CALCULATED IONIZATION-POTENTIALS DETERMINE THE OXIDATION OF VANILLIN PRECURSORS BY LIGNIN PEROXIDASE

Citation
R. Tenhave et al., CALCULATED IONIZATION-POTENTIALS DETERMINE THE OXIDATION OF VANILLIN PRECURSORS BY LIGNIN PEROXIDASE, FEBS letters, 430(3), 1998, pp. 390-392
Citations number
17
Categorie Soggetti
Biology,"Cell Biology",Biophysics
Journal title
ISSN journal
00145793
Volume
430
Issue
3
Year of publication
1998
Pages
390 - 392
Database
ISI
SICI code
0014-5793(1998)430:3<390:CIDTOO>2.0.ZU;2-V
Abstract
In view of the biocatalytic production of vanillin, this research focu sed on the lignin peroxidase (LiP) catalysed oxidation of naturally oc curring phenolic derivatives: O-methyl ethers, O-acetyl esters, and O- glucosyl ethers. The ionisation potential (IP) of a series of model co mpounds was calculated and compared to their experimental conversion b y LiP, defining a relative IP threshold of approximately 9.0 eV. Based on this threshold value only the O-acetyl esters and glucosides of is oeugenol and coniferyl alcohol would be potential LiP substrates. Both O-acetyl eaters were tested and were shown to be converted to O-acety l vanillin in molar yields of 51.8 and 2.3%, respectively. (C) 1998 Fe deration of European Biochemical Societies.