<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hara T</submitter><funding>MEXT | Japan Society for the Promotion of Science</funding><funding>Kyoto University | Institute of Advanced Energy, Kyoto University</funding><pagination>e0192621</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8694117</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(3)</volume><pubmed_abstract>Polychlorinated biphenyls (PCBs) are recalcitrant organohalide pollutants, consisting of 209 congeners. PCB cleanup in natural landscapes is expected to be achieved by the metabolic activity of microorganisms, but aerobic PCB-degrading bacteria that inhabit sites polluted by PCBs cannot degrade all PCB congeners due to the specificity of their enzymes. In this study, we investigated the degradability of PCBs when a genetically modified PCB-degrading bacterium was compounded with wild-type PCB-degrading bacteria. We used two bacterial strains, Comamonas testosteroni YAZ2 isolated from a PCB-uncontaminated natural landscape and Escherichia coli BL21(DE3) transformed with a biphenyl dioxygenase (BphA) gene from a well-known PCB degrader, Burkholderia xenovorans LB400. The enzymatic specificit</pubmed_abstract><journal>Microbiology spectrum</journal><pubmed_title>Augmentation of an Engineered Bacterial Strain Potentially Improves the Cleanup of PCB Water Pollution.</pubmed_title><pmcid>PMC8694117</pmcid><funding_grant_id>JP26550066</funding_grant_id><funding_grant_id>ZE28C-11</funding_grant_id><funding_grant_id>ZE29A-10</funding_grant_id><funding_grant_id>JP18K19881</funding_grant_id><pubmed_authors>Nakata E</pubmed_authors><pubmed_authors>Hara T</pubmed_authors><pubmed_authors>Morii T</pubmed_authors><pubmed_authors>Takatsuka Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Augmentation of an Engineered Bacterial Strain Potentially Improves the Cleanup of PCB Water Pollution.</name><description>Polychlorinated biphenyls (PCBs) are recalcitrant organohalide pollutants, consisting of 209 congeners. PCB cleanup in natural landscapes is expected to be achieved by the metabolic activity of microorganisms, but aerobic PCB-degrading bacteria that inhabit sites polluted by PCBs cannot degrade all PCB congeners due to the specificity of their enzymes. In this study, we investigated the degradability of PCBs when a genetically modified PCB-degrading bacterium was compounded with wild-type PCB-degrading bacteria. We used two bacterial strains, Comamonas testosteroni YAZ2 isolated from a PCB-uncontaminated natural landscape and Escherichia coli BL21(DE3) transformed with a biphenyl dioxygenase (BphA) gene from a well-known PCB degrader, Burkholderia xenovorans LB400. The enzymatic specificit</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2025-05-18T12:04:14.554Z</modification><creation>2025-04-05T20:39:58.076Z</creation></dates><accession>S-EPMC8694117</accession><cross_references><pubmed>34937186</pubmed><doi>10.1128/spectrum.01926-21</doi></cross_references></HashMap>