Engineering of a Stable Whole-Cell Biocatalyst Capable of ( S )-Styrene Oxide Formation for Continuous Two-Liquid-Phase Applications

Author:

Panke Sven1,de Lorenzo Víctor2,Kaiser Arnë1,Witholt Bernard1,Wubbolts Marcel G.1

Affiliation:

1. Institute of Biotechnology, Swiss Federal Institute of Technology Zurich, 8093 Zurich, Switzerland,1 and

2. Centro Nacional de Biotecnologia, Campus de Cantoblanco, 28049 Madrid, Spain2

Abstract

ABSTRACT Recombinant strains of Pseudomonas putida KT2440 carrying genetic expression cassettes with xylene oxygenase- and styrene monooxygenase-encoding genes on their chromosomes could be induced in shaking-flask experiments to specific activities that rivaled those of multicopy-plasmid-based Escherichia coli recombinants. Such strains maintained the introduced styrene oxidation activity in continuous two-liquid-phase cultures for at least 100 generations, although at a lower level than in the shaking-flask experiments. The data suggest that placement of target genes on the chromosome might be a suitable route for the construction of segregationally stable and highly active whole-cell biocatalysts.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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