Lavis V R
Metabolism. 1978 Sep;27(9):1101-8. doi: 10.1016/0026-0495(78)90156-7.
The isozymes of hexokinase in surgical specimens of human subcutaneous adipose tissue were separated by elution from DEAE-cellulose with linear KCl gradients at ph 7.4. Two peaks of activity were found: Peak 1 eluted at 0.05M KCl, and Peak 2 at 0.19M KCl. Michaelis constants (Km) for glucose were: Peak 1, 6.5 x 10-5M; Peak 2, 1.5 x 10-4M. Peak 2 was more susceptible than Peak 1 to inactivation by trypsin, 0.1 mg/ml, and was protected by 0.1M glucose. Both peaks were protected from heat inactivation (45 degrees) by 0.1M glucose. Peak 2 comprised 66 +/- 5 percent of the total hexokinase activity. No activity with the characteristics of hexokinase III was detected in human fat. In all these characteristics, the isozymes of human adipose tissue closely resemble hexokinases I and II from rats.
在pH 7.4条件下,采用线性KCl梯度从DEAE - 纤维素上洗脱的方法,对人皮下脂肪组织手术标本中的己糖激酶同工酶进行分离。发现了两个活性峰:峰1在0.05M KCl处洗脱,峰2在0.19M KCl处洗脱。葡萄糖的米氏常数(Km)分别为:峰1,6.5×10⁻⁵M;峰2,1.5×10⁻⁴M。峰2比峰1更容易被0.1mg/ml的胰蛋白酶灭活,且0.1M葡萄糖可对其起到保护作用。0.1M葡萄糖可保护两个峰免受热失活(45摄氏度)。峰2占总己糖激酶活性的66±5%。在人体脂肪中未检测到具有己糖激酶III特征的活性。在所有这些特性方面,人体脂肪组织的同工酶与大鼠的己糖激酶I和II非常相似。