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So, 'tis the season to start planning the next 12 months of brewing sessions. Normally by this time of year I'd already have squirreled away a case or two of home canned starters for yeast propagation, or at least had a few left over to get an early bird brew session out before the Spring thaw if the weather allowed. This year however, I've been doing so much 'lockdown brewing' that my stash ran completely dry and I've had to resort to actually buying cans of Propper just to make it through 2020. Since I can't fire up the trusty pressure canner outdoors to make my own I've been searching other methods to restock my supply, free of harmful microorganisms.
My tool of implementation for this would be a Fagor-brand electric cooker/pressure cooker. Physically, the canning jars would fit. Pressure-wise, the unit only reaches a pressure of 9 psig, or a little more than .6 bar. USDA guidelines for pressure canning low acid foods to destroy botulism spores is to ensure a temperature of between 240F-250F for at least :10 minutes. At 1 bar, water boils at 250F (sea level), so I would never reach that temperature in the Fagor. Water at 9 psig/0.6 bar boils at 238F which is very close to the minimum temperature recommended for denaturing botulism spores, but close doesn't count for much when dealing with potentially deadly toxins. Although time is also a factor in the process of denaturing botulism spores, USDA cites 240F and below as insufficient to fully and safely denature all spores regardless of time.
It would seem as if this would prevent me from using this pressure cooker/canner, and yet there is a way around this 240F-250F minimum. The need to pressure can a food product is also dependent upon its acidity. High acidity foods are considered safe for canning in a standard water bath boiling at ambient sea level pressure (i.e., tomatoes @ 212F) if they have a pH lower than 4.6. Generally my pre-fermentation beer worts have a pH between 4.9~5.2. While I realize that pH is measured on a non-linear logarithmic scale, it would still seem to be simple enough to acidify starter wort from pH 5.2 to 4.6 or less with ascorbic or citric acid and thus create an inhospitable environment for botulism spores to propagate. Logically if I can safely package tomatoes at 212F and not worry about botulism because of their acidity, why not starter wort?
My methodology would be to start with sterilized jars and canning lids (cleaned, sanitized and "autoclaved" in a 275F oven for :30 mins.), mix in a pre-measured amount of DME for a 1.020 SG wort with boiling distilled water, cap and pressure cook for :20 minutes, and finally slow cool at room temperature until the lids seal. The only differences between this and my usual process of pressure canning in a 'real' pressure canner would be sterilizing the jars/lids and using distilled water instead of filtered tap water. Before I go through the process of actually wasting DME and distilled water on a fool's errand to determine pre-process pH and how much acid addition is needed to achieve <4.6 pH for a quart of wort, I'd like to hear any opinions of the safety or efficacy of this idea. Also, is there any drawback to using an acidic starter wort (pH ~4.6) when culturing yeast? Would phosphoric or lactic acids be better choices for acidification?
I'm not a chemist or microbiologist, so please be gentle with any condescending comments or thoughts about my general lack of knowledge . Thanks in advance!
My tool of implementation for this would be a Fagor-brand electric cooker/pressure cooker. Physically, the canning jars would fit. Pressure-wise, the unit only reaches a pressure of 9 psig, or a little more than .6 bar. USDA guidelines for pressure canning low acid foods to destroy botulism spores is to ensure a temperature of between 240F-250F for at least :10 minutes. At 1 bar, water boils at 250F (sea level), so I would never reach that temperature in the Fagor. Water at 9 psig/0.6 bar boils at 238F which is very close to the minimum temperature recommended for denaturing botulism spores, but close doesn't count for much when dealing with potentially deadly toxins. Although time is also a factor in the process of denaturing botulism spores, USDA cites 240F and below as insufficient to fully and safely denature all spores regardless of time.
It would seem as if this would prevent me from using this pressure cooker/canner, and yet there is a way around this 240F-250F minimum. The need to pressure can a food product is also dependent upon its acidity. High acidity foods are considered safe for canning in a standard water bath boiling at ambient sea level pressure (i.e., tomatoes @ 212F) if they have a pH lower than 4.6. Generally my pre-fermentation beer worts have a pH between 4.9~5.2. While I realize that pH is measured on a non-linear logarithmic scale, it would still seem to be simple enough to acidify starter wort from pH 5.2 to 4.6 or less with ascorbic or citric acid and thus create an inhospitable environment for botulism spores to propagate. Logically if I can safely package tomatoes at 212F and not worry about botulism because of their acidity, why not starter wort?
My methodology would be to start with sterilized jars and canning lids (cleaned, sanitized and "autoclaved" in a 275F oven for :30 mins.), mix in a pre-measured amount of DME for a 1.020 SG wort with boiling distilled water, cap and pressure cook for :20 minutes, and finally slow cool at room temperature until the lids seal. The only differences between this and my usual process of pressure canning in a 'real' pressure canner would be sterilizing the jars/lids and using distilled water instead of filtered tap water. Before I go through the process of actually wasting DME and distilled water on a fool's errand to determine pre-process pH and how much acid addition is needed to achieve <4.6 pH for a quart of wort, I'd like to hear any opinions of the safety or efficacy of this idea. Also, is there any drawback to using an acidic starter wort (pH ~4.6) when culturing yeast? Would phosphoric or lactic acids be better choices for acidification?
I'm not a chemist or microbiologist, so please be gentle with any condescending comments or thoughts about my general lack of knowledge . Thanks in advance!