Webb R, Troyan T, Sherman D, Sherman L A
Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907-1392.
J Bacteriol. 1994 Aug;176(16):4906-13. doi: 10.1128/jb.176.16.4906-4913.1994.
Growth of Synechococcus sp. strain PCC 7942 in iron-deficient media leads to the accumulation of an approximately 34-kDa protein. The gene encoding this protein, mapA (membrane-associated protein A), has been cloned and sequenced (GenBank accession number, L01621). The mapA transcript is not detectable in normally grown cultures but is stably accumulated by cells grown in iron-deficient media. However, the promoter sequence for this gene does not resemble other bacterial iron-regulated promoters described to date. The carboxyl-terminal region of the derived amino acid sequence of MapA resembles bacterial proteins involved in iron acquisition, whereas the amino-terminal end of MapA has a high degree of amino acid identity with the abundant, chloroplast envelope protein E37. An approach employing improved cellular fractionation techniques as well as electron microscopy and immunocytochemistry was essential in localizing MapA protein to the cytoplasmic membrane of Synechococcus sp. strain PCC 7942. When these cells were grown under iron-deficient conditions, a significant fraction of MapA could also be localized to the thylakoid membranes.
聚球藻属(Synechococcus)PCC 7942菌株在缺铁培养基中生长会导致一种约34 kDa蛋白质的积累。编码该蛋白质的基因mapA(膜相关蛋白A)已被克隆和测序(GenBank登录号:L01621)。在正常生长的培养物中检测不到mapA转录本,但在缺铁培养基中生长的细胞会稳定积累该转录本。然而,该基因的启动子序列与迄今描述的其他细菌铁调节启动子不同。MapA推导氨基酸序列的羧基末端区域类似于参与铁摄取的细菌蛋白质,而MapA的氨基末端与丰富的叶绿体包膜蛋白E37具有高度的氨基酸同一性。采用改进的细胞分级分离技术以及电子显微镜和免疫细胞化学的方法对于将MapA蛋白定位到聚球藻属PCC 7942菌株的细胞质膜至关重要。当这些细胞在缺铁条件下生长时,相当一部分MapA也可定位到类囊体膜上。