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A restriction enzyme (or restriction endonuclease) is an enzyme that cuts double-stranded or single stranded DNA at specific recognition nucleotide sequences known asrestriction sites....................refer in this website en.wikipedia.org/wiki/Restriction_enzyme
Restriction enzymes are endonucleases that digest the DNA at a sequence specific site. Hind III for example cut between two As in the sequence AAGCTT in the both strand forming a sticky end. If you use this enzyme to cut in your vector DNA, you have to use the same enzyme in the insert DNA so as they can ligate by DNA ligation. This is the important use of same restriction enzyme in cloning.
Because these enzymes cut the DNA molecule at a particular site. But like scissors these are useful tools in genetic engineering or recombinant DNA technology.
Enzymes derived from recombinant DNA technology as opposed to naturally occurring enzymes
Fasle.
A restriction enzyme, also called a restriction endonuclease, is needed to cleave vector DNA when using recombinant DNA technology.
These sticky ends, if they two pieces match, they will join together to form a recombinant DNA.
A Sticky End, referring to Biology is recombinant DNA. After DNA has been cut by a restriction enzyme it has "sticky ends" or recombinant DNA at the ends.
Actually the answer would be Restriction enzyme and DNA ligase.
A restriction enzyme (or restriction endonuclease) is an enzyme that cuts double-stranded or single stranded DNA at specific recognition nucleotide sequences known asrestriction sites....................refer in this website en.wikipedia.org/wiki/Restriction_enzyme
Recombinant DNA is made by combining DNA from different sources. The most common way is to use a plasmid (a circular piece of prokaryote DNA), cut it with a restriction enzyme and then mix it with your target gene which has also been cut with the same enzymes so the pieces fit together like a jigsaw puzzle.
Such an enzyme is called a restriction endonuclease
Restriction enzymes are endonucleases that digest the DNA at a sequence specific site. Hind III for example cut between two As in the sequence AAGCTT in the both strand forming a sticky end. If you use this enzyme to cut in your vector DNA, you have to use the same enzyme in the insert DNA so as they can ligate by DNA ligation. This is the important use of same restriction enzyme in cloning.
Because these enzymes cut the DNA molecule at a particular site. But like scissors these are useful tools in genetic engineering or recombinant DNA technology.
Restriction enzymes cuts out a specific short nucleotide sequence while as the process of ligation, DNA ligase joins them together. So ligase can be considered the reverse of the restriction enzyme process as it joins DNA fragments together instead of cutting them out.
Enzymes derived from recombinant DNA technology as opposed to naturally occurring enzymes