H2 S works synergistically with rhizobia to modify photosynthetic carbon assimilation and metabolism in nitrogen-deficient soybeans.
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L. Yao | Z. Shangguan | Juan Chen | G. Wei | Yuanyuan Ding | Jian-hua Zhang | Nina Zhang | Bing-Yu Suo
[1] Wei-wei Zhang,et al. H2 S Improves Salt-stress Recovery via Organic Acid Turn-over in Apple Seedlings. , 2022, Plant, cell & environment.
[2] Harun I. Gitari,et al. Effects of Rhizobium inoculum compared with mineral nitrogen fertilizer on nodulation and seed yield of common bean. A meta-analysis , 2022, Agronomy for Sustainable Development.
[3] Juan Chen,et al. Effects of sodium hydrosulfide and rhizobia on the growth rate, nutrient stoichiometry, and nutrient resorption of soybean ( Glycine max L.) , 2021, Journal of Plant Nutrition and Soil Science.
[4] Yang Liu,et al. Hydrogen sulfide alleviates salinity stress in Cyclocarya paliurus by maintaining chlorophyll fluorescence and regulating nitric oxide level and antioxidant capacity. , 2021, Plant physiology and biochemistry : PPB.
[5] A. Millar,et al. The mitochondrial pyruvate carrier (MPC) complex mediates one of three pyruvate-supplying pathways that sustain Arabidopsis respiratory metabolism. , 2021, The Plant cell.
[6] S. Umar,et al. The Crosstalk of Melatonin and Hydrogen Sulfide Determines Photosynthetic Performance by Regulation of Carbohydrate Metabolism in Wheat under Heat Stress , 2021, Plants.
[7] S. Eshghi,et al. The effect of hydrogen sulfide on growth, yield and biochemical responses of strawberry (Fragaria × ananassa cv. Paros) leaves under alkalinity stress , 2021 .
[8] Annie Irshad,et al. Contribution of Rhizobium–Legume Symbiosis in Salt Stress Tolerance in Medicago truncatula Evaluated through Photosynthesis, Antioxidant Enzymes, and Compatible Solutes Accumulation , 2021, Sustainability.
[9] Hai-lei Zheng,et al. Unraveling hydrogen sulfide-promoted lateral root development and growth in mangrove plant Kandelia obovata: Insight into regulatory mechanism by TMT-based quantitative proteomic approaches. , 2021, Tree physiology.
[10] T. Ohyama,et al. Recent Advances in Carbon and Nitrogen Metabolism in C3 Plants , 2020, International journal of molecular sciences.
[11] Yuansong Xiao,et al. Regulation of growth in peach roots by exogenous hydrogen sulfide based on RNA-Seq. , 2020, Plant physiology and biochemistry : PPB.
[12] M. Yusuf,et al. Hydrogen sulfide: A versatile gaseous molecule in plants. , 2020, Plant physiology and biochemistry : PPB.
[13] X. Ai,et al. Hydrogen peroxide is involved in hydrogen sulfide-induced carbon assimilation and photoprotection in cucumber seedlings , 2020 .
[14] C. Kaya,et al. Silicon is dependent on hydrogen sulphide to improve boron toxicity tolerance in pepper plants by regulating the AsA-GSH cycle and glyoxalase system. , 2020, Chemosphere.
[15] C. Kaya,et al. Gibberellic acid-induced generation of hydrogen sulfide alleviates boron toxicity in tomato (Solanum lycopersicum L.) plants. , 2020, Plant physiology and biochemistry : PPB.
[16] P. Doerner,et al. The impact of the rhizobia–legume symbiosis on host root system architecture , 2020, Journal of experimental botany.
[17] J. M. Palma,et al. H2S signaling in plants and applications in agriculture , 2020, Journal of advanced research.
[18] Juan Chen,et al. Hydrogen sulfide is a crucial element of the antioxidant defense system in Glycine max–Sinorhizobium fredii symbiotic root nodules , 2020, Plant and Soil.
[19] Z. Shangguan,et al. Hydrogen sulfide and rhizobia synergistically regulate nitrogen (N) assimilation and remobilization during N deficiency-induced senescence in soybean. , 2020, Plant, cell & environment.
