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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12128/5061
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dc.contributor.authorDzionek, Anna-
dc.contributor.authorWojcieszyńska, Danuta-
dc.contributor.authorHupert-Kocurek, Katarzyna-
dc.contributor.authorAdamczyk-Habrajska, Małgorzata-
dc.contributor.authorGuzik, Urszula-
dc.date.accessioned2018-06-28T12:14:06Z-
dc.date.available2018-06-28T12:14:06Z-
dc.date.issued2018-
dc.identifier.citationCatalysts, Vol. 8, iss. 5 (2018), art. no. 176pl_PL
dc.identifier.issn2073-4344-
dc.identifier.urihttp://hdl.handle.net/20.500.12128/5061-
dc.description.abstractPlanococcus sp. S5, a Gram-positive bacterium isolated from the activated sludge is known to degrade naproxen in the presence of an additional carbon source. Due to the possible toxicity of naproxen and intermediates of its degradation, the whole cells of S5 strain were immobilized onto loofah sponge. The immobilized cells degraded 6, 9, 12 or 15 mg/L of naproxen faster than the free cells. Planococcus sp. cells immobilized onto the loofah sponge were able to degrade naproxen efficiently for 55 days without significant damage and disintegration of the carrier. Analysis of the activity of enzymes involved in naproxen degradation showed that stabilization of S5 cells in exopolysaccharide (EPS) resulted in a significant increase of their activity. Changes in the structure of biofilm formed on the loofah sponge cubes during degradation of naproxen were observed. Developed biocatalyst system showed high resistance to naproxen and its intermediates and degraded higher concentrations of the drug in comparison to the free cells.pl_PL
dc.language.isoenpl_PL
dc.rightsUznanie autorstwa 3.0 Polska*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/pl/*
dc.subjectLoofah spongepl_PL
dc.subjectNaproxenpl_PL
dc.subjectPlanococcus sp. S5pl_PL
dc.subjectWhole-cell immobilizationpl_PL
dc.titleImmobilization of Planococcus sp. S5 strain on the loofah sponge and its application in naproxen removalpl_PL
dc.typeinfo:eu-repo/semantics/articlepl_PL
dc.identifier.doi10.3390/catal8050176-
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