| Literature DB >> 3138982 |
I Vancurová1, J Volc, M Flieger, J Neuzil, J Novotná, J Vlach, V Bĕhal.
Abstract
Anhydrotetracycline oxygenase was purified to homogeneity from Streptomyces aureofaciens, a producer of tetracycline. The enzyme was purified 60-fold in a 40% yield by a two-step procedure using a combination of hydrophobic chromatography and ion-exchange h.p.l.c. Purified anhydrotetracycline oxygenase was homogeneous according to SDS/polyacrylamide-gel electrophoresis, isoelectric focusing, ion-exchange h.p.l.c. on a Mono Q HR 5/5 column and size-exclusion h.p.l.c. on a TSK G 3000 SW column. The enzyme consists of two subunits of Mr 57,500, as determined by SDS/polyacrylamide-gel electrophoresis.Entities:
Mesh:
Year: 1988 PMID: 3138982 PMCID: PMC1149284 DOI: 10.1042/bj2530263
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857