Doyle C M, Arp D J
Department of Biochemistry, University of California, Riverside 92521.
J Bacteriol. 1988 Sep;170(9):3891-6. doi: 10.1128/jb.170.9.3891-3896.1988.
The effects of nickel on the expression of hydrogenase in the hydrogen-oxidizing bacterium Alcaligenes latus were studied. In the absence of added nickel, both hydrogenase activity, measured as O2-dependent H2 uptake, and hydrogenase protein, measured in a Western immunoblot, were very low compared with the levels in cells induced for hydrogenase in the presence of nickel. Hydrogenase activity and protein levels were dependent on the added nickel concentration and were saturated at 30 nM added Ni2+. The amount of hydrogenase protein in a culture at a given nickel concentration was calculated from the H2 uptake activity of the culture at that Ni2+ concentration. Between 0 and 30 nM added Ni2+, the amount of hydrogenase protein (in nanomoles) was stoichiometric with the amount of added Ni2+. Thus, all of the added Ni2+ could be accounted for in hydrogenase. Between 0 and 50 nM added Ni2+, all the Ni present in the cultures was associated with the cells after 12 h; above 50 nM added Ni2+, some Ni remained in the medium. No other divalent metal cations tested were able to substitute for Ni2+ in the formation of active hydrogenase. We suggest two possible mechanisms for the regulation of hydrogenase activity and protein levels by nickel.
研究了镍对产碱杆菌中氢化酶表达的影响。在不添加镍的情况下,以依赖氧气的氢气摄取量衡量的氢化酶活性以及通过蛋白质免疫印迹法测定的氢化酶蛋白水平,与在有镍存在时诱导氢化酶的细胞中的水平相比都非常低。氢化酶活性和蛋白水平取决于添加的镍浓度,在添加30 nM Ni2+时达到饱和。根据给定镍浓度下培养物的氢气摄取活性计算出该镍浓度下培养物中氢化酶蛋白的量。在添加0至30 nM Ni2+之间,氢化酶蛋白的量(以纳摩尔计)与添加的Ni2+量呈化学计量关系。因此,所有添加的Ni2+都可以在氢化酶中找到。在添加0至50 nM Ni2+之间,培养物中存在的所有镍在12小时后都与细胞结合;添加量高于50 nM时,一些镍仍留在培养基中。测试的其他二价金属阳离子都不能替代Ni2+来形成有活性的氢化酶。我们提出了镍调节氢化酶活性和蛋白水平的两种可能机制。