Woynarowska B, Witkowski A, Borowski E
Biochim Biophys Acta. 1985 Jun 24;825(2):199-206. doi: 10.1016/0167-4781(85)90104-6.
A dipeptide antibiotic, tetaine, was found to diminish the rate of incorporation of 3H-labelled precursors into nucleic acids of intact and permeabilized HeLa S3 cells with concomitant negligible effect on protein synthesis. Comparison of the inhibitory effects of tetaine indicates that the antibiotic at 0.03-0.1 mM is a selective inhibitor of cellular DNA biosynthesis and, at higher concentration, of DNA and RNA biosynthesis. Tetaine is also an inhibitor of DNA and RNA polymerase reactions in a cell-free system, as determined using partially purified extracts from HeLa S3 cells that served as a source of the enzymes. The pretreatment experiments showed that tetaine inactivated the polymerases without affecting DNA template function. The tetaine effect on biosynthesis of nucleic acids in HeLa S3 cells can be attributed rather to the intact antibiotic than to the product of its enzymatic cleavage, anticapsin.
一种二肽抗生素,四肽菌素,被发现可降低3H标记前体掺入完整和透化的HeLa S3细胞核酸的速率,同时对蛋白质合成的影响可忽略不计。四肽菌素抑制作用的比较表明,0.03 - 0.1 mM的抗生素是细胞DNA生物合成的选择性抑制剂,而在较高浓度下,则是DNA和RNA生物合成的抑制剂。如使用来自HeLa S3细胞的部分纯化提取物作为酶源所确定的,四肽菌素也是无细胞系统中DNA和RNA聚合酶反应的抑制剂。预处理实验表明,四肽菌素使聚合酶失活而不影响DNA模板功能。四肽菌素对HeLa S3细胞核酸生物合成的影响更多地可归因于完整的抗生素,而非其酶促裂解产物抗蛋白酶。