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1.
J Agric Food Chem ; 68(12): 3711-3721, 2020 Mar 25.
Artigo em Inglês | MEDLINE | ID: mdl-32105067

RESUMO

Elevated atmospheric CO2 concentrations (e[CO2]) can decrease the grain quality of wheat. However, little information exists concerning interactions between e[CO2] and nitrogen fertilization on important grain quality traits. To investigate this, a 2-year free air CO2 enrichment (FACE) experiment was conducted with two CO2 (393 and 600 ppm) and three (deficiency, adequate, and excess) nitrogen levels. Concentrations of flour proteins (albumins/globulins, gliadins, and glutenins) and key minerals (iron, zinc, and sulfur) and baking quality (loaf volume) were markedly increased by increasing nitrogen levels and varied between years. e[CO2] resulted in slightly decreased albumin/globulin and total gluten concentration under all nitrogen conditions, whereas loaf volume and mineral concentrations remained unaffected. Two-dimensional gel electrophoresis revealed strong effects of nitrogen supply and year on the grain proteome. Under adequate nitrogen, the grain proteome was affected by e[CO2] with 19 downregulated and 17 upregulated protein spots. The downregulated proteins comprised globulins but no gluten proteins. e[CO2] resulted in decreased crude protein concentration at maximum loaf volume. The present study contrasts with other FACE studies showing markedly stronger negative impacts of e[CO2] on chemical grain quality, and the reasons for that might be differences between genotypes, soil conditions, or the extent of growth stimulation by e[CO2].


Assuntos
Dióxido de Carbono/metabolismo , Grão Comestível/crescimento & desenvolvimento , Nitrogênio/metabolismo , Triticum/crescimento & desenvolvimento , Produção Agrícola , Grão Comestível/metabolismo , Ferro/metabolismo , Proteínas de Plantas/metabolismo , Enxofre/metabolismo , Triticum/metabolismo , Zinco/metabolismo
2.
Glob Chang Biol ; 24(1): e40-e54, 2018 01.
Artigo em Inglês | MEDLINE | ID: mdl-28715112

RESUMO

A 2-year Free Air CO2 Enrichment (FACE) experiment was conducted with winter wheat. It was investigated whether elevated atmospheric CO2 concentration (e[CO2 ]) inhibit nitrate assimilation and whether better growth and nitrogen acquisition under e[CO2 ] can be achieved with an ammonium-based fertilization as it was observed in hydroponic culture with wheat. Under e[CO2 ] a decrease in nitrate assimilation has been discussed as the cause for observed declines in protein concentration in C3 cereals. Wheat was grown under ambient [CO2 ] and e[CO2 ] (600 ppm) with three levels (deficiency, optimal, and excessive) of nitrate-based fertilization (calcium ammonium nitrate; CAN) or with optimal ammonium-based fertilization. Ammonium fertilization was applied via injection of an ammonium solution into the soil in the 1st year and by surface application of urea combined with nitrification inhibitors (UNI) in the 2nd year. Results showed that ammonium-based fertilization was successfully achieved in the 2nd year with respect to nitrification control, as soil ammonium concentration was considerably higher over the growing season for UNI fertilized plots compared to optimal CAN plots. Also, stem nitrate concentration, flag leaf nitrate reductase activity, and transcript levels were lower in UNI fertilized plants compared to optimal CAN. Regarding the e[CO2 ] effect on nitrate reductase activity and transcript levels, no alteration could be observed for any nitrogen fertilizer treatment. Flag leaf growth was stimulated under e[CO2 ] leading to an enhanced nitrate reductase activity referred to m2 ground area at late flowering being in line with a higher nitrogen acquisition under e[CO2 ]. Moreover, nitrogen acquisition was considerably higher in nitrate fertilized plants compared to ammonium fertilized plants under e[CO2 ]. Our results obtained under field conditions show that a change from nitrate- to ammonium-based fertilization will not lead to a better growth and nitrogen acquisition of winter wheat under future e[CO2 ].


Assuntos
Compostos de Amônio/administração & dosagem , Dióxido de Carbono/administração & dosagem , Nitratos/administração & dosagem , Nitrogênio/metabolismo , Compostos de Amônio Quaternário/administração & dosagem , Triticum/fisiologia , Compostos de Amônio/metabolismo , Dióxido de Carbono/metabolismo , Fertilizantes , Nitratos/metabolismo , Óxidos de Nitrogênio/metabolismo , Folhas de Planta/metabolismo , Compostos de Amônio Quaternário/metabolismo , Triticum/efeitos dos fármacos , Triticum/crescimento & desenvolvimento
3.
Nature ; 479(7374): 552-5, 2011 Oct 23.
Artigo em Inglês | MEDLINE | ID: mdl-22020284

RESUMO

Neuronal exocytosis is catalysed by the SNAP receptor protein syntaxin-1A, which is clustered in the plasma membrane at sites where synaptic vesicles undergo exocytosis. However, how syntaxin-1A is sequestered is unknown. Here we show that syntaxin clustering is mediated by electrostatic interactions with the strongly anionic lipid phosphatidylinositol-4,5-bisphosphate (PIP2). Using super-resolution stimulated-emission depletion microscopy on the plasma membranes of PC12 cells, we found that PIP2 is the dominant inner-leaflet lipid in microdomains about 73 nanometres in size. This high accumulation of PIP2 was required for syntaxin-1A sequestering, as destruction of PIP2 by the phosphatase synaptojanin-1 reduced syntaxin-1A clustering. Furthermore, co-reconstitution of PIP2 and the carboxy-terminal part of syntaxin-1A in artificial giant unilamellar vesicles resulted in segregation of PIP2 and syntaxin-1A into distinct domains even when cholesterol was absent. Our results demonstrate that electrostatic protein-lipid interactions can result in the formation of microdomains independently of cholesterol or lipid phases.


Assuntos
Microdomínios da Membrana/química , Fosfatidilinositol 4,5-Difosfato/química , Fosfatidilinositol 4,5-Difosfato/metabolismo , Ligação Proteica , Eletricidade Estática , Sintaxina 1/química , Sintaxina 1/metabolismo , Animais , Colesterol , Microdomínios da Membrana/metabolismo , Microscopia Confocal , Simulação de Dinâmica Molecular , Proteínas do Tecido Nervoso/metabolismo , Células PC12 , Monoéster Fosfórico Hidrolases/metabolismo , Ratos , Lipossomas Unilamelares/química , Lipossomas Unilamelares/metabolismo
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