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大肠杆菌中二氨基庚二酸脱羧酶合成的调控。II. lysA基因及其调控区域的核苷酸序列。

Regulation of diaminopimelate decarboxylase synthesis in Escherichia coli. II. Nucleotide sequence of the lysA gene and its regulatory region.

作者信息

Stragier P, Danos O, Patte J C

出版信息

J Mol Biol. 1983 Aug 5;168(2):321-31. doi: 10.1016/s0022-2836(83)80021-7.

Abstract

The complete nucleotide sequence of the lysA gene and its regulatory region was determined. At the 3' end of the lysA gene an open reading frame was revealed in the opposite direction and was identified as the galR coding region. Only six base-pairs are present between the two translational stops and thus both transcription units are overlapping in vivo. Translational gene fusions constructed in vitro with the beta-galactosidase gene were used to identify the lysA initiating ATG. The sequence encodes a 420 amino acid long peptide for a predicted molecular weight of 46,099. No attenuation-like sequence was found at the beginning of the lysA gene. A target of the LysR activator protein was localized on a 73 base-pair fragment found 48 base-pairs upstream from the lysA coding region. The presence of this DNA sequence on a multicopy plasmid led to a net decrease of lysA expression, indicating limiting amounts of active LysR protein in the cytoplasm.

摘要

测定了lysA基因及其调控区的完整核苷酸序列。在lysA基因的3'端,发现了一个方向相反的开放阅读框,并被鉴定为galR编码区。两个翻译终止位点之间仅存在六个碱基对,因此两个转录单元在体内是重叠的。体外构建的与β-半乳糖苷酶基因的翻译基因融合体用于鉴定lysA起始ATG。该序列编码一个420个氨基酸长的肽,预测分子量为46,099。在lysA基因起始处未发现类似衰减的序列。LysR激活蛋白的靶标定位在lysA编码区上游48个碱基对处的一个73碱基对片段上。多拷贝质粒上该DNA序列的存在导致lysA表达净减少,表明细胞质中活性LysR蛋白的量有限。

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