Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5021
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dc.contributor.authorVijaykumar, MH
dc.contributor.authorVeeranagouda, Y
dc.contributor.authorNeelakanteshwar, K
dc.contributor.authorKaregoudar, TB
dc.date.accessioned2020-06-12T15:05:58Z-
dc.date.available2020-06-12T15:05:58Z-
dc.date.issued2006
dc.identifier.citationWORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY , Vol. 22 , 2 , p. 157 - 162en_US
dc.identifier.uri10.1007/s11274-005-9013-4
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5021-
dc.description.abstractA fungus Cladosporium cladosporioides isolated from coal sample as a decolorizing microorganism. It decolorized five different azo and triphenylmethane dyes like acid blue 193, acid black 210, crystal violet, reactive black B(S) and reactive black BL/LPR both on solid and in liquid broth medium. Culture broth of this fungus decolorized completely 100 mg of acid blue 193 l(-1) in 8 days. The extracellular enzyme of Cladosporium cladosporioides decolorized acid blue 193 on repeated addition to a total (out of 700 mg l(-1)) concentration of 564 mg l(-1) within 168 h without significant decline in the activity, showing the resistant property of Cladosporium cladosporioides to a high concentration of the dye. The optimal temperature 40 degrees C, pH 5.6 and sugar concentration of 4% required for decolorization of acid blue 193. Cladosporium cladosporioides showed manganese peroxidase activity with 41 U l(-1), laccase activity with 1413 U l(-1) and lignin peroxidase activity was negligible after day 8 of incubation.en_US
dc.publisherSPRINGER
dc.subjectCladosporium cladosporioides
dc.subjectdye decolorization
dc.subjectlaccase
dc.subjectmanganese peroxidase
dc.subjectmetabolites
dc.titleDecolorization of 1 : 2 metal complex dye Acid blue 193 by a newly isolated fungus, Cladosporium cladosporioidesen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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