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Dive into the research topics where Olivier Favre-Bulle is active.

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Biotechnology and Bioengineering | 2000

Biosynthesis of synthons in two‐liquid‐phase media

Marcel G. Wubbolts; Olivier Favre-Bulle; Bernard Witholt

The Pseudomonas oleovorans alkane hydroxylase and xylene oxygenase from Pseudomonas putida are versatile mono-oxygenases for stereo- and regioselective oxidation of aliphatic and aromatic hydrocarbons. Pseudomonas oleovorans and alkanol dehydrogenase deficient mutants of Pseudomonas have previously been used to produce alkanols from various alkanes and optically active epoxides from alkenes. Similarly, P. putida strains have been used to produce aromatic alcohols, aromatic acids, and optically active styrene oxides. A limitation in the use of Pseudomonas strains for bioconversions is that these strains can degrade some of the products formed. To counter this problem, we have constructed Escherichia coli recombinants, which contain the alk genes from the OCT plasmid of P. oleovorans [E. coli HB101 (pGEc47)] and the xylMA genes from the TOL plasmid of P. putida mt-2 [E. coli HB101 (pGB63)], encoding alkane hydroxylase and xylene oxygenase, respectively. Escherichia coli HB101 (pGEc47) was used to produce octanoic acid from n-octane and E. coli HB101 (pBG63) was put to use for the oxidation of styrene to styrene oxide in two-liquid phase biocatalysis at high cell densities. The alk(+) recombinant strain E. coli HB101 (pGEc47) was grown to 40 g/L cell dry mass in the presence of n-octane, which was converted to octanoic acid by the alkane oxidation system, the product accumulating in the aqueous phase. The xyl(+) recombinant E. coli HB101 (pBG63) was grown to a cell density of 26 g/L cell dry mass in the presence of around 7% (v/v) n-dodecane, which contained 2% (v/v) styrene. The recombinant E. coli (xyl(+)) converted styrene to (S)-(+)-styrene oxide at high enantiomeric excess (94% ee) and this compound partitioned almost exclusively into the organic phase. Using these high-cell-density two-liquid-phase cultures, the products accumulated rapidly, yielding high concentrations of products (50 mM octanoic acid and 90 mM styrene oxide) in the respective phases.


Archive | 1996

Enzymes and microorganisms having amidase activity for hydrolysing polyamides

Joel Crouzet; Olivier Favre-Bulle; Catherine Jourdat; Anne-Marie Le Coq; Dominique Petre


Archive | 1995

Enzymatic hydrolysis of 4-methylthiobutyronitriles

Olivier Favre-Bulle; Marie-Claude Bontoux; Denis Largeau; Andre Ariagno


Archive | 1997

Industrial scale process for the preparation of 2-hydroxy-4-methylbutyric acid using a nitrilase

Olivier Favre-Bulle; J{acute over }me Pierrard; Christophe David; Philippe Morel; Dominique Horbez


Archive | 1997

Method for preparing 2-hydroxy 4-methylthio butyric acid using a nitrilase

Olivier Favre-Bulle; Jérome Pierrard; Christophe David; Philippe Morel; Dominique Horbez


Archive | 1996

Enzymes and micro organisms with amidase activity which hydrolyze polyamides

Jo{umlaut over }l Crouzet; Didier Faucher; Olivier Favre-Bulle; Catherine Jourdat; Dominique Petre; J{acute over }me Pierrard; Denis Thibaut; Carole Guitton


Archive | 2000

Method for modulating nitrilase selectivity, nitrilases obtained by said method and use thereof

Jerome Pierrard; Olivier Favre-Bulle; Catherine Jourdat


Archive | 1999

Industrial method for producing heterologous proteins in e.coli and strains useful for said method

Jerome Pierrard; Carole Guitton; Olivier Favre-Bulle


Archive | 1995

Enzymatic hydrolysis of racemic a-substituted 4-methylthiobutyronitriles using a nitrilase from alcaligenes faecalis, gordona terrae or rhodococcus sp

Olivier Favre-Bulle; Maria-Claude Bontoux; Denis Largeau; Andre Ariagno


Archive | 2000

Method for isolating and selecting genes coding for enzymes, and suitable culture medium

Olivier Favre-Bulle; Jerome Pierrard; Debitte Nadine Batisse

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