hops (hop extract was tested, not whole hops) containing the aglycones methyl salicylate, 1-octen-3-ol, and cis-3-hexen-1-ol, but not linalool (it's worth noting that other research using whole hops has shown no significant hop derived aglycones when using beta-glucosidase active ''Saccharomyces'' strains; publication yet to be released <ref>Private correspondence with Daniel Sharp from Oregon State University and Dan Pixley.  05/16/2016.</ref>). None of the ''B. bruxellensis'' strains showed this activity, but the only tested strain of ''B. custersianus'' and both of the ''B. anomala'' strains tested did show cell-associated (intracellular) beta-glucosidase activity.  In particular, the ''B. custersianus'' strain was tested against glycosides from hops, in which case high amounts of the aglycones linalool (citrus, orange, lemon, floral <ref>[http://www.thegoodscentscompany.com/data/rw1007872.html "Linalool."  The Good Scents Company.  Retrieved 05/12/2016.]</ref>), methyl salicylate (minty, wintergreen <ref>[http://www.rsc.org/chemistryworld/2015/09/methyl-salicylate-oil-wintergreen-podcast "Methyl salicylate."  Chemistry World.  Retrieved 05/12/2016.]</ref>), 1-octen-3-ol (mushroom, earthy <ref>[http://www.thegoodscentscompany.com/data/rw1024051.html "1-octen-3-ol."  The Good Scents Company.  Retrieved 05/12/2016.]</ref>) and cis-3-hexen-1-ol (grassy, melon rind <ref>[http://www.thegoodscentscompany.com/data/rw1005932.html "(Z)-3-hexen-1-ol." The Good Scents Company.  Retrieved 05/12/2016.]</ref>) were released from hop extracts <ref name="Daenen1"></ref>.  The beta-glucosidase activity was elevated when co-fermenting ''B. custersianus'' with ''S. cerevisiae''.  The authors also found dihydroedulan 1 and 2 (elderberry aroma) and theaspirane A and B (woody and campfire aromas), which are classified as norisoprenoids, were released from dry hopping <ref>[http://www.asbcnet.org/events/archives/Documents/2008WBCprogbook.pdf World Brewing Congress, 2008.  Pg 80.  Retrieved 05/13/2016.]</ref>.  ''B. custersianus'' has been isolated from the later stages of lambic fermentation, and it is thought that its ability to produce beta-glucosidase, which gives it the ability to ferment cellobiose and cellotriose, is a possible adaptation from living in oak barrels <ref name="Daenen1"></ref>.  Recent studies on hops have linked an increase in fruity thiols from hops (3-mercaptohexan-1-ol and 4-mercapto-4-methylpentan-2-one) being produced during fermentation, and this could also explain anecdotal reports of increased fruity aromas from exposing hops to fermentation (it is unknown what exactly causes the increase in thiols during fermentation) <ref>Private correspondence with Richard Preiss by Dan Pixley.  05/16/2016.</ref><ref>[https://beerandbrewing.com/VuhJRCUAAHMUNfil/article/hops-oils--aroma-uncharted-waters "Hops Oils & Aroma: Uncharted Waters," by Stan Hieronymus.  Beer & Brewing.  03/16/2016.  Retrieved 05/16/2016.]</ref>.
+The same strain of ''B. custersianus'' was screened for beta-glucosidase activity and aglycone byproducts during the refermentation of sour cherries in beer (a very small amount of the byproducts were manufactured by the yeast ''de novo'', particularly linalool, alpha-terpineol, alpha-ionol, and a precursor that leads to beta-damascenone under low pH conditions).  Different portions of the cherries were tested: whole cherries with stones (pits), cherry pulp without stones, cherry juice without stones or other solids from the fruit, and the stones alone.  Benzaldehyde (almond, cherry stone flavor) was produced during fermentation in all cases, and reduced to benzyl alcohol (almond flavor) and benzyl acetate (fruity, jasmine flavor) by the end of fermentation.  There were higher levels of these benzyl based compounds in the whole cherries and cherry stone alone samples, indicating that cherry stones make a big impact on the almond flavors found in cherry sour beers.  Methyl salicylate, linalool, alpha-terpineol (pine), geraniol (rose, lime, floral) and alpha-ionol (floral, violet), eugenol (spicy, clove, medicinal) and isoeugenol (fine delicate clove) levels increased in all forms of cherries added except for stones alone, indicating that these aglycones are more present in the flesh and juice of the cherries <ref name="Daenen2"></ref>.  Another study that performed whole genome sequencing on a strain of ''B. naardenensis'' found that it had two genes that could potentially allow this species to produce beta-glucosidase, but this was not confirmed in the study <ref>[https://www.mdpi.com/2076-2607/7/11/489 Assembly and Analysis of the Genome Sequence of the Yeast Brettanomyces naardenensis CBS 7540.  Ievgeniia A. Tiukova, Huifeng Jiang, Jacques Dainat, Marc P. Hoeppner, Henrik Lantz, Jure Piskur, Mats Sandgren, Jens Nielsen, Zhenglong Gu, and Volkmar Passoth.  2019.  DOI: https://doi.org/10.3390/microorganisms7110489.]</ref>.
-The same strain of ''B. custersianus'' was screened for beta-glucosidase activity and aglycone byproducts during the refermentation of sour cherries in beer (a very small amount of the byproducts were manufactured by the yeast ''de novo'', particularly linalool, alpha-terpineol, alpha-ionol, and a precursor that leads to beta-damascenone under low pH conditions).  Different portions of the cherries were tested: whole cherries with stones (pits), cherry pulp without stones, cherry juice without stones or other solids from the fruit, and the stones alone.  Benzaldehyde (almond, cherry stone flavor) was produced during fermentation in all cases, and reduced to benzyl alcohol (almond flavor) and benzyl acetate (fruity, jasmine flavor) by the end of fermentation.  There were higher levels of these benzyl based compounds in the whole cherries and cherry stone alone samples, indicating that cherry stones make a big impact on the almond flavors found in cherry sour beers.  Methyl salicylate, linalool, alpha-terpineol (pine), geraniol (rose, lime, floral) and alpha-ionol (floral, violet), eugenol (spicy, clove, medicinal) and isoeugenol (fine delicate clove) levels increased in all forms of cherries added except for stones alone, indicating that these aglycones are more present in the flesh and juice of the cherries <ref name="Daenen2"></ref>.
