N. Rothschild et al., Manganese deficiency can replace high oxygen levels needed for lignin peroxidase formation by Phanerochaete chrysosporium, APPL ENVIR, 65(2), 1999, pp. 483-488
The combined effects of Mn and oxygen on lignin peroxidase (LIP) activity a
nd isozyme composition in Phanerochaete chrysosporium were studied by using
shallow stationary cultures grown in the presence of limited or excess N.
When no Mn was added, LIP, was formed in both N-limited and N-excess cultur
es exposed to air, but no LIP activity was observed at Mn concentrations gr
eater than 13 mg/liter. In oxygen-flushed, N-excess cultures, LIP was forme
d at all Mn concentrations, and the peak LIP activity values in the extrace
llular fluid were nearly identical in the presence of Mn concentrations ran
ging from 3 to 1,500 mg/liter. When the availability of oxygen to cultures
exposed to air was increased by growing the fungus under nonimmersed liquid
conditions, higher levels of Mn were needed to suppress LIP formation comp
ared with the levels needed in shallow stationary cultures. The composition
of LIP isozymes was affected by the levels of N and Mn. Addition of veratr
yl alcohol to cultures exposed to air did not eliminate the suppressive eff
ect of Mn on LIP formation. A deficiency of Mn in N-excess cultures resulte
d in lower biomass and a lower rate of glucose consumption than in the pres
ence of Mn. In addition, almost no activity of the antioxidant enzyme Mn su
peroxide dismutase was observed in Mn-deficient, N-excess cultures, but the
activity of this enzyme increased as the Mn concentration increased from 3
to 13 mg/liter. No Zn/Cu superoxide dismutase activity was observed in N-e
xcess cultures regardless of the Mn concentration.