[20] Hai-lei Zheng,et al. Comparative Proteomic Analysis Reveals the Regulatory Effects of H2S on Salt Tolerance of Mangrove Plant Kandelia obovata , 2019, International journal of molecular sciences.
[21] M. Hajirezaei,et al. Proteomic and metabolomic analysis of desiccation tolerance in wheat young seedlings. , 2019, Plant physiology and biochemistry : PPB.
[22] F. J. Corpas. Hydrogen Sulfide: A New Warrior against Abiotic Stress. , 2019, Trends in plant science.
[23] C. Kaya,et al. Responses of nitric oxide and hydrogen sulfide in regulating oxidative defence system in wheat plants grown under cadmium stress. , 2019, Physiologia plantarum.
[24] Juan Chen,et al. Hydrogen Sulfide Promotes Nodulation and Nitrogen Fixation in Soybean-Rhizobia Symbiotic System. , 2019, Molecular plant-microbe interactions : MPMI.
[25] Yun Tian,et al. H2S Alleviates Salinity Stress in Cucumber by Maintaining the Na+/K+ Balance and Regulating H2S Metabolism and Oxidative Stress Response , 2019, Front. Plant Sci..
[26] T. Sharkey,et al. Triose phosphate utilization and beyond: from photosynthesis to end-product synthesis , 2018, bioRxiv.
[27] A. Nicotra,et al. Genes controlling legume nodule numbers affect phenotypic plasticity responses to nitrogen in the presence and absence of rhizobia. , 2018, Plant, cell & environment.
[28] P. Gresshoff,et al. Legume nodulation: The host controls the party. , 2018, Plant, cell & environment.
[29] C. Kaya,et al. Hydrogen sulfide regulates the levels of key metabolites and antioxidant defense system to counteract oxidative stress in pepper (Capsicum annuum L.) plants exposed to high zinc regime , 2018, Environmental Science and Pollution Research.
[30] Na Yang,et al. Metabolomics Reveals Distinct Carbon and Nitrogen Metabolic Responses to Magnesium Deficiency in Leaves and Roots of Soybean [Glycine max (Linn.) Merr.] , 2017, Front. Plant Sci..
[31] Yang Zhang,et al. Hydrogen Sulphide Improves Iron Homeostasis in Wheat Under Iron-Deficiency , 2017 .
[32] Wei Shen,et al. Hydrogen peroxide is involved in hydrogen sulfide-induced lateral root formation in tomato seedlings , 2017, BMC Plant Biology.
[33] L. Romero,et al. Persulfidation proteome reveals the regulation of protein function by hydrogen sulfide in diverse biological processes in Arabidopsis , 2017, Journal of experimental botany.
[34] H. Liao,et al. Characterization of Genetic Basis on Synergistic Interactions between Root Architecture and Biological Nitrogen Fixation in Soybean , 2017, Front. Plant Sci..
[35] P. Sofi,et al. Root architecture and rhizobial inoculation in relation to drought stress response in common bean (Phaseolus vulgaris l.) , 2017 .
[36] Zhong-Guang Li,et al. Hydrogen Sulfide: A Signal Molecule in Plant Cross-Adaptation , 2016, Front. Plant Sci..
[37] B. Buchanan. The carbon (formerly dark) reactions of photosynthesis , 2016, Photosynthesis Research.
[38] A. Nicotra,et al. The presence of nodules on legume root systems can alter phenotypic plasticity in response to internal nitrogen independent of nitrogen fixation. , 2016, Plant, cell & environment.
[39] H. Liao,et al. Improving crop nutrient efficiency through root architecture modifications. , 2016, Journal of integrative plant biology.
[40] M. Fujita,et al. Hydrogen sulfide modulates cadmium-induced physiological and biochemical responses to alleviate cadmium toxicity in rice , 2015, Scientific Reports.
[41] J. Araus,et al. Differential CO2 effect on primary carbon metabolism of flag leaves in durum wheat (Triticum durum Desf.). , 2015, Plant, cell & environment.
[42] Z. Shangguan,et al. Hydrogen sulphide improves adaptation of Zea mays seedlings to iron deficiency , 2015, Journal of experimental botany.
[43] Haitao Shi,et al. Hydrogen sulfide regulates abiotic stress tolerance and biotic stress resistance in Arabidopsis. , 2015, Journal of integrative plant biology.
