On the public citation graph
Phosphorylation systems in symbiotic nitrogen-fixing bacteria and their role in bacterial adaptation to various environmental stresses
0 signed · 145 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/9781119004813.ch24openalex-snapshot
The Two‐Component CheY System in the Chemotaxis ofSinorhizobium Meliloti
inferredcites →https://doi.org/10.1002/9781119053095.ch33openalex-snapshot
Motility and Chemotaxis in the Rhizobia
inferredcites →https://doi.org/10.1002/bies.20343openalex-snapshot
Signal transduction in bacterial chemotaxis
inferredcites →https://doi.org/10.1002/mbo3.567openalex-snapshot
Expression of the arsenite oxidation regulatory operon in Rhizobium sp. str. NT ‐26 is under the control of two promoters that respond to different environmental cues
inferredcites →https://doi.org/10.1007/7171_2007_099openalex-snapshot
The Diversity and Evolution of Rhizobia
inferredcites →https://doi.org/10.1007/s00442-010-1649-6openalex-snapshot
Microbial community shifts influence patterns in tropical forest nitrogen fixation
inferredcites →https://doi.org/10.1016/b978-0-12-398264-3.00005-xopenalex-snapshot
What Determines the Efficiency of N2-Fixing Rhizobium-Legume Symbioses?
inferredcites →https://doi.org/10.1016/b978-0-12-409548-9.00685-0openalex-snapshot
Biological Nitrogen Fixation
inferredcites →https://doi.org/10.1016/b978-044452857-5.50011-4openalex-snapshot
The Rhizobium-Legume Nitrogen-Fixing Symbiosis
inferredcites →https://doi.org/10.1016/j.bbagen.2011.01.006openalex-snapshot
Protein phosphorylation in bacterial signal transduction
inferredcites →https://doi.org/10.1016/j.cell.2009.10.006openalex-snapshot
Serine/Threonine Phosphatases: Mechanism through Structure
inferredcites →https://doi.org/10.1016/j.cub.2011.02.045openalex-snapshot
Two-Component Systems and Their Co-Option for Eukaryotic Signal Transduction
inferredcites →https://doi.org/10.1016/j.femsre.2004.04.002openalex-snapshot
Dicarboxylate transport by rhizobia
inferredcites →https://doi.org/10.1016/j.jmb.2016.08.003openalex-snapshot
Molecular Mechanisms of Two-Component Signal Transduction
inferredcites →https://doi.org/10.1016/j.mib.2010.01.005openalex-snapshot
Diversity of structure and function of response regulator output domains
inferredcites →https://doi.org/10.1016/j.molcel.2007.03.008openalex-snapshot
Activation of the Bacterial Sensor Kinase PhoQ by Acidic pH
inferredcites →https://doi.org/10.1016/j.tibs.2007.03.002openalex-snapshot
Bacterial response regulators: versatile regulatory strategies from common domains
inferredcites →https://doi.org/10.1016/j.tim.2010.02.003openalex-snapshot
Regulatory roles of the bacterial nitrogen-related phosphotransferase system
inferredcites →https://doi.org/10.1016/j.tim.2010.07.004openalex-snapshot
CheV: CheW-like coupling proteins at the core of the chemotaxis signaling network
inferredcites →https://doi.org/10.1016/j.tim.2015.03.003openalex-snapshot
Signaling and sensory adaptation in Escherichia coli chemoreceptors: 2015 update
inferredcites →https://doi.org/10.1016/s0076-6879(06)22003-2openalex-snapshot
Identification of Sensory and Signal‐Transducing Domains in Two‐Component Signaling Systems
inferredcites →https://doi.org/10.1016/s0300-9084(98)80055-2openalex-snapshot
Post-translational modification of proteins by reversible phosphorylation in prokaryotes
inferredcites →https://doi.org/10.1016/s1389-1723(01)80308-xopenalex-snapshot
Bacterial Phosphotransferase System (PTS) in Carbohydrate Uptake and Control of Carbon Metabolism
