Source:http://linkedlifedata.com/resource/pubmed/id/10626375
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2000-2-11
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pubmed:abstractText |
The endoperoxide sesquiterpene lactone artemisinin and its derivatives are a promising new group of drugs against malaria. Artemisinin is a constituent of the annual herb Artemisia annua L. So far only the later steps in artemisinin biosynthesis--from artemisinic acid--have been elucidated and the expected olefinic sesquiterpene intermediate has never been demonstrated. In pentane extracts of A. annua leaves we detected a sesquiterpene with the mass spectrum of amorpha-4,11-diene. Synthesis of amorpha-4,11-diene from artemisinic acid confirmed the identity. In addition we identified several sesquiterpene synthases of which one of the major activities catalysed the formation of amorpha-4,11-diene from farnesyl diphosphate. This enzyme was partially purified and shows the typical characteristics of sesquiterpene synthases, such as a broad pH optimum around 6.5-7.0, a molecular mass of 56 kDa, and a K(m) of 0.6 microM. The structure and configuration of amorpha-4,11-diene, its low content in A. annua and the high activity of amorpha-4,11-diene synthase all support that amorpha-4,11-diene is the likely olefinic sesquiterpene intermediate in the biosynthesis of artemisinin.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Alkyl and Aryl Transferases,
http://linkedlifedata.com/resource/pubmed/chemical/Antimalarials,
http://linkedlifedata.com/resource/pubmed/chemical/Artemisinins,
http://linkedlifedata.com/resource/pubmed/chemical/Drugs, Chinese Herbal,
http://linkedlifedata.com/resource/pubmed/chemical/Ligases,
http://linkedlifedata.com/resource/pubmed/chemical/Polyisoprenyl Phosphates,
http://linkedlifedata.com/resource/pubmed/chemical/Sesquiterpenes,
http://linkedlifedata.com/resource/pubmed/chemical/artemisinine,
http://linkedlifedata.com/resource/pubmed/chemical/farnesyl pyrophosphate
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0031-9422
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
52
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
843-54
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10626375-Alkyl and Aryl Transferases,
pubmed-meshheading:10626375-Antimalarials,
pubmed-meshheading:10626375-Artemisia,
pubmed-meshheading:10626375-Artemisinins,
pubmed-meshheading:10626375-Catalysis,
pubmed-meshheading:10626375-Drugs, Chinese Herbal,
pubmed-meshheading:10626375-Hydrogen-Ion Concentration,
pubmed-meshheading:10626375-Ligases,
pubmed-meshheading:10626375-Molecular Weight,
pubmed-meshheading:10626375-Plant Leaves,
pubmed-meshheading:10626375-Plants, Medicinal,
pubmed-meshheading:10626375-Polyisoprenyl Phosphates,
pubmed-meshheading:10626375-Sesquiterpenes
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pubmed:year |
1999
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pubmed:articleTitle |
Amorpha-4,11-diene synthase catalyses the first probable step in artemisinin biosynthesis.
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pubmed:affiliation |
Research Institute for Agrobiology and Soil Fertility (AB-DLO), Wageningen, Netherlands. h.j.bouwmeester@ab.dlo.nl
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pubmed:publicationType |
Journal Article
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