{"title":"A shared basis for nutrient limitation response in cyanobacteria.","authors":"Hagit Zer,Stav Chen,David Rasin,Miguel Hernandez-Prieto,Nir Keren","doi":"10.1016/j.jbc.2025.110765","DOIUrl":null,"url":null,"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.","PeriodicalId":15140,"journal":{"name":"Journal of Biological Chemistry","volume":"4 1","pages":"110765"},"PeriodicalIF":4.0000,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biological Chemistry","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.jbc.2025.110765","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
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.
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.