Restriction Enzymes
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A Restriction Enzyme (or restriction endonuclease) is an enzyme that cuts double-stranded DNA at specific recognition nucleotide sequences known as restriction sites. Restriction enzymes are found in bacteria.
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To cut the DNA, a restriction enzyme makes two incisions, once through each sugar-phosphate backbone (i.e. each strand) of the DNA double helix.
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Recognition sequences vary between 4 and 8 nucleotides, many of them are palindromic
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Recognition sequences in DNA differ for each restriction enzyme, producing differences in the length, sequence and strand orientation
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There are four classes of restriction endonucleases: types I, II, III and IV. All types of enzymes recognize specific short DNA sequences and carry out the endonucleolytic cleavage of DNA to give specific double-stranded fragments with terminal 5'-phosphates.
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Type II are the most commonly available and used restriction enzymes.
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Each enzyme is named after the bacterium from which it was isolated using a naming system based on bacterial genus, species and strain.
- For example, EcoRI
- E – Escherichia –Genus
- Co – coli –species
- R-strain
- I-order of identification
Applications of Restriction enzymes
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Restriction enzymes are used to assist insertion of genes into plasmid vectors during gene cloning and protein expression experiments.
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Restriction enzymes are used to digest genomic DNA for gene analysis by Southern blot
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Restriction enzymes can also be used to distinguish gene alleles by specifically recognizing single base changes in DNA known as single nucleotide polymorphisms (SNPs).
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Last modified: Tuesday, 15 May 2012, 5:47 AM