Brettanomyces and Saccharomyces Co-fermentation

Brettanomyces and Saccharomyces Co-fermentation, for the purposes of this article, is a type of mixed fermentation that specifically refers to fermentations that contain Saccharomyces and Brettanomyces. They do not contain significant amounts of lactic acid produced by lactic acid bacteria (Lactobacillus and Pediococcus). As such, these beers may have a lightly tart flavor from acetic acid production by Brettanomyces, but are generally not described as being sour if properly brewed (see the Mixed Fermentation page for mixed fermentation sour beers). The flavor of beers fermented with Saccharomyces (generally ale yeast, but they can also be fermented with lager yeast) and Brettanomyces is often dominated by the array of flavor compounds produced by Brettanomyces, unless the beer is young in which case the ester and phenol profile of the fermenting strain of Saccharomyces might still have an impact on the flavor. In the case of young beers, the flavor profile will begin to be changed by Brettanomyces as esters, phenols, and fatty acids are created and metabolized.

Generically speaking, these flavors almost always consist of both fruity esters and phenolic components. Sometimes they also consist of an array of other flavors that are generically described as "funky". Specifically, fruity esters range from tropical fruits to stone fruits to citrus fruits, and are produced by all strains of Brettanomyces to some degree. Phenols, fatty acids, alcohols, aldehydes, and other compounds can also create a wide range of flavors including smoke, "barnyard animal", horse blanket, sweat, body odor, rancid cheese, etc. For more information on the identification of these compounds and the known conditions that impact their production, see Brettanomyces metabolism. For 100% Brettanomyces beers, see 100% Brettanomyces Fermentation.

Brewing Methods

Conceptual graph of dynamics of funk expression and inoculation timing of Brettanomyces. Y-axis for each microbe group depicts relative activity which combines in a conceptual sense: growth, attenuation and production of flavor compounds. Plot drawn by Drew Wham based on concepts discussed in American Sour Beer

Technique	More Funk	Less Funk	Note
Inoculation timing	After Saccharomyces has finished fermentation	At the start of Fermentation	See figure 1
Brettanomyces Inoculation cell count	Lower cell count or higher cell count	Higher cell count or lower cell count	Although more data is needed, pitching rate of Brettanomyces may not have a measured impact on beer flavor. See Brettanomyces secondary fermentation experiment.
Strain of Saccharomyces	Phenol positive strain	Phenol negative strain	POF+ strains of S. cerevisiae form 4-vinylguaiacol by enzymatic decarboxylation of ferulic acid . More recent data suggests that POF+ strains of Saccharomyces are not necessary for Brettanomyces to create phenols because Brettanomyces can create the precursor 4-vinyl phenols on its own as long as ferulic acid and other grain derived percursors are available . See Brettanomyces secondary fermentation experiment.
Ferulic Acid (malt derived)	More Ferulic Acid	Less Ferulic Acid	A precursor of 4-vinylguaiacol. Perform a ferulic acid rest, and use grains that contain more ferulic acid such as wheat.
Time since Inoculation	Aged Beer	Young Beer
Fermentation Temperature	Higher temperature increases esters in some but not all strains of B. bruxellensis.	Lower temperature decreases esters in some but not all strains of B. bruxellensis.	Temperature does not appear to affect the amount of phenol compounds produced by B. bruxellensis in a 100% Brettanomyces fermentation. Therefore, the perception of a more "funky" beer might depend on producing less esters rather than creating more phenols. See Brettanomyces phenols and 100% Brettanomyces Fermentation for more information.

Finishing Funky Mixed Fermentations

Bottling and Kegging

See the Packaging page.

Dosing Clean Beer with Brettanomyces At Bottling

One method that some brewers attempt is adding a small pitch of Brettanomyces to a clean beer at bottling time. This can be done either in the bottling bucket/tank, or added to each bottle individually. If adding Brettanomyces to each bottle individually, a 1 mL dosage of Brettanomyces from a starter should be enough since pitching rate seems to have little impact on the beer . Some brewers believe that adding the Brettanomyces at bottling time results in a more complex beer. It is speculated that the extra stress of pressure within the bottles helps to create this complexity.

One challenge with this approach is that it is difficult to predict how much Brettanomyces will further attenuate the beer once in the bottle. Over-carbonation and bottle bombs can easily be an issue with this method if the brewer is not careful. Each degree Plato adds ~2 volumes of CO2 . Since different species and strains of Brettanomyces ferment different types of sugars, some strains might be better suited for dosing at bottling time. For example, most strains of B. anomulus do not ferment maltose, which is around 50% of sugar in wort, so this makes it a good choice for adding to the beer at bottling.

Daniel Addey-Jibb, co-owner and brewer at Le Castor near Montreal, Quebec advises that the approach that his brewery takes is to ferment their saison wort down to 1°P. Once at 1°P , the beer is cold crashed, fined, and then bottled with Brettanomyces. The beer is then stored at room temperature for three months to condition naturally in the bottle. During bottling conditioning, their Brettanomyces culture takes the beer down below 0°P, and their desired level of carbonation is reached. This process took Addey-Jibb's team dozens of trials to perfect using their specific wort recipe, saison yeast, and Brettanomyces strain. Different species or strains of Brettanomyces might ferment differently, and different wort compositions might also ferment differently. For example, Addey-Jibb's saison is mashed with malted barley, wheat, and rye at a low temperature so there are not many higher chain sugars, allowing the beer to dry out quickly . Other wort compositions that include higher chain sugars from specialty malts and/or higher mashing temperatures might ferment much slower, and thus knowing what the final gravity will be once Brettanomyces is added is difficult to know without running trials on that specific fermentation profile. It is recommended to use Belgian beer bottles of sparkling wine bottles that can withstand higher pressures than regular beer bottles just in case over-carbonation becomes an issue.

