Microbiology: An Evolving Science (Fourth Edition)
Microbiology: An Evolving Science (Fourth Edition)
4th Edition
ISBN: 9780393615098
Author: John W. Foster, Joan L. Slonczewski
Publisher: W. W. Norton & Company
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Chapter 7.2, Problem 3TQ
Summary Introduction

To review:

The reason behind the visibility of nalidixic acid-resistant cells even after containing the mutation in gyrA.

Introduction:

The enzyme that changes the supercoiling of the deoxyribonucleic acid (DNA) or regulates the supercoiling level in DNA (deoxyribonucleic acid) is known as topoisomerase. There are two types of topoisomerase present in a cell, topoisomerase I and topoisomerase II. Type I topoisomerase enzymes function by creating transient a single-stranded breaks while type II introduces transient double-stranded breaks.

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Why would a mutation in a somatic cell of a multicellular organism escape detection?
Cytosine can be deaminated to form Uracil   What type of mutation is this classified as? Discuss what happens to the base-pairing properties from switching from C to U? When U is replicated in two rounds of synthesis, what substitution does this result in? Before Uracil alters the DNA during replication, what repair system can be used to correct this error? Describe how this type of DNA repair works?
Given that a faulty ribosomal protein is the culprit and causes DBA, discuss the possible role of normal ribosomal proteins. Why might bone marrow cells be more susceptible to such a mutation than other cells?
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