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PMID: 8812844 Published · ppublish English Journal Article Review

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

Protein expression and purification ·Vol. 7 ·No. 2 ·1996-03-00 ·Pages 129-36

Murby M, Uhlén M, Ståhl S

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.

MeSH Terms
Endopeptidases/genetics,metabolism Escherichia coli/metabolism Gene Expression Regulation, Bacterial/genetics Heat-Shock Proteins/genetics,metabolism Molecular Chaperones/genetics,metabolism Protease Inhibitors/metabolism Protein Engineering Recombinant Fusion Proteins/genetics Recombinant Proteins/genetics,metabolism Solubility
Chemicals
Heat-Shock Proteins Molecular Chaperones Protease Inhibitors Recombinant Fusion Proteins Recombinant Proteins Endopeptidases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Murby M
Department of Biochemistry and Biotechnology, Royal Institute of Technology, Stockholm, Sweden.
Uhlén M
Ståhl S
Article Info
Journal
Protein expression and purification
Abbr.
Protein Expr Purif
ISSN
1046-5928
Published
1996-03-00
Pages
129-36
Language
English
Region
United States
NLM ID
9101496
Subset
IM
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