Efficient production of soluble recombinant single chain Fv fragments by a Pseudomonas putida strain KT2440 cell factory

Microbial Cell Factories

Research

Sarah-C Krüger¹  Thorben Dammeyer¹  Kenneth N Timmis²  Stefan Dübel³  Miriam Steinwand³  Michael Hust³ 

[1] Environmental Microbiology Laboratory, Helmholtz Centre for Infection Research, Inhoffenstr. 7, 38124, Braunschweig, Germany;Environmental Microbiology Laboratory, Helmholtz Centre for Infection Research, Inhoffenstr. 7, 38124, Braunschweig, Germany;Institut für Mikrobiologie, Technische Universität Braunschweig, Spielmannstr. 7, 38106, Braunschweig, Germany;Institut für Biochemie und Biotechnologie, Technische Universität Braunschweig, Spielmannstr. 7, 38106, Braunschweig, Germany;

关键词: Codon Usage;    Pseudomonas Putida;    Antibody Fragment;    Broad Host Range;    Periplasmic Protein;   

DOI  :  10.1186/1475-2859-10-11

 received in 2011-01-14, accepted in 2011-02-21,  发布年份 2011

来源: Springer

【 摘 要 】

BackgroundRecombinant antibody fragments have a wide range of applications in research, diagnostics and therapy. For many of these, small fragments like single chain fragment variables (scFv) function well and can be produced inexpensively in bacterial expression systems. Although Escherichia coli K-12 production systems are convenient, yields of different fragments, even those produced from codon-optimized expression systems, vary significantly. Where yields are inadequate, alternative production systems are needed. Pseudomonas putida strain KT2440 is a versatile biosafety strain known for good expression of heterologous genes, so we have explored its utility as a cell factory for production of scFvs.ResultsWe have generated new broad host range scFv expression constructs and assessed their production in the Pseudomonas putida KT2440 host. Two scFvs bind either to human C-reactive protein or to mucin1, proteins of significant medical diagnostic and therapeutic interest, whereas a third is a model anti-lysozyme scFv. The KT2440 antibody expression systems produce scFvs targeted to the periplasmic space that were processed precisely and were easily recovered and purified by single-step or tandem affinity chromatography. The influence of promoter system, codon optimization for P. putida, and medium on scFv yield was examined. Yields of up to 3.5 mg/l of pure, soluble, active scFv fragments were obtained from shake flask cultures of constructs based on the original codon usage and expressed from the Ptac expression system, yields that were 2.5-4 times higher than those from equivalent cultures of an E. coli K-12 expression host.ConclusionsPseudomonas putida KT2440 is a good cell factory for the production of scFvs, and the broad host range constructs we have produced allow yield assessment in a number of different expression hosts when yields in one initially selected are insufficient. High cell density cultivation and further optimization and refinement of the KT2440 cell factory will achieve additional increases in the yields of scFvs.

【 授权许可】

CC BY   
© Dammeyer et al; licensee BioMed Central Ltd. 2011