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Nickel-induced changes in carbon metabolism in wheat shoots
In this study, we analyzed the toxic effect of Ni during the development of wheat shoots. Typical developmental alterations in carbon metabolism-related parameters reflecting changes associated with the transition of the seedlings from heterotrophic to autotrophic metabolism were observed in the con...
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Published in: | Journal of plant physiology 2013-03, Vol.170 (4), p.369-377 |
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description | In this study, we analyzed the toxic effect of Ni during the development of wheat shoots. Typical developmental alterations in carbon metabolism-related parameters reflecting changes associated with the transition of the seedlings from heterotrophic to autotrophic metabolism were observed in the control shoots between the 1st and the 4th days. Adverse effects of 50 and 100μM Ni became evident starting from the 4th day of growth on the metal-containing media. We found that Ni-induced stimulation of phosphoenolpyruvate carboxylase (PEPC) activity coincided with decrease in the ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) level and with declines in net photosynthetic rate (PN) and stomatal conductance (gs). Application of Ni resulted in increased activities of several dehydrogenases: glucose-6-phosphate dehydrogenase (G6PDH), 6-phosphogluconate dehydrogenase (6PGDH), isocitrate dehydrogenase (NADP-ICDH) and malate dehydrogenase (NADH-MDH). In contrast, the activities of malic enzymes (NADP-ME and NAD-ME) decreased due to Ni stress. Treatment with Ni led to accumulation of glucose and declined concentration of sucrose as well as considerable increases in concentrations of malic and citric acids. Our results indicate that Ni stress redirects the carbon metabolism of developing wheat shoots to provide carbon skeletons for synthesis of amino acids and organic acids as well as to supply reducing power to sustain normal metabolic processes and to support defense mechanisms against oxidative stress. |
doi_str_mv | 10.1016/j.jplph.2012.10.012 |
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Typical developmental alterations in carbon metabolism-related parameters reflecting changes associated with the transition of the seedlings from heterotrophic to autotrophic metabolism were observed in the control shoots between the 1st and the 4th days. Adverse effects of 50 and 100μM Ni became evident starting from the 4th day of growth on the metal-containing media. We found that Ni-induced stimulation of phosphoenolpyruvate carboxylase (PEPC) activity coincided with decrease in the ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) level and with declines in net photosynthetic rate (PN) and stomatal conductance (gs). Application of Ni resulted in increased activities of several dehydrogenases: glucose-6-phosphate dehydrogenase (G6PDH), 6-phosphogluconate dehydrogenase (6PGDH), isocitrate dehydrogenase (NADP-ICDH) and malate dehydrogenase (NADH-MDH). In contrast, the activities of malic enzymes (NADP-ME and NAD-ME) decreased due to Ni stress. Treatment with Ni led to accumulation of glucose and declined concentration of sucrose as well as considerable increases in concentrations of malic and citric acids. Our results indicate that Ni stress redirects the carbon metabolism of developing wheat shoots to provide carbon skeletons for synthesis of amino acids and organic acids as well as to supply reducing power to sustain normal metabolic processes and to support defense mechanisms against oxidative stress.</description><identifier>ISSN: 0176-1617</identifier><identifier>EISSN: 1618-1328</identifier><identifier>DOI: 10.1016/j.jplph.2012.10.012</identifier><identifier>PMID: 23374731</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>adverse effects ; amino acids ; Carbon ; Carbon - metabolism ; Carbon metabolism enzymes ; citric acid ; defense mechanisms ; Enzyme Activation - drug effects ; Enzymes ; glucose ; glucose-6-phosphate 1-dehydrogenase ; isocitrate dehydrogenase ; Malate ; malate dehydrogenase ; Metabolism ; Nickel ; Nickel - toxicity ; oxidative stress ; phosphoenolpyruvate carboxylase ; Phosphoenolpyruvate Carboxylase - metabolism ; phosphogluconate dehydrogenase ; Photosynthesis ; Photosynthesis - drug effects ; Physiology ; Plant Shoots - growth & development ; Plant Stomata - drug effects ; ribulose-bisphosphate carboxylase ; Ribulose-Bisphosphate Carboxylase - metabolism ; seedlings ; shoots ; stomatal conductance ; Stress concentration ; Stresses ; sucrose ; toxicity ; Triticum - drug effects ; Triticum - metabolism ; Triticum aestivum ; Wheat</subject><ispartof>Journal of plant physiology, 2013-03, Vol.170 (4), p.369-377</ispartof><rights>2012 Elsevier GmbH</rights><rights>Copyright © 2012 