On the public citation graph
Metabolic changes of rhizobia in legume nodules
0 signed · 352 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-94-009-5175-4openalex-snapshot
Nitrogen fixation research progress
inferredcites →https://doi.org/10.1007/978-94-009-5175-4_26openalex-snapshot
A Model of Nutrient Exchange in the Rhizobium-Legume Symbiosis
inferredcites →https://doi.org/10.1007/bf00010013openalex-snapshot
The possible role of homoserine in the development of Rhizobium leguminosarum in the rhizosphere of pea seedlings
inferredcites →https://doi.org/10.1007/pl00000778openalex-snapshot
Ammonia and amino acid transport across symbiotic membranes in nitrogen-fixing legume nodules
inferredcites →https://doi.org/10.1007/s11120-004-1768-1openalex-snapshot
Nitrogen-fixing symbiosis between photosynthetic bacteria and legumes
inferredcites →https://doi.org/10.1016/0038-0717(95)98627-zopenalex-snapshot
Rhizopines—Their role in symbiosis and competition
inferredcites →https://doi.org/10.1016/0038-0717(95)98628-2openalex-snapshot
The distribution of inositol rhizopine genes in Rhizobium populations
inferredcites →https://doi.org/10.1016/s0038-0717(97)00180-6openalex-snapshot
Mimosine, a toxin produced by the tree-legume leucaena provides a nodulation competition advantage to mimosine-degrading rhizobium strains
inferredcites →https://doi.org/10.1016/s0176-1617(11)80385-8openalex-snapshot
Exchange of Metabolites Across the Peribacteroid Membrane in Pea Root Nodules
inferredcites →https://doi.org/10.1016/s0378-1097(03)00620-7openalex-snapshot
Aerobic and anaerobic nitrate and nitrite reduction in free-living cells of Bradyrhizobium sp. ( Lupinus )
inferredcites →https://doi.org/10.1016/s1369-5274(99)00035-1openalex-snapshot
Bacteroid formation in the Rhizobium–legume symbiosis
inferredcites →https://doi.org/10.1023/a:1026290508166openalex-snapshot
The role of root exudates and allelochemicals in the rhizosphere
inferredcites →https://doi.org/10.1038/nature01527openalex-snapshot
Amino-acid cycling drives nitrogen fixation in the legume–Rhizobium symbiosis
inferredcites →https://doi.org/10.1038/nature02039openalex-snapshot
Plant recognition of symbiotic bacteria requires two LysM receptor-like kinases
inferredcites →https://doi.org/10.1038/nrmicro954openalex-snapshot
Genetic regulation of biological nitrogen fixation
inferredcites →https://doi.org/10.1046/j.1365-294x.1999.00640.xopenalex-snapshot
Contribution of calystegine catabolic plasmid to competitive colonization of the rhizosphere of calystegine‐producing plants by Sinorhizobium meliloti Rm41
inferredcites →https://doi.org/10.1046/j.1365-2958.1996.00078.xopenalex-snapshot
The general l ‐amino acid permease of Rhizobium leguminosarum is an ABC uptake system that also influences efflux of solutes
inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01884.xopenalex-snapshot
Identification of alanine dehydrogenase and its role in mixed secretion of ammonium and alanine by pea bacteroids
inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02497.xopenalex-snapshot
Solute‐binding protein‐dependent ABC transporters are responsible for solute efflux in addition to solute uptake
inferredcites →https://doi.org/10.1073/pnas.0400595101openalex-snapshot
A Ca 2+ /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning
inferredcites →https://doi.org/10.1073/pnas.0400975101openalex-snapshot
Computational inference of scenarios for α-proteobacterial genome evolution
inferredcites →https://doi.org/10.1073/pnas.0407269101openalex-snapshot
A dual-genome Symbiosis Chip for coordinate study of signal exchange and development in a prokaryote–host interaction
inferredcites →https://doi.org/10.1073/pnas.95.20.12038openalex-snapshot
Alanine, not ammonia, is excreted from N 2 -fixing soybean nodule bacteroids
inferredcites →https://doi.org/10.1080/07352680490480734openalex-snapshot
Plant Cell Wall Remodelling in the Rhizobium–Legume Symbiosis
inferredcites →https://doi.org/10.1093/dnares/7.6.331openalex-snapshot
Complete Genome Structure of the Nitrogen-fixing Symbiotic Bacterium Mesorhizobium loti
inferredcites →https://doi.org/10.1093/dnares/9.6.189openalex-snapshot
Complete Genomic Sequence of Nitrogen-fixing Symbiotic Bacterium Bradyrhizobium japonicum USDA110
inferredcites →https://doi.org/10.1094/mpmi-18-0067openalex-snapshot
Role of Polyhydroxybutyrate and Glycogen as Carbon Storage Compounds in Pea and Bean Bacteroids
inferredcites →https://doi.org/10.1094/mpmi-4-571openalex-snapshot
Betaine Use by Rhizosphere Bacteria: Genes Essential for Trigonelline, Stachydrine, and Carnitine Catabolism inRhizobium melilotiAre Located on pSym in the Symbiotic Region
inferredcites →https://doi.org/10.1094/mpmi.1998.11.12.1175openalex-snapshot
Plasmid-Encoded Catabolic Genes in Rhizobium leguminosarum bv. trifolii: Evidence for a Plant-Inducible Rhamnose Locus Involved in Competition for Nodulation
