Genetics: From Genes to Genomes
6th Edition
ISBN: 9781259700903
Author: Leland Hartwell Dr., Michael L. Goldberg Professor Dr., Janice Fischer, Leroy Hood Dr.
Publisher: McGraw-Hill Education
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Chapter 7, Problem 6P
Suppose you wanted to study genes controlling the structure of bacterial cell surfaces. You decide to start by isolating bacterial mutants resistant to infection by a bacteriophage that binds to the cell surface. The selection procedure is simple: Spread cells from a culture of sensitive bacteria on a petri plate, expose them to a high concentration of phages, and pick the bacterial colonies that grow. To set up the selection you could (1) spread cells from a single liquid culture of sensitive bacteria on many different plates and pick every resistant colony; or (2) start many different cultures, each grown from a single colony of sensitive bacteria, spread one plate from each culture, and then pick a single mutant from each plate. Which method would ensure that you are isolating many independent mutations?
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You are studying a type of bacteria isolated from the acidic water runoff of a mining operation. You subject two batches of the same bacteria type to different environmental growth conditions. One batch is grown at pH 2, while the other is grown at pH 7. All other environmental parameters are kept identical between the two batches. You then collect their proteins and run a Western blot using an antibody that binds to a proton efflux pump protein (which actively expends energy to pump protons out of a cell). How would you characterize the information obtained in this experiment? What does it tell you, and why is that potentially valuable information?
In Hershey-Chase experiment, bacteriophages protein coats were tagged with radioactive isotope S-32. These phages were used to infect E. coli cells and the cells were further centrifuged to form pellets.
Why was the radioactivity level of S-32 found greater outside the cells compared to the E. coli cell pellets? Explain briefly.
If the experiment is repeated in the same manner but this time the phage protein coats are labelled with isotope X and the phage DNA with isotope Y, which isotope’s radioactivity will be found in greater amounts in the E. coli cell pellets after centrifugation? Explain briefly.
Suppose you wanted to study genes controlling thestructure of bacterial cell surfaces. You decide tostart by isolating bacterial mutants resistant to infection by a bacteriophage that binds to the cellsurface. The selection procedure is simple: Spreadcells from a culture of sensitive bacteria on a petriplate, expose them to a high concentration ofphages, and pick the bacterial colonies that grow.To set up the selection you could (1) spread cellsfrom a single liquid culture of sensitive bacteria onmany different plates and pick every resistant colony; or (2) start many different cultures, eachgrown from a single colony of sensitive bacteria,spread one plate from each culture, and then pick asingle mutant from each plate. Which methodwould ensure that you are isolating many independent mutations?
Chapter 7 Solutions
Genetics: From Genes to Genomes
Ch. 7 - The following is a list of mutational changes. For...Ch. 7 - What explanations can account for the following...Ch. 7 - The DNA sequence of one strand of a gene from...Ch. 7 - Among mammals, measurements of the rate of...Ch. 7 - Over a period of several years, a large hospital...Ch. 7 - Suppose you wanted to study genes controlling the...Ch. 7 - In a genetics lab, Kim and Maria infected a sample...Ch. 7 - The results of the fluctuation test Fig. 7.5 were...Ch. 7 - The following pedigree shows the inheritance of a...Ch. 7 - Autism is a neurological disorder thought to be...
