Inagaki K, Hikita T, Yanagidani S, Nomura Y, Kishimoto N, Tano T, Tanaka H
Division of Bioresources Science, Faculty of Agriculture, Okayama University, Japan.
Biosci Biotechnol Biochem. 1993 Oct;57(10):1716-21. doi: 10.1271/bbb.57.1716.
A restriction endonuclease, Aor13HI, an isoschizomer of BspMII, was purified to homogeneity from cell extracts of Acidiphilium organovorum strain 13H. The enzyme has a molecular mass of 60,000 daltons and consists of two subunits identical in molecular mass of 30,000 daltons. Aor13HI endonuclease, like BspMII, recognizes the palindromic six-base sequence 5'-TCCGGA-3', and cleaves between the T and C to produce a four-base 5' extension. Aor13HI is not inhibited by dam-dependent methylation. The isoelectric point of the enzyme is 5.7. Aor13HI activity was maximum at pH 7.5, 100 mM KCl, 7.5-10 mM MgCl2, and 55 degrees C. The enzyme was stable up to 60 degrees C. The N-terminal amino acid sequence (30 residues) of Aor13HI did not show any similarity with the sequence of other restriction endonucleases reported.
一种限制性内切酶Aor13HI,它是BspMII的同裂酶,从嗜酸有机营养菌13H菌株的细胞提取物中纯化至同质。该酶的分子量为60,000道尔顿,由两个分子量为30,000道尔顿的相同亚基组成。Aor13HI内切酶与BspMII一样,识别回文六碱基序列5'-TCCGGA-3',并在T和C之间切割,产生一个四碱基的5'延伸。Aor13HI不受依赖于dam的甲基化抑制。该酶的等电点为5.7。Aor13HI的活性在pH 7.5、100 mM KCl、7.5 - 10 mM MgCl2和55℃时最高。该酶在高达60℃时稳定。Aor13HI的N端氨基酸序列(30个残基)与已报道的其他限制性内切酶的序列没有任何相似性。