<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2025</volume><submitter>Khwathisi A</submitter><pubmed_abstract>Prokaryotic organisms rely on a limited array of metabolites for survival, which varies according to their natural environment. For example, soil-borne bacteria produce diverse metabolites, such as antibiotics, to thrive in their competitive surroundings, inhibiting the growth of nearby competing bacteria. The structural diversity of these compounds offers great analytical challenges, since there is no universal acquisition setting that can be applied to achieve their comprehensive coverage. Therefore, the use of a single experimental setup inevitably hinders the comprehensive metabolite coverage, which would affect the outputs. To address this, we propose employing a design of experiment (DoE) approach through the central composite design (CCD) to enhance the metabolite detection and broa</pubmed_abstract><journal>International journal of microbiology</journal><pagination>4388417</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12303636</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Multiparametric Optimization of Data-Dependent Acquisition Towards More Holistic Bacterial Metabolite Coverage Through Molecular Networking.</pubmed_title><pmcid>PMC12303636</pmcid><pubmed_authors>Samie A</pubmed_authors><pubmed_authors>Khwathisi A</pubmed_authors><pubmed_authors>Madala NE</pubmed_authors><pubmed_authors>Traore AN</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multiparametric Optimization of Data-Dependent Acquisition Towards More Holistic Bacterial Metabolite Coverage Through Molecular Networking.</name><description>Prokaryotic organisms rely on a limited array of metabolites for survival, which varies according to their natural environment. For example, soil-borne bacteria produce diverse metabolites, such as antibiotics, to thrive in their competitive surroundings, inhibiting the growth of nearby competing bacteria. The structural diversity of these compounds offers great analytical challenges, since there is no universal acquisition setting that can be applied to achieve their comprehensive coverage. Therefore, the use of a single experimental setup inevitably hinders the comprehensive metabolite coverage, which would affect the outputs. To address this, we propose employing a design of experiment (DoE) approach through the central composite design (CCD) to enhance the metabolite detection and broa</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-03-27T16:08:06.633Z</modification><creation>2025-08-30T03:05:19.148Z</creation></dates><accession>S-EPMC12303636</accession><cross_references><pubmed>40727305</pubmed><doi>10.1155/ijm/4388417</doi></cross_references></HashMap>