1961 年 14 巻 3 号 p. 119-122
Nucleoside antibiotics, angustmycins A and C1–3), were observed to exhibit inhibitory activity against experimental infections and transplantable tumors in animals4). Their in vitro antimicrobial activities were demonstrated in synthetic media, but they were markedly decreased in organic media5,6). Their activities were reversed by guanine, guanosine, adenosine, inosine, xanthosine and other related substances5). These results as well as their chemical structures2,3) suggested that angustmycins may act as antimetabolites in nucleic acid biosynthesis. The influence of angustmycins on 32P and 14C-labeled amino acids incorporations of Bacillus subtilis was investigated and the results are described in this report.