Suchergebnisse

El objetivo de este trabajo es abordar las cuestiones que plantea la atribución del uso de la vivienda familiar tras la crisis matrimonial y su solución desde el punto de vista legislativo y jurisprudencial. En las prácticas profesionales desarrolladas en el marco del Máster Universitario en Abogacía estudié asuntos relacionados con el Derecho de Familia y la vivienda familiar, y pude observar que se trata de uno de los objetos principales del procedimiento matrimonial, así como uno de los asuntos que más dificultades genera en la práctica diaria de los abogados. Y es que se trata del bien más preciado en el patrimonio de los cónyuges y donde han desarrollado gran parte de su existencia, por lo que ambos esposos, generalmente, interesan su atribución. Se trata de un tema de gran complejidad y con diversos matices, tanto desde la óptica de la propia vivienda como de las circunstancias de sus ocupantes. Es una materia en constante cambio y evolución, y más ahora debido a la crisis económica por la que estamos atravesando que dificulta el acceso a la vivienda. Desde el punto de vista legislativo, su regulación es más bien escasa centrada en el artículo 96 del Código Civil, lo que hace necesario examinar a fondo la numerosa jurisprudencia existente al respecto. Gracias al nuevo recurso por interés casacional, que introdujo la Ley de Enjuiciamiento Civil en el año 2000, esta materia pudo acceder al Tribunal Supremo, que está creando un cuerpo de doctrina muy importante y generando seguridad jurídica, cuestión de gran importancia ya que existían criterios contradictorios entre las Audiencias Provinciales en cuanto a las cuestiones derivadas de la vivienda familiar se refiere. Asimismo, también está en marcha una reforma del artículo 96 CC contenida en el "Anteproyecto de Ley sobre el Ejercicio de la corresponsabilidad parental en caso de nulidad, separación y divorcio", aprobado por el Consejo de Ministros el pasado 19 de julio de 2013, que pretende dar respuesta a las críticas surgidas en diversos foros, así como ...

10 Pags.- 1 Tabl.- 6 Figs. Copyrights, the Authors. Plant Biotechnology Journal is published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. ; Many metal transporters in plants are promiscuous, accommodating multiple divalent cations including some which are toxic to humans. Previous attempts to increase the iron (Fe) and zinc (Zn) content of rice endosperm by overexpressing different metal transporters have therefore led unintentionally to the accumulation of copper (Cu), manganese (Mn) and cadmium (Cd). Unlike other metal transporters, barley Yellow Stripe 1 (HvYS1) is specific for Fe. We investigated the mechanistic basis of this preference by constitutively expressing HvYS1 in rice under the control of the maize ubiquitin1 promoter and comparing the mobilization and loading of different metals. Plants expressing HvYS1 showed modest increases in Fe uptake, root-to-shoot translocation, seed accumulation and endosperm loading, but without any change in the uptake and root-to-shoot translocation of Zn, Mn or Cu, confirming the selective transport of Fe. The concentrations of Zn and Mn in the endosperm did not differ significantly between the wild-type and HvYS1 lines, but the transgenic endosperm contained significantly lower concentrations of Cu. Furthermore, the transgenic lines showed a significantly reduced Cd uptake, root-to-shoot translocation and accumulation in the seeds. The underlying mechanism of metal uptake and translocation reflects the down-regulation of promiscuous endogenous metal transporters revealing an internal feedback mechanism that limits seed loading with Fe. This promotes the preferential mobilization and loading of Fe, therefore displacing Cu and Cd in the seed. ; We acknowledge support from the European Research Council IDEAS Advanced Grant Program (BIOFORCE) to P.C., and the Spanish Ministry of Economy and Competitivity (MINECO; projects AGL2013-42175-R, co-financed with FEDER) and the Aragón Government (Group A03) to J.A. R.B was supported by a PhD fellowship from the University of Lleida, Spain. ; Peer reviewed

