B. They divide quickly -apex
Bacteria are used in recombinant DNA technology because they can easily take up and replicate recombinant DNA molecules. This makes them useful for producing large quantities of specific genes or proteins of interest. Additionally, bacteria have simple growth requirements and reproduce quickly, making them cost-effective for research and production purposes.
The type of DNA technology used to cause bacteria to produce human insulin is recombinant DNA technology. In this process, the gene for human insulin is inserted into the genome of a bacterium, such as Escherichia coli (E. coli), using techniques such as restriction enzymes and ligase enzymes. Once the gene is inserted, the bacterium is then able to produce human insulin, which can be purified and used for medical purposes. This technology has revolutionized the production of insulin, making it more accessible and affordable for people with diabetes. Recombinant DNA technology has also been used to produce many other human proteins, such as growth hormone and blood clotting factors, with great success.
They divide quickly.
Recombinant DNA technology PCR
PCR and recombinant DNA technology both involve manipulating DNA in the laboratory. PCR is a technique used to amplify specific DNA sequences, while recombinant DNA technology involves combining DNA from different sources to create a new DNA molecule. Both techniques have revolutionized the field of molecular biology and have numerous applications in research and biotechnology.
Bacteria reproduce very quickly.
Bacteria reproduce very quickly.
Recombinant DNA technology
Bacteria are used in recombinant DNA technology because they can easily take up and replicate recombinant DNA molecules. This makes them useful for producing large quantities of specific genes or proteins of interest. Additionally, bacteria have simple growth requirements and reproduce quickly, making them cost-effective for research and production purposes.
Genetic engineering involves the use of recombinant DNA technology, the process by which a DNA sequence is manipulated in vitro, thus creating recombinant DNA molecules that have new combinations of genetic material
I think you must rethink about your question, but still I am giving the answer as I can understand that you are asking about recombinant DNA technology where bacterial DNA is used as it is a cloning vector (plasmid). In recombinant DNA technology the particular sequence of DNA that we want to replicate or want to produce in huge number, is attached either with plasmid of bacteria or a DNA of bacteriophage and thus produce the recombinant or hybrid DNA which is copied each time when the bacteria or bacteriophage multiply. In this way the hybrid DNA will be transferred from parent cell to daughter cells.
The type of DNA technology used to cause bacteria to produce human insulin is recombinant DNA technology. In this process, the gene for human insulin is inserted into the genome of a bacterium, such as Escherichia coli (E. coli), using techniques such as restriction enzymes and ligase enzymes. Once the gene is inserted, the bacterium is then able to produce human insulin, which can be purified and used for medical purposes. This technology has revolutionized the production of insulin, making it more accessible and affordable for people with diabetes. Recombinant DNA technology has also been used to produce many other human proteins, such as growth hormone and blood clotting factors, with great success.
They divide quickly.
Recombinant DNA technology PCR
Bacteria reproduce vary quickly
A recombinant sequence of DNA is a sequence of DNA that comes from more than one source. Examples of recombinant DNA are plasmids that are put into bacteria. The plasmid comes from the bacteria (or a bacteria at least) but a target gene has been added (say the lac operon gene that allows bacteria to thrive on lactose), this plasmid is now a recombinant DNA sequence.
Polymerase chain reaction