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Identification of hexose kinase genes in Kluyveromyces marxianus and thermo-tolerant one step producing glucose-free fructose strain construction

机译:马克斯克鲁维酵母中己糖激酶基因的鉴定及耐热一步法生产无葡萄糖果糖菌株的构建

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摘要

In yeast, the hexose assimilation is started at hexose phosphorylation. However, in Kluyveromyces marxianus, the hexokinase (HXK) and glucokinase (GLK) genes were not identified by experiments. Meanwhile, the glucose-free fructose product requires more cost-efficient method. In this study, the KmHXK1 and KmGLK1 genes were functionally identified through gene disruption, over-expression and recombinant enzymes characterization. Both glucose and fructose assimilation ability decreased significantly in KmHXK1 disrupted strain YLM001, however, this ability was not changed obviously in KmGLK1 disrupted strain YLM002. When over-expressing KmGLK1 in YLM001, only the glucose assimilation ability was recovered in obtained strain (YLM005). The kinetic constant analysis of recombinant enzymes also proved that KmHXK1 could phosphorylate glucose (Vmax 553.01 U/mg, Km 0.83 mM) and fructose (Vmax 609.82 U/mg, Km 0.52 mM), and KmGLK1 only phosphorylate glucose with a Vmax of 0.73 U/mg and a Km 4.09 mM. A thermo-tolerant strain YGR003 which produced glucose-free fructose from Jerusalem artichoke tuber in one step was constructed based on the obtained information. The highest production and fastest productivity were 234.44 g/L and 10.26 g/L/h, respectively, which were several folds of the results in previous reports.
机译:在酵母中,己糖同化在己糖磷酸化时开始。但是,在马克斯克鲁维酵母中,己糖激酶(HXK)和葡萄糖激酶(GLK)基因未通过实验鉴定。同时,无葡萄糖果糖产品需要更具成本效益的方法。在这项研究中,KmHXK1和KmGLK1基因通过基因破坏,过度表达和重组酶表征进行功能鉴定。在KmHXK1破坏菌株YLM001中,葡萄糖和果糖的同化能力均显着降低,但在KmGLK1破坏菌株YLM002中,该能力没有明显改变。当在YLM001中过表达KmGLK1时,在获得的菌株(YLM005)中仅恢复了葡萄糖同化能力。重组酶的动力学常数分析还证明KmHXK1可以磷酸化葡萄糖(Vmax 553.01 U / mg,Km 0.83 mM)和果糖(Vmax 609.82 U / mg,Km 0.52 mM),KmGLK1仅磷酸化葡萄糖,Vmax为0.73 UM。 / mg和Km 4.09 mM。基于所获得的信息,构建了一步制得菊芋块茎的无葡萄糖果糖的耐热菌株YGR003。最高的产量和最快的生产率分别为234.44微克/升和10.26微克/升/小时,这是以前报告的几倍。

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