The enzymatic conversion of exomethylene cephalosporin c into deacetyl cephalosporin c and the role of molecular oxygen in cephalosporin c biosynthesis
- 1 January 1988
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 44 (2) , 643-650
- https://doi.org/10.1016/s0040-4020(01)85852-x
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
- The role of molecular oxygen in cephalosporin C biosynthesisJournal of the Chemical Society, Chemical Communications, 1987
- Stereochemical fate of chiral methyl of valine in the ring expansion of penicillin N to deacetoxycephalosporin CJournal of the American Chemical Society, 1985
- Stereochemical investigation of the α-ketoglutarate-dependent 3′-hydroxylation in cephalosporin biosynthesisJournal of the Chemical Society, Chemical Communications, 1984
- Penicillin biosynthesis: multiple pathways from a modified substrateJournal of the Chemical Society, Chemical Communications, 1984
- .gamma.-Butyrobetaine hydroxylase: primary and secondary tritium kinetic isotope effectsBiochemistry, 1983
- Conversion of 3-exomethylene cephalosporin C into deacetyl cephalosporin C in a cell-free extract from Cephalosporium acremonium(CW-19)Journal of the Chemical Society, Chemical Communications, 1983
- A stereochemical concept for the catalytic mechanism of prolylhydroxylaseJournal of Theoretical Biology, 1982
- Synthesis and incorporation of (2S,3S)-valine-4 13C into .beta.-lactam antibioticsJournal of the American Chemical Society, 1973
- Incorporation of (2RS,3S)-[4-13C]-valine into cephalosporin CJournal of the American Chemical Society, 1973
- Beitrag zur Aminosäurebestimmung auf PapierchromatogrammenHoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1958