inferredcites →https://doi.org/10.1021/cr000225sopenalex-snapshot
Structural Basis for Control by Phosphorylation
inferredcites →https://doi.org/10.1021/cr0002543openalex-snapshot
Protein Phosphatases−A Phylogenetic Perspective
inferredcites →https://doi.org/10.1038/ijos.2012.6openalex-snapshot
Tyrosine phosphorylation and bacterial virulence
inferredcites →https://doi.org/10.1038/nrmicro.2017.171openalex-snapshot
Rhizobia: from saprophytes to endosymbionts
inferredcites →https://doi.org/10.1038/s41467-018-03032-2openalex-snapshot
Molecular-channel driven actuator with considerations for multiple configurations and color switching
inferredcites →https://doi.org/10.1038/s41467-018-07343-2openalex-snapshot
The structure and function of the global citrus rhizosphere microbiome
inferredcites →https://doi.org/10.1038/srep43431openalex-snapshot
The general PTS component HPr determines the preference for glucose over mannitol
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.03240.xopenalex-snapshot
Interaction of EnvZ, a sensory histidine kinase, with phosphorylated OmpR, the cognate response regulator
inferredcites →https://doi.org/10.1073/pnas.52.4.1067openalex-snapshot
PHOSPHATE BOUND TO HISTIDINE IN A PROTEIN AS AN INTERMEDIATE IN A NOVEL PHOSPHO-TRANSFERASE SYSTEM
inferredcites →https://doi.org/10.1074/jbc.270.10.5243openalex-snapshot
The Oxygen Sensor Protein, FixL, of Rhizobium meliloti
inferredcites →https://doi.org/10.1074/jbc.m101982200openalex-snapshot
Evidence for Direct Interaction between Enzyme INtrand Aspartokinase to Regulate Bacterial Oligopeptide Transport
inferredcites →https://doi.org/10.1074/jbc.m114.565762openalex-snapshot
The CpxR/CpxA Two-component Regulatory System Up-regulates the Multidrug Resistance Cascade to Facilitate Escherichia coli Resistance to a Model Antimicrobial Peptide
inferredcites →https://doi.org/10.1074/mcp.m700311-mcp200openalex-snapshot
Phosphoproteome Analysis of E. coli Reveals Evolutionary Conservation of Bacterial Ser/Thr/Tyr Phosphorylation
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/femsre/fuw003openalex-snapshot
Exploring the diversity of protein modifications: special bacterial phosphorylation systems
inferredcites →https://doi.org/10.1093/gbe/evt061openalex-snapshot
Life in an Arsenic-Containing Gold Mine: Genome and Physiology of the Autotrophic Arsenite-Oxidizing Bacterium Rhizobium sp. NT-26
inferredcites →https://doi.org/10.1093/nar/17.8.2947openalex-snapshot
ThenarXandnarLgenes encoding the nitrate-sensing regulators ofEscherichia coliare homologous to a family of prokaryotic two-component regulatory genes
inferredcites →https://doi.org/10.1094/mpmi-05-12-0136-ropenalex-snapshot
FxkR Provides the Missing Link in the fixL-fixK Signal Transduction Cascade in Rhizobium etli CFN42
inferredcites →https://doi.org/10.1094/mpmi-10-17-0255-ropenalex-snapshot
Two Agrobacterium tumefaciens CheW Proteins Are Incorporated into One Chemosensory Pathway with Different Efficiencies
inferredcites →https://doi.org/10.1094/mpmi.2002.15.4.388openalex-snapshot
Rhizobium leguminosarum bv. trifolii PssP Protein Is Required for Exopolysaccharide Biosynthesis and Polymerization
inferredcites →https://doi.org/10.1098/rsob.140133openalex-snapshot
Bacterial genospecies that are not ecologically coherent: population genomics ofRhizobium leguminosarum
inferredcites →https://doi.org/10.1098/rstb.2011.0424openalex-snapshot
Bacterial tyrosine kinases: evolution, biological function and structural insights
