Whelan K F, Sherburne R K, Taylor D E
Department of Medical Microbiology and Immunology, University of Alberta, Edmonton, Canada.
J Bacteriol. 1997 Jan;179(1):63-71. doi: 10.1128/jb.179.1.63-71.1997.
The IncHI2 plasmid R478 specifies resistance to potassium tellurite (Te(r)), to some bacteriophages (Phi), and to pore-forming colicins (PacB). The genes encoding the three phenotypes are linked, and an 8.4-kb fragment of R478 DNA encoding them cannot be subcloned unless cocloned with a second section of the plasmid. Subclone pKFW4A contains a 5.9-kb BamHI-EcoRI fragment which caused some toxicity when present in Escherichia coli cells. Bacterial cells containing freshly transformed pKFW4A, examined by light microscopy and electron microscopy, had a filamentous morphology consistent with a block in septation. Insertion of transposon Tn1000 into terZ, -A, -B, and -C genes of pKFW4A resulted in the loss of the filamentation phenotype. Deletion of several regions of the clone confirmed that these latter components are involved in the filamentation phenotype. The region specifying protection from toxicity caused by the larger 8.4-kb fragment (encompassing this cluster and the entire 5.9-kb section of pKFW4A) was sequenced and analyzed by T7 polymerase expression and Tn1000 mutagenesis. Three open reading frames, terW, terY, and terX, were identified in a 2.6-kb region. Two polypeptides with approximate molecular masses of 18 and 28 kDa were expressed in CSRDE3 cells and were consistent with TerW (17.1 kDa; 155 amino acids [aa]) and TerY (26.9 kDa; 248 aa), whereas a protein of 213 aa deduced from terX was not observed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The terX gene product shows strong identity with the previously identified TerE, TerD, and TerZ polypeptides, and there is a conserved motif of 13 residues, GDN(R/L)TG(E/A)GDGDDE, within this group of polypeptides. Complementation analysis indicated that terW, located approximately 6.0 kb upstream of terZ, brings about protection of cells from toxic effects of components of the Te(r), Phi, and PacB cluster.
IncHI2质粒R478赋予对亚碲酸钾(Te(r))、某些噬菌体(Phi)和成孔大肠杆菌素(PacB)的抗性。编码这三种表型的基因是连锁的,除非与质粒的第二部分共克隆,否则R478 DNA编码它们的8.4 kb片段不能被亚克隆。亚克隆pKFW4A包含一个5.9 kb的BamHI - EcoRI片段,当它存在于大肠杆菌细胞中时会产生一些毒性。通过光学显微镜和电子显微镜检查,含有新转化的pKFW4A的细菌细胞具有丝状形态,这与隔膜形成受阻一致。将转座子Tn1000插入pKFW4A的terZ、-A、-B和-C基因导致丝状化表型丧失。对该克隆的几个区域进行缺失分析证实,这些后面的组分与丝状化表型有关。对指定免受较大的8.4 kb片段(包含该簇和pKFW4A的整个5.9 kb部分)毒性影响的区域进行测序,并通过T7聚合酶表达和Tn1000诱变进行分析。在一个2.6 kb区域内鉴定出三个开放阅读框,terW、terY和terX。在CSRDE3细胞中表达了两种分子量约为18 kDa和28 kDa的多肽,它们与TerW(17.1 kDa;155个氨基酸[aa])和TerY(26.9 kDa;248 aa)一致,而通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳未观察到从terX推导的2