Differential expression of peroxidase and ABC transporter as the key regulatory components for degradation of azo dyes by Penicillium oxalicum SAR-3

dc.contributor.authorSaroj, Samta
dc.contributor.authorKumar, Karunesh
dc.contributor.authorPrasad, Manoj
dc.contributor.authorSingh, R. P.
dc.date.accessioned2015-12-23T06:30:31Z
dc.date.available2015-12-23T06:30:31Z
dc.date.issued2014
dc.descriptionAccepted date: 21 September 2014en_US
dc.description.abstractFungal species are potential dye decomposers since these secrete spectra of extracellular enzymes involved in catabolism. However, cellular mechanisms underlying azo dye catalysis and detoxification are incompletely understood and obscure. A potential strain designated as Penicillium oxalicum SAR-3 demonstrated broad-spectrum catabolic ability of different azo dyes. A forward suppression subtractive hybridization (SSH) cDNA library of P. oxalicum SAR-3 constructed in presence and absence of azo dye Acid Red 183 resulted in identification of 183 unique expressed sequence tags (ESTs) which were functionally classified into 12 functional categories. A number of novel genes that affect specifically organic azo dye degradation were discovered. Although the ABC transporters and peroxidases emerged as prominent hot spot for azo dye detoxification, we also identified a number of proteins that are more proximally related to stress-responsive gene expression. Majority of the ESTs (29.5%) were grouped as hypothetical/unknown indicating the presence of putatively novel genes. Analysis of few ESTs through quantitative real-time reverse transcription polymerase chain reaction revealed their possible role in AR183 degradation. The ESTs identified in the SSH library provide a novel insight on the transcripts that are expressed in P. oxalicum strain SAR-3 in response to AR183.en_US
dc.description.sponsorshipSenior research fellowships awarded to SS by Department of Biotechnology, New Delhi, India, and to KK by Council of Scientific and Industrial Research, India, are gratefully acknowledged. It may please be noted that the manuscript is the original work of authors, and all the authors have no conflict of interest, and they have mutually agreed to submitting the manuscript to Functional and Integrative Genomics.en_US
dc.identifier.citationFunct. Integr. Genomics, 14(4): 631-642en_US
dc.identifier.doi10.1007/s10142-014-0405-0en_US
dc.identifier.issn1438-7948
dc.identifier.officialurlhttp://link.springer.com/article/10.1007%2Fs10142-014-0405-0en_US
dc.identifier.urihttp://172.16.0.77:8080/jspui/handle/123456789/449
dc.language.isoen_USen_US
dc.publisherSpringeren_US
dc.subjectQuantitative real-time PCRen_US
dc.subjectSuppression subtractive hybridizationen_US
dc.subjectAzo dyeen_US
dc.subjectPenicillium oxalicumen_US
dc.subjectBioremediationen_US
dc.titleDifferential expression of peroxidase and ABC transporter as the key regulatory components for degradation of azo dyes by Penicillium oxalicum SAR-3en_US
dc.typeArticleen_US

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