Isolation of an intermediate of 2-deoxystreptamine biosynthesis from a mutant of Bacillus circulans.

نویسندگان

  • T Fujiwara
  • Y Takahashi
  • K Matsumoto
  • E Kondo
چکیده

Eight 2-deoxystreptamine-negative (DOS-) mutants were isolated from various strains of Bacillus circulans, normally producing butirosin, xylostasin and ribostamycin. These mutants were classified into two groups (converter and secretor) by the simple method of cosynthesis using agar plate culture. One of the cosynthetic pairs, 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-amino-cyclohexanetetrol, and the pathway of DOS biosynthesis is discussed here.

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منابع مشابه

Structure elucidation of an intermediate of 2-deoxystreptamine biosynthesis.

The structure of a 2-deoxystreptamine (DOS) precursor named S-11-P, which was isolated by using a DOS negative mutant derived from a xylostasin-producing strain of Bacillus circulans B15M, has been elucidated as (1 L)-1,3,5/2,4,-5-aminocyclohexanetetrol by comparison with an authentic specimen, which was synthesized from kanamycin A.

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عنوان ژورنال:
  • The Journal of antibiotics

دوره 33 8  شماره 

صفحات  -

تاریخ انتشار 1980