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Multiple Choice
What products would result from the complete hydrolysis of the tripeptide Gly-Ala-Ser?
A
Glycine, alanine, and asparagine
B
Glycine, alanine, and serine
C
Alanine, serine, and glutamine
D
Glycine, serine, and threonine
Verified step by step guidance
1
Step 1: Understand the concept of peptide hydrolysis. Hydrolysis of a peptide involves breaking the peptide bonds between amino acids using water, resulting in the release of individual amino acids.
Step 2: Identify the amino acids present in the tripeptide Gly-Ala-Ser. The tripeptide is composed of glycine (Gly), alanine (Ala), and serine (Ser).
Step 3: Recall that during complete hydrolysis, all peptide bonds are cleaved, leaving the individual amino acids as products. For Gly-Ala-Ser, this means breaking the bond between Glycine and Alanine, and the bond between Alanine and Serine.
Step 4: Write the chemical reaction for hydrolysis: Gly-Ala-Ser + H₂O → Glycine + Alanine + Serine. This reaction shows the addition of water molecules to break the peptide bonds.
Step 5: Verify the products. After hydrolysis, the resulting amino acids are glycine, alanine, and serine. These are the correct products of the complete hydrolysis of the tripeptide Gly-Ala-Ser.