M. Hofrichter et al., Mineralization and solubilization of synthetic lignin by manganese peroxidases from Nematoloma frowardii and Phlebia radiata, J BIOTECH, 67(2-3), 1999, pp. 217-228
Crude and purified manganese peroxidase from the white-rot fungi Nematoloma
frowardii and Phlebia radiata catalyzed the partial depolymerization of a
[C-14-ring]labelled synthetic lignin into water-soluble fragments (30-50%).
The in vitro depolymerization of the C-14-labelled lignin was accompanied
by a release of (CO2)-C-14 ranging from 4 to 6%. Small quantities of the th
iol mediator glutathione stimulated the depolymerization of lignin resultin
g in a mineralization and solubilization of up to 10 and 64%, respectively.
Most of the water-soluble substances formed had molecular masses around 0.
7 kDa, although a higher-molecular mass fraction was also detectable (>2 kD
a). Photometric assays using 2,2'-azinobis(3-ethylbenzothiazolinesulphonate
) as an indicator demonstrated that high levels of Mn(IIE), which were very
probably responsible for the depolymerization and mineralization of the C-
14-labelled lignin, were adjusted within the first 24 h of incubation. The
manganese peroxidase catalyzed depolymerization process was not necessarily
dependent on H2O2; also in the absence of the H2O2-generating system gluco
se/glucose oxidase, effective solubilization and mineralization of lignin d
ehydrogenation polymerizate occurred, due to the in part superoxide dismuta
se sensitive, 'oxidase-like' activity of MnP which probably produces radica
l species and peroxides from malonate. (C) 1999 Elsevier Science B.V. All r
ights reserved.