<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Goodall ECA</submitter><funding>The University of Queensland</funding><funding>China Sponsorship Council</funding><funding>National Health and Medical Research Council</funding><funding>Australian research council</funding><funding>Biotechnology and Biological Sciences Research Council</funding><funding>H2020 Marie Skłodowska-Curie Actions</funding><pagination>e1009586</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8741058</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(12)</volume><pubmed_abstract>The cell envelope is essential for viability in all domains of life. It retains enzymes and substrates within a confined space while providing a protective barrier to the external environment. Destabilising the envelope of bacterial pathogens is a common strategy employed by antimicrobial treatment. However, even in one of the best studied organisms, Escherichia coli, there remain gaps in our understanding of how the synthesis of the successive layers of the cell envelope are coordinated during growth and cell division. Here, we used a whole-genome phenotypic screen to identify mutants with a defective cell envelope. We report that loss of yhcB, a conserved gene of unknown function, results in loss of envelope stability, increased cell permeability and dysregulated control of cell size. Us</pubmed_abstract><journal>PLoS genetics</journal><pubmed_title>Loss of YhcB results in dysregulation of coordinated peptidoglycan, LPS and phospholipid synthesis during Escherichia coli cell growth.</pubmed_title><pmcid>PMC8741058</pmcid><funding_grant_id>Strategic Funds</funding_grant_id><funding_grant_id>721484</funding_grant_id><funding_grant_id>APP1140064</funding_grant_id><funding_grant_id>APP1150083</funding_grant_id><funding_grant_id>APP1156489</funding_grant_id><funding_grant_id>MIBTP</funding_grant_id><funding_grant_id>CE140100036</funding_grant_id><pubmed_authors>Icke C</pubmed_authors><pubmed_authors>Cunningham AF</pubmed_authors><pubmed_authors>Da Costa R</pubmed_authors><pubmed_authors>Heinz E</pubmed_authors><pubmed_authors>Jones A</pubmed_authors><pubmed_authors>Boelter G</pubmed_authors><pubmed_authors>Rae J</pubmed_authors><pubmed_authors>Henderson IR</pubmed_authors><pubmed_authors>Winkle M</pubmed_authors><pubmed_authors>Banzhaf M</pubmed_authors><pubmed_authors>Blaskovich MA</pubmed_authors><pubmed_authors>Goodall ECA</pubmed_authors><pubmed_authors>Parton RG</pubmed_authors><pubmed_authors>Zhang B</pubmed_authors><pubmed_authors>Bryant JA</pubmed_authors><pubmed_authors>Vollmer W</pubmed_authors><pubmed_authors>Rooke JL</pubmed_authors><pubmed_authors>Tan WB</pubmed_authors><pubmed_authors>Isom GL</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Warner I</pubmed_authors><pubmed_authors>Chng SS</pubmed_authors><pubmed_authors>Cole JA</pubmed_authors><pubmed_authors>Pullela K</pubmed_authors><pubmed_authors>Delhaye A</pubmed_authors><pubmed_authors>Collet JF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Loss of YhcB results in dysregulation of coordinated peptidoglycan, LPS and phospholipid synthesis during Escherichia coli cell growth.</name><description>The cell envelope is essential for viability in all domains of life. It retains enzymes and substrates within a confined space while providing a protective barrier to the external environment. Destabilising the envelope of bacterial pathogens is a common strategy employed by antimicrobial treatment. However, even in one of the best studied organisms, Escherichia coli, there remain gaps in our understanding of how the synthesis of the successive layers of the cell envelope are coordinated during growth and cell division. Here, we used a whole-genome phenotypic screen to identify mutants with a defective cell envelope. We report that loss of yhcB, a conserved gene of unknown function, results in loss of envelope stability, increased cell permeability and dysregulated control of cell size. Us</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2026-05-08T17:24:42.961Z</modification><creation>2022-02-11T15:10:14.821Z</creation></dates><accession>S-EPMC8741058</accession><cross_references><pubmed>34941903</pubmed><doi>10.1371/journal.pgen.1009586</doi></cross_references></HashMap>