首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Enzymatic epoxidation: synthesis of 78-epoxy-1-octene 12-78-diepoxyoctane and 12-Epoxyoctane by Pseudomonas oleovorans.
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Enzymatic epoxidation: synthesis of 78-epoxy-1-octene 12-78-diepoxyoctane and 12-Epoxyoctane by Pseudomonas oleovorans.

机译:酶促环氧化:油酸假单胞菌合成78-环氧-1-辛烯1278-二环氧辛烷和12-环氧辛烷。

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摘要

The kinetics of the enzymatic formation of 7,8-epoxy-1-octene, 1,2-7,8-diepoxyoctane, and 1,2-epoxyoctane by growing and resting cell suspensions of Pseudomonas oleovorans are described. Formation of 1,2-epoxyoctane occurs concurrently with exponential growth on 1-octene, providing that 1-octene is in excess. Conversion of 1,7-octadiene to 7,8-epoxy-1-octene by cells growing on octane lags behind exponential growth and continues into the stationary phase, terminating upon cell death. Formation of 1,2-7,8-diepoxyoctane does not begin until the cells are well into the stationary phase and also continues until cell death. Results with growing and resting cell suspensions suggest that the various substrates compete for the same enzyme system; that viable cells are essential for substrate transport and epoxidation by whole cells; and that whole cells may concentrate and sequester the epoxides, rendering them unrecoverable by our current methods.
机译:描述了通过油菜假单胞菌的生长和静止细胞悬浮液酶促形成7,8-环氧-1-辛烯,1,2,7,8-二环氧辛烷和1,2-环氧辛烷的动力学。只要1-辛烯过量,就会在1-辛烯上指数增长同时形成1,2-环氧辛烷。在辛烷上生长的细胞将1,7-辛二烯转化为7,8-环氧-1-辛烯的过程要比指数增长滞后,并进入固定相,并在细胞死亡时终止。直到细胞完全进入固定相才开始形成1,2-7,8-二环氧辛烷,并且一直持续到细胞死亡。生长和静止的细胞悬浮液的结果表明,各种底物竞争相同的酶系统。活细胞对于全细胞的底物转运和环氧化至关重要;而且整个细胞可能会浓缩并隔离环氧化合物,从而使它们无法通过我们目前的方法进行回收。

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