inferredcites →https://doi.org/10.1099/ijs.0.014043-0openalex-snapshot
Mesorhizobium alhagi sp. nov., isolated from wild Alhagi sparsifolia in north-western China
inferredcites →https://doi.org/10.1099/mic.0.000239openalex-snapshot
Sinorhizobium meliloti low molecular mass phosphotyrosine phosphatase SMc02309 modifies activity of the UDP-glucose pyrophosphorylase ExoN involved in succinoglycan biosynthesis
inferredcites →https://doi.org/10.1099/mic.0.000284openalex-snapshot
Expanding the regulatory network that controls nitrogen fixation in Sinorhizobium meliloti: elucidating the role of the two-component system hFixL-FxkR
inferredcites →https://doi.org/10.1101/gad.1700308openalex-snapshot
Signal integration in bacterial two-component regulatory systems
inferredcites →https://doi.org/10.1111/1462-2920.12037openalex-snapshot
Analysis of the plant growth‐promoting properties encoded by the genome of the rhizobacterium P seudomonas putida BIRD ‐1
inferredcites →https://doi.org/10.1111/j.1365-2958.1993.tb00915.xopenalex-snapshot
Bacillus subtilis CtaA and CtaB function in haem A biosynthesis
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05515.xopenalex-snapshot
The major chemotaxis gene cluster of Rhizobium leguminosarum bv. viciae is essential for competitive nodulation
inferredcites →https://doi.org/10.1111/j.1365-2958.2012.08014.xopenalex-snapshot
The PTSNtr system globally regulates ATP‐dependent transporters in Rhizobium leguminosarum
inferredcites →https://doi.org/10.1111/j.1574-6968.2007.00841.xopenalex-snapshot
Tyrosine-kinase Wzc fromEscherichia colipossesses an ATPase activity regulated by autophosphorylation
inferredcites →https://doi.org/10.1111/j.1574-6968.2012.02529.xopenalex-snapshot
Regulation of Cu(I)/Ag(I) efflux genes in Escherichia coli by the sensor kinase CusS
inferredcites →https://doi.org/10.1111/mmi.13621openalex-snapshot
Unphosphorylated EIIAN tr induces C lp AP ‐mediated degradation of R po S in A zotobacter vinelandii
inferredcites →https://doi.org/10.1128/aem.02007-09openalex-snapshot
Characterization of the NifA-RpoN Regulon in Rhizobium etli in Free Life and in Symbiosis with Phaseolus vulgaris
inferredcites →https://doi.org/10.1128/aem.03454-15openalex-snapshot
Genetic Analysis Reveals the Essential Role of Nitrogen Phosphotransferase System Components in Sinorhizobium fredii CCBAU 45436 Symbioses with Soybean and Pigeonpea Plants
inferredcites →https://doi.org/10.1128/iai.00476-17openalex-snapshot
Bacterial Chat: Intestinal Metabolites and Signals in Host-Microbiota-Pathogen Interactions
inferredcites →https://doi.org/10.1128/jb.00062-08openalex-snapshot
Fine-Tuning of Galactoglucan Biosynthesis in Sinorhizobium meliloti by Differential WggR (ExpG)-, PhoB-, and MucR-Dependent Regulation of Two Promoters
inferredcites →https://doi.org/10.1128/jb.00251-06openalex-snapshot
FixJ: a Major Regulator of the Oxygen Limitation Response and Late Symbiotic Functions of Sinorhizobium meliloti
inferredcites →https://doi.org/10.1128/jb.00365-06openalex-snapshot
Exo-Oligosaccharides of Rhizobium sp. Strain NGR234 Are Required for Symbiosis with Various Legumes
inferredcites →https://doi.org/10.1128/jb.00614-17openalex-snapshot
Cellular Stoichiometry of Methyl-Accepting Chemotaxis Proteins in Sinorhizobium meliloti
inferredcites →https://doi.org/10.1128/jb.00883-06openalex-snapshot
Functional Analysis of Nine Putative Chemoreceptor Proteins in Sinorhizobium meliloti
inferredcites →https://doi.org/10.1128/jb.01088-07openalex-snapshot
