Covalent chromatography. Preparation of fully active papain from dried papaya latex.
نویسندگان
چکیده
1. A Sepharose-(glutathione-2-pyridyl disulphide) conjugate has been prepared. 2. Its use in a new type of chromatography, covalent chromatography by thiol-disulphide interchange, is described. 3. With this technique, papain containing 1 intact catalytic site [thiol with high reactivity towards 2,2'-dipyridyl disulphide (2-Py-S-S-2-Py) at pH4] per mol of protein is readily prepared both from dried papaya latex and from commercial 2xcrystallized partially active papain. 4. The catalysis of the hydrolysis of alpha-N-benzoyl-l-arginine ethyl ester at pH6.0, 25.0 degrees C, I=0.3 by fully active papain thus prepared is characterized by K(m)=18.2+/-<0.1mm and k(cat.)=16.4+/-0.5s(-1).
منابع مشابه
Affinity purification of the novel cysteine proteinase papaya proteinase IV, and papain from papaya latex.
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ورودعنوان ژورنال:
- The Biochemical journal
دوره 133 3 شماره
صفحات -
تاریخ انتشار 1973