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1
The Pseudomonas aeruginosa transcriptome in planktonic cultures and static biofilms using RNA sequencing.使用 RNA 测序研究浮游培养物和静态生物膜中铜绿假单胞菌的转录组。
PLoS One. 2012;7(2):e31092. doi: 10.1371/journal.pone.0031092. Epub 2012 Feb 3.
2
Evidence that WapB is a 1,2-glucosyltransferase of Pseudomonas aeruginosa involved in Lipopolysaccharide outer core biosynthesis.证据表明，WapB 是铜绿假单胞菌中参与脂多糖外核生物合成的 1,2-葡糖基转移酶。
J Bacteriol. 2011 Jun;193(11):2708-16. doi: 10.1128/JB.00032-11. Epub 2011 Mar 25.
3
Review: Lipopolysaccharide biosynthesis in Pseudomonas aeruginosa.综述：铜绿假单胞菌脂多糖生物合成。
Innate Immun. 2009 Oct;15(5):261-312. doi: 10.1177/1753425909106436. Epub 2009 Aug 26.
4
Ribosomes bind leaderless mRNA in Escherichia coli through recognition of their 5'-terminal AUG.在大肠杆菌中，核糖体通过识别无帽mRNA的5'-末端AUG来结合它。
RNA. 2008 Oct;14(10):2159-69. doi: 10.1261/rna.1089208. Epub 2008 Aug 28.
5
Large-scale computational and statistical analyses of high transcription potentialities in 32 prokaryotic genomes.对32个原核生物基因组中的高转录潜力进行大规模计算和统计分析。
Nucleic Acids Res. 2008 Jun;36(10):3332-40. doi: 10.1093/nar/gkn135. Epub 2008 Apr 25.
6
Functional characterization of MigA and WapR: putative rhamnosyltransferases involved in outer core oligosaccharide biosynthesis of Pseudomonas aeruginosa.MigA和WapR的功能表征：参与铜绿假单胞菌外核心寡糖生物合成的假定鼠李糖基转移酶
J Bacteriol. 2008 Mar;190(6):1857-65. doi: 10.1128/JB.01546-07. Epub 2008 Jan 4.
7
Sigma factors in Pseudomonas aeruginosa.铜绿假单胞菌中的σ因子。
FEMS Microbiol Rev. 2008 Jan;32(1):38-55. doi: 10.1111/j.1574-6976.2007.00092.x. Epub 2007 Dec 7.
8
Multiple sigma subunits and the partitioning of bacterial transcription space.多种σ亚基与细菌转录空间的划分
Annu Rev Microbiol. 2003;57:441-66. doi: 10.1146/annurev.micro.57.030502.090913.
9
Expression stability of six housekeeping genes: A proposal for resistance gene quantification studies of Pseudomonas aeruginosa by real-time quantitative RT-PCR.六个管家基因的表达稳定性：关于通过实时定量逆转录聚合酶链反应对铜绿假单胞菌抗性基因定量研究的一项提议。
J Med Microbiol. 2003 May;52(Pt 5):403-408. doi: 10.1099/jmm.0.05132-0.
10
Small broad-host-range lacZ operon fusion vector with low background activity.具有低背景活性的小型广宿主范围lacZ操纵子融合载体。
Biotechniques. 2001 Dec;31(6):1258, 1260, 1262. doi: 10.2144/01316bm06.

甘露糖基转移酶基因 migA 和 wapR 以不同的方式调节铜绿假单胞菌产生的核心寡糖糖型的数量。

Rhamnosyltransferase genes migA and wapR are regulated in a differential manner to modulate the quantities of core oligosaccharide glycoforms produced by Pseudomonas aeruginosa.

机构信息

Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.

出版信息

J Bacteriol. 2012 Aug;194(16):4295-300. doi: 10.1128/JB.05741-11. Epub 2012 Jun 8.

DOI:10.1128/JB.05741-11
PMID:22685285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3416230/
Abstract

migA and wapR are rhamnosyltransferase genes involved in the biosynthesis of Pseudomonas aeruginosa lipopolysaccharide core oligosaccharide. Here, we show that preferential expression of migA and wapR correlated with the levels of uncapped and O polysaccharide-capped core, respectively. wapR is negatively regulated, while migA is positively regulated by RhlR/RhlI quorum sensing.

摘要

migA 和 wapR 是参与铜绿假单胞菌脂多糖核心寡糖生物合成的鼠李糖基转移酶基因。在这里，我们表明 migA 和 wapR 的优先表达分别与无帽和 O 多糖帽核心的水平相关。wapR 受负调控，而 migA 受群体感应 RhlR/RhlI 的正调控。