Source:http://linkedlifedata.com/resource/pubmed/id/16186924
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
16
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pubmed:dateCreated |
2005-9-27
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pubmed:abstractText |
The hydroxylation of alpha-ionone 1 and beta-ionone 2 to their corresponding mono-hydroxylated derivatives has been examined using a recombinant E. coli whole cell system, in which cytochromes P450 SU1 and SU2, and P450 SOY were over-expressed with their cognate ferrodoxins. Both substrates are hydroxylated with a high degree of regioselectivity and for alpha-ionone 1 the reaction is highly diastereoselective yielding the anti-isomer.
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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 |
Aug
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pubmed:issn |
1477-0520
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
21
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2930-4
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16186924-Actinobacteria,
pubmed-meshheading:16186924-Biotransformation,
pubmed-meshheading:16186924-Catalysis,
pubmed-meshheading:16186924-Cytochrome P-450 Enzyme System,
pubmed-meshheading:16186924-Hydroxylation,
pubmed-meshheading:16186924-Norisoprenoids,
pubmed-meshheading:16186924-Stereoisomerism
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pubmed:year |
2005
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pubmed:articleTitle |
Efficient terpene hydroxylation catalysts based upon P450 enzymes derived from actinomycetes.
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pubmed:affiliation |
School of Chemistry, University of Edinburgh, West Mains Road, Edinburgh, EH9 3JJ, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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