Thermoprecipitation of lysozyme from egg white using copolymers of N-isopropylacrylamide and acidic monomers

Vaidya, A. A. ; Lele, B. S. ; Kulkarni, M. G. ; Mashelkar, R. A. (2001) Thermoprecipitation of lysozyme from egg white using copolymers of N-isopropylacrylamide and acidic monomers Journal of Biotechnology, 87 (2). pp. 95-107. ISSN 0168-1656

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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S01681...

Related URL: http://dx.doi.org/10.1016/S0168-1656(00)00382-5

Abstract

Thermoprecipitation of lysozyme from egg white was demonstrated using copolymers of N-isopropylacrylamide with acrylic acid, methacrylic acid, 2-acryloylamido-2-methylpropane-sulfonic acid and itaconic acid, respectively. Polymers synthesized using molar feed ratio of N-isopropylacrylamide:acidic monomers of 98:2 exhibited lower critical solution temperatures in the range of 33-35°C. These polymers exhibited electrostatic interactions with lysozyme and inhibited its bacteriolytic activity. The concentration of acidic groups required to attain 50% relative inhibition of lysozyme by the polymers, was 104-105 times lower than that required for the corresponding monomers. This was attributed to the multimeric nature of polymer-lysozyme binding. More than 90% lysozyme activity was recovered from egg white. Polymers exhibited reusability up to at least 16 cycles with retention of >85% recovery of specific activity from aqueous solution. In contrast, copolymer comprising natural inhibitor of lysozyme i.e. poly (N-isopropylacrylamide-co-O-acryloyl N-acetylglucosamine) lost 50% recovery of specific activity. Thermoprecipitation using these copolymers, which enables very high recovery of lysozyme from egg white, would be advantageous over pH sensitive polymers, which generally exhibit lower recovery.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Acidic Monomers; Lysozyme; N-isopropylacrylamide; Thermoprecipitation; Thermosensitive Polymers
ID Code:17080
Deposited On:16 Nov 2010 08:33
Last Modified:04 Jun 2011 08:12

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