A plaque assay is performed beginning with 1 mL of a solution containing bacteriophages. This solution is serially diluted 4 times by combining 0.1 mL of each sequential dilution with 9.9 mL of liquid medium. Then 0.1 mL of the final dilution is plated in the plaque assay and yields 28 plaques.What is the initial density of bacteriophages in the original 1 mL? Recall that initial phage density = (plaque number/mL) × (dilution factor). (It is not A or C)
a.2.8 x 106 pfu/ml
b.2.8 x 1016pfu/ml
c.2.8 x 108 pfu/ml
d.1.4 x 108 pfu/ml
e.5.6 x 108 pfu/ml
Given that, 0.1 mL of diluted suspension yielded 28 plaques; therefore, the number of plaque forming units = b.2.8 x 1016pfu/ml
A plaque assay is performed beginning with 1 mL of a solution containing bacteriophages. This solution...
I got half credit for this question and not sure what I got
wrong. Please do the math and explain.
A microbiology student was carrying out an independent research project in which he needed to know the number of infectious phage particles added during a particular step in an experimental protocol. In preparation for the experiment, he passed a crude mixture of phage plus infected bacteria through a 0.45 micrometer filter and collected the filtrate (portrayed below in the green-capped...
1. Vibrio bacteria are abundant in ocean and aquatic environments. Suppose you wish to isolate Vibrio- specific bacteriophages from seawater. You enrich your sample by spiking the seawater with growth medium and Vibrio fischer. You then isolate your phage and plate it on lawns of bacterial growth to enumerate how many PFUs/mL are in your sample. a. You set up a series of 10-fold phage dilutions out to a TDF of 10', and you plate each of those dilutions mixed...