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Tchelet, D.

Publications and source records attributed to Tchelet, D..

2 recordsLinked to original sources

Assessing soluble and insoluble calcium sources for growth, biofilm formation, and biomineralization in Bacillus subtilis.

Biofilms formed by soil microbes hold immense potential for bioremediation, carbon dioxide sequestration, and the development of sustainable cementitious materials. However, quantifying the complex temporal coupling among bacterial growth, extracellular matrix (ECM) production, and mineralization dynamics remains a significant challenge due to the inherent nonlinearity of these processes and signal noise in high-throughput assays. To address this, we utilized an automated kinetic framework to evaluate the biomineralization competence of Bacillus subtilis under varying calcium regimes. Our results demonstrate that calcium carbonate promotes microbial growth as effectively as soluble calcium acetate, indicating that B. subtilis actively solubilizes the crystalline powder. Despite this growth efficacy, calcium carbonate was an inadequate source for macro-calcite production compared to organic salts. By quantifying expression from the sinI promoter, which initiates SinI production to activate matrix synthesis, we suggested that calcium-acetate-driven extracellular matrix (ECM) expression significantly enhances the structural template required for robust biomineralization. Kinetic expression analysis and consolidation assays indicate that overproduced ECM partially mitigates crystalline calcite growth defects, offering a baseline for utilizing mineral-rich construction waste ImportanceBiomineralization in B. subtilis has been studied as a potential avenue for developing engineered living materials. However, organic calcium salts, such as calcium acetate and calcium lactate, typically yield higher bioconversion efficiencies than certain inorganic sources often used in construction. This advantage has been largely attributed to the metabolic utilization of the organic anion as a carbon source, thereby promoting local alkalinity. Here, our experiments indicate that this limitation is influenced by structural and regulatory constraints rather than purely chemical barriers. Moreover, we explored a targeted synthetic biology approach to address this by genetically decoupling matrix production from native environmental sensing, thereby engineering strains with increased matrix production that can partially overcome the limitations of non-inductive substrates. This approach can contribute to the development of sustainable construction technologies, moving toward actively programmed Engineered Living Materials (ELMs).

microbiology↗

Vibrio parahaemolyticus T6SS2 effector repertoires

All strains of the marine bacterium Vibrio parahaemolyticus harbor a type VI secretion system (T6SS) named T6SS2, suggesting that this system plays an important role in the life cycle of this emerging pathogen. Although T6SS2 was recently shown to play a role in interbacterial competition, its effector repertoire remains unknown. Here, we employed proteomics to investigate the T6SS2 secretome of two V. parahaemolyticus strains, and we identified several antibacterial effectors encoded outside of the main T6SS2 gene cluster. We revealed two T6SS2-secreted proteins that are conserved in this species, indicating that they constitute the core secretome of T6SS2; other identified effectors are found only in subsets of strains, suggesting that they comprise an accessory effector arsenal of T6SS2. Remarkably, a conserved Rhs repeat-containing effector serves as a quality control checkpoint and is required for T6SS2 activity. Our results reveal the effector repertoire of a conserved T6SS, some of which have no known activity and have not been previously associated with T6SSs.

microbiology↗