7 Pag., 5 Tabl., 2 Fig. ; A liquid chromatography–electrospray ionization time-of-flight mass spectrometry method has been developed for the direct and simultaneous determination of 10 low molecular mass organic acids in different plant tissue extracts. The method does not include a derivatization step. Quantification was accomplished using 13C-labeled malic and succinic acids as internal standards. Good limits of detection (0.05–1.27 pmol) were obtained for malic, 2-oxoglutaric, succinic, quinic, shikimic, cis-aconitic, and citric acids, whereas for oxalic, ascorbic, and fumaric acids limits of detection were 255, 25, and 11 pmol, respectively. Repeatability values for the retention time and peak area were <5%, with the exception of ascorbic acid. Analyte recovery was between 92% and 110% in most cases, with the exception of oxalic (39–108%), 2-oxoglutaric (44–69%), and ascorbic (22–86%) acids, which may require specific extraction procedures and use of the corresponding 13C-labeled organic acid as internal standards to improve accuracy. The method was applied to three types of plant materials: sugar beet leaf extracts, tomato xylem sap, and commercial orange juice. ; This study was supported by the Spanish Ministry of Science and Innovation (MICINN; Projects AGL2007-61948 and AGL2009-09018, cofinanced with FEDER), the European Commission (Thematic Priority 5—Food Quality and Safety, sixth Framework RTD Programme, Contract FP6-FOOD-CT-2006-016279), the trilateral Project Hot Iron (ERA-NET Plant Genome Research KKBE; MICINN Project EUI2008-03618), and the Aragn Government (group A03). R.R.-A. and S.L.-G. were supported by an FPI-MCINN fellowship and a CSIC Grant (I3P-2005) from the I3P programme, cofinanced by the European Social Fund, respectively. Acquisition of the HPLC–TOFMS apparatus was cofinanced with FEDER. ; Peer reviewed

12 Pags.- 9 Figs.- 4 Tabls.- Suppl. Data. ; Flavin synthesis and secretion is an integral part of the toolbox of root-borne Fe facilitators used by Strategy I species upon Fe deficiency. The Fe-deficiency responses of the wild legume Medicago scutellata grown in nutrient solution have been studied at two different pH values (5.5 and 7.5). Parameters studied include leaf chlorophyll, nutrient solution pH, concentrations and contents of micronutrients, flavin accumulation in roots, flavin export to the medium, and root ferric chelate reductase and acidification activities. Results show that M. scutellata behaves upon Fe deficiency as a Strategy I species, with a marked capacity for synthesizing flavins (riboflavin and three hydroxylated riboflavin derivatives), which becomes more intense at high pH. Results also show that this species is capable of exporting a large amount of flavins to the external medium, both at pH 5.5 and 7.5. This is the first report of a species having a major flavin secretion at pH 7.5, in contrast with the very low flavin secretion found in other flavin-producing species such as Beta vulgaris and M. truncatula. These results provide further support to the hypothesis that flavin secretion is relevant for Fe acquisition at high pH, and open the possibility to improve the Fe-efficiency responses in legumes of agronomic interest. ; Supported by the Ferdowsi University of Mashhad research project on M. scutellata 3/41380, the Spanish State Research Agency (AEI) co-financed by the European Regional Development Fund (FEDER) (project AGL2016-75226-R; AEI/FEDER, UE) and the Aragón Government (group A09-20R). ; Peer reviewed

20 Pags.- 2 Tabls.- 1 Fig. © 2014 Álvarez-Fernández, Díaz-Benito, Abadía, López-Millán and Abadía. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. ; The mechanisms plants use to transport metals from roots to shoots are not completely understood. It has long been proposed that organic molecules participate in metal translocation within the plant. However, until recently the identity of the complexes involved in the long-distance transport of metals could only be inferred by using indirect methods, such as analyzing separately the concentrations of metals and putative ligands and then using in silico chemical speciation software to predict metal species. Molecular biology approaches also have provided a breadth of information about putative metal ligands and metal complexes occurring in plant fluids. The new advances in analytical techniques based on mass spectrometry and the increased use of synchrotron X-ray spectroscopy have allowed for the identification of some metal-ligand species in plant fluids such as the xylem and phloem saps. Also, some proteins present in plant fluids can bind metals and a few studies have explored this possibility. This study reviews the analytical challenges researchers have to face to understand long-distance metal transport in plants as well as the recent advances in the identification of the ligand and metal-ligand complexes in plant fluids. ; This study was supported by the Spanish Ministry of Economy and Competitiveness (projects AGL2010-16515 and AGL2012-31988), and the Aragón Government (group A03). Pablo Díaz-Benito was supported by a MINECO-FPI grant. ; Peer reviewed

