Isolation of an intermediate of 2-deoxystreptamine biosynthesis from a mutant of Bacillus circulans.
- 1 January 1980
- journal article
- research article
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 33 (8) , 824-829
- https://doi.org/10.7164/antibiotics.33.824
Abstract
Eight 2-deoxystreptamine-negative (DOS-) mutants were isolated from various strains of B. circulans, normally producing butirosin, xylostasin and ribostamycin. These mutants were classified into 2 groups (converter and secretor) by the simple method of cosynthesis using agar plate culture. One of the cosynthetic pairs, strain S-11 and strain 236, was selected for further study. From the fermentation broth of strain S-11, an intermediate of DOS biosynthesis, S-11-P, was isolated. This compound was converted to butirosin (BTN) effectively by strain 236. The structure of S-11-P was considered to be (1 L or 1 D)-1,3,5/2,4-5-aminocyclohexanetetrol and the pathway of DOS biosynthesis is discussed here.This publication has 5 references indexed in Scilit:
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