Photosynthetic Metabolism and Nitrogen Reshuffling Are Regulated by Reversible Cysteine Thiol Oxidation Following Nitrogen Deprivation in Chlamydomonas
As global temperatures climb to historic highs, the far-reaching effects of climate change have impacted agricultural nutrient availability. This has extended to low latitude oceans, where a deficit in both nitrogen and phosphorus stores has led to dramatic decreases in carbon sequestration in ocean...
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MDPI AG
2020-06-01
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Online Access: | https://www.mdpi.com/2223-7747/9/6/784 |
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author | Amanda L. Smythers Evan W. McConnell Hailey C. Lewis Saher N. Mubarek Leslie M. Hicks |
author_facet | Amanda L. Smythers Evan W. McConnell Hailey C. Lewis Saher N. Mubarek Leslie M. Hicks |
author_sort | Amanda L. Smythers |
collection | DOAJ |
description | As global temperatures climb to historic highs, the far-reaching effects of climate change have impacted agricultural nutrient availability. This has extended to low latitude oceans, where a deficit in both nitrogen and phosphorus stores has led to dramatic decreases in carbon sequestration in oceanic phytoplankton. Although <i>Chlamydomonas reinhardtii</i>, a freshwater model green alga, has shown drastic systems-level alterations following nitrogen deprivation, the mechanisms through which these alterations are triggered and regulated are not fully understood. This study examined the role of reversible oxidative signaling in the nitrogen stress response of <i>C. reinhardtii</i>. Using oxidized cysteine resin-assisted capture enrichment coupled with label-free quantitative proteomics, 7889 unique oxidized cysteine thiol identifiers were quantified, with 231 significantly changing peptides from 184 proteins following 2 h of nitrogen deprivation. These results demonstrate that the cellular response to nitrogen assimilation, photosynthesis, pigment biosynthesis, and lipid metabolism are regulated by reversible oxidation. An enhanced role of non-damaging oxidative pathways is observed throughout the photosynthetic apparatus that provides a framework for further analysis in phototrophs. |
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issn | 2223-7747 |
language | English |
last_indexed | 2024-03-10T18:56:56Z |
publishDate | 2020-06-01 |
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spelling | doaj.art-05f97bd0eab54a87b2057c02fa81efc22023-11-20T04:39:28ZengMDPI AGPlants2223-77472020-06-019678410.3390/plants9060784Photosynthetic Metabolism and Nitrogen Reshuffling Are Regulated by Reversible Cysteine Thiol Oxidation Following Nitrogen Deprivation in ChlamydomonasAmanda L. Smythers0Evan W. McConnell1Hailey C. Lewis2Saher N. Mubarek3Leslie M. Hicks4Department of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USADepartment of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USADepartment of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USADepartment of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USADepartment of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USAAs global temperatures climb to historic highs, the far-reaching effects of climate change have impacted agricultural nutrient availability. This has extended to low latitude oceans, where a deficit in both nitrogen and phosphorus stores has led to dramatic decreases in carbon sequestration in oceanic phytoplankton. Although <i>Chlamydomonas reinhardtii</i>, a freshwater model green alga, has shown drastic systems-level alterations following nitrogen deprivation, the mechanisms through which these alterations are triggered and regulated are not fully understood. This study examined the role of reversible oxidative signaling in the nitrogen stress response of <i>C. reinhardtii</i>. Using oxidized cysteine resin-assisted capture enrichment coupled with label-free quantitative proteomics, 7889 unique oxidized cysteine thiol identifiers were quantified, with 231 significantly changing peptides from 184 proteins following 2 h of nitrogen deprivation. These results demonstrate that the cellular response to nitrogen assimilation, photosynthesis, pigment biosynthesis, and lipid metabolism are regulated by reversible oxidation. An enhanced role of non-damaging oxidative pathways is observed throughout the photosynthetic apparatus that provides a framework for further analysis in phototrophs.https://www.mdpi.com/2223-7747/9/6/784<i>Chlamydomonas</i>nitrogen deprivationproteomicsoxidative signalingstressphotosynthesis |
spellingShingle | Amanda L. Smythers Evan W. McConnell Hailey C. Lewis Saher N. Mubarek Leslie M. Hicks Photosynthetic Metabolism and Nitrogen Reshuffling Are Regulated by Reversible Cysteine Thiol Oxidation Following Nitrogen Deprivation in Chlamydomonas Plants <i>Chlamydomonas</i> nitrogen deprivation proteomics oxidative signaling stress photosynthesis |
title | Photosynthetic Metabolism and Nitrogen Reshuffling Are Regulated by Reversible Cysteine Thiol Oxidation Following Nitrogen Deprivation in Chlamydomonas |
title_full | Photosynthetic Metabolism and Nitrogen Reshuffling Are Regulated by Reversible Cysteine Thiol Oxidation Following Nitrogen Deprivation in Chlamydomonas |
title_fullStr | Photosynthetic Metabolism and Nitrogen Reshuffling Are Regulated by Reversible Cysteine Thiol Oxidation Following Nitrogen Deprivation in Chlamydomonas |
title_full_unstemmed | Photosynthetic Metabolism and Nitrogen Reshuffling Are Regulated by Reversible Cysteine Thiol Oxidation Following Nitrogen Deprivation in Chlamydomonas |
title_short | Photosynthetic Metabolism and Nitrogen Reshuffling Are Regulated by Reversible Cysteine Thiol Oxidation Following Nitrogen Deprivation in Chlamydomonas |
title_sort | photosynthetic metabolism and nitrogen reshuffling are regulated by reversible cysteine thiol oxidation following nitrogen deprivation in chlamydomonas |
topic | <i>Chlamydomonas</i> nitrogen deprivation proteomics oxidative signaling stress photosynthesis |
url | https://www.mdpi.com/2223-7747/9/6/784 |
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