Oxidative stress in bacteria and protein damage by reactive oxygen species

The advent of O2 in the atmosphere was among the first major pollution events occurred on earth The reaction between ferrous iron, very abundant in the reductive early atmosphere, and oxygen results in the formation of harmful superoxide and hydroxyl radicals, which affect all macromolecules (DNA, lipids and proteins). Living organisms have to build up mechanisms to protect themselves against oxidative stress, with enzymes such as catalase and superoxide dismutase, small proteins like thioredoxin and glutaredoxin, and molecules such as glutathione. Bacterial genetic responses to oxidative stress are controlled by two major transcriptional regulators (OxyR and SoxRS). This paper reviews major key points in the generation of reactive oxygen species in bacteria, defense mechanisms and genetic responses to oxidative stress. Special attention is paid to the oxidative damage to proteins

Grx5 glutaredoxin plays a central role in protection against protein oxidative damage in Saccharomyces cerevisiae

Glutaredoxins are members of a superfamily of thiol disulfide oxidoreductases involved in maintaining the redox state of target proteins. In Saccharomyces cerevisiae, two glutaredoxins (Grx1 and Grx2) containing a cysteine pair at the active site had been characterized as protecting yeast cells against oxidative damage. In this work, another subfamily of yeast glutaredoxins (Grx3, Grx4, and Grx5) that differs from the first in containing a single cysteine residue at the putative active site is described. This trait is also characteristic for a number of glutaredoxins from bacteria to humans, with which the Grx3/4/5 group has extensive homology over two regions. Mutants lacking Grx5 are partially deficient in growth in rich and minimal media and also highly sensitive to oxidative damage caused by menadione and hydrogen peroxide. A significant increase in total protein carbonyl content is constitutively observed in grx5cells, and a number of specific proteins, including transketolase, appear to be highly oxidized in this mutant. The synthetic lethality of the grx5 and grx2 mutations on one hand and ofgrx5 with the grx3 grx4 combination on the other points to a complex functional relationship among yeast glutaredoxins, with Grx5 playing a specially important role in protection against oxidative stress both during ordinary growth conditions and after externally induced damage. Grx5-deficient mutants are also sensitive to osmotic stress, which indicates a relationship between the two types of stress in yeast cells

Acción de algunos acaricidas sobre los fítoseídos y la araña roja Panonychus ulmi (Koch) en manzano

Se han realizado 5 ensayos en manzanos para evaluar la acción de algunos acarici­das sobre la araña roja Panonychus ulmi (Koch) y sus depredadores los fitoseidos. En 4 ensayos la especie era Amblyseius andersoni (Chant) y en la otra A. californicus (McGregor). En total se han ensayado 14 materias activas. Se observa una mayor toxicidad de los productos sobre A. californicus que sobre A. andersoni, y en esta última especie la toxicidad suele ser mayor cuando el nivel de P. ulmi es más elevado. Las materias activas que son mas tóxicas para los fitoseidos son: amitraz, bifentrin y fenpropatrin. En el caso del amitraz se observa incluso una proliferación de P. ulmi. Los productos que son menos tóxicos para los fitoseidos y que dan una mayor relación depredador/presa, a pesar de su baja eficacia sobre P. ulmi, son: benzoximato, dioctil-sulfosuccinato-sodico y fenbutestan. Los acaricidas: cihexaestan, dinobuton, hexitiazox y propargita son medianamente tóxicos para los fitoseidos, pero su poca eficacia sobre P. ulmi provoca como resultado una relación depredador/ presa más baja que el testigo. Los que dan una mayor eficacia sobre P. ulmi, pero son más tóxicos para los fi­toseidos que los productos anteriores, por lo que dan como resultado unas relaciones de­ predador/presa más irregulares son: fenazaquin, fenpiroximato, piridaben y tebufenpirad. Deben realizarse más estudios sobre las dosis, mezclas y momentos de aplicación de todos estos productos para su utilización en el control integrado de la araña roja.Fourteen acaricides have been tested in five field trials to evaluate their efficacy on Panonychus ulmi (Koch) and their toxicity to the phytoseids Amblyseius andersoni (Chant) (4 trials) and Amblyseius californicus (McGregor) (1 trial). In general, the acaricides were more toxic to A. californicus than to A. andersoni. The toxicity to A. andersoni was higher when the population of P. ulmi was great. The more toxic to phytoseids active ingredients were amitraz, bifenthrin and fenpropathrin. An increase in P. ulmi populations was observed after the use of amitraz. The acaricides that gave a better predator/prey relationship were benzoximate, dioctil-sulfosuccinate and fenbutatin-oxide. This products showed the lowest toxicity to phytoseids but their efficacy against P. ulmi was low. The acaricides cyhexatin, dinobuton, hexythiazox and propargite were moderately toxic to phytoseids, but their low efficacy against P. ulmi led to a prey/predator relationship smaller than the observed relation in the control plots. The acaricides belonging to the METI-group (fenazaquin, fenpyroximate, pyridaden and tebufenpyrad) were the most efficient against P. ulmi, but also the most toxic to phytosedis, leading to irregular prey/predator relationships. More trials with this chemicals should be done to assess the correct rate, the mixtures betweend them, and the timing of application for use in IPM programs