2 ± 8.3%, 91.5 ± 16.2%, and 87.8 ± 5.8%, respectively. When other competing substrates indicated in Fig. 3 were tested in the mutant, l-cystine was still transported into the cells despite the absence of the TcyABC system (data not shown), confirming the presence of other cystine transporters in S. mutans. Our results show that in addition to l-cystine transport, the TcyABC transporter participates in the uptake of l-cysteine, dl-cystathionine, l-djenkolic acid, and S-methyl-l-cysteine in S. mutans. The two transcriptional activators CysR and HomR are positive regulators

of the TcyABC and TcyDEFGH l-cystine transport systems, respectively (Sperandio et al., 2010). Our search of the selleck chemicals S. mutans UA159 genome revealed another putative LysR-type transcriptional regulator (LTTR) locus (SMU.2060) designated TcyR with homology (24%, 65/263) to the B. subtilis YtlI regulator. To determine the role of TcyR on the expression of the tcyABC operon, we constructed a TcyR insertion mutant (SmTcyR) and tested it under cystine starvation conditions. Gene expression was analyzed by quantitative real-time RT-PCR using cDNAs derived from S. mutans UA159 and mutant strains grown in modified MM with or without cystine. Relative to their expression in UA159,

the absence of TcyR resulted in an approximate 10.8-, 13.1-, and 5.2-fold induction of tcyA, BYL719 datasheet tcyB, and tcyC respectively, under cystine starvation relative to the cystine-fed state (Fig. 4). These results indicate that TcyR has a negative transcriptional role on the expression of tcyABC during cystine limited conditions. these LTTRs are generally positive regulators in prokaryotes (Leichert et al., 2003). Interestingly, the B. subtilis YtlI regulator with which the TcyR regulator shares homology is also a positive regulator. The negative regulator CymRSA in S. aureus (Coppee et al., 2001) showed no homology to our negative regulator TcyR. We also found that under cystine starvation, UA159 cells showed upregulation of the tcyABC and tcyR genes (Fig. 4). More specifically, the

tcysA, tcyB, and tcyC genes were upregulated by 3.3-, 2.4-, and 2.8-fold, whereas expression of tcyR was increased by c. 2.6-fold, thus suggesting induction of the transporter genes and its regulator under cystine-deprived nutritional conditions. This capability is likely advantageous under dense biofilm growth where conditions can become anaerobic and access to nutrients and free amino acids may be limited. In this environment, where cells are likely trying to scavenge cystine or cystine amino acid analogues, upregulation would be an advantage. To determine the effect of cystine starvation on S. mutans UA159 growth, wild-type and mutant strains were grown in MM medium devoid of cysteine–HCl, and growth was monitored using an automated optical density reader.