Brock Biology of Microorganisms (15th Edition)
15th Edition
ISBN: 9780134261928
Author: Michael T. Madigan, Kelly S. Bender, Daniel H. Buckley, W. Matthew Sattley, David A. Stahl
Publisher: PEARSON
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Chapter 7.10, Problem 2MQ
Summary Introduction
Peptidoglycan otherwise murein is a kind of
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Results from a Kirby Bauer antibiotic assay on a Gram-negative bacterial culture are described as follows: A) the bacterium is resistant to penicillin, an antibiotic that targets synthesis of the peptidoglycan cell wall and B) the bacterium is resistant to tetracycline, an antibiotic that targets the small subunit of the ribosome, inhibiting protein synthesis. Which of the results represents intrinsic resistant and which represents acquired resistants?
Usually, bacteria only make tryptophan when
tryptophan is absent or available in low
concentration. However, a particular bacterial
mutation makes tryptophan all the time
whether or not tryptophan is present. What
could explain this phenotype?
A) the terminator hairpin is unable to form
B) the antiterminator hairpin is unable to form
C) trpE is mutated
D) trpD is mutated
E) trpA is mutated
Various antimicrobial drugs to treat microbial infection have diverse mechanism of action. Consider the following antimicrobial drugs:
A. Seconeolitsine, known as DNA topoisomerase I inhibitor in bacteria.
(i) Explain briefly how inhibiting DNA topoisomerase I is a good mechanism of action for an antibiotic, include possible molecular machineries being targeted.
(ii) What would be an appropriate response if seconeolitsine works well by stating the state of supercoiling in bacteria.
(iii) To prove your answer (ii), you test the condition of bacterial DNA by running gel electrophoresis, one has been treated with seconeolitsine (+ sample) and the other one is not (- sample). Explain the position of each + sample and – sample band on the gel in reference to the point of origin (where you load your samples) or how far each DNA sample travel across agarose gel.
(iv) Explain why you would expect answer (iii) for each + sample and – sample.
B.…
Chapter 7 Solutions
Brock Biology of Microorganisms (15th Edition)
Ch. 7.1 - What is the utility of a reporter gene?Ch. 7.1 - Prob. 2MQCh. 7.1 - Prob. 1CRCh. 7.2 - Prob. 1MQCh. 7.2 - Prob. 2MQCh. 7.2 - Prob. 1CRCh. 7.3 - What is the divisome?Ch. 7.3 - How does FtsZ find the cell midpoint of a...Ch. 7.3 - What is the role of the penicillin-binding protein...Ch. 7.4 - How does MreB control the shape of a rod-shaped...
Ch. 7.4 - What protein is thought to control the shape of...Ch. 7.4 - What relationships exist between cytoskeletal...Ch. 7.4 - What morphology do cells have that lack MreB or...Ch. 7.5 - Prob. 1MQCh. 7.5 - What is transpeptidation and why is it important...Ch. 7.5 - Prob. 1CRCh. 7.6 - How are different sets of genes expressed in the...Ch. 7.6 - Prob. 2MQCh. 7.6 - Prob. 1CRCh. 7.7 - Why are the levels of DnaA protein controlled...Ch. 7.7 - Prob. 2MQCh. 7.7 - Prob. 1CRCh. 7.8 - Prob. 1MQCh. 7.8 - What is the major transcriptional regulator that...Ch. 7.8 - What is meant by "patterning" during heterocyst...Ch. 7.9 - What are the four basic stages of biofilm...Ch. 7.9 - Besides autoinducer synthesis, what intracellular...Ch. 7.9 - What type of genes does c-di-GMP activate during...Ch. 7.10 - Describe two targets of antibiotics and discuss...Ch. 7.10 - Prob. 2MQCh. 7.10 - Prob. 3MQCh. 7.10 - Prob. 1CRCh. 7.11 - Is persistence a heritable trait?Ch. 7.11 - What prevents the toxin component of TA modules...Ch. 7.11 - Prob. 3MQCh. 7.11 - Prob. 1CRCh. 7 - If DnaA was not regulated in Escherichia coli and...Ch. 7 - Explain how cells exhibiting different phenotypes...Ch. 7 - Describe how you would genetically design a...
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- Give two reasons why E. coli is naturally resistant to antibiotics like Penicillin?arrow_forwardWhat would happen to a bacteria that lost a plasmid for antibiotic resistance? Would it still be able to grow in normal growth conditions? Explain.arrow_forwardAntibiotics that target bacterial molecules not previously exploited are desperately needed. One such target is the protein FtsZ. The small molecule 3-methoxybenzamide (3-MBA) is known to inhibit FtsZ in Bacillus subtilis but is not bacteriocidal. Nonetheless, researchers reasoned that 3-MBA offered a good starting point for the synthesis of a molecule that might be a potential drug candidate. Over 500 3-MBA analogues were synthesized and screened; one called PA190723 was extremely potent in its capacity to bind FtsZ and inhibit bacterial growth. In fact, when used in a mouse model, PA190723 was bacteriocidal against methicillinand multidrug-resistant Staphylococcus aureus. What makes FtsZ a good drug target? What preliminary information about 3-MBA would be helpful if you were designing the 3-MBA analogues? As these researchers move forward with clinical (human) testing, what other parameters and outcomes must be assessed besides the bacteriocidal activity of PA190723?arrow_forward
- Resistance to many penicillins is the result of cell wall mutations in a variety of bacteria. True or false?arrow_forwardBelow, you can see a picture of an antimicrobial drug. Regarding semi-synthetic antimicrobial drug development to try to avoid development of antibiotic resistance, use 1 sentence to address what is the significance/value of the presence of the various R-groups (e.g. R4, R5, R6, etc.)?arrow_forwardWhat is the underlying molecular mechanism of action for the antibiotic novobiocin?arrow_forward
- The human intestinal tract is home to a vast, diverse microbial community. The bacteria that comprise this microbial community serve a number of important, beneficial functions. However, some bacterial species have been suggested to play a role in certain forms of cancer. One such bacteria is Fusobacterium nucleatum (i.e., F. nucleatum). Investigators wishing to study the role of F. nucleatum in colorectal cancer developed a new assay for detecting these bacteria in tumor tissue. In controlled experiments, the test was highly sensitive in detecting F. nucleatum and also had high specificity. To examine consistency in their test findings, the investigators also conducted repeat tests in 50 tissue samples. From these repeat tests, the investigators observed that the overall number of samples in which F. nucleatum was detected was almost identical (10 out of 50 on the first test vs. 11 out of 50 on the repeat test); for 9 samples, F. nucleatum was detected on both the initial and the…arrow_forwardWhy are structural analogs of sugar molecules (such as Oseltamivir and zanamivir) effective in treatment of influenza-virus infection?arrow_forwardYou have isolated a beta-lactamase producing Staphylococcus aureus (not a MRSA strain) from an infected surgical site on your patient. If for genetic reasons, your patient is allergic to all antibiotics except beta-lactam antibiotics such as ampicillin ( they can only take Beta-lactam antibiotics such as ampicillin), which strategy below could you use to treat this Staphylococcus aureus infection in your patient? Note different answers compared to previous question. give the patient erythromycin can use a beta-lactamse resistant beta-lactam such as methicillin or oxacillin O give the patient penicillin give the patient an azole drugarrow_forward
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