13 Pags.- 7 Figs.- Online Suppl. Data (6 Figs.- 3 Tabls.). © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Experimental Biology. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. ; Although iron is present in large amounts in the soil, its poor solubility means that plants have to use various strategies to facilitate its uptake. In this study, we show that expression of NtPDR3/NtABCG3, a Nicotiana tabacum plasma-membrane ABC transporter in the pleiotropic drug resistance (PDR) subfamily, is strongly induced in the root epidermis under iron deficiency conditions. Prevention of NtPDR3 expression resulted in N. tabacum plants that were less tolerant to iron-deficient conditions, displaying stronger chlorosis and slower growth than those of the wild-type when not supplied with iron. Metabolic profiling of roots and root exudates revealed that, upon iron deficiency, secretion of catechol-bearing O-methylated coumarins such as fraxetin, hydroxyfraxetin, and methoxyfraxetin to the rhizosphere was compromised in NtPDR3-silenced plants. However, exudation of flavins such as riboflavin was not markedly affected by NtPDR3-silencing. Expression of NtPDR3 in N. tabacum Bright Yellow-2 (BY-2) cells resulted in altered intra- and extracellular coumarin pools, supporting coumarin transport by this transporter. The results demonstrate that N. tabacum secretes both coumarins and flavins in response to iron deficiency and that NtPDR3 plays an essential role in the plant response to iron deficiency by mediating secretion of O-methylated coumarins to the rhizosphere. ; This work was supported by grants from the Belgian National Fund for Scientific Research, the Inter-university Poles of Attraction Program (Belgian State, Scientific, Technical, and Cultural Services) and the 'Communauté française de Belgique – Action de Recherches Concertées' for FL, JF, AB, and MB, and by the Spanish MINECO project (co-financed with FEDER) to JA and AA-F, and by the Aragón Government (group A09_17R) to JA. ; Peer reviewed

18 Pags, 5 Tabls., 7 Figs., 1 Appendix with 1 Tabl. The .pdf Document is Protected by copyright and was first published by Frontiers. ; The metabolite profile changes induced by Fe deficiency in leaves and xylem sap of several Strategy I plant species have been characterized. We have confirmed that Fe deficiency causes consistent changes both in the xylem sap and leaf metabolite profiles. The main changes in the xylem sap metabolite profile in response to Fe deficiency include consistent decreases in amino acids, N-related metabolites and carbohydrates, and increases in TCA cycle metabolites. In tomato, Fe resupply causes a transitory flush of xylem sap carboxylates, but within 1 day the metabolite profile of the xylem sap from Fe-deficient plants becomes similar to that of Fe-sufficient controls. The main changes in the metabolite profile of leaf extracts in response to Fe deficiency include consistent increases in amino acids and N-related metabolites, carbohydrates and TCA cycle metabolites. In leaves, selected pairs of amino acids and TCA cycle metabolites show high correlations, with the sign depending of the Fe status. These data suggest that in low photosynthesis, C-starved Fe-deficient plants anaplerotic reactions involving amino acids can be crucial for short-term survival. ; This study was supported by the Spanish Ministry of Science and Innovation (MICINN; projects AGL2009-09018 and AGL2010-16515, co-financed with FEDER), the trilateral Project Hot Iron (ERA-NET Plant Genome Research KKBE; MICINN EUI2008-03618), the Spanish National Research Council (PA1000990, International Promotion Programme 2007), and the Aragón Government (group A03). Rubén Rellán-Álvarez and Hamdi El-Jendoubi were supported by MICINN-FPI grants. ; Peer reviewed

