{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Sobrinos-Sanguino M"],"funding":["European Social Fund","Spain Ministry of Science and Innovation","Spanish National Research Council","Comisión Sectorial de Investigación Científica","National Institutes of Health","State Agency of Research","European Commission","NIGMS NIH HHS","National Institutes of Health Office of Extramural Research","European Regional Development Fund"],"pagination":["148516"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12693692"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["332(Pt 2)"],"pubmed_abstract":["New strategies are urgently needed against antimicrobial resistance, a major health threat, and the different mechanisms regulating the bacterial cell division machinery offer multiple opportunities for developing novel therapeutics. FtsZ, an essential protein of this process, is targeted by multiple small molecules, and benzodioxane-benzamides (BDOBs) are among the most potent inhibitors in several bacterial species. BDOBs mechanisms are however poorly understood, particularly their impact on FtsZ's interplay with partners and ability to assemble phase-separated biomolecular condensates potentially involved in stress sensing. We show that certain BDOBs shielded FtsZ against depolymerization induced by the nucleoprotein complexes of SlmA, which inhibit Z-ring formation near the nucleoid. I"],"journal":["International journal of biological macromolecules"],"pubmed_title":["Benzodioxane-benzamides targeting bacterial cell division protein FtsZ potentially disrupt SlmA-mediated nucleoid occlusion and reversible biomolecular condensation."],"pmcid":["PMC12693692"],"funding_grant_id":["R35 GM131705","PID2019-104544GB-I00","FPU2020\\u201305620","PID2022-136951NB-I00","GM131705"],"pubmed_authors":["Monterroso B","Valoti E","Sobrinos-Sanguino M","Margolin W","Straniero V","Zorrilla S","Barros-Medina I","Lanzini A","Suigo L"],"additional_accession":[]},"is_claimable":false,"name":"Benzodioxane-benzamides targeting bacterial cell division protein FtsZ potentially disrupt SlmA-mediated nucleoid occlusion and reversible biomolecular condensation.","description":"New strategies are urgently needed against antimicrobial resistance, a major health threat, and the different mechanisms regulating the bacterial cell division machinery offer multiple opportunities for developing novel therapeutics. FtsZ, an essential protein of this process, is targeted by multiple small molecules, and benzodioxane-benzamides (BDOBs) are among the most potent inhibitors in several bacterial species. BDOBs mechanisms are however poorly understood, particularly their impact on FtsZ's interplay with partners and ability to assemble phase-separated biomolecular condensates potentially involved in stress sensing. We show that certain BDOBs shielded FtsZ against depolymerization induced by the nucleoprotein complexes of SlmA, which inhibit Z-ring formation near the nucleoid. I","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Dec","modification":"2026-06-06T00:33:10.309Z","creation":"2026-05-24T03:11:50.006Z"},"accession":"S-EPMC12693692","cross_references":{"pubmed":["41138864"],"doi":["10.1016/j.ijbiomac.2025.148516"]}}