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NaCl-altered oxygen flux profiles and H+-ATPase activity in roots of two contrasting poplar species.

Identifieur interne : 000254 ( Main/Exploration ); précédent : 000253; suivant : 000255

NaCl-altered oxygen flux profiles and H+-ATPase activity in roots of two contrasting poplar species.

Auteurs : Xiuying Ma [République populaire de Chine] ; Jinke Li [République populaire de Chine] ; Chen Deng [République populaire de Chine] ; Jian Sun [République populaire de Chine] ; Jian Liu [République populaire de Chine] ; Niya Li [République populaire de Chine] ; Yanjun Lu [République populaire de Chine] ; Ruigang Wang [République populaire de Chine] ; Rui Zhao [République populaire de Chine] ; Xiaoyang Zhou [République populaire de Chine] ; Cunfu Lu [République populaire de Chine] ; Shaoliang Chen [République populaire de Chine]

Source :

RBID : pubmed:33105484

Abstract

Maintaining mitochondrial respiration is crucial for proving ATP for H+ pumps to continuously exclude Na+ under salt stress. NaCl-altered O2 uptake, mitochondrial respiration, and the relevance to H+-ATPase activity were investigated in two contrasting poplar species, Populus euphratica (salt-tolerant) and P. popularis 35-44 (salt-sensitive). Compared with P. popularis, P. euphratica roots exhibited a greater capacity to extrude Na+ under NaCl stress (150 mM). The cytochemical analysis with Pb(NO3)2 staining revealed that P. euphratica root cells retained higher H+ hydrolysis activity than the salt-sensitive poplar during a long-term (LT) of increasing salt stress (50 to 200 mM NaCl, 4 weeks). Long-sustained activation of proton pumps require long-lasting supply of energy (ATP), delivered by aerobic respiration. Taking advantage of the vibrating-electrodes technology combined with the use of membrane-tipped, polarographic oxygen microelectrodes, the species, spatial, and temporal differences in root O2 uptake were characterized under conditions of salt stress. Oxygen uptake upon NaCl shock (150 mM) was less declined in P. euphratica than in P. popularis, although the salt-induced transient kinetics were distinct from the drastic drop of O2 caused by hyperosmotic shock (255 mM mannitol). Short-term (ST) treatment (150 mM NaCl, 24 h) stimulated O2 influx in P. euphratica roots, and LT-treated P. euphratica displayed an increased O2 influx along root axis, whereas O2 influx declined with increasing salinity in P. popularis roots. The spatial localization of O2 influxes revealed that the apical zone was more susceptible than elongation region upon high NaCl (150, 200 mM) during ST and LT stress. Pharmacological experiments showed that the Na+ extrusion and H+-ATPase activity in salinized roots were correspondingly suppressed when O2 uptake was inhibited by a mitochondrial respiration inhibitor, NaN3. Therefore, we conclude that the stable mitochondrial respiration energized H+-ATPase of P. euphratica root cells for maintaining Na+ homeostasis under salt environments.

