Oesterhelt D, Bauer H, Lynen F
Proc Natl Acad Sci U S A. 1969 Aug;63(4):1377-82. doi: 10.1073/pnas.63.4.1377.
The crystallization of purified fatty acid synthetase from yeast is facilitated by seeding techniques. The first seed crystals appeared as particles with almost negligible enzymatic activity in a solution that had been left at 4 degrees C for 15 months. Subsequently, the crystallization time has been reduced to two days, and the crystals now isolated have retained their full enzymatic activity. The loss of synthetase activity that can result from prolonged exposure during crystallization is attributable specifically to damage of the enzyme component responsible for condensation activity. Crystalline synthetase is identical to purified but noncrystalline synthetase by all criteria so far examined.
接种技术有助于酵母中纯化的脂肪酸合成酶结晶。第一批晶种晶体在4℃下放置15个月的溶液中以酶活性几乎可忽略不计的颗粒形式出现。随后,结晶时间缩短至两天,现在分离出的晶体保留了其全部酶活性。结晶过程中长时间暴露可能导致的合成酶活性丧失具体归因于负责缩合活性的酶成分受损。就目前所检验的所有标准而言,结晶态合成酶与纯化的非结晶态合成酶相同。