New Target Genes Controlled by the Bradyrhizobium japonicum Two-Component Regulatory System RegSR
inferredcites →https://doi.org/10.1128/jb.01694-07openalex-snapshot
Glucomannan-Mediated Attachment ofRhizobium leguminosarumto Pea Root Hairs Is Required for Competitive Nodule Infection
inferredcites →https://doi.org/10.1128/jb.01887-05openalex-snapshot
Structural Classification of Bacterial Response Regulators: Diversity of Output Domains and Domain Combinations
inferredcites →https://doi.org/10.1128/jb.01917-07openalex-snapshot
Sinorhizobium melilotiMutants Lacking Phosphotransferase System Enzyme HPr or EIIA Are Altered in Diverse Processes, Including Carbon Metabolism, Cobalt Requirements, and Succinoglycan Production
inferredcites →https://doi.org/10.1128/jb.06345-11openalex-snapshot
CitA/CitB Two-Component System Regulating Citrate Fermentation in Escherichia coli and Its Relation to the DcuS/DcuR System In Vivo
inferredcites →https://doi.org/10.1128/jb.06357-11openalex-snapshot
Mutation of the Sensor Kinase chvG in Rhizobium leguminosarum Negatively Impacts Cellular Metabolism, Outer Membrane Stability, and Symbiosis
inferredcites →https://doi.org/10.1128/jb.171.9.5087-5094.1989openalex-snapshot
Regulation of glutamine synthetase II activity in Rhizobium meliloti 104A14
inferredcites →https://doi.org/10.1128/jb.172.2.824-834.1990openalex-snapshot
Signal transduction pathway controlling synthesis of a class of degradative enzymes in Bacillus subtilis: expression of the regulatory genes and analysis of mutations in degS and degU
inferredcites →https://doi.org/10.1128/jb.173.7.2180-2186.1991openalex-snapshot
The activities of the Escherichia coli MalK protein in maltose transport, regulation, and inducer exclusion can be separated by mutations
inferredcites →https://doi.org/10.1128/jb.180.15.3853-3863.1998openalex-snapshot
Expression of the fixR-nifA Operon in Bradyrhizobium japonicum Depends on a New Response Regulator, RegR
inferredcites →https://doi.org/10.1128/jb.180.2.395-399.1998openalex-snapshot
Specific Amino Acid Substitutions in the Proline-Rich Motif of the Rhizobium meliloti ExoP Protein Result in Enhanced Production of Low-Molecular-Weight Succinoglycan at the Expense of High-Molecular-Weight Succinoglycan
inferredcites →https://doi.org/10.1128/jb.180.7.1729-1740.1998openalex-snapshot
The Rhizobium etli rpoN Locus: DNA Sequence Analysis and Phenotypical Characterization of rpoN , ptsN , and ptsA Mutants
inferredcites →https://doi.org/10.1128/jb.181.4.1238-1248.1999openalex-snapshot
Identification and Characterization of a Two-Component Sensor-Kinase and Response-Regulator System (DcuS-DcuR) Controlling Gene Expression in Response to C 4 -Dicarboxylates in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.182.6.1459-1471.2000openalex-snapshot
Signaling Components in Bacterial Locomotion and Sensory Reception
inferredcites →https://doi.org/10.1128/jb.183.17.5163-5170.2001openalex-snapshot
The Molecular Weight Distribution of Succinoglycan Produced by Sinorhizobium meliloti Is Influenced by Specific Tyrosine Phosphorylation and ATPase Activity of the Cytoplasmic Domain of the ExoP Protein
inferredcites →https://doi.org/10.1128/jb.185.4.1470-1474.2003openalex-snapshot
Overrepresentation of a Gene Family Encoding Extracytoplasmic Solute Receptors in Bordetella
inferredcites →https://doi.org/10.1128/jb.186.2.445-453.2004openalex-snapshot
The HWE Histidine Kinases, a New Family of Bacterial Two-Component Sensor Kinases with Potentially Diverse Roles in Environmental Signaling