+Many strains of ''B. bruxellensis'' have also been found to have varying degrees of intracellular (produced inside the cell only) or parietal (attached to the cell wall) beta-glucosidase activity.  At least one mutant strain of ''B. bruxellensis'' found in wine (''D. bruxellensis'' BCRC920084 from the Bioresource Collection and Research Center, Hsin-Chu, Taiwan) has been reported to have high extracellular (excreted out of the cell) production of beta-glucosidase that was very efficient at breaking down a glycoside called "piceid" that released resveratrol, which has been marketed as a dietary supplement <ref>[https://www.ncbi.nlm.nih.gov/pubmed/29389552?dopt=Abstract Characterization of an extracellular β-glucosidase from Dekkera bruxellensis for resveratrol production.  Kuo HP, Wang R, Huang CY, Lai JT, Lo YC, Huang ST.  2018.]</ref><ref>[https://en.wikipedia.org/wiki/Resveratrol Wikipedia.  "Resveratrol" article.  Retrieved 02/09/2018.]</ref>. ''Brettanomyces'' has more strains that can produce beta-glucosidase than other genera of yeast, and the strains generally also have a higher rate of beta-glucosidase activity than other genera of yeast <ref>[http://link.springer.com/article/10.1038/sj.jim.2900720 Quantification of glycosidase activities in selected yeasts and lactic acid bacteria.  H McMahon, B W Zoecklein, K Fugelsang, Y Jasinski. 1999.]</ref><ref name="Mansfield"></ref>.  Strains with higher beta-glucosidase activity have been isolated from lambic, suggesting that these strains may have an adapted ability to utilize sugar from glycosides <ref name="Vervoort">[http://onlinelibrary.wiley.com/wol1/doi/10.1111/jam.13200/abstract Characterization of the recombinant Brettanomyces anomalus β-glucosidase and its potential for bioflavoring.  Yannick Vervoort, Beatriz Herrera-Malaver, Stijn Mertens, Victor Guadalupe Medina, Jorge Duitama, Lotte Michiels, Guy Derdelinckx, Karin Voordeckers, and Kevin J. Verstrepen.  2016.]</ref>.  Some ''Brettanomyces'' strains may only be capable of beta-glucosidase activity, and not the other enzymes which are needed to break down disaccharide type glycosides.  Additionally, cell death and autolysis can result in an increase in beta-glucosidase activity in solution due to the cell contents being released into solution <ref name="Mansfield"></ref>.  Strains that can metabolize cellobiose tend to also have higher beta-glucosidase activity because they possess an extra gene for beta-glucosidase enzyme production <ref name="Crauwels1">[http://link.springer.com/article/10.1007/s00253-015-6769-9 Comparative phenomics and targeted use of genomics reveals variation in carbon and nitrogen assimilation among different Brettanomyces bruxellensis strains.  S. Crauwels, A. Van Assche, R. de Jonge, A. R. Borneman, C. Verreth, P. Troels, G. De Samblanx, K. Marchal, Y. Van de Peer, K. A. Willems, K. J. Verstrepen, C. D. Curtin, B. Lievens.  2015]</ref>.
-Many strains of ''B. bruxellensis'' have also been found to have varying degrees of intracellular or parietal (attached to the cell wall) beta-glucosidase activity.  ''Brettanomyces'' has more strains that can produce beta-glucosidase than other genera of yeast, and the strains generally also have a higher rate of beta-glucosidase activity than other genera of yeast <ref>[http://link.springer.com/article/10.1038/sj.jim.2900720 Quantification of glycosidase activities in selected yeasts and lactic acid bacteria.  H McMahon, B W Zoecklein, K Fugelsang, Y Jasinski. 1999.]</ref><ref name="Mansfield"></ref>.  Strains with higher beta-glucosidase activity have been isolated from lambic, suggesting that these strains may have an adapted ability to utilize sugar from glycosides <ref name="Vervoort">[http://onlinelibrary.wiley.com/wol1/doi/10.1111/jam.13200/abstract Characterization of the recombinant Brettanomyces anomalus β-glucosidase and its potential for bioflavoring.  Yannick Vervoort, Beatriz Herrera-Malaver, Stijn Mertens, Victor Guadalupe Medina, Jorge Duitama, Lotte Michiels, Guy Derdelinckx, Karin Voordeckers, and Kevin J. Verstrepen.  2016.]</ref>.  Some ''Brettanomyces'' strains may only be capable of beta-glucosidase activity, and not the other enzymes which are needed to break down disaccharide type glycosides.  Additionally, cell death and autolysis can result in an increase in beta-glucosidase activity in solution due to the cell contents being released into solution <ref name="Mansfield"></ref>.  Strains that can metabolize cellobiose tend to also have higher beta-glucosidase activity because they possess an extra gene for beta-glucosidase enzyme production <ref name="Crauwels1">[http://link.springer.com/article/10.1007/s00253-015-6769-9 Comparative phenomics and targeted use of genomics reveals variation in carbon and nitrogen assimilation among different Brettanomyces bruxellensis strains.  S. Crauwels, A. Van Assche, R. de Jonge, A. R. Borneman, C. Verreth, P. Troels, G. De Samblanx, K. Marchal, Y. Van de Peer, K. A. Willems, K. J. Verstrepen, C. D. Curtin, B. Lievens.  2015]</ref>.
+Sensory analysis of beers with cherries or hops have shown that there is a significantly detectable difference between cherry beers that have been exposed to beta-glucosidase from one strain of ''B. anomalus'' versus not exposed to the enzyme, but no significant difference was found in beers hopped with pellets.  The cherry beers exposed to the enzyme contained more and above odor threshold eugenol (clove, honey aroma), benzyl alcohol (sweet, flower), benzaldehyde (almond, cherry) than cherry beers that were not exposed to the enzyme.  The cherry beers exposed to the enzyme were not only identified in a blind tasting but were also preferred to the cherry beers without exposure to the enzyme, indicating that beta-glucosidase activity in cherry beers provides a significant flavor difference.  Other types of beta-glucosidase enzymes released different levels of different flavor compounds, indicating that the source (bacteria or yeast) of the enzyme make a significant difference in the flavors that are produced <ref name="Vervoort"></ref>.
-Sensory analysis of beers with cherries or hops have shown that there is a significantly detectable difference between cherry beers that have been exposed to beta-glucosidase from one strain of ''B. anomalus'' versus not exposed to the enzyme, but no significant difference was found in beers hopped with pellets.  The cherry beers exposed to the enzyme contained more and above odor threshold eugenol (clove, honey aroma), benzyl alcohol (sweet, flower), benzaldehyde (almond, cherry) than cherry beers that were not exposed to the enzyme.  The cherry beers exposed to the enzyme were not only identified in a blind tasting, but were also preferred to the cherry beers without exposure to the enzyme, indicating that beta-glucosidase activity in cherry beers provides a significant flavor difference.  Other types of beta-glucosidase enzymes released different levels of different flavor compounds, indicating that the source (bacteria or yeast) of the enzyme make a significant difference in the flavors that are produced <ref name="Vervoort"></ref>.
