B. Falconnier et al., VANILLIN AS A PRODUCT OF FERULIC ACID BIOTRANSFORMATION BY THE WHITE-ROT FUNGUS PYCNOPORUS-CINNABARINUS-I-937 - IDENTIFICATION OF METABOLICPATHWAYS, Journal of biotechnology, 37(2), 1994, pp. 123-132
Ferulic acid metabolism was studied in cultures of the white-rot fungu
s Pycnoporus cinnabarinus I-937. After 6 days of growth, during the se
condary metabolism of the fungus, the concentration of vanillin in the
culture medium reached a maximum of 64 mg l(-1), corresponding to a m
olar yield of 27.5%. During the biotransformation process, the propeno
ic side chain of ferulic acid was oxidatively cleaved to yield vanilli
c acid, further decarboxylated to 2-methoxyhydroquinone. In addition,
two reductive routes were evidenced, involving the conversion of ferul
ic and vanillic acids into coniferyl and vanillyl alcohols, respective
ly. The biotransformation process was not easily controlled since the
P. cinnabarinus species is known to release laccase into the growth me
dium. When produced, the enzyme countered the vanillin formation by pr
omoting the polymerization of ferulic acid into lignin-like polymers.