Reusser F
Antimicrob Agents Chemother. 1975 Jan;7(1):32-7. doi: 10.1128/AAC.7.1.32.
Lincomycin does not affect initiation factor-dependent formation of 70S initiation complexes formed with fmet-tRNA(F), the initiation triplet A-U-G, and 70S ribosomes, whereas its 7-chloro-derivative clindamycin substantially stimulates this process. Conversely, lincomycin stimulates nonenzymatic formation of the 70S complex, but clindamycin does not. Both antibiotics stimulate the assembly of non-enzymatically formed 70S initiation complexes with R(17) phage ribonucleic acid and exert little effect on those formed in the presence of initiation factors. The formation of 30S initiation complexes is stimulated or remains unaffected by lincomycin or clindamycin except when initiation occurs in the presence of very low Mg(2+) concentrations. In this case, both antibiotics inhibit the assembly of the 30S complexes regardless of the messenger present.
林可霉素不影响由fmet - tRNA(F)、起始三联体A - U - G和70S核糖体形成的依赖起始因子的70S起始复合物的形成,而其7 - 氯衍生物克林霉素则能显著刺激这一过程。相反,林可霉素能刺激70S复合物的非酶促形成,但克林霉素则不能。两种抗生素都能刺激非酶促形成的70S起始复合物与R(17)噬菌体核糖核酸的组装,而对在起始因子存在下形成的复合物影响很小。30S起始复合物的形成受到林可霉素或克林霉素的刺激或不受影响,除非在极低Mg(2+)浓度下发生起始反应。在这种情况下,无论存在何种信使,两种抗生素都会抑制30S复合物的组装。