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Pathways of nitric oxide metabolism and operation of phytoglobins in legume nodules: Missing links and future directions
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/iub.439openalex-snapshot
Structural and functional properties of class 1 plant hemoglobins
inferredcites →https://doi.org/10.1002/yea.1075openalex-snapshot
The role of Ynt1 in nitrate and nitrite transport in the yeast Hansenula polymorpha
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From Cell Division to Organ Shape: Nitric Oxide Is Involved in Auxin-Mediated Root Development
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Nitric Oxide: A Multitask Player in Plant–Microorganism Symbioses
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Factors Affecting Nitrogen Deposition Impacts on Biodiversity: An Overview
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Acid-base-modulation of nitrate reductase in leaf tissues
inferredcites →https://doi.org/10.1007/bf00239997openalex-snapshot
Nitrate and nitrite uptake and reduction by intact sunflower plants
inferredcites →https://doi.org/10.1007/bf01279263openalex-snapshot
Protective effect of exogenous nitrate on the mitochondrial ultrastructure ofOryza sativa coleoptiles under strict anoxia
inferredcites →https://doi.org/10.1007/pl00000849openalex-snapshot
Nitrate and nitrite transport in bacteria
inferredcites →https://doi.org/10.1007/s00425-003-1172-7openalex-snapshot
Nitric oxide plays a central role in determining lateral root development in tomato
inferredcites →https://doi.org/10.1007/s00425-005-0146-3openalex-snapshot
Nitric oxide scavenging by barley hemoglobin is facilitated by a monodehydroascorbate reductase-mediated ascorbate reduction of methemoglobin
inferredcites →https://doi.org/10.1007/s00425-007-0496-0openalex-snapshot
Nitrite-driven anaerobic ATP synthesis in barley and rice root mitochondria
inferredcites →https://doi.org/10.1007/s00775-005-0046-9openalex-snapshot
Oxyleghemoglobin scavenges nitrogen monoxide and peroxynitrite: a possible role in functioning nodules?
inferredcites →https://doi.org/10.1016/j.bbabio.2006.05.011openalex-snapshot
Nitric oxide and the respiratory enzyme
inferredcites →https://doi.org/10.1016/j.bbabio.2008.06.002openalex-snapshot
Nitrite–nitric oxide control of mitochondrial respiration at the frontier of anoxia
inferredcites →https://doi.org/10.1016/j.cmet.2006.02.011openalex-snapshot
Mitochondrial cytochrome oxidase produces nitric oxide under hypoxic conditions: Implications for oxygen sensing and hypoxic signaling in eukaryotes
inferredcites →https://doi.org/10.1016/j.cub.2005.01.042openalex-snapshot
Symbiotic Leghemoglobins Are Crucial for Nitrogen Fixation in Legume Root Nodules but Not for General Plant Growth and Development
inferredcites →https://doi.org/10.1016/j.febslet.2011.10.036openalex-snapshot
Plant hemoglobins: Important players at the crossroads between oxygen and nitric oxide
inferredcites →https://doi.org/10.1016/j.fgb.2007.10.001openalex-snapshot
Nitrite transport is mediated by the nitrite-specific high-affinity NitA transporter and by nitrate transporters NrtA, NrtB in Aspergillus nidulans
inferredcites →https://doi.org/10.1016/j.jaridenv.2015.02.011openalex-snapshot
Effects of soil water content, temperature and experimental nitrogen deposition on nitric oxide (NO) efflux from semiarid shrubland soil
inferredcites →https://doi.org/10.1016/j.jplph.2009.08.006openalex-snapshot
Involvement of nitric oxide in the inhibition of nitrogenase activity by nitrate in Lotus root nodules
inferredcites →https://doi.org/10.1016/j.jplph.2010.06.019openalex-snapshot
Nitric oxide synthase activity is required for development of functional nodules in soybean
inferredcites →https://doi.org/10.1016/j.jprot.2012.05.024openalex-snapshot
