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Recombinant DNA is formed by using a restriction enzyme that cuts the double strand at a particular point. Genetic engineers use restriction enzymes to remove a gene from a donor organism's chromosome and insert it into a vector, a molecule of DNA that will function as a carrier.
While every effort has been made to follow citation style rules, there may be some discrepancies. A Tozzo Frios conta com uma vasta gama de produtos como: frios, laticA­nios, embutidos, enlatados, congelados e produtos a granel. A restriction enzyme (or restriction endonuclease) is an enzyme that cuts double-stranded DNA.
The chemical bonds that the enzymes cleave can be reformed by other enzymes known as ligases, so that restriction fragments carved from different chromosomes or genes can be spliced together, provided their ends are complementary (more below).
The 1978 Nobel Prize in Medicine was awarded to the well-known scientist Daniel Nathans, Werner Arber and Hamilton Smith for the discovery of restriction endonucleases, leading to the development of recombinant DNA technology.

Because recognition sequences and cleavage sites differ between restriction enzymes, the length and the exact sequence of a sticky-end "overhang", as well as whether it is the 5' end or the 3' end strand that overhangs, depends on which enzyme produced it. Restriction enzymes recognize a specific sequence of nucleotides and produce a double stranded cut in the DNA that prevents the phage from replicating. Bacteria prevent their own DNA from being cut by modifying their nucleotides via methylation. Type I restriction enzymes cut DNA about 100 nucleotides after the recognition site and requires ATP. Type II restriction enzymes cut DNA at the recognition site or near the recognition site (Type IIS) and for this reason are most often used in scientific experimentation. Type III restriction enzymes cut DNA about 20-30 base pairs after the recognition site and requires ATP. Venha conhecer nossa loja pessoalmente ou acesse a pA?gina de produtos e confira alguns dos nossos itens. Many of the procedures of molecular biology and genetic engineering rely on restriction enzymes.

Base-pairing between overhangs with complementary sequences enables two fragments to be joined or "spliced" by a DNA ligase.
Because there are only so many ways to arrange the four nucleotides--A,C,G and T--into a four or eight or twelve nucleotide sequence, recognition sequences tend to "crop up" by chance in any long sequence. While recognition sequences vary widely, with lengths between 4 and 8 nucleotides, many of them are palindromic; that is, the sequence on one strand reads the same in the same direction on the complementary strand. When the fragments are mixed together, the complementary ends of each strand will bind with those of the other, forming a recombinant DNA molecule.
Furthermore, restriction enzymes specific to hundreds of distinct sequences have been identified and synthesized for sale to laboratories.
Restriction enzymes therefore are believed to be a mechanism evolved by bacteria to resist attack from viruses called bacteriophages and to help in the removal of viral sequences.

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