These are due to large conformational rearrangements of certain r

These are due to large conformational rearrangements of certain residues away from the packing interactions. A disruption of this hydrophobic packing would result in serious structural

consequences and thus prevent the correct folding of the molecule, affecting the toxin-inclusion formation, the resistance to proteases and a loss in protein activity. The poor accumulation of the two mutants in B. thuringiensis cells as typical crystals could be the reason for their accessibility to the endogenous proteases and thus their rapid degradation, especially in the case of Cry1Ac′3, which is rapidly converted to a 90-kDa stable form. Bacillus thuringiensis proteases were identified belonging to enzymes of the cysteine, metallo- and serine families (Oppert, 1999). Some researchers have described this type of endogenous protease activity on their mutants or recombinant proteins (Coux et al., 2001; Roh et al., 2004). Together selleck chemical with the toxicity data, structural investigation of the residues Y229 and F603 and their positions indicates a structural

and functional role for the two conserved residues. This work was supported by grants from the Ministère Antidiabetic Compound Library chemical structure de l’Enseignement Supérieur, de la Recherche Scientifique et de la Technologie. “
“The diversity of the equine fecal bacterial community was evaluated using pyrosequencing of 16S rRNA gene amplicons. Fecal samples were obtained from horses fed cool-season grass hay. Fecal bacteria were characterized by amplifying the V4 region of bacterial 16S rRNA gene. Of 5898 mean unique sequences, a mean of 1510 operational taxonomic units were identified in the four fecal samples. Equine fecal bacterial

richness was higher than that reported in humans, but lower than that reported in either cattle feces or soil. Bacterial classified sequences were assigned to 16 phyla, of which 10 were present in all samples. The largest number of reads belonged to Firmicutes (43.7% of total bacterial sequences), Verrucomicrobia (4.1%), Proteobacteria (3.8%), and Bacteroidetes (3.7%). The less abundant Actinobacteria, Cyanobacteria, and TM7 phyla presented here have not been previously described in the gut contents or feces of horses. Unclassified Urease sequences represented 38.1% of total bacterial sequences; therefore, the equine fecal microbiome diversity is likely greater than that described. This is the first study to characterize the fecal bacterial community in horses by the use of 16S rRNA gene amplicon pyrosequencing, expanding our knowledge of the fecal microbiota of forage-fed horses. The horse is a nonruminant herbivore where the hindgut (cecum and colon) is a fermentative chamber for a complex and dynamic microbial population. Gut microorganisms serve the host through energy extraction, immune stimulation, pathogen exclusion, and detoxification of toxic compounds.

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