inferredcites →https://doi.org/10.1128/jb.186.9.2664-2672.2004openalex-snapshot
Chemotactic Signaling by an Escherichia coli CheA Mutant That Lacks the Binding Domain for Phosphoacceptor Partners
inferredcites →https://doi.org/10.1128/mmbr.00001-14openalex-snapshot
The Bacterial Phosphoenolpyruvate:Carbohydrate Phosphotransferase System: Regulation by Protein Phosphorylation and Phosphorylation-Dependent Protein-Protein Interactions
inferredcites →https://doi.org/10.1128/mmbr.00024-06openalex-snapshot
How Phosphotransferase System-Related Protein Phosphorylation Regulates Carbohydrate Metabolism in Bacteria
inferredcites →https://doi.org/10.1146/annurev-ecolsys-102710-145034openalex-snapshot
Functional Ecology of Free-Living Nitrogen Fixation: A Contemporary Perspective
inferredcites →https://doi.org/10.1159/000381215openalex-snapshot
The Bacterial Phosphotransferase System: New Frontiers 50 Years after Its Discovery
inferredcites →https://doi.org/10.1186/s12866-016-0849-6openalex-snapshot
Functional analysis of PrkA - a putative serine protein kinase from Mesorhizobium alhagi CCNWXJ12-2 - in stress resistance
inferredcites →https://doi.org/10.1186/s12934-019-1067-3openalex-snapshot
Engineering an electroactive Escherichia coli for the microbial electrosynthesis of succinate from glucose and CO2
inferredcites →https://doi.org/10.1186/s13568-018-0608-1openalex-snapshot
Azospirillum: benefits that go far beyond biological nitrogen fixation
inferredcites →https://doi.org/10.1371/journal.pgen.1005518openalex-snapshot
Autophosphorylation of the Bacterial Tyrosine-Kinase CpsD Connects Capsule Synthesis with the Cell Cycle in Streptococcus pneumoniae
inferredcites →https://doi.org/10.1371/journal.pone.0023701openalex-snapshot
Functional Assessment of EnvZ/OmpR Two-Component System in Shewanella oneidensis
inferredcites →https://doi.org/10.1371/journal.pone.0042611openalex-snapshot
Role of Specific Quorum-Sensing Signals in the Regulation of Exopolysaccharide II Production within Sinorhizobium meliloti Spreading Colonies
inferredcites →https://doi.org/10.1371/journal.pone.0064682openalex-snapshot
ABC Transport Is Inactivated by the PTSNtr under Potassium Limitation in Rhizobium leguminosarum 3841
inferredcites →https://doi.org/10.1371/journal.pone.0139143openalex-snapshot
Site-Specific Ser/Thr/Tyr Phosphoproteome of Sinorhizobium meliloti at Stationary Phase
inferredcites →https://doi.org/10.1371/journal.pone.0182993openalex-snapshot
Comparative analysis of LytS/LytTR-type histidine kinase/response regulator systems in γ-proteobacteria
inferredcites →https://doi.org/10.1371/journal.ppat.1003201openalex-snapshot
The KdpD/KdpE Two-Component System: Integrating K+ Homeostasis and Virulence
inferredcites →https://doi.org/10.2174/1874285801509010001openalex-snapshot
Plant-microbe Cross-talk in the Rhizosphere: Insight and Biotechnological Potential
inferredcites →https://doi.org/10.3389/fmicb.2015.00402openalex-snapshot
The Pho regulon: a huge regulatory network in bacteria
inferredcites →https://doi.org/10.3389/fmicb.2015.00496openalex-snapshot
Bacterial exopolysaccharides: biosynthesis pathways and engineering strategies
inferredcites →https://doi.org/10.3389/fmicb.2016.01928openalex-snapshot
Interaction between Nitrogen and Phosphate Stress Responses in Sinorhizobium meliloti
inferredcites →https://doi.org/10.3389/fmicb.2017.01348openalex-snapshot
Draft Genome Sequence of the Nitrogen-Fixing Rhizobium sullae Type Strain IS123T Focusing on the Key Genes for Symbiosis with its Host Hedysarum coronarium L.
