Metabolome and Lipidome Profiles of Populus × canescens Twig Tissues During Annual Growth Show Phospholipid-Linked Storage and Mobilization of C, N, and S.
Identifieur interne : 000C58 ( Main/Corpus ); précédent : 000C57; suivant : 000C59Metabolome and Lipidome Profiles of Populus × canescens Twig Tissues During Annual Growth Show Phospholipid-Linked Storage and Mobilization of C, N, and S.
Auteurs : Mutsumi Watanabe ; Florian Netzer ; Takayuki Tohge ; Isabel Orf ; Yariv Brotman ; David Dubbert ; Alisdair R. Fernie ; Heinz Rennenberg ; Rainer Hoefgen ; Cornelia HerschbachSource :
- Frontiers in plant science [ 1664-462X ] ; 2018.
Abstract
The temperate climax tree species Fagus sylvatica and the floodplain tree species Populus × canescens possess contrasting phosphorus (P) nutrition strategies. While F. sylvatica has been documented to display P storage and mobilization (Netzer et al., 2017), this was not observed for Populus × canescens (Netzer et al., 2018b). Nevertheless, changes in the abundance of organic bound P in gray poplar trees indicated adaptation of the P nutrition to different needs during annual growth. The present study aimed at characterizing seasonal changes in metabolite and lipid abundances in gray poplar and uncovering differences in metabolite requirement due to specific needs depending on the season. Seasonal variations in the abundance of (i) sugar-Ps and phospholipids, (ii) amino acids, (iii) sulfur compounds, and (iv) carbon metabolites were expected. It was hypothesized that seasonal changes in metabolite levels relate to N, S, and C storage and mobilization. Changes in organic metabolites binding Pi (Porg) are supposed to support these processes. Variation in triacylglycerols, in sugar-phosphates, in metabolites of the TCA cycle and in the amino acid abundance of poplar twig buds, leaves, bark, and wood were found to be linked to changes in metabolite abundances as well as to C, N, and S storage and mobilization processes. The observed changes support the view of a lack of any P storage in poplar. Yet, during dormancy, contents of phospholipids in twig bark and wood were highest probably due to frost-hardening and to its function in extra-plastidic membranes such as amyloplasts, oleosomes, and protein bodies. Consistent with this assumption, in spring sugar-Ps increased when phospholipids declined and poplar plants entering the vegetative growth period and, hence, metabolic activity increases. These results indicate that poplar trees adopt a policy of P nutrition without P storage and mobilization that is different from their N- and S-nutrition strategies.
DOI: 10.3389/fpls.2018.01292
PubMed: 30233628
PubMed Central: PMC6133996
Links to Exploration step
pubmed:30233628Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Metabolome and Lipidome Profiles of <i>Populus</i> × <i>canescens</i> Twig Tissues During Annual Growth Show Phospholipid-Linked Storage and Mobilization of C, N, and S.</title><author><name sortKey="Watanabe, Mutsumi" sort="Watanabe, Mutsumi" uniqKey="Watanabe M" first="Mutsumi" last="Watanabe">Mutsumi Watanabe</name><affiliation><nlm:affiliation>Max Planck Institute of Molecular Plant Physiology, Wissenschaftspark Potsdam-Golm, Potsdam, Germany.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>NARA Institute of Science and Technology, Ikoma, Japan.</nlm:affiliation></affiliation></author><author><name sortKey="Netzer, Florian" sort="Netzer, Florian" uniqKey="Netzer F" first="Florian" last="Netzer">Florian Netzer</name><affiliation><nlm:affiliation>Chair of Tree Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>Chair of Ecosystem Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Tohge, Takayuki" sort="Tohge, Takayuki" uniqKey="Tohge T" first="Takayuki" last="Tohge">Takayuki Tohge</name><affiliation><nlm:affiliation>Max Planck Institute of Molecular Plant Physiology, Wissenschaftspark Potsdam-Golm, Potsdam, Germany.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>NARA Institute of Science and Technology, Ikoma, Japan.</nlm:affiliation></affiliation></author><author><name sortKey="Orf, Isabel" sort="Orf, Isabel" uniqKey="Orf I" first="Isabel" last="Orf">Isabel Orf</name><affiliation><nlm:affiliation>Max Planck Institute of Molecular Plant Physiology, Wissenschaftspark Potsdam-Golm, Potsdam, Germany.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>Department of Life Sciences, Ben-Gurion University of the Negev, Beersheba, Israel.</nlm:affiliation></affiliation></author><author><name sortKey="Brotman, Yariv" sort="Brotman, Yariv" uniqKey="Brotman Y" first="Yariv" last="Brotman">Yariv Brotman</name><affiliation><nlm:affiliation>Department of Life Sciences, Ben-Gurion University of the Negev, Beersheba, Israel.</nlm:affiliation></affiliation></author><author><name sortKey="Dubbert, David" sort="Dubbert, David" uniqKey="Dubbert D" first="David" last="Dubbert">David Dubbert</name><affiliation><nlm:affiliation>Chair of Ecosystem Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Fernie, Alisdair R" sort="Fernie, Alisdair R" uniqKey="Fernie A" first="Alisdair R" last="Fernie">Alisdair R. 