首页> 外国专利> STRAINS OF ESCHERICHIA COLI MODIFIED BY METABOLIC ENGINEERING FOR THE PRODUCTION OF SUCCINIC ACID FROM GLUCOSE, XYLOSE OR A GLUCOSE-XYLOSE MIX, AS A SOURCE OF CARBON.

STRAINS OF ESCHERICHIA COLI MODIFIED BY METABOLIC ENGINEERING FOR THE PRODUCTION OF SUCCINIC ACID FROM GLUCOSE, XYLOSE OR A GLUCOSE-XYLOSE MIX, AS A SOURCE OF CARBON.

机译:通过代谢工程修饰的埃希氏菌菌株,用于从葡萄糖,木糖或葡萄糖-木糖混合物中生产糖基酸,作为碳源。

摘要

The present disclosure is related to new strains of Escherichia coli that use the phosphoenolpyruvate carboxykinase (Pck) enzyme, as the main carboxylation pathway of phosphoenolpyruvate to oxaloacetate, to produce succinic acid with a high yield from glucose, xylose or a glucose-xylose mixture as a carbon source. The new strain, called MS01 frdA Ptrcpck, was obtained with the integration of the pck gene into a chromosome under the control of an inducible promoter, and the other new strain called MS01 frdA Ptrcpck Appc, was obtained with the elimination of the ppc gene, that encodes the pyruvate carboxylase enzyme. The present invention also comprises a fermentation method in mineral medium with glucose, xylose or a glucose-xylose mixture, as a carbon source, which, using the new strains of E. coli, referred above, is used for the production of succinic acid. Particularly referring to the fermentative methods to produce succinic acid from mineral medium with glucose, xylose or a glucose-xylose mixture, as a carbon source, with low oxygen transfer rates. The reintegration of the frdA gene, into a non-fermentative strain of E. coli, allowed the new strains to produce succinic acid with high yields under low oxygen transfer rates (VTO) conditions, being the best production method, the one that provided a VTO of 2.24 mmol O2 L-1 h-1.
机译:本公开涉及新的大肠杆菌菌株,其使用磷酸烯醇丙酮酸羧激酶(Pck)酶作为磷酸烯醇丙酮酸转化为草酰乙酸的主要羧化途径,以高产率从葡萄糖,木糖或葡萄糖-木糖混合物制备琥珀酸。碳源。通过在诱导型启动子的控制下将pck基因整合到染色体中,获得了名为MS01 frdA Ptrcpck的新菌株,通过消除了ppc基因,获得了另一种名为MS01 frdA Ptrcpck Appc的新菌株,编码丙酮酸羧化酶。本发明还包括在矿物培养基中以葡萄糖,木糖或葡萄糖-木糖混合物作为碳源的发酵方法,其使用上述新的大肠杆菌菌株用于生产琥珀酸。特别是指从矿物质培养基中以葡萄糖,木糖或葡萄糖-木糖混合物作为碳源,以低的氧气转移速率生产琥珀酸的发酵方法。将frdA基因重新整合到大肠杆菌的非发酵菌株中,使新菌株能够在低氧传递速率(VTO)条件下以高收率生产琥珀酸,这是最好的生产方法,它提供了一种VTO为2.24 mmol O2 L-1 h-1。

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