Lin N T, Liu T J, Lee T C, You B Y, Yang M H, Wen F S, Tseng Y H
Institute of Molecular Biology and Department of Botany, National Chung Hsing University, Taichung 402, Taiwan.
J Bacteriol. 1999 Apr;181(8):2465-71. doi: 10.1128/JB.181.8.2465-2471.1999.
Gene III (gIII) of phiLf, a filamentous phage specifically infecting Xanthomonas campestris pv. campestris, was previously shown to encode a virion-associated protein (pIII) required for phage adsorption. In this study, the transcription start site for the gene and the N-terminal sequence of the protein were determined, resulting in the revision of the translation initiation site from the one previously predicted for this gene. For comparative study, the gIII of phiXv, a filamentous phage specifically infecting X. campestris pv. vesicatoria, was cloned and sequenced. The deduced amino acid sequences of these two pIIIs exhibit a high degree of identity in their C-terminal halves and possess the structural features typical of the adsorption proteins of filamentous phages: a signal sequence in the N terminus, a long glycine-rich region near the center, and a hydrophobic membrane anchorage domain in the C terminus. The regions between gIII and the upstream gVIII, 128 nucleotides in both phages, are larger than those of other filamentous phages. A hybrid phage of phiXv, consisting of the phiLf pIII and all the other components derived from phiXv, was able to infect X. campestris pv. campestris but not X. campestris pv. vesicatoria, indicating that gIII is the gene specifying host specificity and demonstrating the interchangeability of the pIIIs.
phiLf是一种特异性感染野油菜黄单胞菌野油菜致病变种的丝状噬菌体,其基因III(gIII)先前已被证明编码噬菌体吸附所需的病毒粒子相关蛋白(pIII)。在本研究中,确定了该基因的转录起始位点和该蛋白的N端序列,从而对该基因的翻译起始位点进行了修正,使其与先前预测的位点不同。为了进行比较研究,克隆并测序了phiXv的gIII,phiXv是一种特异性感染野油菜黄单胞菌疮痂致病变种的丝状噬菌体。这两种pIII的推导氨基酸序列在其C端半部表现出高度的同一性,并具有丝状噬菌体吸附蛋白的典型结构特征:N端有一个信号序列,中心附近有一个富含甘氨酸的长区域,C端有一个疏水膜锚定结构域。gIII与上游gVIII之间的区域,在两种噬菌体中均为128个核苷酸,比其他丝状噬菌体的相应区域大。由phiLf pIII和所有其他来自phiXv的成分组成的phiXv杂交噬菌体能够感染野油菜黄单胞菌野油菜致病变种,但不能感染野油菜黄单胞菌疮痂致病变种,这表明gIII是决定宿主特异性的基因,并证明了pIII的可互换性。