Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction
Scherkus C, Schmidt S, Bornscheuer UT, Gröger H, Kara S, Liese A (2017)
Biotechnology and Bioengineering 114(6): 1215-1221.
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Autor*in
Scherkus, Christian;
Schmidt, Sandy;
Bornscheuer, Uwe T.;
Gröger, HaraldUniBi;
Kara, Selin;
Liese, Andreas
Erscheinungsjahr
2017
Zeitschriftentitel
Biotechnology and Bioengineering
Band
114
Ausgabe
6
Seite(n)
1215-1221
ISSN
0006-3592
eISSN
1097-0290
Page URI
https://pub.uni-bielefeld.de/record/2908777
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Scherkus C, Schmidt S, Bornscheuer UT, Gröger H, Kara S, Liese A. Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction. Biotechnology and Bioengineering. 2017;114(6):1215-1221.
Scherkus, C., Schmidt, S., Bornscheuer, U. T., Gröger, H., Kara, S., & Liese, A. (2017). Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction. Biotechnology and Bioengineering, 114(6), 1215-1221. doi:10.1002/bit.26258
Scherkus, Christian, Schmidt, Sandy, Bornscheuer, Uwe T., Gröger, Harald, Kara, Selin, and Liese, Andreas. 2017. “Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction”. Biotechnology and Bioengineering 114 (6): 1215-1221.
Scherkus, C., Schmidt, S., Bornscheuer, U. T., Gröger, H., Kara, S., and Liese, A. (2017). Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction. Biotechnology and Bioengineering 114, 1215-1221.
Scherkus, C., et al., 2017. Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction. Biotechnology and Bioengineering, 114(6), p 1215-1221.
C. Scherkus, et al., “Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction”, Biotechnology and Bioengineering, vol. 114, 2017, pp. 1215-1221.
Scherkus, C., Schmidt, S., Bornscheuer, U.T., Gröger, H., Kara, S., Liese, A.: Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction. Biotechnology and Bioengineering. 114, 1215-1221 (2017).
Scherkus, Christian, Schmidt, Sandy, Bornscheuer, Uwe T., Gröger, Harald, Kara, Selin, and Liese, Andreas. “Kinetic insights into ϵ-caprolactone synthesis: Improvement of an enzymatic cascade reaction”. Biotechnology and Bioengineering 114.6 (2017): 1215-1221.
Daten bereitgestellt von European Bioinformatics Institute (EBI)
7 Zitationen in Europe PMC
Daten bereitgestellt von Europe PubMed Central.
Biocatalytic conversion of cycloalkanes to lactones using an in-vivo cascade in Pseudomonas taiwanensis VLB120.
Karande R, Salamanca D, Schmid A, Buehler K., Biotechnol Bioeng 115(2), 2018
PMID: 28986995
Karande R, Salamanca D, Schmid A, Buehler K., Biotechnol Bioeng 115(2), 2018
PMID: 28986995
Overcoming the Incompatibility Challenge in Chemoenzymatic and Multi-Catalytic Cascade Reactions.
Schmidt S, Castiglione K, Kourist R., Chemistry 24(8), 2018
PMID: 28877401
Schmidt S, Castiglione K, Kourist R., Chemistry 24(8), 2018
PMID: 28877401
Biocatalytic Oxidation Reactions: A Chemist's Perspective.
Dong J, Fernández-Fueyo E, Hollmann F, Paul CE, Pesic M, Schmidt S, Wang Y, Younes S, Zhang W., Angew Chem Int Ed Engl 57(30), 2018
PMID: 29573076
Dong J, Fernández-Fueyo E, Hollmann F, Paul CE, Pesic M, Schmidt S, Wang Y, Younes S, Zhang W., Angew Chem Int Ed Engl 57(30), 2018
PMID: 29573076
Biocatalytic synthesis of lactones and lactams.