inferredcites →https://doi.org/10.1094/mpmi.2000.13.7.733openalex-snapshot
Nodule Invasion and Symbiosome Differentiation During Rhizobium etli-Phaseolus vulgaris Symbiosis
inferredcites →https://doi.org/10.1094/mpmi.2001.14.6.775openalex-snapshot
Root Mucilage from Pea and Its Utilization by Rhizosphere Bacteria as a Sole Carbon Source
inferredcites →https://doi.org/10.1094/mpmi.2001.14.8.1016openalex-snapshot
Investigation of myo-Inositol Catabolism in Rhizobium leguminosarum bv. viciae and Its Effect on Nodulation Competitiveness
inferredcites →https://doi.org/10.1094/mpmi.2003.16.6.508openalex-snapshot
A Global Analysis of Protein Expression Profiles in Sinorhizobium meliloti: Discovery of New Genes for Nodule Occupancy and Stress Adaptation
inferredcites →https://doi.org/10.1094/mpmi.2004.17.3.292openalex-snapshot
Global Changes in Gene Expression in Sinorhizobium meliloti 1021 under Microoxic and Symbiotic Conditions
inferredcites →https://doi.org/10.1098/rspb.1990.0001openalex-snapshot
Bacteroids from soybean root nodules: respiration and N2-fixation in flow-chamber reactions with oxyleghaemoglobin
inferredcites →https://doi.org/10.1099/00221287-140-10-2787openalex-snapshot
myo-Inositol catabolism and catabolite regulation in Rhizobium leguminosarum bv. viciae
inferredcites →https://doi.org/10.1099/00221287-148-6-1959openalex-snapshot
Reassessment of major products of N2 fixation by bacteroids from soybean root nodules
inferredcites →https://doi.org/10.1099/mic.0.27323-0openalex-snapshot
The C-terminal receiver domain of the Rhizobium leguminosarum bv. viciae FixL protein is required for free-living microaerobic induction of the fnrN promoter
inferredcites →https://doi.org/10.1104/pp.102.019661openalex-snapshot
Root Exudation and Rhizosphere Biology
inferredcites →https://doi.org/10.1104/pp.114.4.1359openalex-snapshot
The Formation of Nitrogen-Fixing Bacteroids Is Delayed but Not Abolished in Soybean Infected by an α--Ketoglutarate Dehydrogenase-Deficient Mutant of Bradyrhizobium japonicum
inferredcites →https://doi.org/10.1104/pp.95.3.740openalex-snapshot
Glutamate Oxaloacetate Transaminase in Pea Root Nodules
inferredcites →https://doi.org/10.1111/j.1365-2958.1994.tb00298.xopenalex-snapshot
Genetic characterization of a Rhizobium meliloti lactose utilization locus
inferredcites →https://doi.org/10.1126/science.1060966openalex-snapshot
The Composite Genome of the Legume Symbiont Sinorhizobium meliloti
inferredcites →https://doi.org/10.1126/science.1090074openalex-snapshot
LysM Domain Receptor Kinases Regulating Rhizobial Nod Factor-Induced Infection
inferredcites →https://doi.org/10.1126/science.3738520openalex-snapshot
A Plant Flavone, Luteolin, Induces Expression of Rhizobium meliloti Nodulation Genes
inferredcites →https://doi.org/10.1128/aem.62.11.3991-3996.1996openalex-snapshot
An Experimental Test of the Rhizopine Concept in Rhizobium meliloti
inferredcites →https://doi.org/10.1128/aem.64.10.3954-3960.1998openalex-snapshot
A New Genetic Locus in Sinorhizobium meliloti Is Involved in Stachydrine Utilization
inferredcites →https://doi.org/10.1128/aem.64.12.4944-4949.1998openalex-snapshot
Detection and Isolation of Novel Rhizopine-Catabolizing Bacteria from the Environment
inferredcites →https://doi.org/10.1128/jb.173.11.3478-3487.1991openalex-snapshot
Influence of oxygen on DNA binding, positive control, and stability of the Bradyrhizobium japonicum NifA regulatory protein
inferredcites →https://doi.org/10.1128/jb.173.9.2879-2887.1991openalex-snapshot
Aspartate aminotransferase activity is required for aspartate catabolism and symbiotic nitrogen fixation in Rhizobium meliloti
inferredcites →https://doi.org/10.1128/jb.178.21.6166-6172.1996openalex-snapshot
The Bradyrhizobium japonicum aconitase gene (acnA) is important for free-living growth but not for an effective root nodule symbiosis
inferredcites →https://doi.org/10.1128/jb.180.21.5739-5748.1998openalex-snapshot
α-Galactoside Uptake in Rhizobium meliloti : Isolation and Characterization of agpA , a Gene Encoding a Periplasmic Binding Protein Required for Melibiose and Raffinose Utilization
inferredcites →https://doi.org/10.1128/jb.182.10.2838-2844.2000openalex-snapshot
Catabolism of α-Ketoglutarate by a sucA Mutant of Bradyrhizobium japonicum : Evidence for an Alternative Tricarboxylic Acid Cycle
inferredcites →https://doi.org/10.1128/jb.183.24.6999-7006.2001openalex-snapshot
Regulation of Gene Expression in Response to Oxygen in Rhizobium etli : Role of FnrN in fixNOQP Expression and in Symbiotic Nitrogen Fixation
inferredcites →https://doi.org/10.1128/jb.183.8.2595-2604.2001openalex-snapshot
A Functional myo -Inositol Dehydrogenase Gene Is Required for Efficient Nitrogen Fixation and Competitiveness of Sinorhizobium fredii USDA191 To Nodulate Soybean ( Glycine max [L.] Merr.)
