Question:

Sulphonamides serve to inhibit the

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Sulphonamide Selectivity: Competitively inhibits bacterial Dihydropteroate Synthase (PABA mimic). Animals lack this enzyme and absorb dietary folate.
  • Growth of cancer cells, since they inhibit mammalian dihydrofolate formation
  • Folate biosynthesis in bacteria
  • Folate biosynthesis in animals
  • Growth of cancer cells since they inhibit thymidylate synthase
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The Correct Option is B

Solution and Explanation


Step 1: Understanding the Concept:

Sulfonamides exhibit selective antibacterial toxicity as structural analogues of para-aminobenzoic acid (PABA), competitively inhibiting bacterial dihydropteroate synthase.
Key Formula or Approach:
\[ \text{PABA} + \text{Pteridine} \xrightarrow[\text{Inhibited by Sulphonamides}]{\text{Dihydropteroate Synthase}} \text{Dihydropteroic Acid} \longrightarrow \text{Tetrahydrofolate (THF)} \]

Step 2: Detailed Explanation:

Mechanism of action of Sulphonamides:
- Bacteria must synthesize folic acid de novo from para-aminobenzoic acid (PABA), pteridine, and glutamate.
- Sulphonamides are structural analogues of PABA that competitively inhibit bacterial Dihydropteroate Synthase, completely blocking de novo folate biosynthesis in bacteria.
- Because animal/mammalian cells cannot synthesize folate de novo and instead obtain preformed dietary folate via specific membrane transporters (lacking dihydropteroate synthase), sulphonamides selectively kill bacteria without harming host mammalian cells.

Step 3: Final Answer:

Hence, sulphonamides inhibit Folate biosynthesis in bacteria, corresponding to option (B).
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