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        <gco:CharacterString>Ruergeria pomeroyi DSS-3 replete proteome Dataset Description:  Methods and Sampling: &amp;lt;p&amp;gt;Cultures (50 ml each) of &amp;lt;em&amp;gt;Ruergeria pomeroyi &amp;lt;/em&amp;gt;DSS-3 and &amp;lt;em&amp;gt;Alteromonas macleodii &amp;lt;/em&amp;gt;MIT1002 were harvested in triplicate, centrifuged at 8000 x g for 10 minutes, flash frozen, stored at -80 degrees C, and shipped to Woods Hole Oceanographic Institution for proteomics analysis. Cultures were filtered and filters were extracted using SDS detergent and a SP3 magnetic bead purification followed by trypsin digestion alkylation and reduction. The methods are described in Saito et al. 2020 and were modified from the methods originally published by Hughes et al. 2014. Analysis was conducted by 2D active modulation Orbitrap mass spectrometry as described in McIlvin and Saito 2021.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;This dataset reports results for the&amp;amp;nbsp;&amp;lt;em&amp;gt;Ruergeria pomeroyi&amp;amp;nbsp;&amp;lt;/em&amp;gt;DSS-3 samples. See related datasets for the&amp;amp;nbsp;&amp;lt;em&amp;gt;Alteromonas macleodii&amp;amp;nbsp;&amp;lt;/em&amp;gt;MIT1002 samples.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Note: the sample ids ending in a1, b1, and c1 differentiate biological triplicates from one another.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/871065.rdf" xlink:title="OCE-2019589" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-2019589 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=2019589</gmx:Anchor>
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                <gco:CharacterString>&amp;lt;p&amp;gt;Cultures (50 ml each) of &amp;lt;em&amp;gt;Ruergeria pomeroyi &amp;lt;/em&amp;gt;DSS-3 and &amp;lt;em&amp;gt;Alteromonas macleodii &amp;lt;/em&amp;gt;MIT1002 were harvested in triplicate, centrifuged at 8000 x g for 10 minutes, flash frozen, stored at -80 degrees C, and shipped to Woods Hole Oceanographic Institution for proteomics analysis. Cultures were filtered and filters were extracted using SDS detergent and a SP3 magnetic bead purification followed by trypsin digestion alkylation and reduction. The methods are described in Saito et al. 2020 and were modified from the methods originally published by Hughes et al. 2014. Analysis was conducted by 2D active modulation Orbitrap mass spectrometry as described in McIlvin and Saito 2021.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;This dataset reports results for the&amp;amp;nbsp;&amp;lt;em&amp;gt;Ruergeria pomeroyi&amp;amp;nbsp;&amp;lt;/em&amp;gt;DSS-3 samples. See related datasets for the&amp;amp;nbsp;&amp;lt;em&amp;gt;Alteromonas macleodii&amp;amp;nbsp;&amp;lt;/em&amp;gt;MIT1002 samples.&amp;lt;/p&amp;gt;

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The raw mass spectra files were searched against the SEQUEST high thread database within Proteome Discoverer software (v2.4). Processed files were then loaded into Proteome Software (Scaffold v5) and filtered to False Discovery Rates less than 1% using Percolator (0.7% peptide FDR and 0.03% Protein FDR using decoy database). Percolator was used for PSM validation based on PEP scoring. The output was reported as exclusive unique spectral counts. No normalization was applied to this dataset.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Raw data files are currently being submitted to the ProteomeXchange repository through PRIDE under accession number &amp;lt;a href=&amp;quot;https://www.ebi.ac.uk/pride/archive/projects/PXD034365&amp;quot; target=&amp;quot;_blank&amp;quot;&amp;gt;PXD034365&amp;lt;/a&amp;gt;. Raw file names are:&amp;lt;em&amp;gt; 220427_CCoMP_AHANA_DSS_3_a1, 220427_CCoMP_AHANA_DSS_3_b1, 220427_CCoMP_AHANA_DSS_3_c1&amp;lt;/em&amp;gt;.&amp;lt;/p&amp;gt;

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