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丝状噬菌体氯仿抗性突变体的分离:在噬菌体结构模型中的定位

Isolation of chloroform-resistant mutants of filamentous phage: localization in models of phage structure.

作者信息

Oh J S, Davies D R, Lawson J D, Arnold G E, Dunker A K

机构信息

Department of Biochemistry and Biophysics, Washington State University, Pullman, WA, 99164, USA.

出版信息

J Mol Biol. 1999 Apr 2;287(3):449-57. doi: 10.1006/jmbi.1999.2599.

Abstract

Interaction of fd or M13 filamentous phage with a chloroform/water interface induces morphological change, contracting the filaments sequentially into shortened rods (I-forms), and then into spheroidal particles (S-forms). To further investigate this phage contraction, 34 and 26 chloroform-resistant isolates of fd and M13, respectively, were selected after chloroform treatment of wild-type phages at pH 8. 2 and 4 degrees C. DNA sequencing of gene VIII of the 34 fd isolates revealed five different mutants: these were D5H, M28L, V31L, I37T, and S50T. All 26 M13 isolates were I37T. These mutants exhibited variable sensitivity to chloroform, but all contracted much more slowly than wild-type phage during treatment at 4 degrees C. They all contracted like wild-type phage at 37 degrees C. Site-directed mutagenesis showed that the indicated single mutations carried the chloroform resistance. In structural models of the phage, the D5H locus is on the outside and the S50T locus is on the inside. The M28L and I37T loci are buried in a mostly hydrophobic region in the middle. Although these four mutants are spread out radially, they are localized in the axial direction into a thin disk in the model. The last mutant locus, V31L, is out of this disk, but this locus is proximal to the M28L and I37T loci and also in contact with the surface via a deep hydrophobic hole or depression. These five mutants, their locations, and their variable affects on contraction suggest that chloroform-induced contraction involves a specific mechanism rather than a generalized solvent-induced denaturation and that the critical structural changes occur in a localized level in the phage. These results add weight to suggestions that the sequential contraction of filaments-->I-forms-->S-forms mimic corresponding steps in phage penetration, and, in the reverse order, for phage assembly.

摘要

丝状噬菌体fd或M13与氯仿/水界面的相互作用会引起形态变化,使丝状结构依次收缩为短杆状(I型),然后变为球状颗粒(S型)。为了进一步研究这种噬菌体收缩现象,在pH 8、4℃条件下对野生型噬菌体进行氯仿处理后,分别筛选出了34株对氯仿具有抗性的fd噬菌体分离株和26株M13噬菌体分离株。对34株fd噬菌体分离株的基因VIII进行DNA测序,发现了5种不同的突变体:分别是D5H、M28L、V31L、I37T和S50T。所有26株M13噬菌体分离株均为I37T。这些突变体对氯仿的敏感性各不相同,但在4℃处理过程中,它们的收缩速度均比野生型噬菌体慢得多。在37℃时,它们的收缩情况与野生型噬菌体相同。定点诱变表明,上述单个突变赋予了氯仿抗性。在噬菌体的结构模型中,D5H位点位于外部,S50T位点位于内部。M28L和I37T位点埋藏在中间一个主要为疏水的区域。尽管这4个突变体在径向呈分散分布,但在模型中它们在轴向被定位到一个薄盘中。最后一个突变位点V31L不在这个盘中,但该位点靠近M28L和I37T位点,并且还通过一个深的疏水孔或凹陷与表面接触。这5个突变体、它们的位置以及它们对收缩的不同影响表明,氯仿诱导的收缩涉及一种特定机制,而不是普遍的溶剂诱导变性,并且关键的结构变化发生在噬菌体的局部水平。这些结果进一步支持了以下观点:丝状结构→I型→S型的顺序收缩模拟了噬菌体穿透过程中的相应步骤,而反过来则是噬菌体组装过程中的相应步骤。

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