Hollmann F, Kara S, Opperman DJ, Wang Y., Chem Asian J 13(23), 2018
PMID: 30256534
Hollmann F, Kara S, Opperman DJ, Wang Y., Chem Asian J 13(23), 2018
PMID: 30256534
Cascades in Compartments: En Route to Machine-Assisted Biotechnology.
Rabe KS, Müller J, Skoupi M, Niemeyer CM., Angew Chem Int Ed Engl 56(44), 2017
PMID: 28691387
Rabe KS, Müller J, Skoupi M, Niemeyer CM., Angew Chem Int Ed Engl 56(44), 2017
PMID: 28691387
High-Throughput Feasible Screening Tool for Determining Enzyme Stabilities against Organic Solvents Directly from Crude Extracts.
Wedde S, Kleusch C, Bakonyi D, Gröger H., Chembiochem 18(24), 2017
PMID: 29024398
Wedde S, Kleusch C, Bakonyi D, Gröger H., Chembiochem 18(24), 2017
PMID: 29024398
26 References
Daten bereitgestellt von Europe PubMed Central.
Towards large-scale synthetic applications of Baeyer-Villiger monooxygenases.
Alphand V, Carrea G, Wohlgemuth R, Furstoss R, Woodley JM., Trends Biotechnol. 21(7), 2003
PMID: 12837617
Alphand V, Carrea G, Wohlgemuth R, Furstoss R, Woodley JM., Trends Biotechnol. 21(7), 2003
PMID: 12837617
Applications of Baeyer-Villiger monooxygenases in organic synthesis
Alphand, Curr Org Chem 14(17), 2010
Alphand, Curr Org Chem 14(17), 2010
Einwirkung des Caro'schen Reagens auf Ketone
Baeyer, Ber Dtsch Chem Ges 32(3), 1899
Baeyer, Ber Dtsch Chem Ges 32(3), 1899
The first 200-L scale asymmetric Baeyer-Villiger oxidation using a whole-cell biocatalyst
Baldwin, Org Process Res Dev 12(4), 2008
Baldwin, Org Process Res Dev 12(4), 2008
Biselli, 2002
The purification and properties of cyclohexanone oxygenase from Nocardia globerula CL1 and Acinetobacter NCIB 9871.
Donoghue NA, Norris DB, Trudgill PW., Eur. J. Biochem. 63(1), 1976
PMID: 1261545
Donoghue NA, Norris DB, Trudgill PW., Eur. J. Biochem. 63(1), 1976
PMID: 1261545
Baeyer-Villiger monooxygenases in aroma compound synthesis.
Fink MJ, Rudroff F, Mihovilovic MD., Bioorg. Med. Chem. Lett. 21(20), 2011
PMID: 21900007
Fink MJ, Rudroff F, Mihovilovic MD., Bioorg. Med. Chem. Lett. 21(20), 2011
PMID: 21900007
Enzyme engineering aspects of biocatalysis: cofactor regeneration as example.
Kragl U, Kruse W, Hummel W, Wandrey C., Biotechnol. Bioeng. 52(2), 1996
PMID: 18629898
Kragl U, Kruse W, Hummel W, Wandrey C., Biotechnol. Bioeng. 52(2), 1996
PMID: 18629898
The Baeyer-Villiger oxidation of ketones and aldehydes
Krow, Org React 3(43), 2004
Krow, Org React 3(43), 2004
Process limitations in a whole-cell catalysed oxidation: Sensitivity analysis
Law, Chem Eng Sci 61(20), 2006
Law, Chem Eng Sci 61(20), 2006
Einfluss der Reaktorkonfiguration auf die Enantioselektivität einer kinetischen Racematspaltung
Liese, Chem Ing Tech 85(6), 2013
Liese, Chem Ing Tech 85(6), 2013
A self-sufficient Baeyer-Villiger biocatalysis system for the synthesis of ɛ-caprolactone from cyclohexanol.
Mallin H, Wulf H, Bornscheuer UT., Enzyme Microb. Technol. 53(4), 2013
PMID: 23931695
Mallin H, Wulf H, Bornscheuer UT., Enzyme Microb. Technol. 53(4), 2013
PMID: 23931695
Mihovilovic, 2012
Towards practical Baeyer-Villiger-monooxygenases: design of cyclohexanone monooxygenase mutants with enhanced oxidative stability.
