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Biotechnology Cutting of DNA MCQ Questions for Class 11 General

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01 Practice Topic Isolation of DNA 294 MCQs

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Question 571/592 Easy Biotechnology Processes of Recombinant DNA Technology Cutting of DNA Class 11 Level 56

Restriction digestion में fill-in reaction का उद्देश्य क्या हो सकता है?

What can be the purpose of a fill-in reaction in restriction digestion work?

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A. sticky ends को blunt ends में बदलनाConverting sticky ends into blunt ends

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DNA polymerase overhangs को fill कर सकता है। इससे blunt-end cloning strategy possible हो सकती है। / DNA polymerase can fill overhangs. This can make blunt-end cloning strategy possible.

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Question 572/592 Easy Biotechnology Processes of Recombinant DNA Technology Cutting of DNA Class 11 Level 56

Restriction digestion में exonuclease treatment कब उपयोगी हो सकता है?

When can exonuclease treatment be useful in restriction digestion work?

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A. specific unwanted ends या single-stranded regions process करने मेंIn processing specific unwanted ends or single-stranded regions

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Exonucleases DNA ends से nucleotides remove करते हैं। उनका use strategy-specific होता है। / Exonucleases remove nucleotides from DNA ends. Their use is strategy-specific.

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Question 573/592 Easy Biotechnology Processes of Recombinant DNA Technology Cutting of DNA Class 11 Level 56

Restriction digestion में nicking enzyme किससे अलग होता है?

How is a nicking enzyme different in restriction digestion context?

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A. यह केवल एक DNA strand में nick लगा सकता हैIt can nick only one DNA strand

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Nicking enzymes double-strand cut की जगह single-strand nick कर सकते हैं। यह special DNA engineering में useful है। / Nicking enzymes can make a single-strand nick instead of a double-strand cut. This is useful in special DNA engineering.

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Question 574/592 Easy Biotechnology Processes of Recombinant DNA Technology Cutting of DNA Class 11 Level 56

Restriction endonuclease और nicking enzyme में मुख्य अंतर क्या है?

What is the main difference between restriction endonuclease and nicking enzyme?

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A. endonuclease often दोनों strands काटता है और nicking enzyme एक strand काटता हैEndonuclease often cuts both strands and nicking enzyme cuts one strand

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Restriction enzymes double-stranded break बना सकते हैं। Nicking enzymes single-strand nick के लिए जाने जाते हैं। / Restriction enzymes can create double-stranded breaks. Nicking enzymes are known for single-strand nicks.

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Question 575/592 Easy Biotechnology Processes of Recombinant DNA Technology Cutting of DNA Class 11 Level 56

Restriction digestion में homing endonuclease को rare cutter क्यों माना जा सकता है?

Why can a homing endonuclease be considered a rare cutter in restriction digestion?

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A. यह बहुत लंबी recognition sequence पहचान सकता हैIt can recognize a very long recognition sequence

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Long recognition sequences genome में कम बार मिलती हैं। इसलिए ऐसे enzymes rare cuts दे सकते हैं। / Long recognition sequences occur less often in genomes. Therefore such enzymes can give rare cuts.

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Question 576/592 Easy Biotechnology Processes of Recombinant DNA Technology Cutting of DNA Class 11 Level 56

Restriction digestion और genome editing nuclease में basic similarity क्या है?

What is the basic similarity between restriction digestion and genome editing nuclease?

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A. दोनों DNA cutting से जुड़े हो सकते हैंBoth can be related to DNA cutting

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Restriction enzymes और genome editing nucleases DNA cuts कर सकते हैं। लेकिन recognition और use अलग हो सकते हैं। / Restriction enzymes and genome editing nucleases can cut DNA. But recognition and use can differ.

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Question 577/592 Easy Biotechnology Processes of Recombinant DNA Technology Cutting of DNA Class 11 Level 56

Restriction enzyme और CRISPR nuclease में school-level अंतर क्या है?

What is a school-level difference between restriction enzyme and CRISPR nuclease?

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A. restriction enzyme DNA sequence पहचानता है और CRISPR guide RNA से target हो सकता हैRestriction enzyme recognizes DNA sequence and CRISPR can be guided by guide RNA

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Restriction enzymes fixed recognition sites पर cut करते हैं। CRISPR systems guide RNA से target select कर सकते हैं। / Restriction enzymes cut at fixed recognition sites. CRISPR systems can select targets using guide RNA.

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Question 578/592 Easy Biotechnology Processes of Recombinant DNA Technology Cutting of DNA Class 11 Level 56

Restriction digestion में ethical use of DNA samples क्यों जरूरी है?

Why is ethical use of DNA samples necessary in restriction digestion?

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A. DNA source और consent का सम्मान करने के लिएTo respect DNA source and consent

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Biological DNA samples rules और consent के अनुसार use होने चाहिए। यह responsible biotechnology है। / Biological DNA samples should be used according to rules and consent. This is responsible biotechnology.

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Question 579/592 Easy Biotechnology Processes of Recombinant DNA Technology Cutting of DNA Class 11 Level 56

Restriction digestion में genetic data privacy कब relevant हो सकती है?

When can genetic data privacy be relevant in restriction digestion?

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A. human DNA samples handle करते समयWhile handling human DNA samples

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Human DNA sensitive genetic information रख सकता है। Privacy और approved handling जरूरी हैं। / Human DNA can contain sensitive genetic information. Privacy and approved handling are necessary.

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Question 580/592 Easy Biotechnology Processes of Recombinant DNA Technology Cutting of DNA Class 11 Level 56

Restriction digestion में GMO-related work में containment क्यों जरूरी है?

Why is containment necessary in GMO-related work involving restriction digestion?

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A. modified DNA और organisms को safe control में रखने के लिएTo keep modified DNA and organisms under safe control

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Recombinant DNA work biosafety guidelines के अनुसार किया जाता है। Containment accidental release risk घटाता है। / Recombinant DNA work is done according to biosafety guidelines. Containment reduces accidental release risk.

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