Literature DB >> 8812844

Upstream strategies to minimize proteolytic degradation upon recombinant production in Escherichia coli.

M Murby1, M Uhlén, S Ståhl.   

Abstract

Proteolytic degradation of recombinant proteins represents a major problem related to production of gene products in heterologous hosts. Recombinant DNA technology offers several alternative strategies for stabilization of expressed gene products. These strategies can often give dramatic stabilization effects and can be combined with strategies involving optimization of fermentation conditions or downstream processing schemes. In this review, various genetic approaches to improve the stability of recombinant proteins will be discussed, including (i) choice of host cell strain, (ii) product localization, (iii) use of gene fusion partners, and (iv) product engineering. In addition, the solubility of the gene product can be influenced by factors such as growth temperature, promoter strength, fusion partners, and site-directed changes. Altogether, a battery of approaches can be used to obtain stable gene products.

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Year:  1996        PMID: 8812844     DOI: 10.1006/prep.1996.0018

Source DB:  PubMed          Journal:  Protein Expr Purif        ISSN: 1046-5928            Impact factor:   1.650


  15 in total

1.  Upscale production of a recombinant cyclodextrin glycosyltransferase from Paenibacillus macerans in Escherichia coli.

Authors:  Yi-Nan Yang; Wen-Xin Shan; Pi-Wu Wang
Journal:  3 Biotech       Date:  2017-06-30       Impact factor: 2.406

Review 2.  Overview of the purification of recombinant proteins.

Authors:  Paul T Wingfield
Journal:  Curr Protoc Protein Sci       Date:  2015-04-01

3.  Proteome-scale purification of human proteins from bacteria.

Authors:  Pascal Braun; Yanhui Hu; Binghua Shen; Allison Halleck; Malvika Koundinya; Ed Harlow; Joshua LaBaer
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-05       Impact factor: 11.205

Review 4.  Understanding the art of producing protein and nonprotein molecules in Escherichia coli.

Authors:  P Balbás
Journal:  Mol Biotechnol       Date:  2001-11       Impact factor: 2.695

5.  Design of self-assembling peptide hydrogelators amenable to bacterial expression.

Authors:  Cem Sonmez; Katelyn J Nagy; Joel P Schneider
Journal:  Biomaterials       Date:  2014-10-28       Impact factor: 12.479

Review 6.  Increasing recombinant protein production in Escherichia coli through metabolic and genetic engineering.

Authors:  Hendrik Waegeman; Wim Soetaert
Journal:  J Ind Microbiol Biotechnol       Date:  2011-09-08       Impact factor: 3.346

Review 7.  Strategies for achieving high-level expression of genes in Escherichia coli.

Authors:  S C Makrides
Journal:  Microbiol Rev       Date:  1996-09

8.  Cloning of a Family 11 Xylanase Gene from Bacillus amyloliquefaciens CH51 Isolated from Cheonggukjang.

Authors:  C U Baek; S G Lee; Y R Chung; I Cho; J H Kim
Journal:  Indian J Microbiol       Date:  2012-03-25       Impact factor: 2.461

9.  Establishing the yeast Saccharomyces cerevisiae as a system for expression of human proteins on a proteome-scale.

Authors:  Caterina Holz; Bianka Prinz; Natalia Bolotina; Volker Sievert; Konrad Büssow; Bernd Simon; Ulf Stahl; Christine Lang
Journal:  J Struct Funct Genomics       Date:  2003

10.  Production of a new non-specific nuclease from Yersinia enterocolitica subsp. palearctica: optimization of induction conditions using response surface methodology.

Authors:  Xiu-Juan Fang; Zhen-Xing Tang; Zhen-Hua Li; Zhi-Liang Zhang; Lu-E Shi
Journal:  Biotechnol Biotechnol Equip       Date:  2014-08-26       Impact factor: 1.632

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