Sulfenylated proteins in the Medicago truncatula–Sinorhizobium meliloti symbiosis
inferredcites →https://doi.org/10.1016/j.mito.2011.03.005openalex-snapshot
The anoxic plant mitochondrion as a nitrite: NO reductase
inferredcites →https://doi.org/10.1016/j.molp.2014.12.010openalex-snapshot
Nitric Oxide: A Multitasked Signaling Gas in Plants
inferredcites →https://doi.org/10.1016/j.niox.2015.01.007openalex-snapshot
Nitric oxide from a “green” perspective
inferredcites →https://doi.org/10.1016/j.pbi.2015.05.010openalex-snapshot
Plant nitrogen assimilation and its regulation: a complex puzzle with missing pieces
inferredcites →https://doi.org/10.1016/j.plantsci.2011.04.007openalex-snapshot
Nitric oxide in legume–rhizobium symbiosis
inferredcites →https://doi.org/10.1016/j.plantsci.2016.03.013openalex-snapshot
Dual targeted poplar ferredoxin NADP+ oxidoreductase interacts with hemoglobin 1
inferredcites →https://doi.org/10.1016/j.tplants.2010.11.007openalex-snapshot
On the origins of nitric oxide
inferredcites →https://doi.org/10.1016/j.tplants.2012.04.006openalex-snapshot
Uptake, allocation and signaling of nitrate
inferredcites →https://doi.org/10.1016/s0014-5793(96)01232-xopenalex-snapshot
Presence of nitric oxide synthase activity in roots and nodules of Lupinus albus
inferredcites →https://doi.org/10.1016/s0014-5793(99)00788-7openalex-snapshot
Nitrite reductase activity is a novel function of mammalian mitochondria
inferredcites →https://doi.org/10.1016/s0065-2296(16)30101-xopenalex-snapshot
Advances in Botanical Research
inferredcites →https://doi.org/10.1016/s0891-5849(97)00440-1openalex-snapshot
Direct Detection of Radicals in Intact Soybean Nodules: Presence of Nitric Oxide-Leghemoglobin Complexes
inferredcites →https://doi.org/10.1023/a:1006424330555openalex-snapshot
Soil-air exchange of nitric oxide: An overview of processes, environmental factors, and modeling studies
inferredcites →https://doi.org/10.1023/a:1009738715891openalex-snapshot
A global inventory of nitric oxide emissions from soils
inferredcites →https://doi.org/10.1042/bj20080746openalex-snapshot
A single channel for nitrate uptake, nitrite export and nitrite uptake by Escherichia coli NarU and a role for NirC in nitrite export and uptake
inferredcites →https://doi.org/10.1073/pnas.0408648102openalex-snapshot
Functional- and abundance-based mechanisms explain diversity loss due to N fertilization
inferredcites →https://doi.org/10.1073/pnas.0709461105openalex-snapshot
Oxygen-regulated isoforms of cytochrome c oxidase have differential effects on its nitric oxide production and on hypoxic signaling
inferredcites →https://doi.org/10.1073/pnas.96.11.6529openalex-snapshot
Dual pathways for regulation of root branching by nitrate
inferredcites →https://doi.org/10.1074/jbc.271.4.2088openalex-snapshot
Nitrate and Nitrite Are Transported by Different Specific Transport Systems and by a Bispecific Transporter in Chlamydomonas reinhardtii
inferredcites →https://doi.org/10.1074/jbc.m700901200openalex-snapshot
Regulation of Root Nitrate Uptake at the NRT2.1 Protein Level in Arabidopsis thaliana
inferredcites →https://doi.org/10.1080/07352688809382257openalex-snapshot
Inhibition of legume nodule formation and N2fixation by nitrate
inferredcites →https://doi.org/10.1080/15216540152845911openalex-snapshot
Respiratory Chain Supercomplexes
inferredcites →https://doi.org/10.1089/ars.2012.5136openalex-snapshot
Hydrogen Peroxide and Nitric Oxide: Key Regulators of the Legume— Rhizobium and Mycorrhizal Symbioses
inferredcites →https://doi.org/10.1093/aob/mcf244openalex-snapshot
Functional Electron Microscopy in Studies of Plant response and adaptation to Anaerobic Stress
inferredcites →https://doi.org/10.1093/aob/mcn100openalex-snapshot
Plant mitochondrial function during anaerobiosis
inferredcites →https://doi.org/10.1093/jxb/erg189openalex-snapshot
