Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4799
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dc.contributor.authorKoti B.A
dc.contributor.authorLakshmikanth M
dc.contributor.authorManohar S
dc.contributor.authorLalitha J.
dc.date.accessioned2020-06-12T15:04:56Z-
dc.date.available2020-06-12T15:04:56Z-
dc.date.issued2012
dc.identifier.citationPreparative Biochemistry and Biotechnology , Vol. 42 , 4 , p. 364 - 377en_US
dc.identifier.uri10.1080/10826068.2011.623210
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4799-
dc.description.abstractThe agarases were purified for the first time an using aqueous two-phase system (ATPS) consisting of polyethylene glycol (PEG) and phosphate salt. The three extracellular, alkaline agarases produced by Pseudomonas aeruginosa AG LSL-11 were efficiently extracted into the top PEG-rich layer. The influencing factors on the partition of agarases-molecular weight of the PEG, system pH, system temperature, and NaCl concentration-were investigated. All the factors were found to have a significant effect on the partition of agarases except NaCl. The optimal ATPS parameters for the partitioning and purification of agarases were found to be 12% PEG 600 and 11.9% (w/w) phosphate salt at pH 8.0 and 4°C. All three agarases were concentrated in the top PEG phase with 6.19-fold purity and 71.21% recovery. The ATPS was found to be more convenient and economical than the conventional ion-exchange chromatography (IEC) method for extraction of three agarases and could be significantly employed for the purification of agarases from fermentation broth. Copyright © Taylor & Francis Group, LLC.en_US
dc.subjectagarase
dc.subjectaqueous two-phase system
dc.subjectPseudomonas aeruginosa AG LSL-11
dc.subjectzymogram
dc.titleAqueous two-phase extraction for the purification of alkaline agarases from culture extracts of pseudomonas aeruginosa AG LSL-11en_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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