| Term 
 
        | Fosfomycin (Monurol®) -- mechanism       |  | Definition 
 
        | Cell Wall Synthesis Inhibitor structural analog of phosphoenol pyruvate (PEP),  blocks  step-1 PDG synthesis 
 
 In Step 1: Synthesis of muramic acid (which ends up becoming the glycocele backbone of peptidoglyan) |  | 
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        | Term 
 
        | Fosfomycin (Monurol®) -- general info |  | Definition 
 
        |   broad spectrum antibiotic Resistance emerges quickly from multiple doses Mild adverse effects = diarrhea, vaginitis Uses = single dose oral treatment of uncomplicated UTIs |  | 
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        | Term 
 | Definition 
 
        | Cell wall synthesis inhibitor structural analog of D-alanine--blocks 2 steps in PDG synthesis (1&2) 
 inhibits conversion of D-alanine dipeptide which ends up becoming the end of the peptide for strength and stability of cell wall.  |  | 
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        | Term 
 
        | D-cycloserine - general info |  | Definition 
 
        | Broad spectrum Serious CNS effects (headache, convulsions)- reversible & dose related Used for second-line TB drug |  | 
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        | Term 
 | Definition 
 
        | Cell wall synthesis inhibitor Inhibits step 3 Depletes lipid carrier for PDG synthesis |  | 
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        | Term 
 
        | Bacitracin - general info |  | Definition 
 
        | topical application only narrow spectrum Severe nephrotoxicity used for skin & opthalmologic infections Good in combo w/ polymyxin B |  | 
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        | Term 
 
        | Vancomycin (Vancocin) - mechanism |  | Definition 
 
        | Cell Wall Synthesis Inhibitor Inhibits step 4 & 5 – Binds D-Ala – D-Ala terminus of pentapeptide – Blocks PDG synthesis (step 4: transglycosylase) and X-linking (step 5: transpeptidase) by binding the substrate |  | 
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