首页> 外文期刊>Bioresource Technology: Biomass, Bioenergy, Biowastes, Conversion Technologies, Biotransformations, Production Technologies >The coupling of glycolysis and the Rubisco-based pathway through the non-oxidative pentose phosphate pathway to achieve low carbon dioxide emission fermentation
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The coupling of glycolysis and the Rubisco-based pathway through the non-oxidative pentose phosphate pathway to achieve low carbon dioxide emission fermentation

机译:糖酵解和基于Rubisco的途径通过非氧化戊糖磷酸途径的耦合,实现低二氧化碳排放发酵

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In this study, Rubisco-based engineered Escherichia coli, containing two heterologous enzymes of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) and phosphoribulokinase (PrkA), has been shown to be capable of the in situ recycling of carbon dioxide (CO2) during glycolysis. Two alternative approaches have been proposed to further enhance the carbon flow from glycolysis to a Rubisco-based pathway through the non-oxidative pentose phosphate pathway (NOPPP). The first is achieved by elevating the expression of transketolase I (TktA) and the second by blocking the native oxidation-decarboxylation reaction of E. coli by deleting the zwf gene from the chromosome (designated as JB/pTA and MZB, respectively). Decreases in the CO2 yield and the CO2 evolution per unit mole of ethanol production by at least 81% and 40% are observed. It is demonstrated in this study that the production of one mole of ethanol using E. coli strain MZB, the upper limit of CO2 emission is 0.052 mol. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在这项研究中,基于Rubisco的工程大肠杆菌被证明能够原位循环利用二氧化碳(1,5-双磷酸羧化酶/加氧酶(Rubisco)和磷酸核糖激酶(PrkA)的两种异源酶。糖酵解期间)。已经提出了两种替代方法来进一步增强碳从糖酵解通过非氧化性戊糖磷酸途径(NOPPP)流向基于Rubisco的途径。第一个是通过提高转酮醇酶I(TktA)的表达来实现的,第二个是通过从染色体上删除zwf基因(分别命名为JB / pTA和MZB)来阻止大肠杆菌的天然氧化-脱羧反应。观察到CO 2产率降低和每单位摩尔乙醇产量CO 2释放至少降低了81%和40%。这项研究表明,使用大肠杆菌MZB菌株生产1摩尔乙醇,CO2排放上限为0.052摩尔。 (C)2015 Elsevier Ltd.保留所有权利。

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