Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/31777
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dc.contributor.authorGhoshal, G-
dc.contributor.authorBanerjee, U C-
dc.contributor.authorShivhare, U S-
dc.date.accessioned2015-07-10T11:52:13Z-
dc.date.available2015-07-10T11:52:13Z-
dc.date.issued2015-07-
dc.identifier.issn0975-1084 (Online); 0022-4456 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/31777-
dc.description400-405en_US
dc.description.abstractCellulase free xylanase is one of the most important upcoming enzyme having industrial application in chemical, biochemical, pharmaceutical and food industry. In the present study, a soil isolate was found to be promising for xylanase production. Biochemical identification tests, Scanning Electron Microscopy (SEM) and 16S rRNA sequencing identified the organism Penicillium citrinum MTCC 9620. Later on, optimization of media composition and environmental factors were investigated. Temperature, pH, agitation speed, carbon sources, nitrogen sources, inoculum concentration, and additives were optimized on the basis of xylanase yield, dry cell weight, extracellular protein content, sugar consumption etc. Optimized media produced 138.73 U/mL xylanase at 120 h (30°C). The purified xylanase was found to have molecular weight approximately 29 KDa.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceJSIR Vol.74(07) [July 2015]en_US
dc.subjectXylanaseen_US
dc.subjectPenicillium citrinumen_US
dc.subjectSubmerged Fermentationen_US
dc.subjectOptimizationen_US
dc.subjectPurificationen_US
dc.subjectMolecular weighten_US
dc.titleIsolation, Screening and Optimization of Xylanase Production in Submerged Fermentation Using P.citrinum.en_US
dc.typeArticleen_US
Appears in Collections:JSIR Vol.74(07) [July 2015]

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