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Physiological and Biochemical Responses of Cucumis melo L. Chloroplasts to Low-Phosphate Stress

Phosphorus (P) is a limiting plant soil nutrient. Long-term low inorganic phosphate (Pi) irreversibly damages plant cells and hinders plant growth. Plants have evolved several adaptive biochemical, physiological, and developmental responses to low-Pi stress. However, little is known about chloroplas...

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Autores principales: Li, Pengli, Weng, Jinyang, Zhang, Qing, Yu, Liyao, Yao, Qi, Chang, Liying, Niu, Qingliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204437/
https://www.ncbi.nlm.nih.gov/pubmed/30405663
http://dx.doi.org/10.3389/fpls.2018.01525
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author Li, Pengli
Weng, Jinyang
Zhang, Qing
Yu, Liyao
Yao, Qi
Chang, Liying
Niu, Qingliang
author_facet Li, Pengli
Weng, Jinyang
Zhang, Qing
Yu, Liyao
Yao, Qi
Chang, Liying
Niu, Qingliang
author_sort Li, Pengli
collection PubMed
description Phosphorus (P) is a limiting plant soil nutrient. Long-term low inorganic phosphate (Pi) irreversibly damages plant cells and hinders plant growth. Plants have evolved several adaptive biochemical, physiological, and developmental responses to low-Pi stress. However, little is known about chloroplast responses to low-Pi stress. In this study, we used physiological and biochemical analyses to investigate melon chloroplast responses to low-Pi stress. The results indicated that low-Pi stress impeded melon seedling growth and reduced its dry matter content by inhibiting the photosynthesis. Low-Pi stress reduced the P content in shoots, which inhibited ATP synthase (ATP-ase) activity, and disturbed the proton and electron transport efficiency on chloroplast photosynthetic electron transport chain. In addition, low-Pi stress induced reactive oxygen species (ROS) production in the leaves, which caused membrane peroxidation. Therefore, redox homeostasis was not maintained, and the melon leaves presented with symptoms of photooxidative stress. To mitigate photoinhibition, the melon plants initiated non-photochemical chlorophyll fluorescence quenching (NPQ) initiated by acidification of the thylakoid lumen to dissipate excess excitation energy, significantly improved ROS-scavenging enzyme activity. Based on these experimental results, we concluded that low Pi inhibited photosystem activity and caused photooxidative stress and photoinhibition. To alleviate these negative effects, the plant activated its NPQ mechanism, alternative electron transport pathways, and antioxidant system to protect its chloroplasts.
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spelling pubmed-62044372018-11-07 Physiological and Biochemical Responses of Cucumis melo L. Chloroplasts to Low-Phosphate Stress Li, Pengli Weng, Jinyang Zhang, Qing Yu, Liyao Yao, Qi Chang, Liying Niu, Qingliang Front Plant Sci Plant Science Phosphorus (P) is a limiting plant soil nutrient. Long-term low inorganic phosphate (Pi) irreversibly damages plant cells and hinders plant growth. Plants have evolved several adaptive biochemical, physiological, and developmental responses to low-Pi stress. However, little is known about chloroplast responses to low-Pi stress. In this study, we used physiological and biochemical analyses to investigate melon chloroplast responses to low-Pi stress. The results indicated that low-Pi stress impeded melon seedling growth and reduced its dry matter content by inhibiting the photosynthesis. Low-Pi stress reduced the P content in shoots, which inhibited ATP synthase (ATP-ase) activity, and disturbed the proton and electron transport efficiency on chloroplast photosynthetic electron transport chain. In addition, low-Pi stress induced reactive oxygen species (ROS) production in the leaves, which caused membrane peroxidation. Therefore, redox homeostasis was not maintained, and the melon leaves presented with symptoms of photooxidative stress. To mitigate photoinhibition, the melon plants initiated non-photochemical chlorophyll fluorescence quenching (NPQ) initiated by acidification of the thylakoid lumen to dissipate excess excitation energy, significantly improved ROS-scavenging enzyme activity. Based on these experimental results, we concluded that low Pi inhibited photosystem activity and caused photooxidative stress and photoinhibition. To alleviate these negative effects, the plant activated its NPQ mechanism, alternative electron transport pathways, and antioxidant system to protect its chloroplasts. Frontiers Media S.A. 2018-10-22 /pmc/articles/PMC6204437/ /pubmed/30405663 http://dx.doi.org/10.3389/fpls.2018.01525 Text en Copyright © 2018 Li, Weng, Zhang, Yu, Yao, Chang and Niu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Li, Pengli
Weng, Jinyang
Zhang, Qing
Yu, Liyao
Yao, Qi
Chang, Liying
Niu, Qingliang
Physiological and Biochemical Responses of Cucumis melo L. Chloroplasts to Low-Phosphate Stress
title Physiological and Biochemical Responses of Cucumis melo L. Chloroplasts to Low-Phosphate Stress
title_full Physiological and Biochemical Responses of Cucumis melo L. Chloroplasts to Low-Phosphate Stress
title_fullStr Physiological and Biochemical Responses of Cucumis melo L. Chloroplasts to Low-Phosphate Stress
title_full_unstemmed Physiological and Biochemical Responses of Cucumis melo L. Chloroplasts to Low-Phosphate Stress
title_short Physiological and Biochemical Responses of Cucumis melo L. Chloroplasts to Low-Phosphate Stress
title_sort physiological and biochemical responses of cucumis melo l. chloroplasts to low-phosphate stress
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204437/
https://www.ncbi.nlm.nih.gov/pubmed/30405663
http://dx.doi.org/10.3389/fpls.2018.01525
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