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Physiological and Agronomical Aspects of Phytohormone Production by Model Plant-Growth-Promoting Rhizobacteria (PGPR) Belonging to the Genus Azospirillum
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/11563280openalex-snapshot
Nitric Oxide in Plant Growth, Development and Stress Physiology
inferredcites →https://doi.org/10.1007/978-3-642-65406-0openalex-snapshot
Plant Growth Substances 1970
inferredcites →https://doi.org/10.1007/978-3-642-67704-5_5openalex-snapshot
Biosynthesis and Metabolism of Plant Hormones
inferredcites →https://doi.org/10.1007/978-3-642-70791-9_16openalex-snapshot
Field Inoculation of Rice Using in Vitro Selected Bacterial and Plant Genotypes
inferredcites →https://doi.org/10.1007/978-3-642-70791-9_20openalex-snapshot
Response of Plant Roots to Inoculation with Azospirillum Brasilense and to Application of Indole Acetic Acid
inferredcites →https://doi.org/10.1007/978-3-642-73072-6_12openalex-snapshot
Influence of Azospirillum Brasilense on Nodulation of Legumes
inferredcites →https://doi.org/10.1007/978-3-642-74545-4openalex-snapshot
Plant Growth Substances 1988
inferredcites →https://doi.org/10.1007/978-3-642-74545-4_7openalex-snapshot
Dwarf Mutants of Maize — Research Tools for the Analysis of Growth
inferredcites →https://doi.org/10.1007/978-94-009-4378-0_3openalex-snapshot
Establishment of inoculated Azospirillum spp. in the rhizosphere and in roots of field grown wheat and sorghum
inferredcites →https://doi.org/10.1007/978-94-011-0177-6openalex-snapshot
Advances in Molecular Genetics of Plant-Microbe Interactions
inferredcites →https://doi.org/10.1007/bf00195339openalex-snapshot
Biosynthesis of indole-3-acetic acid in tomato shoots: Measurement, mass-spectral identification and incorporation of ?2H from ?2H2O into indole-3-acetic acid, d- and l-tryptophan, indole-3-pyruvate and tryptamine
inferredcites →https://doi.org/10.1007/bf00280477openalex-snapshot
Molecular cloning and sequence analysis of an Azospirilium brasilense indole-3-pyruvate decarboxylase gene
inferredcites →https://doi.org/10.1007/bf00395413openalex-snapshot
An alternative explanation for plant growth promotion by bacteria of the genus Azospirillum
inferredcites →https://doi.org/10.1007/bf02220706openalex-snapshot
Phytohormone-like substances produced by single and mixed diazotrophic cultures of Azospirillum and Arthrobacter
inferredcites →https://doi.org/10.1007/bf02277385openalex-snapshot
Establishment of inoculatedAzospirillum spp. in the rhizosphere and in roots of field grown wheat and sorghum
inferredcites →https://doi.org/10.1007/s00248-011-9819-6openalex-snapshot
Transcriptome Analysis of the Rhizosphere Bacterium Azospirillum brasilense Reveals an Extensive Auxin Response
inferredcites →https://doi.org/10.1007/s002480000040openalex-snapshot
Expression of the ACC Deaminase Gene fromEnterobacter cloacae UW4 in Azospirillum brasilense
inferredcites →https://doi.org/10.1007/s00253-004-1696-1openalex-snapshot
Gibberellin production by bacteria and its involvement in plant growth promotion and yield increase
inferredcites →https://doi.org/10.1007/s00253-007-0909-9openalex-snapshot
Plant-growth-promoting compounds produced by two agronomically important strains of Azospirillum brasilense, and implications for inoculant formulation
inferredcites →https://doi.org/10.1007/s00344-005-0128-5openalex-snapshot
Azospirillum sp. Promotes Root Hair Development in Tomato Plants through a Mechanism that Involves Ethylene
inferredcites →https://doi.org/10.1007/s00425-005-1523-7openalex-snapshot
Nitric Oxide is Involved in the Azospirillum brasilense-induced Lateral Root Formation in Tomato
inferredcites →https://doi.org/10.1007/s004250000420openalex-snapshot
Enzymatic characterization of the recombinant Arabidopsis thaliana nitrilase subfamily encoded by the NIT 2/ NIT 1/ NIT 3-gene cluster
inferredcites →https://doi.org/10.1007/s004380000340openalex-snapshot
Physiological evidence for differently regulated tryptophan-dependent pathways for indole-3-acetic acid synthesis in Azospirillum brasilense
inferredcites →https://doi.org/10.1007/s10725-007-9232-9openalex-snapshot
Azospirillum brasilense Sp 245 produces ABA in chemically-defined culture medium and increases ABA content in arabidopsis plants
inferredcites →https://doi.org/10.1007/s11104-007-9462-7openalex-snapshot
Physiological and genetic analysis of root responsiveness to auxin-producing plant growth-promoting bacteria in common bean (Phaseolus vulgaris L.)
inferredcites →https://doi.org/10.1007/s11104-007-9476-1openalex-snapshot
Azospirillum amazonense inoculation: effects on growth, yield and N2 fixation of rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1007/s11104-007-9514-zopenalex-snapshot
Lorenz Hiltner, a pioneer in rhizosphere microbial ecology and soil bacteriology research
inferredcites →https://doi.org/10.1007/s11104-008-9560-1openalex-snapshot
Effects of Azospirillum brasilense indole-3-acetic acid production on inoculated wheat plants
inferredcites →https://doi.org/10.1007/s11104-008-9606-4openalex-snapshot
Effect of Rhizobium–Azospirillum coinoculation on nitrogen fixation and yield of two contrasting Phaseolus vulgaris L. genotypes cultivated across different environments in Cuba
inferredcites →https://doi.org/10.1007/s11104-010-0499-7openalex-snapshot
Azospirillum lipoferum strain AZm5 containing 1-aminocyclopropane-1-carboxylic acid deaminase improves early growth of tomato seedlings under nitrogen deficiency
inferredcites →https://doi.org/10.1007/s11104-011-1009-2openalex-snapshot
The hisC1 gene, encoding aromatic amino acid aminotransferase-1 in Azospirillum brasilense Sp7, expressed in wheat
inferredcites →https://doi.org/10.1016/0021-9673(94)85210-3openalex-snapshot
Chromatography of gibberellins
inferredcites →https://doi.org/10.1016/0024-3205(63)90108-5openalex-snapshot
Zeatin, a factor inducing cell division isolated from
inferredcites →https://doi.org/10.1016/0038-0717(89)90024-2openalex-snapshot
Identification and quantification of IAA and IBA in Azospirillum brasilense-inoculated maize roots
inferredcites →https://doi.org/10.1016/0038-0717(92)90036-wopenalex-snapshot
Azospirillum brasilense produces gibberellin in pure culture on chemically-defined medium and in co-culture on straw
inferredcites →https://doi.org/10.1016/0038-0717(94)90195-3openalex-snapshot
Characterization of two aromatic amino acid aminotransferases and production of indoleacetic acid in Azospirillum strains
inferredcites →https://doi.org/10.1016/0038-0717(94)90311-5openalex-snapshot
Agronomic applications of azospirillum: An evaluation of 20 years worldwide field inoculation
inferredcites →https://doi.org/10.1016/0378-1097(88)90202-9openalex-snapshot
Distribution of sym-homosperimidine in eubacteria, cyanobacteria, algae and ferns
inferredcites →https://doi.org/10.1016/0378-1097(90)90034-nopenalex-snapshot
Polyamines in Rhizobium, Bradyrhizobium, Azorhizobium and Argobacterium
inferredcites →https://doi.org/10.1016/j.ejsobi.2008.05.006openalex-snapshot
Stress-responsive indole-3-acetic acid biosynthesis by Azospirillum brasilense SM and its ability to modulate plant growth
inferredcites →https://doi.org/10.1016/j.ejsobi.2008.07.001openalex-snapshot
Field performance of a liquid formulation of Azospirillum brasilense on dryland wheat productivity
inferredcites →https://doi.org/10.1016/j.ejsobi.2008.08.003openalex-snapshot
Cadaverine production by Azospirillum brasilense and its possible role in plant growth promotion and osmotic stress mitigation
inferredcites →https://doi.org/10.1016/j.ejsobi.2008.08.005openalex-snapshot
Azospirillum brasilense Az39 and Bradyrhizobium japonicum E109, inoculated singly or in combination, promote seed germination and early seedling growth in corn (Zea mays L.) and soybean (Glycine max L.)
