More recently, its spore has been proposed as a platform to display heterologous proteins and as a vehicle for mucosal vaccination. We characterize here the spore surface of four human intestinal strains of B. subtilis, previously identified as able to grow anaerobically and form biofilm. These properties, lost in laboratory strains, are relevant for the colonization of human mucosal sites and likely to improve the efficiency of strains to be used for mucosal delivery. Our characterization is an essential preliminary step for the development of these intestinal strains as display systems and

has indicated that spores of at least one of them are SB203580 more efficient than the laboratory strain for the non-recombinant display of two model heterologous proteins. “
“The enterobacterium Photorhabdus luminescens produces a number of toxins to kill its insect host. By analyzing the genomic sequence of P. luminescens TT01, we found that amino acid sequences encoded by plu1961 and plu1962 showed high similarity to XaxAB binary toxin of Xenorhabuds nematophila, which has both necrotic and apoptotic activities in both insect and mammalian cells in vitro. To evaluate the biological activity of Plu1961/Plu1962, their coding genes were cloned and expressed in Escherichia coli. Both Plu1961 Decitabine and Plu1962 were expressed as

soluble protein in BL21 (DE3) and their mixture caused insect midgut CF-203 cells death via necrosis. Confocal fluorescence microscopy showed that Plu1961/Plu1962 mixture was able to depolymerize microtubule and induce the

increase in plasma membrane permeabilization in CF-203 cells. Moreover, co-expression of Plu1961/Plu1962 in the same cytoplasm exhibited cytotoxic effect against mammalian cells (B16, 4T1, and HeLa cells) and injectable activity against Spodoptera exigua larvae. Until now, two types of binary toxins have been identified in P. luminescens, the first type is PirAB and Plu1961/Plu1962 is the second one. The biological role Methane monooxygenase of Plu1961/Plu1962 binary toxin played in the infection process should attract more attention in future. Photorhabdus luminescens is an entomopathogenic, Gram-negative, bioluminescent bacterium that exists in a state of mutualistic symbiosis with entomopathogenic nematodes of the family Heterorhabditidiae (Ffrench-Constant et al., 2007). Upon entering an insect host, the nematodes release the bacteria directly into the insect hemocoel. Once released into the insect blood system, the bacteria kill their insect host by producing a large number of toxins. Various toxins have been characterized in P. luminescens (Rodou et al., 2010), which can be classified into four major groups: the toxin complexes (Tcs), the ‘makes caterpillars floppy’ (Mcf) toxins, the Photorhabdus insect-related (Pir) proteins, and the Photorhabdus virulence cassettes (PVC).