Enhanced disruption of Candida utilis using enzymatic pretreatment and high‐pressure homogenization
- 5 January 1994
- journal article
- research article
- Published by Wiley in Biotechnology & Bioengineering
- Vol. 43 (1) , 46-56
- https://doi.org/10.1002/bit.260430107
Abstract
The enhancement of the overall disruption of a native strain of Candida utilis (ATCC 9226) was studied using a combination of two methods, namely, pretreatment in the form of partial enzymatic lysis by Zymolyase followed by mechanical disruption in a Microfluidizer high‐pressure homogenizer. The cells were grown in both batch and continuous cultures to examine the effect of specific growth rate on disruption. Cell suspensions ranging in concentration from 7 to 120 g DW/L were disrupted with and without enzymatic pretreatment. For yeast grown in batch culture, final total disruption obtained using the combined protocol approached 95% with four passes at a pressure of 95 MPa, as compared with only 65% disruption using only mechanical homogenization. A modified model was developed to predict the fraction disrupted by the enzymatic pretreatment‐mechanical homogenization two‐stage process. Predicted disruptions agreed favorably with experimental observations (maximum deviation of 20%) over a wide range of operating conditions. © 1994 John Wiley & Sons, Inc.Keywords
This publication has 12 references indexed in Scilit:
- Disruption of native and recombinant Escherichia coli in a high‐pressure homogenizerBiotechnology & Bioengineering, 1989
- The Interactions Between Fermentation and Protein RecoveryNature Biotechnology, 1984
- The isolation of lytic enzymes fromCytophaga and their application to the rupture of yeast cellsBiotechnology & Bioengineering, 1981
- Production of yeast-lytic enzymes byCytophaga species in batch cultureBiotechnology & Bioengineering, 1980
- New method of measuring cell-wall ruptureBiotechnology & Bioengineering, 1979
- Absence of External Causes of Lag in Saccharomyces cerevisiaeJournal of General Microbiology, 1978
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976
- Mechanism of cell disintegration in a high pressure homogenizerBiotechnology & Bioengineering, 1974
- An extreme pressure pump for continuous cell disintegrationBiotechnology & Bioengineering, 1973
- LYSIS OF VIABLE YEAST CELLS BY ENZYMES OF ARTHROBACTER LUTEUSThe Journal of General and Applied Microbiology, 1972