Bioscience, Biotechnology, and Biochemistry
Online ISSN : 1347-6947
Print ISSN : 0916-8451
Microbiology & Fermentation Technology Notes
Asymmetric Reduction of Ethyl 2-methyl 3-oxobutanoate by Chlorella
Takayuki KURAMOTOKenzo IWAMOTOMinoru IZUMIMitsunori KIRIHATAFumiki YOSHIZAKO
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1999 年 63 巻 3 号 p. 598-601

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  Chlorella pyrenoidosa Chick reduced ethyl 2-methyl 3-oxobutanoate to the corresponding alcohols with the diastereomer (anti/syn) ratio of 53/47. The enantiomer excesses of anti-(2S, 3S)- and syn-(2S, 3R)-hydroxy esters were 89 and >99ee% respectively. C. vulgaris and C. regularis afforded predominantly the syn-isomer, contrary to C. pyrenoidosa. The differences in the activity of reducing ethyl 2-methyl 3-oxobutanoate were observed among three strains of Chlorella. Addition of 2% metal salts slightly increased the chemical yield of the hydroxy ester.
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© 1999 by Japan Society for Bioscience, Biotechnology, and Agrochemistry
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