+The effects of beta-glucosidase on hops may be limited even in ideal conditions using pure beta-glucosidase that is highly efficient in beer where beta-glucosidase activity by yeast is limited.  Sharp et al. (2017) determined that hops contain such a small amount of glycosides that their release doesn't contribute much to hop flavor and aroma.  While previous studies focused on hop extracts, they studied glycosides in whole leaf hops for the first time and found non-significant levels of hop-derived monoterpenes from glycosides even when using pure beta-glucosidase extracted from almonds.  For example, linalool was increased by 16.5 μg/L when using the highest hopping rate, but this amount has little impact on the overall aroma and flavor of the beer.  Terpineol, citronellol, nerol, and geraniol were also not increased in significant amounts, however 1-octanol (waxy, green, citrus, orange, aldehydic, fruity <ref>[http://www.thegoodscentscompany.com/data/rw1021071.html Octanol.  The Good Scents Company.  Retrieved 03/31/2017.]</ref>) was increased significantly <ref name="Sharp_2017" />.
+In 2020, whole genome sequencing and glycosidic activity were tested for 84 strains of ''Brettanomyces'' by [https://www.frontiersin.org/articles/10.3389/fmicb.2020.00637/full Colomer et al].  They found that the capability of ''Brettanomyces'' to break down glycosides is determined by possessing two genes: ''BbBGL1'' and ''BbBGL2''.  The genes called ''BbBGL2'' have a major role in whether glycosides are broken down, while the role of ''BbBGL1'' is minimal.  About half of the strains had some level of glycosidic activity, although the majority was low with a couple of strains that had high levels of glycosidic activity, thus these genes alone do not account for the wide variation in glycosidic activity levels in ''Brettanomyces'' (see [https://www.frontiersin.org/files/Articles/495404/fmicb-11-00637-HTML-r1/image_m/fmicb-11-00637-g007.jpg this figure] from the study which maps beta-glucosidase activity for the 84 strains that were sequenced) <ref>[https://www.frontiersin.org/articles/10.3389/fmicb.2020.00637/full Assessing Population Diversity of Brettanomyces Yeast Species and Identification of Strains for Brewing Applications.  Marc Serra Colomer, Anna Chailyan, Ross T. Fennessy, Kim Friis Olsson, Lea Johnsen, Natalia Solodovnikova and Jochen Forster.  2020.  DOI: https://doi.org/10.3389/fmicb.2020.00637.]</ref>.  The beta-glucidase levels were also measured for 5 strains (4 strains of ''B. bruxellensis'' and 1 strain of ''B. anomalus'') that have the genetic make up to produce this enzyme; most of the enzyme was only produced within the cell (intracellular) for all of the strains tested, and only small amounts were produced outside of the cells except for one strain of ''B. anomalus''.  The enzyme therefore wouldn't act on glycosides outside of the cell unless the cell ruptured.  There was also a small amount of beta-glucosidase activity within the cell wall of one of the strains of ''B. anomalus''.  They also fermented a dry hopped beer with these strains and found that the strains with the lowest beta-glucosidase activity had the lowest conversion of geraniol to β‐citronellol, and therefore there was no correlation between beta-glucosidase activity and hop biotransformation (although there was evidence of another unidentified type of biotransformation occurring with the hops (see [[Brettanomyces#Hop_Biotransformation|''Brettanomyces'' hop biotransformation]]) <ref>[https://onlinelibrary.wiley.com/doi/full/10.1002/jib.610 Biotransformation of hop derived compounds by Brettanomyces yeast strains.  Marc Serra Colomer, Birgitte Funch, Natalia Solodovnikova, Timothy John Hobley, Jochen Förster.  2020.  DOI: https://doi.org/10.1002/jib.610.]</ref>.
+Wang et al. (2018) reported another type of glycosidic activity in one strain of ''B bruxellensis'' which is the conversion of the glycoside "mogroside V" into an artificial sweetener called siamenoside I.   Other yeast and bacteria species were tested and did not find this particular glycosidic activity.  [https://en.wikipedia.org/wiki/Mogroside Mogroside V] is found naturally in some fruit, specifically, an Asian fruit called [https://en.wikipedia.org/wiki/Siraitia_grosvenorii Lo Han Kuo (''Siraitia grosvenorii'')].  The artificial sweetener siamenoside is 563 times sweeter tasting than 5% sucrose.  The specific enzyme responsible for this conversion that this strain of ''B. bruxellensis'' produced is called ''Db''Exg1 <ref>[https://www.sciencedirect.com/science/article/pii/S0308814618317473 Dekkera bruxellensis, a beer yeast that specifically bioconverts mogroside extracts into the intense natural sweetener siamenoside I.  Reuben Wang, Yi-Chieh Chen, Yun-Ju Lai, Ting-Jang Lu, Shyue-Tsong Huang, Yi-Chen Lo.  2018.  DOI: https://doi.org/10.1016/j.foodchem.2018.09.163.]</ref>.
+See also:
+* [[Hops#Glycosides|Glycosides in Hops]].
+* [http://scottjanish.com/genetically-modified-gm-yeast-strains-unlocking-bound-hop-thiols-and-engineering-targeted-fermentation-characteristics/ "Genetically Modified (GM) Yeast Strains: Unlocking Bound Hop Thiols and Engineering Targeted Fermentation Characteristics," by Scott Janish.]
+===Activity of Other Yeasts===
+A strain of ''Candida glabrata'' was selected in a study for its high beta-glucosidase activity, its tolerance to ethanol, and its ability to utilize maltose, and was shown to produce novel flavor characteristics in beer fermentation, including a significant increase in geraniol <ref>[https://www.sciencedirect.com/science/article/abs/pii/S0308814622026887#f0020 Application of non-Saccharomyces yeasts with high β-glucosidase activity to enhance terpene-related floral flavor in craft beer. Xiaoyu Han, Qiuxing Qin, Chenyu Li, Xiaoxuan Zhao, Fangxu Song, Mengjiao An, Ying Chen, Xiuqin Wang, Weidong Huang, Jicheng Zhan, Yilin You. 2022.]</ref>. Strains of ''Meyerozyma guilliermondii'' and ''Hanseniaspora uvarum'' that were isolated from a spontaneous wine fermentation have also been found to have positive results when co-fermented with ''S. cerevisiae'' in wine. Specifically, compared to the control wines, there were higher levels of the terpenes: isopulegol, citronellol, geranylacetone, geraniol, trans-nerolidol, and nerol. This was associated with the high beta-glucosidase activity of these yeast strains <ref>[https://www.frontiersin.org/articles/10.3389/fmicb.2022.845837/full Indigenous Non-Saccharomyces Yeasts With β-Glucosidase Activity in Sequential Fermentation With Saccharomyces cerevisiae: A Strategy to Improve the Volatile Composition and Sensory Characteristics of Wines. Gao Pingping, Peng Shuai, Sam Faisal Eudes, Zhu Yatong, Liang Lihong, Li Min, Wang Jing. 2022.]</ref>.
+===Activity of Lactic Acid Bacteria===
+(To do)
+http://www.icfsnmalaysia2017.org/ICFSN2017%20proceedings%20-%20pp%2054-60.pdf
+https://search.proquest.com/docview/752091646?pq-origsite=gscholar
+https://www.researchgate.net/profile/Prafulla_Mahajan/publication/225362291_Production_of_Cell_Membrane-Bound_a-_and_b-Glucosidase_by_Lactobacillus_acidophilus/links/55fd56cd08aeba1d9f56bdbd.pdf
