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肠螯合素钪配合物的抗菌作用研究。

Studies of the antibacterial effect of the scandium complex of enterochelin.

作者信息

Plaha D S, Rogers H J, Williams G W

出版信息

J Antibiot (Tokyo). 1984 May;37(5):588-95. doi: 10.7164/antibiotics.37.588.

Abstract

The scandium complex of enterochelin is known to be assimilated and degraded by enterobacterial pathogens, liberating intracellular scandium. Macromolecular synthesis was inhibited in the order RNA, protein, DNA and phospholipid. Some component of heat-inactivated serum acts in concert with the complex inducing RNA degradation and killing. Both processes are inhibited by dinitrophenol. These biochemical changes resemble those found during complement mediated killing. An examination of the effect on synchronously growing cells suggests that the complex may exert its primary effect during the initiation of chromosome replication.

摘要

已知肠杆菌素的钪络合物可被肠道细菌病原体吸收并降解,释放出细胞内的钪。大分子合成受到抑制,顺序为RNA、蛋白质、DNA和磷脂。热灭活血清的某些成分与该络合物协同作用,诱导RNA降解并导致细胞死亡。这两个过程均被二硝基苯酚抑制。这些生化变化类似于补体介导的细胞杀伤过程中发现的变化。对同步生长细胞的影响研究表明,该络合物可能在染色体复制起始阶段发挥其主要作用。

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