NsrM (All0345) and NsrX (Alr1976), two FurC (PerR)-targeted transcriptional regulators, modulate nitrogen metabolism and heterocyst differentiation genes in the cyanobacterium Anabaena sp. strain PCC 7120.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Jorge Guío, Marta Acero, Anindita Bandyopadhyay, Deng Liu, Himadri B Pakrasi, Isabelle Michaud-Soret, M Teresa Bes, Emma Sevilla, María F Fillat
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引用次数: 0

Abstract

The control of nitrogen metabolism in the model cyanobacterium Anabaena sp. strain PCC7120 is a complex process orchestrated by master regulators such as NtcA, HetR, and FurC (PerR). These proteins establish complex networks with secondary regulators, finely tuning cellular metabolism in response to diverse, often undefined environmental signals. The XRE-like Alr1976 and the MerR-like All0345 proteins are two predicted transcriptional regulators regulated by FurC. While All0345 is widespread, both proteins have homologs conserved across several bacterial phyla, with alr1976 often followed by a gene encoding a Zn-metalloprotease. Previous transcriptomic analyses showed that furC overexpression affected alr1976 expression slightly more under nitrogen-deficient conditions, while changes in all0345 expression were exclusively observed under N deficiency, pointing them as critical candidates for understanding the finer details of nitrogen control in Anabaena. This work shows that both Alr1976 (NsrX) and All0345 (NsrM) are potentially modulated by NtcA and work as nitrogen secondary regulators. Electrophoretic mobility shift assays and transcriptomic analyses of ∆nsrX and ∆nsrM deletion strains indicate that both regulators act as repressors of key genes involved in nitrogen metabolism and heterocyst development. Notably, the ∆nsrM strain showed earlier heterocyst formation at 24 h of nitrogen step-down. NsrX and NsrM display distinct requirements for optimal DNA-binding activity to nitrogen metabolism genes (presence of Mn and reducing environment, respectively), suggesting they respond to different environmental stimuli. This differential signal integration likely enables master regulators FurC and NtcA to exert more precise control over shared targets, thereby refining the intricate network of nitrogen metabolic regulation in Anabaena.

Importance: Filamentous, nitrogen-fixing cyanobacteria are valuable organisms for biotechnology applications and as models for the study of multicellularity in prokaryotes. Understanding the regulation of nitrogen fixation and heterocyst development is essential for optimizing their use in synthetic biology and as biofertilizers. This study identifies two novel nitrogen secondary regulators, Alr1976 (NsrX) and All0345 (NsrM), as part of the intricate regulatory circuit governing nitrogen metabolism in the model cyanobacterium Anabaena sp. strain PCC7120. Genes encoding NsrX and NsrM are regulated by both FurC (PerR) and NtcA, therefore taking part in the NtcA-PerR network that modulates nitrogen metabolism and heterocyst differentiation genes.

NsrM (All0345)和NsrX (Alr1976)是两个FurC (PerR)靶向的转录调控因子,可调节蓝藻Anabaena sp.菌株PCC 7120的氮代谢和异囊分化基因。
模型蓝藻Anabaena sp.菌株PCC7120的氮代谢控制是一个复杂的过程,由NtcA、HetR和FurC (PerR)等主要调控因子精心策划。这些蛋白质与二级调节因子建立了复杂的网络,精细地调节细胞代谢,以响应不同的,通常是不确定的环境信号。类似xre的Alr1976蛋白和类似mrr的All0345蛋白是FurC调控的两个预测的转录调控因子。虽然All0345分布广泛,但这两种蛋白在几个细菌门中都有保守的同源物,alr1976后面通常有一个编码锌金属蛋白酶的基因。先前的转录组学分析表明,在缺氮条件下,furC过表达对alr1976表达的影响略大,而all0345表达的变化仅在缺氮条件下观察到,这表明它们是了解Anabaena氮素控制细节的关键候选物。这项工作表明,Alr1976 (NsrX)和All0345 (NsrM)都可能被NtcA调节,并作为氮二级调节剂。∆nsrX和∆nsrM缺失菌株的电泳迁移率和转录组学分析表明,这两种调节因子都是参与氮代谢和杂种囊发育的关键基因的抑制因子。值得注意的是,在降氮24 h时,∆nsrM菌株的杂种囊形成时间较早。NsrX和NsrM对氮代谢基因的最佳dna结合活性要求不同(分别为Mn存在和还原环境),表明它们对不同的环境刺激有响应。这种差分信号集成可能使主调控因子FurC和NtcA对共享靶标施加更精确的控制,从而完善Anabaena中复杂的氮代谢调控网络。重要性:丝状、固氮的蓝藻是生物技术应用中有价值的生物,也是原核生物多细胞研究的模型。了解固氮和异囊发育的调控对于优化它们在合成生物学和作为生物肥料中的应用至关重要。本研究确定了两种新的氮二级调控因子Alr1976 (NsrX)和All0345 (NsrM),作为模型蓝藻Anabaena sp.菌株PCC7120中氮代谢复杂调控回路的一部分。编码NsrX和NsrM的基因同时受FurC (PerR)和NtcA的调控,因此参与NtcA-PerR网络调节氮代谢和杂种囊分化基因。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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