标题:Biosynthesis of ethylene glycol from D-xylose in recombinant Escherichia coli
作者:Wang, Yuhui; Xian, Mo; Feng, Xinjun; Liu, Min; Zhao, Guang
作者机构:[Wang, Yuhui; Xian, Mo; Feng, Xinjun; Liu, Min; Zhao, Guang] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, CAS Key Lab Biobased Mat, Qin 更多
通讯作者:Liu, M;Zhao, G
通讯作者地址:[Liu, M; Zhao, G]Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao 266101, Peoples R China.
来源:BIOENGINEERED
出版年:2018
卷:9
期:1
页码:233-241
DOI:10.1080/21655979.2018.1478489
关键词:Acetate; aldehyde reductase; biosynthesis; D-xylose; Escherichia coli;; ethylene glycol; glycolate
摘要:Ethylene glycol (EG) is an important chemical used as antifreeze and a raw material in polyester synthesis. The EG biosynthetic pathway from D-xylose with D-xylonate as key intermediate has some advantages, but showed low EG production. Here, we reconstructed and optimized this pathway in Escherichia coli. In view of the greater intracellular prevalence of NADH, an aldehyde reductase FucO using NADH was employed to convert glycoaldehyde into EG, in replacement of NADPH-dependent reductase YqhD. To suppress the accumulation of by-products acetate and glycolate, two genes arcA and aldA were knocked out. The resultant strain Q2843 produced 72 g/L EG under fed-batch fermentation conditions, with the yield of 0.40 g/g D-xylose and EG productivity of 1.38 g/L/h. The use of NADH-dependent enzyme FucO and by-product elimination significantly improved the performance of EG producing strain, which represented the highest titer, yield and productivity of EG reported so far.
收录类别:SCOPUS;SCIE
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055735330&doi=10.1080%2f21655979.2018.1478489&partnerID=40&md5=d5b9ddbdcbe5ae3a9a338c5b57dc0cdb
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