Hofreuter Dirk, Karnholz Arno, Haas Rainer
Max von Pettenkofer Institut für Hygiene und Medizinische Mikrobiologie, LMU München, München, Germany.
Int J Med Microbiol. 2003 Jun;293(2-3):153-65. doi: 10.1078/1438-4221-00258.
The human gastric pathogen Helicobacter pylori is naturally competent for genetic transformation. The H. pylori comB gene duster encodes the VirB4-homologous ATPase ComB4 and the structural proteins ComB7-ComB10, which share significant sequence identity to the Agrobacterium tumefaciens virB-encoded type IV secretion system. To study the topology of the ComB7-10 proteins, we applied TnMax transposon mutagenesis by generating fusions of ComB proteins with mature beta-lactamase (BlaM) or alkaline phosphatase (PhoA). Our data show that the putative lipoprotein ComB7 is secreted and is found membrane-attached, probably by its lipid anchor. According to our topology mapping ComB8 is a bitopic membrane protein with a short N-terminal portion in the cytoplasm and the remainder of the protein expanding into the periplasmic space. ComB9 was verified as a periplasmic protein, tightly attached to the membrane. The N-terminus of ComB10 is anchored in the cytoplasmic membrane and the major portion of the protein, including a putative coiled-coil domain, is located in the periplasm. Limited protease digestion and protein extraction under different salt and pH conditions confirmed the periplasmic localization and the tight membrane association of the ComB protein complex. A hypothetical model of the ComB DNA transformation pore in H. pylori is presented.
人类胃部病原体幽门螺杆菌具有天然的遗传转化能力。幽门螺杆菌的comB基因簇编码与VirB4同源的ATP酶ComB4以及结构蛋白ComB7-ComB10,它们与根癌土壤杆菌virB编码的IV型分泌系统具有显著的序列同一性。为了研究ComB7-10蛋白的拓扑结构,我们通过将ComB蛋白与成熟的β-内酰胺酶(BlaM)或碱性磷酸酶(PhoA)融合,应用TnMax转座子诱变技术。我们的数据表明,推测的脂蛋白ComB7被分泌出来,并通过其脂质锚定附着在膜上。根据我们的拓扑结构图谱,ComB8是一种双拓扑膜蛋白,其短的N端部分位于细胞质中,而蛋白质的其余部分延伸到周质空间。ComB9被证实为周质蛋白,紧密附着在膜上。ComB10的N端锚定在细胞质膜中,蛋白质的主要部分,包括一个推测的卷曲螺旋结构域,位于周质中。在不同盐浓度和pH条件下进行的有限蛋白酶消化和蛋白质提取,证实了ComB蛋白复合物的周质定位和与膜的紧密结合。本文提出了幽门螺杆菌中ComB DNA转化孔的假设模型。