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Overproduction of the membrane-bound [NiFe]-hydrogenase in Thermococcus kodakarensis and its effect on hydrogen production

机译:柯达热球菌膜结合[NiFe]-加氢酶的过量生产及其对产氢的影响

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摘要

The hyperthermophilic archaeon Thermococcus kodakarensis can utilize sugars or pyruvate for growth. In the absence of elemental sulfur, the electrons via oxidation of these substrates are accepted by protons, generating molecular hydrogen (H2). The hydrogenase responsible for this reaction is a membrane-bound [NiFe]-hydrogenase (Mbh). In this study, we have examined several possibilities to increase the protein levels of Mbh in T. kodakarensis by genetic engineering. Highest levels of intracellular Mbh levels were achieved when the promoter of the entire mbh operon (TK2080-TK2093) was exchanged to a strong constitutive promoter from the glutamate dehydrogenase gene (TK1431) (strain MHG1). When MHG1 was cultivated under continuous culture conditions using pyruvate-based medium, a nearly 25% higher specific hydrogen production rate (SHPR) of 35.3 mmol H2 g-dcw−1 h−1 was observed at a dilution rate of 0.31 h−1. We also combined mbh overexpression using an even stronger constitutive promoter from the cell surface glycoprotein gene (TK0895) with disruption of the genes encoding the cytosolic hydrogenase (Hyh) and an alanine aminotransferase (AlaAT), both of which are involved in hydrogen consumption (strain MAH1). At a dilution rate of 0.30 h−1, the SHPR was 36.2 mmol H2 g-dcw−1 h−1, corresponding to a 28% increase compared to that of the host T. kodakarensis strain. Increasing the dilution rate to 0.83 h−1 or 1.07 h−1 resulted in a SHPR of 120 mmol H2 g-dcw−1 h−1, which is one of the highest production rates observed in microbial fermentation.
机译:超嗜热古生球菌Kodakarensis可以利用糖或丙酮酸来生长。在没有元素硫的情况下,质子会接受这些底物氧化产生的电子,从而产生分子氢(H2)。负责该反应的氢化酶是膜结合的[NiFe]-氢化酶(Mbh)。在这项研究中,我们研究了通过基因工程提高柯达喀尔丁香中Mbh蛋白质水平的几种可能性。当将整个mbh操纵子的启动子(TK2080-TK2093)交换为谷氨酸脱氢酶基因(TK1431)的强组成型启动子(菌株MHG1)时,细胞内Mbh的水平最高。当使用丙酮酸基培养基在连续培养条件下培养MHG1时,比氢生产率(SHPR)提高了近25%,为35.3 mmol H2 g-dcw -1 h -1 -1 。我们还使用来自细胞表面糖蛋白基因(TK0895)的更强组成型启动子与破坏胞浆氢化酶(Hyh)和丙氨酸氨基转移酶(AlaAT)的基因相结合来实现mbh过表达,这两者均涉及氢消耗(菌株) MAH1)。稀释率为0.30 h -1 时,SHPR为36.2 mmol H2 g-dcw -1 h -1 ,对应于28相较于宿主柯达卡尔德氏菌菌株,其%增加。将稀释率提高到0.83 h -1 或1.07 h -1 会导致SHPR为120 mmol H2 g-dcw -1 h < sup> -1 ,这是微生物发酵中观察到的最高生产率之一。

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