F. Guillen et Cs. Evans, ANISALDEHYDE AND VERATRALDEHYDE ACTING AS REDOX CYCLING AGENTS FOR H2O2 PRODUCTION BY PLEUROTUS-ERYNGII, Applied and environmental microbiology, 60(8), 1994, pp. 2811-2817
The existence of a redox cycle leading to the production of hydrogen p
eroxide (H2O2) in the white rot fungus Pleurotus eryngii has been conf
irmed by incubations of 10-day-old mycelium with veratryl (3,4-dimetho
xybenzyl) and anisyl (4-methoxybenzyl) compounds (alcohols, aldehydes,
and acids). Veratraldehyde and anisaldehyde were reduced by aryl alco
hol dehydrogenase to their corresponding alcohols, which were oxidized
by aryl-alcohol oxidase, producing H2O2. Veratric and anisic acids we
re incorporated into the cycle after their reduction, which was cataly
zed by aryl-aldehyde dehydrogenase. With the use of different initial
concentrations of either veratryl alcohol, veratraldehyde, or veratric
acid (0.5 to 4.0 mM), around 94% of veratraldehyde and 3% of veratryl
alcohol (compared with initial concentrations) and trace amounts of v
eratric acid were found when equilibrium between reductive and oxidati
ve activities had been reached, regardless of the initial compound use
d. At concentrations higher than 1 mM, veratric acid was not transform
ed, and at 1.0 mM, it produced a negative effect on the activities of
aryl-alcohol oxidase and both dehydrogenases. H2O2 levels were proport
ional to the initial concentrations of veratryl compounds (around 0.5%
), and an equilibrium between aryl-alcohol oxidase and an unknown H2O2
-reducing system kept these levels steady. On the other hand, the conc
omitant production of the three above-mentioned enzymes during the act
ive growth phase of the fungus was demonstrated. Finally, the possibil
ity that anisaldehyde is the metabolite produced by P. eryngii for the
maintenance of this redox cycle is discussed.