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PMID: 6280151 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Digestion of highly modified bacteriophage DNA by restriction endonucleases.

Nucleic acids research ·Vol. 10 ·No. 5 ·1982-03-11 ·Pages 1579-91

Huang LH, Farnet CM, Ehrlich KC, Ehrlich M

Abstract

The ability of thirty Type II restriction endonucleases to cleave five different types of highly modified DNA has been examined. The DNA substrates were derived from relatively large bacteriophage genomes which contain all or most of the cytosine or thymine residues substituted at the 5-position. These substituents were a proton (PBS1 DNA), a hydroxymethyl group (SP01 DNA), a methyl group (XP12 DNA), a glucosylated hydroxymethyl group (T4 DNA), or a phosphoglucuronated, glucosylated 4,5-dihydroxypentyl group (SP15 DNA). Although PBS1 DNA and SP01 DNA were digested by most of the enzymes, they were cleaved much more slowly than was normal DNA by many of them. 5-Methylcytosine-rich XP12 DNA and the multiply modified T4 and SP15 DNAs were resistant to most of these endonucleases. The only enzyme that cleaved all five of these DNAs was TaqI, which fragmented them extensively.

MeSH Terms
Base Sequence DNA Restriction Enzymes/metabolism DNA, Viral Deoxyribonuclease I Deoxyribonucleases Endonucleases Kinetics Phosphoric Diester Hydrolases Substrate Specificity
Chemicals
DNA, Viral Deoxyribonucleases Endonucleases DNA Restriction Enzymes Deoxyribonuclease I Phosphoric Diester Hydrolases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Huang L H
Farnet C M
Ehrlich K C
Ehrlich M
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43 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1982-03-11
Pages
1579-91
Language
English
Region
England
NLM ID
0411011
PMCID
PMC320551
Subset
IM
Grants
NCI NIH HHS · CA-19942 · United States
NIGMS NIH HHS · GM-26986 · United States
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