Mineral nitrogen sources differently affect root glutamine synthetase isoforms and amino acid balance among organs in maize

Glutamine synthetase (GS) catalyzes the first step of nitrogen assimilation in plant cell. The main GS are classified as cytosolic GS1 and plastidial GS2, of which the functionality is variable according to the nitrogen sources, organs and developmental stages. In maize (Zea mays L.) one gene for GS...

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Veröffentlicht in:BMC plant biology 2015-04, Vol.15 (1), p.96-96, Article 96
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description Glutamine synthetase (GS) catalyzes the first step of nitrogen assimilation in plant cell. The main GS are classified as cytosolic GS1 and plastidial GS2, of which the functionality is variable according to the nitrogen sources, organs and developmental stages. In maize (Zea mays L.) one gene for GS2 and five genes for GS1 subunits are known, but their roles in root metabolism are not yet well defined. In this work, proteomic and biochemical approaches have been used to study root GS enzymes and nitrogen assimilation in maize plants re-supplied with nitrate, ammonium or both. The plant metabolic status highlighted the relevance of root system in maize nitrogen assimilation during both nitrate and ammonium nutrition. The analysis of root proteomes allowed a study to be made of the accumulation and phosphorylation of six GS proteins. Three forms of GS2 were identified, among which only the phosphorylated one showed an accumulation trend consistent with plastidial GS activity. Nitrogen availabilities enabled increments in root total GS synthetase activity, associated with different GS1 isoforms according to the nitrogen sources. Nitrate nutrition induced the specific accumulation of GS1-5 while ammonium led to up-accumulation of both GS1-1 and GS1-5, highlighting co-participation. Moreover, the changes in thermal sensitivity of root GS transferase activity suggested differential rearrangements of the native enzyme. The amino acid accumulation and composition in roots, xylem sap and leaves deeply changed in response to mineral sources. Glutamine showed the prevalent changes in all nitrogen nutritions. Besides, the ammonium nutrition was associated with an accumulation of asparagine and reducing sugars and a drop in glutamic acid level, significantly alleviated by the co-provision with nitrate. This work provides new information about the multifaceted regulation of the GS enzyme in maize roots, indicating the involvement of specific isoenzymes/isoforms, post-translational events and biochemical factors. For the first time, the proteomic approach allowed to discriminate the individual contribution of the GS1 isoforms, highlighting the participation of GS1-5 in nitrate metabolism. Moreover, the results give new insights about the influence of amino acid metabolism in plant C/N balance.
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The main GS are classified as cytosolic GS1 and plastidial GS2, of which the functionality is variable according to the nitrogen sources, organs and developmental stages. In maize (Zea mays L.) one gene for GS2 and five genes for GS1 subunits are known, but their roles in root metabolism are not yet well defined. In this work, proteomic and biochemical approaches have been used to study root GS enzymes and nitrogen assimilation in maize plants re-supplied with nitrate, ammonium or both. The plant metabolic status highlighted the relevance of root system in maize nitrogen assimilation during both nitrate and ammonium nutrition. The analysis of root proteomes allowed a study to be made of the accumulation and phosphorylation of six GS proteins. Three forms of GS2 were identified, among which only the phosphorylated one showed an accumulation trend consistent with plastidial GS activity. Nitrogen availabilities enabled increments in root total GS synthetase activity, associated with different GS1 isoforms according to the nitrogen sources. Nitrate nutrition induced the specific accumulation of GS1-5 while ammonium led to up-accumulation of both GS1-1 and GS1-5, highlighting co-participation. Moreover, the changes in thermal sensitivity of root GS transferase activity suggested differential rearrangements of the native enzyme. The amino acid accumulation and composition in roots, xylem sap and leaves deeply changed in response to mineral sources. Glutamine showed the prevalent changes in all nitrogen nutritions. Besides, the ammonium nutrition was associated with an accumulation of asparagine and reducing sugars and a drop in glutamic acid level, significantly alleviated by the co-provision with nitrate. This work provides new information about the multifaceted regulation of the GS enzyme in maize roots, indicating the involvement of specific isoenzymes/isoforms, post-translational events and biochemical factors. For the first time, the proteomic approach allowed to discriminate the individual contribution of the GS1 isoforms, highlighting the participation of GS1-5 in nitrate metabolism. 