Kane S M, Vugrincic C, Finbloom D S, Smith D W
Biochemistry. 1978 Apr 18;17(8):1509-14. doi: 10.1021/bi00601a024.
The histidyl-tRNA synthetase of rabbit reticulocyte cytosol has been purified 84 000-fold to apparent homogeneity with a specific activity of 687 nmol of histidyl-tRNA formed per min per mg of protein. Ten to 15% of the enzyme activity is sedimented with the ribosomes while the remainder is in the cytosol. The purified enzyme has a molecular weight of 122 000 as determined by sucrose density gradient centrifugation. Gel electrophoresis in the presence of 0.1% sodium dodecyl sulfate suggests that it is composed of two similar subunits with a molecular weight of approximately 64 000. The enzyme has a magnesium optimum of 45 mM; however, this is reduced to 5 mM in the presence of an intracellular potassium concentration (160 nM). The enzyme acylates the two histidine tRNA isoacceptors of rabbit reticulocytes with similar Km values and at similar rates.
兔网织红细胞胞质溶胶中的组氨酰 - tRNA合成酶已被纯化84000倍,达到表观均一性,比活性为每分钟每毫克蛋白质形成687 nmol组氨酰 - tRNA。10%至15%的酶活性与核糖体一起沉降,其余部分存在于胞质溶胶中。通过蔗糖密度梯度离心法测定,纯化后的酶分子量为122000。在0.1%十二烷基硫酸钠存在下进行的凝胶电泳表明,它由两个分子量约为64000的相似亚基组成。该酶的最佳镁离子浓度为45 mM;然而,在细胞内钾离子浓度(160 nM)存在的情况下,这一浓度会降至5 mM。该酶以相似的Km值和相似的速率使兔网织红细胞的两种组氨酸tRNA同工受体发生酰化反应。