Ianulaĭtis A A, Stakenas P S, Piatrushite M P, Bitinaĭte Iu B, Klimashauskas S I
Mol Biol (Mosk). 1984 Jan-Feb;18(1):115-29.
Fourteen restriction endonucleases and 4 methylases were isolated and purified from 14 strains of Citrobacter freundii and Escherichia coli, which were isolated from natural sources. To determine the nucleotide sequence recognized by the endonucleases a comparison of DNA cleavage patterns, the evaluation of the cleavage frequency of some DNA with known recognition sequences and mapping was used. It was determined that Cfr101 is a new enzyme recognizing 5'PuCCGGPy. Other restriction enzymes isolated were isoschizomers of: Cfr5I, Cfr11I, Eco60I, Eco61I--EcoRII; Cfr4I, Cfr8I, Cfr13I--Sau96I; Cfr6I--PvuII, Cfr9I--SmaI, Eco26I--HgiJII; Eco32I--EcoRV; Eco52I--XmaIII; Eco56I--NaeI. Some of the enzymes in C. freundii and E. coli were found for the first time. The methylases MCfrI; MCfr6I, MCfr9I and MCfr10I recognize the same nucleotide sequence as specific endonucleases isolated from the same strain. DNA modification in vitro by MCfrI and MCfr10I yields 5-methylcytosine and 4-methylcytosine by MCfr6I and MCfr9I.
从14株自然来源分离的弗氏柠檬酸杆菌和大肠杆菌中分离并纯化出14种限制性核酸内切酶和4种甲基化酶。为了确定这些内切酶识别的核苷酸序列,采用了DNA切割模式比较、对一些具有已知识别序列的DNA的切割频率评估以及图谱绘制等方法。已确定Cfr101是一种识别5'PuCCGGPy的新酶。分离出的其他限制性酶是以下酶的同裂酶:Cfr5I、Cfr11I、Eco60I、Eco61I - EcoRII;Cfr4I、Cfr8I、Cfr13I - Sau96I;Cfr6I - PvuII、Cfr9I - SmaI、Eco26I - HgiJII;Eco32I - EcoRV;Eco52I - XmaIII;Eco56I - NaeI。弗氏柠檬酸杆菌和大肠杆菌中的一些酶是首次发现。甲基化酶MCfrI、MCfr6I、MCfr9I和MCfr10I识别与从同一菌株分离出的特定内切酶相同的核苷酸序列。MCfrI和MCfr10I在体外进行DNA修饰时产生5-甲基胞嘧啶,MCfr6I和MCfr9I产生4-甲基胞嘧啶。