Here, we report a systematic analysis of PAS proteins in Xcc using bioinformatics, molecular genetics and biochemical methods. All putative PAS proteins in Xcc 8004 were genetically inactivated, while a functional

clustering of PAS domains were deployed on the basis of SSTs. Characterization Fulvestrant of the mutants over a wide region of the visible spectrum (red, far-red, blue and white light) identified a number of previously putative PAS proteins that are involved in the regulation of bacterial metabolism and responses to light, including those involved in colony growth, motility and virulence. To our knowledge, this is the first large-scale study and systematic detection of PAS-domain-containing and light-signalling

components in a bacterial strain, and these results may have important and immediate implications for mapping the light-signalling networks in this important bacterial phytopathogen and other bacteria. All bacterial strains and plasmid constructs used in this study are listed in Supporting Information, Table S1. The growth conditions for each strain are described in the Supporting Information. Stem Cell Compound Library in vivo The primer sequences used in this study are given in Table S2. Insertion-deletion and in-frame deletion were used to construct Xcc mutants (11 insertion-deletion and 22 in-frame deletion), and the details of the procedure are described in the Supporting Information. Each insertional Xcc mutant was confirmed by Southern blotting, which is described in the Supporting Information. Xcc strains were carefully cultured to OD600 nm = 0.10 ±  0.01 in NYG media. In light-induced growth assays, 1 mL of culture was then added and growth was allowed in 150-mL MMXC media with 100 r.p.m. agitation at 28 °C under different conditions. The experiments were performed to test light-induced Carnitine palmitoyltransferase II growth under four different sets of light conditions, including blue (763 μW cm−2), red (4.30 mW cm−2), far-red (3.36 mW cm−2) and white light (12 000 lux), using dark as a control. Under each light and dark set of

conditions, the Xcc cell number and viability were estimated by plating on NYG agar at 28 °C, following culture at the 4th and 5th days of light-condition growth (T1) and dark-condition growth (T0). The light-induced growth rate (GR) was calculated as the ratio of the mean value of T1 to that of T0, and the light-induced relative growth rate (RGR) was the ratio of the mutated strain GR compared with that of wild-type Xcc 8004. The same bacterial culture preparation, with a similar performance, and statistical analysis were conducted in the light-induced motility and virulence assays, and the details are given in the Supporting Information. In virulence assays, plant inoculation with Xcc was exposed to two levels of light intensity, and the transmission into leaves was estimated.