+http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2672.2009.04461.x/full
+https://ifst.onlinelibrary.wiley.com/doi/abs/10.1111/jfpp.16368
+https://www.mdpi.com/2076-3921/11/2/305
+https://www.sciencedirect.com/science/article/abs/pii/S2212429224014354
 ===Cyanogenic Glycosides===
-'''(In progress)'''
+All plants contain at least tiny amounts of [https://en.wikipedia.org/wiki/Hydrogen_cyanide hydrogen cyanide] ('''HCN'''), however, some plants also release high amounts of HCN from a class of glycosides called "cyanogenic glycosides", also called "cyanoglycosides".  [https://en.wikipedia.org/wiki/Amygdalin Amygdalin] and [https://en.wikipedia.org/wiki/Linamarin linamarin] are common examples of cyanogenic glycosides <ref name="Gleadow_2014"></ref>.  Amygdalin is sometimes marketed as a cure for cancer by the health food industry, but this claim is not supported by clinical data, and digestion of too much amygdalin can be dangerous <ref>[https://www.quackwatch.org/01QuackeryRelatedTopics/Cancer/laetrile.html Wilson, Benjamin.  "The Rise and Fall of Laetrile".  Quackwatch.org website.  01/07/2017.  retrieved 03/30/2017.]</ref><ref>[http://www.nejm.org/doi/pdf/10.1056/NEJM198201283060403 A Clinical Trial of Amygdalin (Laetrile) in the Treatment of Human Cancer.  Charles G. Moertel, M.D., Thomas R. Fleming, Ph.D., Joseph Rubin, M.D., Larry K. Kvols, M.D., Gregory Sarna, M.D., Robert Koch, M.D., Violante E. Currie, M.D., Charles W. Young, M.D., Stephen E. Jones, M.D., and J. Paul Davignon, Ph.D.  1982.  DOI: 10.1056/NEJM198201283060403.]</ref><ref>[https://www.infona.pl/resource/bwmeta1.element.springer-2c7e4ea1-3683-3bbd-9394-a98a551e7c63 Laetrile for cancer: a systematic review of the clinical evidence.  Stefania Milazzo, Stephane Lejeune, Edzard Ernst.  2007.  DOI: 10.1007/s00520-006-0168-9.]</ref><ref>[http://www.sciencedirect.com/science/article/pii/S0944711316000362 Amygdalin, quackery or cure?  Roman A. Blahetaa, Karen Nelsonb, Axel Haferkampa, Eva Juengela.  2016.]</ref>.  HCN is released from cyanogenic glycosides just like other types of glycosides: beta-glucosidase enzyme or exposure to low pH breaks the bond between a glucose molecule and an unstable compound called "cyanohydrin" (or "alpha-hydroxynnitrile"), which then disassociates into a ketone or benzaldehyde and an HCN molecule.  In cyanogenic glycosides, this reaction is called "cyanogenesis".  Cyanogenesis is stimulated by maceration, and by bacteria in the human gut <ref name="Speijers">[http://www.inchem.org/documents/jecfa/jecmono/v30je18.htm "Cyanogenic Glycosides", First Draft.  Dr G. Speijers.  National Institute of Public Health and Environmental Protection Laboratory for Toxicology, Bilthoven, The Netherlands.  Retrieved 08/25/2016.]</ref>.  Although the optimum pH of cyanogenesis (at least for amygdalin) is 5.0 - 5.8, cyongenesis can occur at a wide range of pH values, and can occur in the presence of acid <ref>[http://www.sciencedirect.com/science/article/pii/S0308814601003132 Total cyanide determination of plants and foods using the picrate and acid hydrolysis methods.  M Rezaul Haque, J Howard Bradbury.  2002.]</ref>.  If seeds containing cyanogenic glycosides are ground up, the coarseness to which they are ground effects how quickly cyanogenesis occurs.  Finely ground seeds extract HCN within an hour, where as coarsely ground seeds extract within 24 hours <ref name="tuncel">[http://www.sciencedirect.com/science/article/pii/030881469599841M The effects of grinding, soaking and cooking on the degradation of amygdalin of bitter apricot seeds.  G Tunçel, M.J.R Nout, L Brimer.  1995.]</ref>.  HCN boils at a relatively low temperature (25.6°C / 78.1°F) <ref name="Gleadow_2014"></ref>.  In some cases, soaking, cooking, and/or sometimes fermenting foods with certain bacteria or yeast (this has not been fully documented with ''Saccharomyces'' or ''Brettanomyces'') that contain cyanogenic glycosides allows the HCN to be released, and then subsequent cooking afterwards will boil off the cyanide <ref>[http://www.sciencedirect.com/science/article/pii/016816059400115M International Journal of Food Microbiology.  M.J.R. Nout, G. Tunçe, L. Brimer.  1995.]</ref><ref name="Chaouali"></ref>.
-All plants contain tiny amounts of [https://en.wikipedia.org/wiki/Hydrogen_cyanide hydrogen cyanide] (HCN), however some plants also release high amounts of HCN from a class of glycosides called "cyanogenic glycosides", also called "cyanoglycosides".  [https://en.wikipedia.org/wiki/Amygdalin Amygdalin] and [https://en.wikipedia.org/wiki/Linamarin linamarin] are common examples of cyanogenic glycosides.  After being released from cyanogenic glycosides, HCN is highly toxic to animals.  HCN boils at a relatively low temperature (25.6°C / 78.1°F).  The human body is used to breaking down trace amounts of cyanide into the less toxic substance thiocyanate with an enzyme called rhodanese, which then leaves the body via urination <ref name="Gleadow_2014">[http://www.annualreviews.org/doi/full/10.1146/annurev-arplant-050213-040027 Cyanogenic Glycosides: Synthesis, Physiology, and Phenotypic Plasticity.  Roslyn M. Gleadow and Birger Lindberg Møller.  2014.]</ref>.  Although there are more than 3,000 plant species that are cyanogenic (a number of them cultivated by farmers perhaps because their cyanogenic properties deter animals from eating them), only a few parts of plants that are considered foods contain enough HCN from cyanogenic glycosides to be considered dangerous (generally, other forms of cyanide are considered more dangerous, such as from exposure to air or water that is polluted with cyanide) <ref name="CDC1">[http://www.atsdr.cdc.gov/toxprofiles/tp8.pdf Toxicology Profile for Cyanide.  Agency for Toxic Substances & Disease Registry.  July 2006.  Retrieved 08/25/2016.]</ref>.  The location of the cyanogenic glycosides and the enzymes that release them are often each located in different (or all) parts of plants, and those locations are diverse across species.  In some plants, the cyanogenic glycosides are concentrated in the stems or leaves of the plant and not the seeds (e.g. sorghum, barley, and lima beans). In fruits sometimes the seeds contain concentrated amounts (e.g. black cherry pits), and other times in the fruit itself (e.g. ''Passiflora edulis'').  In rosaceous stone fruits, cyanogenic glycosides are located in the seeds, but the beta-glucosidase enzyme that the plant uses to release HCN is located in the roots of the plant.  The concentration of cyanogenic glycosides is generally higher in seedling plants compared to mature plants, however this is there are a few exceptions where this is the opposite (e.g. some ''Eucalyptus'' species, and lima beans).  HCN is released from cyanogenic glycosides just like other types of glycosides: beta-glucosidase enzyme or exposure to low pH breaks the bond between a glucose molecule and an unstable compound called "cyanohydrin" (or "alpha-hydroxynnitrile"), which then disassociates into a ketone or benzaldehyde and an HCN molecule.  This reaction is stimulated by maceration, and by bacteria in the human gut.  The cyanogenic glycosides themselves are not toxic until the HCN is released <ref name="Speijers">[http://www.inchem.org/documents/jecfa/jecmono/v30je18.htm "Cyanogenic Glycosides", First Draft.  Dr G. Speijers.  National Institute of Public Health and Environmental Protection Laboratory for Toxicology, Bilthoven, The Netherlands.  Retrieved 08/25/2016.]</ref>.
