Chapter 6: Problem 16
Assume that one counted 67 plaques on a bacterial plate where \(0.1 \mathrm{ml}\) of a \(10^{-5}\) dilution of phage was added to bacterial culture. What was the initial concentration of the undiluted phage?
Chapter 6: Problem 16
Assume that one counted 67 plaques on a bacterial plate where \(0.1 \mathrm{ml}\) of a \(10^{-5}\) dilution of phage was added to bacterial culture. What was the initial concentration of the undiluted phage?
All the tools & learning materials you need for study success - in one app.
Get started for freeDescribe the origin of \(\mathrm{F}^{\prime}\) bacteria and merozygotes.
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.
Describe the basis for chromosome mapping in the Hfr \(\times \mathrm{F}^{-}\) crosses.
Influenza (the flu) is responsible for approximately 250,000 to 500,000 deaths annually, but periodically its toll has been much higher. For example, the 1918 flu pandemic killed approximately 30 million people worldwide and is considered the worst spread of a deadly illness in recorded history. With highly virulent flu strains emerging periodically, it is little wonder that the scientific community is actively studying influenza biology. In \(2007,\) the National Institute of Allergy and Infectious Diseases completed sequencing of 2035 human and avian influenza virus strains. Influenza strains undergo recombination as described in this chapter, and they have a high mutation rate owing to the error-prone replication of their genome (which consists of RNA rather than DNA). In addition, they are capable of chromosome reassortment in which various combinations of their eight chromosomes (or portions thereof) can be packaged into progeny viruses when two or more strains infect the same cell. The end result is that we can make vaccines, but they must change annually, and even then, we can only guess at what specific viral strains will be prevalent in any given year. Based on the above information, consider the following questions: (a) Of what evolutionary value to influenza viruses are high mutation and recombination rates coupled with chromosome reassortment? (b) Why can't humans combat influenza just as they do mumps, measles, or chicken pox? (c) Why are vaccines available for many viral diseases but not influenza?
In recombination studies of the \(r I I\) locus in phage \(\mathrm{T} 4\), what is the significance of the value determined by calculating phage growth in the \(\mathrm{K} 12\) versus the \(\mathrm{B}\) strains of \(E .\) coli following simultaneous infection in \(E .\) coli \(\mathrm{B}\) ? Which value is always greater?
What do you think about this solution?
We value your feedback to improve our textbook solutions.