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Isolation of a series of single missense mutants of a dna gene of phage φ29, gene 1, utilizing their inhibitory effect on E. coli growth

机译:利用它们对大肠杆菌生长的抑制作用,分离噬菌体φ29基因1的dna基因的一系列单一错义突变体

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References(31) Cited-By(1) Gene 1 product (gp1) of Bacillus subtilis phage φ29 is known to promote DNA replication of the phage. Although its role in the DNA replication is not clear, gp1 is reported to exhibit multiple characteristics, including RNA binding, cell membrane localization, and self-association. To investigate these characteristics, we undertook the isolation of a series of missense mutants of gene 1 bearing substitutions at various regions. During cloning of gene 1, we found that its expression severely inhibited the growth of its host Escherichia coli cells. In this study, we utilized this growth-inhibition phenomenon to screen a random library muta-genized by error-prone PCR, expecting that mutants which could not inhibit cell growth would be affected in the authentic functions of gp1. Using this approach, we obtained 31 different mutants bearing single amino acid substitutions at 26 positions along the entire length of gp1. As a preliminary analysis of these mutants, we compared the deduced amino acid sequences of gp1s from φ29 and its related phages PZA, B103 and M2. Alignment of these sequences revealed three conserved regions, i.e. a hydrophobic region near the carboxyl terminus (assumed to be involved in the membrane localization and self-association of gp1), coiled-coil motif (essential for self-association), and a region of unknown function near the amino terminus. Interestingly, many of the substitutions in the isolated mutants occurred at strongly conserved residues in these regions and affected characteristic features of the regions (e.g. hydrophobicity of the hydrophobic region). These substitutions are expected to affect authentic functions of gp1, and the mutants will be useful for studies of the structure and functions of gp1.
机译:参考文献(31)枯草芽孢杆菌噬菌体φ29的被引用的By(1)基因1产物(gp1)可以促进噬菌体的DNA复制。尽管尚不清楚其在DNA复制中的作用,但据报道gp1具有多种特征,包括RNA结合,细胞膜定位和自缔合。为了研究这些特征,我们进行了一系列在各个区域带有取代的基因1的错义突变体的分离。在基因1的克隆过程中,我们发现其表达严重抑制了其宿主大肠杆菌细胞的生长。在这项研究中,我们利用这种生长抑制现象来筛选通过易错PCR诱变的随机文库,期望不能抑制细胞生长的突变体会影响gp1的真实功能。使用这种方法,我们获得了31个不同的突变体,它们沿着gp1的全长在26个位置带有单个氨基酸取代。作为对这些突变体的初步分析,我们比较了从φ29及其相关噬菌体PZA,B103和M2推导的gp1s的氨基酸序列。这些序列的比对揭示了三个保守区域,即羧基末端附近的疏水区域(假定与gp1的膜定位和自缔合有关),卷曲螺旋基序(对自我缔合必不可少)和一个区域。氨基末端附近的功能未知。有趣的是,分离的突变体中的许多取代发生在这些区域中的高度保守的残基处,并影响了该区域的特征(例如,疏水区域的疏水性)。预期这些取代会影响gp1的真实功能,而突变体将对gp1的结构和功能的研究有用。

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