کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10247937 | 48934 | 2005 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Biotransformation of (+)-(1R)- and (â)-(1S)-fenchone by the larvae of common cutworm (Spodoptera litura)
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
کاتالیزور
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چکیده انگلیسی
Biotransformation of (+)-(1R)- and (â)-(1S)-fenchone in Spodoptera litura larvae has been investigated. (+)- and (â)-Fenchone were regio- and stereo-selective hydroxylated. (+)-Fenchone was transformed to one new terpenoid, (+)-(1S,4R)-3-oxo-2,2,4-trimethyl-cyclopentylacetic acid and four known terpenoids, (+)-(1S,6S)-6-exo-hydroxyfenchone, (+)-(1S,6R)-6-endo-hydroxyfenchone, (+)-(1R)-10-hydroxyfenchone and (+)-(1S,5R)-5-exo-hydroxyfenchone. (â)-Fenchone was transformed to one new terpenoid, (â)-(1S)-10-hydroxyfenchone and four known terpenoids, (â)-(1R,6R)-6-exo-hydroxyfenchone, (â)-(1R,6S)-6-endo-hydroxyfenchone, (â)-(1R,5S)-5-exo-hydroxyfenchone and (â)-(1R,4S)-3-oxo-2,2,4-trimethyl-cyclopentylacetic acid. C-6 position of (+)- and (â)-fenchone was progressing to the carboxylic acid, which is characteristically metabolic pathway compared with any other biocatalysts. Intestinal bacteria from the frass of larvae did not participate in the metabolism of (+)- and (â)-fenchone.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Catalysis B: Enzymatic - Volume 32, Issue 4, 1 February 2005, Pages 123-130
Journal: Journal of Molecular Catalysis B: Enzymatic - Volume 32, Issue 4, 1 February 2005, Pages 123-130
نویسندگان
Mitsuo Miyazawa, Yohei Miyamoto,