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Isolation of pure anhydrotetracycline oxygenase from Streptomyces aureofaciens.

作者信息

Vancurová I, Volc J, Flieger M, Neuzil J, Novotná J, Vlach J, Bĕhal V

机构信息

Institute of Microbiology, Czechoslovak Academy of Sciences, Prague.

出版信息

Biochem J. 1988 Jul 1;253(1):263-7. doi: 10.1042/bj2530263.

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.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a833/1149284/cccff42e5de1/biochemj00228-0264-a.jpg

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