Literature DB >> 14537822

Metabolic load and heterologous gene expression.

B R Glick1.   

Abstract

The expression of a foreign protein(s) in a recombinant host cell or organism often utilizes a significant amount of the host cell's resources, removing those resources away from host cell metabolism and placing a metabolic load (metabolic drain, metabolic burden) on the host. As a consequence of the imposed metabolic load, the biochemistry and physiology of the host may be dramatically altered. The numerous physiological changes that may occur often lowers the amount of the target foreign protein that is produced and eventually recovered from the recombinant organism. In this review the physiological changes to host cells, the causes of the phenomenon of metabolic load, and several strategies to avoid some of the problems associated with metabolic load are elaborated and discussed.

Year:  1995        PMID: 14537822     DOI: 10.1016/0734-9750(95)00004-a

Source DB:  PubMed          Journal:  Biotechnol Adv        ISSN: 0734-9750            Impact factor:   14.227


  151 in total

1.  A plasmid cloning vector with precisely regulatable copy number in Escherichia coli.

Authors:  A Herman-Antosiewicz; M Obuchowski; G Wegrzyn
Journal:  Mol Biotechnol       Date:  2001-03       Impact factor: 2.695

2.  Field performance of chitinase transgenic silver birches (Betula pendula): resistance to fungal diseases.

Authors:  H-L Pasonen; S-K Seppänen; Y Degefu; A Rytkönen; K von Weissenberg; A Pappinen
Journal:  Theor Appl Genet       Date:  2004-06-24       Impact factor: 5.699

3.  Expression of Escherichia coli virulence usher protein attenuates wild-type Salmonella.

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Journal:  Virulence       Date:  2012-01-01       Impact factor: 5.882

4.  Stability of soybean recombinant plastome over six generations.

Authors:  Nathalie Dufourmantel; Ghislaine Tissot; Frédéric Garçon; Bernard Pelissier; Manuel Dubald
Journal:  Transgenic Res       Date:  2006-06       Impact factor: 2.788

Review 5.  Review: optimizing inducer and culture conditions for expression of foreign proteins under the control of the lac promoter.

Authors:  R S Donovan; C W Robinson; B R Glick
Journal:  J Ind Microbiol       Date:  1996-03

Review 6.  Plasmid DNA vaccine vector design: impact on efficacy, safety and upstream production.

Authors:  James A Williams; Aaron E Carnes; Clague P Hodgson
Journal:  Biotechnol Adv       Date:  2009-02-20       Impact factor: 14.227

Review 7.  Engineering reduced evolutionary potential for synthetic biology.

Authors:  Brian A Renda; Michael J Hammerling; Jeffrey E Barrick
Journal:  Mol Biosyst       Date:  2014-02-21

8.  Transformation of Azospirillum brasilense Cd with an ACC deaminase gene from enterobacter cloacae UW4 fused to the Tet r gene promoter improves its fitness and plant growth promoting ability.

Authors:  G Holguin; B R Glick
Journal:  Microb Ecol       Date:  2003-05-13       Impact factor: 4.552

9.  Comparative transcription profiling and in-depth characterization of plasmid-based and plasmid-free Escherichia coli expression systems under production conditions.

Authors:  Juergen Mairhofer; Theresa Scharl; Karoline Marisch; Monika Cserjan-Puschmann; Gerald Striedner
Journal:  Appl Environ Microbiol       Date:  2013-04-12       Impact factor: 4.792

10.  The effects of kanamycin concentration on gene transcription levels in Escherichia coli.

Authors:  Xiaozhen Liu; Na Li; Minjun Jia; Shuangli Zhang; Hao Niu; Qiang Li; Pengfei Gu
Journal:  3 Biotech       Date:  2020-02-05       Impact factor: 2.406

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