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000904321 1001_ $$0P:(DE-HGF)0$$aSushko, Tatsiana$$b0
000904321 245__ $$aA new twist of rubredoxin function in M. tuberculosis
000904321 260__ $$aSan Diego, Calif.$$bElsevier$$c2021
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000904321 520__ $$aElectron transfer mediated by metalloproteins drives many biological processes. Rubredoxins are a ubiquitous [1Fe-0S] class of electron carriers that play an important role in bacterial adaptation to changing environmental conditions. In Mycobacterium tuberculosis, oxidative and acidic stresses as well as iron starvation induce rubredoxins expression. However, their functions during M. tuberculosis infection are unknown. In the present work, we show that rubredoxin B (RubB) is able to efficiently shuttle electrons from cognate reductases, FprA and FdR to support catalytic activity of cytochrome P450s, CYP124, CYP125, and CYP142, which are important for bacterial viability and pathogenicity. We solved the crystal structure of RubB and characterized the interaction between RubB and CYPs using site-directed mutagenesis. Mutations that not only neutralize single charge but also change the specific residues on the surface of RubB did not dramatically decrease activity of studied CYPs. Together with isothermal calorimetry (ITC) experiments, the obtained results suggest that interactions are transient and not highly specific. The redox potential of RubB is −264 mV vs. Ag/AgCl and the measured extinction coefficients are 9931 M−1cm−1 and 8371 M−1cm−1 at 380 nm and 490 nm, respectively. Characteristic parameters of RubB along with the discovered function might be useful for biotechnological applications. Our findings suggest that a switch from ferredoxins to rubredoxins might be crucial for M. tuberculosis to support CYPs activity during the infection.
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000904321 7001_ $$0P:(DE-HGF)0$$aKavaleuski, Anton$$b1
000904321 7001_ $$0P:(DE-HGF)0$$aGrabovec, Irina$$b2
000904321 7001_ $$0P:(DE-HGF)0$$aKavaleuskaya, Anna$$b3
000904321 7001_ $$0P:(DE-HGF)0$$aVakhrameev, Daniil$$b4
000904321 7001_ $$0P:(DE-HGF)0$$aBukhdruker, Sergey$$b5
000904321 7001_ $$0P:(DE-HGF)0$$aMarin, Egor$$b6
000904321 7001_ $$0P:(DE-HGF)0$$aKuzikov, Alexey$$b7
000904321 7001_ $$0P:(DE-HGF)0$$aShumyantseva, Victoria$$b8
000904321 7001_ $$0P:(DE-HGF)0$$aMasamrekh, Rami$$b9
000904321 7001_ $$0P:(DE-HGF)0$$aTsumoto, Kouhei$$b10
000904321 7001_ $$0P:(DE-Juel1)191126$$aBorshchevskiy, Valentin$$b11$$ufzj
000904321 7001_ $$0P:(DE-HGF)0$$aStrushkevich, Natallia$$b12
000904321 7001_ $$0P:(DE-HGF)0$$aGilep, Andrei$$b13$$eCorresponding author
000904321 773__ $$0PERI:(DE-600)1462232-4$$a10.1016/j.bioorg.2021.104721$$gVol. 109, p. 104721 -$$p104721 -$$tBioorganic chemistry$$v109$$x0045-2068$$y2021
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