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巴西固氮芽孢杆菌 PB24 中氮固定的遗传与调控。

Genetics and regulation of nitrogen fixation in Paenibacillus brasilensis PB24.

机构信息

Laboratório de Genética Microbiana, Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.

Laboratório de Biologia Computacional e Sistemas, Instituto Oswaldo Cruz, Rio de Janeiro, Brazil.

出版信息

Microbiol Res. 2021 Feb;243:126647. doi: 10.1016/j.micres.2020.126647. Epub 2020 Nov 24.

Abstract

Biological nitrogen fixation (BNF), performed by diazotrophic prokaryotes, is responsible for reducing dinitrogen (N) present in the biosphere into biologically available forms of nitrogen. Paenibacillus brasilensis PB24 is a diazotrophic Gram-positive bacterium and is considered ecologically and industrially important because it is able to produce antimicrobial substances and 2,3-butanediol. However, the genetics and regulation of its nitrogen fixing (nif) genes have never been assessed so far. Therefore, the present study aimed to (i) identify the structural and regulatory genes related to BNF in the PB24 genome, (ii) perform comparative genomics analysis of the nif operon among different Paenibacillus species and (iii) study the expression of these genes in the presence and absence of NH. Strain PB24 showed a nif operon composed of nine genes (nifBHDKENXhesAV), with a conserved synteny (with small variations) among the Paenibacillus species evaluated. BNF regulatory genes, glnK and amtB (encoding GlnK signal transduction protein and AmtB transmembrane protein, respectively) and glnR and glnA genes (encoding the transcription factor GlnR and glutamine synthetase) were found in the PB24 genome. Primers were designed for qPCR amplification of the nitrogenase structural (nifH, nifD and nifK) and regulatory (glnA and amtB) BNF genes. The structural gene expression in PB24 was up- and downregulated in the absence and presence of NH, respectively. The gene expression levels indicated a GlnR-mediated repression of genes associated with ammonium import (amtBglnK) and BNF (nif genes). Additionally, the regulatory mechanism of GlnR in P. brasilensis PB24 differed from the other Paenibacillus evaluated, considering the different distribution of binding sites recognized by GlnR.

摘要

生物固氮(BNF)由固氮原核生物进行,负责将生物圈中存在的二氮(N)还原为生物可利用的氮形式。巴西芽胞杆菌 PB24 是一种固氮革兰氏阳性菌,由于能够产生抗菌物质和 2,3-丁二醇,因此被认为具有生态和工业重要性。然而,迄今为止,其固氮(nif)基因的遗传学和调控尚未得到评估。因此,本研究旨在:(i)鉴定 PB24 基因组中与 BNF 相关的结构和调控基因;(ii)对不同巴西芽胞杆菌种间 nif 操纵子进行比较基因组学分析;(iii)研究这些基因在 NH 存在和不存在时的表达情况。PB24 菌株表现出由九个基因(nifBHDKENXhesAV)组成的 nif 操纵子,在所评估的巴西芽胞杆菌种中具有保守的基因排列(存在微小变化)。在 PB24 基因组中发现了 BNF 调控基因 glnK 和 amtB(分别编码 GlnK 信号转导蛋白和 AmtB 跨膜蛋白)和 glnR 和 glnA 基因(编码转录因子 GlnR 和谷氨酰胺合成酶)。为 nif 结构(nifH、nifD 和 nifK)和调控(glnA 和 amtB)BNF 基因的 qPCR 扩增设计了引物。在 PB24 中,结构基因的表达在 NH 存在和不存在的情况下分别上调和下调。基因表达水平表明 GlnR 介导了与铵导入(amtBglnK)和 BNF(nif 基因)相关的基因的抑制。此外,考虑到 GlnR 识别的结合位点的不同分布,巴西芽胞杆菌 PB24 中的 GlnR 调控机制与其他评估的巴西芽胞杆菌不同。

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