Bacillus subtilis produces multiple cell-cell signaling molecules to control the sophisticated sporulation [30] that is often a temporal, spatial, and dynamic

decision-making process [28]. The outermost protective layers of B. subtilis endospores are the coat and the cortex [31]. The spore coat is a barrier against bactericidal enzymes and destructive chemicals. Therefore, heat resistant spores are also resistant to treatment Geneticin ic50 by various chemicals, such as acids, bases, oxidizing agents, alkylating agents, aldehydes and organic solvents [32]. Thus, we investigated the role of VE-822 clinical trial indole on heat resistance as well as other environmental stresses. In this study, we identified that indole was a stationary phase extracellular molecule in P. alvei and functioned to inhibit spore maturation and to decrease survival rates under several environmental stresses. Additionally, we studied the effect of indole derivatives originated from plants on spore formation in P. alvei. This study provides another important role of indole and indole derivatives. Results Extracellular indole accumulation in P. alvei To be an environmental signal molecule, indole has to be excreted out of cells. Thus, the cell growth of P. alvei and the extracellular indole concentration were measured in Luria-Bertani (LB) medium. Clearly, the level of extracellular indole from P. alvei Tideglusib was growth-dependent (Figure 1A). Indole production

was begun in the middle of exponential growth phase and reached

the maximum amount (300 μM) in the stationary phase. Notably, the level of extracellular indole present was stable over time at 37°C (Figure 1A), which was one of characteristics of the indole molecule [2] while other signaling molecules, such as AHLs, AI-2, and signal peptides, are only temporally present and heat-unstable [2]. The accumulation pattern of extracellular indole was similar to that of other bacteria, such as E. coli [33] and Vibrio cholera [10], while these two bacteria accumulated up to 500-600 μM of extracellular indole within 24 h in LB [10, 33]. The slower accumulation of indole in P. alvei was probably due to the 200-fold lower activity of P. alvei tryptophanase than that of E. coli tryptophanase [22]. Figure 1 Production of extracellular indole in P. Erastin alvei. Cell growth and extracellular indole accumulation in LB (A) and extracellular indole accumulation in LB supplemented with different carbon sources (B) at 37°C at 250 rpm. Cell growth (closed circle) was determined via the optical density at 600 nm (OD600). Glucose (Glu), glycerol (Gly), and lactose (Lac) in 0.5% (w/v) were added at the beginning of the culture and cells were cultured for 36 h and indole production was measured. Experiments were performed in triplicate and one standard deviation is shown. Catabolite repression of P. alvei tryptophanase Since indole production was suppressed by the presence of glucose in E.