Production of Optically Active 1,2,4-Butanetriol from Corresponding Racemate by Microbial Stereoinversion(MICROBIAL PHYSIOLOGY AND BIOTECHNOLOGY)
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概要
- 論文の詳細を見る
Sterigmatomyces elviae DSM 70852 produced 12 g/l (S)-1,2,4-butanetriol (enantiomeric excess >99.9%) from 20 g/l racemate in 82 h. From the results of the inversion of an (R)-isomer to an (S)-isomer and GC-MS, it was suggested that (R)-1,2,4-butanetrioI is oxidized to 1,4-dihydroxy-2-butanone, which is reduced to an (S)-isomer.
- 公益社団法人日本生物工学会の論文
- 2007-05-25
著者
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Tani Yoshiki
Graduate School Of Biological Sciences Nara Institute Of Science And Technology
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YAMAMOTO Hiroaki
Tsukuba Research Center, Daicel Chemical Industries, Ltd.
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Kawada Naoki
Tsukuba Research Center, Daicel Chemical Industries, Ltd.
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Kawada Naoki
Tsukuba Research Center Daicel Chemical Industries Ltd.
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Yamada-onodera Keiko
Graduate School Of Biological Sciences Nara Institute Of Science And Technology
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Norimoto Akihiro
Graduate School of Biological Sciences, Nara Institute of Science and Technology
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Furuya Rika
Tsukuba Research Center, Daicel Chemical Industries, Ltd.
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Tani Yoshiki
Graduate School Of Biological Sciences Advanced Institute Of Science And Technology
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Yamada-onodera Keiko
Graduate School Of Biological Sciences Nara Inst. Of Sci. And Technol.
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Yamamoto Hiroaki
Tsukuba Research Center Daicel Chemical Industries Ltd.
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Norimoto Akihiro
Graduate School Of Biological Sciences Nara Institute Of Science And Technology
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Furuya Rika
Tsukuba Research Center Daicel Chemical Industries Ltd.
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