Andrews S C, Harrison P M, Guest J R
Krebs Institute, Department of Molecular Biology, University of Sheffield, United Kingdom.
J Bacteriol. 1989 Jul;171(7):3940-7. doi: 10.1128/jb.171.7.3940-3947.1989.
The bacterioferritin (BFR) of Escherichia coli K-12 is an iron-storage hemoprotein, previously identified as cytochrome b1. The bacterioferritin gene (bfr) has been cloned, sequenced, and located in the E. coli linkage map. Initially a gene fusion encoding a BFR-lambda hybrid protein (Mr 21,000) was detected by immunoscreening a lambda gene bank containing Sau3A restriction fragments of E. coli DNA. The bfr gene was mapped to 73 min (the str-spc region) in the physical map of the E. coli chromosome by probing Southern blots of restriction digests of E. coli DNA with a fragment of the bfr gene. The intact bfr gene was then subcloned from the corresponding lambda phage from the gene library of Kohara et al. (Y. Kohara, K. Akiyama, and K. Isono, Cell 50:495-508, 1987). The bfr gene comprises 474 base pairs and 158 amino acid codons (including the start codon), and it encodes a polypeptide having essentially the same size (Mr 18,495) and N-terminal sequence as the purified protein. A potential promoter sequence was detected in the 5' noncoding region, but it was not associated with an "iron box" sequence (i.e., a binding site for the iron-dependent Fur repressor protein). BFR was amplified to 14% of the total protein in a bfr plasmid-containing strain. An additional unidentified gene (gen-64), encoding a relatively basic 64-residue polypeptide and having the same polarity as bfr, was detected upstream of the bfr gene.
大肠杆菌K-12的细菌铁蛋白(BFR)是一种铁储存血红蛋白,先前被鉴定为细胞色素b1。细菌铁蛋白基因(bfr)已被克隆、测序并定位在大肠杆菌连锁图谱中。最初,通过免疫筛选一个包含大肠杆菌DNA Sau3A限制片段的λ基因文库,检测到一个编码BFR-λ杂交蛋白(分子量21,000)的基因融合体。通过用bfr基因的一个片段探测大肠杆菌DNA限制酶切片段的Southern印迹,将bfr基因定位到大肠杆菌染色体物理图谱的73分钟处(str-spc区域)。然后从Kohara等人(Y. Kohara、K. Akiyama和K. Isono,《细胞》50:495-508,1987)的基因文库中相应的λ噬菌体亚克隆出完整的bfr基因。bfr基因由474个碱基对和158个氨基酸密码子组成(包括起始密码子),它编码的多肽与纯化蛋白的大小(分子量18,495)和N端序列基本相同。在5'非编码区检测到一个潜在的启动子序列,但它与“铁盒”序列(即铁依赖性Fur阻遏蛋白的结合位点)无关。在一个含有bfr质粒的菌株中,BFR扩增至总蛋白的14%。在bfr基因上游检测到另一个未鉴定的基因(gen-64),它编码一个相对碱性的64个残基的多肽,与bfr具有相同的极性。