More efficient redox biocatalysis by utilising 1,4-butanediol as a 'smart cosubstrate'

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Selin Kara
  • Dominik Spickermann
  • Joerg H. Schrittwieser
  • Christian Leggewie
  • Willem J.H. Van Berkel
  • Isabel W.C.E. Arends
  • Frank Hollmann

Externe Organisationen

  • Delft University of Technology
  • evoxx technologies GmbH
  • Wageningen University and Research
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)330-335
Seitenumfang6
FachzeitschriftGreen chemistry
Jahrgang15
Ausgabenummer2
Frühes Online-Datum20 Dez. 2012
PublikationsstatusVeröffentlicht - Feb. 2013
Extern publiziertJa

Abstract

1,4-Butanediol is shown to be an efficient cosubstrate to promote NAD(P)H-dependent redox biocatalysis. The thermodynamically and kinetically inert lactone coproduct makes the regeneration reaction irreversible. Thereby not only the molar surplus of cosubstrate is dramatically reduced but also faster reaction rates are obtained.

ASJC Scopus Sachgebiete

Zitieren

More efficient redox biocatalysis by utilising 1,4-butanediol as a 'smart cosubstrate'. / Kara, Selin; Spickermann, Dominik; Schrittwieser, Joerg H. et al.
in: Green chemistry, Jahrgang 15, Nr. 2, 02.2013, S. 330-335.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Kara, S, Spickermann, D, Schrittwieser, JH, Leggewie, C, Van Berkel, WJH, Arends, IWCE & Hollmann, F 2013, 'More efficient redox biocatalysis by utilising 1,4-butanediol as a 'smart cosubstrate'', Green chemistry, Jg. 15, Nr. 2, S. 330-335. https://doi.org/10.1039/c2gc36797a
Kara, S., Spickermann, D., Schrittwieser, J. H., Leggewie, C., Van Berkel, W. J. H., Arends, I. W. C. E., & Hollmann, F. (2013). More efficient redox biocatalysis by utilising 1,4-butanediol as a 'smart cosubstrate'. Green chemistry, 15(2), 330-335. https://doi.org/10.1039/c2gc36797a
Kara S, Spickermann D, Schrittwieser JH, Leggewie C, Van Berkel WJH, Arends IWCE et al. More efficient redox biocatalysis by utilising 1,4-butanediol as a 'smart cosubstrate'. Green chemistry. 2013 Feb;15(2):330-335. Epub 2012 Dez 20. doi: 10.1039/c2gc36797a
Kara, Selin ; Spickermann, Dominik ; Schrittwieser, Joerg H. et al. / More efficient redox biocatalysis by utilising 1,4-butanediol as a 'smart cosubstrate'. in: Green chemistry. 2013 ; Jahrgang 15, Nr. 2. S. 330-335.
Download
@article{a158431c3c98415698b95a7362722f43,
title = "More efficient redox biocatalysis by utilising 1,4-butanediol as a 'smart cosubstrate'",
abstract = "1,4-Butanediol is shown to be an efficient cosubstrate to promote NAD(P)H-dependent redox biocatalysis. The thermodynamically and kinetically inert lactone coproduct makes the regeneration reaction irreversible. Thereby not only the molar surplus of cosubstrate is dramatically reduced but also faster reaction rates are obtained.",
author = "Selin Kara and Dominik Spickermann and Schrittwieser, {Joerg H.} and Christian Leggewie and {Van Berkel}, {Willem J.H.} and Arends, {Isabel W.C.E.} and Frank Hollmann",
year = "2013",
month = feb,
doi = "10.1039/c2gc36797a",
language = "English",
volume = "15",
pages = "330--335",
journal = "Green chemistry",
issn = "1463-9262",
publisher = "Royal Society of Chemistry",
number = "2",

}

Download

TY - JOUR

T1 - More efficient redox biocatalysis by utilising 1,4-butanediol as a 'smart cosubstrate'

AU - Kara, Selin

AU - Spickermann, Dominik

AU - Schrittwieser, Joerg H.

AU - Leggewie, Christian

AU - Van Berkel, Willem J.H.

AU - Arends, Isabel W.C.E.

AU - Hollmann, Frank

PY - 2013/2

Y1 - 2013/2

N2 - 1,4-Butanediol is shown to be an efficient cosubstrate to promote NAD(P)H-dependent redox biocatalysis. The thermodynamically and kinetically inert lactone coproduct makes the regeneration reaction irreversible. Thereby not only the molar surplus of cosubstrate is dramatically reduced but also faster reaction rates are obtained.

AB - 1,4-Butanediol is shown to be an efficient cosubstrate to promote NAD(P)H-dependent redox biocatalysis. The thermodynamically and kinetically inert lactone coproduct makes the regeneration reaction irreversible. Thereby not only the molar surplus of cosubstrate is dramatically reduced but also faster reaction rates are obtained.

UR - http://www.scopus.com/inward/record.url?scp=84873321013&partnerID=8YFLogxK

U2 - 10.1039/c2gc36797a

DO - 10.1039/c2gc36797a

M3 - Article

AN - SCOPUS:84873321013

VL - 15

SP - 330

EP - 335

JO - Green chemistry

JF - Green chemistry

SN - 1463-9262

IS - 2

ER -

Von denselben Autoren