inferredcites →https://doi.org/10.1016/j.femsle.2004.01.047openalex-snapshot
Aromatic amino acid aminotransferase activity and indole-3-acetic acid production by associative nitrogen-fixing bacteria
inferredcites →https://doi.org/10.1016/j.femsle.2005.03.048openalex-snapshot
Growth and indole-3-acetic acid biosynthesis ofAzospirillum brasilenseSp245 is environmentally controlled
inferredcites →https://doi.org/10.1016/j.phytochem.2008.08.020openalex-snapshot
Primary or secondary? Versatile nitrilases in plant metabolism
inferredcites →https://doi.org/10.1016/j.resmic.2010.01.005openalex-snapshot
Effects of Azospirillum brasilense with genetically modified auxin biosynthesis gene ipdC upon the diversity of the indigenous microbiota of the wheat rhizosphere
inferredcites →https://doi.org/10.1016/j.soilbio.2008.06.016openalex-snapshot
Effect of Azospirillum brasilense coinoculated with Rhizobium on Phaseolus vulgaris flavonoids and Nod factor production under salt stress
inferredcites →https://doi.org/10.1016/s0031-9422(00)80461-6openalex-snapshot
Plant Growth Substances 1982:
inferredcites →https://doi.org/10.1016/s0031-9422(00)94191-8openalex-snapshot
Encyclopedia of plant physiology, New series
inferredcites →https://doi.org/10.1016/s0038-0717(97)00187-9openalex-snapshot
Proposal for the division of plant growth-promoting rhizobacteria into two classifications: biocontrol-PGPB (plant growth-promoting bacteria) and PGPB
inferredcites →https://doi.org/10.1016/s0065-2113(10)08002-8openalex-snapshot
How the Plant Growth-Promoting Bacterium Azospirillum Promotes Plant Growth—A Critical Assessment
inferredcites →https://doi.org/10.1016/s0065-2296(07)46001-3openalex-snapshot
Nitric Oxide and Plant Growth Promoting Rhizobacteria: Common Features Influencing Root Growth and Development
inferredcites →https://doi.org/10.1016/s0167-7306(08)60488-3openalex-snapshot
Abscisic acid metabolism and its regulation
inferredcites →https://doi.org/10.1016/s0167-7306(08)x6025-9openalex-snapshot
Biochemistry and Molecular Biology of Plant Hormones
inferredcites →https://doi.org/10.1016/s0300-9629(80)80039-9openalex-snapshot
Encyclopedia of plant physiology new series
inferredcites →https://doi.org/10.1016/s0378-1097(03)00694-3openalex-snapshot
Indole-3-butyric acid (IBA) production in culture medium by wild strainAzospirillum brasilense
inferredcites →https://doi.org/10.1016/s0723-2020(98)80035-0openalex-snapshot
Polyamine Distribution Among Authentic Pseudomonads and Azotobacteraceae
inferredcites →https://doi.org/10.1016/s0944-5013(11)80136-9openalex-snapshot
Cytokinin-like substances and ethylene production by Azospirillum in media with different carbon sources
inferredcites →https://doi.org/10.1016/s0966-842x(00)01732-7openalex-snapshot
Indole-3-acetic acid: a reciprocal signalling molecule in bacteria–plant interactions
inferredcites →https://doi.org/10.1016/s1360-1385(00)01790-8openalex-snapshot
Gibberellin metabolism: new insights revealed by the genes
inferredcites →https://doi.org/10.1016/s1360-1385(00)01795-7openalex-snapshot
New interactions between classical plant hormones
inferredcites →https://doi.org/10.1021/ja01610a105openalex-snapshot
KINETIN, A CELL DIVISION FACTOR FROM DEOXYRIBONUCLEIC ACID1
inferredcites →https://doi.org/10.1023/a:1004658000815openalex-snapshot
Phytostimulatory effect of Azospirillum brasilense wild type and mutant strains altered in IAA production on wheat
inferredcites →https://doi.org/10.1023/a:1005730509433openalex-snapshot
Plasticity of polyamine metabolism associated with high osmotic stress in rape leaf discs and with ethylene treatment
inferredcites →https://doi.org/10.1023/a:1005925925127openalex-snapshot
Hydrolysis of [17,17-2H2]gibberellin A20-glucoside and [17,17-2H2]gibberellin A20-glucosyl ester by Azospirillum lipoferum cultured in a nitrogen-free biotin-Based chemically-defined medium
inferredcites →https://doi.org/10.1023/a:1020584627919openalex-snapshot
Gibberellin A3 stimulates adventitious rooting of cuttings from cherry (Prunus avium)
inferredcites →https://doi.org/10.1038/nrm2020openalex-snapshot
Auxin in action: signalling, transport and the control of plant growth and development
inferredcites →https://doi.org/10.1046/j.1365-2672.2003.02047.xopenalex-snapshot
Beijerinckia derxii releases plant growth regulators and amino acids in synthetic media independent of nitrogenase activity
inferredcites →https://doi.org/10.1046/j.1365-2958.1999.01396.xopenalex-snapshot
The ipdC promoter auxin‐responsive element of Azospirillum brasilense, a prokaryotic ancestral form of the plant AuxRE?
inferredcites →https://doi.org/10.1046/j.1472-765x.2003.01373.xopenalex-snapshot
Plant growth regulators and amino acids released by Azospirillum sp. in chemically defined media
inferredcites →https://doi.org/10.1071/pp9930527openalex-snapshot
The Route, Control and Compartmentation of Auxin Synthesis
inferredcites →https://doi.org/10.1073/pnas.22.8.511openalex-snapshot
On the Physiology of the Formation of Nodules on Legume Roots
inferredcites →https://doi.org/10.1073/pnas.81.6.1728openalex-snapshot
Nucleotide sequence of the tms genes of the pTiA6NC octopine Ti plasmid: two gene products involved in plant tumorigenesis.