inferredcites →https://doi.org/10.1128/jb.184.15.4071-4080.2002openalex-snapshot
Rhizobium leguminosarumHas a Second General Amino Acid Permease with Unusually Broad Substrate Specificity and High Similarity to Branched-Chain Amino Acid Transporters (Bra/LIV) of the ABC Family
inferredcites →https://doi.org/10.1128/jb.184.24.7042-7046.2002openalex-snapshot
Analysis of Infection Thread Development Using Gfp- and DsRed-Expressing Sinorhizobium meliloti
inferredcites →https://doi.org/10.1128/jb.186.8.2439-2448.2004openalex-snapshot
Expression Islands Clustered on the Symbiosis Island of the Mesorhizobium loti Genome
inferredcites →https://doi.org/10.1128/jb.187.15.5493-5495.2005openalex-snapshot
De Novo Alanine Synthesis by Bacteroids ofMesorhizobium lotiIs Not Required for Nitrogen Transfer in the Determinate Nodules ofLotus corniculatus
inferredcites →https://doi.org/10.1128/jb.187.5.1581-1590.2005openalex-snapshot
Experimental Identification and Quantification of Glucose Metabolism in Seven Bacterial Species
inferredcites →https://doi.org/10.1128/mmbr.66.2.203-222.2002openalex-snapshot
Key Role of Bacterial NH 4 + Metabolism in Rhizobium-Plant Symbiosis
inferredcites →https://doi.org/10.1128/mmbr.68.2.280-300.2004openalex-snapshot
Infection and Invasion of Roots by Symbiotic, Nitrogen-Fixing Rhizobia during Nodulation of Temperate Legumes
inferredcites →https://doi.org/10.1186/gb-2003-4-2-r15openalex-snapshot
Transcriptome analysis of Sinorhizobium melilotiduring symbiosis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4869493openalex-extracted
Rhizobium-Linked Nutritional and Phytochemical Changes Under Multitrophic Functional Contexts in Sustainable Food Systems
inferred← citeshttps://doi.org/10.1002/9780470015902.a0001388.pub2openalex-snapshot
Amino Acid Degradation
inferred← citeshttps://doi.org/10.1002/9780470015902.a0003720.pub2openalex-snapshot
Root Nodules (Legume–RhizobiumSymbiosis)
inferred← citeshttps://doi.org/10.1002/9780470015902.a0021157openalex-snapshot
Rhizobium and Other N ‐fixing Symbioses
inferred← citeshttps://doi.org/10.1002/9780470959404.ch16openalex-snapshot
Plant Hormones and Initiation of Legume Nodulation and Arbuscular Mycorrhization
inferred← citeshttps://doi.org/10.1002/9780470959404.ch8openalex-snapshot
The Path of Rhizobia: From a Free‐living Soil Bacterium to Root Nodulation
inferred← citeshttps://doi.org/10.1002/9781118015841.ch7openalex-snapshot
Interactions Between Microorganisms and Plants
inferred← citeshttps://doi.org/10.1002/9781119053095.ch73openalex-snapshot
Contribution of the RNA Chaperone Hfq to Environmental Fitness and Symbiosis in Sinorhizobium meliloti
inferred← citeshttps://doi.org/10.1002/9781119409144.ch83openalex-snapshot
Complex dynamics and synchronization of N ‐feedback and C alteration in the nodules of Medicago truncatula under abundant N or sub‐optimal P supply
inferred← citeshttps://doi.org/10.1002/9781119991311.ch3openalex-snapshot
Symbiotic Nitrogen Fixation
inferred← citeshttps://doi.org/10.1002/9781394217786.ch7openalex-snapshot
GABA and Nodulation in Plants
inferred← citeshttps://doi.org/10.1002/cssc.200800125openalex-snapshot
Phytoremediation of Organic Contaminants in Soil and Groundwater
inferred← citeshttps://doi.org/10.1002/mbo3.1006openalex-snapshot
A novel way to synthesize pantothenate in bacteria involves β‐alanine synthase present in uracil degradation pathway
inferred← citeshttps://doi.org/10.1002/mbo3.565openalex-snapshot
Transcriptome analysis and anaerobic C 4 ‐dicarboxylate transport in Actinobacillus succinogenes
inferred← citeshttps://doi.org/10.1002/pmic.200900710openalex-snapshot
An integrated proteomics and transcriptomics reference data set provides new insights into the Bradyrhizobium japonicum bacteroid metabolism in soybean root nodules
inferred← citeshttps://doi.org/10.1007/124_2016_11openalex-snapshot
Physiology and Spatio-temporal Relations of Nutrient Acquisition by Roots and Root Symbionts
inferred← citeshttps://doi.org/10.1007/7171_2008_122openalex-snapshot
Physiology of Actinorhizal Nodules
inferred← citeshttps://doi.org/10.1007/978-1-4939-1357-2_4openalex-snapshot
MALDI-MS-Assisted Molecular Imaging of Metabolites in Legume Plants
inferred← citeshttps://doi.org/10.1007/978-3-031-24181-9_5openalex-snapshot
Diversity and Evolution of Nitrogen Fixing Bacteria
inferred← citeshttps://doi.org/10.1007/978-3-031-68102-8_5openalex-snapshot
Assessment of the Impact of Climate Change on Rice Productivity: Modeling and Simulation Studies
inferred← citeshttps://doi.org/10.1007/978-3-211-99753-6_2openalex-snapshot
Enhancing Rhizobium–Legume Symbiosis Using Signaling Factors
inferred← citeshttps://doi.org/10.1007/978-3-211-99753-6_4openalex-snapshot
Recent Advances in Rhizobium–Legume Interactions: A Proteomic Approach
inferred← citeshttps://doi.org/10.1007/978-3-211-99753-6_8openalex-snapshot
Engineering Nodulation Competitiveness of Rhizobial Bioinoculants in Soils
inferred← citeshttps://doi.org/10.1007/978-3-319-06212-9_4openalex-snapshot
How Does High Temperature Affect Legume Nodule Symbiotic Activity?
inferred← citeshttps://doi.org/10.1007/978-3-319-06511-3_9openalex-snapshot
Defence, Symbiosis and ABCG Transporters
inferred← citeshttps://doi.org/10.1007/978-3-319-55729-8_5openalex-snapshot
Oxygen and the Regulation of N2 Fixation in Legume Nodules Under P Scarcity
inferred← citeshttps://doi.org/10.1007/978-3-319-59174-2_3openalex-snapshot
Flavonoids and Nod Factors: Importance in Legume-Microbe Interactions and Legume Improvement
inferred← citeshttps://doi.org/10.1007/978-3-319-75910-4_4openalex-snapshot
Morphological and Symbiotic Root Modifications for Mineral Acquisition from Nutrient-Poor Soils
inferred← citeshttps://doi.org/10.1007/978-3-540-68638-5_22openalex-snapshot
Biosynthese von Aminosäuren, Nucleotiden und verwandten Molekülen
inferred← citeshttps://doi.org/10.1007/978-3-540-75575-3_7openalex-snapshot
Evolutionary Genomics of the Nitrogen-Fixing Symbiotic Bacteria
