
Martin S. answered 04/12/20
Patient, Relaxed PhD Molecular Biologist for Science and Math Tutoring
To get the original concentration of bacteria, first divide the number of colonies by the volume plated, then multiply by the dilution factor. That assumes that each colony is derived from a single cell. This is statistically valid for plates with between 30 and 300 colonies, so no problem with the data.
The plating volume was 1000 microliters, or 1 milliliter, so there were 32 cells per milliliter in the plating suspension. That in turn was diluted by 10-4 prior to plating. The dilution factor is the inverse of the dilution, so in this case it would be 104. Multiply that by the concentration that was plated, and you have 32 x 104, = 3,2 x 105 cells per milliliter in the original suspension.
Hope this helps.

Martin S.
Glad to help04/13/20
Kokoo A.
Thank you it helped a lot :)04/13/20