Who constituted the first rDNA? Name the vector and host used for the process.
Answer
604.8k+ views
Hint: Recombinant DNA is technology where a piece of DNA which is created by combining DNA fragments from two different sources. It is possible because the molecular structure of DNA all organisms have the same chemical structure, and differ only in the sequence of nucleotides in the whole identical structure.
Complete answer:
The technology to propagate and express recombinant genes was developed by Stanley Cohen and Herbert Boyer in 1973. It made it possible to convert bacterial cells into living factories for the selected proteins to be produced directly. In the Salmonella typhimurium bacterium, they cut a piece of DNA from a plasmid carrying the antibiotic resistance gene and related it to the Escherichia coli plasmid.
The creation of recombinant DNA requires a cloning vector, a DNA molecule that replicates within a living cell. Vectors are typically derived from plasmids or viruses and represent relatively small segments of DNA containing the genetic signals necessary for replication, as well as additional components for ease when injecting foreign DNA, recognize cells containing recombinant DNA and where appropriate, express foreign DNA. The choice of a molecular cloning vector depends on the choice of the host organism, the size of the DNA to be cloned, and whether it is foreign DNA.to be expressed and how. The DNA segments can cut and ligate by using a number of techniques, such as restriction enzyme and DNA ligase respectively.
Note: Recombinant DNA technology is an important tool in vaccine production, insulin, interferon, and human growth hormone. It is also used in production of clotting factors that are used for treatment of haemophilia and also in gene therapy.
Complete answer:
The technology to propagate and express recombinant genes was developed by Stanley Cohen and Herbert Boyer in 1973. It made it possible to convert bacterial cells into living factories for the selected proteins to be produced directly. In the Salmonella typhimurium bacterium, they cut a piece of DNA from a plasmid carrying the antibiotic resistance gene and related it to the Escherichia coli plasmid.
The creation of recombinant DNA requires a cloning vector, a DNA molecule that replicates within a living cell. Vectors are typically derived from plasmids or viruses and represent relatively small segments of DNA containing the genetic signals necessary for replication, as well as additional components for ease when injecting foreign DNA, recognize cells containing recombinant DNA and where appropriate, express foreign DNA. The choice of a molecular cloning vector depends on the choice of the host organism, the size of the DNA to be cloned, and whether it is foreign DNA.to be expressed and how. The DNA segments can cut and ligate by using a number of techniques, such as restriction enzyme and DNA ligase respectively.
Note: Recombinant DNA technology is an important tool in vaccine production, insulin, interferon, and human growth hormone. It is also used in production of clotting factors that are used for treatment of haemophilia and also in gene therapy.
Recently Updated Pages
Master Class 12 Business Studies: Engaging Questions & Answers for Success

Master Class 12 Chemistry: Engaging Questions & Answers for Success

Master Class 12 Biology: Engaging Questions & Answers for Success

Class 12 Question and Answer - Your Ultimate Solutions Guide

Master Class 11 English: Engaging Questions & Answers for Success

Master Class 11 Social Science: Engaging Questions & Answers for Success

Trending doubts
Which are the Top 10 Largest Countries of the World?

Draw a labelled sketch of the human eye class 12 physics CBSE

Differentiate between homogeneous and heterogeneous class 12 chemistry CBSE

Differentiate between Pyramid of energy and pyramid class 12 biology CBSE

Why is the cell called the structural and functional class 12 biology CBSE

Draw the diagram of the pyramid of energy Explain In class 12 biology CBSE

