藻藻中蓝藻氮酶簇的研究:固氮光自养生物工程的蓝图。

IF 5.1 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2025-04-09 Epub Date: 2025-02-25 DOI:10.1128/mbio.04052-24
Deng Liu, Anindita Bandyopadhyay, Michelle Liberton, Himadri B Pakrasi, Maitrayee Bhattacharyya-Pakrasi
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引用次数: 0

摘要

单细胞重氮营养蓝藻(如Cyanothece)的氮酶基因簇经常被大自然选择与真核光养生物建立固氮伙伴关系。在这种伙伴关系中赋予优势的基本集群组成部分仍未得到充分探索。为了利用该植物群开发合成的光合固氮系统,有必要对其组成基因进行全面和系统的分析。初步评估将该菌群改造成非重氮营养光养菌的可能性,产生了具有显著氮酶活性的Synechocystis 6803菌株。在目前的研究中,采用重构方法来确定集群中非结构基因的可有可无性,并定义了一个最小基因集,用于构建光养生物的功能性氮酶。采用自底向上的策略,对蓝藻51142的nif基因进行重组,形成新的操作子。然后,这些基因被无缝地移除,以确定它们在固氮过程中的重要性。我们证明,除了结构基因nifHDK, nifBSUENPVZTXW,以及hesAB,在光养菌中优化氮酶功能是重要的。我们还表明,这些基因的最佳表达对有效的氮酶活性至关重要。我们的发现为生成合成系统提供了坚实的基础,该系统将促进太阳能将大气中的氮转化为富氮化合物,向更绿色的世界迈进了一步。将固氮基因整合到各种光合生物中是一种令人兴奋的策略,可以以一种绿色和节能的方式将大气中的氮转化为富氮产物。为了促进这一过程,我们有必要了解非重氮营养、光自养细胞中原核固氮机制的基本功能。本研究考察了一个由真核光自养生物在多种场合自然选择的固氮伙伴关系的氮酶基因簇,并为设计具有固氮能力的光合生物提供了基本蓝图。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of the Cyanothece nitrogenase cluster in Synechocystis: a blueprint for engineering nitrogen-fixing photoautotrophs.

The nitrogenase gene cluster of unicellular diazotrophic cyanobacteria, such as Cyanothece, is frequently selected by nature for nitrogen-fixing partnerships with eukaryotic phototrophs. The essential cluster components that confer an advantage in such partnerships remain underexplored. To use this cluster for the development of synthetic, phototrophic nitrogen-fixing systems, a thorough and systematic analysis of its constituent genes is necessary. An initial effort to assess the possibility of engineering this cluster into non-diazotrophic phototrophs led to the generation of a Synechocystis 6803 strain with significant nitrogenase activity. In the current study, a refactoring approach was taken to determine the dispensability of the non-structural genes in the cluster and define a minimal gene set for constructing a functional nitrogenase for phototrophs. Using a bottom-up strategy, the nif genes from Cyanothece 51142 were re-organized to form new operons. The genes were then seamlessly removed to determine their essentiality in the nitrogen fixation process. We demonstrate that besides the structural genes nifHDK, nifBSUENPVZTXW, as well as hesAB, are important for optimal nitrogenase function in a phototroph. We also show that optimal expression of these genes is crucial for efficient nitrogenase activity. Our findings provide a solid foundation for generating synthetic systems that will facilitate solar-powered conversion of atmospheric nitrogen into nitrogen-rich compounds, a stride toward a greener world.IMPORTANCEIntegrating nitrogen fixation genes into various photosynthetic organisms is an exciting strategy for converting atmospheric nitrogen into nitrogen-rich products in a green and energy-efficient way. In order to facilitate this process, it is essential that we understand the fundamentals of the functioning of a prokaryotic nitrogen-fixing machinery in a non-diazotrophic, photoautotrophic cell. This study examines a nitrogenase gene cluster that has been naturally selected on multiple occasions for a nitrogen-fixing partnership by eukaryotic photoautotrophs and provides a basic blueprint for designing a photosynthetic organism with nitrogen-fixing ability.

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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
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