DOI: 10.1093/treephys/tpaa142
PubMed: 33105484


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<name sortKey="Zhao, Rui" sort="Zhao, Rui" uniqKey="Zhao R" first="Rui" last="Zhao">Rui Zhao</name>
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<div type="abstract" xml:lang="en">Maintaining mitochondrial respiration is crucial for proving ATP for H+ pumps to continuously exclude Na+ under salt stress. NaCl-altered O2 uptake, mitochondrial respiration, and the relevance to H+-ATPase activity were investigated in two contrasting poplar species, Populus euphratica (salt-tolerant) and P. popularis 35-44 (salt-sensitive). Compared with P. popularis, P. euphratica roots exhibited a greater capacity to extrude Na+ under NaCl stress (150 mM). The cytochemical analysis with Pb(NO3)2 staining revealed that P. euphratica root cells retained higher H+ hydrolysis activity than the salt-sensitive poplar during a long-term (LT) of increasing salt stress (50 to 200 mM NaCl, 4 weeks). Long-sustained activation of proton pumps require long-lasting supply of energy (ATP), delivered by aerobic respiration. Taking advantage of the vibrating-electrodes technology combined with the use of membrane-tipped, polarographic oxygen microelectrodes, the species, spatial, and temporal differences in root O2 uptake were characterized under conditions of salt stress. Oxygen uptake upon NaCl shock (150 mM) was less declined in P. euphratica than in P. popularis, although the salt-induced transient kinetics were distinct from the drastic drop of O2 caused by hyperosmotic shock (255 mM mannitol). Short-term (ST) treatment (150 mM NaCl, 24 h) stimulated O2 influx in P. euphratica roots, and LT-treated P. euphratica displayed an increased O2 influx along root axis, whereas O2 influx declined with increasing salinity in P. popularis roots. The spatial localization of O2 influxes revealed that the apical zone was more susceptible than elongation region upon high NaCl (150, 200 mM) during ST and LT stress. Pharmacological experiments showed that the Na+ extrusion and H+-ATPase activity in salinized roots were correspondingly suppressed when O2 uptake was inhibited by a mitochondrial respiration inhibitor, NaN3. Therefore, we conclude that the stable mitochondrial respiration energized H+-ATPase of P. euphratica root cells for maintaining Na+ homeostasis under salt environments.</div>
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<ELocationID EIdType="doi" ValidYN="Y">10.1093/treephys/tpaa142</ELocationID>
<Abstract>
<AbstractText>Maintaining mitochondrial respiration is crucial for proving ATP for H+ pumps to continuously exclude Na+ under salt stress. NaCl-altered O2 uptake, mitochondrial respiration, and the relevance to H+-ATPase activity were investigated in two contrasting poplar species, Populus euphratica (salt-tolerant) and P. popularis 35-44 (salt-sensitive). Compared with P. popularis, P. euphratica roots exhibited a greater capacity to extrude Na+ under NaCl stress (150 mM). The cytochemical analysis with Pb(NO3)2 staining revealed that P. euphratica root cells retained higher H+ hydrolysis activity than the salt-sensitive poplar during a long-term (LT) of increasing salt stress (50 to 200 mM NaCl, 4 weeks). Long-sustained activation of proton pumps require long-lasting supply of energy (ATP), delivered by aerobic respiration. Taking advantage of the vibrating-electrodes technology combined with the use of membrane-tipped, polarographic oxygen microelectrodes, the species, spatial, and temporal differences in root O2 uptake were characterized under conditions of salt stress. Oxygen uptake upon NaCl shock (150 mM) was less declined in P. euphratica than in P. popularis, although the salt-induced transient kinetics were distinct from the drastic drop of O2 caused by hyperosmotic shock (255 mM mannitol). Short-term (ST) treatment (150 mM NaCl, 24 h) stimulated O2 influx in P. euphratica roots, and LT-treated P. euphratica displayed an increased O2 influx along root axis, whereas O2 influx declined with increasing salinity in P. popularis roots. The spatial localization of O2 influxes revealed that the apical zone was more susceptible than elongation region upon high NaCl (150, 200 mM) during ST and LT stress. Pharmacological experiments showed that the Na+ extrusion and H+-ATPase activity in salinized roots were correspondingly suppressed when O2 uptake was inhibited by a mitochondrial respiration inhibitor, NaN3. Therefore, we conclude that the stable mitochondrial respiration energized H+-ATPase of P. euphratica root cells for maintaining Na+ homeostasis under salt environments.</AbstractText>
<CopyrightInformation>© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Ma</LastName>
<ForeName>Xiuying</ForeName>
<Initials>X</Initials>
<AffiliationInfo>
<Affiliation>Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, College of Biological Sciences and Technology (Box 162), Beijing Forestry University, Beijing 100083, P.R. China.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of life Science and Engineering, Jining University, Qufu 273155, Shandong, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Li</LastName>
<ForeName>Jinke</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, College of Biological Sciences and Technology (Box 162), Beijing Forestry University, Beijing 100083, P.R. China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Deng</LastName>
