等位酶淀粉凝胶电泳技术中的几个应引起重视的问题

本文总结了我们在用淀粉凝胶电泳技术进行等位酶分析的实验过程中的一些经验和教训，主要结论是：1)尽管材料不同，对于不同的酶系统，用特定的缓冲液系统常能获得比较理想的效果，如DIA，CPI，HEX，SOD和TPI用S6(Soltis等，1983)；AMP用S8；MDH用S9和SKD用W2(Wendel和Weeden，1989)等。2)用磷酸缓冲液配制AMP的染色配方较其它配方效果好。3)当胶染时，使用琼脂替代琼脂糖，染色效果不变而成本更低，谱带扩散更慢。4)不同的提取液可能适用于不同的酶系统，如磷酸-PVP提取液(Soltis等，1983)不适用于石荠苎的GPI的提取。5)正确选择凝胶和电极缓冲液，S1虽然适用面广，但效果不一定好，对于位点多和等位基因丰富的材料尤其应警惕，因S1可能掩盖样品之间的差异。

Some Advises for Starch Gel Electrophoresis in Allozyme Analysis

This paper summarized our experience,and lessons while we were doing starch gel electrophoresis experiment for allozyme analysis. High resolution was often achieved on some enzymes with certain buffer systems, for example, DIA, GPI, HEX, SOD and TPI with S6 ( Soltis et al., 1983); AMP with S8;MDH with S9; and SKD with W2 (Wendel and Weeden, 1989). Staining recipe of Soltis and Reiseberg (1986) was recommended for visualizing AMP. Agar staining was preferred to agarose staining for the reason of lower cost and slower diffusion of bands. For GPI, special attention should be paid to the choice of extraction buffer. In some cases, the bands of GPI were significantly reduced using the phosphate grinding buffer of Soltis et al. (1983) in some groups such as Mosla. The use of gel and electrode buffer No. 1 (S1) should be avoided if the materials are isozymes and alleles rich.