Nitrate-independent expression of plant nitrate reductase in Lotus japonicus root nodules
inferredcites →https://doi.org/10.1093/jxb/erh272openalex-snapshot
Nitrate, NO and haemoglobin in plant adaptation to hypoxia: an alternative to classic fermentation pathways
inferredcites →https://doi.org/10.1093/jxb/eri252openalex-snapshot
In higher plants, only root mitochondria, but not leaf mitochondria reduce nitrite to NO, in vitro and in situ
inferredcites →https://doi.org/10.1093/jxb/erj184openalex-snapshot
Reactive oxygen and nitrogen species and glutathione: key players in the legume-Rhizobium symbiosis
inferredcites →https://doi.org/10.1093/jxb/erq323openalex-snapshot
MtNOA1/RIF1 modulates Medicago truncatula–Sinorhizobium meliloti nodule development without affecting its nitric oxide content
inferredcites →https://doi.org/10.1093/jxb/erv051openalex-snapshot
Nitric oxide: a multifaceted regulator of the nitrogen-fixing symbiosis
inferredcites →https://doi.org/10.1093/jxb/erw290openalex-snapshot
Hemoglobin LjGlb1-1 is involved in nodulation and regulates the level of nitric oxide in theLotus japonicus–Mesorhizobium lotisymbiosis
inferredcites →https://doi.org/10.1093/pci/pci001openalex-snapshot
Symbiotic Rhizobium and Nitric Oxide Induce Gene Expression of Non-symbiotic Hemoglobin in Lotus japonicus
inferredcites →https://doi.org/10.1093/pcp/pcm073openalex-snapshot
A Nitrite Transporter Associated with Nitrite Uptake by Higher Plant Chloroplasts
inferredcites →https://doi.org/10.1093/pcp/pcq022openalex-snapshot
Production and Scavenging of Nitric Oxide by Barley Root Mitochondria
inferredcites →https://doi.org/10.1093/pcp/pcr020openalex-snapshot
Nitric Oxide Production Induced in Roots of Lotus japonicus by Lipopolysaccharide from Mesorhizobium loti
inferredcites →https://doi.org/10.1093/pcp/pct167openalex-snapshot
Members of the NPF3 Transporter Subfamily Encode Pathogen-Inducible Nitrate/Nitrite Transporters in Grapevine and Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcw174openalex-snapshot
Nitrite Protects Mitochondrial Structure and Function under Hypoxia
inferredcites →https://doi.org/10.1094/mpmi-05-15-0118-ropenalex-snapshot
Sinorhizobium meliloti Controls Nitric Oxide–Mediated Post-Translational Modification of a Medicago truncatula Nodule Protein
inferredcites →https://doi.org/10.1094/mpmi-19-0441openalex-snapshot
A Class 1 Hemoglobin Gene from Alnus firma Functions in Symbiotic and Nonsymbiotic Tissues to Detoxify Nitric Oxide
inferredcites →https://doi.org/10.1094/mpmi-19-0970openalex-snapshot
Nitric Oxide Is Formed in Medicago truncatula-Sinorhizobium meliloti Functional Nodules
inferredcites →https://doi.org/10.1094/mpmi-21-9-1175openalex-snapshot
Expression of a Class 1 Hemoglobin Gene and Production of Nitric Oxide in Response to Symbiotic and Pathogenic Bacteria in Lotus japonicus
inferredcites →https://doi.org/10.1094/mpmi-23-5-0702openalex-snapshot
Production of Nitric Oxide and Nitrosylleghemoglobin Complexes in Soybean Nodules in Response to Flooding
inferredcites →https://doi.org/10.1094/mpmi-23-6-0748openalex-snapshot
The Response to Nitric Oxide of the Nitrogen-Fixing Symbiont Sinorhizobium meliloti
inferredcites →https://doi.org/10.1098/rstb.2013.0126openalex-snapshot
Processes regulating nitric oxide emissions from soils
inferredcites →https://doi.org/10.1099/mic.0.2006/000059-0openalex-snapshot
The contribution of bacteroidal nitrate and nitrite reduction to the formation of nitrosylleghaemoglobin complexes in soybean root nodules
inferredcites →https://doi.org/10.1104/pp.110.166140openalex-snapshot
Both Plant and Bacterial Nitrate Reductases Contribute to Nitric Oxide Production in Medicago truncatula Nitrogen-Fixing Nodules
inferredcites →https://doi.org/10.1104/pp.111.186056openalex-snapshot
