Assuming you are adding enough healthy cells (not "under seeding" and simply doing a mini-fermentation after limited biomass production), cell density is determined primarily by volume of media, all things standardised, e.g., oxygenated wort (1.040) with sufficient nutrients.My question is about overall number of cells created - beginning numbers vs amount of starter wort used.
The 2ml is more likely to end up with more healthy yeast cells at the end of the final step-up of the same volume after a comparable series of step-ups. I'd say stick with 5X step-ups (by volume) mostly to minimise the chances of under seeding.With the two regimens above, it would appear that the 50ml vial would result in creating more cells in the end. The 2ml would end up with more vitality but would it have cells numbers that were comparable?
Yes, exactly. 'Seeding' in terms of cell culture terminology.I am understanding the term "under seeding" as putting too few cells in too much wort.
The first step is fine at 1.020 and usually the only one I pressure cook. The subsequent steps I have at 1.040 and just double boil then store in the freezer. I use kettle wort and just make a little extra occasionally on brew day. Just simmer it under a lid for 20min after adjusting gravity to 1.040. The lid helps keep it at 1.040. This is effectively sterilised starter wort now. If there were any surviving spores in the kettle wort they’ll ‘germinate’ overnight then get zapped by the second boil the next day. Sometimes it gets left in the fridge for 2-3 days. The trick is to pour it hot into hot, oven sterilised bottles then cap with lids boiled in water at the same time the wort is simmering. Then leave to cool before freezing. I prefer to have each step prepped individually then just pour straight into the next step when ready. Just take it out of the freezer the night or morning before use. Sometimes, for whatever reason, you might want to delay stepping up by storing the just-finished step in the fridge for a few days. It’s just more flexible to have the different steps in separate bottles, I think.@McMullan - I am forecasting for my new yeast starter method from 2ml vials and wanted to ask your opinion - Would you have an issue with keeping the 20ml, 100ml & 500ml propagation steps at 1.020 then moving to 1.035/1.040 for the 2.5L step?
This would make the pressure canning a lot easier. I could make a qt mason jar of the 1.020 wort and use it for the first three steps by pouring a bit out and keeping it sealed in the fridge until the next step.
Thanks again for your help. I am seeing a lot of potential with this approach as overbuilding the starter a little and grabbing a few 2ml vials worth of slurry seems like a better approach than harvesting from a batch.
That should be fine as long as it remains contamination free. It does introduce risks associated with more handling, though. I’m a bit sceptical about pressure cooking something as complex as homemade wort. It’s a different product and likely has reduced nutritional qualities. The first step, like standard lab media, is just to wake up the cells and get them adapted to growing again. Downstream steps, I’m more interested in promoting biomass.Thanks for your input. It is easy to pressure can them all for me but I thought I could limit the amount of small jars by using one larger jar for the first three steps. I will find a way forward. Maybe make the qt. mason jar of 1.040 wort and just dilute with boiled water upon pouring for the first step.
Same here, but when I started making my own starter wort and double boiling it, which was more convenient due to small volumes, I noticed it seemed better. Researched the literature and it became obvious possibly why. Pressure cooking reduces the free amino acid content by quite a lot. I’m a ‘fresh’ wort convert. Simmered not under pressure. For guaranteed sterility and long-term storage at room temperature, pressure cook. But once we get past the initial step starter, we’re in ‘food’ territory and just need to follow basic food hygiene practices. Promote lots of healthy yeast then let the ethanol do the rest.I have been pressure canning wort for a few years and have not noticed anything bad happening. I do 1020 1/4pints and 1040 1/2pint, pints and quarts. A little work to clean and canned the jars but quite convenient to just open a jar to step up a starter.
Only you can answer that, because it’s your decision. For me, it isn’t worth the risk on the first step. After that, it doesn’t bother me.I would ask is this level of risk acceptable?
I had another read-through of your method and I might be able to pull it off. I would need to boil in my 10 gallon boil kettle, let it sit overnight in that same pot with the lid on, then boil the next day and transfer through the outlet into the hot mash jars. Though this would all take place out in my garage. Is that a non-starter or does the temperature eliminate the risks?The first step is fine at 1.020 and usually the only one I pressure cook. The subsequent steps I have at 1.040 and just double boil then store in the freezer. I use kettle wort and just make a little extra occasionally on brew day. Just simmer it under a lid for 20min after adjusting gravity to 1.040. The lid helps keep it at 1.040. This is effectively sterilised starter wort now. If there were any surviving spores in the kettle wort they’ll ‘germinate’ overnight then get zapped by the second boil the next day. Sometimes it gets left in the fridge for 2-3 days. The trick is to pour it hot into hot, oven sterilised bottles then cap with lids boiled in water at the same time the wort is simmering. Then leave to cool before freezing. I prefer to have each step prepped individually then just pour straight into the next step when ready. Just take it out of the freezer the night or morning before use. Sometimes, for whatever reason, you might want to delay stepping up by storing the just-finished step in the fridge for a few days. It’s just more flexible to have the different steps in separate bottles, I think.
I think so.Is it worth it for the free amino acids?
I use lab bottles regardless. Been reusing them for years.BTW, are you able to reuse the mason jar lids since this is not really a pressure canning situation?
Makes sense as freezing the glass mason jars is a little dicey as well. Can you point me to the lab bottles? What material are they? I was picturing glass since you put them in the oven but I guess certain plastics would be fine at low oven temps. 250F 300F?I use lab bottles regardless. Been reusing them for years.
@Bassman2003 : McMullan won't be answering anytime soon.McMullan,
I wanted to revive this thread to get your opinion on a different approach for canning wort. The whole reason for pressure canning is to avoid the risk of Botulism. Canning guidelines say pH 4.6 is the divider between needing to pressure can or just boil. What if one lowered the pH of the starter wort to 4.6 and just boil-canned? So basically brewing a batch of beer without chilling it and storing in mason jars?
Would the yeast performance/activity be affected using pH 4.6 wort for the entire starter?
What is the better of the two choices - decreased performance with pressure canned wort or no-pressure pH 4.6 wort?
One could mix in higher pH wort or add alkalinity if 4.6 is too low for good yeast growth.
Thanks for your input.