A "forced fermentation test" might help to determine the final gravity of a given Brettanomyces strain or blend of strains. Use the same wort composition as the beer in question, and pitch a large cell count of Brettanomyces. Use a stirplate if possible, and an airlock to keep oxygen out (some Brettanomyces strains can attenuate further when fermented aerobically and thus will not give an accurate final gravity reading when fermented aerobically). Keep the temperature around 80-85°F for a month or two, and then measure the gravity. Each gravity point gives produces about 0.5 volumes of CO2. Adjust the priming sugar for the rest of the batch accordingly. Use bottles that are rated for higher pressures, such as Belgian bottles or sparkling wine bottles .

For more information on bottling sour and funky beer in general, see the Packaging page.

Review of Scientific Analysis

The published analysis of beer that is co-fermented with S. cerevisiae and Brettanomyces is rare. In this section, published data on this topic will be reviewed.

Nick Mader of Fremont Brewing (2017 Master Brewers Conference Presentation) compared various flavor compounds produced between a 100% S. cerevisiae (BSI-565, Wallionian Saison yeast) and 100% B. bruxellensis (BSI-Drei), and percentage combinations of 75/25, 50/50, and 25/75 inoculations of the BSI-565 strain and BSI-Drei strain. Fermentations were completed in 35 days, and the beers were analyzed for their ester and phenol content. Attenuation results were about the same for the 100% BSI-565 and the co-fermentation of BSI-565 and BSI-Drei, while the attenuation rate was around 12% lower for the 100% BSI-Drei fermentation, indicating that co-fermentation with these two particular strains did not greatly affect attenuation and that the BSI-Drei did not ferment as well by itself.

The esters that were analyzed were ethyl acetate (pineapple, pear, solventy), ethyl butyrate (tropical fruit), ethyl hexanoate (apple), ethyl decanoate (apple, brandy), ethyl octanoate (waxy, pineapple), isoamyl acetate (banana), isobutyl alcohol (solventy), and isoamyl alcohol (fusel, banana). Ethyl acetate was highest in the 100% BSI-565 fermentation (43 ppm; above the 33 ppm odor threshold), and lowest in the 100% BSI-Drei fermentation (21 ppm; below the 33 ppm odor threshold). The different co-fermentation rates formed a pattern of more ethyl acetate as the pitching rate of BSI-Drei was increased, but they were still lower than the 100% BSI-565 fermentation. The 75/25 ratio produced 27 ppm, 50/50 produced 34 ppm, and the 25/75 produced 42 ppm (BSI-565 to BSI-Drei ratio in percent pitching rate). Ethyl butyrate was highest in the 100% BSI-565, and curved downward as the pitching rate for the BSI-565 strain was decreased. Ethyl butyrate was below odor threshold in the 100% BSI-Drei fermentation. This indicates that the production of ethyl butyrate was dependent on the pitching rate of BSI-565, and that the BSI-Drei strain did not produce significant amounts of this ester. For each of the esters ethyl hexanoate, ethyl decanoate, ethyl octanoate, they had a slight decrease as the pitching rate of BSI-565 decreased, indicating that these esters are produced more by the BSI-565 strain, however the small measured differences may not be reflected in the actual taste/aroma of the beers since the differences were so small. The exception was ethyl decanoate which was around 3x higher in the 100% BSI-Drei, which indicates that ethyl decanoate is a major flavor contributor to 100% BSI-Drei fermentations. Overall, the ester concentrations were significantly lower in the BSI-565/BSI-Drei fermentations compared to the strains of S. cerevisiae and B. bruxellensis used by Lance Shaner and Richard Preiss in their similar experiment, indicating that total ester concentrations are highly dependent on the strains used. Isoamyl acetate, which was above odor threshold in the 100% BSI-565 fermentation, was almost not detectable in any of the fermentations that contained BSI-Drei (it was 0 ppm in the 100% BSI-Drei fermentation), which is in agreement with other studies that Brettanomyces hydrolyzes this ester. The alcohols isobutyl alcohol and isoamyl alcohol were slightly decreased as the pitching rate of BSI-565 decreased, and were extremely low in the 100% BSI-Drei, indicating that these alcohols were produced more so by BSI-565.

The phenols that were measured in Mader's experiment were 4-vinylguaiacol (clove), 4-ethylguaiacol (smokey, spicy), and 4-ethylphenol (medicinal, barnyard). While the 100% BSI-565 fermentation had high levels of 4-VG (1800 ppm), they were less than half the amount in the co-fermented ferments (600-800 ppm) but still above odor threshold (300 ppm) (the different ratios of BSI-565 to BSI-Drei did not have a large impact), and 4-VG was below threshold in the 100% BSI-Drei fermentation. 4-EG and 4-EP had high levels in the co-fermentations with BSI-565 and BSI-Drei and the 100% BSI-Drei, and the ratios did not have a large impact. This is in agreement with another experiment by Lance Shaner and Richard Preiss that showed that pitching rate of Brettanomyces after fermentation with S. cerevisiae did not have a great affect on the levels of phenols produced .

See Also

Additional Articles on MTF Wiki

• Mixed Fermentation
• Brettanomyces
• Saccharomyces
• Mixed Cultures
• Brettanomyces secondary fermentation experiment

External Resources

• White Labs list of Belgian yeast strains and characteristics, including phenols/spiciness.