Kiley P J, Donohue T J, Havelka W A, Kaplan S
J Bacteriol. 1987 Feb;169(2):742-50. doi: 10.1128/jb.169.2.742-750.1987.
The genes for the Rhodobacter sphaeroides light-harvesting B875-beta, and B875-alpha polypeptides (pufB and pufA) are closely linked to the genes for the reaction center L and reaction center M polypeptides (pufL and pufM) on what has been termed the puf operon (gene order, pufB, A, L, M). The DNA sequence of the pufB and pufA structural genes from wild-type R. sphaeroides 2.4.1 was determined and aligned with the available amino acid sequence of the wild-type B875-beta and B875-alpha polypeptides. The relative levels of the B875-beta and B875-alpha and the reaction center L and reaction center M polypeptides synthesized in a homologous cell-free transcription-translation system were compared with those found in vivo. Analysis of the gene products produced in vitro with plasmids containing deletions upstream of the pufB structural gene identified a region of DNA required for expression of the B875-beta and B875-alpha polypeptides. These results support the hypothesis that the mapped 5' termini of the large and small puf operon transcripts represent transcription initiation sites.
球形红杆菌捕光B875-β和B875-α多肽(pufB和pufA)的基因与反应中心L和反应中心M多肽(pufL和pufM)的基因紧密相连,位于所谓的puf操纵子上(基因顺序为pufB、A、L、M)。测定了野生型球形红杆菌2.4.1的pufB和pufA结构基因的DNA序列,并与野生型B875-β和B875-α多肽的可用氨基酸序列进行比对。将在同源无细胞转录-翻译系统中合成的B875-β和B875-α以及反应中心L和反应中心M多肽的相对水平与体内发现的水平进行比较。用含有pufB结构基因上游缺失的质粒对体外产生的基因产物进行分析,确定了B875-β和B875-α多肽表达所需的DNA区域。这些结果支持了这样的假说,即大的和小的puf操纵子转录本的定位5'末端代表转录起始位点。