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食油假单胞菌对1,7-辛二烯的环氧化作用:在环己烷存在下的发酵过程

Epoxidation of 1,7-octadiene by Pseudomonas oleovorans: fermentation in the presence of cyclohexane.

作者信息

Schwartz R D, McCoy C J

出版信息

Appl Environ Microbiol. 1977 Jul;34(1):47-9. doi: 10.1128/aem.34.1.47-49.1977.

Abstract

A very efficient conversion of 1,7-octadiene to 7,8-epoxy-1-octene and 1,2-7,8-diepoxyoctane was achieved by incorporating a high concentration of cyclohexane into the conventional fermentation medium. In the presence of cyclohexane, a 90-ml% conversion of substrate to product was accomplished within 72 h, compared with an 18,5-mol% conversion in the absence of cyclohexane. Furthermore, the products were simultaneously separated and concentrated in the organic phase.

摘要

通过在传统发酵培养基中加入高浓度的环己烷,实现了1,7-辛二烯高效转化为7,8-环氧-1-辛烯和1,2-7,8-二环氧辛烷。在环己烷存在的情况下,72小时内底物到产物的转化率达到90毫升%,而在没有环己烷的情况下转化率为18.5摩尔%。此外,产物在有机相中同时被分离和浓缩。

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本文引用的文献

1
Stereoselective epoxidation of octadiene catalyzed by an enzyme system of Pseudomonas oleovorans.
J Am Chem Soc. 1974 Jun 12;96(12):4031-2. doi: 10.1021/ja00819a060.
7
On the role of superoxide in reactions catalyzed by rubredoxin of Pseudomonas oleovorans.
Biochem Biophys Res Commun. 1973 Oct 15;54(4):1540-5. doi: 10.1016/0006-291x(73)91161-3.
8
Structural effects on the reactivity of substrates and inhibitors in the epoxidation system of Pseudomonas oleovorans.
Biochim Biophys Acta. 1975 Sep 22;403(1):245-55. doi: 10.1016/0005-2744(75)90026-1.

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