Genome mining of 2-phenylethanol biosynthetic genes from Enterobacter sp CGMCC 5087 and heterologous overproduction in Escherichia coli
Liu, Changqing1,2; Zhang, Kai1,2; Cao, Wenyan1,2; Zhang, Ge1,2,3; Chen, Guoqiang1,2,3; Yang, Haiyan1,2; Wang, Qian3; Liu, Haobao3; Xian, Mo1,2; Zhang, Haibo1,2
刊名BIOTECHNOLOGY FOR BIOFUELS
2018-11-08
卷号11页码:15
关键词2-Phenylethanol Enterobacter sp CGMCC 5087 2-Keto acid decarboxylase Alcohol dehydrogenase Phenylpyruvate pathway Metabolic engineering
ISSN号1754-6834
DOI10.1186/s13068-018-1297-3
英文摘要Background2-Phenylethanol (2-PE) is a higher aromatic alcohol that is widely used in the perfumery, cosmetics, and food industries and is also a potentially valuable next-generation biofuel. In our previous study, a new strain Enterobacter sp. CGMCC 5087 was isolated to produce 2-PE from glucose through the phenylpyruvate pathway.ResultsIn this study, candidate genes for 2-PE biosynthesis were identified from Enterobacter sp. CGMCC 5087 by draft whole-genome sequence, metabolic engineering, and shake flask fermentation. Subsequently, the identified genes encoding the 2-keto acid decarboxylase (Kdc) and alcohol dehydrogenase (Adh) enzymes from Enterobacter sp. CGMCC 5087 were introduced into E. coli BL21(DE3) to construct a high-efficiency microbial cell factory for 2-PE production using the prokaryotic phenylpyruvate pathway. The enzymes Kdc4427 and Adh4428 from Enterobacter sp. CGMCC 5087 showed higher performances than did the corresponding enzymes ARO10 and ADH2 from Saccharomyces cerevisiae, respectively. The E. coli cell factory was further improved by overexpressing two upstream shikimate pathway genes, aroF/aroG/aroH and pheA, to enhance the metabolic flux of the phenylpyruvate pathway, which resulted in 2-PE production of 260mg/L. The combined overexpression of tktA and ppsA increased the precursor supply of erythrose-4-phosphate and phosphoenolpyruvate, which resulted in 2-PE production of 320mg/L, with a productivity of 13.3mg/L/h.ConclusionsThe present study achieved the highest titer of de novo 2-PE production of in a recombinant E. coli system. This study describes a new, efficient 2-PE producer that lays foundation for the industrial-scale production of 2-PE and its derivatives in the future.
资助项目National Natural Science Foundation of China (NSF)[31400084] ; Hainan's Key Project of Research and Development Plan[ZDYF2017155] ; Taishan Scholars Climbing Program of Shandong[TSPD20150210] ; Youth Innovation Promotion Association CAS[2017252]
WOS关键词SACCHAROMYCES-CEREVISIAE ; EHRLICH PATHWAY ; L-PHENYLALANINE ; PHENYLPYRUVATE DECARBOXYLASE ; PHENYLACETALDEHYDE SYNTHASE ; BIOTECHNOLOGICAL PRODUCTION ; METABOLISM ; BIOFUELS ; YEAST ; BIOCATALYSTS
WOS研究方向Biotechnology & Applied Microbiology ; Energy & Fuels
语种英语
出版者BMC
WOS记录号WOS:000449850300004
资助机构National Natural Science Foundation of China (NSF) ; Hainan's Key Project of Research and Development Plan ; Taishan Scholars Climbing Program of Shandong ; Youth Innovation Promotion Association CAS
内容类型期刊论文
源URL[http://ir.qibebt.ac.cn/handle/337004/10998]  
专题中国科学院青岛生物能源与过程研究所
通讯作者Xian, Mo; Zhang, Haibo
作者单位1.Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, CAS Key Lab Biobased Mat, 189 Songling Rd, Qingdao 266101, Peoples R China
2.Univ Chinese Acad Sci, Beijing, Peoples R China
3.Chinese Acad Agr Sci, Key Lab Tobacco Gene Resources, Tobacco Res Inst, Qingdao 266101, Peoples R China
推荐引用方式
GB/T 7714
Liu, Changqing,Zhang, Kai,Cao, Wenyan,et al. Genome mining of 2-phenylethanol biosynthetic genes from Enterobacter sp CGMCC 5087 and heterologous overproduction in Escherichia coli[J]. BIOTECHNOLOGY FOR BIOFUELS,2018,11:15.
APA Liu, Changqing.,Zhang, Kai.,Cao, Wenyan.,Zhang, Ge.,Chen, Guoqiang.,...&Zhang, Haibo.(2018).Genome mining of 2-phenylethanol biosynthetic genes from Enterobacter sp CGMCC 5087 and heterologous overproduction in Escherichia coli.BIOTECHNOLOGY FOR BIOFUELS,11,15.
MLA Liu, Changqing,et al."Genome mining of 2-phenylethanol biosynthetic genes from Enterobacter sp CGMCC 5087 and heterologous overproduction in Escherichia coli".BIOTECHNOLOGY FOR BIOFUELS 11(2018):15.
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