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超高压多肽的鉴定及其在大肠杆菌K-12磷酸糖转运系统外源诱导中作用的证据

Identification of uhp polypeptides and evidence for their role in exogenous induction of the sugar phosphate transport system of Escherichia coli K-12.

作者信息

Weston L A, Kadner R J

出版信息

J Bacteriol. 1987 Aug;169(8):3546-55. doi: 10.1128/jb.169.8.3546-3555.1987.

Abstract

Cells of Escherichia coli possess a transport system that catalyzes the accumulation, in unaltered form, of a variety of sugar phosphates. Induction of the transport activity occurs in response to external glucose 6-phosphate and does not require detectable entry of this inducer. To define the genes that encode the Uhp transport system and those that mediate its exogenous induction, transposon insertions were isolated and mapped within a 6.5-kilobase HindIII-BamHI fragment that carries the entire uhp region. The transposon insertions were transferred by homologous recombination onto the chromosome to test their effect on Uhp expression when all genes were present in single copy number. The complementation behavior of plasmids carrying the insertions or subcloned fragments of the region was compared with their polypeptide coding capacity in maxicells. These studies defined three uhp regulatory genes (uhpABC), all of which are necessary for expression of the uhpT gene, which encodes the transporter. The products of uhpB and uhpC are not required when uhpA is present on a multicopy plasmid. The four genes, uhpA, uhpB, uhpC, and uhpT, are transcribed in the same direction, and their products have apparent molecular weights of 25,000, 48,000, 20,000, and 38,000, respectively. The UhpB and UhpT polypeptides are associated with the membrane fraction. These results led to a model of regulation in which the UhpB and UhpC regulatory proteins prevent the ability of UhpA to activate transcription of the uhpT gene under noninducing conditions.

摘要

大肠杆菌细胞拥有一种转运系统,该系统能催化多种磷酸糖以未改变的形式积累。转运活性的诱导是对外部6-磷酸葡萄糖做出的反应,且不需要该诱导剂的可检测进入。为了确定编码Uhp转运系统的基因以及介导其外源诱导的基因,分离了转座子插入并将其定位在一个携带整个uhp区域的6.5千碱基的HindIII - BamHI片段内。通过同源重组将转座子插入转移到染色体上,以测试当所有基因以单拷贝数存在时它们对Uhp表达的影响。比较了携带该区域插入片段或亚克隆片段的质粒的互补行为与其在大细胞中的多肽编码能力。这些研究确定了三个uhp调控基因(uhpABC),所有这些基因对于编码转运蛋白的uhpT基因的表达都是必需的。当uhpA存在于多拷贝质粒上时,不需要uhpB和uhpC的产物。uhpA、uhpB、uhpC和uhpT这四个基因按相同方向转录, 它们的产物的表观分子量分别为25,000、48,000、20,000和38,000。UhpB和UhpT多肽与膜部分相关。这些结果导致了一种调控模型,其中UhpB和UhpC调控蛋白在非诱导条件下阻止UhpA激活uhpT基因转录的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e4d/212431/7904b2e2e6e0/jbacter00198-0168-a.jpg

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