+After being released from cyanogenic glycosides, HCN is highly toxic to animals.  The human body is used to breaking down trace amounts of cyanide into the less toxic substance thiocyanate with an enzyme called rhodanese, which then leaves the body via urination <ref name="Gleadow_2014">[http://www.annualreviews.org/doi/full/10.1146/annurev-arplant-050213-040027 Cyanogenic Glycosides: Synthesis, Physiology, and Phenotypic Plasticity.  Roslyn M. Gleadow and Birger Lindberg Møller.  2014.]</ref>.  Although there are more than 3,000 plant species that are cyanogenic (a number of them cultivated by farmers perhaps because their cyanogenic properties deter animals from eating them), only a few parts of plants that are considered foods contain enough HCN from cyanogenic glycosides to be considered dangerous (generally, other forms of cyanide are considered more dangerous, such as from exposure to air or water that is polluted with cyanide) <ref name="CDC1">[http://www.atsdr.cdc.gov/toxprofiles/tp8.pdf Toxicology Profile for Cyanide.  Agency for Toxic Substances & Disease Registry.  July 2006.  Retrieved 08/25/2016.]</ref>.  The location of the cyanogenic glycosides and the enzymes that release them are often each located in different (or all) parts of plants, and those locations are diverse across species.  In some plants, the cyanogenic glycosides are concentrated in the stems or leaves of the plant and not the seeds (e.g. sorghum, barley, and lima beans). In fruits sometimes the seeds contain concentrated amounts (e.g. black cherry pits), and other times in the fruit itself (e.g. ''Passiflora edulis'').  In rosaceous stone fruits, cyanogenic glycosides are located in the seeds, but the beta-glucosidase enzyme that the plant uses to release HCN is located in the roots of the plant.  The concentration of cyanogenic glycosides is generally higher in seedling plants compared to mature plants, however there are a few exceptions where this is the opposite (e.g. some ''Eucalyptus'' species, and lima beans).  The HCN potential of plants varies highly depending on the species, strain, and climate/environmental conditions of the crop year <ref name="Gleadow_2014"></ref>.
-Although rare, there have been a few reported deaths due to cyanide poisoning from foods containing cyanogenic glycosides.  These reports include deaths from elderberry juice that was thought to contain stems and/or leaves (the stems and leaves contain much higher cyanogenic glycosides than the berries, and ripe berries by themselves are considered safe) <ref>[http://www.cdc.gov/mmwr/preview/mmwrhtml/00000311.htm Poisoning from Elderberry Juice -- California.  CDC website.  1998.  Retrieved 08/30/2016.]</ref>, apricot pits, choke cherry pits, and improperly processed cassava (a staple food in parts of North Africa) <ref name="who"></ref>.  A lethal dosage of cyanide in humans is estimated to be around 1.52 mg per kilogram of body weight, with 0.56 mg per kilogram of body weight being the lowest recorded (although this lowest figure was obtained from a historical case when the measurements taken may not have been accurate) <ref>[http://www.atsdr.cdc.gov/toxprofiles/tp8.pdf Toxicology Profile for Cyanide.  Agency for Toxic Substances & Disease Registry.  July 2006.  Pg 42.  Retrieved 08/25/2016.]</ref>.  High exposure can cause light-headedness, nausea, vomiting, stomach cramps, diarrhea, convulsions, harm to the brain and heart, comas, and death.  Exposure to 0.05 mg of cyanide per kilogram of body weight per day for 15-364 days is considered to be the minimum accumulative cyanide exposure by the US CDC.  Accumulative exposure can cause health risks, such as reproductive, respiratory, neurological, thyroid, and gastrointestinal issues <ref>[http://www.atsdr.cdc.gov/toxprofiles/tp8.pdf Toxicology Profile for Cyanide.  Agency for Toxic Substances & Disease Registry.  July 2006.  Pg 21.  Retrieved 08/25/2016.]</ref>.
+Although rare, there have been a few reported deaths due to cyanide poisoning from foods containing cyanogenic glycosides.  These reports include deaths from elderberry juice that was thought to contain stems and/or leaves (the stems and leaves contain much higher cyanogenic glycosides than the berries, and ripe berries by themselves are considered safe) <ref>[http://www.cdc.gov/mmwr/preview/mmwrhtml/00000311.htm Poisoning from Elderberry Juice -- California.  CDC website.  1998.  Retrieved 08/30/2016.]</ref>, apricot kernels (pits), choke cherry pits, and improperly processed cassava (a staple food in parts of North Africa) <ref name="who"></ref>.  A lethal dosage of cyanide in humans is estimated to be around 1.52 mg per kilogram of body weight, with 0.56 mg per kilogram of body weight being the lowest recorded (although this lowest figure was obtained from a historical case when the measurements taken may not have been accurate) <ref>[http://www.atsdr.cdc.gov/toxprofiles/tp8.pdf Toxicology Profile for Cyanide.  Agency for Toxic Substances & Disease Registry.  July 2006.  Pg 42.  Retrieved 08/25/2016.]</ref>.  High exposure can cause light-headedness, nausea, vomiting, stomach cramps, diarrhea, convulsions, harm to the brain and heart, comas, and death.  Exposure to 0.05 mg of cyanide per kilogram of body weight per day for 15-364 days is considered to be the minimum accumulative cyanide exposure by the US CDC.  Accumulative exposure can cause health risks, such as reproductive, respiratory, neurological, thyroid, and gastrointestinal issues <ref>[http://www.atsdr.cdc.gov/toxprofiles/tp8.pdf Toxicology Profile for Cyanide.  Agency for Toxic Substances & Disease Registry.  July 2006.  Pg 21.  Retrieved 08/25/2016.]</ref>.  In some foods, such as marzipan and persipan (made from bitter apricot seeds), the processing of this food destroys the natural beta-glucosidase enzyme (which denatures at 75°C), leaving the flora in the human gut to break down the cyanogenic glycosides.  Even if an abnormally large portion of marzipan or persipan is ingested, the lack of beta-glucosidase along with the high calories in the food acts as a slow release of cyanide into the human body which the body can deal with <ref>[http://link.springer.com/article/10.1007%2Fs00204-015-1479-8 Bioavailability of cyanide after consumption of a single meal of foods containing high levels of cyanogenic glycosides: a crossover study in humans.  Klaus Abraham, Thorsten Buhrke, Alfonso Lampen.  2015.]</ref>.