Opperman DJ, Reetz MT., Chembiochem 11(18), 2010
PMID: 21080396
Opperman DJ, Reetz MT., Chembiochem 11(18), 2010
PMID: 21080396
Characterization and Crystal Structure of a Robust Cyclohexanone Monooxygenase.
Romero E, Castellanos JR, Mattevi A, Fraaije MW., Angew. Chem. Int. Ed. Engl. 55(51), 2016
PMID: 27873437
Romero E, Castellanos JR, Mattevi A, Fraaije MW., Angew. Chem. Int. Ed. Engl. 55(51), 2016
PMID: 27873437
A fed-batch synthetic strategy for a three-step enzymatic synthesis of poly-ϵ-caprolactone
Scherkus, ChemCatChem 8(22), 2016
Scherkus, ChemCatChem 8(22), 2016
Biocatalytic access to chiral polyesters by an artificial enzyme cascade synthesis
Schmidt, ChemCatChem 7(23), 2015
Schmidt, ChemCatChem 7(23), 2015
An enzyme cascade synthesis of ε-caprolactone and its oligomers.
Schmidt S, Scherkus C, Muschiol J, Menyes U, Winkler T, Hummel W, Groger H, Liese A, Herz HG, Bornscheuer UT., Angew. Chem. Int. Ed. Engl. 54(9), 2015
PMID: 25597635
Schmidt S, Scherkus C, Muschiol J, Menyes U, Winkler T, Hummel W, Groger H, Liese A, Herz HG, Bornscheuer UT., Angew. Chem. Int. Ed. Engl. 54(9), 2015
PMID: 25597635
A novel, efficient regenerating method of NADPH using a new formate dehydrogenase
Seelbach, Tetrahedron Lett 37(9), 1996
Seelbach, Tetrahedron Lett 37(9), 1996
Direct biocatalytic one-pot-transformation of cyclohexanol with molecular oxygen into ɛ-caprolactone.
Staudt S, Bornscheuer UT, Menyes U, Hummel W, Groger H., Enzyme Microb. Technol. 53(4), 2013
PMID: 23931696
Staudt S, Bornscheuer UT, Menyes U, Hummel W, Groger H., Enzyme Microb. Technol. 53(4), 2013
PMID: 23931696
The Baeyer-Villiger reaction: new developments toward greener procedures.
ten Brink GJ, Arends IW, Sheldon RA., Chem. Rev. 104(9), 2004
PMID: 15352787
ten Brink GJ, Arends IW, Sheldon RA., Chem. Rev. 104(9), 2004
PMID: 15352787
Stabilization of cyclohexanone monooxygenase by a computationally designed disulfide bond spanning only one residue.
van Beek HL, Wijma HJ, Fromont L, Janssen DB, Fraaije MW., FEBS Open Bio 4(), 2014
PMID: 24649397
van Beek HL, Wijma HJ, Fromont L, Janssen DB, Fraaije MW., FEBS Open Bio 4(), 2014
PMID: 24649397
Cloning, expression, and characterization of an ®-specific alcohol dehydrogenase from Lactobacillus kefir
Weckbecker, Biocatal Biotransform 24(5), 2006
Weckbecker, Biocatal Biotransform 24(5), 2006
Weissermel, 2003
Regeneration of NAD(P)H using glucose-6-sulfate and glucose-6-phosphate dehydrogenase
Wong, J Org Chem 46(23), 1981
Wong, J Org Chem 46(23), 1981
Relaxing the nicotinamide cofactor specificity of phosphite dehydrogenase by rational design.
Woodyer R, van der Donk WA, Zhao H., Biochemistry 42(40), 2003
PMID: 14529270
Woodyer R, van der Donk WA, Zhao H., Biochemistry 42(40), 2003
PMID: 14529270
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