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Appl Environ Microbiol. 2005 Dec;71(12):8221-7.

Engineering of solvent-tolerant Pseudomonas putida S12 for bioproduction of phenol from glucose.

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  • 1TNO Quality of Life, P.O. Box 342, 7300 AH Apeldoorn, The Netherlands. nick.wierckx@tno.nl

Abstract

Efficient bioconversion of glucose to phenol via the central metabolite tyrosine was achieved in the solvent-tolerant strain Pseudomonas putida S12. The tpl gene from Pantoea agglomerans, encoding tyrosine phenol lyase, was introduced into P. putida S12 to enable phenol production. Tyrosine availability was a bottleneck for efficient production. The production host was optimized by overexpressing the aroF-1 gene, which codes for the first enzyme in the tyrosine biosynthetic pathway, and by random mutagenesis procedures involving selection with the toxic antimetabolites m-fluoro-dl-phenylalanine and m-fluoro-l-tyrosine. High-throughput screening of analogue-resistant mutants obtained in this way yielded a P. putida S12 derivative capable of producing 1.5 mM phenol in a shake flask culture with a yield of 6.7% (mol/mol). In a fed-batch process, the productivity was limited by accumulation of 5 mM phenol in the medium. This toxicity was overcome by use of octanol as an extractant for phenol in a biphasic medium-octanol system. This approach resulted in accumulation of 58 mM phenol in the octanol phase, and there was a twofold increase in the overall production compared to a single-phase fed batch.

PMID:
16332806
PMCID:
PMC1317433
DOI:
10.1128/AEM.71.12.8221-8227.2005
[PubMed - indexed for MEDLINE]
Free PMC Article
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