-Upon learning about cyanogenic glycosides, brewers often question the toxicity of cherry pits in beer.  Cherry pits have traditionally been used in [[lambic]] kriek beers in Belgium.  However, the dilution of HCN from cherry pits in beer results in benign levels.  Assuming full breakdown of these glycosides, and that none of the HCN boils off (25.6°C boiling temperature), levels of HCN introduced from cherry pits are too low to cause harm to adult humans.  The EU regulates that alcoholic beverages cannot exceed 1 mg of HCN per ABV percentage (v/v%) per liter <ref>[http://ec.europa.eu/food/fs/sfp/addit_flavor/flav09_en.pdf  COUNCIL DIRECTIVE of 22 June 1988 on the approximation of the laws of the Member States relating to flavourings for use in foodstuffs and to source materials for their production (88/388/EEC).  The European Food Commission, Food Safety.  Retrieved 08/26/2016</ref>.  Luk Daenen, a glycoside researcher, calculated that for a 4% ABV alcohol beer, 4 mg of HCN per liter is allowed.  With 200 grams of cherries per liter, and the pits being 10-14 grams of that weight, there is 22 - 30.8 amygdalin per liter of beer.  Around 6% of the weight of amygdalin is converted into HCN.  Assuming maximum extraction of HCN from the amygdalin glycoside, which is unlikely because the pits are not ground up when used in beer, this equates to 1.3 - 1.82 mg of HCN per liter of beer, which is less than the 4 mg of HCN per liter that the EU regulation states.  Considering that ~42 mg of HCN is required to kill a person that weighs 70 kilograms (154 pounds), that person would need to drink around 23 liters of beer <ref name="daenen">[https://www.uclouvain.be/cps/ucl/doc/inbr/documents/presentation-luk-daenen.pdf "Use of beta-glucosidase activity for flavour enhancement in specialty beers," slideshow by Luk Daenen.  2012.  Retrieved 08/26/2016.]</ref>.  350 mL of alcohol would kill a 70 kilogram adult <ref>[http://www.alcohol.org.nz/alcohol-its-effects/health-effects/alcohol-poisoning "Alcohol Poisoning".  NZ Health Promotion Agency.  Retrieved 08/26/2016.]</ref>.  The amount of 4% ABV beer required to kill a 70 kg adult from alcohol poisoning is around 8.75 liters.  Alcohol would kill such a person far before cyanide poisoning would become a concern.
+Upon learning about cyanogenic glycosides, brewers often question the toxicity of ingredients such as cherry pits or apricot kernels in beer.  Cherry pits have traditionally been used in [[lambic]] kriek beers in Belgium.  However, the dilution of HCN from cherry pits in beer results in benign levels.  Assuming full breakdown of these glycosides, and that none of the HCN boils off (25.6°C boiling temperature), levels of HCN introduced from cherry pits are too low to cause harm to adult humans.  The EU regulates that alcoholic beverages cannot exceed 1 mg of HCN per ABV percentage (v/v%) per liter <ref>[http://ec.europa.eu/food/fs/sfp/addit_flavor/flav09_en.pdf  COUNCIL DIRECTIVE of 22 June 1988 on the approximation of the laws of the Member States relating to flavourings for use in foodstuffs and to source materials for their production (88/388/EEC).  The European Food Commission, Food Safety.  Retrieved 08/26/2016.]</ref>.  Luk Daenen, a glycoside researcher, calculated that for a 4% ABV alcohol beer, 4 mg of HCN per liter is allowed.  With 200 grams of cherries per liter, and the pits being 10 - 14 grams of that weight, there is 22 - 30.8 mg amygdalin per liter of beer.  Around 6% of the weight of amygdalin is converted into HCN.  Assuming maximum extraction of HCN from the amygdalin glycoside, which is unlikely because the pits are not ground up when used in beer, this equates to 1.3 - 1.82 mg of HCN per liter of beer.  This amount is less than the 4 mg of HCN per liter that the EU regulation states.  Considering that ~42 mg of HCN is required to kill a person that weighs 70 kilograms (154 pounds), that person would need to drink around 23 liters of beer <ref name="daenen">[https://www.uclouvain.be/cps/ucl/doc/inbr/documents/presentation-luk-daenen.pdf "Use of beta-glucosidase activity for flavour enhancement in specialty beers," slideshow by Luk Daenen.  2012.  Retrieved 08/26/2016.]</ref>.  Considering that 350 mL of pure alcohol would kill a 70 kilogram adult <ref>[http://www.alcohol.org.nz/alcohol-its-effects/health-effects/alcohol-poisoning "Alcohol Poisoning".  NZ Health Promotion Agency.  Retrieved 08/26/2016.]</ref>, the amount of 4% ABV beer required to kill a 70 kg adult from alcohol poisoning is around 8.75 liters.  Alcohol would kill such a person far before cyanide poisoning would become a concern.  In general, the potential cyanide in most plants will become too dilute to have any health problems when added to beer in normal amounts, however there might still be plants that are extremely high in HCN content that should be avoided in beer (see the table below).  If there is a concern that an ingredient containing potentially high levels of HCN could reach unhealthy levels in beer, the beer should be sent for lab analysis so that the HCN levels can be determined before being consumed.
-Because of the high boiling point of HCN, cooking or boiling foods that contain high levels of cyanide will greatly eliminate the HCN (90-100% in some cases) <ref name="Chaouali"></ref>.
+Some cyanogenic foods can have their cyanogenic glycosides reduced by cooking them at 230°C for 15 minutes (flaxseed, for example) <ref name="Chaouali"></ref><ref name="flax"></ref>, however some amygdalin based cyanogenic plants may have their amygdalin content reduced to about 25% by cooking alone (apricot seeds, for example; only the cooking temperature of 100°C was tested <ref name="tuncel"></ref>).  Fermentation by certain species of microbes can have a greater effect on reducing amygdalin to HCN than cooking alone.  Microbes that have been shown to break down amygdalin include some species of lactic acid bacteria including ''Lactobacillus plantarum'', and fungi such as ''Endomyces fibuliger'', ''Pichia etchellsii'', and ''Hanseniaspora  valbyensis''.  Some strains of ''Brettanomyces'' that have high beta-glucosidase activity might be able to break down amygdalin by around 64%, and some strains of ''S. cerevisiae'' might be able to break down up to around 10% of amygdalin, but this needs to be verified by science.  Once the amygdalin is broken down into HCN, the HCN can then be volatilized off by cooking in a ventilated space <ref>[http://link.springer.com/article/10.1007/BF00151870 Simple screening procedure for microorganisms to degrade amygdalin.  L. Brimer, G. Tunçel, M. J. R. Nout.  1993.]</ref><ref>[http://www.ncbi.nlm.nih.gov/pubmed/7710917 Microbial degradation of amygdalin of bitter apricot seeds (Prunus armeniaca).  Nout MJ, Tunçel G, Brimer L.  1995.]</ref><ref name="Daenen1"></ref>.  In normal brewing procedures, however, the beer is not cooked nor ventilated, so any HCN that is produced by the breakdown of cyanogenic glycosides should be presumed to remain in the beer.
