Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/45096
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dc.contributor.authorJose, Divya-
dc.contributor.authorMohandas, A-
dc.contributor.authorSingh, I S Bright-
dc.date.accessioned2018-10-03T10:19:16Z-
dc.date.available2018-10-03T10:19:16Z-
dc.date.issued2018-04-
dc.identifier.issn0975-0967 (Online); 0972-5849 (Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/45096-
dc.description284-289en_US
dc.description.abstractLasB protease, also known as the elastase enzyme was purified from an environmental isolate of Pseudomonas aeruginosa MCCB 123. The enzyme production was optimized by response surface methodology (RSM) which yielded 24754.17 U/mL protease activity and 654.14 U/ml elastase activity. The yields were 1.83 fold and 2.39 fold higher for protease and elastase activities, respectively. Scale up study of enzyme production was carried in a 5 L bioreactor. Bioprocess technology for enzyme production was successfully developed.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.sourceIJBT Vol.17(2) [April 2018]en_US
dc.subjectPseudomonas aeruginosaen_US
dc.subjectLasB proteaseen_US
dc.subjectElastaseen_US
dc.subjectOptimizationen_US
dc.titleBioprocess technology for LasB protease (elastase) production from Pseudomonas aeruginosa MCCB 123en_US
dc.typeArticleen_US
Appears in Collections:IJBT Vol.17(2) [April 2018]

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