inferred← citeshttps://doi.org/10.1007/978-3-540-85546-0_3openalex-snapshot
Genomics of Root–Microbe Interactions
inferred← citeshttps://doi.org/10.1007/978-3-642-23524-5_14openalex-snapshot
Molecular Signals and Receptors: Communication Between Nitrogen-Fixing Bacteria and Their Plant Hosts
inferred← citeshttps://doi.org/10.1007/978-3-642-39317-4_2openalex-snapshot
A Roadmap Towards a Systems Biology Description of Bacterial Nitrogen Fixation
inferred← citeshttps://doi.org/10.1007/978-81-322-2068-8_12openalex-snapshot
Legume-Rhizobia Symbiosis Under Stress
inferred← citeshttps://doi.org/10.1007/978-90-481-2666-8_32openalex-snapshot
Symbiotic Nitrogen Fixation in Legume Nodules: Process and Signaling: A Review
inferred← citeshttps://doi.org/10.1007/978-981-10-5511-9_6openalex-snapshot
Gaining Insight into Plant Responses to Beneficial and Pathogenic Microorganisms Using Metabolomic and Transcriptomic Approaches
inferred← citeshttps://doi.org/10.1007/978-981-13-0253-4_1openalex-snapshot
Legumes and Sustainable Use of Soils
inferred← citeshttps://doi.org/10.1007/978-981-16-2922-8_7openalex-snapshot
Role of Nitrogen-Fixing Microorganisms for Plant and Soil Health
inferred← citeshttps://doi.org/10.1007/bf03179989openalex-snapshot
Nitrogen and carbon costs of soybean and lupin root systems during phosphate starvation
inferred← citeshttps://doi.org/10.1007/s00203-013-0874-xopenalex-snapshot
Phenotype profiling of Rhizobium leguminosarum bv. trifolii clover nodule isolates reveal their both versatile and specialized metabolic capabilities
inferred← citeshttps://doi.org/10.1007/s00374-014-0969-9openalex-snapshot
Proteins involved in nodulation competitiveness of two Bradyrhizobium diazoefficiens strains induced by soybean root exudates
inferred← citeshttps://doi.org/10.1007/s00425-010-1148-3openalex-snapshot
Metabolic and structural rearrangement during dark-induced autophagy in soybean (Glycine max L.) nodules: an electron microscopy and 31P and 13C nuclear magnetic resonance study
inferred← citeshttps://doi.org/10.1007/s00438-007-0246-9openalex-snapshot
Dissection of the Bradyrhizobium japonicum NifA+σ54 regulon, and identification of a ferredoxin gene (fdxN) for symbiotic nitrogen fixation
inferred← citeshttps://doi.org/10.1007/s11104-008-9833-8openalex-snapshot
Nitrogen-fixing bacteria associated with leguminous and non-leguminous plants
inferred← citeshttps://doi.org/10.1007/s11104-010-0471-6openalex-snapshot
3-Phosphoglycerate dehydrogenase in Mesorhizobioum loti is essential for maintaining symbiotic nitrogen fixation of Lotus japonicus root nodules
inferred← citeshttps://doi.org/10.1007/s12275-013-2335-2openalex-snapshot
Interrelationship of Bradyrhizobium sp. and plant growth-promoting bacteria in cowpea: Survival and symbiotic performance
inferred← citeshttps://doi.org/10.1007/s42398-023-00286-5openalex-snapshot
Nodulation in the absence of nod genes induction: alternative mechanisms involved in the symbiotic interaction between Cupriavidus sp. UYMMa02A and Mimosa pudica
inferred← citeshttps://doi.org/10.1007/s42994-024-00193-1openalex-snapshot
Enacting partner specificity in legume–rhizobia symbioses
inferred← citeshttps://doi.org/10.1016/b978-0-12-384986-1.00011-9openalex-snapshot
Nitrogen fixation enables plants to use the nitrogen of the air for growth
inferred← citeshttps://doi.org/10.1016/b978-0-12-815355-0.00003-5openalex-snapshot
Nod factor signaling in legume-Rhizobium symbiosis: Specificity and molecular genetics of nod factor signaling
inferred← citeshttps://doi.org/10.1016/b978-0-12-823831-8.00008-6openalex-snapshot
Adaptive phytoremediation practices for sustaining ecosystem services
inferred← citeshttps://doi.org/10.1016/b978-0-443-19150-3.00013-8openalex-snapshot
Beneficial soil microorganisms and their role in sustainable agriculture
inferred← citeshttps://doi.org/10.1016/b978-012373944-5.00046-8openalex-snapshot
Development, Prokaryotic: Variety and Versatility
inferred← citeshttps://doi.org/10.1016/bs.abr.2022.02.019openalex-snapshot
Insights into soybean with high photosynthetic efficiency
inferred← citeshttps://doi.org/10.1016/bs.agron.2014.09.001openalex-snapshot
Advances in Host Plant and Rhizobium Genomics to Enhance Symbiotic Nitrogen Fixation in Grain Legumes
inferred← citeshttps://doi.org/10.1016/j.agwat.2018.08.021openalex-snapshot
Do metabolic changes underpin physiological responses to water limitation in alfalfa (Medicago sativa) plants during a regrowth period?
inferred← citeshttps://doi.org/10.1016/j.apsoil.2020.103703openalex-snapshot
Rhizobium leguminosarum strain combination effects on nodulation and biological nitrogen fixation with Vicia villosa
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117972openalex-snapshot
Proteomic and metabolomic profiling depicts the functional landscape of the Medicago truncatula symbiosome
inferred← citeshttps://doi.org/10.1016/j.comptc.2018.08.015openalex-snapshot
A density functional theory investigation of the fragmentation mechanism of deprotonated asparagine
inferred← citeshttps://doi.org/10.1016/j.cub.2012.02.032openalex-snapshot
Cell Size Control in Bacteria
inferred← citeshttps://doi.org/10.1016/j.eja.2025.127880openalex-snapshot
Mixed plantation of milk vetch (Astragalus sinicus L.) and ryegrass (Lolium perenne L.) promotes biological nitrogen fixation by modulating diazotrophic community
inferred← citeshttps://doi.org/10.1016/j.ejsobi.2011.12.003openalex-snapshot
Curing of a non-symbiotic plasmid of the Rhizobium tropici strain CIAT 899 affected nodule occupancy and competitiveness of the bacteria in symbiosis with common beans
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2007.10.027openalex-snapshot
VuNIP1 (NOD26-like) and VuHSP17.7 gene expression are regulated in response to heat stress in cowpea nodule
inferred← citeshttps://doi.org/10.1016/j.envres.2024.118923openalex-snapshot
Organic amendments increased Chinese milk vetch symbiotic nitrogen fixation by enriching Mesorhizobium in rhizosphere.
