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Both Plant and Bacterial Nitrate Reductases Contribute to Nitric Oxide Production in Medicago truncatula Nitrogen-Fixing Nodules

https://doi.org/10.1104/pp.110.166140
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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/10.1016/j.mito.2011.03.005openalex-snapshot
The anoxic plant mitochondrion as a nitrite: NO reductase
inferred← citeshttps://doi.org/10.1016/j.niox.2014.06.008openalex-snapshot
Detection and function of nitric oxide during the hypersensitive response in Arabidopsis thaliana: Where there’s a will there’s a way
inferred← citeshttps://doi.org/10.1016/j.niox.2016.09.005openalex-snapshot
Nitric oxide synthase in plants: Where do we stand?
inferred← citeshttps://doi.org/10.1016/j.niox.2019.04.006openalex-snapshot
Characterization of plant glutamine synthetase S-nitrosation
inferred← citeshttps://doi.org/10.1016/j.niox.2019.09.006openalex-snapshot
A forty year journey: The generation and roles of NO in plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2013.06.020openalex-snapshot
Nitric oxide and reactive oxygen species in plant biotic interactions
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.03.018openalex-snapshot
The emerging roles of nitric oxide (NO) in plant mitochondria
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.04.007openalex-snapshot
Nitric oxide in legume–rhizobium symbiosis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.07.014openalex-snapshot
The hunt for plant nitric oxide synthase (NOS): Is one really needed?
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112393openalex-snapshot
Differential regulation of the “phytoglobin-nitric oxide respiration” in Medicago truncatula roots and nodules submitted to flooding
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112851openalex-snapshot
Pivotal role of nitric oxide in regulating beneficial plant–microbe interactions under both physiological and stress conditions
inferred← citeshttps://doi.org/10.1016/j.plaphy.2013.04.004openalex-snapshot
Nitrosative responses in citrus plants exposed to six abiotic stress conditions
inferred← citeshttps://doi.org/10.1016/j.plaphy.2013.10.030openalex-snapshot
Nitrate reductase (NR)-dependent NO production mediates ABA- and H2O2-induced antioxidant enzymes
inferred← citeshttps://doi.org/10.1016/j.plaphy.2017.04.011openalex-snapshot
Evidence towards the involvement of nitric oxide in drought tolerance of sugarcane
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.08.005openalex-snapshot
The outcomes of the functional interplay of nitric oxide and hydrogen sulfide in metal stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/j.scienta.2016.12.006openalex-snapshot
Nitric oxide is involved in ethylene-induced adventitious root development in cucumber (Cucumis sativus L.) explants
inferred← citeshttps://doi.org/10.1016/j.scienta.2025.114607openalex-snapshot
Multi-omics reveal tiered adaptation and critical thresholds for fertilizer substitution in an arid agroecosystem
inferred← citeshttps://doi.org/10.1016/j.soilbio.2014.09.025openalex-snapshot
A review of soil NO transformation: Associated processes and possible physiological significance on organisms
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100191openalex-snapshot
Mechanisms of nitric oxide involvement in plant-microbe interaction and its enhancement of stress resistance
inferred← citeshttps://doi.org/10.1016/j.stress.2025.101102openalex-snapshot
Biosynthesis and multifaceted roles of reactive species in plant defense mechanisms during environmental cues
inferred← citeshttps://doi.org/10.1038/s41598-022-12285-3openalex-snapshot
Common gene expression patterns are observed in rice roots during associations with plant growth-promoting bacteria, Herbaspirillum seropedicae and Azospirillum brasilense
inferred← citeshttps://doi.org/10.1038/s41598-022-17462-yopenalex-snapshot
Intracellular production of reactive oxygen species and a DAF-FM-related compound in Aspergillus fumigatus in response to antifungal agent exposure
inferred← citeshttps://doi.org/10.1042/bj20150880openalex-snapshot
An integrated biochemical system for nitrate assimilation and nitric oxide detoxification in Bradyrhizobium japonicum
inferred← citeshttps://doi.org/10.1042/bst20110732openalex-snapshot
The nitric oxide response in plant-associated endosymbiotic bacteria
inferred← citeshttps://doi.org/10.1042/bst20110733openalex-snapshot
Denitrification in Sinorhizobium meliloti
