<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Naka H</submitter><funding>FIC NIH HHS</funding><pubmed_abstract>&lt;i>Teredinibacter turnerae&lt;/i> is an intracellular bacterial symbiont that resides in the gills of shipworms, wood-eating bivalve mollusks. This bacterium produces a catechol siderophore, turnerbactin, required for the survival of this bacterium under iron limiting conditions. The turnerbactin biosynthetic genes are contained in one of the secondary metabolite clusters conserved among &lt;i>T. turnerae&lt;/i> strains. However, Fe(III)-turnerbactin uptake mechanisms are largely unknown. Here, we show that the first gene of the cluster, &lt;i>fttA&lt;/i> a homologue of Fe(III)-siderophore TonB-dependent outer membrane receptor (TBDR) genes is indispensable for iron uptake via the endogenous siderophore, turnerbactin, as well as by an exogenous siderophore, amphi-enterobactin, ubiquitously produced by ma</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2023.02.23.529781</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9980095</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The dual role of TonB genes in turnerbactin uptake and carbohydrate utilization in the shipworm symbiont &lt;i>Teredinibacter turnerae&lt;/i>.</pubmed_title><pmcid>PMC9980095</pmcid><funding_grant_id>U01 TW008163</funding_grant_id><pubmed_authors>Naka H</pubmed_authors><pubmed_authors>Haygood MG</pubmed_authors></additional><is_claimable>false</is_claimable><name>The dual role of TonB genes in turnerbactin uptake and carbohydrate utilization in the shipworm symbiont &lt;i>Teredinibacter turnerae&lt;/i>.</name><description>&lt;i>Teredinibacter turnerae&lt;/i> is an intracellular bacterial symbiont that resides in the gills of shipworms, wood-eating bivalve mollusks. This bacterium produces a catechol siderophore, turnerbactin, required for the survival of this bacterium under iron limiting conditions. The turnerbactin biosynthetic genes are contained in one of the secondary metabolite clusters conserved among &lt;i>T. turnerae&lt;/i> strains. However, Fe(III)-turnerbactin uptake mechanisms are largely unknown. Here, we show that the first gene of the cluster, &lt;i>fttA&lt;/i> a homologue of Fe(III)-siderophore TonB-dependent outer membrane receptor (TBDR) genes is indispensable for iron uptake via the endogenous siderophore, turnerbactin, as well as by an exogenous siderophore, amphi-enterobactin, ubiquitously produced by ma</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-05-09T03:15:32.235Z</modification><creation>2026-05-09T03:08:32.344Z</creation></dates><accession>S-EPMC9980095</accession><cross_references><pubmed>36865190</pubmed><doi>10.1101/2023.02.23.529781</doi></cross_references></HashMap>