Inhibitors of Cell Wall Synthesis Flashcards
Which class shouldn’t be used in combination with a beta lactam?
carbapenams (cuse increase in beta lactamases)
Fosfomycin MoA
inhibits conversion of NAG to NAM by inhibiting enolpyruvate transferase enzyme
Cycloserine MoA
inhibits incorporation of D-alanine into pentapeptide by inhibiting alanine racemase - also inhibits creation of d-alanine dipeptide by inhibiting its ligase Inhibits conversion of L-ala to D-ala*
Bacitracin MoA
inhibits the binding of NAM to the cell membrane by inhibiting the dephosphorylation step in the cycling of the lipid carrier bactoprenol
Vancomycin MoA
binds to the D-ala-D-ala terminus noncovalently, and the the pentaglycine bridge of the pentapeptide - inhibits transglycosylation and transpeptidation, preventing elongation of peptidoglycan
Vancomycin resistance
bacteria can alter the D-ala-D-ala strain to prevent binding by replacing D-alanine with D-lactate. This is done by enterococci and VRSA strains. The other way is through VISA strains thickening the cell wall with increased D-ala residue
Dalbavancin
lipoglycopeptide - the same as vancomycin, but has a lipophilic side chain that allows for enhanced binding
Telavancin
disrupts the cell membrane depolarization - also a lipoglycopeptide. Depolarization is due to lipophilic side chain
Oritavancin
also a lipoglycopeptide - increases membrane permeability - can dimerize and anchor to the cell membrane, can also inhibit bacterial RNA synthesis, has an affinity for binding with D-ala-D-lactate, so effective for bacteria with vancomycin resistance