Ch. 7 - Like the yellow Labrador retrievers featured in...Ch. 7 - Remember that Balancer chromosomes prevent the...Ch. 7 - Figure 7.14 shows examples of base substitutions...Ch. 7 - Figure 7.14a shows the mutagen 5-bromouracil 5-BU,...Ch. 7 - So-called two-way mutagens can induce both a...Ch. 7 - In 1967, J. B. Jenkins treated wild-type male...Ch. 7 - When a particular mutagen identified by the Ames...Ch. 7 - Prob. 18PCh. 7 - The Ames test uses the reversion rate His- to His...Ch. 7 - The mutant FMR-1 allele that causes fragile X...Ch. 7 - The physicist Stephen Hawking, famous for his...Ch. 7 - Aflatoxin B1 is a highly mutagenic and...Ch. 7 - In human DNA, 70 of cytosine residues that are...Ch. 7 - Bromodeoxyuridine BrdU is a synthetic nucleoside...Ch. 7 - Albinism in animals is caused by recessive...Ch. 7 - a. In Figure 7.22b, what can you say about the...Ch. 7 - Imagine that you caught a female albino mouse in...Ch. 7 - Plant breeders studying genes influencing leaf...Ch. 7 - In humans, albinism is normally inherited in an...Ch. 7 - a. Seymour Benzers fine structure analysis of the...Ch. 7 - a. You have a test tube containing 5 ml of a...Ch. 7 - Prob. 32PCh. 7 - The rosy ry gene of Drosophila encodes an enzyme...Ch. 7 - Nine rII- mutants of bacteriophage T4 were used in...Ch. 7 - In a haploid yeast strain, eight recessive...Ch. 7 - In Problem 24, you learned that Bloom syndrome is...Ch. 7 - The pathway for arginine biosynthesis in...Ch. 7 - In corn snakes, the wild-type color is brown. One...Ch. 7 - In a certain species of flowering plants with a...Ch. 7 - The intermediates A, B, C, D, E, and F all occur...Ch. 7 - In each of the following cross schemes, two...Ch. 7 - Prob. 42PCh. 7 - The following complementing E. coli mutants were...Ch. 7 - In 1952, an article in the British Medical Journal...Ch. 7 - Mutations in an autosomal gene in humans cause a...Ch. 7 - Antibodies were made that recognize six proteins...Ch. 7 - Prob. 47PCh. 7 - Prob. 48PCh. 7 - In addition to the predominant adult hemoglobin,...Ch. 7 - Most mammals, including New World primates such as...Ch. 7 - Humans are normally trichromats; we have three...
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- In transformation, a bacterial cell takes up DNA fragments from its surroundings. The figure shows the process of natural transformation. Position the labels below with the correct images. (A) Donor and recipient genomes The donor strand is integrated into the recipient chromosome and the displaced bacterial DNA is degraded. A wild-type donor cell is in the vicinity of a double auxotroph. If the wild-type cell lyses, it releases DNA into the environment. One cell is identical to the original recipient, while the other carries the wild-type genes. A competent recipient cells a receptor site on its surface. One strand of donor DNA enters the cell and pairs with a homologous region of the bacterial chromosome The remaining DNA strand is degraded. A donor DNA strand binds to the receptor site. Reset trpC1 Wild-type donor cell Mechanism of natural transformation Donor DNA hal Receptor site- trpc/his double auxotroph Recipient cell Competent cell recipient -Bacterial chromosome (had.bpC") Ma…arrow_forwardImagine that you are a student in Alfred Hershey and Martha Chase’s lab in the late 1940s. You are given five test tubes containing E. coli bacteria infected with T2 bacteriophages that have been labeled with either 32P or 35S. Unfortunately, you forget to mark the tubes and are now uncertain about which were labeled with 32P and which with 35S. You place the contents of each tube in a blender and turn it on for a few seconds to shear off the phage protein coats. You then centrifuge the contents to separate the protein coats and the cells. You check for thepresence of radioactivity and obtain the following results. Which tubes contained E. coli infected with 32P-labeled phage? Explain your answer.arrow_forwardYou have found that two types of bacteria (one large, one small) can undergo horizontal gene transfer. The smaller cells encode the green fluorescent protein (GFP), and the large cells do not glow. You mix the two types of cells together, and allow them to grow together on an agar plate. The next day, you find that some of the larger cells have acquired the gfp gene and now glow green, indicating that the gene has moved from the smaller cells to the larger cells. You want to determine whether this is occurring via conjugation, transformation, or transduction. You have available a few different experimental tools: -Pure cultures of the large, non-glowing bacteria -Pure cultures of the small, gfp-expressing, glowing bacteria -0.2 µm filters (will trap both types of cells, but will let other smaller materials through) -DNase enzyme (degrades DNA) -Fluorescent microscopes and electron microscopes -All other necessary test tubes, liquid growth media, agar plates, etc Briefly outline a…arrow_forward
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