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

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

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摘要

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.
机译:通过使用聚合酶链反应或mini-Mu克隆扩增的DNA对psi :: lacZ(Mu d1)染色体接头进行测序,分析了由Mu d1(lacZbla)制成的二十四个独立的磷酸饥饿诱导(psi)转录融合体。我们的DNA序列分析表明,Mu d1中的MuR DNA具有意外的结构,该结构由104个碱基的MuR DNA组成,呈大的反向重复序列,我们将其称为Mu d1-R。此外,尽管Mu d1整体插入基因组中具有随机性,但磷酸盐调节子的phoA和phn(psiD)位点中的Mu d1s显示了插入位点的区域特异性。通过搜索DNA数据库中Mu d1s相邻和上游的序列,鉴定了7种psi :: lacZ(Mu d1)转录融合的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性的sn-甘油-3-磷酸结合蛋白。 gltB基因中有两个psiQ :: lacZ(Mu d1),而gltBDF操纵子的gltD基因中有一个psiQ :: lacZ(Mu d1),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3-磷酸甘油脱氢酶。 psiE和psiF :: lacZ(Mu d1)s分别位于xylE和phoA基因附近的开放阅读框中。其他六个psi :: lacZ(Mu d1)位于尚未报告的大肠杆菌序列中。

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