15 páginas, 4 figuras, 2 tablas.-- et al. ; [Background]: Plants grown under iron deficiency show different morphological, biochemical and physiological changes. These changes include, among others, the elicitation of different strategies to improve the acquisition of Fe from the rhizosphere, the adjustment of Fe homeostasis processes and a reorganization of carbohydrate metabolism. The application of modern techniques that allow the simultaneous and untargeted analysis of multiple proteins and metabolites can provide insight into multiple processes taking place in plants under Fe deficiency. The objective of this study was to characterize the changes induced in the root tip proteome and metabolome of sugar beet plants in response to Fe deficiency and resupply. [Results]: Root tip extract proteome maps were obtained by 2-D isoelectric focusing polyacrylamide gel electrophoresis, and approximately 140 spots were detected. Iron deficiency resulted in changes in the relative amounts of 61 polypeptides, and 22 of them were identified by mass spectrometry (MS). Metabolites in root tip extracts were analyzed by gas chromatography-MS, and more than 300 metabolites were resolved. Out of 77 identified metabolites, 26 changed significantly with Fe deficiency. Iron deficiency induced increases in the relative amounts of proteins and metabolites associated to glycolysis, tri-carboxylic acid cycle and anaerobic respiration, confirming previous studies. Furthermore, a protein not present in Fe-sufficient roots, dimethyl-8-ribityllumazine (DMRL) synthase, was present in high amounts in root tips from Fe-deficient sugar beet plants and gene transcript levels were higher in Fe-deficient root tips. Also, a marked increase in the relative amounts of the raffinose family of oligosaccharides (RFOs) was observed in Fe-deficient plants, and a further increase in these compounds occurred upon short term Fe resupply. [Conclusions]: The increases in DMRL synthase and in RFO sugars were the major changes induced by Fe deficiency and resupply in root tips of sugar beet plants. Flavin synthesis could be involved in Fe uptake, whereas RFO sugars could be involved in the alleviation of oxidative stress, C trafficking or cell signalling. Our data also confirm the increase in proteins and metabolites related to carbohydrate metabolism and TCA cycle pathways. ; RRA and SA were supported by FPI fellowships from the Spanish Ministry of Science and Innovation (MICINN). JRC was supported by an I3P-CSIC predoctoral fellowship. Work supported by the Spanish MICINN (projects AGL2004-00194 and AGL2007-61948, co-financed with FEDER), the Spain-Italy Integrated Action HI2007-0228, the European Commission (Thematic Priority 5- Food Quality and Safety, 6th Framework RTD Programme, Contract no. FP6-FOOD-CT-2006-016279) and the Aragón Government (group A03). Acquisition of the HPLC-MS apparatus was cofinanced with FEDER. ; Peer reviewed

17 Pags.- 7 Figs.- 1 Tabl. Copyright © 2018 Díaz-Benito, Banakar, Rodríguez-Menéndez, Capell, Pereiro, Christou, Abadía, Fernández and Álvarez-Fernández. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. ; Iron and Zn deficiencies are worldwide nutritional disorders that can be alleviated by increasing the metal concentration of rice (Oryza sativa L.) grains via bio-fortification approaches. The overproduction of the metal chelator nicotianamine (NA) is among the most effective ones, but it is still unclear whether this is due to the enrichment in NA itself and/or the concomitant enrichment in the NA derivative 2′-deoxymugineic acid (DMA). The endosperm is the most commonly consumed portion of the rice grain and mediates the transfer of nutrients from vegetative tissues to the metal rich embryo. The impact of contrasting levels of DMA and NA on the metal distribution in the embryo and endosperm of rice seeds has been assessed using wild-type rice and six different transgenic lines overexpressing nicotianamine synthase (OsNAS1) and/or barley nicotianamine amino transferase (HvNAATb). These transgenic lines outlined three different DMA/NA scenarios: (i) in a first scenario, an enhanced NA level (via overexpression of OsNAS1) would not be fully depleted because of a limited capacity to use NA for DMA synthesis (lack of -or low- expression of HvNAATb), and results in consistent enrichments in NA, DMA, Fe and Zn in the endosperm and NA, DMA and Fe in the embryo; (ii) in a second scenario, an enhanced NA level (via overexpression of OsNAS1) would be depleted by an enhanced capacity to use NA for DMA synthesis (via expression of HvNAATb), and results in enrichments only for DMA and Fe, both in the endosperm and embryo, and (iii) in a third scenario, the lack of sufficient NA replenishment would limit DMA synthesis, in spite of the enhanced capacity to use NA for this purpose (via expression of HvNAATb), and results in decreases in NA, variable changes in DMA and moderate decreases in Fe in the embryo and endosperm. Also, quantitative LA-ICP-MS metal map images of the embryo structures show that the first and second scenarios altered local distributions of Fe, and to a lesser extent of Zn. The roles of DMA/NA levels in the transport of Fe and Zn within the embryo are thoroughly discussed. ; This work was supported by the grants of the Spanish Ministry of Science, Innovation and Universities (AGL2016-75226-R, BIO2014-54426-P and AGL2017-85377-R, all co-financed with FEDER), Aragón Government (Group A09_17R) and Generalitat de Catalunya (Grant 2017 SGR 828). PD-B was supported by a MINECO-FPI contract. RB was supported by a Ph.D. fellowship from the University of Lleida. SR-M was supported by a research contract from the Fundación Universidad de Oviedo (FUO-069-17). BF was supported by a MINECO research contract (RYC-2014-14985; "Ramón y Cajal Program"). ; Peer reviewed

