Ross C
Department of Botany and Plant Pathology, Colorado State University, Fort Collins, Colorado 80521.
Plant Physiol. 1974 Apr;53(4):635-7. doi: 10.1104/pp.53.4.635.
Concentrations of cycloheximide as low as 3 mug/ml inhibited incorporation of labeled orotic acid or uridine into RNA cytidylic acid of soybean (Glycine max) hypocotyl sections. Even lower concentrations of this well known protein synthesis inhibitor interfered with conversion of labeled cytidine into RNA uridylic acid. Both cycloheximide and puromycin inhibited absorption of (3)H-phenylalanine and its incorporation into protein, but puromycin did not significantly affect the labeling patterns of RNA cytidylic and uridylic acids when orotic acid-6-(14)C was fed. Results give further support to the hypothesis that cycloheximide inhibits the interconversion of uridine and cytidine nucleotides, presumably by acting as a glutamine antagonist in the glutamine-dependent reaction catalyzed by cytidine triphosphate synthetase.
低至3微克/毫升的放线菌酮浓度可抑制标记的乳清酸或尿苷掺入大豆(Glycine max)下胚轴切片的RNA胞苷酸中。这种著名的蛋白质合成抑制剂的更低浓度会干扰标记的胞苷转化为RNA尿苷酸。放线菌酮和嘌呤霉素都抑制了(3)H-苯丙氨酸的吸收及其掺入蛋白质中,但当喂食乳清酸-6-(14)C时,嘌呤霉素对RNA胞苷酸和尿苷酸的标记模式没有显著影响。结果进一步支持了放线菌酮抑制尿苷和胞苷核苷酸相互转化的假说,推测是通过在胞苷三磷酸合成酶催化的谷氨酰胺依赖性反应中作为谷氨酰胺拮抗剂起作用。