inferredcites →https://doi.org/10.1093/dnares/dsp026openalex-snapshot
Complete Genomic Structure of the Cultivated Rice Endophyte Azospirillum sp. B510
inferredcites →https://doi.org/10.1093/jxb/erj045openalex-snapshot
Nitric oxide modulates the expression of cell cycle regulatory genes during lateral root formation in tomato
inferredcites →https://doi.org/10.1093/jxb/ert080openalex-snapshot
Auxin biosynthesis and storage forms
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a077841openalex-snapshot
Quantitative Analysis of Endogenous Gibberellins in Normal and Dwarf Cultivars of Rice
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078554openalex-snapshot
Inoculation with Azospirillum lipoferum Affects Growth and Gibberellin Status of Corn Seedling Roots
inferredcites →https://doi.org/10.1093/pcp/pcd018openalex-snapshot
Regulation of Elongation Growth by Gibberellin in Root Segments of Lemna minor
inferredcites →https://doi.org/10.1093/pcp/pce099openalex-snapshot
Azospirillum spp. metabolize[ 17,17-2H2]gibberellin A20 to[ 17,17-2H2]gibberellin A1 in vivo in dy rice mutant seedlings
inferredcites →https://doi.org/10.1093/treephys/22.6.373openalex-snapshot
Effects of exogenous diamines on the interaction between ectomycorrhizal fungi and adventitious root formation in Scots pine in vitro
inferredcites →https://doi.org/10.1094/mpmi-07-10-0148openalex-snapshot
The Pseudomonas Secondary Metabolite 2,4-Diacetylphloroglucinol Is a Signal Inducing Rhizoplane Expression of Azospirillum Genes Involved in Plant-Growth Promotion
inferredcites →https://doi.org/10.1094/mpmi-18-0311openalex-snapshot
Transcriptional Analysis of the Azospirillum brasilense Indole-3-Pyruvate Decarboxylase Gene and Identification of a cis -Acting Sequence Involved in Auxin Responsive Expression
inferredcites →https://doi.org/10.1094/mpmi-21-7-1001openalex-snapshot
Aerobic Nitric Oxide Production by Azospirillum brasilense Sp245 and Its Influence on Root Architecture in Tomato
inferredcites →https://doi.org/10.1094/mpmi-6-609openalex-snapshot
Azospirillum brasilense Indole-3-Acetic Acid Biosynthesis: Evidence for a Non-Tryptophan Dependent Pathway
inferredcites →https://doi.org/10.1099/00221287-93-1-177openalex-snapshot
Ethylene Production by Bacteria
inferredcites →https://doi.org/10.1104/pp.010546openalex-snapshot
Auxin and Ethylene Response Interactions during Arabidopsis Root Hair Development Dissected by Auxin Influx Modulators
inferredcites →https://doi.org/10.1104/pp.124.3.1315openalex-snapshot
Inward Potassium Channel in Guard Cells As a Target for Polyamine Regulation of Stomatal Movements
inferredcites →https://doi.org/10.1104/pp.125.2.627openalex-snapshot
Gibberellin Biosynthesis Mutations and Root Development in Pea
inferredcites →https://doi.org/10.1104/pp.125.4.2053openalex-snapshot
Azospirillum brasilense and Azospirillum lipoferum Hydrolyze Conjugates of GA20 and Metabolize the Resultant Aglycones to GA1 in Seedlings of Rice Dwarf Mutants
inferredcites →https://doi.org/10.1104/pp.41.2.234openalex-snapshot
On the Ability of Taphrina deformans to Produce Indoleacetic Acid from Tryptophan by Way of Tryptamine
inferredcites →https://doi.org/10.1104/pp.43.7.1069openalex-snapshot
Ethylene Formation in Pea Seedlings; Its Relation to the Inhibition of Bud Growth Caused by Indole-3-Acetic Acid
inferredcites →https://doi.org/10.1104/pp.90.1.45openalex-snapshot
Identification of Gibberellins A1, A3, and Iso-A3 in Cultures of Azospirillum lipoferum
inferredcites →https://doi.org/10.1104/pp.97.2.778openalex-snapshot
Cadaverine, an Essential Diamine for the Normal Root Development of Germinating Soybean (Glycine max) Seeds
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Production of Plant Growth Regulators by Rhizosphere Phosphate‐solubilizing Bacteria
inferredcites →https://doi.org/10.1111/j.1365-2672.2007.03366.xopenalex-snapshot
Early interactions between legumes and rhizobia: disclosing complexity in a molecular dialogue
inferredcites →https://doi.org/10.1111/j.1462-2920.2005.00848.xopenalex-snapshot
Comparative in situ analysis of ipdC–gfp mut3 promoter fusions of Azospirillum brasilense strains Sp7 and Sp245
inferredcites →https://doi.org/10.1111/j.1462-2920.2007.01529.xopenalex-snapshot
Organization of the ipdC region regulates IAA levels in different Azospirillum brasilense strains: molecular and functional analysis of ipdC in strain SM
inferredcites →https://doi.org/10.1111/j.1574-6941.2006.00082.xopenalex-snapshot
Phylogeny of the 1-aminocyclopropane-1-carboxylic acid deaminase-encoding gene acdS in phytobeneficial and pathogenic Proteobacteria and relation with strain biogeography
inferredcites →https://doi.org/10.1111/j.1574-6976.2007.00072.xopenalex-snapshot
Indole-3-acetic acid in microbial and microorganism-plant signaling
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Plant Growth Substances Produced by Azospirillum brasilense and Their Effect on the Growth of Pearl Millet ( Pennisetum americanum L.)
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Analysis of Indole-3-Acetic Acid and Related Indoles in Culture Medium from Azospirillum lipoferum and Azospirillum brasilense
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Promotion of nod Gene Inducers and Nodulation in Common Bean (Phaseolus vulgaris) Roots Inoculated with Azospirillum brasilense Cd
inferredcites →https://doi.org/10.1128/aem.71.4.1803-1810.2005openalex-snapshot
Azospirillum brasilense Produces the Auxin-Like Phenylacetic Acid by Using the Key Enzyme for Indole-3-Acetic Acid Biosynthesis
inferredcites →https://doi.org/10.1128/jb.181.4.1338-1342.1999openalex-snapshot
Auxins Upregulate Expression of the Indole-3-Pyruvate Decarboxylase Gene in Azospirillum brasilense
inferredcites →https://doi.org/10.1134/s000629790901012xopenalex-snapshot
Expression and functional analysis of aminotransferase involved in indole-3-acetic acid biosynthesis in Azospirillum brasilense Yu62
inferredcites →https://doi.org/10.1134/s1021443706050025openalex-snapshot
Polyamines and stress: Biological role, metabolism, and regulation
inferredcites →https://doi.org/10.1139/b09-023openalex-snapshot
Participation of abscisic acid and gibberellins produced by endophytic Azospirillum in the alleviation of drought effects in maize
inferredcites →https://doi.org/10.1139/m83-143openalex-snapshot
Determination of the most frequent N2-fixing bacteria in a rice rhizosphere
inferredcites →https://doi.org/10.1139/m83-147openalex-snapshot
Isolation and characterization of Azospirillum mutants excreting high amounts of indoleacetic acid
inferredcites →https://doi.org/10.1139/m88-125openalex-snapshot
Alteration of size of wheat root systems and nitrogen fixation by associative nitrogen-fixing bacteria measured under field conditions
inferredcites →https://doi.org/10.1139/m90-003openalex-snapshot
Possible mode of action of Azospirillum brasilense strain Cd on the root morphology and nodule formation in burr medic (Medicago polymorpha)
inferredcites →https://doi.org/10.1139/m90-105openalex-snapshot
Current status of Azospirillum inoculation technology: Azospirillum as a challenge for agriculture
inferredcites →https://doi.org/10.1139/m93-011openalex-snapshot
Tryptophan conversion to indole-3-acetic acid via indole-3-acetamide in Azospirillum brasilense Sp7
inferredcites →https://doi.org/10.1139/m93-026openalex-snapshot
Indoleacetic acid production by the rhizosphere bacterium Azospirillum brasilense Cd under in vitro conditions
inferredcites →https://doi.org/10.1139/m95-070openalex-snapshot
A novel procedure for rapid isolation of plant growth promoting pseudomonads
