Vaidya, A. A. ; Lele, B. S. ; Deshmukh, M. V. ; Kulkarni, M. G. (2001) Design and evaluation of new ligands for lysozyme recovery by affinity thermoprecipitation Chemical Engineering Science, 56 (19). pp. 5681-5692. ISSN 0009-2509
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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00092...
Related URL: http://dx.doi.org/10.1016/S0009-2509(01)00169-5
Abstract
Ligands containing acetamido group and a spacer were conjugated with an acrylic monomer and copolymerized with N-isopropylacrylamide (NIPAM) to yield a thermoprecipitating polymer. The ability of the ligand to bind to lysozyme, which is the first step in the separation of lysozyme, is quantified in terms of I50, the ligand concentration required to achieve 50% of the maximum attainable inhibition of lysozyme. The copolymers containing acetamido groups inhibit lysozyme far more efficiently than the corresponding polymers containing N-acetylglucosamine, the natural inhibitor for lysozyme. The amount and activity of lysozyme recovered from the aqueous solution as well as lysozyme-ovalbumin mixture increased with the length and the hydrophilicity of the spacer. These polymers also exhibited better recyclability.
Item Type: | Article |
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Source: | Copyright of this article belongs to Elsevier Science. |
Keywords: | Affinity Precipitation; Ligands; Lysozyme; Acetamido; N-isopropylacrylamide |
ID Code: | 17090 |
Deposited On: | 16 Nov 2010 08:32 |
Last Modified: | 04 Jun 2011 08:13 |
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