Grzelakowska-Sztabert B, Balińska M
Biochim Biophys Acta. 1980 Oct 1;632(2):164-72. doi: 10.1016/0304-4165(80)90074-4.
Betaine when present in the culture medium could induce the activity of betaine: homocysteine methyltransferase (EC 2.1.1.5) in mouse L-cells, and leukemic L1210 cells, as well as in mouse embryo fibroblasts grown in vitro. We found this process to be time- and concentration-dependent. A persisting contact of the cells with betaine was indispensible for expressing and maintaining the enzyme activity. The treatment of cells with cycloheximide or actinomycin D abolished the process of induction. Methionine as well as homocysteine, when present either in the culture medium or in the reaction mixture, strongly depressed the activity of this enzyme. The L-cells with the induced betaine:homocysteine methyltransferase survived but did not multiply in the methionine-deficient medium, therefore, they did not become prototrophs with respect to methionine.
当培养基中存在甜菜碱时,它可诱导小鼠L细胞、白血病L1210细胞以及体外培养的小鼠胚胎成纤维细胞中甜菜碱:同型半胱氨酸甲基转移酶(EC 2.1.1.5)的活性。我们发现这一过程具有时间和浓度依赖性。细胞与甜菜碱持续接触对于表达和维持酶活性必不可少。用环己酰亚胺或放线菌素D处理细胞可消除诱导过程。当甲硫氨酸以及同型半胱氨酸存在于培养基或反应混合物中时,会强烈抑制该酶的活性。诱导出甜菜碱:同型半胱氨酸甲基转移酶的L细胞在甲硫氨酸缺乏的培养基中存活但不增殖,因此,它们在甲硫氨酸方面并未成为原养型细胞。