D. Li et al., REGULATION OF MANGANESE PEROXIDASE GENE-TRANSCRIPTION BY HYDROGEN-PEROXIDE, CHEMICAL STRESS, AND MOLECULAR-OXYGEN, Applied and environmental microbiology, 61(1), 1995, pp. 341-345
The expression of manganese peroxidase (MnP) in nitrogen-limited cultu
res of the lignin-degrading fungus Phanerochaete chrysosporium is regu
lated at the level of gene transcription by H2O2 and various chemicals
, including ethanol, sodium arsenite, and 2,4-dichlorophenol, as well
as by Mn(II) and heat shock Northern (RNA) blot analysis demonstrates
that the addition of 1.0 mM H2O2 to 5-day old cultures grown in the ab
sence of Mn results in the appearance of mnp mRNA within 15 min. Highe
r levels of mnp mRNA are obtained with simultaneous induction by Mn an
d H2O2 than with H2O2 alone. Although neither MnP activity nor associa
ted protein is detectable in H2O2-induced cultures groan in the absenc
e of Mn, simultaneous induction with Mn and H2O2 results in a 1.6-fold
increase in MnP activity compared with the MnP activity resulting fro
m Mn induction alone. In the presence of Mn, purging of low-nitrogen c
ultures with 100% O-2, in contrast to incubation under air, results in
an increase in the accumulation of mnp mRNA and a 13-fold increase in
MnP activity on day 5. However, in contrast to the effects of H2O2 an
d heat shock, O-2 purging of Mn-deficient cultures results in negligib
le accumulation of mnp mRNA.