Spectrophotometric assay of alpha-acetolactate decarboxylase

被引:15
作者
Dulieu, C [1 ]
Poncelet, D [1 ]
机构
[1] ENSAIA, Lab Fermentations Bioconversions Ind, F-54505 Vandoeuvre Nancy, France
关键词
alpha-acetolactate decarboxylase; spectrophotometric determination; activity;
D O I
10.1016/S0141-0229(99)00079-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The usual colorimetric method to determine a-acetolactate decarboxylase activity is long, is of poor accuracy (35%), and does not suit brewing fermentation conditions. By simple modification in the procedure, it was possible to improve the measurement to an accuracy of 11%, to allow more samples to be analyzed in a shorter period, and to reduce the cost per analysis. The recommended changes are easy to set up: the temperature of work should be decreased, the number of buffers should be reduced from two to one, and the chosen buffer should be maleate instead of 4-morpholineethanesulfonic acid. We also mention a way to measure both diacetyl and acetoin contents in the same set of measurement, based on absorbance readings of the reaction medium at two different times. These improvements are in accordance with brewing fermentation conditions. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:537 / 542
页数:6
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