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Enhanced hydrogen production by insertional inactivation of adhE gene in Klebsiella oxytoca HP1

机译:催产克雷伯菌HP1中adhE基因的插入失活提高了产氢量

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Ethanol is the main byproduct of anaerobic H_2-producing fermentation in Klebsiella oxytoca HP1. Two moles of NAD(P)H are consumed to yield one mole of ethanol that may decrease bacterial hydrogen production. In this article the adhE gene that codes for acetaldehyde dehydrogenase was disrupted for the first time. A homologous recombination vector pTA-Str was constructed in which the adhE gene was disrupted by inserting an aminoglycoside-3'-adenyltransferase (aadA) gene. As expected, the vector includes the insertion 5'-adhE-aadA-adhE-3'. The amplified DNA fragment 5'-adhE-aadA-adhE-3' from pTA-Str was transformed into K. oxytoca HP1 and one recombinant was obtained. PCR analysis of the resulting genomic DNA indicated the appropriate deletion and insertion. Compared with the H_2-production of wild type K. oxytoca HP1, the hydrogen yield of the mutant increased by 16.07% and ethanol concentration decreased by 77.47%, suggesting that inactivation of the adhE gene in K. oxytoca HP1 is a potential method for enhancing bacterial H_2-production.
机译:乙醇是产氧克雷伯菌HP1中产生厌氧H_2发酵的主要副产物。消耗了2摩尔的NAD(P)H,以产生1摩尔的乙醇,这可能会减少细菌的产氢量。在本文中,编码乙醛脱氢酶的adhE基因首次被破坏。构建了同源重组载体pTA-Str,其中通过插入氨基糖苷-3'-腺苷酸转移酶(aadA)基因破坏了adhE基因。如所期望的,载体包括插入物5'-adhE-aadA-adhE-3'。将来自pTA-Str的扩增的DNA片段5'-adhE-aadA-adhE-3'转化到产氧假单胞菌HP1中,得到一个重组体。所得基因组DNA的PCR分析表明适当的缺失和插入。与野生型产氧假单胞菌HP1的H_2产生相比,该突变体的氢产率提高了16.07%,乙醇浓度降低了77.47%,这表明产氧假单胞菌HP1中的adhE基因失活是一种潜在的增强方法。细菌H_2的产生。

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