Edman U, Edman J C, Lundgren B, Santi D V
Intercampus Program for Molecular Parasitology, University of California, San Francisco 94143.
Proc Natl Acad Sci U S A. 1989 Sep;86(17):6503-7. doi: 10.1073/pnas.86.17.6503.
The thymidylate synthase (TS) gene from Pneumocystis carinii has been isolated from complementary and genomic DNA libraries and expressed in Escherichia coli. The coding sequence of TS is 891 nucleotides, encoding a 297-amino acid protein of Mr 34,269. The deduced amino acid sequence is similar to TS from other organisms and is most closely related to the enzyme from Saccharomyces cerevisiae with 65% identity. TS is found on a 330-kilobase-pair chromosome in P. carinii. While TS and dihydrofolate reductase reside on a single polypeptide chain in all protozoa studied to date, TS is not linked to dihydrofolate reductase in P. carinii. The TS gene shows the presence of four small intervening sequences, some of which interrupt the coding sequence in highly ordered structural regions of the protein. Heterologous expression of P. carinii TS in E. coli was accomplished by cloning the coding sequence into plasmid vectors under control of the lac and tac promoters. These constructs direct the synthesis of catalytically active enzyme to the extent of 2% of total soluble protein.
卡氏肺孢子虫的胸苷酸合成酶(TS)基因已从互补DNA文库和基因组DNA文库中分离出来,并在大肠杆菌中表达。TS的编码序列为891个核苷酸,编码一个297个氨基酸的蛋白质,分子量为34,269。推导的氨基酸序列与其他生物的TS相似,与酿酒酵母的酶关系最为密切,同一性为65%。TS存在于卡氏肺孢子虫的一条330千碱基对的染色体上。虽然在迄今为止研究的所有原生动物中,TS和二氢叶酸还原酶位于单一多肽链上,但在卡氏肺孢子虫中,TS与二氢叶酸还原酶不相连。TS基因显示存在四个小的间隔序列,其中一些在蛋白质的高度有序结构区域中断了编码序列。通过将编码序列克隆到受lac和tac启动子控制的质粒载体中,实现了卡氏肺孢子虫TS在大肠杆菌中的异源表达。这些构建体指导合成具有催化活性的酶,其产量达到总可溶性蛋白的2%。