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The pathway ofD-cycloserine biosynthesis inStreptomyces garyphalus
Authors:Marie-Louise Svensson  Sten Gatenbeck
Affiliation:(1) Department of Biochemistry and Biotechnology, Royal Institute of Technology, S-100 44 Stockholm, Sweden
Abstract:
Incubation experiments using washed cells and toluene treated cells ofStreptomyces garyphalus showed that O-acetyl-L-serine and hydroxyurea are intermediates in the biosynthesis ofD-cycloserine. The formation of [14C]O-ureidoserine from O-acetyl-L-serine and hydroxyurea was demonstrated by incubating an enzyme solution with14C-labelled substrates. Desalted cell-free extract catalyzed the conversion of O-ureido-D-serine toD-cycloserine in a reaction requiring ATP and Mg2+. The results suggested the following pathway forD-cycloserine biosynthesis.
Keywords:D-Cycloserine  O-Ureido-D-serine  Biosynthesis  Streptomyces garyphalus
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