The isolates were identified based on colony characteristics and biochemical profile including oxidase, indole production, methyl red, VP, citrate utilization, glucose fermentation, lactose fermentation, Na requirement, tripple sugar iron, motility tests and growth on EMB agar
Prior to testing samples, the efficiency of the two media was assessed, under controlled conditions using five standard strains mentioned above and was found to be 100% for both EMB agar
and Hicrome E.
Samples were cultured on blood agar & EMB agar
The growth medium's used during the entire process include Nutrient agar, Macconkey's agar, EMB agar
and Mannitol salt agar
Growth patterns were observed using EMB agar
and KKA agar.
In order to test this, goose fecal, influent, effluent, and river water samples were collected and isolated by being streaked onto EMB agar
The loopful of culture, from the positive presumptive tube was streaked on sterilized EMB agar
was isolated, by placing EMB agar
plate in open in room for 20 minutes and then incubating it for 24 hours at 37degC.
coli, while picked up and streaked upon EMB agar
radioresistens delayed bacterial identification, and it was not until the organism was later observed growing on EMB agar
that an incorrect diagnosis was suspected.
No Test Pseudomonas Enterococcus aeruginosa faecalis 1 Nutrient Agar + + 2 MacConkey agar Pink color White 3 Blood agar Beta hemolytic - 4 EMB agar
- - 5 Manital salt agar.