inferredcites →https://doi.org/10.1139/m96-032openalex-snapshot
Bacterial biosynthesis of indole-3-acetic acid
inferredcites →https://doi.org/10.1142/p130openalex-snapshot
Biochemical and Genetic Mechanisms Used by Plant Growth Promoting Bacteria
inferredcites →https://doi.org/10.1146/annurev.arplant.51.1.501openalex-snapshot
G ROWTH R ETARDANTS : Effects on Gibberellin Biosynthesis and Other Metabolic Pathways
inferredcites →https://doi.org/10.1146/annurev.arplant.53.091401.143329openalex-snapshot
S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS
inferredcites →https://doi.org/10.1146/annurev.arplant.56.032604.144046openalex-snapshot
ABSCISIC ACID BIOSYNTHESIS AND CATABOLISM
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105231openalex-snapshot
CYTOKININS: Activity, Biosynthesis, and Translocation
inferredcites →https://doi.org/10.1146/annurev.pp.13.060162.001405openalex-snapshot
The Physiology of Ethylene Formation
inferredcites →https://doi.org/10.1146/annurev.pp.22.060171.001005openalex-snapshot
Biochemistry of Symbiotic Nitrogen Fixation in Legumes
inferredcites →https://doi.org/10.1186/1471-2164-12-409openalex-snapshot
Genomic insights into the versatility of the plant growth-promoting bacterium Azospirillum amazonense
inferredcites →https://doi.org/10.1371/journal.pgen.1002430openalex-snapshot
Azospirillum Genomes Reveal Transition of Bacteria from Aquatic to Terrestrial Environments
inferredcites →https://doi.org/10.3390/genes3040576openalex-snapshot
Genome Sequence of Azospirillum brasilense CBG497 and Comparative Analyses of Azospirillum Core and Accessory Genomes provide Insight into Niche Adaptation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Transcriptomics of Plants Interacting with Pathogens and Beneficial Microbes
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Plant Probiotics for Nutrient Acquisition by Agriculturally Important Grasses: A Comprehensive Review of the Science and the Application
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Performance of soybeans inoculated with multifunctional microorganisms under water‐deficit stress
inferred← citeshttps://doi.org/10.1007/978-3-030-17597-9_4openalex-snapshot
Azospirillum as Biofertilizer for Sustainable Agriculture: Azospirillum brasilense AZ39 as a Model of PGPR and Field Traceability
inferred← citeshttps://doi.org/10.1007/978-3-030-17597-9_6openalex-snapshot
Challenges, Regulations and Future Actions in Biofertilizers in the European Agriculture: From the Lab to the Field
inferred← citeshttps://doi.org/10.1007/978-3-030-23169-9_3openalex-snapshot
Microbial Applications for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-030-30926-8_11openalex-snapshot
Regulatory Role of Rhizobacteria to Induce Drought and Salt Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1007/978-3-030-30926-8_12openalex-snapshot
Growth and Yield of Field Crops Grown Under Drought Stress Condition Is Influenced by the Application of PGPR
inferred← citeshttps://doi.org/10.1007/978-3-030-30926-8_2openalex-snapshot
Bacterial Mixtures, the Future Generation of Inoculants for Sustainable Crop Production
inferred← citeshttps://doi.org/10.1007/978-3-031-05427-3_14openalex-snapshot
Role of Phytohormones in Plant-Microbial Interaction
inferred← citeshttps://doi.org/10.1007/978-3-031-21079-2_13openalex-snapshot
Soil Salinity and Climate Change: Microbiome-Based Strategies for Mitigation of Salt Stress to Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-031-53590-1_13openalex-snapshot
Strengthening Tree Nutrition Through the Application of Biofertilizers
inferred← citeshttps://doi.org/10.1007/978-3-031-67837-0_12openalex-snapshot
Enhancing Adaptation and Stress Tolerance in Urban Plants Through Plant Growth-Promoting Rhizobacteria (PGPR)
inferred← citeshttps://doi.org/10.1007/978-3-031-76886-6_10openalex-snapshot
Physiological Mechanisms Behind the Plants and Microbes Induced Soil Remediation
inferred← citeshttps://doi.org/10.1007/978-3-031-90139-3_17openalex-snapshot
Priestia flexa—A Phosphate-Solubilizing and IAA-Producing Actinobacterium from the Rhizosphere of Oryza sativa Showing In Vitro Antagonism Against Bipolaris oryzae
inferred← citeshttps://doi.org/10.1007/978-3-032-09222-9_10openalex-snapshot
Phytohormones, Plant Growth Regulators, and Other Related Metabolites Produced by Azospirillum
inferred← citeshttps://doi.org/10.1007/978-3-032-11438-9_8openalex-snapshot
Microbial Biotechnology in Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-319-06542-7_7openalex-snapshot
Phytohormones and Other Plant Growth Regulators Produced by PGPR: The Genus Azospirillum
inferred← citeshttps://doi.org/10.1007/978-3-319-08216-5_1openalex-snapshot
Microphos: Principles, Production and Application Strategies
inferred← citeshttps://doi.org/10.1007/978-3-319-08575-3_26openalex-snapshot
Plant Hormones Produced by Microbes
inferred← citeshttps://doi.org/10.1007/978-3-319-24654-3_2openalex-snapshot
Azospirillum sp. as a Challenge for Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-319-24654-3_7openalex-snapshot
Phytohormone-Producing PGPR for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-319-54401-4_2openalex-snapshot
Plant Growth-Promoting Bacteria: Importance in Vegetable Production
inferred← citeshttps://doi.org/10.1007/978-3-319-54401-4_7openalex-snapshot
Beneficial Role of Plant Growth-Promoting Bacteria in Vegetable Production Under Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-3-319-59174-2_11openalex-snapshot
Inoculation Effects of Associative Plant Growth-Promoting Rhizobacteria on the Performance of Legumes
inferred← citeshttps://doi.org/10.1007/978-3-642-30197-1_300openalex-snapshot
The Family Rhodospirillaceae
inferred← citeshttps://doi.org/10.1007/978-981-10-0388-2_3openalex-snapshot
Plant Growth-Promoting Rhizobacteria: Key Mechanisms of Action
inferred← citeshttps://doi.org/10.1007/978-981-10-2555-6_14openalex-snapshot
The Contribution of the Use of Azospirillum sp. in Sustainable Agriculture: Learnings from the Laboratory to the Field
inferred← citeshttps://doi.org/10.1007/978-981-10-2854-0_10openalex-snapshot
PGPR-Mediated Amelioration of Crops Under Salt Stress
inferred← citeshttps://doi.org/10.1007/978-981-10-4059-7_2openalex-snapshot
The Interactions of Soil Microbes Affecting Stress Alleviation in Agroecosystems
inferred← citeshttps://doi.org/10.1007/978-981-10-6593-4_12openalex-snapshot
Harnessing the Plant Microbiome: A Key Towards Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-10-7284-0_6openalex-snapshot
Plant Growth-Promoting Rhizobacteria: Diversity and Applications
inferred← citeshttps://doi.org/10.1007/978-981-13-0149-0_14openalex-snapshot
The Role of Microbes to Improve Crop Productivity and Soil Health
inferred← citeshttps://doi.org/10.1007/978-981-13-0347-0_2openalex-snapshot
Role of Functional Bacterial Phylum Proteobacteria in Glycine max Growth Promotion Under Abiotic Stress: A Glimpse on Case Study
inferred← citeshttps://doi.org/10.1007/978-981-13-8335-9_10openalex-snapshot
Role of Halotolerant Microbes in Plant Growth Promotion Under Salt Stress Conditions
inferred← citeshttps://doi.org/10.1007/978-981-13-8495-0_10openalex-snapshot
Influence of the Rhizospheric Microbiome in Plant Health Management
inferred← citeshttps://doi.org/10.1007/978-981-15-3204-7_6openalex-snapshot
Mechanisms of Plant Growth Promotion and Functional Annotation in Mitigation of Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-981-15-6125-2_10openalex-snapshot
Rhizosphere Plant–Microbe Interactions Under Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-981-15-7447-4_8openalex-snapshot