<ForeName>Chen</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, College of Biological Sciences and Technology (Box 162), Beijing Forestry University, Beijing 100083, P.R. China.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Sun</LastName>
<ForeName>Jian</ForeName>
<Initials>J</Initials>
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<Affiliation>Institute of Integrative Plant Biology, School of Life Science, Jiangsu Normal University, Xuzhou 221116, Jiangsu Province, People's Republic of China.</Affiliation>
</AffiliationInfo>
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<LastName>Liu</LastName>
<ForeName>Jian</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, College of Biological Sciences and Technology (Box 162), Beijing Forestry University, Beijing 100083, P.R. China.</Affiliation>
</AffiliationInfo>
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<LastName>Li</LastName>
<ForeName>Niya</ForeName>
<Initials>N</Initials>
<AffiliationInfo>
<Affiliation>Department of Biology, College of Life Science, Hainan Normal University, Haikou 571158, China.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Lu</LastName>
<ForeName>Yanjun</ForeName>
<Initials>Y</Initials>
<AffiliationInfo>
<Affiliation>College of Forestry, Northwest Agriculture & Forestry University of China, Taicheng Road 3, 712100, Yangling, Shaanxi Province, P.R. China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Wang</LastName>
<ForeName>Ruigang</ForeName>
<Initials>R</Initials>
<AffiliationInfo>
<Affiliation>Agro-Environmental Protection Institute, Ministry of Agriculture and Rural Affairs, Tianjin, 300191, PR China.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Zhao</LastName>
<ForeName>Rui</ForeName>
<Initials>R</Initials>
<AffiliationInfo>
<Affiliation>Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, College of Biological Sciences and Technology (Box 162), Beijing Forestry University, Beijing 100083, P.R. China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Zhou</LastName>
<ForeName>Xiaoyang</ForeName>
<Initials>X</Initials>
<AffiliationInfo>
<Affiliation>Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, College of Biological Sciences and Technology (Box 162), Beijing Forestry University, Beijing 100083, P.R. China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Lu</LastName>
<ForeName>Cunfu</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, College of Biological Sciences and Technology (Box 162), Beijing Forestry University, Beijing 100083, P.R. China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Chen</LastName>
<ForeName>Shaoliang</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, College of Biological Sciences and Technology (Box 162), Beijing Forestry University, Beijing 100083, P.R. China.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2020</Year>
<Month>10</Month>
<Day>26</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>Canada</Country>
<MedlineTA>Tree Physiol</MedlineTA>
<NlmUniqueID>100955338</NlmUniqueID>
<ISSNLinking>0829-318X</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">NaCl</Keyword>
<Keyword MajorTopicYN="N">O2 influx</Keyword>
<Keyword MajorTopicYN="N">Root</Keyword>
<Keyword MajorTopicYN="N">cytochemical staining</Keyword>
<Keyword MajorTopicYN="N">mitochondrial respiration</Keyword>
<Keyword MajorTopicYN="N">non-invasive micro-test (NMT) system</Keyword>
<Keyword MajorTopicYN="N">plasma membrane H+-ATPase</Keyword>
<Keyword MajorTopicYN="N">polarographic oxygen microelectrodes</Keyword>
<Keyword MajorTopicYN="N">poplar</Keyword>
</KeywordList>
</MedlineCitation>
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<Day>26</Day>
<Hour>20</Hour>
<Minute>18</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2020</Year>
<Month>10</Month>
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<PubMedPubDate PubStatus="medline">
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<PublicationStatus>aheadofprint</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">33105484</ArticleId>
<ArticleId IdType="pii">5940447</ArticleId>
<ArticleId IdType="doi">10.1093/treephys/tpaa142</ArticleId>
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<affiliations>
<list>
<country>
<li>République populaire de Chine</li>
</country>
<settlement>
<li>Pékin</li>
</settlement>
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<name sortKey="Deng, Chen" sort="Deng, Chen" uniqKey="Deng C" first="Chen" last="Deng">Chen Deng</name>
<name sortKey="Li, Jinke" sort="Li, Jinke" uniqKey="Li J" first="Jinke" last="Li">Jinke Li</name>
<name sortKey="Li, Niya" sort="Li, Niya" uniqKey="Li N" first="Niya" last="Li">Niya Li</name>
<name sortKey="Liu, Jian" sort="Liu, Jian" uniqKey="Liu J" first="Jian" last="Liu">Jian Liu</name>
<name sortKey="Lu, Cunfu" sort="Lu, Cunfu" uniqKey="Lu C" first="Cunfu" last="Lu">Cunfu Lu</name>
<name sortKey="Lu, Yanjun" sort="Lu, Yanjun" uniqKey="Lu Y" first="Yanjun" last="Lu">Yanjun Lu</name>
<name sortKey="Ma, Xiuying" sort="Ma, Xiuying" uniqKey="Ma X" first="Xiuying" last="Ma">Xiuying Ma</name>
<name sortKey="Sun, Jian" sort="Sun, Jian" uniqKey="Sun J" first="Jian" last="Sun">Jian Sun</name>
<name sortKey="Wang, Ruigang" sort="Wang, Ruigang" uniqKey="Wang R" first="Ruigang" last="Wang">Ruigang Wang</name>
<name sortKey="Zhao, Rui" sort="Zhao, Rui" uniqKey="Zhao R" first="Rui" last="Zhao">Rui Zhao</name>
<name sortKey="Zhou, Xiaoyang" sort="Zhou, Xiaoyang" uniqKey="Zhou X" first="Xiaoyang" last="Zhou">Xiaoyang Zhou</name>
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