inferred← citeshttps://doi.org/10.1042/bst20200989openalex-snapshot
Rhizobia: highways to NO
inferred← citeshttps://doi.org/10.1071/fp11066openalex-snapshot
Progress on research on actinorhizal plants
inferred← citeshttps://doi.org/10.1073/pnas.1116559109openalex-snapshot
Leghemoglobin green derivatives with nitrated hemes evidence production of highly reactive nitrogen species during aging of legume nodules
inferred← citeshttps://doi.org/10.1080/17429145.2023.2251511openalex-snapshot
Rhizobium etli is able to emit nitrous oxide by connecting assimilatory nitrate reduction with nitrite respiration in the bacteroids of common bean nodules
inferred← citeshttps://doi.org/10.1080/19476337.2019.1621949openalex-snapshot
The role of nitric oxide in the mechanism of lactic acid bacteria substituting for nitrite
inferred← citeshttps://doi.org/10.1089/ars.2012.5136openalex-snapshot
Hydrogen Peroxide and Nitric Oxide: Key Regulators of the Legume— Rhizobium and Mycorrhizal Symbioses
inferred← citeshttps://doi.org/10.1093/aob/mcv023openalex-snapshot
Spatial and temporal regulation of the metabolism of reactive oxygen and nitrogen species during the early development of pepper (Capsicum annuum) seedlings
inferred← citeshttps://doi.org/10.1093/femsle/fny041openalex-snapshot
Overexpression of the periplasmic nitrate reductase supports anaerobic growth by Ensifer meliloti
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/eraa421openalex-snapshot
Nitric oxide production and signalling in algae
inferred← citeshttps://doi.org/10.1093/jxb/erab008openalex-snapshot
Molecular responses of legumes to abiotic stress: post-translational modifications of proteins and redox signaling
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/erad455openalex-snapshot
Dynamics of hemoglobins during nodule development, nitrate response, and dark stress in Lotus japonicus
inferred← citeshttps://doi.org/10.1093/jxb/eraf160openalex-snapshot
Oxygen and derived reactive species in legume–rhizobia interactions: paradoxes and dual roles
inferred← citeshttps://doi.org/10.1093/jxb/eraf175openalex-snapshot
The role of reactive oxygen, nitrogen, and sulfur species in the integration of (a)biotic stress signals in legumes
inferred← citeshttps://doi.org/10.1093/jxb/eraf353openalex-snapshot
Nitrate reductase-mediated nitric oxide synthesis in shaping stress resilience in plants
inferred← citeshttps://doi.org/10.1093/jxb/erv051openalex-snapshot
Nitric oxide: a multifaceted regulator of the nitrogen-fixing symbiosis
inferred← citeshttps://doi.org/10.1093/jxb/ery159openalex-snapshot
Redefining nitric oxide production in legume nodules through complementary insights from electron paramagnetic resonance spectroscopy and specific fluorescent probes
inferred← citeshttps://doi.org/10.1093/jxb/erz117openalex-snapshot
Nitric oxide in plants: pro- or anti-senescence
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/pcp/pcy245openalex-snapshot
Stably TransformedLotus japonicusPlants Overexpressing Phytoglobin LjGlb1-1 Show Decreased Nitric Oxide Levels in Roots and Nodules as Well as Delayed Nodule Senescence
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/10.1094/mpmi-05-15-0118-ropenalex-snapshot
Sinorhizobium meliloti Controls Nitric Oxide–Mediated Post-Translational Modification of a Medicago truncatula Nodule Protein
inferred← citeshttps://doi.org/10.1094/mpmi-05-22-0118-scopenalex-snapshot
Role of Nitric Oxide of Bacterial Origin in the Medicago truncatula–Sinorhizobium meliloti Symbiosis
inferred← citeshttps://doi.org/10.1094/mpmi-07-21-0180-ropenalex-snapshot
Specialization in a Nitrogen-Fixing Symbiosis: Proteome Differences Between Sinorhizobium medicae Bacteria and Bacteroids
inferred← citeshttps://doi.org/10.1094/mpmi-09-12-0214-cropenalex-snapshot
Nitric Oxide as a Mediator for Defense Responses
inferred← citeshttps://doi.org/10.1094/mpmi-12-11-0322openalex-snapshot
Inhibition of Glutamine Synthetase by Phosphinothricin Leads to Transcriptome Reprograming in Root Nodules of Medicago truncatula
inferred← citeshttps://doi.org/10.1094/mpmi-34-12openalex-snapshot
Full Issue PDF
inferred← citeshttps://doi.org/10.1101/2024.05.31.596865openalex-snapshot
Nitrate reductase activity is required in Medicago truncatula - Sinorhizobium meliloti nitrogen-fixing symbiosis
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1104/pp.112.196444openalex-snapshot
Functional Assessment of the Medicago truncatula NIP/LATD Protein Demonstrates That It Is a High-Affinity Nitrate Transporter
inferred← citeshttps://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?
