Walker J E, Gay N J, Saraste M, Eberle A N
Biochem J. 1984 Dec 15;224(3):799-815. doi: 10.1042/bj2240799.
The nucleotide sequence is described of a region of the Escherichia coli chromosome extending from oriC to phoS that also includes the loci gid, unc and glmS. Taken with known sequences for asnA and phoS this completes the sequence of a segment of about 17 kilobases or 0.4 min of the E. coli genome. Sequences that are probably transcriptional promoters for unc and phoS can be detected and the identity of the unc promoter has been confirmed by experiments in vitro with RNA polymerase. Upstream of the promoter sequence is an extensive region that appears to be non-coding. Conserved sequences are found that may serve to concentrate RNA polymerase in the vicinity of the unc promoter. Hairpin loop structures resembling known rho-independent transcription termination signals are evident following the unc operon and glmS. The glmS gene encoding the amidotransferase, glucosamine synthetase, has been identified by homology with glutamine 5-phosphoribosylpyrophosphate amidotransferase.
描述了大肠杆菌染色体上从oriC延伸至phoS的一个区域的核苷酸序列,该区域还包括gid、unc和glmS基因座。结合已知的asnA和phoS序列,这就完成了大肠杆菌基因组中一段约17千碱基或0.4分钟片段的序列测定。可以检测到可能是unc和phoS转录启动子的序列,并且通过用RNA聚合酶进行的体外实验证实了unc启动子的特性。在启动子序列上游是一个似乎是非编码的广泛区域。发现了保守序列,其可能有助于将RNA聚合酶集中在unc启动子附近。在unc操纵子和glmS之后,明显存在类似于已知的不依赖ρ因子的转录终止信号的发夹环结构。通过与谷氨酰胺5-磷酸核糖焦磷酸酰胺转移酶的同源性鉴定出了编码氨基转移酶——葡糖胺合成酶的glmS基因。