Nohno T, Noji S, Taniguchi S, Saito T
Department of Pharmacology, Kawasaki Medical School, Japan.
Nucleic Acids Res. 1989 Apr 25;17(8):2947-57. doi: 10.1093/nar/17.8.2947.
The nucleotide sequence of a 4.4-kilobase SacII-SspI fragment encoding the narXL operon and a part of the narK gene of Escherichia coli has been determined. The narX and narL genes encode proteins of molecular weight 67,275 and 23,927, respectively, and are transcribed from a common promoter, narXp, locating within 429 bases upstream of narX. Transcription from narXp is not significantly induced by nitrate under anaerobiosis, whereas transcription from narK promoter, which overlaps narXp region and is transcribed divergently, is fully induced by nitrate. The N-terminal two-thirds of the NarL protein has extensive homology with those of a diverse set of prokaryotic regulatory proteins, including OmpR, PhoB, SfrA, UhpA, CheY, CheB, NtrC, DctD, FixJ, VirG, SpoOF, and SpoOA. A segment locating in the C-terminal half of the NarL protein seems to have potential most likely to form the helix-turn-helix structure characteristic of a class of DNA-binding protein. The protein is considered to play a role as a transcriptional activator of the nitrate reductase operon, narCHJI, and the narK gene. The C-terminal region of the NarX protein also has homology with other regulatory proteins known as counterparts of two-component regulatory systems, such as EnvZ, PhoR, PhoM, CpxA, NtrB, DctB, FixL, and VirA. Presence of two copies of hydrophobic segments in the N-terminal half of the NarX protein suggests the role as a transmembrane receptor sensing nitrate.
已确定编码大肠杆菌narXL操纵子和部分narK基因的一个4.4千碱基的SacII - SspI片段的核苷酸序列。narX和narL基因分别编码分子量为67275和23927的蛋白质,它们从位于narX上游429个碱基内的一个共同启动子narXp转录。在厌氧条件下,来自narXp的转录不会被硝酸盐显著诱导,而来自与narXp区域重叠且转录方向相反的narK启动子的转录则会被硝酸盐完全诱导。NarL蛋白的N端三分之二与多种原核调节蛋白具有广泛的同源性,包括OmpR、PhoB、SfrA、UhpA、CheY、CheB、NtrC、DctD、FixJ、VirG、SpoOF和SpoOA。位于NarL蛋白C端一半的一个片段似乎最有可能形成一类DNA结合蛋白特有的螺旋 - 转角 - 螺旋结构。该蛋白被认为作为硝酸盐还原酶操纵子narCHJI和narK基因的转录激活剂发挥作用。NarX蛋白的C端区域也与其他被称为双组分调节系统对应物的调节蛋白具有同源性,如EnvZ、PhoR、PhoM、CpxA、NtrB、DctB、FixL和VirA。NarX蛋白N端一半存在两个疏水片段表明其作为感知硝酸盐的跨膜受体的作用。