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2008.11.006openalex-snapshot
A portal for rhizobial genomes: RhizoGATE integrates a Sinorhizobium meliloti genome annotation update with postgenome data
inferred← citeshttps://doi.org/10.1016/j.jgg.2024.06.013openalex-snapshot
Nitrogen inhibition of nitrogenase activity involves the modulation of cytosolic invertase in soybean nodule
inferred← citeshttps://doi.org/10.1016/j.jprot.2015.04.034openalex-snapshot
Quantitative time-course proteome analysis of Mesorhizobium loti during nodule maturation
inferred← citeshttps://doi.org/10.1016/j.pbi.2009.05.010openalex-snapshot
The unbearable naivety of legumes in symbiosis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.04.015openalex-snapshot
Metabolic changes of iron uptake in N2-fixing common bean nodules during iron deficiency
inferred← citeshttps://doi.org/10.1016/j.plaphy.2016.08.002openalex-snapshot
Rhizobial strains exert a major effect on the amino acid composition of alfalfa nodules under NaCl stress
inferred← citeshttps://doi.org/10.1016/j.ram.2015.06.006openalex-snapshot
Interrogantes en la tecnología de la inoculación de semillas de soja con Bradyrhizobium spp.
inferred← citeshttps://doi.org/10.1016/j.resmic.2010.05.004openalex-snapshot
Identification of a TRAP transporter for malonate transport and its expression regulated by GtrA from Sinorhizobium meliloti
inferred← citeshttps://doi.org/10.1016/j.sajb.2016.10.025openalex-snapshot
Rhizobial diversity and function in rooibos (Aspalathus linearis) and honeybush (Cyclopia spp.) plants: A review
inferred← citeshttps://doi.org/10.1016/j.sajb.2025.06.049openalex-snapshot
The morphological, symbiotic and molecular physiological below-ground adaptations for nutrient scarce environments: A South African perspective
inferred← citeshttps://doi.org/10.1016/j.sajb.2026.02.033openalex-snapshot
Transcriptomic landscapes across plant biology: Insights from in vitro cultivation to orchid flowering and legume-rhizobia symbiosis
inferred← citeshttps://doi.org/10.1016/j.soilbio.2013.09.001openalex-snapshot
Metabolism of nitrogen and carbon: Optimization of biological nitrogen fixation and cowpea development
inferred← citeshttps://doi.org/10.1016/j.tim.2009.07.004openalex-snapshot
Establishing nitrogen-fixing symbiosis with legumes: how many rhizobium recipes?
inferred← citeshttps://doi.org/10.1016/j.tim.2024.03.010openalex-snapshot
Bradyrhizobium japonicum (diazoefficiens)
inferred← citeshttps://doi.org/10.1016/j.vas.2025.100524openalex-snapshot
Identification and evaluation of agroecosystem compartments as forage sources for free-ranging goats in smallholder farming systems of western Democratic Republic of Congo
inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101636openalex-snapshot
Symbiosome membrane-localized cationic amino acid transporters support symbiotic nitrogen fixation in Medicago truncatula
inferred← citeshttps://doi.org/10.1016/j.ymben.2026.102553openalex-snapshot
Kinetic model of a determinate legume root nodule reveals plant metabolic characteristics for more efficient nitrogen fixation symbiosis
inferred← citeshttps://doi.org/10.1017/cbo9780511790461.007openalex-snapshot
Biosynthesis and microbial growth
inferred← citeshttps://doi.org/10.1021/acs.jproteome.8b00209openalex-snapshot
Bradyrhizobium diazoefficiens USDA 110– Glycine max Interactome Provides Candidate Proteins Associated with Symbiosis
inferred← citeshttps://doi.org/10.1038/nrmicro1705openalex-snapshot
How rhizobial symbionts invade plants: the Sinorhizobium–Medicago model
inferred← citeshttps://doi.org/10.1038/s41396-019-0517-6openalex-snapshot
Comparative proteomics of related symbiotic mussel species reveals high variability of host–symbiont interactions
inferred← citeshttps://doi.org/10.1038/s41598-017-11372-0openalex-snapshot
Transcriptional analysis of genes involved in competitive nodulation in Bradyrhizobium diazoefficiens at the presence of soybean root exudates
inferred← citeshttps://doi.org/10.1038/s41598-018-30884-xopenalex-snapshot
The intertwined metabolism during symbiotic nitrogen fixation elucidated by metabolic modelling
inferred← citeshttps://doi.org/10.1038/s41598-020-57861-7openalex-snapshot
Magnetic Resonance Microscopy at Cellular Resolution and Localised Spectroscopy of Medicago truncatula at 22.3 Tesla
inferred← citeshttps://doi.org/10.1039/c6mb00553eopenalex-snapshot
Construction and simulation of the Bradyrhizobium diazoefficiens USDA110 metabolic network: a comparison between free-living and symbiotic states
inferred← citeshttps://doi.org/10.1051/agro:2006030openalex-snapshot
Symbiotic nitrogen fixation in legume nodules: process and signaling. A review
inferred← citeshttps://doi.org/10.1055/s-0035-1545880openalex-snapshot
The ABC of Phytohormone Translocation
inferred← citeshttps://doi.org/10.1071/fp11066openalex-snapshot
Progress on research on actinorhizal plants
inferred← citeshttps://doi.org/10.1071/fp11095openalex-snapshot
New perspectives on nodule nitrogen assimilation in actinorhizal symbioses
inferred← citeshttps://doi.org/10.1071/fp13189openalex-snapshot
On the relationship between C and N fixation and amino acid synthesis in nodulated alfalfa (Medicago sativa)
inferred← citeshttps://doi.org/10.1071/fp16377openalex-snapshot
Cell differentiation in nitrogen-fixing nodules hosting symbiosomes
inferred← citeshttps://doi.org/10.1073/pnas.0808048105openalex-snapshot
A mutant GlnD nitrogen sensor protein leads to a nitrogen-fixing but ineffective Sinorhizobium meliloti symbiosis with alfalfa
inferred← citeshttps://doi.org/10.1073/pnas.0903653106openalex-snapshot
Legumes regulate Rhizobium bacteroid development and persistence by the supply of branched-chain amino acids
inferred← citeshttps://doi.org/10.1073/pnas.1409642111openalex-snapshot
A nonpyrrolysine member of the widely distributed trimethylamine methyltransferase family is a glycine betaine methyltransferase
inferred← citeshttps://doi.org/10.1080/09064710802609527openalex-snapshot
Influence of root-zone temperature on growth and nitrogen fixation in three Iranian grasspea landraces
inferred← citeshttps://doi.org/10.1093/femsec/fiz067openalex-snapshot
Phylogenetic evidence of allopatric speciation of bradyrhizobia nodulating cowpea (Vigna unguiculata L. walp) in South African and Mozambican soils
inferred← citeshttps://doi.org/10.1093/hr/uhae321openalex-snapshot
Nutrient-dependent regulation of symbiotic nitrogen fixation in legumes
inferred← citeshttps://doi.org/10.1093/jxb/erab198openalex-snapshot
Split-root assays for studying legume–rhizobia symbioses, rhizodeposition, and belowground nitrogen transfer in legumes
inferred← citeshttps://doi.org/10.1093/jxb/eru260openalex-snapshot
Reassimilation of ammonium in Lotus japonicus
inferred← citeshttps://doi.org/10.1093/jxb/erv357openalex-snapshot
Small-peptide signals that control root nodule number, development, and symbiosis
inferred← citeshttps://doi.org/10.1094/mpmi-05-11-0140openalex-snapshot
A Comparative Transcriptome Analysis of Rhizobium etli Bacteroids: Specific Gene Expression During Symbiotic Nongrowth
inferred← citeshttps://doi.org/10.1094/mpmi-06-11-0152openalex-snapshot
Bacteroid Development in Legume Nodules: Evolution of Mutual Benefit or of Sacrificial Victims?
