PRESCOTT'S MICROBIO W/PROCTORIO
PRESCOTT'S MICROBIO W/PROCTORIO
11th Edition
ISBN: 9781264731060
Author: WILLEY
Publisher: MCG
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Chapter 14.6, Problem 6CC
Summary Introduction

To describe: The three stages of CRISPR/Cas response to viral infection.

Introduction: Microbial cells have various systems to fight against viral infections. The examples of such defensive systems include restriction-modification (innate system) and CRISPR/Cas system (adaptive immune system). The genetic elements of the invading virus are used as a memory by the CRISPR/Cas system to prepare for a possible future attack.

Summary Introduction

To explain: The role of quorum sensing in the CRISPR/Cas system.

Introduction: Quorum sensing is a mechanism for gene regulation in bacteria. This mechanism is dependent upon the population density and the signal molecules. This mechanism was first observed by a microbiologist Alexander Tomasz in the mid-1960s.

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19. On the diagram below a. Label the three pictures as: DNA; polypeptide; or RNA. b. Label the arrows as: translation or transcription/RNA processing. c. Add the following details to the diagram. Promoter region TATA box Transcription start site Transcription terminator Intron (A,B,C,D) Exons (1,2,3,4,5) Splice sites 5' cap 5' UTR (untranslated region) 3' poly A tail 3' UTR (untranslated region) Translational start (AUG) Translational stop (UGA, UAG, or UAA) N and C ends of polypeptide 0000
Match the letter labels in the figure below to the terms. Some letter labels are not used. MNNNNNNIN M C B A M D F E H K G 8
The diagram below illustrates a quorum sensing pathway from Staphylococcus aureus. Please answer the following questions. 1. Autoinduction is part of the quorum sensing system. Which promoter (P2 or P3) is critical for autoinduction? 2)This staphylococcus aureus grows on human wounds, causing severe infections. You would like to start a clinical trial to treat these wound infections. Please describe: a) What molecule do you recommend for the trial. Why? b) Your trial requires that Staphylococcus aureus be isolated from the wound and submitted to genome sequencing before admittance. Why? What are you testing for?  3) If a mutation arises where the Promoter P3 is constitutively active, how would that influence sensitivity to AIP? Please explain your rationale. 4) This pathway is sensitive to bacterial cell density. Describe two separate mutation that would render the pathway active independent of cell density. Briefly explain your rationale. Mutation 1 Mutation 2

Chapter 14 Solutions

PRESCOTT'S MICROBIO W/PROCTORIO

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