A shared basis for nutrient limitation response in cyanobacteria.

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hagit Zer,Stav Chen,David Rasin,Miguel Hernandez-Prieto,Nir Keren
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引用次数: 0

Abstract

Cyanobacteria possess diverse regulatory mechanisms to adapt to nutrient limitation, yet the extent to which these responses are shared across different nutrient stresses remains unclear. Understanding these commonalities can reveal fundamental principles of cellular resource allocation and survival strategies. In this work, we investigated the transcriptional responses of Synechocystis sp. PCC 6803 to nitrogen, sulphur or phosphate limitation and found a core set of genes consistently regulated across all three conditions. This shared response includes repression of genes related to photosynthesis and respiratory electron transport, as well as genes encoding components of the Calvin-Benson cycle, ribosome function and cellular metabolism. Amongst the highest affected pathways is chlorophyll biosynthesis. A subset of regulatory genes, mostly kinases, are upregulated under all three limitation conditions. These results were further validated by a study of the composition and the function of the photosynthetic machinery. Chlorophyll accumulation was arrested immediately upon transition to limiting media, photosynthetic activities were reduced and protein complexes were degraded. Our findings reveal a conserved program in cyanobacteria that modulates cellular metabolism and photosynthesis in response to diverse nutrient limitations. Based on these findings, we suggest that chlorophyll biosynthesis is a key regulated pathway driving structural and physiological responses in photosynthesis.
蓝藻中营养限制反应的共同基础。
蓝藻拥有多种调节机制来适应营养限制,但这些反应在不同营养胁迫下共享的程度尚不清楚。了解这些共性可以揭示细胞资源分配和生存策略的基本原则。在这项工作中,我们研究了Synechocystis sp. PCC 6803对氮、硫或磷酸盐限制的转录反应,并发现了一组核心基因在这三种条件下一致受到调控。这种共同的反应包括抑制与光合作用和呼吸电子传递相关的基因,以及编码卡尔文-本森循环成分、核糖体功能和细胞代谢的基因。受影响最大的途径之一是叶绿素生物合成。调控基因的一个子集,主要是激酶,在所有三种限制条件下上调。对光合机制的组成和功能的研究进一步证实了这些结果。在过渡到限制培养基后,叶绿素积累立即被阻止,光合活性降低,蛋白质复合物降解。我们的研究结果揭示了蓝细菌中一个保守的程序,该程序调节细胞代谢和光合作用,以响应不同的营养限制。基于这些发现,我们认为叶绿素生物合成是驱动光合作用结构和生理反应的关键调控途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
自引率
4.20%
发文量
1233
期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
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