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
This question requires matching antibiotics from Group I with their respective molecular targets in Group II.
We need to determine the specific mechanism of action for each antibiotic listed:
Based on the mechanisms described above, the correct pairings are:
Therefore, the correct combination is P-3, Q-4, R-2, S-1.
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] Influenza A virus | 1. Isoniazid |
| [Q] Fungus | 2. Amantadine |
| [R] Plasmodium | 3. Fluconazole |
| [S] Mycobacterium | 4. Artemisinin |
| 5. Iodoquinol |
A bacterial culture (200 µl containing $1.8 \times 10^9$ cells) was treated with an antibiotic Z (50 µg per ml) for 4 h at 37°C. After this treatment, the culture was divided into two equal aliquots.
Set A: 100 µl was plated on Luria agar.
Set B: 100 µl was centrifuged, the cell pellet washed and plated on Luria agar.
After incubating these two plates for 24 h at 37°C, Set A plate showed no colonies, whereas the Set B plate showed $0.9 \times 10^9$ cells. This experiment showed that the antibiotic Z is