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嗜温绿色硫细菌绿热栖菌的铁氧化还原蛋白-NAD(P)还原酶催化的NADP/NADPH氧化还原动力学。

Kinetics of NADP/NADPH reduction-oxidation catalyzed by the ferredoxin-NAD(P) reductase from the green sulfur bacterium Chlorobaculum tepidum.

作者信息

Seo Daisuke, Kitashima Masaharu, Sakurai Takeshi, Inoue Kazuhito

机构信息

Division of Material Science, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma, Kanazawa, Ishikawa, 920-1192, Japan.

Department of Biological Sciences, Kanagawa University, Tsuchiya, Hiratsuka, Kanagawa, 259-1293, Japan.

出版信息

Photosynth Res. 2016 Dec;130(1-3):479-489. doi: 10.1007/s11120-016-0285-3. Epub 2016 Jun 24.

Abstract

Ferredoxin-NAD(P) oxidoreductase (FNR, [EC 1.18.1.2], [EC 1.18.1.3]) from the green sulfur bacterium Chlorobaculum tepidum (CtFNR) is a homodimeric flavoprotein with significant structural homology to bacterial NADPH-thioredoxin reductases. CtFNR homologs have been found in many bacteria, but only in green sulfur bacteria among photoautotrophs. In this work, we examined the reactions of CtFNR with NADP, NADPH, and (4S-H)-NADPD by stopped-flow spectrophotometry. Mixing CtFNR with NADPH yielded a rapid decrease of the absorbance in flavin band I centered at 460 nm within 1 ms, and then the absorbance further decreased gradually. The magnitude of the decrease increased with increasing NADPH concentration, but even with ~50-fold molar excess NADPH, the absorbance change was only ~45 % of that expected for fully reduced protein. The absorbance in the charge transfer (CT) band centered around 600 nm increased rapidly within 1 ms, then slowly decreased to about 70 % of the maximum. When CtFNR was mixed with excess NADP, the absorbance in the flavin band I increased to about 70 % of that of CtFNR with an apparent rate of ~4 s, whereas almost no absorption changes were observed in the CT band. Obtained data suggest that the reaction between CtFNR and NADP/NADPH is reversible, in accordance with its physiological function.

摘要

来自绿硫细菌嗜温绿菌(CtFNR)的铁氧化还原蛋白-NAD(P)氧化还原酶(FNR,[EC 1.18.1.2],[EC 1.18.1.3])是一种同型二聚体黄素蛋白,与细菌NADPH-硫氧还蛋白还原酶具有显著的结构同源性。在许多细菌中都发现了CtFNR同源物,但仅在光合自养生物中的绿硫细菌中存在。在这项工作中,我们通过停流分光光度法研究了CtFNR与NADP、NADPH和(4S-H)-NADPD的反应。将CtFNR与NADPH混合后,黄素I带中以460nm为中心的吸光度在1毫秒内迅速下降,然后吸光度进一步逐渐下降。下降幅度随NADPH浓度的增加而增加,但即使NADPH摩尔过量约50倍,吸光度变化也仅为完全还原蛋白预期值的约45%。电荷转移(CT)带中以600nm为中心的吸光度在1毫秒内迅速增加,然后缓慢下降至最大值的约70%。当CtFNR与过量NADP混合时,黄素I带中的吸光度增加至CtFNR吸光度的约70%,表观速率约为4秒,而在CT带中几乎未观察到吸收变化。获得的数据表明,CtFNR与NADP/NADPH之间的反应是可逆的,这与其生理功能一致。

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