Difficulty: Easy
Correct Answer: Restriction endonuclease
Explanation:
Introduction / Context:Restriction endonucleases underpin recombinant DNA technology, cloning, and genomic mapping. They evolved as bacterial defense mechanisms against foreign DNA such as bacteriophages, providing sequence-specific cleavage.
Given Data / Assumptions:
Concept / Approach:Restriction enzymes (e.g., EcoRI, HindIII) recognize palindromic sequences and cleave DNA to produce sticky or blunt ends. In bacteria, methylation systems protect host DNA from self-cleavage. Other enzymes listed do not perform sequence-specific restriction: transposase moves DNA elements, helicase unwinds DNA, and reverse transcriptase copies RNA into DNA.
Step-by-Step Solution:Identify the requirement: sequence-specific recognition and cleavage.Match to restriction endonucleases from bacteria.Exclude enzymes with unrelated functions (helicase, transposase, reverse transcriptase).Select restriction endonuclease.
Verification / Alternative check:Restriction–modification systems pair endonucleases with methyltransferases; this pairing is well documented in microbial genetics.
Why Other Options Are Wrong:Transposase: catalyzes transposition; not a defense nuclease against foreign DNA sequences.Helicase: unwinds duplex DNA; no site-specific cutting.Reverse transcriptase: synthesizes DNA from RNA; no sequence-specific DNA cutting.
Common Pitfalls:Confusing general nucleases with sequence-specific restriction enzymes; only the latter recognize defined motifs.
Final Answer:Restriction endonuclease
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