scholarly journals Increased cellular resistance to oxidative stress by expression of cyanobacterium catalase-peroxidase in animal cells

FEBS Letters ◽  
1998 ◽  
Vol 426 (2) ◽  
pp. 221-224 ◽  
Author(s):  
Takahiro Ishikawa ◽  
Yuriko Ohta ◽  
Toru Takeda ◽  
Shigeru Shigeoka ◽  
Morimitsu Nishikimi
2006 ◽  
Vol 6 (1) ◽  
pp. 57-62 ◽  
Author(s):  
Y. Pedreño ◽  
P. González-Párraga ◽  
S. Conesa ◽  
M. Martínez-Esparza ◽  
A. Aguinaga ◽  
...  

2000 ◽  
Vol 68 (7) ◽  
pp. 3861-3866 ◽  
Author(s):  
Jeong-a Kim ◽  
Zengyu Sha ◽  
John E. Mayfield

ABSTRACT All aerobic organisms have mechanisms that protect against oxidative compounds. Catalase, peroxidase, superoxide dismutase, glutathione, and thioredoxin are widely distributed in many taxa and constitute elements of a nearly ubiquitous antioxidant metabolic strategy. Interestingly, the regulatory mechanisms that control these elements are rather different depending on the nature of the oxidative stress and the organism. Catalase is well documented to play an important role in protecting cells from oxidative stress. In particular, pathogenic bacteria seem to use this enzyme as a defensive tool against attack by the host. To investigate the significance of catalase in hostile environments, we made catalase deletion mutations in two different B. abortus strains and used two-dimensional gel analysis, survival tests, and adaptation experiments to explore the behavior and role of catalase under several oxidative stress conditions. These studies show that B. abortus strains that do not express catalase activity exhibit increased sensitivity to hydrogen peroxide. We also demonstrate that catalase expression is regulated in this species, and that preexposure to a sublethal concentration of hydrogen peroxide allows B. abortus to adapt so as to survive subsequent exposure to higher concentrations of hydrogen peroxide.


2017 ◽  
Vol 19 (10) ◽  
pp. 4365-4378 ◽  
Author(s):  
Guohong Li ◽  
Anni Fan ◽  
Guoxiong Peng ◽  
Nemat O. Keyhani ◽  
Jiankang Xin ◽  
...  

2006 ◽  
Vol 6 (2) ◽  
pp. 319-319 ◽  
Author(s):  
Yolanda Pendreño ◽  
Pilar González-Párraga ◽  
Sergio Conesa ◽  
María Martínez-Esparza ◽  
Ana Aguinaga ◽  
...  

Author(s):  
J. Lock ◽  
A. H. Price

It is no longer doubted that calcium functions as a second messenger in animals and plants. This is only possible because cells maintain cytosolic calcium concentrations many orders of magnitude below that of extracellular or organelle calcium. Environmental stimuli are perceived by receptor proteins which trigger transient elevation of cytosolic calcium using internal or external sources. The spatial and temporal distribution and the magnitude of calcium elevation determines the specific cellular response at the molecular level (Cheek 1991). The fine balance of cytosolic calcium homeostasis in animal cells is highly sensitive to oxidising conditions (Duncan 1991). Elevated cytosolic calcium resulting from oxidative perturbation of calcium homeostasis is believed to be responsible for the subsequent cellular injury and death (Nicotera et al. 1991). Transient stimulation of cytosolic calcium in sublethal oxidative stress may be a mechanism by which oxidative attack is perceived by the animal cell (Nicotera et al. 1991). Our understanding of oxidative stress and plant responses to it would be greatly advanced if it can be shown that similar processes occur in plant cells. This paper briefly presents the mechanism of oxidative disruption of calcium homeostasis in animal cells and summarises the evidence that the same scenario applies to plants.


2004 ◽  
Vol 50 (1) ◽  
pp. 41-49 ◽  
Author(s):  
Charles D Miller ◽  
Drauzio Rangel ◽  
Gilberto UL Braga ◽  
Stephan Flint ◽  
Sun-Il Kwon ◽  
...  

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 catalase–peroxidase, glutathione reductase, and superoxide dismutase when compared with the less resistant strain 2575. A transient loss in activity of catalase–peroxidase 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 catalase–peroxidases and glutathione reductase in germlings changed with growth phase. UV-B exposure from lamps reduced the activity of isozymes displaying catalase–peroxidase 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 catalase–peroxidases 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: catalase–peroxidase, germination, glutathione reductase, Metarhizium anisopliae, near-UV, protein oxidation, superoxide dismutase.


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