Q.6 The anti-parallel nature of double standard DNA is due to: 1. Phosphodiester bonds 2. Hydrogen bonds 3. Disulphide bonds 4. Glycosidic bond

Q.6 The anti-parallel nature of double standard DNA is due to:

1. Phosphodiester bonds

2. Hydrogen bonds

3. Disulphide bonds

4. Glycosidic bond

DNA’s double helix features two antiparallel strands running 5′ to 3′ in opposite directions, a key feature discovered by Watson and Crick. This MCQ tests the molecular basis of that polarity, fundamental for replication and transcription understanding.

Correct Answer: 1. Phosphodiester bonds

Phosphodiester bonds link the 3′ hydroxyl of one deoxyribose sugar to the 5′ phosphate of the next nucleotide, creating the sugar-phosphate backbone with inherent 5′-3′ directionality. In the double helix, one strand’s 5’→3′ orientation opposes the other’s 3’→5′, enforcing antiparallelism. This polarity is crucial as DNA polymerase synthesizes only 5’→3′.

Why Not the Other Options?

  • 2. Hydrogen bonds
    Hydrogen bonds (2 between A-T, 3 between G-C) hold complementary bases together across strands but don’t dictate directionality; they allow parallel or antiparallel alignment equally.

  • 3. Disulphide bonds
    Disulfide bonds form between cysteine residues in proteins, irrelevant to nucleic acids or DNA structure; DNA lacks sulfur-containing amino acids.

  • 4. Glycosidic bond
    N-glycosidic bonds attach nitrogenous bases to the 1′ carbon of deoxyribose but are identical on both strands, contributing nothing to antiparallel polarity.

Structural Implications

Antiparallel strands enable semiconservative replication, with leading/lagging strand synthesis. This design stabilizes the helix via backbone interactions and base stacking. For students, visualize: phosphodiester bonds create polarity arrows pointing oppositely in the ladder-like model.

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