ENNIS H L, LUBIN M
Science. 1964 Dec 11;146(3650):1474-6. doi: 10.1126/science.146.3650.1474.
Cycloheximide and acetoxy-cycloheximide specifically inhibit protein synthesis in L-cells growing in suspension culture. In extracts of rat liver, the drugs inhibit transfer of amino acid from soluble RNA to polypeptide. Unlike puromycin, these drugs do not accelerate release of nascent polypeptide chains. The drugs have no effect on protein synthesis in extracts of Escherichia coli.
放线菌酮和乙酰氧基放线菌酮能特异性抑制悬浮培养的L细胞中的蛋白质合成。在大鼠肝脏提取物中,这些药物会抑制氨基酸从可溶性RNA转移至多肽。与嘌呤霉素不同,这些药物不会加速新生多肽链的释放。这些药物对大肠杆菌提取物中的蛋白质合成没有影响。