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The Role of the ncRNA RgsA in the Oxidative Stress Response and Biofilm Formation in Azotobacter vinelandii.ncRNA RgsA 在土壤固氮菌氧化应激反应和生物膜形成中的作用。
Curr Microbiol. 2016 Jun;72(6):671-9. doi: 10.1007/s00284-016-1003-2. Epub 2016 Feb 9.
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Cross-talk between a regulatory small RNA, cyclic-di-GMP signalling and flagellar regulator FlhDC for virulence and bacterial behaviours.一种调控性小RNA、环二鸟苷信号传导与鞭毛调节因子FlhDC之间关于毒力和细菌行为的相互作用。
Environ Microbiol. 2015 Nov;17(11):4745-63. doi: 10.1111/1462-2920.13029. Epub 2015 Oct 14.
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Genomics and Ecophysiology of Heterotrophic Nitrogen-Fixing Bacteria Isolated from Estuarine Surface Water.从河口表层水分离出的异养固氮细菌的基因组学与生态生理学
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Evolution of molybdenum nitrogenase during the transition from anaerobic to aerobic metabolism.从厌氧代谢向需氧代谢转变过程中钼固氮酶的演化
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Differential RNA-seq of Vibrio cholerae identifies the VqmR small RNA as a regulator of biofilm formation.霍乱弧菌的差异RNA测序确定VqmR小RNA为生物膜形成的调节因子。
Proc Natl Acad Sci U S A. 2015 Feb 17;112(7):E766-75. doi: 10.1073/pnas.1500203112. Epub 2015 Feb 2.
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The nitrogen-fixation island insertion site is conserved in diazotrophic Pseudomonas stutzeri and Pseudomonas sp. isolated from distal and close geographical regions.固氮岛插入位点在从远近距离不同地理区域分离出的重氮营养型施氏假单胞菌和假单胞菌属中是保守的。
PLoS One. 2014 Sep 24;9(9):e105837. doi: 10.1371/journal.pone.0105837. eCollection 2014.
7
Transcriptional response of Corynebacterium glutamicum ATCC 13032 to hydrogen peroxide stress and characterization of the OxyR regulon.谷氨酸棒杆菌ATCC 13032对过氧化氢胁迫的转录反应及OxyR调控子的表征
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Genome-wide profiling of Hfq-binding RNAs uncovers extensive post-transcriptional rewiring of major stress response and symbiotic regulons in Sinorhizobium meliloti.苜蓿中华根瘤菌中Hfq结合RNA的全基因组分析揭示了主要应激反应和共生调控子广泛的转录后重排。
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新型调控非编码RNA NfiS通过与斯氏假单胞菌A1501中的固氮酶基因nifK mRNA碱基配对来优化固氮作用。

The novel regulatory ncRNA, NfiS, optimizes nitrogen fixation via base pairing with the nitrogenase gene nifK mRNA in Pseudomonas stutzeri A1501.

作者信息

Zhan Yuhua, Yan Yongliang, Deng Zhiping, Chen Ming, Lu Wei, Lu Chao, Shang Liguo, Yang Zhimin, Zhang Wei, Wang Wei, Li Yun, Ke Qi, Lu Jiasi, Xu Yuquan, Zhang Liwen, Xie Zhihong, Cheng Qi, Elmerich Claudine, Lin Min

机构信息

National Key Facility for Crop Gene Resources and Genetic Improvement, Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China;

Key Laboratory of Coastal Biology and Bioresource Utilization, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003, China;

出版信息

Proc Natl Acad Sci U S A. 2016 Jul 26;113(30):E4348-56. doi: 10.1073/pnas.1604514113. Epub 2016 Jul 12.

DOI:10.1073/pnas.1604514113
PMID:27407147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4968741/
Abstract

Unlike most Pseudomonas, the root-associated bacterium Pseudomonas stutzeri A1501 fixes nitrogen after the horizontal acquisition of a nitrogen-fixing (nif) island. A genome-wide search for small noncoding RNAs (ncRNAs) in P. stutzeri A1501 identified the novel P. stutzeri-specific ncRNA NfiS in the core genome, whose synthesis was significantly induced under nitrogen fixation or sorbitol stress conditions. The expression of NfiS was RNA chaperone Hfq-dependent and activated by the sigma factor RpoN/global nitrogen activator NtrC/nif-specific activator NifA regulatory cascade. The nfiS-deficient mutant displayed reduced nitrogenase activity, as well as increased sensitivity to multiple stresses, such as osmotic and oxidative stresses. Secondary structure prediction and complementation studies confirmed that a stem-loop structure was essential for NfiS to regulate the nitrogenase gene nifK mRNA synthesis and thus nitrogenase activity. Microscale thermophoresis and physiological analysis showed that NfiS directly pairs with nifK mRNA and ultimately enhances nitrogenase activity by increasing the translation efficiency and the half-life of nifK mRNA. Our data also suggest structural and functional divergence of NfiS evolution in diazotrophic and nondiazotrophic backgrounds. It is proposed that NfiS was recruited by nifK mRNA as a novel regulator to integrate the horizontally acquired nif island into host global networks.

摘要

与大多数假单胞菌不同,根部相关细菌施氏假单胞菌A1501在水平获得固氮(nif)岛后能够固氮。对施氏假单胞菌A1501进行全基因组范围内的小非编码RNA(ncRNA)搜索,在核心基因组中鉴定出了新型的施氏假单胞菌特异性ncRNA NfiS,其合成在固氮或山梨醇胁迫条件下显著诱导。NfiS的表达依赖于RNA伴侣蛋白Hfq,并由σ因子RpoN/全局氮激活因子NtrC/nif特异性激活因子NifA调控级联激活。nfiS缺陷型突变体表现出固氮酶活性降低,以及对多种胁迫(如渗透胁迫和氧化胁迫)的敏感性增加。二级结构预测和互补研究证实,茎环结构对于NfiS调节固氮酶基因nifK mRNA的合成从而调节固氮酶活性至关重要。微量热泳动和生理学分析表明,NfiS直接与nifK mRNA配对,并最终通过提高nifK mRNA的翻译效率和半衰期来增强固氮酶活性。我们的数据还表明,NfiS在固氮和非固氮背景下的进化存在结构和功能差异。有人提出,NfiS被nifK mRNA招募为一种新型调节因子,以将水平获得的nif岛整合到宿主全局网络中。