Chapter 6: Problem 12
Define plaque, lysogeny, and prophage.
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Chapter 6: Problem 12
Define plaque, lysogeny, and prophage.
These are the key concepts you need to understand to accurately answer the question.
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A plaque assay is performed beginning with \(1 \mathrm{mL}\) of a solution containing bacteriophages. This solution is serially diluted three times by combining 0.1 mL of each sequential dilution with \(9.9 \mathrm{mL}\) of liquid medium. Then 0.1 mL of the final dilution is plated in the plaque assay and yields 17 plaques. What is the initial density of bacteriophages in the original 1 mL?
Describe the basis for chromosome mapping in the Hfr \(\times \mathbf{F}^{-}\) crosses.
Explain the observations that led Zinder and Lederberg to conclude that the prototrophs recovered in their transduction experiments were not the result of \(\mathrm{F}^{+}\) mediated conjugation.
Why are the recombinants produced from an Hfr \(\times \mathrm{F}^{-}\) cross rarely, if ever, \(\mathrm{F}^{+}\) ?
Two theoretical genetic strains of a virus \(\left(a^{-} b^{-} c^{-} \text {and } a^{+} b^{+} c^{+}\right)\) were used to simultaneously infect a culture of host bacteria. Of 10,000 plaques scored, the following genotypes were observed. Determine the genetic map of these three genes on the viral chromosome. Decide whether interference was positive or negative.
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