<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Webb J</submitter><funding>RCUK | Biotechnology and Biological Sciences Research Council</funding><funding>Biotechnology and Biological Sciences Research Council</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>e00187-19</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6561320</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4(4)</volume><pubmed_abstract>Productivity of bacterial cell factories is frequently compromised by stresses imposed by recombinant protein synthesis and carbon-to-product conversion, but little is known about these bioprocesses at a systems level. Production of the unnatural metabolite citramalate in &lt;i>Escherichia coli&lt;/i> requires the expression of a single gene coding for citramalate synthase. Multiomic analyses of a fermentation producing 25  g liter&lt;sup>-1&lt;/sup> citramalate were undertaken to uncover the reasons for its productivity. Metabolite, transcript, protein, and lipid profiles of high-cell-density, fed-batch fermentations of &lt;i>E. coli&lt;/i> expressing either citramalate synthase or an inactivated enzyme were similar. Both fermentations showed downregulation of flagellar genes and upregulation of chaperones</pubmed_abstract><journal>mSystems</journal><pubmed_title>Systems Analyses Reveal the Resilience of Escherichia coli Physiology during Accumulation and Export of the Nonnative Organic Acid Citramalate.</pubmed_title><pmcid>PMC6561320</pmcid><funding_grant_id>BB/N01040X/1</funding_grant_id><funding_grant_id>BB/N010493/1</funding_grant_id><funding_grant_id>BB/N01037X/1</funding_grant_id><funding_grant_id>EP/K039660/1</funding_grant_id><funding_grant_id>EP/M028127/1</funding_grant_id><pubmed_authors>Kelly DJ</pubmed_authors><pubmed_authors>Lilley K</pubmed_authors><pubmed_authors>Stephens G</pubmed_authors><pubmed_authors>Webb J</pubmed_authors><pubmed_authors>Langer S</pubmed_authors><pubmed_authors>Green J</pubmed_authors><pubmed_authors>Larson T</pubmed_authors><pubmed_authors>Thomas GH</pubmed_authors><pubmed_authors>Minde DP</pubmed_authors><pubmed_authors>Eastham G</pubmed_authors><pubmed_authors>Alstrom-Moore A</pubmed_authors><pubmed_authors>Rossoni L</pubmed_authors><pubmed_authors>Springthorpe V</pubmed_authors><pubmed_authors>Walker H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Systems Analyses Reveal the Resilience of Escherichia coli Physiology during Accumulation and Export of the Nonnative Organic Acid Citramalate.</name><description>Productivity of bacterial cell factories is frequently compromised by stresses imposed by recombinant protein synthesis and carbon-to-product conversion, but little is known about these bioprocesses at a systems level. Production of the unnatural metabolite citramalate in &lt;i>Escherichia coli&lt;/i> requires the expression of a single gene coding for citramalate synthase. Multiomic analyses of a fermentation producing 25  g liter&lt;sup>-1&lt;/sup> citramalate were undertaken to uncover the reasons for its productivity. Metabolite, transcript, protein, and lipid profiles of high-cell-density, fed-batch fermentations of &lt;i>E. coli&lt;/i> expressing either citramalate synthase or an inactivated enzyme were similar. Both fermentations showed downregulation of flagellar genes and upregulation of chaperones</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2026-06-14T05:32:49.642Z</modification><creation>2020-05-22T11:07:06Z</creation></dates><accession>S-EPMC6561320</accession><cross_references><pubmed>31186337</pubmed><doi>10.1128/mSystems.00187-19</doi></cross_references></HashMap>