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dc.contributor.authorYildirim, Selçuk-
dc.contributor.authorFranko, Telma T.-
dc.contributor.authorWohlgemuth, Roland-
dc.contributor.authorKohler, Hans-Peter E.-
dc.contributor.authorWitholt, Bernard-
dc.contributor.authorSchmid, Andreas-
dc.date.accessioned2018-06-18T13:51:27Z-
dc.date.available2018-06-18T13:51:27Z-
dc.date.issued2005-
dc.identifier.issn1615-4150de_CH
dc.identifier.issn1615-4169de_CH
dc.identifier.urihttps://digitalcollection.zhaw.ch/handle/11475/7073-
dc.description.abstractAn 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.de_CH
dc.language.isoende_CH
dc.publisherWileyde_CH
dc.relation.ispartofAdvanced Synthesis & Catalysisde_CH
dc.rightsLicence according to publishing contractde_CH
dc.subjectNnitrilede_CH
dc.subjectFermentationde_CH
dc.subjectDihydroxylationde_CH
dc.subjectBiocatalysisde_CH
dc.subject.ddc572: Biochemiede_CH
dc.subject.ddc660.6: Biotechnologiede_CH
dc.titleRecombinant chlorobenzene dioxygenase from Pseudomonas sp. P51: a biocatalyst for regioselective oxidation of aromatic nitrilesde_CH
dc.typeBeitrag in wissenschaftlicher Zeitschriftde_CH
dcterms.typeTextde_CH
zhaw.departementLife Sciences und Facility Managementde_CH
zhaw.organisationalunitInstitut für Lebensmittel- und Getränkeinnovation (ILGI)de_CH
dc.identifier.doi10.1002/adsc.200505075de_CH
zhaw.funding.euNode_CH
zhaw.issue7-8de_CH
zhaw.originated.zhawNode_CH
zhaw.pages.end1072de_CH
zhaw.pages.start1060de_CH
zhaw.publication.statuspublishedVersionde_CH
zhaw.volume347de_CH
zhaw.publication.reviewPeer review (Publikation)de_CH
zhaw.webfeedLM-Verpackungde_CH
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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