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c482t-68867594e450ed7e800e98976c9b98aa743f2b981c2a5d9169e026852be4cf0b3</citedby><cites>FETCH-LOGICAL-c482t-68867594e450ed7e800e98976c9b98aa743f2b981c2a5d9169e026852be4cf0b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23374731$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gajewska, Ewa</creatorcontrib><creatorcontrib>Niewiadomska, Ewa</creatorcontrib><creatorcontrib>Tokarz, Krzysztof</creatorcontrib><creatorcontrib>Słaba, Mirosława</creatorcontrib><creatorcontrib>Skłodowska, Maria</creatorcontrib><title>Nickel-induced changes in carbon metabolism in wheat shoots</title><title>Journal of plant physiology</title><addtitle>J Plant Physiol</addtitle><description>In this study, we analyzed the toxic effect of Ni during the development of wheat shoots. Typical developmental alterations in carbon metabolism-related parameters reflecting changes associated with the transition of the seedlings from heterotrophic to autotrophic metabolism were observed in the control shoots between the 1st and the 4th days. Adverse effects of 50 and 100μM Ni became evident starting from the 4th day of growth on the metal-containing media. We found that Ni-induced stimulation of phosphoenolpyruvate carboxylase (PEPC) activity coincided with decrease in the ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) level and with declines in net photosynthetic rate (PN) and stomatal conductance (gs). Application of Ni resulted in increased activities of several dehydrogenases: glucose-6-phosphate dehydrogenase (G6PDH), 6-phosphogluconate dehydrogenase (6PGDH), isocitrate dehydrogenase (NADP-ICDH) and malate dehydrogenase (NADH-MDH). In contrast, the activities of malic enzymes (NADP-ME and NAD-ME) decreased due to Ni stress. Treatment with Ni led to accumulation of glucose and declined concentration of sucrose as well as considerable increases in concentrations of malic and citric acids. Our results indicate that Ni stress redirects the carbon metabolism of developing wheat shoots to provide carbon skeletons for synthesis of amino acids and organic acids as well as to supply reducing power to sustain normal metabolic processes and to support defense mechanisms against oxidative stress.</description><subject>adverse effects</subject><subject>amino acids</subject><subject>Carbon</subject><subject>Carbon - metabolism</subject><subject>Carbon metabolism enzymes</subject><subject>citric acid</subject><subject>defense mechanisms</subject><subject>Enzyme Activation - drug effects</subject><subject>Enzymes</subject><subject>glucose</subject><subject>glucose-6-phosphate 1-dehydrogenase</subject><subject>isocitrate dehydrogenase</subject><subject>Malate</subject><subject>malate dehydrogenase</subject><subject>Metabolism</subject><subject>Nickel</subject><subject>Nickel - toxicity</subject><subject>oxidative stress</subject><subject>phosphoenolpyruvate carboxylase</subject><subject>Phosphoenolpyruvate Carboxylase - metabolism</subject><subject>phosphogluconate dehydrogenase</subject><subject>Photosynthesis</subject><subject>Photosynthesis - drug effects</subject><subject>Physiology</subject><subject>Plant Shoots - growth & development</subject><subject>Plant Stomata - drug effects</subject><subject>ribulose-bisphosphate carboxylase</subject><subject>Ribulose-Bisphosphate Carboxylase - metabolism</subject><subject>seedlings</subject><subject>shoots</subject><subject>stomatal conductance</subject><subject>Stress concentration</subject><subject>Stresses</subject><subject>sucrose</subject><subject>toxicity</subject><subject>Triticum - drug effects</subject><subject>Triticum - metabolism</subject><subject>Triticum aestivum</subject><subject>Wheat</subject><issn>0176-1617</issn><issn>1618-1328</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkctOwzAQRS0EoqXwBUiQJZsUvxI7QixQxUuqYAGsLceZUJckLnYC4u9xKbCE1Z25OjO25iJ0SPCUYJKfLqfLVbNaTCkmNDrTKFtoTHIiU8Ko3EZjTESeRkOM0F4ISxz7TLJdNKKMCS4YGaOzO2teoEltVw0GqsQsdPcMIbFdYrQvXZe00OvSNTa0a_N9AbpPwsK5PuyjnVo3AQ6-dYKeri4fZzfp_P76dnYxTw2XtE9zKXORFRx4hqESIDGGQhYiN0VZSK0FZzWNFTFUZ1VB8gIwzWVGS-CmxiWboJPN3pV3rwOEXrU2GGga3YEbgiKCc0Exp_h_NCOMC0wJ-R9llFEqsygTxDao8S4ED7Vaedtq_6EIVuss1FJ9ZaHWWazNKHHq6PuBoWyh-p35OX4EjjdArZ3Sz94G9fQQN2Q4JiUZ55E43xAQz_tmwatgLHQxKOvB9Kpy9s8vfAKEL6G5</recordid><startdate>20130301</startdate><enddate>20130301</enddate><creator>Gajewska, Ewa</creator><creator>Niewiadomska, Ewa</creator><creator>Tokarz, Krzysztof</creator><creator>Słaba, Mirosława</creator><creator>Skłodowska, Maria</creator><general>Elsevier GmbH</general><scope>FBQ</scope><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>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20130301</creationdate><title>Nickel-induced changes in carbon metabolism in wheat shoots</title><author>Gajewska, Ewa ; Niewiadomska, Ewa ; Tokarz, Krzysztof ; Słaba, Mirosława ; Skłodowska, Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c482t-68867594e450ed7e800e98976c9b98aa743f2b981c2a5d9169e026852be4cf0b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>adverse effects</topic><topic>amino acids</topic><topic>Carbon</topic><topic>Carbon - metabolism</topic><topic>Carbon metabolism enzymes</topic><topic>citric acid</topic><topic>defense mechanisms</topic><topic>Enzyme Activation - drug effects</topic><topic>Enzymes</topic><topic>glucose</topic><topic>glucose-6-phosphate 1-dehydrogenase</topic><topic>isocitrate dehydrogenase</topic><topic>Malate</topic><topic>malate dehydrogenase</topic><topic>Metabolism</topic><topic>Nickel</topic><topic>Nickel - toxicity</topic><topic>oxidative stress</topic><topic>phosphoenolpyruvate carboxylase</topic><topic>Phosphoenolpyruvate Carboxylase - metabolism</topic><topic>phosphogluconate dehydrogenase</topic><topic>Photosynthesis</topic><topic>Photosynthesis - drug effects</topic><topic>Physiology</topic><topic>Plant Shoots - growth & development</topic><topic>Plant Stomata - drug effects</topic><topic>ribulose-bisphosphate carboxylase</topic><topic>Ribulose-Bisphosphate Carboxylase - metabolism</topic><topic>seedlings</topic><topic>shoots</topic><topic>stomatal conductance</topic><topic>Stress concentration</topic><topic>Stresses</topic><topic>sucrose</topic><topic>toxicity</topic><topic>Triticum - drug effects</topic><topic>Triticum - metabolism</topic><topic>Triticum aestivum</topic><topic>Wheat</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gajewska, Ewa</creatorcontrib><creatorcontrib>Niewiadomska, Ewa</creatorcontrib><creatorcontrib>Tokarz, Krzysztof</creatorcontrib><creatorcontrib>Słaba, Mirosława</creatorcontrib><creatorcontrib>Skłodowska, Maria</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of plant physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gajewska, Ewa</au><au>Niewiadomska, Ewa</au><au>Tokarz, Krzysztof</au><au>Słaba, Mirosława</au><au>Skłodowska, Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nickel-induced changes in carbon metabolism in wheat shoots</atitle><jtitle>Journal of plant physiology</jtitle><addtitle>J Plant Physiol</addtitle><date>2013-03-01</date><risdate>2013</risdate><volume>170</volume><issue>4</issue><spage>369</spage><epage>377</epage><pages>369-377</pages><issn>0176-1617</issn><eissn>1618-1328</eissn><abstract>In this study, we analyzed the toxic effect of Ni during the development of wheat shoots. Typical developmental alterations in carbon metabolism-related parameters reflecting changes associated with the transition of the seedlings from heterotrophic to autotrophic metabolism were observed in the control shoots between the 1st and the 4th days. Adverse effects of 50 and 100μM Ni became evident starting from the 4th day of growth on the metal-containing media. We found that Ni-induced stimulation of phosphoenolpyruvate carboxylase (PEPC) activity coincided with decrease in the ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) level and with declines in net photosynthetic rate (PN) and stomatal conductance (gs). Application of Ni resulted in increased activities of several dehydrogenases: glucose-6-phosphate dehydrogenase (G6PDH), 6-phosphogluconate dehydrogenase (6PGDH), isocitrate dehydrogenase (NADP-ICDH) and malate dehydrogenase (NADH-MDH). In contrast, the activities of malic enzymes (NADP-ME and NAD-ME) decreased due to Ni stress. Treatment with Ni led to accumulation of glucose and declined concentration of sucrose as well as considerable increases in concentrations of malic and citric acids. Our results indicate that Ni stress redirects the carbon metabolism of developing wheat shoots to provide carbon skeletons for synthesis of amino acids and organic acids as well as to supply reducing power to sustain normal metabolic processes and to support defense mechanisms against oxidative stress.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>23374731</pmid><doi>10.1016/j.jplph.2012.10.012</doi><tpages>9</tpages></addata></record> |
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subjects | adverse effects amino acids Carbon Carbon - metabolism Carbon metabolism enzymes citric acid defense mechanisms Enzyme Activation - drug effects Enzymes glucose glucose-6-phosphate 1-dehydrogenase isocitrate dehydrogenase Malate malate dehydrogenase Metabolism Nickel Nickel - toxicity oxidative stress phosphoenolpyruvate carboxylase Phosphoenolpyruvate Carboxylase - metabolism phosphogluconate dehydrogenase Photosynthesis Photosynthesis - drug effects Physiology Plant Shoots - growth & development Plant Stomata - drug effects ribulose-bisphosphate carboxylase Ribulose-Bisphosphate Carboxylase - metabolism seedlings shoots stomatal conductance Stress concentration Stresses sucrose toxicity Triticum - drug effects Triticum - metabolism Triticum aestivum Wheat |
title | Nickel-induced changes in carbon metabolism in wheat shoots |
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