Young E T, Nicholls D M
Biochem J. 1978 Jun 15;172(3):479-86. doi: 10.1042/bj1720479.
Homogenates of liver were obtained from control rats and from rats that had received DDT [1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane]. The postmicrosomal supernatant fractions were used for the purification of elongation factor 1 by hydroxyapatite chromatography and phosphocellulose chromarography. The amount of binding factor present was essentially the same for both groups of animals, but the specific activity, as measured by the binding assay, was about twice as high in the DDT-treated preparations. After sucrose-gradient sedimentation, the difference in specific activity was found to reside in the low-molecular-weight (50000) form of elongation factor 1. The implications of an increased reactivity of elongation factor 1 during the induction of membrane enzymes are discussed.
从对照大鼠和接受滴滴涕[1,1,1-三氯-2,2-双(对氯苯基)乙烷]的大鼠中获取肝脏匀浆。微粒体后上清液部分用于通过羟基磷灰石色谱法和磷酸纤维素色谱法纯化延伸因子1。两组动物中存在的结合因子量基本相同,但通过结合测定法测得的比活性在滴滴涕处理的制剂中约高两倍。蔗糖梯度沉降后,发现比活性的差异存在于低分子量(50000)形式的延伸因子1中。讨论了膜酶诱导过程中延伸因子1反应性增加的影响。