Tetracycline is an antibiotic medication used to treat various bacterial infections. Its effectiveness comes from selectively inhibiting bacterial protein synthesis.
Tetracycline targets the bacterial ribosome, specifically the 30S ribosomal subunit. Its primary mechanism is:
This prevents the correct amino acid, carried by the tRNA, from entering the ribosome to be added to the growing polypeptide chain. Consequently, protein synthesis is halted.
Therefore, Tetracycline's action is specifically preventing the delivery of new amino acids to the ribosome via tRNA.
| Group I | Group II |
| [P] Influenza A virus | 1. Isoniazid |
| [Q] Fungus | 2. Amantadine |
| [R] Plasmodium | 3. Fluconazole |
| [S] Mycobacterium | 4. Artemisinin |
| 5. Iodoquinol |
Match the antibiotics in Group I with their modes of action in Group II.
| Group I | Group II |
| P) Chloramphenicol | 1) Inhibits protein synthesis by acting on 30S ribosomal subunit |
| Q) Rifampicin | 2) Interferes with DNA replication by inhibiting DNA gyrase |
| R) Tetracycline | 3) Inhibits protein synthesis by acting on 50S ribosomal subunit |
| S) Quinolone | 4) Interferes with RNA polymerase activity |
| 5) Inhibits $\beta$-lactamase activity |
| Group I | Group II |
| P. Sulfonamide | 1. Peptidoglycan synthesis |
| Q. Quinolones | 2. Peptide chain elongation |
| R. Erythromycin | 3. Folic acid biosynthesis |
| S. Cephalosporin | 4. Topoisomerase |