Kobayashi T, Takao M, Oikawa A, Yasui A
Research Institute for Tuberculosis and Cancer, Tohoku University, Sendai, Japan.
Nucleic Acids Res. 1989 Jun 26;17(12):4731-44. doi: 10.1093/nar/17.12.4731.
By using a synthetic DNA probe derived from an amino acid sequence in the most conserved region of three known photolyases (Escherichia coli, Anacystis nidulans and Saccharomyces cerevisiae), we isolated a DNA fragment containing two long open reading frames (ORFs) from a genomic DNA library of Streptomyces griseus. One ORF encodes a polypeptide of 455 amino acids (Mr 50594), which exhibits substantial similarities with the other three photolyases. Photoreactivation-repair deficient E. coli cells could be converted into photoreactivatable ones by introduction of plasmids harboring this ORF, indicating that this is the photolyase gene of S. griseus. The deduced aa sequence of Streptomyces photolyase was most similar to that of E. coli. The putative DNA binding site as well as cofactor binding regions were proposed.
通过使用源自三种已知光解酶(大肠杆菌、集胞藻和酿酒酵母)最保守区域氨基酸序列的合成DNA探针,我们从灰色链霉菌的基因组DNA文库中分离出一个包含两个长开放阅读框(ORF)的DNA片段。其中一个ORF编码一个由455个氨基酸组成的多肽(Mr 50594),它与其他三种光解酶具有显著的相似性。通过导入携带该ORF的质粒,光复活修复缺陷的大肠杆菌细胞可以转化为可光复活的细胞,这表明这就是灰色链霉菌的光解酶基因。链霉菌光解酶推导的氨基酸序列与大肠杆菌的最为相似。还提出了假定的DNA结合位点以及辅因子结合区域。