Snyder J A, Harrison J H
J Exp Zool. 1977 Oct;202(1):89-96. doi: 10.1002/jez.1402020111.
Frog Lysozyme has been purified by sequential application of acid extraction, salt fractionation, CM-cellulose chromatography, heat treatment, and gel filtration. Eight isozymes of purified lysozyme were found to be stable during prolonged storage. Isozymes were separated by preparative polyacrylamide gel electrophoresis, Ninety percent of the lytic activity of frog ovarian egg was represented by forms 7 and 8, the most highly charged isozymes. Seventy-eight percent of frog liver lysozyme activity was that of form 4. Forms 7 and 8 differed from form 4 by being larger (apparent molecular weight of 18,000 vs. 16,000), by remaining active in more acidic environment, and by exhibiting a dependency upon NaCl for activity. Antiserum prepared against frog form 4 did not react with frog forms 7 and 8 and antiserum to chicken egg-white lysozyme did not react with any frog lysozymes. All frog lysozymes showed identical reversible binding to deaminated chitin. Apparent size differences and lack of immunological cross-reactivity suggest that at least some of the isozymes are non-allelic.
通过依次进行酸提取、盐分级分离、CM - 纤维素色谱法、热处理和凝胶过滤,青蛙溶菌酶已被纯化。纯化后的溶菌酶的八种同工酶在长期储存过程中被发现是稳定的。同工酶通过制备型聚丙烯酰胺凝胶电泳进行分离,青蛙卵巢卵的溶菌活性的90%由形式7和8代表,这两种是电荷最高的同工酶。青蛙肝脏溶菌酶活性的78%是形式4的活性。形式7和8与形式4的不同之处在于更大(表观分子量分别为18,000和16,000)、在更酸性的环境中仍保持活性以及其活性依赖于氯化钠。针对青蛙形式4制备的抗血清不与青蛙形式7和8发生反应,针对鸡蛋白溶菌酶的抗血清不与任何青蛙溶菌酶发生反应。所有青蛙溶菌酶对脱氨基几丁质表现出相同的可逆结合。表观大小差异和缺乏免疫交叉反应表明至少一些同工酶是非等位基因的。