Well, after all the times I’ve told S. Cerevisiae that I’ve tried it and didn’t \care for the results, I decided it was time to give his procedure a fair trial. Here’s what happened…Old Dog…New Tricks | Experimental Brewing
That’s my problem, timing high krausen. So, ive been using 2L oxygenated and shook wort, pitching the smack pack about 6pm before brew day. Brew morning, ~12 hrs later, I put it in the fridge. Then I end up decanting about 80% and pitching about 6pm after brewing two batches that brew day. That works great, but I’d be curious to know how the masters of this technique are timing it for a 1L high krausen total contents pitch.
After discussing it with Mark, I’m not sure being exactly at high krausen makes a world of difference. I was close and judging by the looks of things, it was close enough. I was using a 3 month old smack pack and I wanted to be sure it had enough time. I decided that was more important than being exactly at high krausen when I pitched. I also decided that 1 qt. of starter wort in my beer probably wouldn’t have much noticeable effect. That part remains to be tested.
Mark, if you had to quantify a general time frame for predicting high krausen in a shook or oxygenated 1L starter with a fresh smack pack, what would it be? Would it be different for ale vs lager?
I think I’m in the ball park. My last starters were 6 day old 1056 that were in starters for 12 hrs before putting in the fridge. I gave them a little swirl and the wife saw it, thought they were going to explode. Then about 10 maybe 12 hrs later I removed from the fridge, decanted and pitched. Had blowoff in 12 hrs after that.
But I’m wondering if I should make my starters with 1L, morning of brew day, and pitch the whole thing that evening (12 hrs later) Maybe 2L for lagers 1L for ales.
Jim, it sounds like you have the process dialed-in for your environment. As much as I would like say that culture X pitched into 1L of starter wort is going reach high krausen at time X, yeast behavior just cannot be quantified to that level of precision in a general way, especially when things such as water composition, wort composition, incubation time, and incubation temperature are factored into the equation. That’s why I give a window of between 12 and 18 hours after inoculation. The best thing that one can do is what you are doing; namely, inoculating, observing, and adjusting the incubation time frame per one’s observations.
In your case, I would feel comfortable making the starter in the morning and pitching 12 hours later. The worst case scenario is that you have to place a chilled batch of wort in your fermentation chamber for a few hours. The one area where Wyeast absolutely blows White Labs out of the water is that one knows something about how the culture will perform before pitching it into starter wort. Wyeast smack packs have built-in proofing. If the pack swells, the culture is good. The rate at which the pack swells also provides insight into the condition of the culture as well as to how well it will respond when pitched into starter wort.
I used the shaken method last weekend and pitched a very active 1.6 liter starter (with 160g of dme) pitched about 18 hours after making the starter.
I was surprised at the gravity reading I took yesterday, 6 days after brewing, which had gone from 1.048 to 1.020. I really expected it to be finished by now.
It’s a Belgian Witbier recipe that I’ve made a dozen times or so using Wyeast 3944, fermented in the mid 60’sF.
So that’s one variable that would be measurable, if it’s not an anomaly.
So, basically this way I can use a smaller starter and still be good.
I usually use dry yeast, but this easy smaller starter method would make using more liquid yeast a good option.
The smaller starter volume comes from pitching at high krausen. As I mentioned above, it is important to use a vessel that is at least four times the volume of the starter, and the media must be shaken until there is more foam than liquid, preferably as much foam as the media can produce (it is very difficult to shake a starter that vigorously without a screw on cap). For example, using a 2L flask to prepare a 1L shaken, not stirred starter is a no-no, and so is using a 1 gallon jug or 5L flask to prepare a greater than 1L starter. I used a 1 gallon jug to prepare 1 quart and 1 liter starters for years before I found NOS 5L and 10L media bottles at price points that I was willing to pay.
With the above said, I shared this method with the community because I felt that there was a need for a low-cost, low-tech, shear stress-free method for producing a healthy starter. I hope that people do not attempt to generalize the method in the way that many specific methods have been generalized by the community. It usually works without fail if all of the conditions are met.
Wow…why is that Mark? I made a 1 qt. starter in a gal. jug, but I often use that same jug for 2-3 qt. starters. How does vessel size relate to starter quality? Thanks!
I think low cost and low tech are great, but I don’t know anyone who has experienced shear stress so it seems weird to worry about it. It seems like worrying about HSA all over again.
The requirement has mostly to do with expansion into foam. The method is dependent on turning the media into as much foam as is possible because foam has a very high specific surface area, and gas dissolves into a liquid at the interface between the gas and the liquid. A liquid-gas foam composed of gas entrapped in very thin layers of liquid.
I would appreciate your adding the vessel volume to starter volume ratio requirement to the blog entry because methods have a way of getting blown out of proportion on the Internet. Yeast rinsing is an example of what happens when a very specific method is let loose in the home brewing community without bounds being placed on it. Yeast rinsing is a generalization of a method used to store colony forming units under autoclaved distilled water in a laboratory setting. However, the generalization does not meet the original requirements for having an absolutely nutrient-free culture, nor does it include that the storage solution has to be autoclaved distilled water. There’s no way to rinse a cropped culture completely free of nutrients in a home setting, as the process requires a centrifuge.