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What is the term for a plasmid that contains a foreign gene?

Recombiant DNA


What occurs first in the production of a recombinant plasmid?

In the production of a recombinant plasmid, the DNA of interest (insert) and the plasmid vector are both cut with restriction enzymes to create compatible ends. These cut fragments are then ligated together using DNA ligase to produce the recombinant plasmid.


When is a plasmid considered a recombinant plasmid?

A plasmid is considered recombinant when it contains DNA sequences from two different sources that have been artificially combined, often through genetic engineering techniques like restriction enzyme digestion and ligation. This results in a plasmid with modified or additional genetic material compared to its original form.


What is recombinant Plasmid?

A plasmid is a small, circular, double-stranded DNA molecule that is distinct from a cell's chromosomal DNA. ... Researchers can insert DNA fragments or genes into a plasmid vector, creating a so-called recombinant plasmid. This plasmid can be introduced into a bacterium by way of the process called transformation.


What is the most logical sequence of steps for splicing foreign DNA into a plasmid and inserting the plasmis into a bacterium?

Cut the plasmid and foreign DNA with the same restriction enzyme to create complementary sticky ends. Mix the cut plasmid and foreign DNA together and ligate them using DNA ligase. Introduce the ligated plasmid into the bacterium using a method like transformation, where the bacterium uptakes the plasmid. Select for transformed bacteria using antibiotic resistance or another selectable marker on the plasmid.

Related Questions

What is the term for a plasmid that contains a foreign gene?

Recombiant DNA


What occurs first in the production of a recombinant plasmid?

In the production of a recombinant plasmid, the DNA of interest (insert) and the plasmid vector are both cut with restriction enzymes to create compatible ends. These cut fragments are then ligated together using DNA ligase to produce the recombinant plasmid.


When is a plasmid considered a recombinant plasmid?

A plasmid is considered recombinant when it contains DNA sequences from two different sources that have been artificially combined, often through genetic engineering techniques like restriction enzyme digestion and ligation. This results in a plasmid with modified or additional genetic material compared to its original form.


How can a plasmid be engineered to include a piece of foreign DNA?

A plasmid can be engineered to include a piece of foreign DNA by using restriction enzymes to cut both the plasmid and the foreign DNA at specific sites. The two fragments are then ligated together using DNA ligase. The resulting recombinant plasmid can be introduced into a host organism for replication and expression of the foreign DNA.


Which includes the others plasmid foreign gene transformed bacterium recombinant DNA?

I have the same question


How is the meaning recombine related to the production of recombinant DNA?

recombine joins together with means that the plasmid and the foreign dna join together to make recombinant dna


What is recombinant Plasmid?

A plasmid is a small, circular, double-stranded DNA molecule that is distinct from a cell's chromosomal DNA. ... Researchers can insert DNA fragments or genes into a plasmid vector, creating a so-called recombinant plasmid. This plasmid can be introduced into a bacterium by way of the process called transformation.


What is the most logical sequence of steps for splicing foreign DNA into a plasmid and inserting the plasmis into a bacterium?

Cut the plasmid and foreign DNA with the same restriction enzyme to create complementary sticky ends. Mix the cut plasmid and foreign DNA together and ligate them using DNA ligase. Introduce the ligated plasmid into the bacterium using a method like transformation, where the bacterium uptakes the plasmid. Select for transformed bacteria using antibiotic resistance or another selectable marker on the plasmid.


How are restriction enzymes utilized in the process of creating recombinant DNA?

Restriction enzymes are used to cut DNA at specific sequences, allowing scientists to insert desired genes into a plasmid. This creates recombinant DNA, which can be used in genetic engineering to produce desired traits in organisms.


How can bacteria be transformed with recombinant plasmid?

Bacteria can be transformed with recombinant plasmid by introducing the plasmid into the bacterial cell through a process called transformation. This allows the bacteria to take up the recombinant DNA from the plasmid and express the desired gene or trait encoded in the DNA.


Why use bam h1 ans sau3a1 in plasmid transformation?

BamHI and Sau3A1 are restriction enzymes that can be used to linearize or digest plasmid DNA during the transformation process. Linearizing the plasmid with these enzymes makes it easier for the foreign DNA to be inserted and integrated into the plasmid. This helps in efficiently producing recombinant plasmids with the desired DNA insert.


How can one create recombinant DNA?

Recombinant DNA is created by combining DNA from different sources using enzymes called restriction enzymes. These enzymes cut the DNA at specific points, allowing the desired DNA fragments to be inserted into a vector, such as a plasmid. The vector is then introduced into a host cell, where it replicates and produces the desired recombinant DNA.