首页> 美国卫生研究院文献>Nucleic Acids Research >The Neisseria gonorrhoeae S.NgoVIII restriction/modification system: a type IIs system homologous to the Haemophilus parahaemolyticus HphI restriction/modification system.
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The Neisseria gonorrhoeae S.NgoVIII restriction/modification system: a type IIs system homologous to the Haemophilus parahaemolyticus HphI restriction/modification system.

机译:淋病奈瑟氏球菌S.NgoVIII限制/修饰系统:与副溶血嗜血杆菌HphI限制/修饰系统同源的IIs型系统。

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摘要

Strains of Neisseria gonorrhoeae possess numerous restriction-modification (R-M) systems. One of these systems, which has been found in all strains tested, encodes the S. NgoVIII specificity (5'TCACC 3') R-M system. We cloned two adjacent methyltransferase genes (dcmH and damH), each encoding proteins whose actions protect DNA from digestion by R.HphI or R.Ngo BI (5'TCACC 3'). The damH gene product is a N 6-methyladenine methyltransferase that recognizes this sequence. We constructed a plasmid containing multiple copies of the S.NgoVIII sequence, grew it in the presence of damH and used the HPLC to demonstrate the presence of N 6-methyladenine in the DNA. A second plasmid, containing overlapping damH and Escherichia coli dam recognition sequences in combination with various restriction digests, was used to identify which adenine in the recognition sequence was modified by damH. The predicted dcmH gene product is homologous to 5-methylcytosine methyltransferases. The products of both the dcmH and damH genes, as well as an open reading frame downstream of the damH gene are highly similar to the Haemophilus parahaemolyticus hphIMC , hphIMA and hphIR gene products, encoding the Hph I Type IIs R-M system. The S.NgoVIII R-M genes are flanked by a 97 bp direct repeat that may be involved in the mobility of this R-M system.
机译:淋病奈瑟氏球菌菌株具有许多限制性修饰(R-M)系统。在所有测试菌株中都发现了其中一种系统,该系统编码S. NgoVIII特异性(5'TCACC 3')R-M系统。我们克隆了两个相邻的甲基转移酶基因(dcmH和damH),每个基因编码的蛋白质的作用是保护DNA免于被R.HphI或R.Ngo BI消化(5'TCACC 3')。 damH基因产物是识别该序列的N 6-甲基腺嘌呤甲基转移酶。我们构建了一个包含S.NgoVIII序列多个副本的质粒,在damH存在下使其生长,并使用HPLC证明了DNA中存在N 6-甲基腺嘌呤。第二个质粒包含重叠的damH和大肠杆菌dam识别序列以及各种限制性酶切消化,用于鉴定识别序列中哪个腺嘌呤被damH修饰。预测的dcmH基因产物与5-甲基胞嘧啶甲基转移酶同源。 dcmH和damH基因的产物以及damH基因下游的开放阅读框与副溶血嗜血杆菌hphIMC,hphIMA和hphIR基因产物高度相似,编码Hph I型IIs R-M系统。 S.NgoVIII R-M基因的侧面是一个97 bp的直接重复序列,可能与该R-M系统的移动性有关。

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