<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Karoyo AH</submitter><funding>Natural Sciences and Engineering Research Council of Canada</funding><pagination>403</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6141685</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6</volume><pubmed_abstract>Dual function polymer materials with immobilized &lt;i>Sphingobium Chorophenolicum&lt;/i> (SpC) bacterium cells are reported herein that undergo tandem adsorption and biodegradation of phenolic compounds. The cross-linked polymer materials contain β-cyclodextrin (β-CD) with incremental hexamethylene diisocyanate (HDI) cross-linker at variable mole ratios (X = 1, 3, or 6), denoted as HDI-X systems. The adsorptive uptake properties of the insoluble HDI-X polymers (X = 3 and 6) with various phenolic compounds [pentachlorophenol (PCP), 2,4,6-trichlorophenol (TCP), and 2,4,6-trimethylphenol (TMP)] were studied using batch adsorption isotherms. The molecular selective phenol removal (S&lt;sub>R&lt;/sub>) capacity of the HDI-3 and HDI-6 materials was evaluated by electrospray ionization mass spectrometry (ESI-MS). The results were compared against granular activated carbon (GAC) and native β-CD, where 1D/2D &lt;sup>1&lt;/sup>H NMR spectral characterization of the complexes formed between phenolic guests and a soluble polymer (HDI-1) in aqueous solution provide insight on the intermolecular interactions and the role of cross-linking effects. Immobilization of SpC onto HDI-3 was shown to form a composite polymer/bacterium material. The composite system displays synergistic removal effects due to tandem PCP adsorption and SpC biodegradation to yield by-products such as 2,6-dichloro-1,4-hydroquinone (DCHQ). Apoptosis and cytotoxicity of DCHQ were evaluated using three breast cancer cell lines.</pubmed_abstract><journal>Frontiers in chemistry</journal><pubmed_title>Cyclodextrin-Based Polymer-Supported Bacterium for the Adsorption and &lt;i>in-situ&lt;/i> Biodegradation of Phenolic Compounds.</pubmed_title><pmcid>PMC6141685</pmcid><funding_grant_id>RGPIN 2016-06197</funding_grant_id><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Karoyo AH</pubmed_authors><pubmed_authors>Wilson LD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cyclodextrin-Based Polymer-Supported Bacterium for the Adsorption and &lt;i>in-situ&lt;/i> Biodegradation of Phenolic Compounds.</name><description>Dual function polymer materials with immobilized &lt;i>Sphingobium Chorophenolicum&lt;/i> (SpC) bacterium cells are reported herein that undergo tandem adsorption and biodegradation of phenolic compounds. The cross-linked polymer materials contain β-cyclodextrin (β-CD) with incremental hexamethylene diisocyanate (HDI) cross-linker at variable mole ratios (X = 1, 3, or 6), denoted as HDI-X systems. The adsorptive uptake properties of the insoluble HDI-X polymers (X = 3 and 6) with various phenolic compounds [pentachlorophenol (PCP), 2,4,6-trichlorophenol (TCP), and 2,4,6-trimethylphenol (TMP)] were studied using batch adsorption isotherms. The molecular selective phenol removal (S&lt;sub>R&lt;/sub>) capacity of the HDI-3 and HDI-6 materials was evaluated by electrospray ionization mass spectrometry (ESI-MS). The results were compared against granular activated carbon (GAC) and native β-CD, where 1D/2D &lt;sup>1&lt;/sup>H NMR spectral characterization of the complexes formed between phenolic guests and a soluble polymer (HDI-1) in aqueous solution provide insight on the intermolecular interactions and the role of cross-linking effects. Immobilization of SpC onto HDI-3 was shown to form a composite polymer/bacterium material. The composite system displays synergistic removal effects due to tandem PCP adsorption and SpC biodegradation to yield by-products such as 2,6-dichloro-1,4-hydroquinone (DCHQ). Apoptosis and cytotoxicity of DCHQ were evaluated using three breast cancer cell lines.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2026-05-06T02:56:35.997Z</modification><creation>2025-05-18T13:24:04.938Z</creation></dates><accession>S-EPMC6141685</accession><cross_references><pubmed>30255014</pubmed><doi>10.3389/fchem.2018.00403</doi></cross_references></HashMap>