Hirshfield I N, Yeh F M, Zamecnik P C
Biochim Biophys Acta. 1976 Jul 2;435(3):290-305. doi: 10.1016/0005-2787(76)90110-6.
Lysyl-tRNA synthetase was purified to 70-90% of homogeneity from Escherichia coli K-12. The enzyme was purified from wild-type cells grown in minimal medium, or minimal medium containing either 20 mM L-alanine or 3 mM glycly-L-leucine. The synthetase was similarly purified from a mutant strain grown in minimal medium plus 20 mM L-alanine. Results based on sodium dodecyl sulfate-polyacrylamide gel electrophoresis, gel filtration, and trypsin inactivation studies indicate (A) that the presence of L-alanine of glycyl-L-leucine in the culture medium alters the properties of the wild-type enzyme; (B) that the alteration of the synthetase by l-alanine and glycyl-L-leucine is different; and (c) that the molecular weight of lysyl-tRNA synthetase is at least 135000--140000. The results suggest that most likely the metabolites modify the structure of lysyl-tRNA synthetase, but the possibility that the metabolites induce the synthesis of a new lysyl-tRNA synthetase cannot be completely eliminated.
赖氨酰 - tRNA合成酶从大肠杆菌K - 12中纯化至70 - 90%的纯度。该酶从在基本培养基中生长的野生型细胞,或含有20 mM L - 丙氨酸或3 mM甘氨酰 - L - 亮氨酸的基本培养基中生长的野生型细胞中纯化得到。合成酶也从在添加了20 mM L - 丙氨酸的基本培养基中生长的突变株中以类似方式纯化得到。基于十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳、凝胶过滤和胰蛋白酶失活研究的结果表明:(A) 培养基中L - 丙氨酸或甘氨酰 - L - 亮氨酸的存在改变了野生型酶的性质;(B) L - 丙氨酸和甘氨酰 - L - 亮氨酸对合成酶的改变不同;(C) 赖氨酰 - tRNA合成酶的分子量至少为135000 - 140000。结果表明,最有可能的是代谢产物改变了赖氨酰 - tRNA合成酶的结构,但代谢产物诱导合成新的赖氨酰 - tRNA合成酶的可能性也不能完全排除。