Enzyme Activities Associated With Oxidative Stress in Metarhizium Anisopliae During Germination, Mycelial Conidiation and in Response to Near-UV Irradiation
Canadia Journal of Microbiology
Metarhizium anisopliae isolates have a wide insect host range, but an impediment to their commercial use as a biocontrol agent of above-ground insects is the high susceptibility of spores to the near-UV present in solar irradiation. To understand stress responses in M. anisopliae, we initiated studies of enzymes that protect against oxidative stress in two strains selected because their spores differed in sensitivity to UV-B. Spores of the more near-UV resistant strain in M. anisopliae 324 displayed different isozyme profiles for catalaseperoxidase, glutathione reductase, and superoxide dismutase when compared with the less resistant strain 2575. A transient loss in activity of catalaseperoxidase and glutathione reductase was observed during germination of the spores, whereas the intensity of isozymes displaying superoxide dismutase did not change as the mycelium developed. Isozyme composition for catalaseperoxidases and glutathione reductase in germlings changed with growth phase. UV-B exposure from lamps reduced the activity of isozymes displaying catalaseperoxidase and glutathione reductase activities in 2575 more than in 324. The major effect of solar UV-A plus UV-B also was a reduction in catalaseperoxidases isozyme level, a finding confirmed by measurement of catalase specific activity. Impaired growth of M. anisopliae after near-UV exposure may be related to reduced abilities to handle oxidative stress.Key words: catalaseperoxidase, germination, glutathione reductase, Metarhizium anisopliae, near-UV, protein oxidation, superoxide dismutase.
Miller, C.D., D. Rangel, G.U.L. Braga, S. Flint, Sun-Il Kwon, C.L. Messias, D.W. Roberts and A.J. Anderson. 2004. Enzyme activities associated with oxidative stress in Metarhizium anisopliae during germination, mycelial conidiation and in response to near-UV irradiation. Canadian Journal of Microbiology. 50 (1): 41-49.