Liu Fei, Fang Bai-Shan
Province Key Laboratory of Industrial Biotechnology( Huaqiao University), Quanzhou 362021, China.
Sheng Wu Gong Cheng Xue Bao. 2007 Jan;23(1):133-7.
Degenerate PCR primers were designed by multiple alignment of the protein sequences of known structural genes encoding the catalytic subunits of NiFe-hydrogenases obtained from Swiss-Prot Protein Sequence Database through CLUSTAL-W software and compared for conserved sequence motifs. An amplified PCR product 1 kb in size was obtained from the genomic DNA of Klebsiella pneumoniae using a set of degenerate primers, and then inverse PCR technique was used to obtain the full hydrogenase coding region. A predicted secondary structure and 3D structural model were constructed by homology modeling and docking. On the basis of these results, it was inferred that NiFe-hydrogenase from Klebsiella pneumoniae belongs to the membrane-bound H2 evolving hydrogenase group (Ech hydrogenase group).
通过CLUSTAL-W软件对从瑞士蛋白质数据库(Swiss-Prot Protein Sequence Database)获得的编码NiFe氢化酶催化亚基的已知结构基因的蛋白质序列进行多重比对,设计简并PCR引物,并比较保守序列基序。使用一组简并引物从肺炎克雷伯菌的基因组DNA中获得了大小为1 kb的扩增PCR产物,然后使用反向PCR技术获得完整的氢化酶编码区。通过同源建模和对接构建了预测的二级结构和三维结构模型。基于这些结果,推断肺炎克雷伯菌的NiFe氢化酶属于膜结合产氢氢化酶组(Ech氢化酶组)。