[44] W. Frommer,et al. SWEETs, transporters for intracellular and intercellular sugar translocation. , 2015, Current opinion in plant biology.
[45] C. Körner. Paradigm shift in plant growth control. , 2015, Current opinion in plant biology.
[46] T. Altmann,et al. Phenotypic and metabolic responses to drought and salinity of four contrasting lentil accessions , 2015, Journal of experimental botany.
[47] D. Huhman,et al. Integrated Metabolomics and Transcriptomics Reveal Enhanced Specialized Metabolism in Medicago truncatula Root Border Cells1[OPEN] , 2015, Plant Physiology.
[48] Joel L. Sachs,et al. Lotus hosts delimit the mutualism–parasitism continuum of Bradyrhizobium , 2015, Journal of evolutionary biology.
[49] Y. Ruan. Sucrose metabolism: gateway to diverse carbon use and sugar signaling. , 2014, Annual review of plant biology.
[50] S. Smeekens,et al. Sugar signals and the control of plant growth and development. , 2014, Journal of experimental botany.
[51] W. Shen,et al. Auxin-induced hydrogen sulfide generation is involved in lateral root formation in tomato. , 2014, Plant physiology and biochemistry : PPB.
[52] U. Flügge,et al. Role of metabolite transporters in source-sink carbon allocation , 2013, Front. Plant Sci..
[53] M. Udvardi,et al. Transport and metabolism in legume-rhizobia symbioses. , 2013, Annual review of plant biology.
[54] M. Peoples,et al. Nitrogen contributions from faba bean (Vicia faba L.) reliant on soil rhizobia or inoculation , 2013, Plant and Soil.
[55] S. Rudaz,et al. Metabolomics reveals herbivore-induced metabolites of resistance and susceptibility in maize leaves and roots. , 2013, Plant, cell & environment.
[56] M. Tegeder,et al. Soybean ureide transporters play a critical role in nodule development, function and nitrogen export. , 2012, The Plant journal : for cell and molecular biology.
[57] A. Fernie,et al. The use of metabolomics to dissect plant responses to abiotic stresses , 2012, Cellular and Molecular Life Sciences.
[58] Anne Guiboileau,et al. Autophagy machinery controls nitrogen remobilization at the whole-plant level under both limiting and ample nitrate conditions in Arabidopsis. , 2012, The New phytologist.
[59] L. Nussaume,et al. Root developmental adaptation to phosphate starvation: better safe than sorry. , 2011, Trends in plant science.
[60] Z. Pei,et al. Hydrogen sulphide enhances photosynthesis through promoting chloroplast biogenesis, photosynthetic enzyme expression, and thiol redox modification in Spinacia oleracea seedlings , 2011, Journal of experimental botany.
[61] W. Frommer,et al. Sugar transporters for intercellular exchange and nutrition of pathogens , 2010, Nature.
[62] Mark Stitt,et al. Metabolic and signaling aspects underpinning the regulation of plant carbon nitrogen interactions. , 2010, Molecular plant.
[63] M. Burger,et al. Carbon Dioxide Enrichment Inhibits Nitrate Assimilation in Wheat and Arabidopsis , 2010, Science.
[64] Ken E. Giller,et al. Are the rates of photosynthesis stimulated by the carbon sink strength of rhizobial and arbuscular mycorrhizal symbioses , 2009 .
[65] M. Stitt,et al. Adjustment of growth and central metabolism to a mild but sustained nitrogen-limitation in Arabidopsis. , 2009, Plant, cell & environment.
[66] N. Baker. Chlorophyll fluorescence: a probe of photosynthesis in vivo. , 2008, Annual review of plant biology.
[67] M. Akhtar,et al. Biocontrol of a root-rot disease complex of chickpea by Glomus intraradices, Rhizobium sp. and Pseudomonas straita , 2008 .
[68] E. Baena-González,et al. Sugar sensing and signaling in plants: conserved and novel mechanisms. , 2006, Annual review of plant biology.
[69] T. Nielsen,et al. Fructose-2,6-bisphosphate: a traffic signal in plant metabolism. , 2004, Trends in plant science.
