Kuliszewski M J, Nicholls D M
Biochem J. 1980 Sep 15;190(3):791-7. doi: 10.1042/bj1900791.
Rats received two injections (each 2.6 mg/kg body wt.) of CdCl2, and the kidneys were removed 24 h later. Postmicrosomal supernatant fractions of the homogenized kidneys were used as a source of elongation factors 1 and 2 in assays for [14C]phenylalanyl-tRNA binding to ribosomes and for peptide-bond synthesis. After purification of these preparations by precipitation with (NH4)2SO4 and gel filtration on Sephadex G-200 and G-100, elongation factor 1 activity was significantly increased. A significant increase in the activity of purified elongation factor 2 was also found. The results are discussed in relation to the reported effects of CdCl2 and of HgCl2 on renal tissue.
给大鼠注射两次氯化镉(每次2.6毫克/千克体重),24小时后摘除肾脏。将匀浆后的肾脏微粒体后上清液组分用作延伸因子1和2的来源,用于检测[14C]苯丙氨酰 - tRNA与核糖体的结合以及肽键合成。通过硫酸铵沉淀和在葡聚糖凝胶G - 200和G - 100上进行凝胶过滤对这些制剂进行纯化后,延伸因子1的活性显著增加。还发现纯化后的延伸因子2的活性也显著增加。结合已报道的氯化镉和氯化汞对肾组织的影响对结果进行了讨论。