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Comprehensive study on Escherichia coli genomic expression: Does position really matter?
Goormans, Anke R; Snoeck, Nico; Decadt, Hannes; Vermeulen, Karel; Peters, Gert; Coussement, Pieter; Van Herpe, Dries; Beauprez, Joeri J; De Maeseneire, Sofie L; Soetaert, Wim K.
Afiliación
  • Goormans AR; Centre for Industrial Biotechnology and Biocatalysis (InBio.be), Department of Biotechnology, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000, Ghent, Belgium.
  • Snoeck N; Centre for Industrial Biotechnology and Biocatalysis (InBio.be), Department of Biotechnology, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000, Ghent, Belgium.
  • Decadt H; Centre for Industrial Biotechnology and Biocatalysis (InBio.be), Department of Biotechnology, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000, Ghent, Belgium.
  • Vermeulen K; Department of Data Analysis and Mathematical Modelling, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000, Ghent, Belgium.
  • Peters G; Inbiose N.V., Technologiepark Zwijnaarde 3 - Bus 41, 9052, Ghent, Belgium.
  • Coussement P; Inbiose N.V., Technologiepark Zwijnaarde 3 - Bus 41, 9052, Ghent, Belgium.
  • Van Herpe D; Inbiose N.V., Technologiepark Zwijnaarde 3 - Bus 41, 9052, Ghent, Belgium.
  • Beauprez JJ; Inbiose N.V., Technologiepark Zwijnaarde 3 - Bus 41, 9052, Ghent, Belgium.
  • De Maeseneire SL; Centre for Industrial Biotechnology and Biocatalysis (InBio.be), Department of Biotechnology, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000, Ghent, Belgium. Electronic address: sofie.demaeseneire@ugent.be.
  • Soetaert WK; Centre for Industrial Biotechnology and Biocatalysis (InBio.be), Department of Biotechnology, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000, Ghent, Belgium; Inbiose N.V., Technologiepark Zwijnaarde 3 - Bus 41, 9052, Ghent, Belgium.
Metab Eng ; 62: 10-19, 2020 11.
Article en En | MEDLINE | ID: mdl-32795614
As a biorefinery platform host, Escherichia coli has been used extensively to produce metabolites of commercial interest. Integration of foreign DNA onto the bacterial genome allows for stable expression overcoming the need for plasmid expression and its associated instability. Despite the development of numerous tools and genome editing technologies, the question of where to incorporate a synthetic pathway remains unanswered. To address this issue, we studied the genomic expression in E. coli and linked it not only to 26 rationally selected genomic locations, but also to the gene direction in relation to the DNA replication fork, to the carbon and nitrogen source, to DNA folding and supercoiling, and to metabolic burden. To enable these experiments, we have designed a fluorescent expression cassette to eliminate specific local effects on gene expression. Overall it can be concluded that although the expression range obtained by changing the genomic location of a pathway is small compared to the range typically seen in promoter-RBS libraries, the effect of culture medium, environmental stress and metabolic burden can be substantial. The characterization of multiple effects on genomic expression, and the associated libraries of well-characterized strains, will only stimulate and improve the creation of stable production hosts fit for industrial settings.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Escherichia coli / Edición Génica Idioma: En Revista: Metab Eng Asunto de la revista: ENGENHARIA BIOMEDICA / METABOLISMO Año: 2020 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Bélgica

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Escherichia coli / Edición Génica Idioma: En Revista: Metab Eng Asunto de la revista: ENGENHARIA BIOMEDICA / METABOLISMO Año: 2020 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Bélgica