22 Pags.- 3 Tabls.- 8 Figs. This Document is Protected by copyright and was first published by Frontiers (http://journal.frontiersin.org/journal/373). All rights reserved. it is reproduced with permission. ; Root secretion of coumarin-phenolic type compounds has been recently shown to be related to Arabidopsis thaliana tolerance to Fe deficiency at high pH. Previous studies revealed the identity of a few simple coumarins occurring in roots and exudates of Fe-deficient A. thaliana plants, and left open the possible existence of other unknown phenolics. We used HPLC-UV/VIS/ESI-MS(TOF), HPLC/ESI-MS(ion trap) and HPLC/ESI-MS(Q-TOF) to characterize (identify and quantify) phenolic-type compounds accumulated in roots or secreted into the nutrient solution of A. thaliana plants in response to Fe deficiency. Plants grown with or without Fe and using nutrient solutions buffered at pH 5.5 or 7.5 enabled to identify an array of phenolics. These include several coumarinolignans not previously reported in A. thaliana (cleomiscosins A, B, C, and D and the 5′-hydroxycleomiscosins A and/or B), as well as some coumarin precursors (ferulic acid and coniferyl and sinapyl aldehydes), and previously reported cathecol (fraxetin) and non-cathecol coumarins (scopoletin, isofraxidin and fraxinol), some of them in hexoside forms not previously characterized. The production and secretion of phenolics were more intense when the plant accessibility to Fe was diminished and the plant Fe status deteriorated, as it occurs when plants are grown in the absence of Fe at pH 7.5. Aglycones and hexosides of the four coumarins were abundant in roots, whereas only the aglycone forms could be quantified in the nutrient solution. A comprehensive quantification of coumarins, first carried out in this study, revealed that the catechol coumarin fraxetin was predominant in exudates (but not in roots) of Fe-deficient A. thaliana plants grown at pH 7.5. Also, fraxetin was able to mobilize efficiently Fe from a Fe(III)-oxide at pH 5.5 and pH 7.5. On the other hand, non-catechol coumarins were much less efficient in mobilizing Fe and were present in much lower concentrations, making unlikely that they could play a role in Fe mobilization. The structural features of the array of coumarin type-compounds produced suggest some can mobilize Fe from the soil and others can be more efficient as allelochemicals. ; Work supported by the Spanish Ministry of Economy and Competitiveness (MINECO) (grant AGL2013-42175-R, co-financed with FEDER) and the Aragón Government (group A03). PS-T and AL-V were supported by MINECO-FPI contracts. ; Peer reviewed

12 Pags., 1 Tabl., 8 Figs. ; A dual-stable isotope tracer experiment was carried out with Fe-deficient sugar beet plants grown hydroponically and resupplied with differentially Fe labeled racemic and meso Fe(III)-chelates of the ethylendiamine di(o-hydroxyphenylacetic) acid (o,oEDDHA). No short-term Fe isotope exchange reactions occurred in the nutrient solution and plants did not discriminate between 54Fe and 57Fe. After 3–6 h, stable Fe isotopes, chelating agents and chelates were analyzed in roots, xylem sap and leaves by ICP-MS and HPLC-ESI/TOFMS. Ferric chelate reductase rates, xylem transport and total uptake were 2-fold higher with the meso isomer than with the racemic one. Both chelating agent isomers were incorporated and distributed by plants at similar rates, in amounts one order of magnitude lower than those of Fe. After 6 h of Fe resupply, most of the Fe acquired was localized in roots, whereas most of the chelating agent was in leaves. In a separate experiment, Fe-deficient sugar beet and tomato plants were treated with different concentrations of Fe(III)-o,oEDDHA (with a meso/racemic ratio of 1). The xylem sap Fe concentration at 24 h was unaffected by the chelate concentration, with xylem Fe(III)-o,oEDDHA accounting for 1–18% of total Fe and xylem meso/racemic ratio close to 1. Although most of the Fe coming from Fe(III)-o,oEDDHA was taken up through a reductive dissociative mechanism, a small part of the Fe may be taken up via non-dissociative mechanisms. ; This work was supported by the Spanish Ministry of Science and Innovation (MICINN) (projects AGL2007-61948 and AGL2009-09018, co-financed with FEDER), the Commission of European Communities (ISAFRUIT Project, Thematic Priority 5-Food Quality and Safety, of the 6th Framework Programme of RTD; Contract No. FP6-FOOD-CT-2006- 016279), the trilateral Project Hot Iron (ERA-NET Plant Genome Research KKBE; MICINN EUI2008-03618) and the Arago´ n Government (Group A03). IO was supported by a CONAID-DGA predoctoral fellowship and a CAI-Europa grant. ; Peer reviewed

