I had some questions about dry yeast that I emailed Ferments about recently. I thought the group would enjoy the discussion.
Q: I have enjoyed using Fermentis dry yeast because of the storage convenience. I especially like the beer brewed with the 34/70 lager strain. I was surprised that the cell count per gram was lower than expected, specifically on the lager yeast. Can you briefly explain why dry yeast is “different” from liquid cultures and why it initially needs less? Also, why is the lager cfu/g significantly lower than the ale?
I have read that dry yeast has more sterols and glycogen in reserve before they are put into stasis (which is why it doesn’t need aeration) and was wondering if that was why the initially required cell count is lower than the 1 million cells per ml per degree Plato guidelines.
Thanks for your help.
Response:
KREITER Bryan - Fermentis
Jan 31, 2023, 10:07 AM
to me
Hi Keith,
I’m happy to hear Fermentis yeast is working well for you. The primary advantage vs liquid is ease of use, which includes the ability to direct pitch or rehydrate as well as shelf stability. With performance comparable to liquid cultures, it just makes a lot of sense for many brewers. The advantage of liquid is the sheer variety of strains and genetics. Not all strains can be dried successfully, so we will never have the same variety.
The difference in the cell concentration is mainly related to a difference in cell size. Cell size varies between strains, and lager cells tend to be larger than ale cells, thus fewer per gram. Another factor, though minimal, is that pastorianus is more difficult to dry. This resulted in slightly lower viable cells per gram for lager vs ale. Improvements in the past ten years or so have closed this gap and the viability for ale and lager is now virtually the same. I was told that we may adjust the spec for SafLager upward to be in line with SafAle in the near future, but this has not happened yet.
What you heard about sterols and glycogen is accurate. Fermentis yeast is produced in purely aerobic condition in a batch fed process, maintaining sugar concentrations below 0.5%. This ensures all the sugars are used for biomass and no alcohol is produced during propagation (no alcohol stress). Most liquid producers do not achieve pure aerobic condition (but close) and do not batch feed the sugars. When sugar concentration is higher than about 0.5%, the Crabtree effect comes into play and alcohol is produced. Alcohol is a stressor and our yeast have never been exposed to this stress. The saturation with oxygen allows the yeast to produce ample fatty acids, sterols, glycogen, then we dry them and preserve them in this state. They have all the building blocks they need for growth and a complete fermentation. This is why we say, when pitching a fresh brick, that oxygenation is not necessary (no harm if you do). For lack of a better term, they are “pre-oxygenated.” In dry form, the fatty acids, sterols, viability, vitality and all other factors are stable. In a liquid culture, the cells can be consuming these reserves and viability and vitality will be decreasing steadily from packaging to the time of use. Our yeast can begin growing with the reserves they already have and liquid cultures will need to synthesize the fatty acids and sterols they need to grow (oxygen required).
If you are fermenting >18 plato, I would recommend rehydrating the yeast and oxygenating the wort. I say this because our studies were all in conditions below this, so we can’t say with certainty that there is no benefit above this point.
Lastly, we may in the future make some refinements to pitching rates for some strains. The rates will still be dry mass based, but might be more like grams/ml/Plato. Pitching rates are more important for some strains than others. In our studies of SafLager W-34/70, pitching rate had little effect on fermentation kinetics or flavor. For BE-256, if you pitch too much in lower gravity wort, you can get sulfur….
I hope this helps! Take care!
Bryan