+====Determining HCN Potential====
+The [http://nordicfoodlab.org/blog/2013/8/hydrogen-cyanide The DIY picric acid test for HCN] could help in measuring HCN content in beer.  Make sure that this test is performed against the finished beer after any glycosides would be broken down.  Toxicology labs, if available, should be able to offer services that measure HCN in beer.  The following table also lists potential HCN content for various food items.  For finding the HCN content based on amygdalin content, approximately 6% of amygdalin by weight is converted to HCN.
 {| class="wikitable sortable"
 |-
-! Plant !! mg HCN/kg or mg/liter
+! Plant !! mg HCN/kg or mg/liter <nowiki>*</nowiki> || Prominent Glycoside
 |-
-| Cereal grains and their products || 0.001-0.45 <ref name="who">[http://www.who.int/ipcs/publications/cicad/en/cicad61.pdf Concise International Chemical Assessment Document 61.  HYDROGEN CYANIDE AND CYANIDES: HUMAN HEALTH ASPECTS.  World Health Organization.  2004.  Pg 13.  Retrieved 08/29/2016.]</ref>
+| Cereal grains and their products || 0.001-0.45 <ref name="who">[http://www.who.int/ipcs/publications/cicad/en/cicad61.pdf Concise International Chemical Assessment Document 61.  HYDROGEN CYANIDE AND CYANIDES: HUMAN HEALTH ASPECTS.  World Health Organization.  2004.  Pg 13.  Retrieved 08/29/2016.]</ref> ||
 |-
-| Soy protein products || 0.07-0.3 <ref name="who"></ref>
+| Soy protein products || 0.07-0.3 <ref name="who"></ref> || Linmarin <ref name="soybean"></ref>
 |-
-| Soybean hulls || 1.24 <ref name="who"></ref>
+| Soybean hulls || 1.24 <ref name="who"></ref> || Linmarin <ref name="soybean"></ref>
 |-
-| Apricot pits, wet weight || 89-2170 (depends on region/strain) <ref name="Chaouali"></ref><ref name="who"></ref>
+| Home-made cherry juice from pitted fruits || 5.1 <ref name="who"></ref> || Amygdalin <ref name="Gleadow_2014"></ref>
 |-
-| Home-made cherry juice from pitted fruits || 5.1 <ref name="who"></ref>
+| Home-made cherry juice containing 100% crushed pits || 23 <ref name="who"></ref> || Amydalin <ref name="Gleadow_2014"></ref>
 |-
-| Home-made cherry juice containing 100% crushed pits || 23 <ref name="who"></ref>
+| Almonds (wild bitter) || 1062-4690 <ref name="Chaouali">[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793392/ Potential Toxic Levels of Cyanide in Almonds (Prunus amygdalus), Apricot Kernels (Prunus armeniaca), and Almond Syrup.  Nadia Chaouali, Ines Gana, Amira Dorra, Fathia Khelifi, Anouer Nouioui, Wafa Masri, Ines Belwaer, Hayet Ghorbel, and Abderazzek Hedhili.  2013.]</ref><ref>[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1273391/ Cyanide poisoning after bitter almond ingestion.  T A Shragg, T E Albertson, and C J Fisher, Jr.  1982.]</ref> || Amygdalin <ref name="wikipedia_almond">[https://en.wikipedia.org/wiki/Almond "Almond".  Wikipedia.  Retrieved 09/06/2016.]</ref>
 |-
-| Almonds (wild bitter) || 1062-4690 <ref name="Chaouali">[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793392/ Potential Toxic Levels of Cyanide in Almonds (Prunus amygdalus), Apricot Kernels (Prunus armeniaca), and Almond Syrup.  Nadia Chaouali, Ines Gana, Amira Dorra, Fathia Khelifi, Anouer Nouioui, Wafa Masri, Ines Belwaer, Hayet Ghorbel, and Abderazzek Hedhili.  2013.</ref><ref>[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1273391/ Cyanide poisoning after bitter almond ingestion.  T A Shragg, T E Albertson, and C J Fisher, Jr.  1982.]</ref>
+| Almonds (sweet domesticated) || 25 <ref name="Chaouali"></ref> || Amygdalin <ref name="wikipedia_almond"></ref>
 |-
-| Almonds (sweet domesticated) || 25 <ref name="Chaouali"></ref>
+| Cherries with pit || 6.5-9.1 <ref name="daenen"></ref> || Amygdalin <ref name="Gleadow_2014"></ref>
 |-
-| Cherries with pit || 6.5-9.1 <ref name="daenen"></ref>
+| Cherry pits only (black) || 161 <ref name="Bolarinwa_2014" /> || Amygdalin <ref name="Bolarinwa_2014" />
 |-
-| Fresh Apricots with kernel ||
+| Cherry pits only (red) || 233 <ref name="Bolarinwa_2014" /> || Amygdalin <ref name="Bolarinwa_2014" />
 |-
-| '''Commercial fruit juices''' ||
+| Cherry pits only (morello) || 3900 <ref name="VOLDŘICH_1992" /> || Amygdalin <ref name="VOLDŘICH_1992" />
 |-
-| Cherry || 4.6 <ref name="who"></ref>
+| Apricot pits, wet weight || 89-2170 (depends on region/variety) <ref name="Chaouali"></ref><ref name="who"></ref> || Amgydalin <ref name="Gleadow_2014"></ref>
 |-
-| Apricot || 2.2 <ref name="who"></ref>
+| Sweet Apricots with kernel (14-24 fruits for 1 kg; single kernel avg weight is 6 grams <ref name="calapricot">[http://www.califapricot.com/marking_regulations.html California Apricots.  Marking Regulations.  Retrieved 09/01/16.]</ref>) || 4.2 - 7.2 (avg 0.3 mg per kernel <ref name="wiki_apric_kernel">[https://en.wikipedia.org/wiki/Apricot_kernel "Apricot Kernel".  Wikipedia.  Retrieved 09/01/2016.]</ref>) || Amygdalin <ref name="Gleadow_2014"></ref>
 |-
-| Prune || 1.9 <ref name="who"></ref>
+| Bitter Apricots with kernel (14-24 fruits for 1 kg; single kernel avg weight is 6 grams <ref name="calapricot"></ref>) || 25.2 - 43.2 (avg 1.8 mg per kernel <ref name="wiki_apric_kernel"></ref>) || Amygdalin <ref name="Gleadow_2014"></ref>
 |-
-| '''Tropical foodstuffs''' ||
+| Elderflower (leaves/stems) || 1600 <ref name="nordicfoodlab">[https://web.archive.org/web/20190812014649/http://nordicfoodlab.org:80/blog/2013/10/elder-a-love-story "Elder – a love story".  Justine de Valicourt.  Nordic Food Lab.  10/03/2013.  Retrieved 09/07/2016.]</ref> || Sambunigrin (or sometimes prunasin, holocalin, or zierin) <ref name="elderflowers">[https://www.researchgate.net/publication/233262135_Cyanogenic_Glycosides_from_Sambucus_Nigra Cyanogenic Glycosides from Sambucus Nigra.  Marina Dellagreca, Antonio Fiorentino, Pietro Monaco, Lucio Previtera & Ana M. Simonet.  2006.]</ref>
 |-
-| Cassava(bitter)/dried root cortex || 2360-2450 <ref name="who"></ref><ref name="Speijers"></ref>
+| Elderberries (fully ripe; under-ripe will contain more) || 30 <ref name="nordicfoodlab"></ref> || Sambunigrin (or sometimes prunasin, holocalin, or zierin) <ref name="elderflowers"></ref>
 |-
-| Cassava(bitter)/leaves || 300-310 <ref name="who"></ref><ref name="Speijers"></ref>
