{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Medic A"],"funding":["Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja"],"pagination":["23696-23710"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9069449"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["9(41)"],"pubmed_abstract":["The <i>Pseudomonas aeruginosa</i> san ai strain was investigated for its capability to degrade the 2,6-di-<i>tert</i>-butylphenol (2,6-DTBP) plastic additive, a hazardous and toxic substance for aquatic life. This investigation was performed under different parameter values: 2,6-DTBP concentration, inoculum size, pH, and temperature. The GC-MS study showed that <i>P. aeruginosa</i> efficiently degraded 2,6-DTBP in the pH range of 5-8 at higher temperatures. Under exposure to 2,6-DTBP concentrations of 2, 10, and 100 mg L<sup>-1</sup>, the strain degraded by 100, 100, and 85%, respectively, for 7 days. Crude enzyme preparation from the biomass of <i>P. aeruginosa</i> san ai showed higher efficiency in 2,6-DTBP removal than that shown by whole microbial cells. Gene encoding for the enzymes i"],"journal":["RSC advances"],"pubmed_title":["A comprehensive study of conditions of the biodegradation of a plastic additive 2,6-di-<i>tert</i>-butylphenol and proteomic changes in the degrader <i>Pseudomonas aeruginosa</i> san ai."],"pmcid":["PMC9069449"],"funding_grant_id":["43004","176006"],"pubmed_authors":["Beskoski V","Stojanovic K","Loncarevic B","Izrael-Zivkovic L","Medic A","Kazazic S","Karadzic I"],"additional_accession":[]},"is_claimable":false,"name":"A comprehensive study of conditions of the biodegradation of a plastic additive 2,6-di-<i>tert</i>-butylphenol and proteomic changes in the degrader <i>Pseudomonas aeruginosa</i> san ai.","description":"The <i>Pseudomonas aeruginosa</i> san ai strain was investigated for its capability to degrade the 2,6-di-<i>tert</i>-butylphenol (2,6-DTBP) plastic additive, a hazardous and toxic substance for aquatic life. This investigation was performed under different parameter values: 2,6-DTBP concentration, inoculum size, pH, and temperature. The GC-MS study showed that <i>P. aeruginosa</i> efficiently degraded 2,6-DTBP in the pH range of 5-8 at higher temperatures. Under exposure to 2,6-DTBP concentrations of 2, 10, and 100 mg L<sup>-1</sup>, the strain degraded by 100, 100, and 85%, respectively, for 7 days. Crude enzyme preparation from the biomass of <i>P. aeruginosa</i> san ai showed higher efficiency in 2,6-DTBP removal than that shown by whole microbial cells. Gene encoding for the enzymes i","dates":{"release":"2019-01-01T00:00:00Z","publication":"2019 Jul","modification":"2026-05-30T15:18:36.516Z","creation":"2025-04-04T10:02:14.106Z"},"accession":"S-EPMC9069449","cross_references":{"pubmed":["35530597"],"doi":["10.1039/c9ra04298a"]}}