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Engineering the α-ketoglutarate overproduction from raw glycerol by overexpression of the genes encoding NADP~+-dependent isocitrate dehydrogenase and pyruvate carboxylase in Yarrowia lipolytica

机译:通过解脂耶氏酵母中编码NADP〜+依赖性异柠檬酸脱氢酶和丙酮酸羧化酶的基因的过表达来工程化粗甘油中α-酮戊二酸的过量生产

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摘要

To establish and develop a biotechnological process of α-ketoglutaric acid (KGA) production by Yarrowia lipolytica, it is necessary to increase the KGA productivity and to reduce the amounts of by-products, e.g. pyruvic acid(PA) as major by-product and fumarate, malate and succinate as minor by-products. The aim of this study was the improvement of KGA overproduction with Y. lipolytica by a gene dose-dependent overexpression of genes encoding NADP~+- dependent isocitrate dehydrogenase (IDP1) and pyruvate carboxylase(PYC1) under KGA production conditions from the renewable carbon source raw glycerol. Recombinant Y. lipolytica strains were constructed, which harbour multiple copies of the respective IDP1, PYC1 or IDP1 and PYC1 genes together. We demonstrated that a selective increase in IDP activity in IDP1 multicopy transformants changes the produced amount of KGA. Overexpression of the gene IDP1 in combination with PYC1 had the strongest effect on increasing the amount of secreted KGA. About 19 % more KGA compared to strain H355 was produced in bioreactor experiments with raw glycerol as carbon source. The applied cultivation conditions with this strain significantly reduced the main by-product PA and increased the KGA selectivity to more than 95 % producing up to 186 g l~(-1) KGA. This proved the high potential of this multicopy transformant for developing a biotechnological KGA production process
机译:为了建立和发展解脂耶氏酵母生产α-酮戊二酸(KGA)的生物技术方法,有必要提高KGA的生产率并减少副产物的量,例如通过化学方法。丙酮酸(PA)为主要副产物,富马酸酯,苹果酸和琥珀酸酯为次要产物。这项研究的目的是通过在可再生碳源的KGA生产条件下,通过编码NADP〜+依赖性异柠檬酸脱氢酶(IDP1)和丙酮酸羧化酶(PYC1)的基因的剂量依赖性过表达来改善解脂耶氏酵母的KGA过量生产。生甘油。构建了重组解脂耶氏酵母菌株,它们一起携带各自的IDP1,PYC1或IDP1和PYC1基因的多个副本。我们证明IDP1多拷贝转化体中IDP活性的选择性增加改变了KGA的产生量。 IDP1基因与PYC1的过表达对增加分泌的KGA的影响最强。在以生甘油为碳源的生物反应器实验中,与菌株H355相比,KGA的产量增加了约19%。在该菌株上施加的培养条件显着降低了主要副产物PA,并将KGA选择性提高到95%以上,从而产生高达186 g l〜(-1)KGA。这证明了这种多拷贝转化体在开发生物技术KGA生产工艺方面的巨大潜力

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