Farchaus J W, Barz W P, Grünberg H, Oesterhelt D
Max-Planck Institut für Biochemie, Martinsried, Germany.
EMBO J. 1992 Aug;11(8):2779-88. doi: 10.1002/j.1460-2075.1992.tb05345.x.
The puf operon in Rhodobacter sphaeroides contains the genes for the light-harvesting antenna complex I (LHI), the reaction centre (RC) L and M subunits and an additional small open reading frame identified as pufX. It has been demonstrated before that a photosynthetically incompetent pufLMX deletion strain was not complemented by a plasmid-borne truncated puf operon version lacking only pufX, although expression of the pufL and pufM gene products was restored. We demonstrate here that the functional reinsertion of only the pufX open reading frame into the same construct is sufficient and necessary for complementation of the non-photosynthetic phenotype. We also demonstrate that the observed lack of photoheterotrophic growth in the absence of pufX is not the result of decreased light-harvesting ability, but rather the result of an impairment in light-driven cyclic electron transfer. Western blots using polyclonal antibodies against a synthetic peptide corresponding to a portion of the DNA-derived pufX amino acid sequence showed that the pufX open reading frame is expressed and that the gene product has an M(r) of 8-10,000 on SDS gels; a value close to the predicted mass of 9 kDa. The pufX polypeptide was localized to the intracytoplasmic membrane fraction and appeared to co-purify with the RC-LHI complex. It is suggested that the pufX polypeptide is associated with the RC-LHI complex and that it may play a critical role in facilitating the interaction between this complex and other components required for light-driven cyclic electron transfer.
球形红杆菌中的puf操纵子包含编码光捕获天线复合体I(LHI)、反应中心(RC)的L和M亚基以及另一个被鉴定为pufX的小开放阅读框的基因。之前已经证明,一个光合功能缺失的pufLMX缺失菌株不能被仅缺少pufX的质粒携带的截短puf操纵子版本互补,尽管pufL和pufM基因产物的表达得以恢复。我们在此证明,仅将pufX开放阅读框功能性重新插入到同一构建体中对于非光合表型的互补是充分且必要的。我们还证明,在没有pufX的情况下观察到的光异养生长缺乏不是光捕获能力降低的结果,而是光驱动循环电子传递受损的结果。使用针对与DNA衍生的pufX氨基酸序列的一部分相对应的合成肽的多克隆抗体进行的蛋白质免疫印迹显示,pufX开放阅读框被表达,并且该基因产物在SDS凝胶上的分子量为8 - 10,000;该值接近预测的9 kDa质量。pufX多肽定位于胞内膜部分,并且似乎与RC-LHI复合体共纯化。有人提出,pufX多肽与RC-LHI复合体相关联,并且它可能在促进该复合体与光驱动循环电子传递所需的其他组分之间的相互作用中起关键作用。