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Polyhydroxyalkanoate production from sucrose by Cupriavidus necator strains harboring csc genes from Escherichia coli W

机译:从大肠杆菌W的Cupriavidus Necator菌株蔗糖产生的聚羟基烷烃生产来自大肠杆菌W的CSC基因

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Cupriavidus necator H16 is the most promising bacterium for industrial production of polyhydroxyalkanoates (PHAs) because of their remarkable ability to accumulate them in the cells. With genetic modifications, this bacterium can produce poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHHx), which has better physical properties, as well as poly(3-hydroxybutyrate) (PHB) using plant oils and sugars as a carbon source. Considering production cost, sucrose is a very attractive raw material because it is inexpensive; however, this bacterium cannot assimilate sucrose. Here, we used the sucrose utilization (csc) genes of Escherichia coli W to generate C. necator strains that can assimilate sucrose. Especially, glucose-utilizing recombinant C. necator strains harboring the sucrose hydrolase gene (cscA) and sucrose permease gene (cscB) of E. coli W grew well on sucrose as a sole carbon source and accumulated PHB. In addition, strains introduced with a crotonyl-CoA reductase gene (ccr), ethylmalonyl-CoA decarboxylase gene (emd), and some other genetic modifications besides the csc genes and the glucose-utilizing mutations produced PHBHHx with a 3-hydroxyhexanoate (3HHx) content of maximum approximately 27 mol% from sucrose. Furthermore, when one of the PHBHHx-producing strains was cultured with sucrose solution in a fed-batch fermentation, PHBHHx with a 3HHx content of approximately 4 mol% was produced and reached 113 g/L for 65 h, which is approximately 1.5-fold higher than that produced using glucose solution.
机译:Cupriavidus Necator H16是最有前途的用于工业生产的多羟基烷烃(PHA),因为它们在细胞中积聚它们的显着能力。通过遗传修饰,该细菌可以产生聚(3-羟基丁酸酯-CO-3-羟基己酸酯)(PHBHHX),其具有更好的物理性质,以及使用植物油和糖作为碳的聚(3-羟基丁酸酯)(PHB)来源。考虑生产成本,蔗糖是一种非常有吸引力的原料,因为它廉价;然而,这种细菌不能吸收蔗糖。这里,我们使用大肠杆菌W的蔗糖利用(CSC)基因产生可以吸收蔗糖的C.菌株。特别是,利用重组C.含有大肠杆菌W的蔗糖水解基因(CSCA)和蔗糖允许基因(CSCB)的葡萄糖菌株在蔗糖作为唯一的碳源和积累的PHB中。此外,除了CSC基因之外,用克罗托隆-CoA还原酶基因(CCR),乙基甘油基-COA脱羧酶基因(EMD)和一些其他遗传修饰引入的菌株和一些其他遗传修饰。用3-羟基己酸酯(3HHX)产生pHBHHX蔗糖最大约27mol%的含量。此外,当在FED分批发酵中用蔗糖溶液培养PHBHHX产生菌株之一时,产生3HHx含量约为4mol%的PHBHHX,达到115小时,达到65小时,约为1.5倍高于使用葡萄糖溶液产生的。

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