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通过psi::lacZ(Mu d1)转录融合的DNA序列分析鉴定大肠杆菌K-12中的磷酸盐饥饿诱导基因。

Identification of phosphate starvation-inducible genes in Escherichia coli K-12 by DNA sequence analysis of psi::lacZ(Mu d1) transcriptional fusions.

作者信息

Metcalf W W, Steed P M, Wanner B L

机构信息

Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907.

出版信息

J Bacteriol. 1990 Jun;172(6):3191-200. doi: 10.1128/jb.172.6.3191-3200.1990.

Abstract

Twenty-four independent phosphate starvation-inducible (psi) transcriptional fusions made with Mu d1(lacZbla) were analyzed by sequencing the psi::lacZ(Mu d1) chromosomal junctions by using DNAs amplified with the polymerase chain reaction or mini-Mu cloning. Our DNA sequence analysis showed that the MuR DNA in Mu d1 has an unexpected structure that is comprised of 104 bases of MuR DNA in the form of a large inverted repeat, which we denoted Mu d1-R. Also, Mu d1s in the phoA and phn (psiD) loci of the phosphate regulon showed regional specificities for the insertion sites despite the randomness of Mu d1 insertions into the genome as a whole. Gene products or open reading frames were identified for seven unknown psi::lacZ(Mu d1) transcriptional fusions by searching DNA data bases with the sequences adjacent and upstream of the Mu d1s. One psiC::lacZ(Mu d1) lies in the ugpB gene of the ugpBAEC operon, which encodes a periplasmic sn-glycerol-3-phosphate-binding protein; two psiQ::lacZ(Mu d1)s lie in the gltB gene, and one psiQ::lacZ(Mu d1) lies in the gltD gene of the gltBDF operon, encoding the large and small subunits of glutamate synthase, respectively; and the psi-51::lacZ(Mu d1) lies in the glpB gene of the glpABC operon, which codes for the anaerobically regulated glycerol-3-phosphate dehydrogenase. psiE and psiF::lacZ(Mu d1)s lie in uncharacterized open reading frames near the xylE and phoA genes, respectively. Six other psi::lacZ(Mu d1)s lie in yet unreported Escherichia coli sequences.

摘要

利用聚合酶链反应扩增的DNA或mini-Mu克隆对psi::lacZ(Mu d1)染色体连接点进行测序,分析了24个独立的用Mu d1(lacZbla)构建的磷酸盐饥饿诱导型(psi)转录融合体。我们的DNA序列分析表明,Mu d1中的MuR DNA具有意想不到的结构,它由104个碱基的MuR DNA组成,呈大的反向重复形式,我们将其命名为Mu d1-R。此外,尽管Mu d1作为一个整体随机插入基因组,但磷酸盐调控子的phoA和phn(psiD)位点中的Mu d1在插入位点上表现出区域特异性。通过用Mu d1s相邻和上游的序列搜索DNA数据库,为7个未知的psi::lacZ(Mu d1)转录融合体鉴定了基因产物或开放阅读框。一个psiC::lacZ(Mu d1)位于ugpBAEC操纵子的ugpB基因中,该基因编码一种周质sn-甘油-3-磷酸结合蛋白;两个psiQ::lacZ(Mu d1)位于gltB基因中,一个psiQ::lacZ(Mu d1)位于gltBDF操纵子的gltD基因中,分别编码谷氨酸合酶的大亚基和小亚基;psi-51::lacZ(Mu d1)位于glpABC操纵子的glpB基因中,该基因编码厌氧调节的甘油-3-磷酸脱氢酶。psiE和psiF::lacZ(Mu d1)分别位于xylE和phoA基因附近未鉴定的开放阅读框中。另外6个psi::lacZ(Mu d1)位于尚未报道的大肠杆菌序列中。

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