inferred← citeshttps://doi.org/10.1104/pp.113.228312openalex-snapshot
An RNA Sequencing Transcriptome Analysis Reveals Novel Insights into Molecular Aspects of the Nitrate Impact on the Nodule Activity of Medicago truncatula
inferred← citeshttps://doi.org/10.1104/pp.113.229369openalex-snapshot
Hydrogen Peroxide Acts Upstream of Nitric Oxide in the Heat Shock Pathway in Arabidopsis Seedlings
inferred← citeshttps://doi.org/10.1104/pp.17.01187openalex-snapshot
The Nitrate Transporter Family Protein LjNPF8.6 Controls the N-Fixing Nodule Activity
inferred← citeshttps://doi.org/10.1111/1462-2920.13948openalex-snapshot
The nitrate‐reduction gene cluster components exert lineage‐dependent contributions to optimization of Sinorhizobium symbiosis with soybeans
inferred← citeshttps://doi.org/10.1111/1751-7915.13517openalex-snapshot
Effectiveness of nitrogen fixation in rhizobia
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2012.02505.xopenalex-snapshot
Nitric oxide production mediates oligogalacturonide‐triggered immunity and resistance to Botrytis cinerea in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2012.05100.xopenalex-snapshot
Oxidative and nitrosative‐based signaling and associated post‐translational modifications orchestrate the acclimation of citrus plants to salinity stress
inferred← citeshttps://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
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/jac.12471openalex-snapshot
Hypoxia and Anoxia Stress: Plant responses and tolerance mechanisms
inferred← citeshttps://doi.org/10.1111/mmi.14465openalex-snapshot
Nitric oxide as a developmental and metabolic signal in filamentous fungi
inferred← citeshttps://doi.org/10.1111/mpp.12095openalex-snapshot
Nitric oxide: an effective weapon of the plant or the pathogen?
inferred← citeshttps://doi.org/10.1111/nph.15969openalex-snapshot
The role of nitrite and nitric oxide under low oxygen conditions in plants
inferred← citeshttps://doi.org/10.1111/nph.16462openalex-snapshot
Medicago truncatula Phytoglobin 1.1 controls symbiotic nodulation and nitrogen fixation via the regulation of nitric oxide concentration
inferred← citeshttps://doi.org/10.1111/nph.16615openalex-snapshot
The power of the phytoglobin–NO cycle in the regulation of nodulation and symbiotic nitrogen fixation
inferred← citeshttps://doi.org/10.1111/nph.16728openalex-snapshot
The functional characterization of LjNRT2.4 indicates a novel, positive role of nitrate for an efficient nodule N 2 ‐fixation activity
inferred← citeshttps://doi.org/10.1111/nph.18434openalex-snapshot
Signaling by reactive molecules and antioxidants in legume nodules
inferred← citeshttps://doi.org/10.1111/pce.12204openalex-snapshot
Polyamines reprogram oxidative and nitrosative status and the proteome of citrus plants exposed to salinity stress
inferred← citeshttps://doi.org/10.1111/pce.12295openalex-snapshot
Interplays between nitric oxide and reactive oxygen species in cryptogein signalling
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/pce.12715openalex-snapshot
New insights into reactive oxygen species and nitric oxide signalling under low oxygen in plants
inferred← citeshttps://doi.org/10.1111/pce.12884openalex-snapshot
The occurrence and control of nitric oxide generation by the plant mitochondrial electron transport chain
inferred← citeshttps://doi.org/10.1111/pce.13151openalex-snapshot
Pathways of nitric oxide metabolism and operation of phytoglobins in legume nodules: Missing links and future directions
inferred← citeshttps://doi.org/10.1111/pce.13850openalex-snapshot
Physiological significance of pedospheric nitric oxide for root growth, development and organismic interactions
inferred← citeshttps://doi.org/10.1111/pce.14505openalex-snapshot
Group VII ethylene response factors, MtERF74 and MtERF75, sustain nitrogen fixation in Medicago truncatula microoxic nodules
inferred← citeshttps://doi.org/10.1111/plb.13319openalex-snapshot
Crosstalk between H2S and NO: an emerging signalling pathway during waterlogging stress in legume crops
