Kumar Ravinder, Pinnaka Anil Kumar, Krishnan Beena
Microbial Type Culture Collection and Gene Bank (MTCC), CSIR-Institute of Microbial Technology, Chandigarh, India.
G.N. Ramachandran Protein Centre, CSIR-Institute of Microbial Technology, Chandigarh, India.
Extremophiles. 2017 May;21(3):523-535. doi: 10.1007/s00792-017-0922-6. Epub 2017 Mar 18.
A moderately thermophilic Gram-negative bacterium isolated from the Polok hot spring, Sikkim, India, was identified as a strain (PL17) of Tepidimonas fonticaldi by 16S rDNA sequencing. T. fonticaldi PL17 produces a Type IIP restriction endonuclease; named TfoI. Restriction mapping, run-off sequencing of TfoI-digests of dsDNA fragments, and end compatibility of TfoI with NdeI confirmed that the enzyme recognizes and cleaves the sequence 5'-T^TAA-3', and is thus an isoschizomer of MseI. The TfoI restriction-modification genes in the T. fonticaldi PL17 genome were identified, and the annotated TfoI protein encodes a protein of 181 amino acid residues that shares 47.2% sequence identity with MseI. The native enzyme was purified using a four-column chromatography protocol, and its functional homogeneity was confirmed by standard quality control tests. The ESI-MS measured molecular weight of purified TfoI (20.696 kDa) is in agreement with that of the calculated monomeric molecular weight of the predicted TfoI protein sequence (20.694 kDa). TfoI exhibits optimal activity in the temperature range of 55-70 °C with Mg or Co as cofactor. Similar to its isoschizomers, TfoI can be used as the frequent cutter for genome analysis.
从印度锡金邦波洛克温泉分离出的一株中度嗜热革兰氏阴性菌,经16S rDNA测序鉴定为丰蒂卡温泉单胞菌菌株(PL17)。丰蒂卡温泉单胞菌PL17产生一种IIP型限制性内切酶,命名为TfoI。通过限制性图谱分析、双链DNA片段的TfoI酶切产物的 runoff测序以及TfoI与NdeI的末端兼容性分析,证实该酶识别并切割序列5'-T^TAA-3',因此是MseI的同裂酶。鉴定了丰蒂卡温泉单胞菌PL17基因组中的TfoI限制修饰基因,注释的TfoI蛋白编码一个由181个氨基酸残基组成的蛋白质,与MseI的序列同一性为47.2%。使用四柱层析方案纯化天然酶,并通过标准质量控制测试确认其功能均一性。电喷雾电离质谱法测得的纯化TfoI的分子量(20.696 kDa)与预测的TfoI蛋白序列的计算单体分子量(20.694 kDa)一致。TfoI在以Mg或Co作为辅因子的情况下,在55-70°C的温度范围内表现出最佳活性。与其同裂酶类似,TfoI可作为基因组分析的常用切割酶。