It has been assumed www.selleckchem.com/products/PLX-4032.html that the LuxS protein localizes in the cytosol. A chromosomal translational fusion was made between LuxS and the periplasmic reporter protein β-lactamase. Expression of a β-lactamase results in resistance against β-lactam antibiotics such as ampicillin. However, to confer this resistance in Gram-negative bacteria, β-lactamase has to be exported outside the cytoplasm since formation of disulfide bridges is a prerequisite for enzyme activity [28, 29]. An in frame gene construct encoding LuxS followed by a truncated

β-lactamase lacking its native signal peptide was inserted into the chromosome of S. Typhimurium. The strain with the fusion construct was subsequently analyzed for growth at 37°C in liquid LB medium containing variable concentrations of ampicillin. As expected, a wildtype strain is highly sensitive to ampicillin. The luxSβla

fusion strain, however, showed a clear increase in ampicillin resistance (Figure 3A). As the two strains differ also in synthesis of AI-2 because Fulvestrant molecular weight the LuxS-βla fusion protein is not expected to have AI-2 synthase activity, synthetic DPD was also added to the growth medium. However, this did not alter the observed difference in ampicillin resistance (data not shown). Increased ampicillin resistance and thus an active β-lactamase implies that the LuxS-βla fusion protein is translocated across the cytoplasmic membrane. Figure 3 Analysis of LuxS localization. (A) Growth of S. Typhimurium wildtype and luxSβla with ampicillin. The minimal inhibitory concentration (MIC) for sensitivity to ampicillin (μg ml-1) in liquid culture was determined for each strain as described in the Methods section. These data are representative for three

biological repeats. (B) Strains were grown on LB plates containing the chromogenic alkaline phosphatase substrate BCIP. Active alkaline phosphatase converts this substrate into a blue product. Negative and positive Thymidylate synthase control strains express PhoA either without or with signal peptide (SP) from a constitutive promoter (pCMPG5748 and pCMPG5734); pCMPG5730 expresses a LuxS-PhoA fusion protein. All strains carry a ΔphoN mutation (CMPG5726). (C) Strains were grown to mid-exponential phase (OD595 1) and a PhoA activity test was performed. Average results of at least 3 biological replicates are shown with standard deviations. (D) Cellular fractionation of LuxS-PhoA fusion and control strains. (E) Cellular fractionation of S. Typhimurium expressing chromosomally FLAG-tagged LuxS. Total cells (T), grown to OD595 1, were separated into periplasmic (P), cytoplasmic (C) and membrane (M) fractions as described in the Methods section. The proteins maltose binding protein (MBP), alkaline phosphatase without signal peptide (PhoA-SP) and outer membrane protein A (OmpA) were used as periplasmic, cytoplasmic and membrane associated control proteins, respectively. All antibodies used are listed in the Methods section.