Table of Contents
Cell Wall Synthesis Inhibitors
A peptidoglycan monomer consists of 2 joined amino-sugars, N-acetyl glucosamine (NAG) and N-acetyle muramic acid (NAM), with a pentapeptide coming off of the NAM. So, a peptidoglycan monomer is a NAG-NAM-pentapeptide. These peptidoglycan monomers are synthesized in cytosol and transported across cytoplasmic membrane by Bactoprenols (BP). Transglycosylase (Transglycosidase) enzymes insert and link new peptidoglycan monomers into the breaks in peptidoglycan (chain elongation). Finally, transpeptidase enzymes reform the peptide cross-links between the rows and layers of peptidoglycan to make the wall strong (cross-linking).
Enolpyruvate transferase converts UDP-N-acetylglucosamine to UDP-N-acetylmuramic acid. L-alanine racemase, forms D-alanine from L-alanine, and D-alanylalanine synthetase (ligase) incorporates D-alanine into the pentapeptide.
Mnemonic: Firmly Bind to Bacterial Cell Vall – EaT BAT
The cell wall inhibitor antimicrobials and the steps they inhibit are:
- Fosfomycin: Enoylpyruvate transferase (EPT) – NAG to NAM conversion
- Beta-lactam: Transpeptidase (TP) – Cross-linking
- Bacitracin: Bactoprenol (BP) dephosphorylation (Transfer of NAG-NAM-pentapeptide from cytosol to cell membrane)
- Cycloserine: Alanine racemase and ligase (Pentapeptide formation)
- Vancomycin: Transglycolase (Chain elongation)
All these drugs are BACTERICIDAL.
Beta-lactams include: Penicillins, Cephalosporins, Monobactams and Carabapenems
Mycobacterial cell wall = Peptidoglycan + Mycolic acid + Arabinogalactan
- Isoniazid and Pyrazinamide: Prevents mycolic acid synthesis (Action of pyrazinamide is often mentioned as unknown in books)
- Ethambutol: Prevents mycolic acid incorportation into cell wall (inhibits arabinogalactan transferase)
All 1st line ATT drugs are bactericidal except ethambutol which is bacteriostatic.
Fungal cell wall = Beta-glucan polymers equivalent to bacterial peptidoglycan
- Echinocandins: Inhibit beta-glucan synthesis (fungicidal against yeasts like candida and fungistatic against molds)
We can understand the translation using a cook book analogy. Suppose:
- Restaurant = Cell
- Recipe book = DNA
- A single recipe page = Gene
- Photocopier = RNA polymerase
- Photocopied recipe page = mRNA
- Chef and his spectacles = Ribosome (Suppose 50S ribosome is the chef and 30S ribosome is his spectacles)
- Kitchen hands = tRNA
- Ingredients = Amino acids
- Final food = Protein
Chef reads photocopied recipe page and kitchen hands bring ingredients to the chef to make food (protein).
a. Tetracycline and Tigecycline: Prevents meeting of kitchen hand with the chef (bind to 30S subunit of ribosome and interfere with binding of tRNA to ribosomal complex)
b. Aminoglycosides: Replaces the spectacles of chef, so that he reads the recipe incorrectly (bind to 30S subunit of ribosome and causes mRNA codon to misread)
c. Linezolide (Oxazolidinone): Doesn’t allow chef to wear spectacles to start cooking (bind to 50S subunit of ribosome and prevents formation of 50S/30S initiation complex)
d. Macrolides, Clindamycin (Lincosamides), Streptogramins (Quinupristin, Dalfopristin) and Pleuromutilin: Prevents chef from reading of further steps in photocopied recipe page (bind to 50S subunit of ribosome and prevents translocation-movement of ribosome along mRNA)
e. Chloramphenicol: Prevents kitchen assistant from adding ingredients (bind to 50S subunit of ribosome and prevents peptide bond formation)
f. Rifampicin: It damages the photocopier (inhibits RNA polymerase)
Mnemonic: ATT 30 and CELLS 50
- Binds to 30S: Aminoglycoside, Tetracycline, Tigecycline
- Binds to 50S: Chloramphenicol, Erythromycin (Macrolides), Linezolid, Lincosamide (Clindamycin), Streptogramins (-pristins)
Mnemonic: Take the 1st letter of drug for mechanism of action
- Tetracycline and Tigecycline: inhibits incoming T-RNA attachment to ribosome
- Aminoglycoside: Alters ribosome
- Linezolid: Link disruption between 50S and 30S ribosome
- Chloramphenicol: Chain elongation inhibition of protein
- Rifampicin: RNA polymerase inhibitor (inhibits transcription)
- All other: Preven translocation
All these drugs are BACTERIOSTATIC except Aminoglycosides and Streptogramins.
Affecting Cell Membranes
a. Polypeptides: Polymixin B, Colistin, Tyrothricin (Binds to lipopolysacharide and phospholipid of outer cell membrane in gram negative organism and eventually breaks inner cell membrane as well; bactericidal)
b. Glycolipopetides: Daptomycin (disrupts the action potential of gram positive cell membrane; bactericidal)
c. Polyene: Amphotericin B, Nystatin, Hamycin, Natamycin (Binds to ergosterol; fungistatic)
d. Azoles: Ketoconazole, Fluconazole, Itraconazole (Inhibits ergosterol synthesis by inhibiting 14-alpha-demethylase; fungistatic against yeasts and fungicidal against molds)
e. Allylamines: Terbinafine, Naftifine (Inhibits ergosterol synthesis by inhibiting squalene epoxidase; fungicidal)
DNA synthesis inhibitor:
- DNA gyrase inhibitor: Fluoroquinolones (bactericidal)
- Dihydrofolate synthase inhibitor: Sulfonamides, PAS, Dapsone
- Dihydrofolate reductase inhibitor: Trimethoprim, Pyrimethamine, Proguanil
These Sulfone drugs are BACTERIOSTATIC.
DNA destruction: Metronidazole (free nitro-radicals; bactericidal against anaerobes) and Nitrofurantoin (bacteriostatic)
- Bacteriostatic + Bacteriostatic = Additive
- Bactericidal + Bactericidal = Frequently additive and sometimes synergistic
- Bactericidal + Bacteriostatic = Additive if lower sensitivity to bactericidal drug and Antagonistic if higher snesitivity to bactericidal drug
He is the section editor of Orthopedics in Epomedicine. He searches for and share simpler ways to make complicated medical topics simple. He also loves writing poetry, listening and playing music.