Moore P M, Peberdy J F
Can J Microbiol. 1976 Jul;22(7):915-21. doi: 10.1139/m76-132.
Chitin synthase (ED 2.4.1.16) has been characterized in Aspergillus flavus. A K(m) value of 2.5 m(M) was obtained for the substrate UDPGlcNAc. The enzyme had a requirement for GlcNAc, and Mg2+ and activity was increased in the presence of soluble chitodextrins F1 and F2. The optimum activity was obtained using Tris--HCl buffer, pH 7.5, with a secondary peak at pH 6.2 and an incubation temperature of 29.5 degrees C. Distribution patterns of chitin synthase in protoplasts and mycelial material were very similar. The highest specific activity was found in a 200 000 X g fraction. Enzyme levels in growing mycelium increased during the exponential growth phase after which they declined. Activity also increased during the early stages of regeneration of both conidial and mycelial protoplasts, despite an initial lack in net protein synthesis. Chitin synthase levels were also dependent upon the carbon source available during regeneration.
几丁质合酶(EC 2.4.1.16)已在黄曲霉中得到鉴定。底物UDPGlcNAc的米氏常数(K(m))为2.5 mM。该酶需要GlcNAc和Mg2+,并且在可溶性几丁质糊精F1和F2存在的情况下活性会增加。使用pH 7.5的Tris-HCl缓冲液可获得最佳活性,在pH 6.2时有一个次要峰值,孵育温度为29.5摄氏度。几丁质合酶在原生质体和菌丝体材料中的分布模式非常相似。在200 000 X g的组分中发现了最高的比活性。生长中的菌丝体中的酶水平在指数生长期增加,之后下降。分生孢子和菌丝体原生质体再生的早期阶段活性也会增加,尽管最初净蛋白质合成缺乏。几丁质合酶水平还取决于再生过程中可用的碳源。