Source:http://linkedlifedata.com/resource/pubmed/id/15070349
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
14
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pubmed:dateCreated |
2004-4-8
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pubmed:abstractText |
Jadomycin B, an antifungal antibiotic with a unique 8H-benz[b]oxazolo[3,2-f]phenanthridine pentacyclic skeleton produced by the bacterium Streptomyces venezuelae ISP 5230, exists in a dynamic equilibrium of two diastereomers differing in the configuration of C-3a. Several novel jadomycins with various amino acid-derived 1-side chains could be generated, by replacing isoleucine in the production medium of S. venezuelae with other amino acids. These two findings led to the conclusion that a nonenzymatic reaction with the amino acid followed by a likewise nonenzymatic cyclization cascade are crucial for its late biosynthesis.
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pubmed:grant | |
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 |
Apr
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pubmed:issn |
0002-7863
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
14
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pubmed:volume |
126
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4496-7
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pubmed:dateRevised |
2008-1-17
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pubmed:meshHeading |
pubmed-meshheading:15070349-Amino Acids,
pubmed-meshheading:15070349-Hydrogen Bonding,
pubmed-meshheading:15070349-Isoleucine,
pubmed-meshheading:15070349-Isoquinolines,
pubmed-meshheading:15070349-Models, Molecular,
pubmed-meshheading:15070349-Molecular Conformation,
pubmed-meshheading:15070349-Nuclear Magnetic Resonance, Biomolecular,
pubmed-meshheading:15070349-Stereoisomerism
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pubmed:year |
2004
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pubmed:articleTitle |
The dynamic structure of jadomycin B and the amino acid incorporation step of its biosynthesis.
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pubmed:affiliation |
Division of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, 907 Rose Street, Lexington, Kentucky 40536-0082, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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