Bioremediation of Polluted Soil by Using Plant Growth–Promoting Rhizobacteria
inferred← citeshttps://doi.org/10.1007/978-981-16-1350-0_15openalex-snapshot
A Promising Approach of Managing Seed-Borne Pathogens Through Plant Growth-Promoting Microbes
inferred← citeshttps://doi.org/10.1007/978-981-16-3840-4_6openalex-snapshot
Rhizospheric Microbes and Their Mechanism
inferred← citeshttps://doi.org/10.1007/978-981-16-7759-5_13openalex-snapshot
Role of Plant–Microbe Interactions in Combating Salinity Stress
inferred← citeshttps://doi.org/10.1007/978-981-19-4124-5_7openalex-snapshot
Plant Growth-Promoting Microbes: Key Players in Organic Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-96-3425-5_12openalex-snapshot
Mechanistic Insights of Plant-Microbe Interactions in Mitigation of Salinity Stress
inferred← citeshttps://doi.org/10.1007/978-981-97-0672-3_17openalex-snapshot
Plant Growth-Promoting Rhizobacteria (PGPR) and Plant Growth-Promoting Fungi (PGPF) for Alleviating Abiotic Stress in Plants
inferred← citeshttps://doi.org/10.1007/978-981-97-3473-3_9openalex-snapshot
Plant Growth-Promoting Rhizobacteria and Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-99-9388-8_11openalex-snapshot
Zinc-Solubilizing Microorganisms: Contributions in Nutrient Availability and Implications for Crop Productivity in Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/s00203-017-1357-2openalex-snapshot
Development and nitrate reductase activity of sugarcane inoculated with five diazotrophic strains
inferred← citeshttps://doi.org/10.1007/s00203-017-1422-xopenalex-snapshot
Revealing strategies of quorum sensing in Azospirillum brasilense strains Ab-V5 and Ab-V6
inferred← citeshttps://doi.org/10.1007/s00203-018-1535-xopenalex-snapshot
Antioxidant activity and induction of mechanisms of resistance to stresses related to the inoculation with Azospirillum brasilense
inferred← citeshttps://doi.org/10.1007/s00203-018-1594-zopenalex-snapshot
Modulation of nitrogen metabolism of maize plants inoculated with Azospirillum brasilense and Herbaspirillum seropedicae
inferred← citeshttps://doi.org/10.1007/s00203-021-02361-zopenalex-snapshot
The auxin-producing Bacillus thuringiensis RZ2MS9 promotes the growth and modifies the root architecture of tomato (Solanum lycopersicum cv. Micro-Tom)
inferred← citeshttps://doi.org/10.1007/s00203-024-03890-zopenalex-snapshot
Metabolic and physiological adaptations of microalgal growth-promoting bacterium Azospirillum brasilense growing under biogas atmosphere: a microarray-based transcriptome analysis
inferred← citeshttps://doi.org/10.1007/s00248-017-1139-zopenalex-snapshot
Azospirillum brasilense Increases CO2 Fixation on Microalgae Scenedesmus obliquus, Chlorella vulgaris, and Chlamydomonas reinhardtii Cultured on High CO2 Concentrations
inferred← citeshttps://doi.org/10.1007/s00253-019-10045-4openalex-snapshot
Drought tolerance improvement in plants: an endophytic bacterial approach
inferred← citeshttps://doi.org/10.1007/s00253-022-12220-6openalex-snapshot
Chitosan/starch beads as bioinoculants carrier: long-term survival of bacteria and plant growth promotion
inferred← citeshttps://doi.org/10.1007/s00284-023-03570-zopenalex-snapshot
Assessment of Plant Growth-Promoting Parameters of Endophytes Isolated from Calotropis procera and Their Performance Under Irrigated and Non-irrigated Conditions
inferred← citeshttps://doi.org/10.1007/s00299-018-2328-zopenalex-snapshot
Salt stress alleviation in citrus plants by plant growth-promoting rhizobacteria Pseudomonas putida and Novosphingobium sp.
inferred← citeshttps://doi.org/10.1007/s00344-017-9712-8openalex-snapshot
Auxin, Cytokinin, and Ethylene Involved in Rice N Availability Improvement Caused by Endophyte Phomopsis liquidambari
inferred← citeshttps://doi.org/10.1007/s00344-020-10065-9openalex-snapshot
Inoculation with Azospirillum lipoferum or Azotobacter chroococcum Reinforces Maize Growth by Improving Physiological Activities Under Saline Conditions
inferred← citeshttps://doi.org/10.1007/s00344-020-10241-xopenalex-snapshot
Comparative Effects of Azospirillum brasilense Sp245 and Pseudomonas aeruginosa PAO1 Lipopolysaccharides on Wheat Seedling Growth and Peroxidase Activity
inferred← citeshttps://doi.org/10.1007/s00344-021-10457-5openalex-snapshot
Halotolerant Plant Growth-Promoting Rhizobacteria Induce Salinity Tolerance in Wheat by Enhancing the Expression of SOS Genes
inferred← citeshttps://doi.org/10.1007/s00344-024-11534-1openalex-snapshot
Seed Priming Alters the Microbial Community Composition in Seedlings of Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s00344-025-11954-7openalex-snapshot
Halo-Tolerant Phosphate-Solubilising Bacterium from Coral Reef: A Potential Bioagent for Phosphate Reclamation and Soil Fertility Enhancement
inferred← citeshttps://doi.org/10.1007/s00374-020-01453-0openalex-snapshot
Changes in root morphological traits in soybean co-inoculated with Bradyrhizobium spp. and Azospirillum brasilense or treated with A. brasilense exudates
inferred← citeshttps://doi.org/10.1007/s00374-020-01463-yopenalex-snapshot
Everything you must know about Azospirillum and its impact on agriculture and beyond
inferred← citeshttps://doi.org/10.1007/s00374-024-01795-zopenalex-snapshot
Enhancement of late-sown maize production with immobilized bacteria in chitosan/starch beads in different crop management conditions
inferred← citeshttps://doi.org/10.1007/s00374-026-01992-yopenalex-snapshot
Synergistic effects from combining foliar and soil inoculation of plant growth promoting microbes: enhanced sugarcane physiology and rhizosphere modulation via organic acid exudation and nitrogen - cycling
inferred← citeshttps://doi.org/10.1007/s00411-022-00985-3openalex-snapshot
Phytoremediation of 137Cs: factors and consequences in the environment
inferred← citeshttps://doi.org/10.1007/s00425-026-05134-4openalex-snapshot
More is not always better: phosphorus context shapes the effectiveness of single-strain and consortium plant growth-promoting bacteria in tomato
inferred← citeshttps://doi.org/10.1007/s00438-018-1439-0openalex-snapshot
Genomic characterization of Nitrospirillum amazonense strain CBAmC, a nitrogen-fixing bacterium isolated from surface-sterilized sugarcane stems
inferred← citeshttps://doi.org/10.1007/s00449-023-02947-5openalex-snapshot
Synergic association of the consortium Arthrospira maxima with the microalga growth-promoting bacterium Azospirillum cultured under the stressful biogas composition
inferred← citeshttps://doi.org/10.1007/s00709-020-01552-7openalex-snapshot
The nature of the interaction Azospirillum-Arabidopsis determine the molecular and morphological changes in root and plant growth promotion
inferred← citeshttps://doi.org/10.1007/s10343-023-00861-0openalex-snapshot
Fungal Root Rots of Sugar Beets: A Review of Common Causal Agents and Management Strategies
inferred← citeshttps://doi.org/10.1007/s10343-025-01254-1openalex-snapshot
Metabolic profiling and characterization of plant growth promoting traits of endophytic bacteria to ensure their potential as bio-inoculants
inferred← citeshttps://doi.org/10.1007/s10482-018-1108-7openalex-snapshot
Multifunctional potential of endophytic and rhizospheric microbial isolates associated with Butia purpurascens roots for promoting plant growth
inferred← citeshttps://doi.org/10.1007/s10482-025-02100-0openalex-snapshot
The role of endophytic bacteria in enhancing plant growth and health for sustainable agriculture
inferred← citeshttps://doi.org/10.1007/s10529-021-03114-0openalex-snapshot
Lipopeptide production by Bacillus atrophaeus strain B44 and its biocontrol efficacy against cotton rhizoctoniosis