inferred← citeshttps://doi.org/10.1126/scisignal.aad4403openalex-snapshot
Occurrence, structure, and evolution of nitric oxide synthase–like proteins in the plant kingdom
inferred← citeshttps://doi.org/10.1128/aem.01458-12openalex-snapshot
Characterization of the Twin-Arginine Transport Secretome in Sinorhizobium meliloti and Evidence for Host-Dependent Phenotypes
inferred← citeshttps://doi.org/10.1134/s1021443722602713openalex-snapshot
Participation of Nitric Oxide in the Regulation of Plants’ Development and Their Resistance to Water Deficit
inferred← citeshttps://doi.org/10.1186/1471-2180-14-142openalex-snapshot
Genetic basis for denitrification in Ensifer meliloti
inferred← citeshttps://doi.org/10.1186/s12864-021-08130-yopenalex-snapshot
Effects of nitrogen levels on gene expression and amino acid metabolism in Welsh onion
inferred← citeshttps://doi.org/10.1186/s12870-019-1974-9openalex-snapshot
Cyclic nucleotide-gated ion channel 6 mediates thermotolerance in Arabidopsis seedlings by regulating nitric oxide production via cytosolic calcium ions
inferred← citeshttps://doi.org/10.12794/metadc2048610openalex-snapshot
Medicago truncatula NPF1.7: Structure-Function Assessment and Potential as a Phytohormone Transporter
inferred← citeshttps://doi.org/10.12794/metadc407822openalex-snapshot
Functional Characterization of Mtnip/latd’s Biochemical and Biological Function
inferred← citeshttps://doi.org/10.1360/ssv-2022-0075openalex-snapshot
A perspective view of nitric oxide: biosynthesis, metabolism and signaling in plants
inferred← citeshttps://doi.org/10.1371/journal.pone.0045526openalex-snapshot
Detection of S-Nitrosothiol and Nitrosylated Proteins in Arachis hypogaea Functional Nodule: Response of the Nitrogen Fixing Symbiont
inferred← citeshttps://doi.org/10.1371/journal.pone.0070531openalex-snapshot
High-Resolution Transcriptomic Analyses of Sinorhizobium sp. NGR234 Bacteroids in Determinate Nodules of Vigna unguiculata and Indeterminate Nodules of Leucaena leucocephala
inferred← citeshttps://doi.org/10.15389/agrobiology.2017.5.878engopenalex-snapshot
ANTIOXIDANT DEFENSE SYSTEM IN SYMBIOTIC NODULES OF LEGUMES (review)
inferred← citeshttps://doi.org/10.15407/frg2019.05.371openalex-snapshot
Nitrate reductase and its role in legume-rhizobia symbiosis
inferred← citeshttps://doi.org/10.1590/1678-992x-2017-0195openalex-snapshot
Nitrogen source influences the antioxidative system of soybean plants under hypoxia and re-oxygenation
inferred← citeshttps://doi.org/10.21685/1680-0826-2023-17-1-2openalex-snapshot
Second nitrate reductase of Dunaliella salina: functional redundancy or greater?
inferred← citeshttps://doi.org/10.31590/ejosat.683895openalex-snapshot
Reaktif Azot Türlerinin (RNS) Üretimi, Fonksiyonu ve Stres Koşullarındaki Durumu
inferred← citeshttps://doi.org/10.31857/s0015330322600437openalex-snapshot
Involvement of Nitric Oxide in Regulation of Plant Development and Resistance to Moisture Deficiency
inferred← citeshttps://doi.org/10.3389/fagro.2023.1175524openalex-snapshot
Genomic analysis of Sinorhizobium meliloti LPU63, an acid-tolerant and symbiotically efficient alfalfa-nodulating rhizobia
inferred← citeshttps://doi.org/10.3389/fmicb.2015.00537openalex-snapshot
Anoxic growth of Ensifer meliloti 1021 by N2O-reduction, a potential mitigation strategy
inferred← citeshttps://doi.org/10.3389/fmicb.2019.01526openalex-snapshot
The Nitrate Assimilatory Pathway in Sinorhizobium meliloti: Contribution to NO Production
inferred← citeshttps://doi.org/10.3389/fmicb.2019.02915openalex-snapshot
The Hemoglobin Bjgb From Bradyrhizobium diazoefficiens Controls NO Homeostasis in Soybean Nodules to Protect Symbiotic Nitrogen Fixation
inferred← citeshttps://doi.org/10.3389/fpls.2013.00372openalex-snapshot
Possible role of glutamine synthetase in the NO signaling response in root nodules by contributing to the antioxidant defenses
inferred← citeshttps://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?
