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Subjects

Biotechnology

Genetic Engineering

In this Class 11 Biotechnology topic under Principles of Biotechnology, students learn how genetic engineering deliberately changes an organism’s DNA to obtain a desired trait or product. The topic introduces recombinant DNA technology, including the roles of restriction enzymes, DNA ligase, vectors, host cells, transformation, and selection of modified cells. It also connects these steps to applications such as producing useful proteins and improving crops, while encouraging attention to biological safety, ethical questions, and the limits of genetic modification.

Easy · Level 5 · 25 questions

Practice questions

01When is expression of a foreign gene considered successful in genetic engineering?

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02Why is a human gene used in recombinant insulin production?

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03Bt gene is considered related to which organism?

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04What is a plant called when a gene from another organism is stably introduced into its genome through genetic engineering?

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05Why is the gene gun method useful in plant cells?

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06Agrobacterium is used for what purpose?

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07Why is risk assessment done before inserting a new gene into an organism?

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08What problem can contamination cause in a genetic engineering experiment?

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09In DNA fingerprinting, how are individual patterns generally except identical twins?

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10What is the primary use of DNA technology in forensic science?

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11What is the basic idea of gene therapy?

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12After inserting a foreign gene into a host, what should be checked immediately?

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13Why are all host cells not successfully transformed?

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14What can be the importance of a colony in cloning?

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15Why is gene cloning useful in research?

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16Why is a control group useful in genetic engineering experiments?

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17Which is an example of a desired product in genetic engineering?

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18Why should genetically modified organisms be tested in a controlled environment?

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19Why can adding a promoter with a gene be useful?

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20In which condition is recombinant DNA technology considered successful?

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21Which statement about sticky ends is correct?

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22What is the main difference between blunt ends and sticky ends?

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23Which technique is most useful if the DNA sample is very small?

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24What causes the negative charge of DNA in gel electrophoresis?

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25A student says every plasmid is a good vector. Why is this not correct?

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