Pregled bibliografske jedinice broj: 56651
Enantioselective enzymatic oxidation with indirect electrochemical NAD+ regeneration
Enantioselective enzymatic oxidation with indirect electrochemical NAD+ regeneration // Reactive intermediates in organic and biological electrochemistry in honor of late professor Eberhard Steckhan / Yoshida, J. ; Peters, D.G. ; Workentin, M.S. (ur.).
Washington (MD): The Electrochemical Society (ECS), 2001. str. 00-00 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 56651 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Enantioselective enzymatic oxidation with indirect electrochemical NAD+ regeneration
Autori
Schroeder, Iris ; Vasić-Rački, Đurđa ; Wandrey, Christian ; Liese, Andreas
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Reactive intermediates in organic and biological electrochemistry in honor of late professor Eberhard Steckhan
/ Yoshida, J. ; Peters, D.G. ; Workentin, M.S. - Washington (MD) : The Electrochemical Society (ECS), 2001, 00-00
Skup
The 199th Meeting of The Electrochemical Society
Mjesto i datum
Sjedinjene Američke Države, 25.03.2001. - 29.03.2001
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
enantioselective enzymatic oxidation; electrochemical NAD regeneration
Sažetak
For production of 2-hydroxyketones and racemic resolution of vicinal diols glycerol dehydrogenase (GDH) [EC 1.1.1.6] from Cellulomonas species was used as production enzyme.1 Since GDH is NAD + dependent and strongly
inhibited by its reduced form NADH, an effective and cost efficient cofactor regeneration is necessary. For this regeneration ABTS+.was used as oxidizing agent, which itself was prepared in situ by anodic oxidation. Though electrochemical cofactor regeneration needs no cosubstrate nor additional enzymes, until now it is not used in industrial biotransformations.2, 3 The kinetic parameters were determined and a kinetic model for the electrochemically driven
enzymatic reaction was developed. Based on this model the ratios of the reactants were optimized and the model proved by experiments. Synthesis of 2-hydroxyketones and racemic resolution were performed in different reactor
types, avoiding product inhibition by continuous extraction of the formed 2-hydroxyketones. GDH was retained by using ultrafiltration membranes.
Lit: 1 A. Liese, M. Karutz, J. Kamphuis, C. Wandrey, U. Kragl, Biotech. Bioeng. 1996, 51, 544-550
2 A. Liese, K. Seelbach, C. Wandrey, Industrial Biotransformations, VCH Weinheim 2000
3 E. Steckhan, Top. Curr. Chem 1994, 170, 83-111
Financial support by BASF AG Ludwigshafen (Germany) is gratefully acknowledged.
Izvorni jezik
Engleski
Znanstvena područja
Prehrambena tehnologija
POVEZANOST RADA
Projekti:
125021
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Đurđa Vasić-Rački
(autor)