inferred← citeshttps://doi.org/10.1094/mpmi-08-25-0108-fiopenalex-snapshot
Not All Allies Are Welcome: Partner Discrimination in Legume–Rhizobium Symbiosis
inferred← citeshttps://doi.org/10.1094/mpmi-10-19-0289-ropenalex-snapshot
Feedback Regulation of N Fixation in Frankia-Alnus Symbiosis Through Amino Acids Profiling in Field and Greenhouse Nodules
inferred← citeshttps://doi.org/10.1094/mpmi-12-16-0264-ropenalex-snapshot
The Bacteroid Periplasm in Soybean Nodules Is an Interkingdom Symbiotic Space
inferred← citeshttps://doi.org/10.1094/mpmi-20-11-1353openalex-snapshot
Genome-Wide Transcript Analysis of Bradyrhizobium japonicum Bacteroids in Soybean Root Nodules
inferred← citeshttps://doi.org/10.1094/mpmi-21-2-0219openalex-snapshot
Identification of Genes Relevant to Symbiosis and Competitiveness in Sinorhizobium meliloti Using Signature-Tagged Mutants
inferred← citeshttps://doi.org/10.1094/mpmi-22-8-1032openalex-snapshot
A Metabolic Signature of the Beneficial Interaction of the Endophyte Paenibacillus sp. Isolate and In Vitro–Grown Poplar Plants Revealed by Metabolomics
inferred← citeshttps://doi.org/10.1094/mpmi-23-4-0355openalex-snapshot
Role of the Sinorhizobium meliloti Global Regulator Hfq in Gene Regulation and Symbiosis
inferred← citeshttps://doi.org/10.1094/mpmi-23-6-0784openalex-snapshot
Rhizobial Adaptation to Hosts, a New Facet in the Legume Root-Nodule Symbiosis
inferred← citeshttps://doi.org/10.1094/pbiomes-03-19-0014-ropenalex-snapshot
A Biosensor-Based Assay ( GlnLux -Agar) Shows Defoliation Triggers Rapid Release of Glutamine from Nodules and Young Roots of Forage Legumes
inferred← citeshttps://doi.org/10.1094/pbiomes-07-18-0031-taopenalex-snapshot
Visualizing Glutamine Accumulation in Root Systems Involved in the Legume–Rhizobia Symbiosis by Placement on Agar Embedded with Companion Biosensor Cells
inferred← citeshttps://doi.org/10.1098/rsos.150708openalex-snapshot
Metabolic constraints for a novel symbiosis
inferred← citeshttps://doi.org/10.1098/rspb.2015.2563openalex-snapshot
Ecological genomics of mutualism decline in nitrogen-fixing bacteria
inferred← citeshttps://doi.org/10.1099/mic.0.001471openalex-snapshot
Aspartate aminotransferase of Rhizobium leguminosarum has extended substrate specificity and metabolizes aspartate to enable N2 fixation in pea nodules
inferred← citeshttps://doi.org/10.1099/mic.0.058370-0openalex-snapshot
Biosynthesis of branched-chain amino acids is essential for effective symbioses between betarhizobia and Mimosa pudica
inferred← citeshttps://doi.org/10.1101/067348openalex-snapshot
The intertwined metabolism of Medicago truncatula and its nitrogen fixing symbiont Sinorhizobium meliloti elucidated by genome-scale metabolic models
inferred← citeshttps://doi.org/10.1101/2024.09.24.614788openalex-snapshot
Sanctioning of bacterial cheaters by the host plant in nitrogen-fixing symbiosis between Medicago truncatula and Sinorhizobium meliloti
inferred← citeshttps://doi.org/10.1101/663849openalex-snapshot
De novo β-alanine synthesis in α-proteobacteria involves a β-alanine synthase from the uracil degradation pathway
inferred← citeshttps://doi.org/10.1104/pp.107.097741openalex-snapshot
Nutrient Sharing between Symbionts
inferred← citeshttps://doi.org/10.1104/pp.110.157800openalex-snapshot
Soybean Metabolites Regulated in Root Hairs in Response to the Symbiotic BacteriumBradyrhizobium japonicum
inferred← citeshttps://doi.org/10.1104/pp.112.197061openalex-snapshot
A Medicago truncatula Tobacco Retrotransposon Insertion Mutant Collection with Defects in Nodule Development and Symbiotic Nitrogen Fixation
inferred← citeshttps://doi.org/10.1105/tpc.15.00108openalex-snapshot
Nitrogen-Fixing Nodules Are an Important Source of Reduced Sulfur, Which Triggers Global Changes in Sulfur Metabolism in Lotus japonicus
inferred← citeshttps://doi.org/10.1111/1462-2920.13757openalex-snapshot
A conserved α‐proteobacterial small RNA contributes to osmoadaptation and symbiotic efficiency of rhizobia on legume roots
inferred← citeshttps://doi.org/10.1111/1462-2920.70178openalex-snapshot
EcoFoldDB : Protein Structure‐Guided Functional Profiling of Ecologically Relevant Microbial Traits at the Metagenome Scale
inferred← citeshttps://doi.org/10.1111/1574-6968.12124openalex-snapshot
An overview of the metabolic differences betweenBradyrhizobium japonicum110 bacteria and differentiated bacteroids from soybean (Glycine max) root nodules: anin vitro13C- and31P-nuclear magnetic resonance spectroscopy study
inferred← citeshttps://doi.org/10.1111/1758-2229.70183openalex-snapshot
Disinfection Efficiency Among Black Alder and Hybrid Alder Genotypes and Their Influence on Alder Seed Germination In Vitro
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2007.06036.xopenalex-snapshot
Multiple Ku orthologues mediate DNA non‐homologous end‐joining in the free‐living form and during chronic infection of Sinorhizobium meliloti
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2009.06769.xopenalex-snapshot
The PhyR‐σEcfG signalling cascade is involved in stress response and symbiotic efficiency in Bradyrhizobium japonicum
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2009.06794.xopenalex-snapshot
Sinorhizobium meliloti CpdR1 is critical for co‐ordinating cell cycle progression and the symbiotic chronic infection
