Literature DB >> 21125387

Recent developments in difficult protein expression: a guide to E. coli strains, promoters, and relevant host mutations.

James C Samuelson1.   

Abstract

Escherichia coli is a versatile and popular tool for heterologous protein production. Some of the reasons for its popularity include rapid growth, a variety of portable vectors, relatively simple genetics, and the potential for high-density cultivation. In addition, the extensive laboratory use of E. coli has resulted in technologies to target protein overexpression to various intracellular compartments. This is advantageous because these compartments have different environments that may facilitate folding of particular proteins of interest. This chapter discusses the properties of many of the E. coli strains available for protein expression in order to facilitate the choice of the best expression host for a particular protein of interest.

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Year:  2011        PMID: 21125387     DOI: 10.1007/978-1-61737-967-3_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  13 in total

1.  Strategies for production of active eukaryotic proteins in bacterial expression system.

Authors:  Orawan Khow; Sunutcha Suntrarachun
Journal:  Asian Pac J Trop Biomed       Date:  2012-02

Review 2.  Overcoming the Solubility Problem in E. coli: Available Approaches for Recombinant Protein Production.

Authors:  Claudia Ortega; Pablo Oppezzo; Agustín Correa
Journal:  Methods Mol Biol       Date:  2022

3.  The structural model of Salmonella typhimurium ethanolamine ammonia-lyase directs a rational approach to the assembly of the functional [(EutB-EutC)₂]₃ oligomer from isolated subunits.

Authors:  Adonis Miguel Bovell; Kurt Warncke
Journal:  Biochemistry       Date:  2013-02-14       Impact factor: 3.162

4.  Chaperone-Assisted Soluble Expression of a Humanized Anti-EGFR ScFv Antibody in E. Coli.

Authors:  Kamal Veisi; Safar Farajnia; Nosratollah Zarghami; Hamid Reza Khoram Khorshid; Nasser Samadi; Shiva Ahdi Khosroshahi; Hossein Zarei Jaliani
Journal:  Adv Pharm Bull       Date:  2015-12-31

5.  A stepwise approach for the reproducible optimization of PAMO expression in Escherichia coli for whole-cell biocatalysis.

Authors:  Edwin van Bloois; Hanna M Dudek; Wouter A Duetz; Marco W Fraaije
Journal:  BMC Biotechnol       Date:  2012-06-21       Impact factor: 2.563

6.  Heterologous production of active ribonuclease inhibitor in Escherichia coli by redox state control and chaperonin coexpression.

Authors:  Juozas Šiurkus; Peter Neubauer
Journal:  Microb Cell Fact       Date:  2011-08-08       Impact factor: 5.328

7.  Engineering and Validation of a Vector for Concomitant Expression of Rare Transfer RNA (tRNA) and HIV-1 nef Genes in Escherichia coli.

Authors:  Siti Aisyah Mualif; Sin-Yeang Teow; Tasyriq Che Omar; Yik Wei Chew; Narazah Mohd Yusoff; Syed A Ali
Journal:  PLoS One       Date:  2015-07-06       Impact factor: 3.240

8.  Hyper secretion of Thermobifida fusca β-glucosidase via a Tat-dependent signal peptide using Streptomyces lividans.

Authors:  Takaya Miyazaki; Shuhei Noda; Tsutomu Tanaka; Akihiko Kondo
Journal:  Microb Cell Fact       Date:  2013-10-01       Impact factor: 5.328

9.  Comparative Single-Cell Analysis of Different E. coli Expression Systems during Microfluidic Cultivation.

Authors:  Dennis Binder; Christopher Probst; Alexander Grünberger; Fabienne Hilgers; Anita Loeschcke; Karl-Erich Jaeger; Dietrich Kohlheyer; Thomas Drepper
Journal:  PLoS One       Date:  2016-08-15       Impact factor: 3.240

10.  The tunable pReX expression vector enables optimizing the T7-based production of membrane and secretory proteins in E. coli.

Authors:  Grietje Kuipers; Alexandros Karyolaimos; Zhe Zhang; Nurzian Ismail; Gianluca Trinco; David Vikström; Dirk Jan Slotboom; Jan-Willem de Gier
Journal:  Microb Cell Fact       Date:  2017-12-16       Impact factor: 5.328

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