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枯草芽孢杆菌噬菌体SPP1和SF6基因1产物的分析:一种参与头部充满式包装起始的蛋白质。

Analysis of the Bacillus subtilis bacteriophages SPP1 and SF6 gene 1 product: a protein involved in the initiation of headful packaging.

作者信息

Chai S, Kruft V, Alonso J C

机构信息

Max-Planck-Institut für molekulare Genetik, Berlin, Federal Republic of Germany.

出版信息

Virology. 1994 Aug 1;202(2):930-9. doi: 10.1006/viro.1994.1415.

Abstract

Gene 1 product (G1P) of the related Bacillus subtilis bacteriophages SPP1, SF6, and rho 15 is essential for DNA maturation and packaging. A DNA segment containing gene 1 of phage SF6 or rho 15 origin was cloned and sequenced. SF6 and rho 15 G1P (both with predicted molecular mass of 16.7 kDa) share 71% identity with G1P of SPP1. The G1P of all three phages contains three conserved segments (I, II, and III). Within segments I and II helix-turn-helix DNA binding and nucleotide binding motifs were predicted. G1P of both SPP1 and SF6 origin was purified. SPP1 G1P protein (20.7 kDa), purified from cells overexpressing the cloned gene, purifies together with another polypeptide, having a molecular mass of about 13 kDa. The 13-kDa polypeptide results from a translation start signal within gene 1, and hence was termed SPP1 G1P*. G1P of both SPP1 and SF6 binds specifically to a pac-containing DNA fragment, whereas G1P*, which lacks segment I, does not. Chimeric G1P proteins were obtained by domain swapping between gene 1 of SPP1 and SF6. The results presented here suggest that the G1P DNA binding motif lies in segment I and the major determinant for G1P::G1P interaction might lie in segment II. Segment III and the extended C-terminal part of SPP1 G1P are dispensable. The G1P::G2P interacting region remains uncharacterized.

摘要

枯草芽孢杆菌相关噬菌体SPP1、SF6和rho 15的基因1产物(G1P)对DNA成熟和包装至关重要。克隆并测序了包含噬菌体SF6或rho 15基因1的DNA片段。SF6和rho 15的G1P(预测分子量均为16.7 kDa)与SPP1的G1P具有71%的同一性。所有三种噬菌体的G1P均包含三个保守区段(I、II和III)。在区段I和II内预测到了螺旋-转角-螺旋DNA结合基序和核苷酸结合基序。纯化了源自SPP1和SF6的G1P。从过表达克隆基因的细胞中纯化得到的SPP1 G1P蛋白(20.7 kDa)与另一种分子量约为13 kDa的多肽一起纯化。13 kDa的多肽来自基因1内的一个翻译起始信号,因此被称为SPP1 G1P*。SPP1和SF6的G1P均特异性结合含pac的DNA片段,而缺少区段I的G1P*则不结合。通过SPP1和SF6的基因1之间的结构域交换获得了嵌合G1P蛋白。此处给出的结果表明,G1P的DNA结合基序位于区段I中,G1P::G1P相互作用的主要决定因素可能位于区段II中。SPP1 G1P的区段III和延伸的C末端部分是可有可无的。G1P::G2P相互作用区域仍未明确。

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