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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1999-1-26
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pubmed:abstractText |
The novel phospholipid 2, which bears a tert-butyl moiety in place of the natural trimethyl ammonium group of phosphatidylcholine, has been enzymatically synthesized via a transphosphatidylation reaction mediated by phospholipase D. The change from the choline headgroup in 1 to the tert-butyl group in 2 reduced the efficiency of hydrolysis by the phosphatidylcholine-preferring phospholipase C from Bacillus cereus by a factor of greater than 10(3).
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
17
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
593-6
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:9871566-Bacillus cereus,
pubmed-meshheading:9871566-Kinetics,
pubmed-meshheading:9871566-Models, Chemical,
pubmed-meshheading:9871566-Mutagenesis, Site-Directed,
pubmed-meshheading:9871566-Phosphatidylcholines,
pubmed-meshheading:9871566-Phospholipase D,
pubmed-meshheading:9871566-Type C Phospholipases
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pubmed:year |
1998
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pubmed:articleTitle |
Enzymatic synthesis of a modified phospholipid and its evaluation as a substrate for B. cereus phospholipase C.
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pubmed:affiliation |
Department of Chemistry and Biochemistry, University of Texas at Austin 78712, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|