2019
Modifications of the Aerobic Respiratory Chain of Paracoccus Denitrificans in Response to Superoxide Oxidative Stress
SEDLÁČEK, Vojtěch a Igor KUČERAZákladní údaje
Originální název
Modifications of the Aerobic Respiratory Chain of Paracoccus Denitrificans in Response to Superoxide Oxidative Stress
Autoři
SEDLÁČEK, Vojtěch (203 Česká republika, domácí) a Igor KUČERA (203 Česká republika, domácí)
Vydání
Microorganisms, Basel, MDPI, 2019, 2076-2607
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10600 1.6 Biological sciences
Stát vydavatele
Švýcarsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.152
Kód RIV
RIV/00216224:14310/19:00107871
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000506646400058
Klíčová slova anglicky
NADH dehydrogenase; succinate dehydrogenase; terminal oxidase; iron-sulfur cluster; FnrP transcription factor; superoxide
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 26. 3. 2020 17:14, Mgr. Marie Šípková, DiS.
Anotace
V originále
Paracoccus denitrificans is a strictly respiring bacterium with a core respiratory chain similar to that of mammalian mitochondria. As such, it continuously produces and has to cope with superoxide and other reactive oxygen species. In this work, the effects of artificially imposed superoxide stress on electron transport were examined. Exposure of aerobically growing cells to paraquat resulted in decreased activities of NADH dehydrogenase, succinate dehydrogenase, and N,N,N’,N’-tetramethyl-p-phenylenediamine (TMPD) oxidase. Concomitantly, the total NAD(H) pool size in cells was approximately halved, but the NADH/NAD+ ratio increased twofold, thus partly compensating for inactivation losses of the dehydrogenase. The inactivation of respiratory dehydrogenases, but not of TMPD oxidase, also took place upon treatment of the membrane fraction with xanthine/xanthine oxidase. The decrease in dehydrogenase activities could be fully rescued by anaerobic incubation of membranes in a mixture containing 2-mercaptoethanol, sulfide and ferrous iron, which suggests iron–sulfur clusters as targets for superoxide. By using cyanide titration, a stress-sensitive contribution to the total TMPD oxidase activity was identified and attributed to the cbb3-type terminal oxidase. This response (measured by both enzymatic activity and mRNA level) was abolished in a mutant defective for the FnrP transcription factor. Therefore, our results provide evidence of oxidative stress perception by FnrP.
Návaznosti
GA16-18476S, projekt VaV |
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