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首页> 外文期刊>Nucleic acids research >Tsp49I (ACGT↓), a Thermostable Neoschizomer of the Type II Restriction Endonuclease MaeII (A↓CGT), Discovered in Isolates of the Genus Thermus from the Azores, Iceland and New Zealand
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Tsp49I (ACGT↓), a Thermostable Neoschizomer of the Type II Restriction Endonuclease MaeII (A↓CGT), Discovered in Isolates of the Genus Thermus from the Azores, Iceland and New Zealand

机译:Tsp49I(ACGT↓)是II型限制性内切核酸酶MaeII(A↓CGT)的耐高温新分裂体,位于亚速尔群岛,冰岛和新西兰的栖热菌属分离物中

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摘要

One hundred and forty eight isolates of the genus Thermus, from neutral and alkaline hot water springs on four continents, have been screened for the presence of restriction endonuclease activity. An isolate (SM49) from the island of Sao Miguel, in the Azores, showed a high level of restriction endonuclease activity when a cell-free extract was incubated with λ phage DNA at 65°C. A Type II restriction endonuclease (Tsp49I) has been partially purified from this isolate and the recognition and cleavage site determined. Tsp49I recognizes the four base sequence ACGT, which is the same as the recognition sequence of the mesophilic Type II restriction endonuclease MaeII. However, unlike MaeII, which cleaves DNA between the first and second base of the recognition sequence (A↓CGT), Tsp49I hydrolyses the phosphodiester bond in both strands of the substrate after the last base of the recognition sequence 5′-ACGT↓-3′, producing four base 3′-OH overhangs (sticky ends). The enzyme has a pH optimum of 9.0, requires 2 mM MgCl2 for maximum activity and retains full enzyme activity following incubation for 10 min at temperatures up to 80°C. Two further examples of the same restriction endonuclease specificity as Tsp49I were detected in Thermus isolates from Iceland (TspIDSI) and New Zealand (TspWAM8AI). The three MaeII neoschizomers, Tsp49I, TspIDSI and TspWA-M8AI, exhibit similar pH optima, heat stabilities and MgCl2 requirements, but differ in their requirements for NaCl and KCl.
机译:筛选了来自四大洲中性和碱性热水泉的Thermus属的148个分离株是否存在限制性核酸内切酶活性。当无细胞提取物与λ噬菌体DNA在65°C孵育时,来自亚速尔群岛圣米格尔岛的分离株(SM49)显示出高水平的限制性核酸内切酶活性。已从该分离物中部分纯化了II型限制性核酸内切酶(Tsp49I),并确定了识别位点和切割位点。 Tsp49I识别四个碱基序列ACGT,与嗜温II型限制性核酸内切酶MaeII的识别序列相同。但是,与MaeII不同,MaeII在识别序列的第一个碱基和第二个碱基之间切割DNA(A↓CGT),而Tsp49I在识别序列的5'-ACGT↓-3的最后一个碱基之后水解底物两条链中的磷酸二酯键。 ',产生四个碱基3'-OH突出端(粘性末端)。该酶的最适pH值为9.0,需要2 mM MgCl 2 才能发挥最大活性,并在高达80°C的温度下孵育10分钟后仍保持完整的酶活性。在来自冰岛(TspIDSI)和新西兰(TspWAM8AI)的Thermus分离物中检测到与Tsp49I相同的限制性内切酶特异性的另外两个例子。三种MaeII新近异构体Tsp49I,TspIDSI和TspWA-M8AI表现出相似的pH最佳值,热稳定性和MgCl 2 要求,但对NaCl和KCl的要求不同。

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