The Central Region Laboratory, Center of Research and Diagnostics, Centers for Disease Control, Taichung City 40855, Taiwan.
Int J Med Microbiol. 2010 Jun;300(5):296-303. doi: 10.1016/j.ijmm.2009.11.003. Epub 2009 Dec 22.
Pulsed-field gel electrophoresis (PFGE) analysis revealed that the genomes of some pathogenic Escherichia coli O157:H7 strains, including EDL933, were resistant to NotI digestion. An amino acid sequence comparison suggested that the z2389 gene carried on prophage CP-933R in strain EDL933 is likely to encode a C(5)-cytosine methyltransferase. The z2389-equivalent gene was found in the NotI-resistant strains tested, but it was not detected in the NotI-susceptible strains. PFGE analysis of the wild-type EDL933 strain and of a z2389 null mutant revealed that z2389 was associated with full genome protection against NotI digestion and partial protection against EagI digestion. In vitro methylation experiments with purified recombinant protein demonstrated that Z2389 is capable of methylating NotI and EagI sites. Sequencing of bisulfite-treated DNA indicated that the methylation occurred at the first cytosine residue of the NotI recognition sequence, whereas EagI sites remained unmethylated or were methylated at the first cytosine residue. Thus, z2389 encodes a DNA cytosine methyltransferase that confers full protection to NotI sites.
脉冲场凝胶电泳(PFGE)分析表明,一些致病性大肠杆菌 O157:H7 菌株的基因组,包括 EDL933,对 NotI 消化具有抗性。氨基酸序列比较表明,在 EDL933 菌株的 CP-933R 噬菌体上携带的 z2389 基因可能编码 C(5)-胞嘧啶甲基转移酶。在测试的耐 NotI 菌株中发现了 z2389 等效基因,但在不耐 NotI 的菌株中未检测到。对野生型 EDL933 菌株和 z2389 缺失突变体的 PFGE 分析表明,z2389 与完全保护基因组免受 NotI 消化和部分保护免受 EagI 消化有关。用纯化的重组蛋白进行的体外甲基化实验表明,Z2389 能够甲基化 NotI 和 EagI 位点。亚硫酸氢盐处理的 DNA 测序表明,甲基化发生在 NotI 识别序列的第一个胞嘧啶残基上,而 EagI 位点保持未甲基化或在第一个胞嘧啶残基上甲基化。因此,z2389 编码一种 DNA 胞嘧啶甲基转移酶,可完全保护 NotI 位点。