<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>61(51)</volume><submitter>Couturier C</submitter><pubmed_abstract>Herein, we describe the myxobacterial natural product Corramycin isolated from Corallococcus coralloides. The linear peptide structure contains an unprecedented (2R,3S)-γ-N-methyl-β-hydroxy-histidine moiety. Corramycin exhibits anti-Gram-negative activity against Escherichia coli (E. coli) and is taken up via two transporter systems, SbmA and YejABEF. Furthermore, the Corramycin biosynthetic gene cluster (BGC) was identified and a biosynthesis model was proposed involving a 12-modular non-ribosomal peptide synthetase/polyketide synthase. Bioinformatic analysis of the BGC combined with the development of a total synthesis route allowed for the elucidation of the molecule's absolute configuration. Importantly, intravenous administration of 20 mg kg&lt;sup>-1&lt;/sup> of Corramycin in an E. coli mo</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pagination>e202210747</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10099666</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Structure Elucidation, Total Synthesis, Antibacterial In Vivo Efficacy and Biosynthesis Proposal of Myxobacterial Corramycin.</pubmed_title><pmcid>PMC10099666</pmcid><pubmed_authors>Vermat T</pubmed_authors><pubmed_authors>Bauer A</pubmed_authors><pubmed_authors>Cazals V</pubmed_authors><pubmed_authors>Schummer D</pubmed_authors><pubmed_authors>Muller R</pubmed_authors><pubmed_authors>Taillier T</pubmed_authors><pubmed_authors>Deckarm S</pubmed_authors><pubmed_authors>Couturier C</pubmed_authors><pubmed_authors>Dubarry N</pubmed_authors><pubmed_authors>Leroi-Geissler C</pubmed_authors><pubmed_authors>Sizun P</pubmed_authors><pubmed_authors>Rey A</pubmed_authors><pubmed_authors>Toti L</pubmed_authors><pubmed_authors>Haag Richter S</pubmed_authors><pubmed_authors>Renard S</pubmed_authors><pubmed_authors>Kurz M</pubmed_authors><pubmed_authors>Poverlein C</pubmed_authors><pubmed_authors>Harmrolfs K</pubmed_authors><pubmed_authors>von Tesmar A</pubmed_authors><pubmed_authors>Silve S</pubmed_authors><pubmed_authors>Stump H</pubmed_authors><pubmed_authors>Wink J</pubmed_authors><pubmed_authors>Groß S</pubmed_authors><pubmed_authors>Mourez M</pubmed_authors><pubmed_authors>Bacque E</pubmed_authors><pubmed_authors>Fievet A</pubmed_authors><pubmed_authors>Lessoud E</pubmed_authors><pubmed_authors>Fraisse L</pubmed_authors><pubmed_authors>Versluys S</pubmed_authors><pubmed_authors>Hoffmann J</pubmed_authors><pubmed_authors>Zaburannyi N</pubmed_authors><pubmed_authors>Hoffmann M</pubmed_authors><pubmed_authors>Prasad Awal R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Structure Elucidation, Total Synthesis, Antibacterial In Vivo Efficacy and Biosynthesis Proposal of Myxobacterial Corramycin.</name><description>Herein, we describe the myxobacterial natural product Corramycin isolated from Corallococcus coralloides. The linear peptide structure contains an unprecedented (2R,3S)-γ-N-methyl-β-hydroxy-histidine moiety. Corramycin exhibits anti-Gram-negative activity against Escherichia coli (E. coli) and is taken up via two transporter systems, SbmA and YejABEF. Furthermore, the Corramycin biosynthetic gene cluster (BGC) was identified and a biosynthesis model was proposed involving a 12-modular non-ribosomal peptide synthetase/polyketide synthase. Bioinformatic analysis of the BGC combined with the development of a total synthesis route allowed for the elucidation of the molecule's absolute configuration. Importantly, intravenous administration of 20 mg kg&lt;sup>-1&lt;/sup> of Corramycin in an E. coli mo</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-05T12:13:16.062Z</modification><creation>2025-04-05T12:13:16.062Z</creation></dates><accession>S-EPMC10099666</accession><cross_references><pubmed>36197755</pubmed><doi>10.1002/anie.202210747</doi></cross_references></HashMap>