Recombinant DNA Technology Overview
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Questions and Answers

In what year did the foundation for recombinant DNA technology emerge with the discovery of restriction enzymes?

  • 1995
  • 1968 (correct)
  • 1982
  • 1975

Which of the following is NOT a technique used to insert modified genes into target cells during transformation?

  • Gene guns
  • Microscopy (correct)
  • Microfibers
  • Electroporation

What is the main purpose of gene cloning in the process of recombinant DNA technology?

  • To create multiple copies of a specific gene (correct)
  • To introduce a modified gene into a host organism
  • To identify and isolate genes for further manipulation
  • To study the function of a specific gene

What is the significance of 'gene design' in the context of recombinant DNA technology?

<p>All of the above (D)</p> Signup and view all the answers

What is the other widely used term for Recombinant DNA technology?

<p>Genetic engineering (B)</p> Signup and view all the answers

Flashcards

Recombinant DNA

Artificially created DNA from two or more sources.

Genetic Engineering

Also known as recombinant DNA technology, altering genetic material.

Restriction Enzymes

Enzymes that cut DNA at specific sequences, crucial for cloning.

Gene Cloning

Process to create numerous copies of a specific gene.

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Transformation

Inserting a modified gene into target cells.

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Study Notes

Recombinant DNA Technology

  • Recombinant DNA is artificially created DNA from two or more sources, combined into a single molecule.
  • This creates new genetic combinations useful for science, medicine, agriculture, and industry.
  • Recombinant DNA technology is also known as genetic engineering.
  • It emerged in 1968 with the discovery of restriction enzymes by Werner Arber.

Process of Recombinant DNA Technology

  • DNA Extraction: Scientists extract DNA from the organism containing the gene of interest.

  • Gene Cloning: Scientists isolate and create many copies of the desired gene.

  • Gene Design: Genetic engineers modify the gene to function in a new organism. This is done in a test tube, cutting and rearranging gene sections.

  • Transformation: The modified gene is inserted into the desired recipient cell using techniques like gene guns, agrobacterium, microfibers, or electroporation.

  • Maintaining the recombinant DNA in the host and passing it to offspring is crucial.

  • Inserting the desired gene into a host organism is challenging and requires careful selection of the vector and the host.

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Description

This quiz explores the fundamentals of Recombinant DNA Technology and its processes. Discover key concepts such as DNA extraction, gene cloning, and transformation techniques. Gain insights into the applications of genetic engineering in science and industry.

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