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首页> 外文期刊>British Journal of Cancer >Utilization of preformed and endogenously synthesized methionine by cells in tissue culture
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Utilization of preformed and endogenously synthesized methionine by cells in tissue culture

机译:细胞在组织培养中对预制的和内源性合成的蛋氨酸的利用

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Some malignant and transformed cell lines are unable to proliferate in vitro in a L-methionine-depleted medium supplemented with L-homocysteine. To investigate the utilization of preformed and endogenously synthesized methionine 4 cell lines have been chosen with a range of abilities to proliferate under such nutritional conditions. The order of the ability of these cell lines to proliferate in an L-methionine-depleted medium containing 0.1 mM L-homocysteine parallels the minimal concentration of L-methionine required for optimal growth, L-methionine auxotrophs having a greater minimal requirement. In the presence of 0.1 mM L-homocysteine all of the cell lines synthesize macromolecules from [5-14C]methyltetrahydrofolic acid during a 24 h period, and the cell line with the highest methionine requirement shows the most extensive incorporation of radiolabel into DNA and RNA, both in depleted medium and in medium containing 6.7 microM L-methionine. Double-label experiments using [5-14C]methyltetrahydrofolic acid and L-(methyl-3H) methionine show preferential incorporation of preformed over endogenously synthesized methionine by methionine auxotrophs. There is no alteration in the intracellular level of S-adenosyl-L-homocysteine (SAH) or SAH hydrolase activity in cells incubated for 24 h in methionine-depleted medium supplemented with 0.1 mM L-homocysteine. These results suggest that certain cell lines are unable to effectively use endogenously synthesized methionine.
机译:一些恶性和转化细胞系无法在补充了L-高半胱氨酸的L-蛋氨酸贫化的培养基中体外增殖。为了研究利用预先形成的和内源性合成的蛋氨酸4种细胞系,这些细胞系在这种营养条件下具有一定的增殖能力。这些细胞系在含有0.1mM L-高半胱氨酸的L-蛋氨酸贫化的培养基中增殖的能力的顺序与最佳生长所需的L-蛋氨酸的最低浓度平行,L-蛋氨酸营养缺陷型具有更高的最低要求。在存在0.1 mM L-高半胱氨酸的情况下,所有细胞系在24小时内均由[5-14C]甲基四氢叶酸合成大分子,蛋氨酸需求量最高的细胞系显示出放射性标记最广泛地掺入DNA和RNA ,无论是在耗尽的培养基中还是在含有6.7 microM L-蛋氨酸的培养基中。使用[5-14C]甲基四氢叶酸和L-(甲基-3H)甲硫氨酸的双标记实验显示,相比于内源合成的甲硫氨酸,蛋氨酸营养缺陷型可以优先掺入预制的蛋氨酸。在补充有0.1 mM L-高半胱氨酸的蛋氨酸贫化培养基中孵育24小时的细胞中,S-腺苷-L-高半胱氨酸(SAH)或SAH水解酶活性的细胞内水平没有改变。这些结果表明某些细胞系不能有效地使用内源性合成的蛋氨酸。

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