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Fluorometabolite biosynthesis: isotopically labelled glycerol incorporations into the antibiotic nucleocidin in Streptomyces calvus.
Bartholomé, Axel; Janso, Jeffrey E; Reilly, Usa; O'Hagan, David.
  • Bartholomé A; University of St Andrews, School of Chemistry and Centre for Biomolecular Sciences, North Haugh, St Andrews, Fife KY16 9ST, UK. do1@st-andrews.ac.uk.
  • Janso JE; Worldwide Research and Development, Medicinal Sciences, Pfizer, 445 Eastern Point Rd, Groton, CT 06340, USA.
  • Reilly U; Worldwide Research and Development, Medicinal Sciences, Pfizer, 445 Eastern Point Rd, Groton, CT 06340, USA.
  • O'Hagan D; University of St Andrews, School of Chemistry and Centre for Biomolecular Sciences, North Haugh, St Andrews, Fife KY16 9ST, UK. do1@st-andrews.ac.uk.
Org Biomol Chem ; 15(1): 61-64, 2016 Dec 20.
Article en En | MEDLINE | ID: mdl-27845468
ABSTRACT
Deuterium and carbon-13 labelled glycerols have been fed to Streptomyces calvus fermentations and isotope incorporation into the fluorine containing antibiotic nucleocidin have been evaluated by 19F-NMR. A single deuterium atom was incorporated from [2H5]- and (R)-[2H2]-glycerol into C-5' of the antibiotic, suggesting that an oxidation occurs at this carbon after ribose ring assembly from glycerol (pentose phosphate pathway), during nucleocidin biosynthesis.
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Banco de datos: MEDLINE Asunto principal: Streptomyces / Adenosina / Glicerol / Antibacterianos Idioma: En Año: 2016 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Streptomyces / Adenosina / Glicerol / Antibacterianos Idioma: En Año: 2016 Tipo del documento: Article