hylander0
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- Jan 8, 2015
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I want to lay out a problem we as us home brewers deal with from time to time and get some feedback. Pitch rates and proper, healthy yeast propagation.
Situation: You have your 10 Gallons of 1.058 OG beer planned out. You have one healthy vial of yeast containing approx. 90 billon cells and that is the all you can get![Frown :( :(](data:image/gif;base64,R0lGODlhAQABAIAAAAAAAP///yH5BAEAAAAALAAAAAABAAEAAAIBRAA7)
Problem: You need 405 Billion and you can only use your stir plate & 2L Erlenmeyer flask
Facts (see source below):
Healthy Yeast Propagation Wort should be between 1.020 SP & 1.030 SP, Limit # of steps - More stepping introduces more chances for contamination and Keep as close to 72 degrees F as possible
Source
My Solution (Calculator)
1. Start and finish 1.5 L starter @ 1.030 with 90 B cells
2. Decant Starter and Remove 3/4 of the slurry in to Sanitized Jar for pitching
3. Start and finished 1.5 L @ 1.030 with 65 B cells
4. Decant Starter and Remove All of the slurry in to Sanitized Jar for pitching
5. Done
Given the growth rate is next to nothing after 200 B in a 2L flask then I would have no choice but to do this.
I would like some feedback on this conquer and divide stepping up technique. Thoughts on this? Given my situation what have to done in the past (obviously besides using a bigger flask to step up)?
Situation: You have your 10 Gallons of 1.058 OG beer planned out. You have one healthy vial of yeast containing approx. 90 billon cells and that is the all you can get
Problem: You need 405 Billion and you can only use your stir plate & 2L Erlenmeyer flask
Facts (see source below):
Healthy Yeast Propagation Wort should be between 1.020 SP & 1.030 SP, Limit # of steps - More stepping introduces more chances for contamination and Keep as close to 72 degrees F as possible
Source
My Solution (Calculator)
1. Start and finish 1.5 L starter @ 1.030 with 90 B cells
a. Cells propagated: 262 B
2. Decant Starter and Remove 3/4 of the slurry in to Sanitized Jar for pitching
a. Cells in Flask: 65 B
b. Cells in Jar: 197 B
3. Start and finished 1.5 L @ 1.030 with 65 B cells
a. Cells propagated: 209 B
4. Decant Starter and Remove All of the slurry in to Sanitized Jar for pitching
a. Cells in Jar: 197 B + 209 B = 406 B
5. Done
Given the growth rate is next to nothing after 200 B in a 2L flask then I would have no choice but to do this.
I would like some feedback on this conquer and divide stepping up technique. Thoughts on this? Given my situation what have to done in the past (obviously besides using a bigger flask to step up)?