Furmanek B, Gromek K, Sektas M, Kaczorowski T
Department of Microbiology, University of Gdansk, Kladki 24, 80-822 Gdansk, Poland.
FEMS Microbiol Lett. 2001 Mar 15;196(2):171-6. doi: 10.1111/j.1574-6968.2001.tb10560.x.
Neisseria cuniculi produces the restriction enzyme NcuI which is an isoschizomer of MboII. We have demonstrated that NcuI recognizes a pentanucleotide sequence (5'-GAAGA-3'/3'-CTTCT-5'), and cleaves the DNA 8 and 7 nucleotides downstream from the recognition site leaving a single 3'-protruding nucleotide. We have purified this enzyme to electrophoretic homogeneity using a four-step chromatographic procedure. NcuI endonuclease is a monomeric protein with a M(r)=48,000+/-1000 under denaturing conditions. The properties of NcuI are consistent with those for MboII, the position of the cleavage site being identical and the pH profile and divalent cation requirements being similar. Moreover, NcuI cross-reacts strongly with anti-MboII serum suggesting the presence of similar antigenic determinants. We have determined the sequence of 20 N-terminal amino acids for NcuI and concluded that this sequence is identical to the N-terminal portion of the MboII enzyme.
兔奈瑟菌产生限制性内切酶NcuI,它是MboII的同裂酶。我们已经证明NcuI识别一个五核苷酸序列(5'-GAAGA-3'/3'-CTTCT-5'),并在识别位点下游8个和7个核苷酸处切割DNA,留下一个单一的3'-突出核苷酸。我们使用四步色谱法将该酶纯化至电泳纯。NcuI内切酶是一种单体蛋白,在变性条件下M(r)=48,000±1000。NcuI的特性与MboII一致,切割位点的位置相同,pH曲线和二价阳离子需求相似。此外,NcuI与抗MboII血清发生强烈交叉反应,表明存在相似的抗原决定簇。我们已经确定了NcuI的20个N端氨基酸序列,并得出该序列与MboII酶的N端部分相同的结论。