inferred← citeshttps://doi.org/10.1007/s10705-020-10100-xopenalex-snapshot
Nitrogen acquisition and 15N-fertiliser recovery efficiency of sugarcane cultivar RB92579 inoculated with five diazotrophs
inferred← citeshttps://doi.org/10.1007/s10725-026-01463-2openalex-snapshot
Frontiers in Azotobacter-mediated plant development and stress mitigation: proteomic, nanobiotechnology, and genomic insights
inferred← citeshttps://doi.org/10.1007/s10811-019-01862-1openalex-snapshot
Azospirillum brasilense-microalga interaction increases growth and accumulation of cell compounds in Chlorella vulgaris and Tetradesmus obliquus cultured under nitrogen stress
inferred← citeshttps://doi.org/10.1007/s10811-020-02202-4openalex-snapshot
Biofertilization with Macrocystis pyrifera algae extracts combined with PGPR-enhanced growth in Lactuca sativa seedlings
inferred← citeshttps://doi.org/10.1007/s11033-020-05676-0openalex-snapshot
Plant growth promoting Pseudomonas aeruginosa from Valeriana wallichii displays antagonistic potential against three phytopathogenic fungi
inferred← citeshttps://doi.org/10.1007/s11104-015-2546-xopenalex-snapshot
Beneficial microorganisms for soybean (Glycine max (L.) Merr), with a focus on low root-zone temperatures
inferred← citeshttps://doi.org/10.1007/s11104-019-04101-1openalex-snapshot
Inoculation with five diazotrophs alters nitrogen metabolism during the initial growth of sugarcane varieties with contrasting responses to added nitrogen
inferred← citeshttps://doi.org/10.1007/s11104-019-04124-8openalex-snapshot
The ammonium excreting Azospirillum brasilense strain HM053: a new alternative inoculant for maize
inferred← citeshttps://doi.org/10.1007/s11104-019-04201-yopenalex-snapshot
Transcriptome and proteome profiles of the diazotroph Nitrospirillum amazonense strain CBAmC in response to the sugarcane apoplast fluid
inferred← citeshttps://doi.org/10.1007/s11104-019-04388-0openalex-snapshot
Interaction of phytohormone-producing rhizobia with sugarcane mini-setts and their effect on plant development
inferred← citeshttps://doi.org/10.1007/s11104-023-06120-5openalex-snapshot
Growth response and bacterial colonization of Urochloa cultivars inoculated with different species of diazotrophs
inferred← citeshttps://doi.org/10.1007/s11104-025-08178-9openalex-snapshot
A century of research on Azospirillum and still so much to discover
inferred← citeshttps://doi.org/10.1007/s11270-017-3309-5openalex-snapshot
Rhizobacterial Pseudomonas spp. Strains Harbouring acdS Gene Could Enhance Metallicolous Legume Nodulation in Zn/Pb/Cd Mine Tailings
inferred← citeshttps://doi.org/10.1007/s11274-014-1669-1openalex-snapshot
Phosphate solubilization potential and modeling of stress tolerance of rhizobacteria from rice paddy soil in northern Iran
inferred← citeshttps://doi.org/10.1007/s11274-025-04708-wopenalex-snapshot
Unlocking phosphorus in saline environments: simplified bacterial communities enhance P cycling and maize growth
inferred← citeshttps://doi.org/10.1007/s11274-026-05141-3openalex-snapshot
Co-cultivation of diazotrophic bacteria enhances auxin-mediated root development in maize: implications for microbial inoculants
inferred← citeshttps://doi.org/10.1007/s11356-023-27820-6openalex-snapshot
Exploration of plant growth promoting traits and regulatory mechanisms of Bacillus anthracis PM21 in enhancing salt stress tolerance in maize
inferred← citeshttps://doi.org/10.1007/s11540-020-09465-xopenalex-snapshot
Molecular Identification and In Vitro Plant Growth-Promoting Activities of Culturable Potato (Solanum tuberosum L.) Rhizobacteria in Tanzania
inferred← citeshttps://doi.org/10.1007/s12223-024-01195-8openalex-snapshot
Biopriming with multifarious sulphur-oxidizing bacteria improve in vitro Vigna radiata L. (mung bean) and Brassica juncea L. (mustard) seed germination
inferred← citeshttps://doi.org/10.1007/s12298-021-01036-9openalex-snapshot
Azospirillum brasilense Sp245 triggers cytokinin signaling in root tips and improves biomass accumulation in Arabidopsis through canonical cytokinin receptors
inferred← citeshttps://doi.org/10.1007/s12355-022-01133-3openalex-snapshot
Integrated Application of Nitrogen, Molybdenum and Plant Growth-Promoting Rhizobacterium can Enhance the Sugarcane Growth
inferred← citeshttps://doi.org/10.1007/s13199-017-0536-xopenalex-snapshot
The benefits of foliar inoculation with Azospirillum brasilense in soybean are explained by an auxin signaling model
inferred← citeshttps://doi.org/10.1007/s13199-018-00589-wopenalex-snapshot
Dynamics of endogenous hormone regulation in plants by phytohormone secreting rhizobacteria under water-stress
inferred← citeshttps://doi.org/10.1007/s13199-018-0568-xopenalex-snapshot
Improvement of soybean grain nutritional quality under foliar inoculation with Azospirillum brasilense strain Az39
inferred← citeshttps://doi.org/10.1007/s13199-020-00730-8openalex-snapshot
Field response of two seed propagated elephant grass genotypes to diazotrophic bacterial inoculation and in situ confocal microscopy colonization analyses
inferred← citeshttps://doi.org/10.1007/s13199-024-00980-wopenalex-snapshot
Unlocking the Secrets of Rhizosphere Microbes: A New Dimension for Agriculture
inferred← citeshttps://doi.org/10.1007/s13205-018-1428-3openalex-snapshot
A resourceful methodology to profile indolic auxins produced by rhizo-fungi using spectrophotometry and HPTLC
inferred← citeshttps://doi.org/10.1007/s13205-025-04243-3openalex-snapshot
Unlocking the potential of ecofriendly guardians for biological control of plant diseases, crop protection and production in sustainable agriculture
inferred← citeshttps://doi.org/10.1007/s13213-015-1154-6openalex-snapshot
Agronomic and environmental aspects of diazotrophic bacteria in rice fields
inferred← citeshttps://doi.org/10.1007/s13399-021-01543-5openalex-snapshot
Comparative assessment of different biofertilizers in maize (Zea mays L.) cultivation
inferred← citeshttps://doi.org/10.1007/s41348-023-00824-7openalex-snapshot
Biological control of soil-borne pathogens in arid lands: a review
inferred← citeshttps://doi.org/10.1007/s42398-018-0025-zopenalex-snapshot
Plant growth promoting potential of Aspergillus sp. NPF7, isolated from wheat rhizosphere in South Gujarat, India
inferred← citeshttps://doi.org/10.1007/s42452-025-06468-6openalex-snapshot
Employing plant growth-promoting rhizobacteria for abiotic stress mitigation in plants: with a focus on drought stress
inferred← citeshttps://doi.org/10.1007/s42535-022-00415-1openalex-snapshot
Convoluted role of cyanobacteria as biofertilizer: an insight of sustainable agriculture
inferred← citeshttps://doi.org/10.1007/s42535-023-00763-6openalex-snapshot
Effect of different concentrations of pyridoxine on physiological indices of Brassica rapa varieties
inferred← citeshttps://doi.org/10.1007/s42729-022-00909-6openalex-snapshot
Modulation of Maize Rhizosphere Microbiota Composition by Inoculation with Azospirillum argentinense Az39 (Formerly A. brasilense Az39)
inferred← citeshttps://doi.org/10.1007/s42729-022-00948-zopenalex-snapshot
Previous Incubation of Bradyrhizobium japonicum E109 and Azospirillum argentinense Az39 (formerly A. brasilense Az39) Improves the Bradyrhizobium-Soybean Symbiosis
inferred← citeshttps://doi.org/10.1007/s42729-026-03315-4openalex-snapshot
Elucidating the Functional Role of PGPR in Modulating Plant Physiology for Improved Drought Resilience and Yield Enhancement: A Review
inferred← citeshttps://doi.org/10.1007/s42770-021-00618-9openalex-snapshot
Brief history of biofertilizers in Brazil: from conventional approaches to new biotechnological solutions
