The RpiR-Like Repressor IolR Regulates Inositol Catabolism in Sinorhizobium meliloti

Sinorhizobium meliloti , the nitrogen-fixing symbiont of alfalfa, has the ability to catabolizemyo -,scyllo -, andd -chiro -inositol. Functional inositol catabolism (iol ) genes are required for growth on these inositol isomers, and they play a role during plant-bacterium interactions. The inositol catabolism genes comprise the chromosomally encodediolA (mmsA ) and theiolY (smc01163 )RCDEB genes, as well as theidhA gene located on the pSymB plasmid. Reverse transcriptase assays showed that theiolYRCDEB genes are transcribed as one operon. Theiol genes were weakly expressed without induction, but their expression was strongly induced bymyo -inositol. The putative transcriptional regulator of theiol genes, IolR, belongs to the RpiR-like repressor family. Electrophoretic mobility shift assays demonstrated that IolR recognized a conserved palindromic sequence (5′-GGAA-N6 -TTCC-3′) in the upstream regions of theidhA ,iolY ,iolR , andiolC genes. Complementation assays found IolR to be required for the repression of its own gene and for the downregulation of theidhA -encodedmyo -inositol dehydrogenase activity in the presence and absence of inositol. Further expression studies indicated that the late pathway intermediate 2-keto-5-deoxy-d -gluconic acid 6-phosphate (KDGP) functions as the true inducer of theiol genes. TheiolA (mmsA ) gene encoding methylmalonate semialdehyde dehydrogenase was not regulated by IolR. TheS. meliloti iolA (mmsA ) gene product seems to be involved in more than only the inositol catabolic pathway, since it was also found to be essential for valine catabolism, supporting its more recent annotation asmmsA .