首页> 外文OA文献 >Type II DNA restriction-modification system and an endonuclease from the ruminal bacterium Fibrobacter succinogenes S85.
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Type II DNA restriction-modification system and an endonuclease from the ruminal bacterium Fibrobacter succinogenes S85.

机译:II型DNA限制性修饰系统和瘤胃细菌琥珀酸纤维杆菌S85的核酸内切酶。

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摘要

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.
机译:琥珀酸纤维杆菌是在食草动物的瘤胃和盲肠中发现的一种重要的纤维素分解细菌。将外源DNA引入琥珀酸短杆菌S85的许多尝试均以失败告终,表明该生物体中存在遗传屏障。这项研究的结果清楚地表明,琥珀酸镰刀菌S85具有II型限制性核酸内切酶FsuI,该酶识别5'-GG(A / T)CC-3'序列。在测序凝胶上对限制性产物的分析表明,FsuI在两个脱氧鸟苷残基之间裂解,产生3碱基的5'突出端。这些数据证明FsuI是AvaII的同分异构体。已在琥珀酸杆菌S85的细胞提取物中鉴定出甲基转移酶活性。这种活性在体外修饰了DNA,并保护DNA不受FsuI和AvaII的限制。体内由克隆的甲基化酶基因修饰的DNA编码M.Eco47II,也保护DNA不受FsuI的限制,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。琥珀酸葡萄球菌S85中的甲基转移酶活性可能会修饰相同的脱氧胞嘧啶残基,但确切位点尚不清楚。还从该生物的细胞提取物中分离出高活性的DNase(DNase A)。 DNase A是一种核酸内切酶,对所有形式的DNA(单链,双链,线性和环状)均显示高活性,但对RNA无活性。在体外,DNase A广泛地水解了琥珀酸短螺旋杆菌S85 DNA,表明缺乏针对这种酶水解的保护作用。在存在Mg2 +的情况下,DNA水解为8至10个核苷酸长的片段。 DNase A的存在和琥珀酸镰刀菌S85的II型限制性修饰系统可能是阻止将外源DNA引入该细菌的障碍。

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