Staining electrophoretic gels for laccase and peroxidase activity using 1,8-diaminonaphthalene

被引:20
作者
Hoopes, JT [1 ]
Dean, JFD
机构
[1] Univ Georgia, Warnell Sch Forest Resources, Athens, GA 30602 USA
[2] Univ Georgia, Dept Biochem & Mol Biol, Athens, GA 30602 USA
关键词
electrophoresis; densitometry; histochemistry; zymogram; oxidase; peroxidase; laccase; plant;
D O I
10.1006/abio.2001.5112
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new chromogenic substrate for laccases and peroxidases, 1,8-diaminonapthalene, was used to detect phenoloxidase activity in gels after SDS-PAGE. This substrate has several advantages over other widely used phenoloxidase stains in that it is inexpensive, and the oxidized product has both high molar absorptivity and very low solubility. Furthermore, neither the substrate nor the product is known to have toxicity problems of the type associated with many other phenoloxidase stains. The sensitivity of detection using 1,8-diaminonapthalene was comparable to that obtained using the most sensitive stains commonly used for phenoloxidases, e.g., 3,3-diaminobenzidine, and was close to that attainable for protein detection using silver staining. Zymograms developed with 1,8-diaminonapthalene can be used with video densitometry to monitor the specific enzymatic activity of phenoloxidases during enzyme purification. (C) 2001 Academic Press.
引用
收藏
页码:96 / 101
页数:6
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