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噬菌体末端酶对DNA的包装与切割:噬菌体T4中通过一种突触机制进行的调控

DNA packaging and cutting by phage terminases: control in phage T4 by a synaptic mechanism.

作者信息

Black L W

机构信息

Department of Biological Chemistry, University of Maryland Medical School, Baltimore 21201, USA.

出版信息

Bioessays. 1995 Dec;17(12):1025-30. doi: 10.1002/bies.950171206.

Abstract

Phage DNA packaging occurs by DNA translocation into a prohead. Terminases are enzymes which initiate DNA packaging by cutting the DNA concatemer, and they are closely fitted structurally to the portal vertex of the prohead to form a 'packasome'. Analysis among a number of phages supports an active role of the terminases in coupling ATP hydrolysis to DNA translocation through the portal. In phage T4 the small terminase subunit promotes a sequence-specific terminase gene amplification within the chromosome. This link between recombination and packaging suggests a DNA synapsis mechanism by the terminase to control packaging initiation, formally homologous to eukaryotic chromosome segregation.

摘要

噬菌体DNA包装是通过将DNA转运到原头部来实现的。末端酶是通过切割DNA多联体来启动DNA包装的酶,它们在结构上与原头部的门户顶点紧密契合,形成一个“包装体”。对多种噬菌体的分析支持末端酶在将ATP水解与通过门户的DNA转运偶联中发挥积极作用。在噬菌体T4中,小末端酶亚基促进染色体中序列特异性的末端酶基因扩增。重组与包装之间的这种联系表明,末端酶存在一种DNA联会机制来控制包装起始,这在形式上与真核染色体分离同源。

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