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. 1971 Jan;121(2):161–168. doi: 10.1042/bj1210161

Enzyme purification by electrodecantation

B G Winchester 1, M Caffrey 1, D Robinson 1
PMCID: PMC1176551  PMID: 5000643

Abstract

1. Electrodecantation has been applied to the initial fractionation from crude material of pig kidney β-d-glucosidase and sheep testicular N-acetylglucosaminidase. 2. The isoelectric points determined by isoelectric focusing were pH4.9 for the β-d-glucosidase and pH6.3 for the N-acetylglucosaminidase. 3. Electrodecantation of pig kidney extract and sheep testicular extract was carried out at pH4.9 and 6.3 respectively. 4. A six- to ten-fold increase in specific activity could be obtained with good recoveries after a single cycle of electrodecantation. 5. The technique has also been used to purify further an extracellular Bacillus subtilis protease preparation. 6. Attempts to use electrodecantation for the concentration of very dilute enzyme solutions resulted in considerable loss of activity. 7. The limitations and potential use of the technique in laboratory-scale enzyme preparation are discussed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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