Recombinant DNA Technology Overview
5 Questions
1 Views

Choose a study mode

Play Quiz
Study Flashcards
Spaced Repetition
Chat to lesson

Podcast

Play an AI-generated podcast conversation about this lesson

Questions and Answers

What is the primary role of restriction endonuclease enzymes in recombinant DNA technology?

  • To ligate the DNA insert to the vector
  • To introduce the rDNA into host cells
  • To cleave the DNA insert enzymatically (correct)
  • To isolate the target DNA segment
  • Which of the following statements accurately describes a cloning vector?

  • It only works with bacterial cells like E.coli.
  • It is a type of enzyme used to cleave DNA.
  • It is a self-replicating DNA molecule that integrates the DNA insert. (correct)
  • It is a foreign DNA segment intended for cloning.
  • In which step of recombinant DNA technology are transformed cells separated from non-transformed cells?

  • Selection of Transformed Host Cells (correct)
  • Introduction of DNA-Insert into Vector
  • Selection of Suitable Cloning Vector
  • Expression and Multiplication of DNA Insert
  • What is the purpose of introducing the rDNA molecule into a suitable host cell?

    <p>To ensure expression and multiplication of the DNA insert</p> Signup and view all the answers

    What generally occurs during the expression and multiplication step of recombinant DNA technology?

    <p>The foreign DNA must express desired characteristics and is multiplied.</p> Signup and view all the answers

    Study Notes

    Steps in Recombinant DNA Technology

    • Selection and Isolation of DNA Insert: The first step is selecting a specific DNA segment (target DNA) to be cloned. This segment is then isolated enzymatically.

    • Selection of Suitable Cloning Vector: A self-replicating DNA molecule, called a cloning vector, is chosen to integrate the DNA insert. Common vectors include plasmids and bacteriophages.

    • Introduction of DNA Insert into Vector to Form rDNA Molecule: The target DNA (or DNA insert) is extracted and cut enzymatically by restriction enzymes. The resulting fragments are joined (ligated) to the vector DNA using an enzyme called ligase, creating a recombinant DNA (rDNA) molecule (also called cloning-vector-insert DNA construct).

    • Recombinant DNA Molecule into a Suitable Host: The rDNA is introduced into selected host cells (often bacterial cells like E. coli, though yeast and fungi can be used). This introduction process is called transformation.

    • Selection of Transformed Host Cells: Transformed cells that have taken up the rDNA molecule are separated from non-transformed cells using marker genes. Various methods are used for this separation.

    • Expression and Multiplication of DNA Insert in the Host: The foreign DNA expresses its desired characteristics within the host cells. The transformed host cells are multiplied to yield numerous copies. These genes may be transferred to other organisms, if needed.

    Studying That Suits You

    Use AI to generate personalized quizzes and flashcards to suit your learning preferences.

    Quiz Team

    Related Documents

    Description

    This quiz covers the essential steps and processes involved in recombinant DNA technology. Learn about the selection and isolation of DNA, the use of cloning vectors, and the transformation into host cells. Get ready to test your understanding of this crucial biotechnological method.

    More Like This

    Use Quizgecko on...
    Browser
    Browser