inferredcites →https://doi.org/10.3390/genes8120360openalex-snapshot
Synthesis of Rhizobial Exopolysaccharides and Their Importance for Symbiosis with Legume Plants
inferredcites →https://doi.org/10.3390/genes9070369openalex-snapshot
Mutation in the pssZ Gene Negatively Impacts Exopolysaccharide Synthesis, Surface Properties, and Symbiosis of Rhizobium leguminosarum bv. trifolii with Clover
inferredcites →https://doi.org/10.3390/ijms12117898openalex-snapshot
Environmental Signals and Regulatory Pathways That Influence Exopolysaccharide Production in Rhizobia
inferredcites →https://doi.org/10.3390/ijms19102872openalex-snapshot
Hanks-Type Serine/Threonine Protein Kinases and Phosphatases in Bacteria: Roles in Signaling and Adaptation to Various Environments
inferredcites →https://doi.org/10.3390/ijms20122905openalex-snapshot
Transcriptomic Studies Reveal that the Rhizobium leguminosarum Serine/Threonine Protein Phosphatase PssZ has a Role in the Synthesis of Cell-Surface Components, Nutrient Utilization, and Other Cellular Processes
inferredcites →https://doi.org/10.5772/48277openalex-snapshot
Bacterial Two-Component Systems: Structures and Signaling Mechanisms
inferredcites →https://doi.org/10.5772/51202openalex-snapshot
Exopolysaccharide Biosynthesis in Rhizobium leguminosarum: From Genes to Functions
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.4764125openalex-extracted
Integrated Tea Polyphenols and Polydopamine Bidirectional Modified Graphene as Anode for Improved Bioelectricity Generation and Cr(Vi) Reduction in Microbial Fuel Cells
inferred← citeshttps://doi.org/10.1007/978-3-030-83270-4_9openalex-snapshot
Can Bacterial Populations Go Extinct? Evolutionary Biology and Bacterial Studies in Cuatro Ciénegas Shed Light on the Extinction Process
inferred← citeshttps://doi.org/10.1007/s11104-023-06302-1openalex-snapshot
Invasive plant species interact with drought to shift key functions and families in the native rhizosphere
inferred← citeshttps://doi.org/10.1007/s11274-023-03785-zopenalex-snapshot
Chromosomal gene of hybrid multisensor histidine kinase is involved in motility regulation in the rhizobacterium Azospirillum baldaniorum Sp245 under mechanical and water stress
inferred← citeshttps://doi.org/10.1007/s11368-026-04303-yopenalex-snapshot
Slope aspect dominates over treeline position in structuring nitrogen-fixing microbial communities in Tibetan alpine ecotones
inferred← citeshttps://doi.org/10.1007/s15010-020-01547-9openalex-snapshot
Are antibacterial effects of non-antibiotic drugs random or purposeful because of a common evolutionary origin of bacterial and mammalian targets?
inferred← citeshttps://doi.org/10.1016/b978-0-443-18486-4.00006-3openalex-snapshot
Prospective manipulation of plant growth-promoting bacteria as biofertilizers and biopesticides in agriculture
inferred← citeshttps://doi.org/10.1016/j.apsoil.2020.103815openalex-snapshot
Proteome responses of Rhizobium tropici CIAT 899 upon apigenin and salt stress induction
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2024.142858openalex-snapshot
Integrated tea polyphenols and polydopamine functionalized graphene anode for improved bioelectricity generation and Cr(VI) reduction in microbial fuel cells
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.139141openalex-snapshot
Rhizobial symbiosis modulates mercury accumulation and metabolic adaptation under hydrological extremes
inferred← citeshttps://doi.org/10.1016/j.jwpe.2023.104716openalex-snapshot
Microbial community structure characteristics and gene distribution of sulfur-siderite/limestone autotrophic denitrification
inferred← citeshttps://doi.org/10.1016/j.pedsph.2026.01.019openalex-snapshot
Biochar application affects respiration and concomitant biological activities in agricultural soils: A global meta-analysis
inferred← citeshttps://doi.org/10.1016/j.soilbio.2025.109863openalex-snapshot
Signal molecules and enzymes produced by Rhizobium leguminosarum sv. trifolii strains originating from the subpolar and temperate climate zones as elements of adaptation to low temperature stress
inferred← citeshttps://doi.org/10.1038/s41598-026-39563-8openalex-snapshot
Genomic and in vitro characterization of two lytic bacteriophages infecting multidrug-resistant Erwinia sp. strain AnSW2-5
inferred← citeshttps://doi.org/10.1039/d4en00511bopenalex-snapshot
Silica nanoparticles enhance plant disease resistance by modulating the endophyte community structure in tomato ( Solanum lycopersicum L.) roots
inferred← citeshttps://doi.org/10.1089/omi.2023.0272openalex-snapshot
Pomegranate Rhizosphere Microbial Diversity Revealed by Metagenomics: Toward Organic Farming, Plant Growth Promotion and Biocontrol?
