RESUMEN
Legionella pneumophila uses aquatic protozoa as replication niche and protection from harsh environments. Although L. pneumophila is not known to have a circadian clock, it encodes homologues of the KaiBC proteins of Cyanobacteria that regulate circadian gene expression. We show that L. pneumophila kaiB, kaiC and the downstream gene lpp1114, are transcribed as a unit under the control of the stress sigma factor RpoS. KaiC and KaiB of L. pneumophila do not interact as evidenced by yeast and bacterial two-hybrid analyses. Fusion of the C-terminal residues of cyanobacterial KaiB to Legionellaâ KaiB restores their interaction. In contrast, KaiC of L. pneumophila conserved autophosphorylation activity, but KaiB does not trigger the dephosphorylation of KaiC like in Cyanobacteria. The crystal structure of L. pneumophilaâ KaiB suggests that it is an oxidoreductase-like protein with a typical thioredoxin fold. Indeed, mutant analyses revealed that the kai operon-encoded proteins increase fitness of L. pneumophila in competitive environments, and confer higher resistance to oxidative and sodium stress. The phylogenetic analysis indicates that L. pneumophilaâ KaiBC resemble Synechosystisâ KaiC2B2 and not circadian KaiB1C1. Thus, the L. pneumophilaâ Kai proteins do not encode a circadian clock, but enhance stress resistance and adaption to changes in the environments.
Asunto(s)
Proteínas Bacterianas/metabolismo , Péptidos y Proteínas de Señalización del Ritmo Circadiano/metabolismo , Legionella pneumophila/genética , Operón , Estrés Fisiológico , Acanthamoeba castellanii/microbiología , Acanthamoeba castellanii/fisiología , Adaptación Fisiológica , Proteínas Bacterianas/genética , Relojes Circadianos , Péptidos y Proteínas de Señalización del Ritmo Circadiano/genética , Perfilación de la Expresión Génica , Regulación Bacteriana de la Expresión Génica , Aptitud Genética , Legionella pneumophila/fisiología , Fosforilación , Filogenia , Estructura Terciaria de Proteína , ARN Bacteriano/genéticaRESUMEN
The crystal structure of Escherichia coli MoaB was determined by multiwavelength anomalous diffraction phasing and refined at 1.6-A resolution. The molecule displayed a modified Rossman fold. MoaB is assembled into a hexamer composed of two trimers. The monomers have high structural similarity with two proteins, MogA and MoeA, from the molybdenum cofactor synthesis pathway in E. coli, as well as with domains of mammalian gephyrin and plant Cnx1, which are also involved in molybdopterin synthesis. Structural comparison between these proteins and the amino acid conservation patterns revealed a putative active site in MoaB. The structural analysis of this site allowed to advance several hypothesis that can be tested in further studies.