Glutamine Synthetase Is a Molecular Target of Nitric Oxide in Root Nodules of Medicago truncatula and Is Regulated by Tyrosine Nitration
inferredcites →https://doi.org/10.1104/pp.112.208538openalex-snapshot
Expression Dynamics of the Medicago truncatula Transcriptome during the Symbiotic Interaction with Sinorhizobium meliloti: Which Role for Nitric Oxide?
inferredcites →https://doi.org/10.1104/pp.99.2.712openalex-snapshot
Tissue-Specific Expression of the Alternative Oxidase in Soybean and Siratro
inferredcites →https://doi.org/10.1105/tpc.12.8.1441openalex-snapshot
The Chlamydomonas reinhardtii Nar1 Gene Encodes a Chloroplast Membrane Protein Involved in Nitrite Transport
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02335.xopenalex-snapshot
Nitric oxide emission from tobacco leaves and cell suspensions: rate limiting factors and evidence for the involvement of mitochondrial electron transport
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03519.xopenalex-snapshot
A gene expression atlas of the model legume Medicago truncatula
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03689.xopenalex-snapshot
Overexpression of class 1 plant hemoglobin genes enhances symbiotic nitrogen fixation activity between Mesorhizobium loti and Lotus japonicus
inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01314.xopenalex-snapshot
Anoxic nitric oxide cycling in plants: participating reactions and possible mechanisms
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03527.xopenalex-snapshot
Regulation of nonsymbiotic and truncated hemoglobin genes of Lotus japonicus in plant organs and in response to nitric oxide and hormones
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03693.xopenalex-snapshot
Nitric oxide is required for an optimal establishment of the Medicago truncatula–Sinorhizobium meliloti symbiosis
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04166.xopenalex-snapshot
Alternative oxidase modulates leaf mitochondrial concentrations of superoxide and nitric oxide
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04282.xopenalex-snapshot
Nitric oxide ( NO ): a key player in the senescence of Medicago truncatula root nodules
inferredcites →https://doi.org/10.1111/nph.12120openalex-snapshot
Hydrogen peroxide‐regulated genes in the Medicago truncatula–Sinorhizobium meliloti symbiosis
inferredcites →https://doi.org/10.1111/nph.12358openalex-snapshot
Characterization of nitrite uptake in Arabidopsis thaliana: evidence for a nitrite‐specific transporter
inferredcites →https://doi.org/10.1111/pce.12312openalex-snapshot
What happens to plant mitochondria under low oxygen? An omics review of the responses to low oxygen and reoxygenation
inferredcites →https://doi.org/10.1111/pce.13081openalex-snapshot
Rice phytoglobins regulate responses under low mineral nutrients and abiotic stresses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1128/aem.44.6.1385-1388.1982openalex-snapshot
Nitrite and Nitric Oxide as Inhibitors of Nitrogenase from Soybean Bacteroids
inferredcites →https://doi.org/10.1128/mmbr.61.4.533-616.1997openalex-snapshot
Cell biology and molecular basis of denitrification
inferredcites →https://doi.org/10.1134/s0003683808040108openalex-snapshot
Effect of nitric oxide and other nitrogen compounds on the adhesion and penetration of nodule bacteria into root tissues and on growth of etiolated pea seedlings
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092839openalex-snapshot
Coordinating Nodule Morphogenesis with Rhizobial Infection in Legumes
inferredcites →https://doi.org/10.1186/1471-2229-7-21openalex-snapshot
Auxin and nitric oxide control indeterminate nodule formation
inferredcites →https://doi.org/10.3389/fpls.2013.00384openalex-snapshot
Which role for nitric oxide in symbiotic N2-fixing nodules: toxic by-product or useful signaling/metabolic intermediate?
