<?xml version='1.0' encoding='utf-8'?>
<?xml-stylesheet type="text/xsl" href="/v2/static/oai2.xsl"?>
<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd">
  <responseDate>2026-10-14T11:09:03Z</responseDate>
  <request identifier="oai:figshare.com:article/33847450" metadataPrefix="oai_dc" verb="GetRecord">https://api.figshare.com/v2/oai</request>
  <GetRecord>
    <record>
      <header>
        <identifier>oai:figshare.com:article/33847450</identifier>
        <datestamp>2026-09-16T12:40:01Z</datestamp>
        <setSpec>category_8</setSpec>
        <setSpec>portal_316</setSpec>
        <setSpec>item_type_3</setSpec>
        <setSpec>month_year_09_2026</setSpec>
      </header>
      <metadata>
        <oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"  xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>Supplementary file 1_Utahmycin C, a new glycosylated derivative of a rare azaanthraquinone produced by Streptomyces sp. YD248.docx</dc:title>
          <dc:creator>Fatemeh M. Tajabadi (24981514)</dc:creator>
          <dc:creator>Andrew M. Piggott (1335855)</dc:creator>
          <dc:creator>Jeff Errington (366288)</dc:creator>
          <dc:creator>Yousef Dashti (3876511)</dc:creator>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>azaanthraquinone</dc:subject>
          <dc:subject>polyketide</dc:subject>
          <dc:subject>glycoside</dc:subject>
          <dc:subject>streptomyces</dc:subject>
          <dc:subject>type II PKS</dc:subject>
          <dc:description>&lt;p&gt;Chemical investigation of Streptomyces sp. YD248 led to the isolation of utahmycin C (1), a new glycosylated member of the rare bacterial 1,3-dimethyl-2-azaanthraquinone family. Its structure was established by NMR spectroscopy and high-resolution mass spectrometry, revealing a β-D-glucuronic acid substituent attached to the azaanthraquinone core. Unusual long-range &lt;sup&gt;5&lt;/sup&gt;J HMBC correlations prompted validation by density functional theory (DFT) through NMR chemical shift calculations, which showed excellent agreement with the experimental data. Bioinformatics analysis identified a biosynthetic gene cluster (BGC) homologous to the reported Erd gene cluster associated with utahmycin A biosynthesis. This study expands the structural diversity of bacterial azaanthraquinones.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-16T12:40:01Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fmicb.2026.1921234.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Supplementary_file_1_Utahmycin_C_a_new_glycosylated_derivative_of_a_rare_azaanthraquinone_produced_by_Streptomyces_sp_YD248_docx/33847450</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
        </oai_dc:dc>
      </metadata>
    </record>
  </GetRecord>
</OAI-PMH>
