Identification and Functional Characterization of Small Alarmone Synthetases in .

The hyperphosphorylated guanosine derivatives ppGpp and pppGpp represent global regulators of the bacterial stress response, as they act as central elements of the stringent response system. Although it was assumed that both, (p)ppGpp synthesis and hydrolysis, are catalyzed by one bifunctional RSH-protein in the actinobacterial model organism ATCC 13032, two putative short alarmone synthetases (SASs) were identified by bioinformatic analyses. The predicted sequences of both enzymes, designated as RelP and RelS, exhibit high similarities to the conserved (p)ppGpp synthetase catalytic domain. In the context of sequence analysis, significant differences were found between the RelP variants of different isolates. In contrast to the bifunctional RelA/SpoT homolog (RSH) protein Rel, whose gene deletion results in a reduced growth rate, no change in growth characteristics were observed for deletion mutants of the putative SAS proteins under standard growth conditions. The growth deficit of the Δ strain could be restored by the additional deletion of the gene encoding RelS, which clearly indicates a functional relationship between both enzymes. The predicted pyrophosphokinase activity of RelS was demonstrated by means of genetic complementation of an ΔΔ strain. For the expression of RelP , as well as the slightly differing variant RelP from AS1.542, no complementation was observed, concluding that both RelP versions possess no significant pyrophosphokinase activity . The results were confirmed by characterization of the corresponding proteins. In the course of this investigation, the additional conversion of GMP to pGpp was determined for the enzyme RelS. Since the SAS species analyzed extend both the network of stringent response related enzymes and the number of substances involved, the study of this class of enzymes is an important component in understanding the bacterial stress response. In addition to the comprehension of important biological processes, such as growth rate regulation and the survival of pathogenic species in the host organism, SAS enzymes can be used to produce novel hyperphosphorylated nucleotide species, such as pGpp.