Metabolic profiling of the sink-to-source transition in developing leaves of quaking aspen.
Identifieur interne : 004233 ( Main/Exploration ); précédent : 004232; suivant : 004234Metabolic profiling of the sink-to-source transition in developing leaves of quaking aspen.
Auteurs : Mijeong Lee Jeong [États-Unis] ; Hongying Jiang ; Huann-Sheng Chen ; Chung-Jui Tsai ; Scott A. HardingSource :
- Plant physiology [ 0032-0889 ] ; 2004.
Descripteurs français
- KwdFr :
- Acides aminés (métabolisme), Feuilles de plante (croissance et développement), Feuilles de plante (enzymologie), Feuilles de plante (métabolisme), Malates (métabolisme), Métabolisme glucidique (MeSH), Photosynthèse (physiologie), Populus (croissance et développement), Populus (métabolisme), Respiration cellulaire (physiologie), Régulation de l'expression des gènes végétaux (MeSH).
- MESH :
- croissance et développement : Feuilles de plante, Populus.
- enzymologie : Feuilles de plante.
- métabolisme : Acides aminés, Feuilles de plante, Malates, Populus.
- physiologie : Photosynthèse, Respiration cellulaire.
- Métabolisme glucidique, Régulation de l'expression des gènes végétaux.
English descriptors
- KwdEn :
- Amino Acids (metabolism), Carbohydrate Metabolism (MeSH), Cell Respiration (physiology), Gene Expression Regulation, Plant (MeSH), Malates (metabolism), Photosynthesis (physiology), Plant Leaves (enzymology), Plant Leaves (growth & development), Plant Leaves (metabolism), Populus (growth & development), Populus (metabolism).
- MESH :
- chemical , metabolism : Amino Acids, Malates.
- enzymology : Plant Leaves.
- growth & development : Plant Leaves, Populus.
- metabolism : Plant Leaves, Populus.
- physiology : Cell Respiration, Photosynthesis.
- Carbohydrate Metabolism, Gene Expression Regulation, Plant.
Abstract
Profiles of small polar metabolites from aspen (Populus tremuloides Michx.) leaves spanning the sink-to-source transition zone were compared. Approximately 25% of 250 to 300 routinely resolved peaks were identified, with carbohydrates, organic acids, and amino acids being most abundant. Two-thirds of identified metabolites exhibited greater than 4-fold changes in abundance during leaf ontogeny. In the context of photosynthetic and respiratory measurements, profile data yielded information consistent with expected developmental trends in carbon-heterotrophic and carbon-autotrophic metabolism. Suc concentration increased throughout leaf expansion, while hexose sugar concentrations peaked at mid-expansion and decreased sharply thereafter. Amino acid contents generally decreased during leaf expansion, but an early increase in Phe and a later one in Gly and Ser reflected growing commitments to secondary metabolism and photorespiration, respectively. The assimilation of nitrate and utilization of stored Asn appeared to be marked by sequential changes in malate concentration and Asn transaminase activity. Principal component and hierarchical clustering analysis facilitated the grouping of cell wall maturation (pectins, hemicelluloses, and oxalate) and membrane biogenesis markers in relation to developmental changes in carbon and nitrogen assimilation. Metabolite profiling will facilitate investigation of nitrogen use and cellular development in Populus sp. varying widely in their growth and pattern of carbon allocation during sink-to-source development and in response to stress.
DOI: 10.1104/pp.104.044776
PubMed: 15448196
PubMed Central: PMC523395
Affiliations:
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Harding</name></author></analytic><series><title level="j">Plant physiology</title><idno type="ISSN">0032-0889</idno><imprint><date when="2004" type="published">2004</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amino Acids (metabolism)</term><term>Carbohydrate Metabolism (MeSH)</term><term>Cell Respiration (physiology)</term><term>Gene Expression Regulation, Plant (MeSH)</term><term>Malates (metabolism)</term><term>Photosynthesis (physiology)</term><term>Plant Leaves (enzymology)</term><term>Plant Leaves (growth & development)</term><term>Plant Leaves (metabolism)</term><term>Populus (growth & development)</term><term>Populus (metabolism)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Acides aminés (métabolisme)</term><term>Feuilles de plante (croissance et développement)</term><term>Feuilles de plante (enzymologie)</term><term>Feuilles de plante (métabolisme)</term><term>Malates (métabolisme)</term><term>Métabolisme glucidique (MeSH)</term><term>Photosynthèse (physiologie)</term><term>Populus (croissance et développement)</term><term>Populus (métabolisme)</term><term>Respiration cellulaire (physiologie)</term><term>Régulation de l'expression des gènes végétaux (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Amino Acids</term><term>Malates</term></keywords><keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr"><term>Feuilles de plante</term><term>Populus</term></keywords><keywords scheme="MESH" qualifier="enzymologie" xml:lang="fr"><term>Feuilles de plante</term></keywords><keywords scheme="MESH" qualifier="enzymology" xml:lang="en"><term>Plant Leaves</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Plant Leaves</term><term>Populus</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Plant Leaves</term><term>Populus</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Acides aminés</term><term>Feuilles de plante</term><term>Malates</term><term>Populus</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Photosynthèse</term><term>Respiration cellulaire</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Cell Respiration</term><term>Photosynthesis</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Carbohydrate Metabolism</term><term>Gene Expression Regulation, Plant</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Métabolisme glucidique</term><term>Régulation de l'expression des gènes végétaux</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Profiles of small polar metabolites from aspen (Populus tremuloides Michx.) leaves spanning the sink-to-source transition zone were compared. Approximately 25% of 250 to 300 routinely resolved