期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：2013
卷号：110
期号：52
页码：21142-21147
DOI：10.1073/pnas.1316629111
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：The bacterial phosphoenolpyruvate:sugar phosphotransferase system (PTS) is a multicomponent system that participates in a variety of physiological processes in addition to the phosphorylation-coupled transport of numerous sugars. In Escherichia coli and other enteric bacteria, enzyme IIAGlc (EIIAGlc) is known as the central processing unit of carbon metabolism and plays multiple roles, including regulation of adenylyl cyclase, the fermentation/respiration switch protein FrsA, glycerol kinase, and several non-PTS transporters, whereas the only known regulatory role of the E. coli histidine-containing phosphocarrier protein HPr is in the activation of glycogen phosphorylase. Because HPr is known to be more abundant than EIIAGlc in enteric bacteria, we assumed that there might be more regulatory mechanisms connected with HPr. The ligand fishing experiment in this study identified Rsd, an anti-sigma factor known to complex with {sigma}70 in stationary-phase cells, as an HPr-binding protein in E. coli. Only the dephosphorylated form of HPr formed a tight complex with Rsd and thereby inhibited complex formation between Rsd and {sigma}70. Dephosphorylated HPr, but not phosphorylated HPr, antagonized the inhibitory effect of Rsd on {sigma}70-dependent transcriptions both in vivo and in vitro, and also influenced the competition between {sigma}70 and {sigma}S for core RNA polymerase in the presence of Rsd. Based on these data, we propose that the anti-{sigma}70 activity of Rsd is regulated by the phosphorylation state-dependent interaction of HPr with Rsd.
