Q85. Match the resistance mechanism in Group I with the antibiotic in Group II Group I Group II P. β-Lactamases Q. Enhanced folate metabolism R. Drug efflux S. Phosphorylation of the drug T. Mutant RNA polymerase 1. Aminoglycosides 2. Penicillins 3. Sulfa drugs 4. Tetracyclins 5. Nalidixic acid 6. Rifamycin P-2, Q-3, R-4, S-5, T-6 P-3, Q-4, R-1, S-6, T-5 P-2, Q-3, R-4, S-1, T-6 P-1, Q-2, R-3, S-4, T-6

Q85. Match the resistance mechanism in Group I with the antibiotic in Group II

Group I Group II
P. β-Lactamases
Q. Enhanced folate metabolism
R. Drug efflux
S. Phosphorylation of the drug
T. Mutant RNA polymerase
1. Aminoglycosides
2. Penicillins
3. Sulfa drugs
4. Tetracyclins
5. Nalidixic acid
6. Rifamycin
  1. P-2, Q-3, R-4, S-5, T-6
  2. P-3, Q-4, R-1, S-6, T-5
  3. P-2, Q-3, R-4, S-1, T-6
  4. P-1, Q-2, R-3, S-4, T-6

    Antibiotic Resistance Mechanisms Matching: Correct Answer & Detailed Analysis

    β-Lactamases and other resistance strategies help bacteria evade antibiotics like penicillins and tetracyclines. This guide reveals the correct Group I to Group II matching for exam prep in microbiology and biochemistry.

    Correct Answer

    The right match is P-2, Q-3, R-4, S-1, T-6.
    This pairs each resistance mechanism with its primary antibiotic target accurately.
    β-Lactamases hydrolyze penicillins, while efflux pumps eject tetracyclins, based on standard mechanisms in bacterial resistance.

    Matching Breakdown

    • P. β-Lactamases → 2. Penicillins: Enzymes like β-lactamases cleave the β-lactam ring in penicillins, inactivating them before they bind penicillin-binding proteins.
      This is the most common resistance to β-lactams in Gram-negative bacteria.

    • Q. Enhanced folate metabolism → 3. Sulfa drugs: Bacteria bypass sulfa drug inhibition by overproducing folate pathway enzymes or using alternative pathways.
      Sulfa drugs block para-aminobenzoic acid incorporation into folic acid.

    • R. Drug efflux → 4. Tetracyclins: Efflux pumps actively export tetracyclins from the cell, reducing intracellular levels needed to inhibit protein synthesis.
      Common in Gram-negative pathogens.

    • S. Phosphorylation of the drug → 1. Aminoglycosides: Kinases phosphorylate aminoglycosides, preventing ribosomal binding and protein synthesis inhibition.
      This modifies the drug for expulsion or inactivation.

    • T. Mutant RNA polymerase → 6. Rifamycin: Mutations alter rifamycin’s binding site on RNA polymerase, blocking transcription inhibition.
      Rifamycins like rifampicin target bacterial RNA synthesis.

    Options Analysis

    Evaluate all choices to understand distractors:

    Option P Q R S T Why Incorrect
    P-2, Q-3, R-4, S-5, T-6 2 3 4 5 6 S wrong: Phosphorylation fits aminoglycosides (1), not nalidixic acid (5) .
    P-3, Q-4, R-1, S-6, T-5 3 4 1 6 5 Multiple errors: P not sulfa (3); R not aminoglycosides (1) .
    P-2, Q-3, R-4, S-1, T-6 2 3 4 1 6 Correct: Matches all mechanisms precisely .
    P-1, Q-2, R-3, S-4, T-6 1 2 3 4 6 Wrong across: P not aminoglycosides (1); Q not penicillins (2) .

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