Serrano R
Biochem Biophys Res Commun. 1984 Jun 15;121(2):735-40. doi: 10.1016/0006-291x(84)90243-2.
The plasma membrane ATPase from oat roots has been purified near homogeneity by a simple procedure. Plasma membranes isolated from sucrose gradients are first extracted with Triton X-100 and KC1 and the residue solubilized with lysolecithin. Rate-zonal centrifugation in a vertical rotor with a glycerol gradient results in a preparation of very high specific activity (6 mumoles min-1 mg protein-1 at 30 degrees C) and where over 70% of the protein corresponds to a polypeptide of about 100 kilodaltons previously identified as the ATPase. The purified enzyme could be reconstituted in proteoliposomes catalyzing ATP-driven proton transport sensitive to vanadate.
通过一个简单的程序,燕麦根的质膜ATP酶已被纯化至接近均一状态。首先用Triton X-100和KCl提取从蔗糖梯度中分离出的质膜,然后用溶血卵磷脂溶解残余物。在垂直转子中进行甘油梯度速率区带离心,得到的制剂具有非常高的比活性(30℃时为6微摩尔·分钟⁻¹·毫克蛋白⁻¹),其中超过70%的蛋白质对应于一种先前鉴定为ATP酶的约100千道尔顿的多肽。纯化后的酶可以在蛋白脂质体中重建,催化对钒酸盐敏感的ATP驱动的质子运输。