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固氮菌 PAL5 株对铁限制的转录组响应及调控网络的表征。

Transcriptomic Response of the Diazotrophic Bacteria Strain PAL5 to Iron Limitation and Characterization of the Regulatory Network.

机构信息

Embrapa Agrobiologia, Rodovia BR 465, Km 07, Seropédica 23891-000, RJ, Brazil.

Departamento de Bioquímica e Biologia Molecular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Jardim das Américas, Curitiba 81531-980, PR, Brazil.

出版信息

Int J Mol Sci. 2022 Aug 1;23(15):8533. doi: 10.3390/ijms23158533.

Abstract

has been the focus of several studies aiming to understand the mechanisms behind this endophytic diazotrophic bacterium. The present study is the first global analysis of the early transcriptional response of exponentially growing to iron, an essential cofactor for many enzymes involved in various metabolic pathways. RNA-seq, targeted gene mutagenesis and computational motif discovery tools were used to define the regulon. The data analysis showed that genes encoding functions related to iron homeostasis were significantly upregulated in response to iron limitations. Certain genes involved in secondary metabolism were overexpressed under iron-limited conditions. In contrast, it was observed that the expression of genes involved in Fe-S cluster biosynthesis, flagellar biosynthesis and type IV secretion systems were downregulated in an iron-depleted culture medium. Our results support a model that controls transcription in by function. The protein was able to complement an mutant. These results provide new insights into the effects of iron on the metabolism of , as well as demonstrate the essentiality of this micronutrient for the main characteristics of plant growth promotion by .

摘要

一直是多项研究的焦点,旨在了解这种内生固氮细菌背后的机制。本研究是对指数生长期 对铁的早期转录响应的首次全球分析,铁是参与各种代谢途径的许多酶的必需辅因子。RNA-seq、靶向基因诱变和计算基序发现工具被用于定义 调控子。数据分析表明,编码与铁稳态相关功能的基因在铁限制时显著上调。某些参与次生代谢的基因在缺铁条件下过度表达。相比之下,在缺铁培养基中观察到与 Fe-S 簇生物合成、鞭毛生物合成和 IV 型分泌系统相关的基因表达下调。我们的结果支持了一种由 功能控制转录的模型。 蛋白能够补充 突变体。这些结果提供了关于铁对 的代谢影响的新见解,并证明了这种微量元素对 通过促进植物生长的主要特征的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2f1/9368920/6679774201ea/ijms-23-08533-g001.jpg

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