Crystal structure of the plasmid maintenance system ε/ζ:: Functional mechanism of toxin ζ and inactivation by ε2ζ2 complex formation

被引:105
作者
Meinhart, A
Alonso, JC
Sträter, N
Saenger, W
机构
[1] Free Univ Berlin, Inst Kristallog, D-14195 Berlin, Germany
[2] Ctr Nacl Biotecnol, Dep Biotechnol Microbiana, Madrid 28049, Spain
关键词
programmed; cell death; epsilon protein; zeta protein; toxin inactivation; phosphotransferase;
D O I
10.1073/pnas.0434325100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Programmed cell death in prokaryotes is frequently found as postsegregational killing. It relies on antitoxin/toxin systems that secure stable inheritance of low and medium copy number plasmids during cell division and kill cells that have lost the plasmid. The broad-host-range, low-copy-number plasmid pSM19035 from Streptococcus pyogenes carries the genes encoding the antitoxin/toxin system epsilon/zeta and antibiotic resistance proteins, among others. The crystal structure of the biologically nontoxic epsilon(2)zeta(2) protein complex at a 1.95-Angstrom resolution and site-directed mutagenesis showed that free zeta acts as phosphotransferase by using ATP/GTP. In epsilon(2)zeta(2), the toxin zeta is inactivated because the N-terminal helix of the antitoxin epsilon blocks the ATP/GTP-binding site. To our knowledge, this is the first prokaryotic postsegregational killing system that has been entirely structurally characterized.
引用
收藏
页码:1661 / 1666
页数:6
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