peaks were identified, with carbohydrates, organic acids, and amino acids being most abundant. Two-thirds of identified metabolites exhibited greater than 4-fold changes in abundance during leaf ontogeny. In the context of photosynthetic and respiratory measurements, profile data yielded information consistent with expected developmental trends in carbon-heterotrophic and carbon-autotrophic metabolism. Suc concentration increased throughout leaf expansion, while hexose sugar concentrations peaked at mid-expansion and decreased sharply thereafter. Amino acid contents generally decreased during leaf expansion, but an early increase in Phe and a later one in Gly and Ser reflected growing commitments to secondary metabolism and photorespiration, respectively. The assimilation of nitrate and utilization of stored Asn appeared to be marked by sequential changes in malate concentration and Asn transaminase activity. Principal component and hierarchical clustering analysis facilitated the grouping of cell wall maturation (pectins, hemicelluloses, and oxalate) and membrane biogenesis markers in relation to developmental changes in carbon and nitrogen assimilation. Metabolite profiling will facilitate investigation of nitrogen use and cellular development in Populus sp. varying widely in their growth and pattern of carbon allocation during sink-to-source development and in response to stress.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">15448196</PMID><DateCompleted><Year>2005</Year><Month>01</Month><Day>03</Day></DateCompleted><DateRevised><Year>2018</Year><Month>12</Month><Day>24</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">0032-0889</ISSN><JournalIssue CitedMedium="Print"><Volume>136</Volume><Issue>2</Issue><PubDate><Year>2004</Year><Month>Oct</Month></PubDate></JournalIssue><Title>Plant physiology</Title><ISOAbbreviation>Plant Physiol</ISOAbbreviation></Journal><ArticleTitle>Metabolic profiling of the sink-to-source transition in developing leaves of quaking aspen.</ArticleTitle><Pagination><MedlinePgn>3364-75</MedlinePgn></Pagination><Abstract><AbstractText>Profiles of small polar metabolites from aspen (Populus tremuloides Michx.) leaves spanning the sink-to-source transition zone were compared. Approximately 25% of 250 to 300 routinely resolved peaks were identified, with carbohydrates, organic acids, and amino acids being most abundant. Two-thirds of identified metabolites exhibited greater than 4-fold changes in abundance during leaf ontogeny. In the context of photosynthetic and respiratory measurements, profile data yielded information consistent with expected developmental trends in carbon-heterotrophic and carbon-autotrophic metabolism. Suc concentration increased throughout leaf expansion, while hexose sugar concentrations peaked at mid-expansion and decreased sharply thereafter. Amino acid contents generally decreased during leaf expansion, but an early increase in Phe and a later one in Gly and Ser reflected growing commitments to secondary metabolism and photorespiration, respectively. The assimilation of nitrate and utilization of stored Asn appeared to be marked by sequential changes in malate concentration and Asn transaminase activity. Principal component and hierarchical clustering analysis facilitated the grouping of cell wall maturation (pectins, hemicelluloses, and oxalate) and membrane biogenesis markers in relation to developmental changes in carbon and nitrogen assimilation. Metabolite profiling will facilitate investigation of nitrogen use and cellular development in Populus sp. varying widely in their growth and pattern of carbon allocation during sink-to-source development and in response to stress.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Jeong</LastName><ForeName>Mijeong Lee</ForeName><Initials>ML</Initials><AffiliationInfo><Affiliation>Plant Biotechnology Research Center, School of Forest Resources and Environmental Science , Michigan Technological University, Houghton, Michigan 49931, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Jiang</LastName><ForeName>Hongying</ForeName><Initials>H</Initials></Author><Author ValidYN="Y"><LastName>Chen</LastName><ForeName>Huann-Sheng</ForeName><Initials>HS</Initials></Author><Author ValidYN="Y"><LastName>Tsai</LastName><ForeName>Chung-Jui</ForeName><Initials>CJ</Initials></Author><Author ValidYN="Y"><LastName>Harding</LastName><ForeName>Scott A</ForeName><Initials>SA</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2004</Year><Month>09</Month><Day>24</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Plant Physiol</MedlineTA><NlmUniqueID>0401224</NlmUniqueID><ISSNLinking>0032-0889</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000596">Amino Acids</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008293">Malates</NameOfSubstance></Chemical><Chemical><RegistryNumber>817L1N4CKP</RegistryNumber><NameOfSubstance UI="C030298">malic acid</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000596" MajorTopicYN="N">Amino Acids</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D050260" MajorTopicYN="N">Carbohydrate Metabolism</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D019069" MajorTopicYN="N">Cell Respiration</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018506" MajorTopicYN="N">Gene Expression Regulation, Plant</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008293" MajorTopicYN="N">Malates</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010788" MajorTopicYN="N">Photosynthesis</DescriptorName><QualifierName UI="Q000502" 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Harding</name><name sortKey="Jiang, Hongying" sort="Jiang, Hongying" uniqKey="Jiang H" first="Hongying" last="Jiang">Hongying Jiang</name><name sortKey="Tsai, Chung Jui" sort="Tsai, Chung Jui" uniqKey="Tsai C" first="Chung-Jui" last="Tsai">Chung-Jui Tsai</name></noCountry><country name="États-Unis"><noRegion><name sortKey="Jeong, Mijeong Lee" sort="Jeong, Mijeong Lee" uniqKey="Jeong M" first="Mijeong Lee" last="Jeong">Mijeong Lee Jeong</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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