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Subjects

Biotechnology

Cloning Vectors

In Class 11 Biotechnology, this topic explains how cloning vectors carry a selected DNA fragment into a suitable host cell for replication and study. As part of Principles of Biotechnology, students explore the essential features of vectors, including an origin of replication, selectable markers, cloning sites, and a suitable size. They also learn how restriction enzymes and DNA ligase help insert a gene, how recombinant DNA is introduced into host cells, and how transformed cells may be identified during the cloning process.

Easy · Level 5 · 25 questions

Practice questions

01What is the best easy-level summary of a cloning vector?

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02What is the most important comparison in the topic Cloning Vectors?

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03A plasmid vector has ori but no marker. What will be the main difficulty?

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04A vector has a selectable marker but no ori. What problem will occur in the host?

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05If insert DNA joins in the MCS what is the benefit?

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06A colony grows on an antibiotic plate. What can this simply indicate?

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07What is the main difference between antibiotic selection and blue-white screening?

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08Which result can indicate a non-recombinant vector in blue-white screening?

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09Which result can indicate a recombinant clone in blue-white screening?

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10A plasmid vector has ampR gene. What is its use on an ampicillin plate?

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11A tetR gene in a vector is disrupted. This can be linked with which concept?

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12If a vector is very large what may happen to transformation?

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13When is a high copy number useful in a cloning vector?

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14Which vector can be considered more suitable for very large DNA fragments?

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15Which vector is called bacterial artificial chromosome?

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16Which vector is called yeast artificial chromosome?

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17Ti plasmid is associated with which bacterium?

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18Which part of Ti plasmid is transferred into plants?

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19Which vector can be based on a virus that infects bacteria?

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20Cos sites in a cosmid vector are related to what?

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21Which option gives the correct basic structure of a plasmid vector?

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22Which enzyme is useful after vector and insert ends are ready to join?

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23What does directional cloning vector design help with?

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24Which vector may be sufficient only for making DNA copies?

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25Why can restriction digestion be used to confirm insert in a cloning vector?

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