+| Peach seeds/kernels || 54-2600 (variety dependent; mostly reported between 54-666) <ref name="VOLDŘICH_1992">[https://www.scopus.com/record/display.uri?eid=2-s2.0-84987336720&origin=inward&txGid=713c7a86664b8d2865e54a25eaafc9b5 Cyanogenesis in Canned Stone Fruits.  VOLDŘICH, M.,  KYZLINK, V.  1992.  DOI: 10.1111/j.1365-2621.1992.tb05446.x.]</ref><ref name="Bolarinwa_2014">[https://www.sciencedirect.com/science/article/pii/S0308814613016245 Amygdalin content of seeds, kernels and food products commercially-available in the UK.  Islamiyat F. Bolarinwa, Caroline Orfila, Michael R.A. Morgan.  2014.  DOI: https://doi.org/10.1016/j.foodchem.2013.11.002.]</ref><ref>[https://www.scopus.com/record/display.uri?eid=2-s2.0-0021674858&origin=inward&txGid=ee159dc998e0469bc88f0685e8d41ecb The cyanide content of laetrile preparations, apricot, peach and apple seeds.  Holzbecher, M.D.,  Moss, M.A.,  Ellenberger, H.A 1984.]</ref> || Amygdalin <ref name="Bolarinwa_2014" />
 |-
-| Cassava(bitter)/whole tubers || 380-395 <ref name="who"></ref><ref name="Speijers"></ref>
+| Nectarine seeds (summer fire) || 7.2 <ref name="Bolarinwa_2014" /> || Amygdalin <ref name="Bolarinwa_2014" />
 |-
-| Cassava(sweet)/leaves || 451-468 <ref name="who"></ref><ref name="Speijers"></ref>
+| Plum seeds (green) || 1050 <ref name="Bolarinwa_2014" /> || Amygdalin <ref name="Bolarinwa_2014" />
 |-
-| Cassava(sweet)/whole tubers || 445-462 <ref name="who"></ref><ref name="Speijers"></ref>
+| Plum seeds (black; firar black) || 600 <ref name="Bolarinwa_2014" /> || Amygdalin <ref name="Bolarinwa_2014" />
 |-
-| Gari flour (Nigeria) || 10.6-22.1 <ref name="who"></ref>
+| Plum seeds (purple; larry anne) || 130 <ref name="Bolarinwa_2014" /> || Amygdalin <ref name="Bolarinwa_2014" />
 |-
-| Sorghum/whole immature plant || 2400-2500 <ref name="who"></ref><ref name="Speijers"></ref>
+| Plum seeds (yellow; son gold) || 92 <ref name="Bolarinwa_2014" /> || Amygdalin <ref name="Bolarinwa_2014" />
 |-
-| Bamboo/immature shoot tip || 7700-8000 <ref name="who"></ref><ref name="Speijers"></ref>
+| Plum seeds (red; laetitia) || 26 <ref name="Bolarinwa_2014" /> || Amygdalin <ref name="Bolarinwa_2014" />
 |-
-| Lima beans from Java (coloured)  || 3000-3120 <ref name="who"></ref><ref name="Speijers"></ref>
+| Apple seeds (royal gala) || 178 <ref name="Bolarinwa_2014" /> || Amygdalin <ref name="Bolarinwa_2014" />
 |-
-| Lima beans from Puerto Rico (black)  || 2900-3000 <ref name="who"></ref><ref name="Speijers"></ref>
+| Pear (conference) || 77 <ref name="Bolarinwa_2014" /> || Amygdalin <ref name="Bolarinwa_2014" />
 |-
-| Lima beans from Burma (white) || 2000-2100 <ref name="who"></ref><ref name="Speijers"></ref>
+| Non-Rosaceae fruit seeds (courgette, cucumber, marrow, honey dew melon, squash varieties) || 0.6-12.6 <ref name="Bolarinwa_2014" /> || Amygdalin <ref name="Bolarinwa_2014" />
+|-
+| '''Commercial fruit juices'''
+|-
+| Cherry || 4.6 <ref name="who"></ref> || Amygdalin <ref name="Gleadow_2014"></ref>
+|-
+| Apricot || 2.2 <ref name="who"></ref> || Amygdalin <ref name="Gleadow_2014"></ref>
+|-
+| Prune || 1.9 <ref name="who"></ref> || Amygdalin <ref name="Gleadow_2014"></ref>
+|-
+| '''Tropical foodstuffs'''
+|-
+| Cassava(bitter)/dried root cortex || 2360-2450 <ref name="who"></ref><ref name="Speijers"></ref> || Linamarin <ref name="Gleadow_2014"></ref>
+|-
+| Cassava(bitter)/leaves || 300-310 <ref name="who"></ref><ref name="Speijers"></ref> || Linamarin <ref name="Gleadow_2014"></ref>
+|-
+| Cassava(bitter)/whole tubers || 380-395 <ref name="who"></ref><ref name="Speijers"></ref> || Linamarin <ref name="Gleadow_2014"></ref>
+|-
+| Cassava(sweet)/leaves || 451-468 <ref name="who"></ref><ref name="Speijers"></ref> || Linamarin <ref name="Gleadow_2014"></ref>
+|-
+| Cassava(sweet)/whole tubers || 445-462 <ref name="who"></ref><ref name="Speijers"></ref> || Linamarin <ref name="Gleadow_2014"></ref>
+|-
+| Gari flour (Nigeria) || 10.6-22.1 <ref name="who"></ref> || Linamarin <ref name="Gleadow_2014"></ref>
+|-
+| Sorghum/whole immature plant || 2400-2500 <ref name="who"></ref><ref name="Speijers"></ref> || Dhurrin <ref name="Gleadow_2014"></ref>
+|-
+| Bamboo/immature shoot tip || 7700-8000 <ref name="who"></ref><ref name="Speijers"></ref> || Taxiphyllin <ref>[http://www.ingentaconnect.com/contentone/ben/cnf/2016/00000012/00000002/art00012 Cyanogenic Toxicity and Human Health.  Singhal, Poonam; Satya, Santosh; N . Naik, Satya.  2016.]</ref>
+|-
+| Lima beans from Java (coloured)  || 3000-3120 <ref name="who"></ref><ref name="Speijers"></ref> || Linmarin <ref name="soybean">[http://pubs.acs.org/doi/abs/10.1021/jf00116a021 Determination of cyanide in soybeans and soybean products. David H. Honig, M. Elaine Hockridge, Robert M. Gould, Joseph J. Rackis.  1983.]</ref>
+|-
+| Lima beans from Puerto Rico (black)  || 2900-3000 <ref name="who"></ref><ref name="Speijers"></ref> || Linmarin <ref name="soybean"></ref>
+|-
+| Lima beans from Burma (white) || 2000-2100 <ref name="who"></ref><ref name="Speijers"></ref> || Linmarin <ref name="soybean"></ref>
+|-
+| Flaxseed || 910 <ref name="flax">[http://pubs.acs.org/doi/abs/10.1021/bk-1997-0662.ch010 Cyanogenic Glycosides of Flaxseeds.  Fereidoon Shahidi and P. K. J. P. D. Wanasundara.  1997.]</ref> || Linamarin, linustatin and neolinustatin <ref name="flax"></ref>
 |-
 |}
+: <nowiki>*</nowiki> Amounts are averages, or are single examples.  Actual levels may vary greatly between strains and growth conditions.
+See also:
+* [https://www.facebook.com/groups/MilkTheFunk/permalink/1401402279887982/ MTF thread on cyanide potential in beer.]
 ==See Also==
 ===Additional Articles on MTF Wiki===
+* [[Hops#Hop_Derived_Compounds_In_Beer_and_Biotransformations|Hop Biotransformations]]
 * [[Brettanomyces]]
+* [[Pediococcus]]
 * [[Mixed Fermentation]]
+* [[Soured Fruit Beer]]
+* [[Soured Herb, Spice, and Vegetable Beer]]
 ===External Resources===
@@ Line 108: / Line 195: @@
 * [https://www.uclouvain.be/cps/ucl/doc/inbr/documents/presentation-jean-marie-rock.pdf "Dry Hopping Myths versus Reality," slideshow by Jean-Marie Rock, ex-brewmaster for Orval.]
 * [https://www.uclouvain.be/cps/ucl/doc/inbr/documents/presentation-luk-daenen.pdf "Use of beta-glucosidase activity for flavour enhancement in specialty beers," slideshow by Luk Daenen.]
+* [http://nordicfoodlab.org/blog/2013/10/elder-a-love-story "Elder: a love story", by Justine de Valicourt (cyanide in elderberries).]
+* [http://www.dpi.nsw.gov.au/__data/assets/pdf_file/0013/111190/prussic-acid-poisoning-in-livestock.pdf Overview of HCN in various grass/straw/hay/livestock feed species.]
+* [http://scottjanish.com/?s=glycosides Scott Janish blog articles about glycosides.]
 ==References==

Difference between revisions of "Glycosides"

Latest revision as of 16:26, 28 August 2024

Contents

Glycosides and Beta-Glucosidase Activity

Monoterpenes and Glycosides

Acidic Hydrolysis

Beta-Glucosidase

Activity of Brettanomyces and Saccharomyces

Activity of Other Yeasts

Activity of Lactic Acid Bacteria

Cyanogenic Glycosides

Determining HCN Potential

See Also

Additional Articles on MTF Wiki

External Resources

References

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