Let me try to touch on a few things that have been brought up.
The plates are from White Labs online shop at yeastman.com - anyone can set up an account and order online. Be aware that some selective media plates have a very short shelf life. One product that I wish I bought in quantity is their sterile 50mL vials. They have a conical bottom, but also a ring to keep it upright. It’s a great vessel for the first step of growing up some yeast. I did have one contaminated agar plate from them. I’m hoping that it was a fluke and not a QC problem on their end. As an aside, I picked two colonies from the contaminated plate to step up and they are putting out some serious honey aroma. I know pentanedione is supposed to be a flaw, but right now is smells really nice to me. I’ll post more about my experience with WLP??? in the future.
As far as the experiment setup goes, I was not as concerned with the overall microbicidal activity of each sanitizer as I was in simply checking the effectiveness of each as a surface sanitizer for typical use in my home brewery. I am starting with equipment that I consider sufficiently clean of organic soils - everything cold side gets an extended soak and/or circulation with PBW and inspected for crud. I’m sure there are more accurate ways to test this out, but I still contend that my setup is a decent surrogate for this.
I am not claiming that the Star San is a superior disinfectant for treating heavily contaminated equipment. For those you need something broad spectrum (or just toss it if it’s easily replaceable). But I do think that it passes the “close enough for government work” sniff test for clean equipment that will be innoculated with an active and/or sizeable pitch of brewer’s yeast. I also think that an important part of sanitization that is easy to overlook is the “must remain wet for the entire required contact time” part of things. The foaming action of Star San is a big asset in this department. I suspect that once I flipped the agar plates to dry that some Star San clung to the plate for a while, essentially extending its contact time for a bit.
FYI - One of the reasons I chose tap water over an untreated plate as my control was to rule out a simple mechanical action of washing the contaminants off the surface as the primary mechanism of action. That certainly wasn’t the case here. That seems to strengthen the case that at least some antimicrobial activity is at work here.
Regardless of my results, if I were working with a slant of a culture that costs well beyond the total of all my other ingredients in a batch, I would certainly be using something as broad-spectrum as possible and ensuring it stayed wet for an extended contact time. Or just flamed anything possible.
Personally, my motivation for performing this experiment was that I felt myself falling into the trap of applying my medical knowledge of disinfectants to the brewery. But the goals are completely different - in medicine your goal is to reduce the count of pathogens to as close to zero as possible. In the brewery, we just need to reduce the amount of contaminants to a level where your pitch of yeast can rapidly outcompete them. Frankly, looking at the sparse dozen or so colonies on the iodophor plate, that’s probably well within the acceptable window.
One more random tangent I’ve thought of while mulling this all over - a solution containing both concentrated Iodophor and Star San diluted to the appropriate concentrations may pose the best of both worlds. The acidity of the Star San enhances the effect of iodophor, and the surfactant will keep it in place longer. Or I could just be half-asleep and rambling lol.