NESTER'S MICROBIOLOGY: A HUMAN PERSPECT
NESTER'S MICROBIOLOGY: A HUMAN PERSPECT
9th Edition
ISBN: 9781260161373
Author: Anderson, SALM
Publisher: MCGRAW-HILL HIGHER EDUCATION
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Chapter 7, Problem 10SA
Summary Introduction

To review:

The reasons for the difficulties encountered in locating the protein-coding regions in a genomic sequence.

Introduction:

The amino acids are the building blocks of proteins. Protein encoding is initiated when a stretch of DNA (deoxyribonucleic acid) encodes genetic information for the amino acid sequence specific for the future protein. This is followed by the transcription process, in which this genetic information is transferred to mRNA (messenger ribonucleic acid) from any of the two strands of the DNA. Once the mRNA is formed, it undergoes processing steps like splicing, tailing, and capping. This removes the introns or the noncoding sequences. Ultimately, the final step occurs in protein synthesis called translation. Locating anonymous protein-codingregionsin a genomic sequence can lead to ambiguity.

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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
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