Publication type: Article in scientific journal
Type of review: Peer review (publication)
Title: Recombinant chlorobenzene dioxygenase from Pseudomonas sp. P51: a biocatalyst for regioselective oxidation of aromatic nitriles
Authors: Yildirim, Selçuk
Franko, Telma T.
Wohlgemuth, Roland
Kohler, Hans-Peter E.
Witholt, Bernard
Schmid, Andreas
DOI: 10.1002/adsc.200505075
Published in: Advanced Synthesis & Catalysis
Volume(Issue): 347
Issue: 7-8
Page(s): 1060
Pages to: 1072
Issue Date: 2005
Publisher / Ed. Institution: Wiley
ISSN: 1615-4150
1615-4169
Language: English
Subjects: Nnitrile; Fermentation; Dihydroxylation; Biocatalysis
Subject (DDC): 572: Biochemistry
660.6: Biotechnology
Abstract: An efficient biocatalyst was developed for the cis-dihydroxylation of aromatic nitriles. The chlorobenzene dioxygenase (CDO) genes of Pseudomonas sp. strain P51 were cloned under the strict control of the Palk promoter of Pseudomonas putida GPo1. Escherichia coli JM101 cells carrying the resulting plasmid pTEZ30 were used for the biotransformation of benzonitrile in a 2-L stirred tank bioreactor. Use of a stable expression system resulted in an average specific activity and an average volumetric productivity of 1.47 U/g cdw and 120 mg of product/h/L, respectively. The values represent a three-fold increase compared to the results of the similar biotransformations with E. coli JM101 (pTCB144) where the genes of CDO were expressed under the control of lac promoter. The productivity of the cis-dihydroxylation process was limited by product toxicity. Removal of the products at toxic concentrations by means of an external charcoal column resulted in an additional increase in product concentration by 43%. E. coli JM101 (pTEZ30) was further used for the regio- and stereospecific dihydroxylations of various monosubstituted benzonitriles, benzyl cyanide, and cinnamonitrile. Biotransformations resulted in products with 42.9-97.1% enantiomeric excess. Initial enzymatic activities and isolated yields were obtained in the range of 1.7-4.7 U/g cdw and of 3-62%, respectively.
URI: https://digitalcollection.zhaw.ch/handle/11475/7073
Fulltext version: Published version
License (according to publishing contract): Licence according to publishing contract
Departement: Life Sciences and Facility Management
Organisational Unit: Institute of Food and Beverage Innovation (ILGI)
Appears in collections:Publikationen Life Sciences und Facility Management

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Yildirim, S., Franko, T. T., Wohlgemuth, R., Kohler, H.-P. E., Witholt, B., & Schmid, A. (2005). Recombinant chlorobenzene dioxygenase from Pseudomonas sp. P51: a biocatalyst for regioselective oxidation of aromatic nitriles. Advanced Synthesis & Catalysis, 347(7-8), 1060–1072. https://doi.org/10.1002/adsc.200505075
Yildirim, S. et al. (2005) ‘Recombinant chlorobenzene dioxygenase from Pseudomonas sp. P51: a biocatalyst for regioselective oxidation of aromatic nitriles’, Advanced Synthesis & Catalysis, 347(7-8), pp. 1060–1072. Available at: https://doi.org/10.1002/adsc.200505075.
S. Yildirim, T. T. Franko, R. Wohlgemuth, H.-P. E. Kohler, B. Witholt, and A. Schmid, “Recombinant chlorobenzene dioxygenase from Pseudomonas sp. P51: a biocatalyst for regioselective oxidation of aromatic nitriles,” Advanced Synthesis & Catalysis, vol. 347, no. 7-8, pp. 1060–1072, 2005, doi: 10.1002/adsc.200505075.
YILDIRIM, Selçuk, Telma T. FRANKO, Roland WOHLGEMUTH, Hans-Peter E. KOHLER, Bernard WITHOLT und Andreas SCHMID, 2005. Recombinant chlorobenzene dioxygenase from Pseudomonas sp. P51: a biocatalyst for regioselective oxidation of aromatic nitriles. Advanced Synthesis & Catalysis. 2005. Bd. 347, Nr. 7-8, S. 1060–1072. DOI 10.1002/adsc.200505075
Yildirim, Selçuk, Telma T. Franko, Roland Wohlgemuth, Hans-Peter E. Kohler, Bernard Witholt, and Andreas Schmid. 2005. “Recombinant Chlorobenzene Dioxygenase from Pseudomonas Sp. P51: A Biocatalyst for Regioselective Oxidation of Aromatic Nitriles.” Advanced Synthesis & Catalysis 347 (7-8): 1060–72. https://doi.org/10.1002/adsc.200505075.
Yildirim, Selçuk, et al. “Recombinant Chlorobenzene Dioxygenase from Pseudomonas Sp. P51: A Biocatalyst for Regioselective Oxidation of Aromatic Nitriles.” Advanced Synthesis & Catalysis, vol. 347, no. 7-8, 2005, pp. 1060–72, https://doi.org/10.1002/adsc.200505075.


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