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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5024
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dc.contributor.authorPatil, NK
dc.contributor.authorKundapur, R
dc.contributor.authorShouche, YS
dc.contributor.authorKaregoudar, TB
dc.date.accessioned2020-06-12T15:05:58Z-
dc.date.available2020-06-12T15:05:58Z-
dc.date.issued2006
dc.identifier.citationCURRENT MICROBIOLOGY , Vol. 52 , 5 , p. 369 - 374en_US
dc.identifier.uri10.1007/s00284-005-5258-2
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5024-
dc.description.abstractBacterial strain Delftia sp. TBKNP-05, isolated by para-hydroxybenzoate enrichment technique, is capable of degrading di-n-butylphthalate (DBP) as a sole source of carbon and energy. Analysis of intermediates by thin-layer chromatography and high-performance liquid chromatography indicated the presence of monobutylphthalate (MBP), phthalate (PA), and protocatechuate (PCA). The washed cells grown on DBP and PA showed appreciable oxidation of DBP, MBP, PA, and PCA. The enzyme activities in cell-free extracts of Delftia sp. TBKNP-05 exhibited the presence of DBP esterase, MBP esterase, PA-dioxygenase, and PCA 4,5-dioxygenase. The PCA is metabolized by meta-cleavage pathway, leading to further mineralization of the compound in this bacterium.en_US
dc.publisherSPRINGER
dc.titleDegradation of plasticizer Di-n-butylphthalate by Delftia sp TBKNP-05en_US
dc.typeArticle
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