I am trying to identify the spoilage organisms associated with tomatoes and malay apple wax. Generally, what is the appropriate number of serial dilution one has to perform to achieve best results for a colony count.
It is difficult to determine in advance the best number of serial dilution. In the case of contaminated plants I used to apply the third and fourth dilution respectively the seventh and eight.
Ten fold serial dilutions up to10^-8 needs to made. 100 µl of the third and fourth dilution respectively the seventh and eight dilution have to be plated onto agar medium with a glass rod, then incubated.
If I understand you, I will make about eight ten fold serial dilutions, plate third, fourth, seventh and eighth dilution for incubation and then find the average for the colony counts.
Depending on the incubation of preparation. Maintain consistent incubation period, then do tenfold dilutions. For example: E. coli, 20 hours of incubation at 30-35 will yield 10^9, but Pseudomonas only yield 10^8.