<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Peng F</submitter><funding>Deutsche Forschungsgemeinschaft (DFG)</funding><funding>Deutsche Forschungsgemeinschaft</funding><pagination>e0285924</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11898615</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(3)</volume><pubmed_abstract>Structural maintenance of chromosomes (SMC) are ubiquitously distributed proteins involved in chromosome organization. Deletion of &lt;i>smc&lt;/i> causes severe growth phenotypes in many organisms. Surprisingly, &lt;i>smc&lt;/i> can be deleted in &lt;i>Corynebacterium glutamicum&lt;/i>, a member of the &lt;i>Actinomycetota&lt;/i> phylum, without any apparent growth phenotype. SMC in &lt;i>C. glutamicum&lt;/i> is loaded in a ParB-dependent fashion to the chromosome and functions in replichore cohesion. The unexpected absence of a growth phenotype in the &lt;i>smc&lt;/i> mutant prompted us to screen for synthetic interactions within &lt;i>C. glutamicum&lt;/i>. We generated a high-density Tn5 library from wild-type and &lt;i>smc&lt;/i>-deleted &lt;i>C. glutamicum&lt;/i> strains. Transposon sequencing data revealed that the DNA translocase FtsK </pubmed_abstract><journal>mBio</journal><pubmed_title>Early onset of septal FtsK localization allows for efficient DNA segregation in SMC-deleted &amp;lt;i&amp;gt;Corynebacterium glutamicum&amp;lt;/i&amp;gt; strains.</pubmed_title><pmcid>PMC11898615</pmcid><funding_grant_id>INST 257/645-1</funding_grant_id><funding_grant_id>BR2815/6-2</funding_grant_id><pubmed_authors>Linder M</pubmed_authors><pubmed_authors>Ruckert-Reed C</pubmed_authors><pubmed_authors>Bramkamp M</pubmed_authors><pubmed_authors>Haak M</pubmed_authors><pubmed_authors>Peng F</pubmed_authors><pubmed_authors>Kalinowski J</pubmed_authors><pubmed_authors>Meyer F</pubmed_authors><pubmed_authors>Weiß M</pubmed_authors><pubmed_authors>Giacomelli G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Early onset of septal FtsK localization allows for efficient DNA segregation in SMC-deleted &amp;lt;i&amp;gt;Corynebacterium glutamicum&amp;lt;/i&amp;gt; strains.</name><description>Structural maintenance of chromosomes (SMC) are ubiquitously distributed proteins involved in chromosome organization. Deletion of &lt;i>smc&lt;/i> causes severe growth phenotypes in many organisms. Surprisingly, &lt;i>smc&lt;/i> can be deleted in &lt;i>Corynebacterium glutamicum&lt;/i>, a member of the &lt;i>Actinomycetota&lt;/i> phylum, without any apparent growth phenotype. SMC in &lt;i>C. glutamicum&lt;/i> is loaded in a ParB-dependent fashion to the chromosome and functions in replichore cohesion. The unexpected absence of a growth phenotype in the &lt;i>smc&lt;/i> mutant prompted us to screen for synthetic interactions within &lt;i>C. glutamicum&lt;/i>. We generated a high-density Tn5 library from wild-type and &lt;i>smc&lt;/i>-deleted &lt;i>C. glutamicum&lt;/i> strains. Transposon sequencing data revealed that the DNA translocase FtsK </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-04-03T23:57:36.823Z</modification><creation>2025-04-03T23:57:36.823Z</creation></dates><accession>S-EPMC11898615</accession><cross_references><pubmed>39873485</pubmed><doi>10.1128/mbio.02859-24</doi></cross_references></HashMap>