inferred← citeshttps://doi.org/10.1007/s42770-021-00651-8openalex-snapshot
Stimulatory effects of defective and effective 3-indoleacetic acid-producing bacterial strains on rice in an advanced stage of its vegetative cycle
inferred← citeshttps://doi.org/10.1007/s42770-023-01236-3openalex-snapshot
Maize—Azospirillum brasilense interaction: accessing maize’s miRNA expression under the effect of an inhibitor of indole-3-acetic acid production by the plant
inferred← citeshttps://doi.org/10.1007/s42770-025-01802-xopenalex-snapshot
Diversity of grass-associated Nitrospirillum and proposal of six novel species
inferred← citeshttps://doi.org/10.1007/s42976-023-00464-5openalex-snapshot
Identification and comparative analysis of differential proteins expression in rice under biotic stress by protein sequencing
inferred← citeshttps://doi.org/10.1007/s42976-024-00570-yopenalex-snapshot
Foliar application of Azospirillum brasilense, salicylic acid and zinc on wheat Performance under rain–fed condition
inferred← citeshttps://doi.org/10.1007/s43538-025-00537-5openalex-snapshot
Isolation and characterization of plant growth-promoting bacteria exhibiting ACC deaminase production in soil samples
inferred← citeshttps://doi.org/10.1007/s43621-026-02778-wopenalex-snapshot
Plant growth-promoting bacteria as biological controls for sustainable crop protection against agricultural biodeterioration
inferred← citeshttps://doi.org/10.1007/s44279-025-00177-9openalex-snapshot
Harnessing biostimulants for sustainable agriculture: innovations, challenges, and future prospects
inferred← citeshttps://doi.org/10.1007/s44447-026-00187-zopenalex-snapshot
Integrating intercropping, nitrogen fertilization and Azospirillum spp. to enhance growth, yield, and quality of sweet corn-sweet potato systems in sandy land
inferred← citeshttps://doi.org/10.1016/b978-0-12-801535-3.00008-5openalex-snapshot
Soybeans, Stress, and Plant Growth-Promoting Rhizobacteria
inferred← citeshttps://doi.org/10.1016/b978-0-12-816483-9.00020-7openalex-snapshot
Impact of Climate Change on Soil Carbon Exchange, Ecosystem Dynamics, and Plant–Microbe Interactions
inferred← citeshttps://doi.org/10.1016/b978-0-12-818204-8.00003-5openalex-snapshot
Salinity and its tolerance strategies in plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-821667-5.00021-xopenalex-snapshot
Bacillus spp.: A bio-inoculant factory for plant growth promotion and immune enhancement
inferred← citeshttps://doi.org/10.1016/b978-0-323-89973-4.00014-4openalex-snapshot
Rhizosphere engineering through pesticides-degrading beneficial bacteria
inferred← citeshttps://doi.org/10.1016/b978-0-323-91132-0.00003-4openalex-snapshot
Microbiological impact and control strategies to monitor postharvest losses in fruits and vegetables
inferred← citeshttps://doi.org/10.1016/b978-0-323-91875-6.00012-8openalex-snapshot
Plant growth-promoting microbiomes: History and their role in agricultural crop improvement
inferred← citeshttps://doi.org/10.1016/b978-0-323-91883-1.00016-4openalex-snapshot
Role of phytohormones in biotic vs abiotic stresses with respect to PGPR and autophagy
inferred← citeshttps://doi.org/10.1016/b978-0-443-15924-4.00001-1openalex-snapshot
Precision biotechnology using beneficial microbes as a fundamental approach to the circular economy
inferred← citeshttps://doi.org/10.1016/b978-0-443-18446-8.00012-7openalex-snapshot
Plant growth-promoting microorganisms: Ecology and use in sustainable agricultural systems
inferred← citeshttps://doi.org/10.1016/b978-0-443-18446-8.00014-0openalex-snapshot
Plant growth promoting rhizobacteria (PGPR): A green approach to manage soil-borne fungal pathogens and plant growth promotion
inferred← citeshttps://doi.org/10.1016/b978-0-443-18446-8.00019-xopenalex-snapshot
Bioprospecting of microbial bioactive molecules for the management of biotic and abiotic stress
inferred← citeshttps://doi.org/10.1016/b978-0-443-23560-3.00024-3openalex-snapshot
Microbial inoculants as crop enhancers
inferred← citeshttps://doi.org/10.1016/b978-0-443-33594-5.00007-xopenalex-snapshot
Regulation of metabolites in plants by stress-tolerant plant growth promoting rhizobacteria
inferred← citeshttps://doi.org/10.1016/b978-0-443-34055-0.00018-7openalex-snapshot
Azospirillum and its influence on efficient nutrient acquisition by plants: a model beyond phytohormones
inferred← citeshttps://doi.org/10.1016/b978-0-444-63504-4.00003-7openalex-snapshot
Role of Rhizobacterial Secondary Metabolites in Crop Protection Against Agricultural Pests and Diseases
inferred← citeshttps://doi.org/10.1016/bs.abr.2025.04.001openalex-snapshot
Genetic engineering of rhizosphere microbes towards crop improvement
inferred← citeshttps://doi.org/10.1016/bs.agron.2025.03.006openalex-snapshot
Deciphering PGPR mechanisms in saline soils: Enhancing plant productivity
inferred← citeshttps://doi.org/10.1016/j.apsoil.2018.08.015openalex-snapshot
Rooting and growth of pre-germinated sugarcane seedlings inoculated with diazotrophic bacteria
inferred← citeshttps://doi.org/10.1016/j.apsoil.2024.105416openalex-snapshot
Unravelling the role of plant growth promoting rhizobacteria in boosting plant growth and phytoremediation of heavy metals
inferred← citeshttps://doi.org/10.1016/j.apsoil.2024.105591openalex-snapshot
Biofilm-forming microorganisms in the rhizosphere to improve plant growth: Coping with abiotic stress and environmental pollution
inferred← citeshttps://doi.org/10.1016/j.apsoil.2026.107483openalex-snapshot
Mechanisms and evidence for nitrous oxide mitigation by microbial inoculants in agricultural soils: A critical review
inferred← citeshttps://doi.org/10.1016/j.bcab.2020.101842openalex-snapshot
Role of plant growth-promoting bacteria in sustainable agriculture
inferred← citeshttps://doi.org/10.1016/j.bcab.2020.101878openalex-snapshot
Plant growth-promoting rhizobacteria: Potential improvement in antioxidant defense system and suppression of oxidative stress for alleviating salinity stress in Triticum aestivum (L.) plants
inferred← citeshttps://doi.org/10.1016/j.bcab.2023.102730openalex-snapshot
Isolation and screening of multi-trait plant growth-promoting rhizobacteria (PGPR) colonizing saffron (Crocus sativus L.) rhizosphere
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2020.107612openalex-snapshot
Potential of phytohormones as a strategy to improve microalgae productivity for biotechnological applications
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2024.142431openalex-snapshot
The halotolerant exopolysaccharide-producing Rhizobium azibense increases the salt tolerance mechanism in Phaseolus vulgaris (L.) by improving growth, ion homeostasis, and antioxidant defensive enzymes
inferred← citeshttps://doi.org/10.1016/j.cpb.2019.100116openalex-snapshot
Proficiency of biocontrol agents as plant growth promoters and hydrolytic enzyme producers in Ganoderma boninense infected oil palm seedlings
inferred← citeshttps://doi.org/10.1016/j.crmicr.2021.100094openalex-snapshot
Biofertilizers: An ecofriendly technology for nutrient recycling and environmental sustainability
inferred← citeshttps://doi.org/10.1016/j.crmicr.2024.100285openalex-snapshot
Drought stress mitigation through bioengineering of microbes and crop varieties for sustainable agriculture and food security
inferred← citeshttps://doi.org/10.1016/j.ejbt.2016.02.001openalex-snapshot
Indole acetic acid and ACC deaminase from endophytic bacteria improves the growth of Solanum lycopersicum
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104529openalex-snapshot
Does inoculation with associative bacteria improve tolerance to nitrogen deficiency in seedlings of Neotropical tree species?
