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PROCESS FOR THE BIOLOGICAL MANUFACTURE OF 1,3-PROPANDIOL

机译:1,3-丙二醇的生物制备过程

摘要

The present invention provides an improved method for the biological production of 1,3-propanediol from a fermentable carbon source in a single microorganism. In one aspect of the present invention, an improved process for the conversion of glucose to 1,3-propanediol is achieved by the use of an E. coli transformed with the Klebsiella pneumoniae dha regulon genes dhaR, orfY, dhaT, orfX, orfW, dhaB1, dhaB2, dhaB3, and orfZ, all these genes arranged in the same genetic organization as found in wild type Klebsiella pneumoniae. In another aspect of the present invention, an improved process for the production of 1,3-propanediol from glucose using a recombinant E. coli containing genes encoding a G3PDH, a G3P phosphatase, a dehydratase, and a dehydratase reactivation factor compared to an identical process using a recombinant E. coli containing genes encoding a G3PDH, a G3P phosphatase, a dehydratase, a dehydratase reactivation factor and a 1,3-propanediol oxidoreductase (dhaT). The dramatically improved process relies on the presence in E. coli of a gene encoding a non-specific catalytic activity sufficient to convert 3-hydroxypropionaldehyde to 1,3-propanediol.
机译:本发明提供了一种在单一微生物中从可发酵碳源生物生产1,3-丙二醇的改进方法。在本发明的一个方面,通过使用转化为肺炎克雷伯氏菌dha regulon基因dhaR,orfY,dhaT,orfX或orfW的大肠杆菌来实现将葡萄糖转化为1,3-丙二醇的改进方法。 dhaB1,dhaB2,dhaB3和orfZ,所有这些基因都以与野生型肺炎克雷伯菌相同的遗传组织排列。在本发明的另一方面,使用重组大肠杆菌从葡萄糖生产1,3-丙二醇的改进方法,所述重组大肠杆菌包含与相同的基因相比编码G3PDH,G3P磷酸酶,脱水酶和脱水酶再活化因子的基因。使用包含编码G3PDH,G3P磷酸酶,脱水酶,脱水酶再活化因子和1,3-丙二醇氧化还原酶(dhaT)的基因的重组大肠杆菌进行酶切过程。显着改善的过程依赖于大肠杆菌中存在的基因,该基因编码的非特异性催化活性足以将3-羟基丙醛转化为1,3-丙二醇。

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