Lee S F, Forsberg C W, Gibbins A M
Department of Microbiology, University of Guelph, Ontario, Canada.
J Bacteriol. 1992 Aug;174(16):5275-83. doi: 10.1128/jb.174.16.5275-5283.1992.
Fibrobacter succinogenes is an important cellulolytic bacterium found in the rumen and cecum of herbivores. Numerous attempts to introduce foreign DNA into F. succinogenes S85 have failed, suggesting the presence of genetic barriers in this organism. Results from this study clearly demonstrate that F. succinogenes S85 possesses a type II restriction endonuclease, FsuI, which recognizes the sequence 5'-GG(A/T)CC-3'. Analysis of the restriction products on sequencing gels showed that FsuI cleaves between the two deoxyguanosine residues, yielding a 3-base 5' protruding end. These data demonstrate that FsuI is an isoschizomer of AvaII. A methyltransferase activity has been identified in the cell extract of F. succinogenes S85. This activity modified DNA in vitro and protected the DNA from the restriction by FsuI and AvaII. DNA modified in vivo by a cloned methylase gene, which codes for M.Eco47II, also protected the DNA from restriction by FsuI, suggesting that FsuI is inhibited by methylation at one or both deoxycytosine residues of the recognition sequence. The methyltransferase activity in F. succinogenes S85 is likely modifying the same deoxycytosine residues, but the exact site(s) is unknown. A highly active DNase (DNase A) was also isolated from the cell extract of this organism. DNase A is an endonuclease which showed high activity on all forms of DNA (single stranded, double-stranded, linear, and circular) but no activity on RNA. In vitro, the DNase A hydrolyzed F. succinogenes S85 DNA extensively, indicating the lack of protection against hydrolysis by this enzyme. In the presence of Mg2+, DNA was hydrolyzed to fragments of 8 to 10 nucleotides in length. The presence of DNase A and the type II restriction-modification system of F. succinogenes S85 may be the barriers preventing the introduction of foreign DNA into this bacterium.
琥珀酸纤维杆菌是在食草动物瘤胃和盲肠中发现的一种重要的纤维素分解细菌。许多将外源DNA导入琥珀酸纤维杆菌S85的尝试均告失败,这表明该生物体中存在遗传障碍。本研究结果清楚地表明,琥珀酸纤维杆菌S85拥有一种II型限制性内切酶FsuI,其识别序列为5'-GG(A/T)CC-3'。对测序凝胶上的限制性产物进行分析表明,FsuI在两个脱氧鸟苷残基之间切割,产生一个3碱基的5'突出末端。这些数据表明FsuI是AvaII的同裂酶。在琥珀酸纤维杆菌S85的细胞提取物中已鉴定出一种甲基转移酶活性。这种活性在体外修饰DNA,并保护DNA免受FsuI和AvaII的限制。由编码M.Eco47II的克隆甲基化酶基因在体内修饰的DNA也保护DNA免受FsuI的限制,这表明FsuI在识别序列的一个或两个脱氧胞嘧啶残基处被甲基化抑制。琥珀酸纤维杆菌S85中的甲基转移酶活性可能修饰相同的脱氧胞嘧啶残基,但确切位点未知。还从该生物体的细胞提取物中分离出一种高活性的DNA酶(DNA酶A)。DNA酶A是一种内切酶,对所有形式的DNA(单链、双链、线性和环状)均表现出高活性,但对RNA无活性。在体外,DNA酶A广泛水解琥珀酸纤维杆菌S85的DNA,表明该酶缺乏对水解的保护作用。在Mg2+存在的情况下,DNA被水解成长度为8至10个核苷酸的片段。DNA酶A的存在以及琥珀酸纤维杆菌S85的II型限制修饰系统可能是阻止外源DNA导入该细菌的障碍。