国家自然科学基金(39770071)和四川省青年科技基金资助项目.
This work was supported by grants from The National Natural Sciences Foundation of China (39770071) and The Youth Science and Technology Foundation of Sichuan Province.
采用分离胶中加入0.25%明胶作为底物的SDS-聚丙烯酰胺凝胶电泳,对光系统Ⅱ颗粒及其1 mol/L NaCl抽提液中存在的蛋白酶进行了分离、活性检测和部分性质分析.在PSⅡ颗粒的1 mol/L NaCl抽提液中检测到有6条酶带存在,分子质量分别为34、37、50、54、58和68 ku.初步分析了还原剂、离子强度等对蛋白酶活性的影响.此方法分离与检测同步,具有灵敏度高、方便等优点.
In order to detect the proteases in the 1 mol/L NaCl extract of plant PSⅡ particles and its 1 mol/L NaCl extract, gelatin-SDS-polyacrylamide gel electrophoresis was used. Six proteases with molecular mass of 34,37,50,54,58 and 68 ku were detected. Influence of reducer and ion strength on the activity of proteases was analyzed preliminary. The new approach is convenient and highly sensitive for separation and detection of proteases at the same time.
周昊,杜林方,朱晓峰.用于植物光系统Ⅱ蛋白酶检测的活性染色方法[J].生物化学与生物物理进展,2002,29(4):651-654
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