Malic acid production by an electrochemical reduction system combined with the use of diaphorase and methylviologen
- 1 May 1985
- journal article
- research article
- Published by Wiley in Biotechnology & Bioengineering
- Vol. 27 (5) , 596-602
- https://doi.org/10.1002/bit.260270508
Abstract
A regenerating reaction combined with the use of native malate dehydrogenase, native diaphorase, methylviologen, NAD, oxalacetic acid as the substrate and lipoamide as a stabilizer was carried out in the presence of electrolysis. Consequently, malic acid was efficiently produced from oxalacetic acid in the regenerating reaction. A glassy carbon bead electrode was used as a cathode. Twenty four milliamperes were passed at a rotation speed of 500 rpm, 29.8 ± 0.3°C and −1.0 V. It was found that lipoamide has a stabilizing effect on malate dehydrogenase and diaphorase. Low concentration (50 μM) of NAD was also effective for the stabilization of malate dehydrogenase. NADH regeneration activity based on malic acid production rate was 4.7 U/mg of the enzyme protein of the commercial diaphorase preparation. The current efficiency was more than 74%, compared with the theoretical yield, in the presence of enough oxalacetic acid.This publication has 5 references indexed in Scilit:
- Purification and properties of soluble hydrogenase from Alcaligenes eutrophus H 16Published by Elsevier ,2003
- Glycerol protection and purification of Bacillus subtilis glucose dehydrogenase.Journal of Biological Chemistry, 1983
- Enzyme-catalyzed organic synthesis: electrochemical regeneration of NAD(P)H from NAD(P) using methyl viologen and flavoenzymesThe Journal of Organic Chemistry, 1981
- Purification and Properties of Formaldehyde Dehydrogenase and Formate Dehydrogenase from Candida boidiniiEuropean Journal of Biochemistry, 1976
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951