inferred← citeshttps://doi.org/10.3389/fpls.2015.00899openalex-snapshot
Understanding nitrate assimilation and its regulation in microalgae
inferred← citeshttps://doi.org/10.3389/fpls.2016.00369openalex-snapshot
Reactive Nitrogen Species in Mitochondria and Their Implications in Plant Energy Status and Hypoxic Stress Tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2016.00471openalex-snapshot
When Bad Guys Become Good Ones: The Key Role of Reactive Oxygen Species and Nitric Oxide in the Plant Responses to Abiotic Stress
inferred← citeshttps://doi.org/10.3389/fpls.2016.00472openalex-snapshot
Cross-Regulation between N Metabolism and Nitric Oxide (NO) Signaling during Plant Immunity
inferred← citeshttps://doi.org/10.3389/fpls.2019.00578openalex-snapshot
Exploring Legume-Rhizobia Symbiotic Models for Waterlogging Tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2019.01496openalex-snapshot
Molecular Weapons Contribute to Intracellular Rhizobia Accommodation Within Legume Host Cell
inferred← citeshttps://doi.org/10.3389/fpls.2020.00521openalex-snapshot
The Role of Nitric Oxide in Nitrogen Fixation by Legumes
inferred← citeshttps://doi.org/10.3389/fpls.2020.01177openalex-snapshot
Potential Pathway of Nitrous Oxide Formation in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2020.01313openalex-snapshot
Plant Nitrate Reductases Regulate Nitric Oxide Production and Nitrogen-Fixing Metabolism During the Medicago truncatula–Sinorhizobium meliloti Symbiosis
inferred← citeshttps://doi.org/10.3389/fpls.2021.658679openalex-snapshot
NO Network for Plant–Microbe Communication Underground: A Review
inferred← citeshttps://doi.org/10.3389/fpls.2021.683601openalex-snapshot
Nitrogen and Phosphorus Signaling and Transport During Legume–Rhizobium Symbiosis
inferred← citeshttps://doi.org/10.3389/fpls.2021.685334openalex-snapshot
Structural Modeling and in planta Complementation Studies Link Mutated Residues of the Medicago truncatula Nitrate Transporter NPF1.7 to Functionality in Root Nodules
inferred← citeshttps://doi.org/10.3389/fpls.2021.688187openalex-snapshot
The Lotus japonicus NPF3.1 Is a Nodule-Induced Gene That Plays a Positive Role in Nodule Functioning
inferred← citeshttps://doi.org/10.3389/fpls.2021.744445openalex-snapshot
Importance of the Rhizosphere Microbiota in Iron Biofortification of Plants
inferred← citeshttps://doi.org/10.3389/fpls.2022.997308openalex-snapshot
What do we know from the transcriptomic studies investigating the interactions between plants and plant growth-promoting bacteria?
inferred← citeshttps://doi.org/10.3389/fpls.2023.1114840openalex-snapshot
Control of the rhizobium–legume symbiosis by the plant nitrogen demand is tightly integrated at the whole plant level and requires inter-organ systemic signaling
inferred← citeshttps://doi.org/10.3389/fpls.2024.1290700openalex-snapshot
The underestimated role of plant root nitric oxide emission under low-oxygen stress
inferred← citeshttps://doi.org/10.3389/fsufs.2020.618230openalex-snapshot
PGPR Mediated Alterations in Root Traits: Way Toward Sustainable Crop Production
inferred← citeshttps://doi.org/10.3390/agriculture13112092openalex-snapshot
Enhancing Rhizobium–Legume Symbiosis and Reducing Nitrogen Fertilizer Use Are Potential Options for Mitigating Climate Change
inferred← citeshttps://doi.org/10.3390/antiox10020332openalex-snapshot
The Oxidative Paradox in Low Oxygen Stress in Plants
inferred← citeshttps://doi.org/10.3390/antiox8120641openalex-snapshot
Assessment of Subcellular ROS and NO Metabolism in Higher Plants: Multifunctional Signaling Molecules
inferred← citeshttps://doi.org/10.3390/bacteria5030041openalex-snapshot
Stress-Responsive Regulatory Networks in Legume–Rhizobium Symbiosis: Implications for Climate-Smart Agriculture
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