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2012.08014.xopenalex-snapshot
The PTSNtr system globally regulates ATP‐dependent transporters in Rhizobium leguminosarum
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2012.08064.xopenalex-snapshot
The conserved polarity factor PodJ1 impacts multiple cell envelope‐associated functions in Sinorhizobium meliloti
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2010.02214.xopenalex-snapshot
Phloem‐derived γ‐aminobutyric acid (GABA) is involved in upregulating nodule N2 fixation efficiency in the model legume Medicago truncatula
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2007.01284.xopenalex-snapshot
The Rhizobium etli opt operon is required for symbiosis and stress resistance
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2012.04099.xopenalex-snapshot
Widespread fitness alignment in the legume–rhizobium symbiosis
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2011.01139.xopenalex-snapshot
Soil factors exhibit greater influence than bacterial inoculation on alfalfa growth and nitrogen fixation
inferred← citeshttps://doi.org/10.1111/j.1574-6968.2010.02034.xopenalex-snapshot
Histidine is a source of the antioxidant, α-ketoglutarate, in Pseudomonas fluorescens challenged by oxidative stress
inferred← citeshttps://doi.org/10.1111/j.1744-7348.2006.00104.xopenalex-snapshot
Asparagine in plants
inferred← citeshttps://doi.org/10.1111/nph.12227openalex-snapshot
Isotope discrimination provides new insight into biological nitrogen fixation
inferred← citeshttps://doi.org/10.1111/nph.12714openalex-snapshot
RbohB, a Phaseolus vulgaris NADPH oxidase gene, enhances symbiosome number, bacteroid size, and nitrogen fixation in nodules and impairs mycorrhizal colonization
inferred← citeshttps://doi.org/10.1111/pce.12116openalex-snapshot
Peribacteroid space acidification: a marker of mature bacteroid functioning in M edicago truncatula nodules
inferred← citeshttps://doi.org/10.1111/ppl.12222openalex-snapshot
Effect of shoot removal on remobilization of carbon and nitrogen during regrowth of nitrogen‐fixing alfalfa
inferred← citeshttps://doi.org/10.1111/tpj.14815openalex-snapshot
Metabolomic profiling of wild‐type and mutant soybean root nodules using laser‐ablation electrospray ionization mass spectrometry reveals altered metabolism
inferred← citeshttps://doi.org/10.1126/science.1184057openalex-snapshot
Plant Peptides Govern Terminal Differentiation of Bacteria in Symbiosis
inferred← citeshttps://doi.org/10.1128/aem.00667-10openalex-snapshot
Genetic and Metabolic Divergence within aRhizobium leguminosarumbv.trifoliiPopulation Recovered from Clover Nodules
inferred← citeshttps://doi.org/10.1128/aem.00823-15openalex-snapshot
A Putative Type III Secretion System Effector Encoded by the MA20_12780 Gene in Bradyrhizobium japonicum Is-34 Causes Incompatibility with Rj 4 Genotype Soybeans
inferred← citeshttps://doi.org/10.1128/aem.01304-25openalex-snapshot
XoxF and the Calvin-Benson cycle mediate lanthanide-dependent growth on methanol in Bradyrhizobium and Sinorhizobium
inferred← citeshttps://doi.org/10.1128/aem.01670-17openalex-snapshot
Concomitant Loss of the Glyoxalase System and Glycolysis Makes the Uncultured Pathogen “Candidatus Liberibacter asiaticus” an Energy Scavenger
inferred← citeshttps://doi.org/10.1128/aem.03314-13openalex-snapshot
A Link between Arabinose Utilization and Oxalotrophy in Bradyrhizobium japonicum
inferred← citeshttps://doi.org/10.1128/jb.00020-10openalex-snapshot
BacA Is Essential for Bacteroid Development in Nodules of Galegoid, but not Phaseoloid, Legumes
inferred← citeshttps://doi.org/10.1128/jb.00165-09openalex-snapshot
Transcriptomic Analysis of Rhizobium leguminosarum Biovar viciae in Symbiosis with Host Plants Pisum sativum and Vicia cracca
inferred← citeshttps://doi.org/10.1128/jb.00206-10openalex-snapshot
The Twin Arginine Transport System Appears To Be Essential for Viability in Sinorhizobium meliloti
inferred← citeshttps://doi.org/10.1128/jb.00252-09openalex-snapshot
An Alternative Succinate (2-Oxoglutarate) Transport System in Rhizobium tropici Is Induced in Nodules of Phaseolus vulgaris
inferred← citeshttps://doi.org/10.1128/jb.00294-10openalex-snapshot
Pyruvate Is Synthesized by Two Pathways in Pea Bacteroids with Different Efficiencies for Nitrogen Fixation
inferred← citeshttps://doi.org/10.1128/jb.00539-20openalex-snapshot
How Rhizobia Adapt to the Nodule Environment
inferred← citeshttps://doi.org/10.1128/jb.00751-12openalex-snapshot
Increased Production of the Exopolysaccharide Succinoglycan Enhances Sinorhizobium meliloti 1021 Symbiosis with the Host Plant Medicago truncatula
inferred← citeshttps://doi.org/10.1128/jb.00776-16openalex-snapshot
Regulation of Polyhydroxybutyrate Accumulation in Sinorhizobium meliloti by the Trans -Encoded Small RNA MmgR
inferred← citeshttps://doi.org/10.1128/jb.00926-08openalex-snapshot
Characterization of a γ-Aminobutyric Acid Transport System of Rhizobium leguminosarum bv. viciae 3841
inferred← citeshttps://doi.org/10.1128/jb.01190-07openalex-snapshot
Influence of the Poly-3-Hydroxybutyrate (PHB) Granule-Associated Proteins (PhaP1 and PhaP2) on PHB Accumulation and Symbiotic Nitrogen Fixation in Sinorhizobium meliloti Rm1021
