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DC Field | Value | Language |
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dc.contributor.author | Koti B.A | |
dc.contributor.author | Lakshmikanth M | |
dc.contributor.author | Manohar S | |
dc.contributor.author | Lalitha J. | |
dc.date.accessioned | 2020-06-12T15:04:56Z | - |
dc.date.available | 2020-06-12T15:04:56Z | - |
dc.date.issued | 2012 | |
dc.identifier.citation | Preparative Biochemistry and Biotechnology , Vol. 42 , 4 , p. 364 - 377 | en_US |
dc.identifier.uri | 10.1080/10826068.2011.623210 | |
dc.identifier.uri | http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4799 | - |
dc.description.abstract | The 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.subject | agarase | |
dc.subject | aqueous two-phase system | |
dc.subject | Pseudomonas aeruginosa AG LSL-11 | |
dc.subject | zymogram | |
dc.title | Aqueous two-phase extraction for the purification of alkaline agarases from culture extracts of pseudomonas aeruginosa AG LSL-11 | en_US |
dc.type | Article | |
Appears in Collections: | 1. Journal Articles |
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