inferredcites →https://doi.org/10.3389/fpls.2016.00369openalex-snapshot
Reactive Nitrogen Species in Mitochondria and Their Implications in Plant Energy Status and Hypoxic Stress Tolerance
inferredcites →https://doi.org/10.3389/fpls.2016.00454openalex-snapshot
Reactive Oxygen Species and Nitric Oxide Control Early Steps of the Legume – Rhizobium Symbiotic Interaction
inferredcites →https://doi.org/10.3389/fpls.2016.00472openalex-snapshot
Cross-Regulation between N Metabolism and Nitric Oxide (NO) Signaling during Plant Immunity
inferredcites →https://doi.org/10.3390/ijms15058186openalex-snapshot
Transport Pathways—Proton Motive Force Interrelationship in Durum Wheat Mitochondria
inferredcites →https://doi.org/10.4161/psb.25923openalex-snapshot
Control of NO level in rhizobium-legume root nodules
inferredcites →https://doi.org/10.4161/psb.5.12.14041openalex-snapshot
Endogenous NO levels regulate nodule functioning
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/s00425-026-04979-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11738-021-03291-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.ampbs.2021.05.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jenvman.2025.124162openalex-snapshot
Legumes reduce the effects of salt stress on co-existing grass
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112393openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.03.025openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tplants.2019.09.007openalex-snapshot
The PHYTOGLOBIN-NO Cycle Regulates Plant Mycorrhizal Symbiosis
inferred← citeshttps://doi.org/10.1038/s41477-020-0683-6openalex-snapshot
Transfer cells mediate nitrate uptake to control root nodule symbiosis
inferred← citeshttps://doi.org/10.1093/jxb/eraa403openalex-snapshot
Nitrate reductases and hemoglobins control nitrogen-fixing symbiosis by regulating nitric oxide accumulation
inferred← citeshttps://doi.org/10.1093/jxb/erad399openalex-snapshot
The emerging roles of nitric oxide and its associated scavengers—phytoglobins—in plant symbiotic interactions
inferred← citeshttps://doi.org/10.1093/jxb/erz159openalex-snapshot
Nitric oxide signaling, metabolism and toxicity in nitrogen-fixing symbiosis
inferred← citeshttps://doi.org/10.1093/plphys/kiag377openalex-snapshot
Functional divergence and symbiotic significance of nitrate reductase isoforms in Medicago truncatula
inferred← citeshttps://doi.org/10.1101/2024.05.31.596865openalex-snapshot
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Effectiveness of nitrogen fixation in rhizobia
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The role of nitrite and nitric oxide under low oxygen conditions in plants
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The power of the phytoglobin–NO cycle in the regulation of nodulation and symbiotic nitrogen fixation
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The Nitrate Assimilatory Pathway in Sinorhizobium meliloti: Contribution to NO Production
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Redirecting Cell Fate During in vitro Embryogenesis: Phytoglobins as Molecular Switches
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Molecular Weapons Contribute to Intracellular Rhizobia Accommodation Within Legume Host Cell
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Contribution des phytoglobines et des nitrate réductases à la régulation de l’oxyde nitrique et de la fixation de l’azote dans la symbiose Medicago truncatula / Sinorhizobium meliloti
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