Abstract

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.

Highlights

  • Recombinant antibody fragments have a wide range of applications in research, diagnostics and therapy

  • We further modified the chassis by equipping it with the G10L ribosome binding site (RBS) with epsilon enhancer [27] and the Erwinia carotovora pelB leader sequence [28] to effect the export of expressed polypeptides to the periplasm

  • The single chain fragment variables (scFv) format consists of variable regions of the antibody heavy and light chains (VH and antibody variable domain of the light chain (VL), respectively), joined by a 15-25 amino acid linker [29]

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Summary

Introduction

Recombinant antibody fragments have a wide range of applications in research, diagnostics and therapy. Its certification as a biosafety strain [13,14], its ability to express a broad spectrum of foreign proteins at high levels and the availability of powerful customized tools for genetic analysis and manipulation [15], make KT2440 an important prokaryotic cell factory. These features suggest that it might be a useful production system for antibody fragments

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