inferred← citeshttps://doi.org/10.1128/jb.01429-09openalex-snapshot
Proteomic Alterations Explain Phenotypic Changes in Sinorhizobium meliloti Lacking the RNA Chaperone Hfq
inferred← citeshttps://doi.org/10.1128/jb.01456-08openalex-snapshot
Characterization of a Mesorhizobium loti α-Type Carbonic Anhydrase and Its Role in Symbiotic Nitrogen Fixation
inferred← citeshttps://doi.org/10.1128/jb.01521-07openalex-snapshot
A Highly Conserved Protein of Unknown Function Is Required by Sinorhizobium meliloti for Symbiosis and Environmental Stress Protection
inferred← citeshttps://doi.org/10.1128/jb.01657-09openalex-snapshot
GlnB/GlnK PII Proteins and Regulation of the Sinorhizobium meliloti Rm1021 Nitrogen Stress Response and Symbiotic Function
inferred← citeshttps://doi.org/10.1128/jb.01714-08openalex-snapshot
Pathway of γ-Aminobutyrate Metabolism in Rhizobium leguminosarum 3841 and Its Role in Symbiosis
inferred← citeshttps://doi.org/10.1128/jb.01834-06openalex-snapshot
The Symbiosis Regulator CbrA Modulates a Complex Regulatory Network Affecting the Flagellar Apparatus and Cell Envelope Proteins
inferred← citeshttps://doi.org/10.1128/mbio.01251-15openalex-snapshot
Specific Hopanoid Classes Differentially Affect Free-Living and Symbiotic States of Bradyrhizobium diazoefficiens
inferred← citeshttps://doi.org/10.1128/msystems.00438-20openalex-snapshot
Evolutionary Timeline and Genomic Plasticity Underlying the Lifestyle Diversity in Rhizobiales
inferred← citeshttps://doi.org/10.1128/msystems.01071-26openalex-snapshot
Shifts in vegetation impact estuary microbiomes
inferred← citeshttps://doi.org/10.1128/spectrum.02016-26openalex-snapshot
The preprotein translocase YajC mediates biofilm formation and symbiotic nitrogen-fixation in Mesorhizobium huakuii
inferred← citeshttps://doi.org/10.1134/s0003683813010109openalex-snapshot
Novel NADPH-dependent L-aspartate dehydrogenases from the mesophilic nitrogen-fixing bacteria Rhodopseudomonas palustris and Bradyrhizobium japonicum
inferred← citeshttps://doi.org/10.1134/s1022795409090014openalex-snapshot
Genetic resources of nodule bacteria
inferred← citeshttps://doi.org/10.1134/s1022795413030150openalex-snapshot
Factor analysis of interactions between alfalfa nodule bacteria (Sinorhizobium meliloti) genes that regulate symbiotic nitrogen fixation
inferred← citeshttps://doi.org/10.1139/cjm-2014-0306openalex-snapshot
Physiology, genetics, and biochemistry of carbon metabolism in the alphaproteobacteriumSinorhizobium meliloti
inferred← citeshttps://doi.org/10.1146/annurev.genet.42.110807.091427openalex-snapshot
Molecular Determinants of a Symbiotic Chronic Infection
inferred← citeshttps://doi.org/10.1155/2011/702947openalex-snapshot
Composite Actinorhizal Plants with Transgenic Roots for the Study of Symbiotic Associations with Frankia
inferred← citeshttps://doi.org/10.1186/1471-2164-15-420openalex-snapshot
Comparative genomics of Bradyrhizobium japonicum CPAC 15 and Bradyrhizobium diazoefficiens CPAC 7: elite model strains for understanding symbiotic performance with soybean
inferred← citeshttps://doi.org/10.1186/1471-2180-10-177openalex-snapshot
The role of iron uptake in pathogenicity and symbiosis in Photorhabdus luminescens TT01
inferred← citeshttps://doi.org/10.1186/1471-2180-10-71openalex-snapshot
The Sinorhizobium meliloti RNA chaperone Hfq influences central carbon metabolism and the symbiotic interaction with alfalfa
inferred← citeshttps://doi.org/10.1186/1471-2180-12-74openalex-snapshot
A comparative genomics screen identifies a Sinorhizobium meliloti 1021 sodM-like gene strongly expressed within host plant nodules
inferred← citeshttps://doi.org/10.1186/1471-2180-13-180openalex-snapshot
Disclosure of the differences of Mesorhizobium loti under the free-living and symbiotic conditions by comparative proteome analysis without bacteroid isolation
inferred← citeshttps://doi.org/10.1186/1752-0509-5-120openalex-snapshot
Systems biology of bacterial nitrogen fixation: High-throughput technology and its integrative description with constraint-based modeling
inferred← citeshttps://doi.org/10.1186/s12864-017-4200-xopenalex-snapshot
Genes for asparagine metabolism in Lotus japonicus: differential expression and interconnection with photorespiration
inferred← citeshttps://doi.org/10.1264/jsme2.me10213openalex-snapshot
Identification of Mesorhizobium loti Genes Relevant to Symbiosis by Using Signature-Tagged Mutants
inferred← citeshttps://doi.org/10.1264/jsme2.me19151openalex-snapshot
Mutants Disrupted in the Type III Secretion System of Bradyrhizobium elkanii BLY3-8 Overcame Nodulation Restriction by Rj3-genotype Soybean
inferred← citeshttps://doi.org/10.12794/metadc801877openalex-snapshot
Forward Genetic Characterization of Medicago truncatula Tnt1 Insertion Mutants Defective in Nodule Development and Symbiotic Nitrogen Fixation
inferred← citeshttps://doi.org/10.1371/journal.pbio.0060068openalex-snapshot
Functional Adaptation of a Plant Receptor- Kinase Paved the Way for the Evolution of Intracellular Root Symbioses with Bacteria
inferred← citeshttps://doi.org/10.1371/journal.pcbi.0030192openalex-snapshot
Metabolic Reconstruction and Modeling of Nitrogen Fixation in Rhizobium etli
showing the first 200 of 288 · page through all 288
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.