Iron and Zn deficiencies are worldwide nutritional disorders that can be alleviated by increasing the metal concentration of rice (Oryza sativa L.) grains via bio-fortification approaches. The overproduction of the metal chelator nicotianamine (NA) is among the most effective ones, but it is still unclear whether this is due to the enrichment in NA itself and/or the concomitant enrichment in the NA derivative 20-deoxymugineic acid (DMA). The endosperm is the most commonly consumed portion of the rice grain and mediates the transfer of nutrients from vegetative tissues to the metal rich embryo. The impact of contrasting levels of DMA and NA on the metal distribution in the embryo and endosperm of rice seeds has been assessed using wild-type rice and six different transgenic lines overexpressing nicotianamine synthase (OsNAS1) and/or barley nicotianamine amino transferase (HvNAATb). These transgenic lines outlined three different DMA/NA scenarios: (i) in a first scenario, an enhanced NA level (via overexpression of OsNAS1) would not be fully depleted because of a limited capacity to use NA for DMA synthesis (lack of -or low- expression of HvNAATb), and results in consistent enrichments in NA, DMA, Fe and Zn in the endosperm and NA, DMA and Fe in the embryo; (ii) in a second scenario, an enhanced NA level (via overexpression of OsNAS1) would be depleted by an enhanced capacity to use NA for DMA synthesis (via expression of HvNAATb), and results in enrichments only for DMA and Fe, both in the endosperm and embryo, and (iii) in a third scenario, the lack of sufficient NA replenishment would limit DMA synthesis, in spite of the enhanced capacity to use NA for this purpose (via expression of HvNAATb), and results in decreases in NA, variable changes in DMA and moderate decreases in Fe in the embryo and endosperm. Also, quantitative LA-ICP-MS metal map images of the embryo structures show that the first and second scenarios altered local distributions of Fe, and to a lesser extent of Zn. The roles of DMA/NA levels in the transport of Fe and Zn within the embryo are thoroughly discussed. ; This work was supported by the grants of the Spanish Ministry of Science, Innovation and Universities (AGL2016-75226-R, BIO2014-54426-P and AGL2017-85377-R, all co-financed with FEDER), Aragón Government (Group A09_17R) and Generalitat de Catalunya (Grant 2017 SGR 828). PD-B was supported by a MINECO-FPI contract. RB was supported by a Ph.D. fellowship from the University of Lleida. SR-M was supported by a research contract from the Fundación Universidad de Oviedo (FUO-069-17). BF was supported by a MINECO research contract (RYC-2014-14985; "Ramón y Cajal Program").

This work was supported by the grants of the Spanish Ministry of Science, Innovation and Universities (AGL2016-75226-R, BIO2014-54426-P and AGL2017-85377-R, all co-financed with FEDER), Aragón Government (Group A09_17R) and Generalitat de Catalunya (Grant 2017 SGR 828). PD-B was supported by a MINECO-FPI contract. RB was supported by a Ph.D. fellowship from the University of Lleida. SR-M was supported by a research contract from the Fundación Universidad de Oviedo (FUO069-17). BF was supported by a MINECO research contract (RYC-2014-14985; "Ramón y Cajal Program").

