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Tomazetto, G.

Publications and source records attributed to Tomazetto, G..

2 recordsLinked to original sources

arfA antisense RNA regulates MscL excretory activity

Bacteria adapt to acute changes in their environment by processing multiple input stimuli through signal integration and crosstalk to allow fine tuning of gene expression in response to stress. The response to hypoosmotic shock and ribosome stalling occurs through the action of mechanosensitive channels and ribosome rescue mechanisms respectively. However, it is not known if a mechanistic link exists between these stress response pathways. Here we report that the corresponding Large-conductance mechanosensitive channel (mscL) and Alternative ribosome-rescue factor A (arfA) genes are commonly co-located on the genomes of Gammaproteobacteria and display overlap in their respective 3 UTR and 3 CDS. We show this unusual genomic arrangement permits an antisense RNA mediated regulatory control between mscL and arfA and this modulates MscL excretory activity in E. coli. These findings highlight a mechanistic link between osmotic and translational stress responses in E. coli, and further elucidates the previously unknown regulatory function of arfA sRNA.

molecular biology↗

An insight into cellulolytic capacity of the Trichoderma harzianum P49P11 revealed by omics approaches

Cellulases are a group of enzymes with several applications in biofuel production, and the paper, food, pharmaceutical, and chemical industries. Trichoderma harzianum P49P11 secrete all cellulases with high efficiency, representing an alternative to the current filamentous fungi in biotechnological industries. In this study, the cellulolytic mechanisms employed by the strain P49P11 to degrade crystalline cellulose in batch fermentation culture mode were elucidated by combining genome and secretome analysis. The strain P49P11 encodes nineteen cellulase genes from five different CAZyme families (GH5, GH6, GH7, GH12, and GH45), followed by several enzyme families for hemicellulose, pectin, and alpha-and beta-glucans degradation. The diverse CAZymes were also observed in the secretome, including cellulases, hemicellulases, and glucanases. In addition, {beta}-glucosidases and xylanase activities detected during the fermentation process validated our secretome analysis. Taken together, our results revealed all enzymatic machinery used by the T. harzianum P49P11 to degrade cellulose in batch fermentation mode. HighlightsO_LIWe described a high-quality genome assembly and annotation of the T. harzianum P49P11. C_LIO_LIThe T. harzianum P49P11 genome possesses a complete set of genes for lignocellulose degradation. C_LIO_LIThe first report on T. harzianum P49P11 secretome obtained from batch fermentation strategy. C_LIO_LIT. harzianum P49P11 produced cellulases, lignocellulases, and auxiliary enzymes produced in response to crystalline cellulose. C_LI

microbiology↗