Step 1: Understanding the role of terminal saccharide moieties.
Terminal saccharides like N-Acetylneuraminic acid (also known as sialic acid) are often found on glycoproteins, and these modifications play a crucial role in preventing their recognition and degradation by the liver. This modification protects plasma glycoproteins from premature clearance.
Step 2: Analyzing the options.
(A)N-Acetylneuraminic acid: Correct — N-Acetylneuraminic acid (sialic acid) is a terminal sugar that protects glycoproteins from uptake and degradation by hepatocytes.
(B)N-Acetylgalactosamine: This sugar is found in glycoproteins but does not have the same protective role as N-Acetylneuraminic acid.
(C)D-Galactose: While D-galactose is important in glycoproteins, it does not have the specific protective function mentioned in the question.
(D)D-Mannose: This sugar is involved in glycoprotein recognition but does not directly protect glycoproteins from degradation in the liver.
Step 3: Conclusion.
The correct answer is (A)N-Acetylneuraminic acid, as it is the saccharide responsible for protecting glycoproteins from degradation.
Which one of the following matches is CORRECT between the inhibitors given in Group A with their modes of action in Group B?
\[\begin{array}{|c|c|} \hline Group A & Group B \\ \hline \text{(P) Antimycin A} & \text{(i) Inhibits cytochrome c oxidase} \\ \hline \text{(Q) Amytal} & \text{(ii) Blocks electron transfer from cyt b to cyt c1} \\ \hline \text{(R) Carbon monoxide} & \text{(iii) Inhibits adenine nucleotide translocase} \\ \hline \text{(S) Atractyloside} & \text{(iv) Prevents electron transfer from Fe-S centers of complex 1 to ubiquinone} \\ \hline \end{array}\]