标题:Pathway engineering results the altered polyhydroxyalkanoates composition in recombinant Escherichia coli
作者:Qiang Li;Quan Chen;Ming-Ji Li;Feng-Shan Wang;Qing-Sheng Qi
作者机构:[Li, Q] State Key Laboratory of Microbial Technology, Shandong University, Jinan, China, School of Pharmaceutical Sciences, Shandong University, Jinan 更多
通讯作者:Qi, QS
通讯作者地址:[Qi, QS]Univ Jinan, Sch Med & Life Sci, Jinan, Peoples R China.
来源:New biotechnology
出版年:2011
卷:28
期:1
页码:92-95
DOI:10.1016/j.nbt.2010.08.007
关键词:Pathway;engineering;composition
摘要:To efficiently produce short-chain-length–medium-chain-length polyhydroxyalkanoates copolymer from substrate mixture containing sugars and/or fatty acids, fadA gene mutant was constructed in Escherichia coli DH5a phosphotransferase system (PTS) disrupted strain. Plasmids pCJY02, pBHR68 and pBHR71 were separately introduced into E. coli DH5a (DptsG, DFadA) by transformation, then the recombinants were cultivated in the medium containing glucose and/or decanoate as carbon resource,respectively. When cultivated in the medium containing decanoate, only pCJY02-harboring recombinant was able to accumulate SCL–MCL PHAs consisting of 3HB, 3HHx, 3HO and 3HD with mol ratios: 43.2:12.8:10.3:33.6. The copolymer content was 1.90 wt% with 2.69 g L~(-1) cell dry weight. When cultivated in the medium containing both decanoate and glucose, the recombinant was found to utilize the mixture of glucose and fatty acids and accumulate SCL–MCL PHAs copolymer consisting of 3HB,3HHx, 3HO and3HD with mol ratios: 83.4:4.0:5.6:7.0. About 4.90 g L~(-1) cell dry weight was harvested and total PHAs content was 7.3 wt% of CDW. This result indicated that the low-substrate-specificity PHA synthase PhaC2_Ps endued hosts with the capability of synthesizing PHA copolymers, and the monomer composition of the synthesized PHA could be modulated by controlling the addition of carbon sources and by modifying metabolic pathways in the hosts.
收录类别:EI;SCOPUS;SCIE
WOS核心被引频次:10
Scopus被引频次:13
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-78650281263&doi=10.1016%2fj.nbt.2010.08.007&partnerID=40&md5=2f788a054fece68b538150cbab68612e
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