Kolosov V L, Zolotarev A S
Bioorg Khim. 1990 Aug;16(8):1060-8.
EcoRI and BamHI fragments of rye chloroplast DNA comprising psbA gene were cloned and a 2729 bp region was sequenced. Cloning of EcoRI fragment into pTZ19R plasmid led to a single nucleotide deletion in the coding region of psbA gene. A scheme of full-length psbA gene cloning is proposed, allowing one to escape the damage effect of the psbA gene expression product on the host cell. The differences between monocot and dicot in nucleotide sequences of DNA downstream of psbA genes are discussed. Gene rps19 is located 131 bp downstream from psbA gene on the complementary strand. The amino acid sequences of D1 and S19 proteins of different species are compared.
克隆了包含psbA基因的黑麦叶绿体DNA的EcoRI和BamHI片段,并对一个2729 bp的区域进行了测序。将EcoRI片段克隆到pTZ19R质粒中导致psbA基因编码区出现单个核苷酸缺失。提出了全长psbA基因克隆方案,可避免psbA基因表达产物对宿主细胞的损伤作用。讨论了单子叶植物和双子叶植物在psbA基因下游DNA核苷酸序列上的差异。基因rps19位于互补链上psbA基因下游131 bp处。比较了不同物种D1和S19蛋白的氨基酸序列。