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Potential Pathogenicity of Candida maltosa IAM 12248
Authors:Minoru Yoshida  Kazunori Hashimoto
Affiliation:National Institute of Animal Health, Kannondai 3–1–1, Yatabe-machi, Tsukuba-gun, Ibaraki 305, Japan
Abstract:The stereochemistry of (+)-(2Z,4E)-trans-1′,4′-dihydroxy-γ-ionylideneacetic acid, a major metabolite from Cercospora cruenta, a fungus found to produce (+)-abscisic acid, was reexamined as to its 1H?1H-Cosy and Noesy 2D-NMR spectra, and it was proved to have a chair conformation with an axial pentadienoate moiety. Further, the metabolism of (+)-[14C]-1′,4′-dihydroxy-γ-ionylideneacetic acid in tomato plants suggested the possibility of it being a biosynthetic intermediate of ABA in plants.
Keywords:
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