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Fernie</name><affiliation><nlm:affiliation>Max Planck Institute of Molecular Plant Physiology, Wissenschaftspark Potsdam-Golm, Potsdam, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Rennenberg, Heinz" sort="Rennenberg, Heinz" uniqKey="Rennenberg H" first="Heinz" last="Rennenberg">Heinz Rennenberg</name><affiliation><nlm:affiliation>Chair of Tree Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Hoefgen, Rainer" sort="Hoefgen, Rainer" uniqKey="Hoefgen R" first="Rainer" last="Hoefgen">Rainer Hoefgen</name><affiliation><nlm:affiliation>Max Planck Institute of Molecular Plant Physiology, Wissenschaftspark Potsdam-Golm, Potsdam, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Herschbach, Cornelia" sort="Herschbach, Cornelia" uniqKey="Herschbach C" first="Cornelia" last="Herschbach">Cornelia Herschbach</name><affiliation><nlm:affiliation>Chair of Tree Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>Chair of Ecosystem Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Frontiers in plant science</title><idno type="ISSN">1664-462X</idno><imprint><date when="2018" type="published">2018</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The temperate climax tree species <i>Fagus sylvatica</i> and the floodplain tree species <i>Populus</i> × <i>canescens</i> possess contrasting phosphorus (P) nutrition strategies. While <i>F. sylvatica</i> has been documented to display P storage and mobilization (Netzer et al., 2017), this was not observed for <i>Populus</i> × <i>canescens</i> (Netzer et al., 2018b). Nevertheless, changes in the abundance of organic bound P in gray poplar trees indicated adaptation of the P nutrition to different needs during annual growth. The present study aimed at characterizing seasonal changes in metabolite and lipid abundances in gray poplar and uncovering differences in metabolite requirement due to specific needs depending on the season. Seasonal variations in the abundance of (i) sugar-Ps and phospholipids, (ii) amino acids, (iii) sulfur compounds, and (iv) carbon metabolites were expected. It was hypothesized that seasonal changes in metabolite levels relate to N, S, and C storage and mobilization. Changes in organic metabolites binding P<sub>i</sub> (P<sub>org</sub>) are supposed to support these processes. Variation in triacylglycerols, in sugar-phosphates, in metabolites of the TCA cycle and in the amino acid abundance of poplar twig buds, leaves, bark, and wood were found to be linked to changes in metabolite abundances as well as to C, N, and S storage and mobilization processes. The observed changes support the view of a lack of any P storage in poplar. Yet, during dormancy, contents of phospholipids in twig bark and wood were highest probably due to frost-hardening and to its function in extra-plastidic membranes such as amyloplasts, oleosomes, and protein bodies. Consistent with this assumption, in spring sugar-Ps increased when phospholipids declined and poplar plants entering the vegetative growth period and, hence, metabolic activity increases. These results indicate that poplar trees adopt a policy of P nutrition without P storage and mobilization that is different from their N- and S-nutrition strategies.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">30233628</PMID><DateRevised><Year>2020</Year><Month>10</Month><Day>01</Day></DateRevised><Article PubModel="Electronic-eCollection"><Journal><ISSN IssnType="Print">1664-462X</ISSN><JournalIssue CitedMedium="Print"><Volume>9</Volume><PubDate><Year>2018</Year></PubDate></JournalIssue><Title>Frontiers in plant science</Title><ISOAbbreviation>Front Plant Sci</ISOAbbreviation></Journal><ArticleTitle>Metabolome and Lipidome Profiles of <i>Populus</i> × <i>canescens</i> Twig Tissues During Annual Growth Show Phospholipid-Linked Storage and Mobilization of C, N, and S.</ArticleTitle><Pagination><MedlinePgn>1292</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.3389/fpls.2018.01292</ELocationID><Abstract><AbstractText>The temperate climax tree species <i>Fagus sylvatica</i> and the floodplain tree species <i>Populus</i> × <i>canescens</i> possess contrasting phosphorus (P) nutrition strategies. While <i>F. sylvatica</i> has been documented to display P storage and mobilization (Netzer et al., 2017), this was not observed for <i>Populus</i> × <i>canescens</i> (Netzer et al., 2018b). Nevertheless, changes in the abundance of organic bound P in gray poplar trees indicated adaptation of the P nutrition to different needs during annual growth. The present study aimed at characterizing seasonal changes in metabolite and lipid abundances in gray poplar and uncovering differences in metabolite requirement due to specific needs depending on