[70] Matthew J Paul,et al. Carbon metabolite sensing and signalling. , 2003, Plant biotechnology journal.
[71] S. Yanagisawa,et al. Differential regulation of EIN3 stability by glucose and ethylene signalling in plants , 2003, Nature.
[72] Filip Rolland,et al. Role of the Arabidopsis Glucose Sensor HXK1 in Nutrient, Light, and Hormonal Signaling , 2003, Science.
[73] Yves Gibon,et al. Steps towards an integrated view of nitrogen metabolism. , 2002, Journal of experimental botany.
[74] Thomas D. Schmittgen,et al. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.
[75] M. Paul,et al. Sink regulation of photosynthesis. , 2001, Journal of experimental botany.
[76] S. Huber,et al. Regulation of Sucrose Metabolism in Higher Plants: Localization and Regulation of Activity of Key Enzymes , 2000 .
[77] N. Matsuki,et al. The possible role of hydrogen sulfide as an endogenous smooth muscle relaxant in synergy with nitric oxide. , 1997, Biochemical and biophysical research communications.
[78] M. Stitt,et al. Nitrate Acts as a Signal to Induce Organic Acid Metabolism and Repress Starch Metabolism in Tobacco. , 1997, The Plant cell.
[79] Ichiro Terashima,et al. A model of the acclimation of photosynthesis in the leaves of C3 plants to sun and shade with respect to nitrogen use , 1995 .
[80] James F. Reynolds,et al. Modelling photosynthesis of cotton grown in elevated CO2 , 1992 .
[81] J. Beltrán,et al. Changes in invertase activities precede ovary growth induced by gibberellic acid in , 1991 .
[82] P. Kerr,et al. Effect of Photoperiod on Photosynthate Partitioning and Diurnal Rhythms in Sucrose Phosphate Synthase Activity in Leaves of Soybean (Glycine max L. [Merr.]) and Tobacco (Nicotiana tabacum L.). , 1984, Plant physiology.
[83] A. Wellburn,et al. Formulae and Program to Determine Total Carotenoids and Chlorophylls A and B of Leaf Extracts in Different Solvents , 1984 .
[84] S. Huber. Role of sucrose-phosphate synthase in partitioning of carbon in leaves. , 1983, Plant physiology.
[85] A. Walkley,et al. AN EXAMINATION OF THE DEGTJAREFF METHOD FOR DETERMINING SOIL ORGANIC MATTER, AND A PROPOSED MODIFICATION OF THE CHROMIC ACID TITRATION METHOD , 1934 .
[86] Z. Fei,et al. Decreased sorbitol synthesis leads to abnormal stamen development and reduced pollen tube growth via an MYB transcription factor, MdMYB39L, in apple (Malus domestica). , 2018, The New phytologist.
[87] A. Rogers,et al. How can we make plants grow faster? A source-sink perspective on growth rate. , 2016, Journal of experimental botany.
[88] A. Fukushima,et al. Metabolomic screening applied to rice FOX Arabidopsis lines leads to the identification of a gene-changing nitrogen metabolism. , 2010, Molecular plant.
[89] T. Kuyper,et al. Differences in photosynthetic behaviour and leaf senescence of soybean (Glycine max [L.] Merrill) dependent on N2 fixation or nitrate supply. , 2010, Plant biology.
[90] R. Molinié,et al. Metabolic profiling of maize mutants deficient for two glutamine synthetase isoenzymes using 1H-NMR-based metabolomics. , 2010, Phytochemical analysis : PCA.
[91] P. Gresshoff,et al. Molecular analysis of legume nodule development and autoregulation. , 2010, Journal of integrative plant biology.
[92] J. R. Evans. Photosynthesis and nitrogen relationships in leaves of C3 plants , 2004, Oecologia.
[93] Mark Stitt,et al. Tobacco mutants with a decreased number of functional nia genes compensate by modifying the diurnal regulation of transcription, post-translational modification and turnover of nitrate reductase , 1997, Planta.
[94] Donald R. Geiger,et al. Diurnal Regulation of Photosynthetic Carbon Metabolism in C3 Plants , 1994 .
[95] E. Paul,et al. Carbon flow, photosynthesis, and N2 fixation in mycorrhizal and nodulated faba beans (Vicia faba L.) , 1982 .