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An Engineered Rare Codon Device for Optimization of Metabolic Pathways.
Wang, You; Li, Chunying; Khan, Md Rezaul Islam; Wang, Yushu; Ruan, Yunfeng; Zhao, Bin; Zhang, Bo; Ma, Xiaopan; Zhang, Kaisi; Zhao, Xiwen; Ye, Guanhao; Guo, Xizhi; Feng, Guoyin; He, Lin; Ma, Gang.
Affiliation
  • Wang Y; Bio-X institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.
  • Li C; 2011 SJTU-BioX-Shanghai Team for The International Genetically Engineered Machine Competition (iGEM), Shanghai Jiao Tong University, Shanghai, PR China.
  • Khan MR; Bio-X institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.
  • Wang Y; 2011 SJTU-BioX-Shanghai Team for The International Genetically Engineered Machine Competition (iGEM), Shanghai Jiao Tong University, Shanghai, PR China.
  • Ruan Y; Bio-X institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.
  • Zhao B; Bio-X institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.
  • Zhang B; Bio-X institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.
  • Ma X; 2011 SJTU-BioX-Shanghai Team for The International Genetically Engineered Machine Competition (iGEM), Shanghai Jiao Tong University, Shanghai, PR China.
  • Zhang K; Bio-X institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.
  • Zhao X; 2011 SJTU-BioX-Shanghai Team for The International Genetically Engineered Machine Competition (iGEM), Shanghai Jiao Tong University, Shanghai, PR China.
  • Ye G; Bio-X institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.
  • Guo X; 2011 SJTU-BioX-Shanghai Team for The International Genetically Engineered Machine Competition (iGEM), Shanghai Jiao Tong University, Shanghai, PR China.
  • Feng G; Bio-X institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.
  • He L; 2011 SJTU-BioX-Shanghai Team for The International Genetically Engineered Machine Competition (iGEM), Shanghai Jiao Tong University, Shanghai, PR China.
  • Ma G; Bio-X institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.
Sci Rep ; 6: 20608, 2016 Feb 08.
Article in En | MEDLINE | ID: mdl-26852704
Rare codons generally arrest translation due to rarity of their cognate tRNAs. This property of rare codons can be utilized to regulate protein expression. In this study, a linear relationship was found between expression levels of genes and copy numbers of rare codons inserted within them. Based on this discovery, we constructed a molecular device in Escherichia coli using the rare codon AGG, its cognate tRNA (tRNA(Arg) (CCU)), modified tRNA(Asp) (GUC → CCU), and truncated aspartyl-tRNA synthetase (TDRS) to switch the expression of reporter genes on or off as well as to precisely regulate their expression to various intermediate levels. To underscore the applicability of our work, we used the rare codon device to alter the expression levels of four genes of the fatty acid synthesis II (FASII) pathway (i.e. fabZ, fabG, fabI, and tesA') in E. coli to optimize steady-state kinetics, which produced nearly two-fold increase in fatty acid yield. Thus, the proposed method has potential applications in regulating target protein expression at desired levels and optimizing metabolic pathways by precisely tuning in vivo molar ratio of relevant enzymes.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Escherichia coli / Metabolic Engineering Language: En Journal: Sci Rep Year: 2016 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Escherichia coli / Metabolic Engineering Language: En Journal: Sci Rep Year: 2016 Document type: Article Country of publication: United kingdom