the season. Seasonal variations in the abundance of (i) sugar-Ps and phospholipids, (ii) amino acids, (iii) sulfur compounds, and (iv) carbon metabolites were expected. It was hypothesized that seasonal changes in metabolite levels relate to N, S, and C storage and mobilization. Changes in organic metabolites binding P<sub>i</sub> (P<sub>org</sub>) are supposed to support these processes. Variation in triacylglycerols, in sugar-phosphates, in metabolites of the TCA cycle and in the amino acid abundance of poplar twig buds, leaves, bark, and wood were found to be linked to changes in metabolite abundances as well as to C, N, and S storage and mobilization processes. The observed changes support the view of a lack of any P storage in poplar. Yet, during dormancy, contents of phospholipids in twig bark and wood were highest probably due to frost-hardening and to its function in extra-plastidic membranes such as amyloplasts, oleosomes, and protein bodies. Consistent with this assumption, in spring sugar-Ps increased when phospholipids declined and poplar plants entering the vegetative growth period and, hence, metabolic activity increases. These results indicate that poplar trees adopt a policy of P nutrition without P storage and mobilization that is different from their N- and S-nutrition strategies.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Watanabe</LastName><ForeName>Mutsumi</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Max Planck Institute of Molecular Plant Physiology, Wissenschaftspark Potsdam-Golm, Potsdam, Germany.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>NARA Institute of Science and Technology, Ikoma, Japan.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Netzer</LastName><ForeName>Florian</ForeName><Initials>F</Initials><AffiliationInfo><Affiliation>Chair of Tree Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Chair of Ecosystem Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Tohge</LastName><ForeName>Takayuki</ForeName><Initials>T</Initials><AffiliationInfo><Affiliation>Max Planck Institute of Molecular Plant Physiology, Wissenschaftspark Potsdam-Golm, Potsdam, Germany.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>NARA Institute of Science and Technology, Ikoma, Japan.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Orf</LastName><ForeName>Isabel</ForeName><Initials>I</Initials><AffiliationInfo><Affiliation>Max Planck Institute of Molecular Plant Physiology, Wissenschaftspark Potsdam-Golm, Potsdam, Germany.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Department of Life Sciences, Ben-Gurion University of the Negev, Beersheba, Israel.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Brotman</LastName><ForeName>Yariv</ForeName><Initials>Y</Initials><AffiliationInfo><Affiliation>Department of Life Sciences, Ben-Gurion University of the Negev, Beersheba, Israel.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Dubbert</LastName><ForeName>David</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Chair of Ecosystem Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Fernie</LastName><ForeName>Alisdair R</ForeName><Initials>AR</Initials><AffiliationInfo><Affiliation>Max Planck Institute of Molecular Plant Physiology, Wissenschaftspark Potsdam-Golm, Potsdam, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Rennenberg</LastName><ForeName>Heinz</ForeName><Initials>H</Initials><AffiliationInfo><Affiliation>Chair of Tree Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Hoefgen</LastName><ForeName>Rainer</ForeName><Initials>R</Initials><AffiliationInfo><Affiliation>Max Planck Institute of Molecular Plant Physiology, Wissenschaftspark Potsdam-Golm, Potsdam, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Herschbach</LastName><ForeName>Cornelia</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>Chair of Tree Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Chair of Ecosystem Physiology, Institute of Forest Sciences, Albert Ludwigs University of Freiburg, Freiburg, Germany.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2018</Year><Month>09</Month><Day>05</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Front Plant Sci</MedlineTA><NlmUniqueID>101568200</NlmUniqueID><ISSNLinking>1664-462X</ISSNLinking></MedlineJournalInfo><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Populus × canescens</Keyword><Keyword MajorTopicYN="N">annual growth cycle</Keyword><Keyword MajorTopicYN="N">nutrient mobilization</Keyword><Keyword MajorTopicYN="N">nutrient storage</Keyword><Keyword MajorTopicYN="N">phospholipids</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2018</Year><Month>05</Month><Day>28</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2018</Year><Month>08</Month><Day>16</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2018</Year><Month>9</Month><Day>21</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate 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