Abstract
The salIR and salM genes of Streptomyces albus G specify the SalGI (SalI) restriction enzyme and its cognate methyltransferase, respectively. These enzymes are responsible for restriction and modification of bacteriophages. Some phages carry genes that interfere with SalI-specific modification. The sal genes have been cloned in a Streptomyces host-vector system. Use of the cloned DNA as a hybridization probe reveals that sal mutants frequently arise from transposition of a DNA segment of approx. 1 kb into the sal genes. Some, but not all, other bacteria that produce SalGI isoschizomers contain nucleotide sequences that hybridize with sal DNA.
MeSH terms
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Bacterial Proteins / genetics
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Bacterial Proteins / metabolism*
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DNA, Bacterial / metabolism
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DNA, Viral / metabolism
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Deoxyribonucleases, Type II Site-Specific / genetics
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Deoxyribonucleases, Type II Site-Specific / metabolism*
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Genes, Bacterial
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Recombinant Proteins / genetics
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Site-Specific DNA-Methyltransferase (Adenine-Specific) / genetics
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Site-Specific DNA-Methyltransferase (Adenine-Specific) / metabolism
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Streptomyces / enzymology*
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Streptomyces / genetics
Substances
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Bacterial Proteins
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DNA, Bacterial
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DNA, Viral
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Recombinant Proteins
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DNA modification methylase SalGI
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Site-Specific DNA-Methyltransferase (Adenine-Specific)
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Deoxyribonucleases, Type II Site-Specific
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GTCGAC-specific type II deoxyribonucleases