This SOP is intended for people who have ample knowledge in micro, lab, and sterile techniques. You must also be comfortable and able to work with agar petri dishes and culture media without contamination issues.
The Goals of this SOP is to.
1. Describe the laboratory step-up procedure of yeast from a pure culture (from a slant of ordered culture) to a large enough volume to pitch the 3 barrel propagator
2. Detail Yeast Propagation in the 100 Gallon Propagator
3. Deliver 1st generation yeast to the brewery at pitchable quantities(40-60bbl fermentations) in a short period of time(about two weeks) without the cost associated with buying large pitches
First of all you'll want to obtain a clean culture from your culture collection (Refrigerated petri dishes with colonies, Slants, or your LHBS vials)


streak out your yeast onto YPD(yeast peptone dextrose) agar plates. and incubate them at 22-24C for a couple days until you get nice distinct isolated colonies. It will take some practice to achieve good streak plates if you've never done this before
The objective here is to get nice individual colonies to pick, these colonies will be the inoculant for 100mL flasks as the first stage of propagation.
you want to avoid petite colonies and ones that otherwise look out of the ordinary.



picked colonies will get transferred directly into 250mL flasks filled with 100mL of sterilized wort with very low BUs or none.
The wort you use for propagation should be about 8-12 plato
as you can see in the above pictures 500mL media bottles were used to collect and autoclave the wort. the flasks were autoclaved separately with their stoppers on a dry cycle. then the sterilized wort is transferred into the flasks leave the trub behind, remember good sterile technique in transferring the sterile wort to the flasks, I like to transfer the wort at boiling temperatures into the flasks and then let it cool in the flasks. You can see the trub left behind in the media bottles, you don't want to let that stuff get into the flasks.
Pick a bunch of colonies from your YPD plate with a sterilized inoculation loop and inoculate the wort in the flasks, flame the lip of the bottle for transfers and inoculation (good micro technique)
target for inoculation is 15-20 million cells per mL
Incubate the flasks with agitation on an orbital shaker at 150 RPM for 2-3 days at 22-24C
you should end up with 100-200 million cells per mL
The Goals of this SOP is to.
1. Describe the laboratory step-up procedure of yeast from a pure culture (from a slant of ordered culture) to a large enough volume to pitch the 3 barrel propagator
2. Detail Yeast Propagation in the 100 Gallon Propagator
3. Deliver 1st generation yeast to the brewery at pitchable quantities(40-60bbl fermentations) in a short period of time(about two weeks) without the cost associated with buying large pitches
First of all you'll want to obtain a clean culture from your culture collection (Refrigerated petri dishes with colonies, Slants, or your LHBS vials)
streak out your yeast onto YPD(yeast peptone dextrose) agar plates. and incubate them at 22-24C for a couple days until you get nice distinct isolated colonies. It will take some practice to achieve good streak plates if you've never done this before
The objective here is to get nice individual colonies to pick, these colonies will be the inoculant for 100mL flasks as the first stage of propagation.
you want to avoid petite colonies and ones that otherwise look out of the ordinary.
picked colonies will get transferred directly into 250mL flasks filled with 100mL of sterilized wort with very low BUs or none.
The wort you use for propagation should be about 8-12 plato
as you can see in the above pictures 500mL media bottles were used to collect and autoclave the wort. the flasks were autoclaved separately with their stoppers on a dry cycle. then the sterilized wort is transferred into the flasks leave the trub behind, remember good sterile technique in transferring the sterile wort to the flasks, I like to transfer the wort at boiling temperatures into the flasks and then let it cool in the flasks. You can see the trub left behind in the media bottles, you don't want to let that stuff get into the flasks.
Pick a bunch of colonies from your YPD plate with a sterilized inoculation loop and inoculate the wort in the flasks, flame the lip of the bottle for transfers and inoculation (good micro technique)
target for inoculation is 15-20 million cells per mL
Incubate the flasks with agitation on an orbital shaker at 150 RPM for 2-3 days at 22-24C
you should end up with 100-200 million cells per mL
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