首页> 外文期刊>Bioresource Technology: Biomass, Bioenergy, Biowastes, Conversion Technologies, Biotransformations, Production Technologies >Co-fermentation of glycerol and glucose by a co-culture system of engineered Escherichia coli strains for 1,3-propanediol production without vitamin B-12 supplementation
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Co-fermentation of glycerol and glucose by a co-culture system of engineered Escherichia coli strains for 1,3-propanediol production without vitamin B-12 supplementation

机译:通过维生素B-12的工程化学大肠杆菌菌株的甘油和葡萄糖的共同发酵通过维生素B-12的1,3-丙二醇生产

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摘要

The necessity of costly co-enzyme B-12 for the activity of glycerol dehydratase (GDHt) is considered as a major bottleneck in sustainable bioproduction of 1,3-propanediol (1,3-PD) from glycerol. Here, an E. coil RosettadhaB1-dhaB2 strain was constructed by overexpressing a B-12-independent GDHt (dhaB1) and its activating factor (dhaB2) from Clostridium butyricum. Subsequently, it was used in designing a co-culture with E. coli BL21-dhaT that overexpressed 1,3-PD oxidoreductase (dhaT), to produce 1,3-PD during co-fermentation of glycerol and glucose. The optimum initial ratio of BL21-dhaT to Rosetta-dhaB1-dhaB2 strains in the co-culture was 1.5. Compared to the fermentation of glycerol alone, co-fermentation approach provided 1.3-folds higher 1,3-PD. Finally, co-fermentation was done in a 10 L bioreactor that produced 41.65 g/L 1,3-PD, which corresponded to 0.69 g/L/h productivity and 0.67 mol/mol yield of 1,3-PD. Hence, the developed co-culture could produce 1,3-PD cost-effectively without requiring vitamin B-12.
机译:甘油脱水酶(GDHt)活性需要昂贵的辅酶B-12,这被认为是从甘油可持续生物生产1,3-丙二醇(1,3-PD)的主要瓶颈。在这里,通过从酪酸梭菌中过度表达B-12非依赖性GDHt(dhaB1)及其激活因子(dhaB2),构建了E.coil Rosettab1-dhaB2菌株。随后,它被用于设计与过度表达1,3-PD氧化还原酶(dhaT)的大肠杆菌BL21 dhaT的共培养物,以在甘油和葡萄糖的共发酵期间产生1,3-PD。在共培养中,BL21 dhaT与Rosetta-dhaB1-dhaB2菌株的最佳初始比例为1.5。与单独发酵甘油相比,共发酵法提供的1,3-PD高出1.3倍。最后,在10L生物反应器中进行共发酵,产生41.65g/L 1,3-PD,对应于0.69g/L/h的生产率和0.67mol/mol的1,3-PD产量。因此,开发的共培养物可以在不需要维生素B-12的情况下经济高效地生产1,3-PD。

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