Yoon Jang W, Minnich Scott A, Ahn Jong S, Park Yong H, Paszczynski Andrzej, Hovde Carolyn J
Department of Microbiology, Molecular Biology and Biochemistry, University of Idaho, Moscow, ID 83844-3052, USA.
Mol Microbiol. 2004 Jan;51(2):419-35. doi: 10.1046/j.1365-2958.2003.03827.x.
Escherichia coli O157:H7 survives in diverse environments from the ruminant gastrointestinal tract to cool nutrient-dilute water. We hypothesized that the gene regulation required for this flexibility includes intrinsically curved DNA that responds to environmental changes. Three intrinsically curved DNAs were cloned from the E. coli O157:H7 virulence plasmid (pO157), sequenced and designated Bent 1 through Bent 3 (BNT1, BNT2 and BNT3). Compared to BNT1 and BNT3, BNT2 had characteristics typical of intrinsically curved DNA including electrophoretic gel retardation at 4 degrees C, six partially phased adenine:thymine tracts and transcriptional activation. BNT2::lacZ operon fusions showed that BNT2 activated transcription at 24 degrees C compared to 37 degrees C and was partially repressed by a bacterial nucleoid-associated protein H-NS. BNT2 regulated the E. coli attaching and effacing gene-positive conserved fragments 1-4 (ecf1-4) that are conserved in Shiga toxin-producing E. coli associated with human disease. Experimental analyses showed that ecf1-4 formed an operon. ecf1, 2 and 3 encoded putative proteins associated with bacterial surface polysaccharide biosynthesis and invasion and ecf4 complemented a chromosomal deletion of lpxM encoding lipid A myristoyl transferase. Mass spectrometric analysis of lipid A from ecf and lpxM single and double mutants showed that myristoylation was altered at lower temperature.
大肠杆菌O157:H7能在从反刍动物胃肠道到低温、营养稀薄水体等多种环境中存活。我们推测,这种适应性所需的基因调控包括对环境变化作出反应的固有弯曲DNA。从大肠杆菌O157:H7毒力质粒(pO157)中克隆出三个固有弯曲DNA,测序后命名为弯曲1至弯曲3(BNT1、BNT2和BNT3)。与BNT1和BNT3相比,BNT2具有固有弯曲DNA的典型特征,包括在4℃时的电泳凝胶阻滞、六个部分相位的腺嘌呤:胸腺嘧啶序列以及转录激活。BNT2::lacZ操纵子融合实验表明,与37℃相比,BNT2在24℃时激活转录,并且受到一种细菌类核相关蛋白H-NS的部分抑制。BNT2调控大肠杆菌紧密黏附并抹平基因阳性保守片段1至4(ecf1 - 4),这些片段在与人类疾病相关的产志贺毒素大肠杆菌中是保守的。实验分析表明,ecf1 - 4形成一个操纵子。ecf1、2和3编码与细菌表面多糖生物合成和侵袭相关的假定蛋白,ecf4补充了编码脂多糖A肉豆蔻酰转移酶的lpxM基因的染色体缺失。对ecf和lpxM单突变体及双突变体的脂多糖A进行质谱分析表明,在较低温度下肉豆蔻酰化发生了改变。