Suppr超能文献

通过非氧化戊糖磷酸途径将糖酵解和 Rubisco 途径偶联起来,以实现低二氧化碳排放发酵。

The coupling of glycolysis and the Rubisco-based pathway through the non-oxidative pentose phosphate pathway to achieve low carbon dioxide emission fermentation.

机构信息

Department of Chemical Engineering, National Chung Hsing University, Taichung 402, Taiwan.

Department of Chemical Engineering, National Chung Hsing University, Taichung 402, Taiwan.

出版信息

Bioresour Technol. 2015;187:189-197. doi: 10.1016/j.biortech.2015.03.090. Epub 2015 Mar 25.

Abstract

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 0.052mol.

摘要

在这项研究中,含有两种异源酶——核酮糖-1,5-二磷酸羧化酶/加氧酶(Rubisco)和磷酸核酮糖激酶(PrkA)的基于 Rubisco 的工程化大肠杆菌被证明能够在糖酵解过程中就地回收二氧化碳(CO2)。已经提出了两种替代方法来进一步通过非氧化戊糖磷酸途径(NOPPP)增强碳从糖酵解流向基于 Rubisco 的途径的流动。第一种方法是通过提高转酮醇酶 I(TktA)的表达来实现的,第二种方法是通过从染色体中删除 zwf 基因来阻断大肠杆菌的天然氧化脱羧反应(分别命名为 JB/pTA 和 MZB)。观察到 CO2 产率和单位摩尔乙醇产量的 CO2 释放量分别至少降低了 81%和 40%。本研究表明,使用大肠杆菌菌株 MZB 生产 1 摩尔乙醇时,CO2 排放量的上限为 0.052mol。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验