Vignais P M, Dimon B, Zorin N A, Colbeau A, Elsen S
CEA/Grenoble, Laboratoire de Biochimie Microbienne (Centre National de la Recherche Scientifique Unité de Recherche Associée no. 1130)/Département de Biologie Moléculaire et Structurale, France.
J Bacteriol. 1997 Jan;179(1):290-2. doi: 10.1128/jb.179.1.290-292.1997.
The H-D exchange reaction has been measured with the D2-H2O system, for Rhodobacter capsulatus JP91, which lacks the hupSL-encoded hydrogenase, and R. capsulatus BSE16, which lacks the HupUV proteins. The hupUV gene products, expressed from plasmid pAC206, are shown to catalyze an H-D exchange reaction distinguishable from the H-D exchange due to the membrane-bound, hupSL-encoded hydrogenase. In the presence of O2, the uptake hydrogenase of BSE16 cells catalyzed a rapid uptake and oxidation of H2, D2, and HD present in the system, and its activity (H-D exchange, H2 evolution in presence of reduced methyl viologen [MV+]) depended on the external pH, while the H-D exchange due to HupUV remained insensitive to external pH and O2. These data suggest that the HupSL dimer is periplasmically oriented, while the HupUV proteins are in the cytoplasmic compartment.
已对缺乏hupSL编码氢化酶的荚膜红细菌JP91和缺乏HupUV蛋白的荚膜红细菌BSE16,在D2-H2O体系中进行了H-D交换反应的测定。从质粒pAC206表达的hupUV基因产物可催化一种H-D交换反应,该反应与由膜结合的hupSL编码氢化酶引起的H-D交换不同。在O2存在的情况下,BSE16细胞的摄取氢化酶催化体系中存在的H2、D2和HD的快速摄取和氧化,其活性(H-D交换、在还原甲基紫精[MV+]存在下的H2释放)取决于外部pH值,而由HupUV引起的H-D交换对外部pH值和O2不敏感。这些数据表明,HupSL二聚体位于周质空间,而HupUV蛋白位于细胞质区室。