inferred← citeshttps://doi.org/10.1016/j.foodchem.2025.146713openalex-snapshot
A simple and rapid screening method for 2,4-dichlorophenoxyacetic acid (2,4-D) determination in environmental and vegetable samples by colorimetry combined with multivariate optimization
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e14618openalex-snapshot
Agronomic performance and quality of baby corn in response to the inoculation of seeds with Azospirillum brasilense and nitrogen fertilization in the summer harvest
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e28754openalex-snapshot
Impact of historical soil management on the interaction of plant-growth-promoting bacteria with maize (Zea mays L.)
inferred← citeshttps://doi.org/10.1016/j.jenvman.2019.109779openalex-snapshot
Understanding the molecular mechanisms for the enhanced phytoremediation of heavy metals through plant growth promoting rhizobacteria: A review
inferred← citeshttps://doi.org/10.1016/j.jenvman.2020.111118openalex-snapshot
Unlocking the potential of plant growth-promoting rhizobacteria on soil health and the sustainability of agricultural systems
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.132142openalex-snapshot
Response of peanut plant and soil N-fixing bacterial communities to conventional and biodegradable microplastics
inferred← citeshttps://doi.org/10.1016/j.jplph.2015.11.007openalex-snapshot
Native plant growth promoting bacteria Bacillus thuringiensis and mixed or individual mycorrhizal species improved drought tolerance and oxidative metabolism in Lavandula dentata plants
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153437openalex-snapshot
Interactive effects of plant growth-promoting rhizobacteria and a seaweed extract on the growth and physiology of Allium cepa L. (onion)
inferred← citeshttps://doi.org/10.1016/j.micres.2017.04.007openalex-snapshot
In vitro PGPR properties and osmotic tolerance of different Azospirillum native strains and their effects on growth of maize under drought stress
inferred← citeshttps://doi.org/10.1016/j.micres.2017.09.007openalex-snapshot
Screening of tropically derived, multi-trait plant growth- promoting rhizobacteria and evaluation of corn and soybean colonization ability
inferred← citeshttps://doi.org/10.1016/j.micres.2018.01.003openalex-snapshot
Isolation, identification, and the growth promoting effects of two antagonistic actinomycete strains from the rhizosphere of Mikania micrantha Kunth
inferred← citeshttps://doi.org/10.1016/j.micres.2019.04.005openalex-snapshot
Beneficial effects of inoculation of growth-promoting bacteria in strawberry
inferred← citeshttps://doi.org/10.1016/j.micres.2020.126516openalex-snapshot
Isolation of a novel rhizobacteria having multiple plant growth promoting traits and antifungal activity against certain phytopathogens
inferred← citeshttps://doi.org/10.1016/j.micres.2020.126585openalex-snapshot
Endophytic bacteria of garlic roots promote growth of micropropagated meristems
inferred← citeshttps://doi.org/10.1016/j.micres.2022.127218openalex-snapshot
The key role of indole-3-acetic acid biosynthesis by Bacillus thuringiensis RZ2MS9 in promoting maize growth revealed by the ipdC gene knockout mediated by the CRISPR-Cas9 system
inferred← citeshttps://doi.org/10.1016/j.micres.2024.127650openalex-snapshot
Phenogenetic profile and agronomic contribution of Azospirillum argentinense Az39T, a reference strain for the South American inoculant industry
inferred← citeshttps://doi.org/10.1016/j.microb.2025.100361openalex-snapshot
How protists contribute to plant growth and health: Exploring new interactions with the plant microbiome
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131200openalex-snapshot
Preparation and evaluation of Ca/Mg-layered double hydroxide as a novel modifier for electrochemical determination of gibberellic acid
inferred← citeshttps://doi.org/10.1016/j.nbt.2016.01.009openalex-snapshot
Mining the genome of Rhodococcus fascians, a plant growth-promoting bacterium gone astray
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113098openalex-snapshot
Phytohormone-microbial nexus targeting-next-generation strategy for fruit growth and postharvest resilience
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.07.021openalex-snapshot
Enhanced drought tolerance in seedlings of Neotropical tree species inoculated with plant growth-promoting bacteria
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110579openalex-snapshot
Co-inoculation of Bradyrhizobium and Azospirillum mitigates the deleterious effects of waterlogging in soybean plants in a scenario of enhanced atmospheric CO2
inferred← citeshttps://doi.org/10.1016/j.pmpp.2021.101753openalex-snapshot
Dry root rot disease, an emerging threat to citrus industry worldwide under climate change: A review
inferred← citeshttps://doi.org/10.1016/j.pmpp.2025.102615openalex-snapshot
Harnessing Achromobacter xylosoxidans SPSB-5 for enhanced P-solubilization, biotic/abiotic stress tolerance, and improved growth of Brassica juncea (L.) seedlings in saline environment
inferred← citeshttps://doi.org/10.1016/j.resmic.2018.04.002openalex-snapshot
New insights into auxin metabolism in Bradyrhizobium japonicum
inferred← citeshttps://doi.org/10.1016/j.resmic.2021.103814openalex-snapshot
Molecular and physiological analysis of indole-3-acetic acid degradation in Bradyrhizobium japonicum E109
inferred← citeshttps://doi.org/10.1016/j.resmic.2025.104295openalex-snapshot
MibR and LibR are involved in the transcriptional regulation of the ipdC gene in Azospirillum brasilense Sp7
inferred← citeshttps://doi.org/10.1016/j.rhisph.2024.100873openalex-snapshot
Seed bio-priming with ACC deaminase-producing bacterial strains alleviates impact of drought stress in Soybean (Glycine max (L.) Merr.)
inferred← citeshttps://doi.org/10.1016/j.scienta.2015.07.020openalex-snapshot
Role of plant growth promoting rhizobacteria in sustainable production of vegetables: Current perspective
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.09.298openalex-snapshot
Stable and radioactive cesium: A review about distribution in the environment, uptake and translocation in plants, plant reactions and plants' potential for bioremediation
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2018.10.312openalex-snapshot
Strontium in the environment: Review about reactions of plants towards stable and radioactive strontium isotopes
inferred← citeshttps://doi.org/10.1016/j.soilbio.2016.08.020openalex-snapshot
Azospirillum sp. in current agriculture: From the laboratory to the field
inferred← citeshttps://doi.org/10.1016/j.soilbio.2023.109292openalex-snapshot
The interplay between Azospirillum brasilense and the native bacterial communities in the soil and rhizosphere of maize (Zea mays L.)
inferred← citeshttps://doi.org/10.1016/j.stress.2025.101164openalex-snapshot
Integrated transcriptomic and metabolomic analysis reveals plant growth-promoting bacteria consortia-induced isoflavonoid biosynthesis as a key mechanism alleviating drought stress in Sophora tonkinensis Gagnep
inferred← citeshttps://doi.org/10.1016/j.syapm.2019.05.003openalex-snapshot
Metatranscriptomics and nitrogen fixation from the rhizoplane of maize plantlets inoculated with a group of PGPRs
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