MICB 201 Study Guide - Midterm Guide: Enol, Depolymerization, Ciprofloxacin

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22 Jun 2016
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They disrupt a cellular process or structure in the target organism without disrupting the same process of structure in the producing organism. Most antibiotics interfere with: peptidoglycan synthesis, translation, transcription or dna replication. A few directly disrupt membranes: using the process of peptidoglycan synthesis explain how -lactam antibiotics and vancomycin work to kill bacteria. To add new peptidoglycan, bonds have to be broken in the pre-existing mesh, autolysins do this. They catalyze the breaking of the covalent o-glycosidic bonds between the nam and nag sugars creating a free end to add new pg. Transglycosylase enzyme (tg) catalyzes the joining of nam and nag extending the glycan chain. Transpeptidase enzyme (tp) catalyzes the x-linking of the glycan chains via their tetrapeptides. Penicillin prevents x-link formation by binding to and inhibiting the transpeptidase enzyme. Therefore, the new pg does not have x-links.

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