首页> 外文OA文献 >Identification of the iron-sulfur clusters in a ferredoxin from the archaeon Sulfolobus acidocaldarius. Evidence for a reduced [3Fe-4S] cluster with pH-dependent electronic properties.
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Identification of the iron-sulfur clusters in a ferredoxin from the archaeon Sulfolobus acidocaldarius. Evidence for a reduced [3Fe-4S] cluster with pH-dependent electronic properties.

机译:鉴定古细菌Sulfolobus acidocaldarius中铁氧还蛋白中的铁硫簇。有减少的[3Fe-4S]团簇的证据,其具有pH依赖的电子特性。

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摘要

A ferredoxin isolated from the archaeon Sulfolobus acidocaldarius strain DSM 639 has been shown to contain one [3Fe-4S]1 + 10 cluster with a reduction potential of -275 mV and one [4Fe-4S]2+/1+ cluster with a reduction potential of -529 mV at pH 6.4, in the temperature range 0-50 degrees C. The monomer molecular mass was confirmed to be 10907.5 +/- 1.0 Da by electrospray mass spectrometry, as calculated from the published amino acid sequence [Minami, Y. Wakabayashi. S., Wada, K., Matsubara, H., Kerscher, L. and Oesterhelt, D. (1985) J. Biochem. (Tokyo) 97, 745-751], while the holoprotein molecular mass was found to be 11,550 +/- 1.0 Da. The reduced [3Fe-4S]0 cluster was also shown by direct electrochemistry and magnetic circular dichroic spectroscopy to undergo a one-proton uptake reaction as first observed for Azotobacter chroococcum ferredoxin I [George, S. J., Richards, A. J. M., Thomson, A. J. and Yates, M. G. (1984) Biochem. J. 224, 247-251]. The pKa of the protonation step has been determined by a novel thin film electrochemical method to be 5.8. This is significantly different from the pKa of 7.7 determined for A. vinelandii ferredoxin I [Shen, B., Martin, L. L., Butt, J. N., Armstrong, F. A., Stout, C. D., Jensen, J. M., Stephens, P. J., LaMar, G. N., Gorst, C. M. and Burgess, B. K. (1993) J. Biol. Chem. 268, 25928-25939] and indicates that the polypeptide chain around the [3Fe-4S] cluster controls this reaction. Although this appears to be only the second reported case of protonation at or near the reduced [3Fe-4S]0 cluster, its observation in S. acidocaldarius ferredoxin raises the question of the generality of this chemistry for 3Fe clusters. The similarity of the pKa to the estimated intracellular pH of S. acidocaldarius strongly suggests a physiological role for this process.
机译:从古细菌Sulfolobus acidocaldarius菌株DSM 639中分离出的铁氧还蛋白已显示含有一个还原电位为-275 mV的[3Fe-4S] 1 + 10簇和一个还原电位为[4Fe-4S] 2 + / 1 +的簇pH值为6.4,在0-50℃的温度下,电势为-529 mV。根据公开的氨基酸序列[Minami,Y],通过电喷雾质谱法确定单体分子量为10907.5 +/- 1.0 Da若林S.,Wada,K.,Matsubara,H.,Kerscher,L。和Oesterhelt,D。(1985)J.Biochem。 (东京)97,745-751],而发现全蛋白分子量为11,550 +/- 1.0Da。还原的[3Fe-4S] 0团簇还通过直接电化学和磁圆二向色光谱显示出发生了一个质子吸收反应,首次观察到嗜铬绿球菌铁氧还蛋白I [George,SJ,Richards,AJM,Thomson,AJ和Yates ,MG(1984)生物化学。 J. 224,247-251]。通过新颖的薄膜电化学方法已经确定了质子化步骤的pKa为5.8。这与针对A. vinelandii ferredoxin I的pKa值7.7显着不同[Shen,B.,Martin,LL,Butt,JN,Armstrong,FA,Stout,CD,Jensen,JM,Stephens,PJ,LaMar,GN, Gorst,CM和Burgess,BK(1993)J.Biol。化学268,25928-25939],并指出[3Fe-4S]簇周围的多肽链控制了该反应。尽管这似乎只是在还原的[3Fe-4S] 0簇上或附近出现质子化的第二个报道案例,但它在嗜酸链球菌铁氧还蛋白中的观察提出了这种化学对3Fe簇的普遍性的问题。 pKa与嗜酸链球菌的估计细胞内pH的相似性强烈暗示了该过程的生理作用。

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