14 Pag., 3 Tabl., 5 Fig. The definitive version is available at: www3.interscience.wiley.com ; Three-week-old alfalfa (Medicago sativa), barley (Hordeum vulgare) and maize (Zea mays) were exposed for 7 d to 30 µm of mercury (HgCl2) to characterize the Hg speciation in root, with no symptoms of being poisoned. The largest pool (99%) was associated with the particulate fraction, whereas the soluble fraction (SF) accounted for a minor proportion (<1%). Liquid chromatography coupled with electro-spray/time of flight mass spectrometry showed that Hg was bound to an array of phytochelatins (PCs) in root SF, which was particularly varied in alfalfa (eight ligands and five stoichiometries), a species that also accumulated homophytochelatins. Spatial localization of Hg in alfalfa roots by microprobe synchrotron X-ray fluorescence spectroscopy showed that most of the Hg co-localized with sulphur in the vascular cylinder. Extended X-ray Absorption Fine Structure (EXAFS) fingerprint fitting revealed that Hg was bound in vivo to organic-S compounds, i.e. biomolecules containing cysteine. Albeit a minor proportion of total Hg, Hg–PCs complexes in the SF might be important for tolerance to Hg, as was found with Arabidopsis thaliana mutants cad2-1 (with low glutathione content) and cad1-3 (unable to synthesize PCs) in comparison with wild type plants. Interestingly, high-performance liquid chromatography-electrospray ionization-time of flight analysis showed that none of these mutants accumulated Hg–biothiol complexes. ; This work was supported by Fundación Ramón Areces (http://www.fundacionareces.es), the Spanish Ministry of Science and Innovation (AGL2010-15151-PROBIOMET and AGL2007-61948), Comunidad de Madrid (EIADES S2009/AMB-1478), Junta Comunidades Castilla-La Mancha (FITOALMA, PBI07-0091-3644) and the Aragón Government (Group A03). The HPLC-ESI-TOFMS equipment was co-financed with EU FEDER funds. Portions of this research were carried out at the Stanford Synchrotron Radiation Lightsource, through the Structural Molecular Biology Program supported by the Department of Energy, Office of Biological and Environmental Research, and by the National Institute of Health, National Centre for Research Resources, Biomedical Technology Program. ; Peer reviewed

13 Pags.- 5 Figs. © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Experimental Biology. ; Symbiotic nitrogen fixation carried out in legume root nodules requires transition metals. These nutrients are delivered by the host plant to the endosymbiotic nitrogen-fixing bacteria living within the nodule cells, a process in which vascular transport is essential. As members of the Yellow Stripe-Like (YSL) family of metal transporters are involved in root to shoot transport, they should also be required for root to nodule metal delivery. The genome of the model legume Medicago truncatula encodes eight YSL proteins, four of them with a high degree of similarity to Arabidopsis thaliana YSLs involved in long-distance metal trafficking. Among them, MtYSL3 is a plasma membrane protein expressed by vascular cells in roots and nodules and by cortical nodule cells. Reducing the expression level of this gene had no major effect on plant physiology when assimilable nitrogen was provided in the nutrient solution. However, nodule functioning was severely impaired, with a significant reduction of nitrogen fixation capabilities. Further, iron and zinc accumulation and distribution changed. Iron was retained in the apical region of the nodule, while zinc became strongly accumulated in the nodule veins in the ysl3 mutant. These data suggest a role for MtYSL3 in vascular delivery of iron and zinc to symbiotic nitrogen fixation. ; This research was funded by a European Research Council Starting Grant (ERC-2013-StG-335284) and the Spanish State Research Agency (AEI) grant (AGL2015-65866-P) to MGG, and a AEI grant (AGL2016-75226-R) to JA and AA-F co-financed by the European Regional Development Fund (FEDER). RC-R and FJJ-P were supported by a Formación del Personal Investigador fellowship (BES2013-062674 and BES-2017-082913, respectively). IA was the recipient of a Juan de la Cierva- Formación postdoctoral fellowship from Ministerio de Ciencia, Innovación y Universidades (FJCI-2017- 33222). VE was partially funded by the Severo Ochoa Programme for Centres of Excellence in R&D from the AEI (grant SEV-2016- 0672) received by the Centro de Biotecnología y Genómica de Plantas (UPM-INIA). Development of the M. truncatula Tnt1 mutant population was, in part, funded by the National Science Foundation, USA (DBI-0703285) to KSM. AM and HK and the µXRF measurements were supported by the Ministry of Education, Youth and Sports of the Czech Republic with co-financing from the European Union (grant 'KOROLID', CZ.02.1.01/0.0/0.0/15_003/0000336) and the Czech Academy of Sciences (RVO: 60077344). ; Peer reviewed