Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
19
|
pubmed:dateCreated |
1983-1-7
|
pubmed:abstractText |
To determine which functional groups of bases within the grooves of double-helical DNA interact with the HpaI endonuclease, we have employed chemically synthesized octanucleotides containing base analogues. The 5-methyl group of thymine was probed as a contact between the HpaI endonuclease and its recognition sequence by using the oligonucleotides d(G-G-T-T-A-A-C-C), d(G-G-T-U-A-A-C-C), and d(G-G-T-U(Br)-A-A-C-C). The 2-amino group of guanine was probed as a contact for the HpaI endonuclease by using the octanucleotide d(G-I-T-T-A-A-C-C). The HpaI endonuclease cleaves octanucleotides d(G-G-T-T-A-A-C-C) and d(G-G-T-B-A-A-C-C) according to Michaelis-Menten kinetics. However, both the Km and turnover number for d(G-G-T-B-A-A-C-C) were severalfold lower than those for cleavage of d(G-G-T-T-A-A-C-C). In addition, d(G-G-T-U-A-A-C-C) was not cleaved by HpaI endonuclease, suggesting that the 5-methyl group of thymine is a contact between the HpaI endonuclease and its recognition sequence. d(G-I-T-T-A-A-C-C) was not cleaved by the HpaI endonuclease which may be due in part to the low thermal stability of the duplex. Nevertheless, our results suggest that the 2-amino group of guanine is a contact for the HpaI endonuclease. A phosphate group 5' external to the HpaI recognition sequence has been identified as a contact between the HpaI endonuclease and DNA. The HpaI endonuclease cleaved 5'-phosphorylated octanucleotide 30-fold faster than unphosphorylated octanucleotide. In addition, the Km of the d(G-G-T-T-A-A-C-C) was 8000-fold higher than the Km of the phage f1 RFI DNA, suggesting that the octanucleotide is too short to take advantage of the entire DNA binding site of the enzyme.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA Restriction Enzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxyribonucleases, Type II...,
http://linkedlifedata.com/resource/pubmed/chemical/Oligodeoxyribonucleotides,
http://linkedlifedata.com/resource/pubmed/chemical/Oligonucleotides,
http://linkedlifedata.com/resource/pubmed/chemical/endodeoxyribonuclease HpaI
|
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0006-2960
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
14
|
pubmed:volume |
21
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
4693-700
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:6291587-DNA Restriction Enzymes,
pubmed-meshheading:6291587-Deoxyribonucleases, Type II Site-Specific,
pubmed-meshheading:6291587-Kinetics,
pubmed-meshheading:6291587-Oligodeoxyribonucleotides,
pubmed-meshheading:6291587-Oligonucleotides,
pubmed-meshheading:6291587-Structure-Activity Relationship,
pubmed-meshheading:6291587-Substrate Specificity
|
pubmed:year |
1982
|
pubmed:articleTitle |
Interaction of the HpaI endonuclease with synthetic oligonucleotides.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|