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Garron, M.-L.

Publications and source records attributed to Garron, M.-L..

2 recordsLinked to original sources

Genomic-Based Prediction of Exopolysaccharide Composition and Structure: Insights from Rhizobium and Sinorhizobium Species

Bacterial exopolysaccharides (EPS) are key components in biofilm formation, stress protection, and symbiosis in Rhizobiaceae. While EPS structural diversity is extensive, experimental characterization remains limited. In this study, we experimentally determined and compared four distinct EPS structures produced by ten Rhizobium alamii strains. Using genomic data, we bioinformatically identified supra-operonic clusters (SOCs) responsible for these EPS biosynthesis. We introduced a computational framework to predict, score, and compare EPS SOCs across 84 Rhizobium and Sinorhizobium species, linking gene content to structural and functional EPS diversity. A total of 743 EPS SOCs was selected for network analyses, allowing the identification of 36 major groups of orthologous EPS SOCs, successfully recovering all known EPS biosynthetic loci and two novels SOCs potentially encoding uncharacterized EPS (xEPS-I, xEPS-II). Profiles of EPS SOCs correlated with taxonomical groups, with a single EPS SOC conserved through all 84 genomes and distinct additional EPS SOCs depending on the group, but do not strictly explain symbiotic capacity. Genetic comparisons of transporters (Wzx, Wzy) and glycosyltransferase sequences indicated these proteins as key markers of EPS structure. Overall, this computational framework accurately identified and classified EPS SOCs, providing a scalable, genome-based method for predicting EPS biosynthetic potential in Rhizobiaceae and usable in other microbial genera.

bioinformatics↗

Screening for Polysaccharide Utilization Loci Targeting Marine Polysaccharides

Polysaccharide utilization loci (PULs) have been a goldmine for the characterization of novel carbohydrate active enzymes (CAZymes) and the understanding of their synergistic degradation of complex polysaccharides. We collected PUL predictions containing CAZymes from glycoside hydrolase families GH29, GH50 and GH117, expected to participate in marine polysaccharide breakdown. We explored the evolutionary diversity in these families in terms of sequences and PUL composition, based on sulfatases and CAZymes. From 41 selected PULs, more than 400 putative enzymes were produced, purified and screened on a large collection of carbohydrates. We attributed a function to more than 130 enzymes from five sulfatase subfamilies, 29 known CAZymes families and discovered an activity for 4 families previously of unknown function, including an -L-galactosidase structurally and functionally characterized with mutants. Finally, our detailed analysis of the enzymatic synergies in five PULs, two targeting marine polysaccharides and three targeting eukaryotic polysaccharides, by marine and human gut organisms, highlight the efficiency of our exploratory strategy.

biochemistry↗