inferred← citeshttps://doi.org/10.1093/ismeco/ycag027openalex-snapshot
Land-use intensification reshapes microbial phosphorus cycling, organic matter composition, and phosphorus fractions in Amazonian soils
inferred← citeshttps://doi.org/10.1101/2020.03.13.990432openalex-snapshot
Fast eco-evolutionary changes in bacterial genomes after anthropogenic perturbation
inferred← citeshttps://doi.org/10.1101/2023.10.31.564804openalex-snapshot
Unraveling the Genomic and Environmental Diversity of the Ubiquitous Solirubrobacter
inferred← citeshttps://doi.org/10.1101/2025.10.14.682339openalex-snapshot
Microbial and organic matter composition jointly drive phosphorus cycling genes and phosphorus availability in Amazonian soils
inferred← citeshttps://doi.org/10.1111/1462-2920.16685openalex-snapshot
Unravelling the genomic and environmental diversity of the ubiquitous Solirubrobacter
inferred← citeshttps://doi.org/10.1111/gcb.70057openalex-snapshot
Navigating Climate Change: Exploring the Dynamics Between Plant–Soil Microbiomes and Their Impact on Plant Growth and Productivity
inferred← citeshttps://doi.org/10.1134/s0026261725601423openalex-snapshot
Analysis of Biofilms Formed in Soil by Bacteria of the Genus Azospirillum
inferred← citeshttps://doi.org/10.1134/s0026261725603215openalex-snapshot
Motility and Biofilm Formation as a Basis of Adaptation to Rhizosphere in Azospirillum Bacteria
inferred← citeshttps://doi.org/10.13057/biodiv/d230740openalex-snapshot
Long-term changes in floristic diversity, composition and stand structure in Acacia auriculiformis plantation in Mount Makiling Forest Reserve, Philippines
inferred← citeshttps://doi.org/10.17116/molgen20254303147openalex-snapshot
The effect of the hybrid histidine kinase gene inactivation on cell morphology in Azospirillum baldaniorum and Azospirillum brasilense
inferred← citeshttps://doi.org/10.24326/mon.2021.6openalex-snapshot
Wybrane zagadnienia z zakresu ochrony i zagrożeń środowiska
inferred← citeshttps://doi.org/10.3103/s0891416825700223openalex-snapshot
The Effect of Hybrid Histidine Kinase Gene Inactivation on Cell Morphology in Azospirillum baldaniorum and Azospirillum brasilense
inferred← citeshttps://doi.org/10.3389/fmicb.2020.563885openalex-snapshot
Evolutionary Rescue of an Environmental Pseudomonas otitidis in Response to Anthropogenic Perturbation
inferred← citeshttps://doi.org/10.3389/fmicb.2020.615775openalex-snapshot
A Novel OmpR-Type Response Regulator Controls Multiple Stages of the Rhizobium etli – Phaseolus vulgaris N2-Fixing Symbiosis
inferred← citeshttps://doi.org/10.3389/fmicb.2021.669404openalex-snapshot
Rhizobial–Host Interactions and Symbiotic Nitrogen Fixation in Legume Crops Toward Agriculture Sustainability
inferred← citeshttps://doi.org/10.3389/fmicb.2021.738780openalex-snapshot
Phosphorylation of Extracellular Proteins in Acinetobacter baumannii in Sessile Mode of Growth
inferred← citeshttps://doi.org/10.3390/ijms22126233openalex-snapshot
Rhizobial Exopolysaccharides: Genetic Regulation of Their Synthesis and Relevance in Symbiosis with Legumes
inferred← citeshttps://doi.org/10.3390/ijms232415536openalex-snapshot
The Ros/MucR Zinc-Finger Protein Family in Bacteria: Structure and Functions
inferred← citeshttps://doi.org/10.3390/jof7080610openalex-snapshot
Histidine Kinase Sln1 and cAMP/PKA Signaling Pathways Antagonistically Regulate Sporisorium scitamineum Mating and Virulence via Transcription Factor Prf1
inferred← citeshttps://doi.org/10.5513/jcea01/25.1.4129openalex-snapshot
The role of biochar and organic fertilizers on the growth and yields of soybean
inferred← citeshttps://doi.org/10.58475/2023.61.1.1826openalex-snapshot
EFFICIENCY OF NITROGEN FIXING, NODULATION FORMATION, PHOSPHATE SOLUBILIZING BACTERIA AND PLANT GROWTH PROMOTING RHIZOBACTERIA ON YIELD OF CHICKPEA
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.