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与噬菌体Mu和D108的ner基因高度同源的大肠杆菌基因nlp的克隆与测序。

Cloning and sequencing of an Escherichia coli gene, nlp, highly homologous to the ner genes of bacteriophages Mu and D108.

作者信息

Choi Y L, Nishida T, Kawamukai M, Utsumi R, Sakai H, Komano T

机构信息

Department of Agricultural Chemistry, Kyoto University, Japan.

出版信息

J Bacteriol. 1989 Sep;171(9):5222-5. doi: 10.1128/jb.171.9.5222-5225.1989.

Abstract

An nlp (Ner-like protein) gene was isolated from Escherichia coli. The nucleotide sequence of a 1,342-base-pair chromosomal DNA fragment containing the nlp gene was analyzed. It contained two open reading frames; one encoded 91 amino acid residues with an Mr of 10,361, and the other (ORFX) encoded 131 amino acid residues of the carboxyl-terminal region of a truncated polypeptide. The amino acid sequence deduced from the DNA sequence of nlp was highly homologous (62 to 63%) to the Ner proteins of bacteriophages Mu and D108. The amino-terminal region of Nlp deduced from the complete open reading frame contained a presumed DNA-binding region. The nlp gene was located at 69.3 min on the E. coli genetic map.

摘要

从大肠杆菌中分离出一个nlp(类Ner蛋白)基因。对包含nlp基因的1342个碱基对的染色体DNA片段的核苷酸序列进行了分析。它包含两个开放阅读框;一个编码91个氨基酸残基,Mr为10361,另一个(ORFX)编码截短多肽羧基末端区域的131个氨基酸残基。从nlp的DNA序列推导的氨基酸序列与噬菌体Mu和D108的Ner蛋白高度同源(62%至63%)。从完整开放阅读框推导的Nlp氨基末端区域包含一个推测的DNA结合区域。nlp基因位于大肠杆菌遗传图谱的69.3分钟处。

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本文引用的文献

1
Isolation of the lac repressor.乳糖阻遏蛋白的分离
Proc Natl Acad Sci U S A. 1966 Dec;56(6):1891-8. doi: 10.1073/pnas.56.6.1891.
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New M13 vectors for cloning.用于克隆的新型M13载体。
Methods Enzymol. 1983;101:20-78. doi: 10.1016/0076-6879(83)01005-8.
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Ner, a cro-like function of bacteriophage Mu.Ner,噬菌体Mu的一种cro样功能。
Virology. 1982 Nov;123(1):19-28. doi: 10.1016/0042-6822(82)90291-4.
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Protein-DNA recognition.蛋白质-脱氧核糖核酸识别
Annu Rev Biochem. 1984;53:293-321. doi: 10.1146/annurev.bi.53.070184.001453.

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