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The main GS are classified as cytosolic GS1 and plastidial GS2, of which the functionality is variable according to the nitrogen sources, organs and developmental stages. In maize (Zea mays L.) one gene for GS2 and five genes for GS1 subunits are known, but their roles in root metabolism are not yet well defined. In this work, proteomic and biochemical approaches have been used to study root GS enzymes and nitrogen assimilation in maize plants re-supplied with nitrate, ammonium or both. The plant metabolic status highlighted the relevance of root system in maize nitrogen assimilation during both nitrate and ammonium nutrition. The analysis of root proteomes allowed a study to be made of the accumulation and phosphorylation of six GS proteins. Three forms of GS2 were identified, among which only the phosphorylated one showed an accumulation trend consistent with plastidial GS activity. Nitrogen availabilities enabled increments in root total GS synthetase activity, associated with different GS1 isoforms according to the nitrogen sources. Nitrate nutrition induced the specific accumulation of GS1-5 while ammonium led to up-accumulation of both GS1-1 and GS1-5, highlighting co-participation. Moreover, the changes in thermal sensitivity of root GS transferase activity suggested differential rearrangements of the native enzyme. The amino acid accumulation and composition in roots, xylem sap and leaves deeply changed in response to mineral sources. Glutamine showed the prevalent changes in all nitrogen nutritions. Besides, the ammonium nutrition was associated with an accumulation of asparagine and reducing sugars and a drop in glutamic acid level, significantly alleviated by the co-provision with nitrate. This work provides new information about the multifaceted regulation of the GS enzyme in maize roots, indicating the involvement of specific isoenzymes/isoforms, post-translational events and biochemical factors. For the first time, the proteomic approach allowed to discriminate the individual contribution of the GS1 isoforms, highlighting the participation of GS1-5 in nitrate metabolism. Moreover, the results give new insights about the influence of amino acid metabolism in plant C/N balance.</description><subject>amino acid metabolism</subject><subject>Amino Acid Sequence</subject><subject>Amino Acids - metabolism</subject><subject>ammonium</subject><subject>Ammonium Compounds - metabolism</subject><subject>asparagine</subject><subject>Blotting, Western</subject><subject>Chromatography, Liquid</subject><subject>corn</subject><subject>developmental stages</subject><subject>Gene Expression Regulation, Enzymologic - drug effects</subject><subject>Gene Expression Regulation, Plant - drug effects</subject><subject>genes</subject><subject>glutamate-ammonia ligase</subject><subject>Glutamate-Ammonia Ligase - genetics</subject><subject>Glutamate-Ammonia Ligase - metabolism</subject><subject>glutamic acid</subject><subject>glutamine</subject><subject>isozymes</subject><subject>leaves</subject><subject>Molecular Sequence Data</subject><subject>nitrates</subject><subject>Nitrates - metabolism</subject><subject>nitrogen</subject><subject>nutrition</subject><subject>phosphorylation</subject><subject>Plant Proteins - genetics</subject><subject>Plant Proteins - metabolism</subject><subject>Plant Roots - metabolism</subject><subject>Protein Isoforms - genetics</subject><subject>Protein Isoforms - metabolism</subject><subject>proteins</subject><subject>proteomics</subject><subject>reducing sugars</subject><subject>root systems</subject><subject>roots</subject><subject>sap</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><subject>Tandem Mass Spectrometry</subject><subject>xylem</subject><subject>Zea mays</subject><subject>Zea mays - genetics</subject><subject>Zea mays - metabolism</subject><issn>1471-2229</issn><issn>1471-2229</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkltrFjEQhhdRbK3-AG8k4I1ebM1xN7kRSvFQqAgerkM2O9lGdpOaZMVP_7xZvlr6gSC5yDDzvDPM8DbNU4JPCZHdq0yo7HGLiWgxl7RV95pjwnvSUkrV_TvxUfMo528Yk15y9bA5okLKTtLuuPn9wQdIZkbBlxQnCCjHNVnIaPTOQYJQ5h0yNbQFpRgLmua1mKWqUN6FcgXFZEA-RxfTkpEJI9qqERnrRzSY2QQLNRXDhGKaTMjIB7QY_wseNw-cmTM8uflPmq9v33w5f99efnx3cX522VrBWGlHoGzAgySEj25UnLkBejYaLC3HgmAnlKCOkZ5gyYyzRhAuVKeYwp3rRcdOmtf7vtfrsMBo6051Y32d_GLSTkfj9WEl-Cs9xR-aM8VkL2qDFzcNUvy-Qi568dnCXHeDuGZNMcaCd1LS_6Kk63mnsOSyos_36GRm0D64WIfbDddnghPWd6RXlTr9B1XfCIu3MYDzNX8geHkgqEyBn2Uya8764vOnQ5bsWZtizgnc7VEI1pvF9N5iulpMbxbTm-bZ3WveKv56iv0B2SLMiA</recordid><startdate>20150403</startdate><enddate>20150403</enddate><creator>Prinsi, Bhakti</creator><creator>Espen, Luca</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20150403</creationdate><title>Mineral nitrogen sources differently affect root glutamine synthetase isoforms and amino acid balance among organs in maize</title><author>Prinsi, Bhakti ; Espen, Luca</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c533t-de23b0b8114dfd943fbe73da08c40510f5952f3171083afca51459693906f7563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>amino acid metabolism</topic><topic>Amino Acid Sequence</topic><topic>Amino Acids - metabolism</topic><topic>ammonium</topic><topic>Ammonium Compounds - metabolism</topic><topic>asparagine</topic><topic>Blotting, Western</topic><topic>Chromatography, Liquid</topic><topic>corn</topic><topic>developmental stages</topic><topic>Gene Expression Regulation, Enzymologic - drug effects</topic><topic>Gene Expression Regulation, Plant - drug effects</topic><topic>genes</topic><topic>glutamate-ammonia ligase</topic><topic>Glutamate-Ammonia Ligase - genetics</topic><topic>Glutamate-Ammonia Ligase - metabolism</topic><topic>glutamic acid</topic><topic>glutamine</topic><topic>isozymes</topic><topic>leaves</topic><topic>Molecular Sequence Data</topic><topic>nitrates</topic><topic>Nitrates - metabolism</topic><topic>nitrogen</topic><topic>nutrition</topic><topic>phosphorylation</topic><topic>Plant Proteins - genetics</topic><topic>Plant Proteins - metabolism</topic><topic>Plant Roots - metabolism</topic><topic>Protein Isoforms - genetics</topic><topic>Protein Isoforms - metabolism</topic><topic>proteins</topic><topic>proteomics</topic><topic>reducing sugars</topic><topic>root systems</topic><topic>roots</topic><topic>sap</topic><topic>Spectrometry, Mass, Electrospray Ionization</topic><topic>Tandem Mass Spectrometry</topic><topic>xylem</topic><topic>Zea mays</topic><topic>Zea mays - genetics</topic><topic>Zea mays - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prinsi, Bhakti</creatorcontrib><creatorcontrib>Espen, Luca</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC plant biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Prinsi, Bhakti</au><au>Espen, Luca</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mineral nitrogen sources differently affect root glutamine synthetase isoforms and amino acid balance among organs in maize</atitle><jtitle>BMC plant biology</jtitle><addtitle>BMC Plant Biol</addtitle><date>2015-04-03</date><risdate>2015</risdate><volume>15</volume><issue>1</issue><spage>96</spage><epage>96</epage><pages>96-96</pages><artnum>96</artnum><issn>1471-2229</issn><eissn>1471-2229</eissn><abstract>Glutamine synthetase (GS) catalyzes the first step of nitrogen assimilation in plant cell. The main GS are classified as cytosolic GS1 and plastidial GS2, of which the functionality is variable according to the nitrogen sources, organs and developmental stages. In maize (Zea mays L.) one gene for GS2 and five genes for GS1 subunits are known, but their roles in root metabolism are not yet well defined. In this work, proteomic and biochemical approaches have been used to study root GS enzymes and nitrogen assimilation in maize plants re-supplied with nitrate, ammonium or both. The plant metabolic status highlighted the relevance of root system in maize nitrogen assimilation during both nitrate and ammonium nutrition. The analysis of root proteomes allowed a study to be made of the accumulation and phosphorylation of six GS proteins. Three forms of GS2 were identified, among which only the phosphorylated one showed an accumulation trend consistent with plastidial GS activity. Nitrogen availabilities enabled increments in root total GS synthetase activity, associated with different GS1 isoforms according to the nitrogen sources. Nitrate nutrition induced the specific accumulation of GS1-5 while ammonium led to up-accumulation of both GS1-1 and GS1-5, highlighting co-participation. Moreover, the changes in thermal sensitivity of root GS transferase activity suggested differential rearrangements of the native enzyme. The amino acid accumulation and composition in roots, xylem sap and leaves deeply changed in response to mineral sources. Glutamine showed the prevalent changes in all nitrogen nutritions. Besides, the ammonium nutrition was associated with an accumulation of asparagine and reducing sugars and a drop in glutamic acid level, significantly alleviated by the co-provision with nitrate. This work provides new information about the multifaceted regulation of the GS enzyme in maize roots, indicating the involvement of specific isoenzymes/isoforms, post-translational events and biochemical factors. For the first time, the proteomic approach allowed to discriminate the individual contribution of the GS1 isoforms, highlighting the participation of GS1-5 in nitrate metabolism. Moreover, the results give new insights about the influence of amino acid metabolism in plant C/N balance.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>25886826</pmid><doi>10.1186/s12870-015-0482-9</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects amino acid metabolism
Amino Acid Sequence
Amino Acids - metabolism
ammonium
Ammonium Compounds - metabolism
asparagine
Blotting, Western
Chromatography, Liquid
corn
developmental stages
Gene Expression Regulation, Enzymologic - drug effects
Gene Expression Regulation, Plant - drug effects
genes
glutamate-ammonia ligase
Glutamate-Ammonia Ligase - genetics
Glutamate-Ammonia Ligase - metabolism
glutamic acid
glutamine
isozymes
leaves
Molecular Sequence Data
nitrates
Nitrates - metabolism
nitrogen
nutrition
phosphorylation
Plant Proteins - genetics
Plant Proteins - metabolism
Plant Roots - metabolism
Protein Isoforms - genetics
Protein Isoforms - metabolism
proteins
proteomics
reducing sugars
root systems
roots
sap
Spectrometry, Mass, Electrospray Ionization
Tandem Mass Spectrometry
xylem
Zea mays
Zea mays - genetics
Zea mays - metabolism
title Mineral nitrogen sources differently affect root glutamine synthetase isoforms and amino acid balance among organs in maize
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