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在固氮条件下,自由生活弗兰克氏菌 CcI3 菌株的胞外多糖产生和转录谱的改变。

Alteration of the exopolysaccharide production and the transcriptional profile of free-living Frankia strain CcI3 under nitrogen-fixing conditions.

机构信息

Department of Biology, University of Texas, Arlington, TX, 76019, USA.

出版信息

Appl Microbiol Biotechnol. 2013 Dec;97(24):10499-509. doi: 10.1007/s00253-013-5277-z. Epub 2013 Oct 6.

Abstract

We investigated the effect of different nitrogen (N) sources on exopolysaccharide (EPS) production and composition by Frankia strain CcI3, a N2-fixing actinomycete that forms root nodules with Casuarina species. Frankia cells grown in the absence of NH4Cl (i.e., under N2-fixing conditions) produced 1.7-fold more EPS, with lower galactose (45.1 vs. 54.7 mol%) and higher mannose (17.3 vs. 9.7 mol%) contents than those grown in the presence of NH4Cl as a combined N-source. In the absence of the combined N-source, terminally linked and branched residue contents were nearly twice as high with 32.8 vs. 15.1 mol% and 15.1 vs. 8.7 mol%, respectively, than in its presence, while the content of linearly linked residues was lower with 52.1 mol% compared to 76.2 mol%. To find out clues for the altered EPS production at the transcriptional level, we performed whole-gene expression profiling using quantitative reverse transcription PCR and microarray technology. The transcription profiles of Frankia strain CcI3 grown in the absence of NH4Cl revealed up to 2 orders of magnitude higher transcription of nitrogen fixation-related genes compared to those of CcI3 cells grown in the presence of NH4Cl. Unexpectedly, microarray data did not provide evidence for transcriptional regulation as a mechanism for differences in EPS production. These findings indicate effects of nitrogen fixation on the production and composition of EPS in Frankia strain CcI3 and suggest posttranscriptional regulation of enhanced EPS production in the absence of the combined N-source.

摘要

我们研究了不同氮(N)源对弗兰克氏菌菌株 CcI3 产生胞外多糖(EPS)的影响,弗兰克氏菌是一种固氮放线菌,能与 Casuarina 物种形成根瘤。在没有氯化铵(即在固氮条件下)的情况下生长的弗兰克氏菌细胞产生的 EPS 增加了 1.7 倍,其半乳糖(45.1 比 54.7mol%)和甘露糖(17.3 比 9.7mol%)含量较低,而在有氯化铵作为组合氮源的情况下生长的弗兰克氏菌细胞含量较高。在没有组合氮源的情况下,末端连接和分支残基的含量几乎是其存在时的两倍,分别为 32.8 比 15.1mol%和 15.1 比 8.7mol%,而线性连接残基的含量则较低,为 52.1mol%,而不是 76.2mol%。为了在转录水平上找到改变 EPS 产生的线索,我们使用定量逆转录 PCR 和微阵列技术进行了全基因表达谱分析。在没有氯化铵的情况下生长的弗兰克氏菌菌株 CcI3 的转录谱显示,与在有氯化铵的情况下生长的 CcI3 细胞相比,氮固定相关基因的转录高达 2 个数量级。出乎意料的是,微阵列数据并未提供转录调控作为 EPS 产生差异的机制的证据。这些发现表明,氮固定对弗兰克氏菌菌株 CcI3 产生和组成 EPS 的影响,并表明在没有组合氮源的情况下,EPS 产量的增强是转录后调控的结果。

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