Uesawa Y, Sugiura Y
Institute for Chemical Research, Kyoto University, Japan.
Biochemistry. 1991 Sep 24;30(38):9242-6. doi: 10.1021/bi00102a016.
Esperamicin A1 effectively breaks DNA strands upon heating at 50 degrees C. The preferential DNA cutting sites of heat-activated esperamicin A1 are random and clearly differ from those of thiol- or UV-light-mediated DNA breakage with esperamicin A1. The absence of heat-induced DNA cleavage by esperamicin Z and the induction of the DNA breakage by esperamicin A1 disulfide indicate that (1) the enediyne core plays a significant role in this DNA strand scission and (2) the DNA cutting with the heat-activated esperamicin antibiotics does not necessarily require a trisulfide trigger in the aglycon portion. On the basis of the present results, a probable mechanism for the heat-induced DNA cleavage of esperamicin A1 has been proposed.
埃斯佩拉霉素A1在50摄氏度加热时能有效切断DNA链。热激活的埃斯佩拉霉素A1的优先DNA切割位点是随机的,且明显不同于硫醇或紫外线介导的埃斯佩拉霉素A1导致的DNA断裂位点。埃斯佩拉霉素Z不存在热诱导的DNA切割,而埃斯佩拉霉素A1二硫化物能诱导DNA断裂,这表明:(1)烯二炔核心在这种DNA链断裂中起重要作用;(2)热激活的埃斯佩拉霉素类抗生素切割DNA不一定需要苷元部分的三硫化物触发。基于目前的结果,已提出了埃斯佩拉霉素A1热诱导DNA切割的可能机制。