Smith E T, Blamey J M, Zhou Z H, Adams M W
Department of Biochemistry, University of Georgia, Athens 30602, USA.
Biochemistry. 1995 May 30;34(21):7161-9. doi: 10.1021/bi00021a030.
The hyperthermophilic bacterium Thermotoga maritima and the hyperthermophilic archaeon Pyrococcus furiosus grow optimally at 80 and 100 degrees C, respectively, by the fermentation of carbohydrates to organic acids, CO2, and H2. Pyruvate is a major source of reductant for H2 production during fermentation, and pyruvate ferredoxin oxidoreductase (POR), a 4Fe-type ferredoxin, and hydrogenase have been previously purified from both species. P. furiosus utilizes a copper-iron-containing POR and a nickel-iron-containing hydrogenase, whereas the POR of T. maritima lacks copper and its hydrogenase lacks nickel. For all four enzymes and for the two ferredoxins, we have determined their reduction potentials (E degrees') and, where possible, thermodynamic parameters associated with electron transfer (delta S degrees and delta H degrees), using differential pulse voltammetry at temperatures ranging from 25 to 95 degrees C. At ambient temperature, the E degrees' values for all six proteins were comparable and spanned less than 50 mV, but their temperature dependence varied dramatically, even between analogous proteins, such that in the physiological-relevant temperature range the E degrees' values became widely separated. In most cases, transition points were observed in E degrees'/temperature profiles, and these generally corresponded with significant increases in catalytic activity, but occurred at lower temperatures in T. maritima than in P. furiosus. The two ferredoxins (and also P. furiosus rubredoxin) had much more negative entropy terms than were calculated for POR and hydrogenase, and these values were also more negative than those previously reported for mesophilic redox proteins. The reduction potentials measured at high temperatures and likely efficiencies of electron transfer between the various proteins were consistent with in vitro activity measurements.(ABSTRACT TRUNCATED AT 250 WORDS)
嗜热细菌嗜热栖热袍菌和嗜热古菌激烈火球菌分别在80℃和100℃下生长最佳,通过将碳水化合物发酵为有机酸、二氧化碳和氢气。丙酮酸是发酵过程中产生氢气的主要还原剂来源,丙酮酸铁氧化还原酶(POR)、一种4Fe型铁氧化还原蛋白和氢化酶此前已从这两个物种中纯化出来。激烈火球菌利用含铜铁的POR和含镍铁的氢化酶,而嗜热栖热袍菌的POR不含铜,其氢化酶不含镍。对于所有这四种酶和两种铁氧化还原蛋白,我们使用差分脉冲伏安法在25至95℃的温度范围内测定了它们的还原电位(E°'),并在可能的情况下测定了与电子转移相关的热力学参数(ΔS°和ΔH°)。在环境温度下,所有六种蛋白质的E°'值相当,跨度小于50 mV,但它们对温度的依赖性差异很大,即使在类似的蛋白质之间也是如此,因此在生理相关温度范围内,E°'值变得广泛分离。在大多数情况下,在E°'/温度曲线中观察到转变点,这些点通常与催化活性的显著增加相对应,但在嗜热栖热袍菌中出现的温度低于激烈火球菌。这两种铁氧化还原蛋白(以及激烈火球菌红素铁氧化还原蛋白)的熵项比为POR和氢化酶计算的值更负,这些值也比先前报道的嗜温氧化还原蛋白的值更负。在高温下测得的还原电位以及各种蛋白质之间可能的电子转移效率与体外活性测量结果一致。(摘要截断于250字)