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Bacterial biosynthesis of indole-3-acetic acid
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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The complete nucleotide sequence of the TL‐DNA of the Agrobacterium tumefaciens plasmid pTiAch5.
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Characterization of High-Frequency Deletions in the iaa-Containing Plasmid, pIAA2, of Pseudomonas syringae pv. savastanoi
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Conversion of Tryptophan, Indole-3-Pyruvic Acid, Indole-3-Lactic Acid and Indole to Indole-3-Acetic Acid by Azospirillum brasilense Sp7
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Involvement of IAA in the interaction between Azospirillum brasilense and Panicum miliaceum roots
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Plant Hormones and their Role in Plant Growth and Development
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Acetobacter diazotrophicus, an indoleacetic acid producing bacterium isolated from sugarcane cultivars of M�xico
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Control of cell proliferation during plant development
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Isolation and functional analysis of a set of auxin genes with low root-inducing activity from an Agrobacterium tumefaciens biotype III strain
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Molecular cloning of the gene for indolepyruvate decarboxylase from Enterobacter cloacae
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/bf00293823openalex-snapshot
Mutants of Nicotiana plumbaginifolia with increased sensitivity to auxin
inferredcites →https://doi.org/10.1007/bf00337774openalex-snapshot
Transposon Tn5 mutagenesis in Azospirillum lipoferum: isolation of indole acetic acid mutants
inferredcites →https://doi.org/10.1007/bf00380852openalex-snapshot
Endogenous and exogenous auxin in the control of root growth
inferredcites →https://doi.org/10.1007/bf00383526openalex-snapshot
Genetic analysis of the individual T-DNA genes of Agrobacterium tumefaciens; further evidence that two genes are involved in indole-3-acetic acid synthesis
inferredcites →https://doi.org/10.1007/bf00396089openalex-snapshot
Effect of applied and endogenous indol-3-yl-acetic acid on maize root growth
inferredcites →https://doi.org/10.1007/bf00398689openalex-snapshot
Endogenous indoles and the biosynthesis and metabolism of indole-3-acetic acid in cultures of Rhizobium phaseoli
inferredcites →https://doi.org/10.1007/bf00425657openalex-snapshot
Genetic evidence that the tryptophan 2-mono-oxygenase gene of Pseudomonas savastonoi is functionally equivalent to one of the T-DNA genes involved in plant tumour formation by Agrobacterium tumefaciens
inferredcites →https://doi.org/10.1007/bf01577732openalex-snapshot
Tryptophan catabolism to indolepyruvic and indoleacetic acids byRhizobium japonicum L-259 mutants
inferredcites →https://doi.org/10.1007/bf02902155openalex-snapshot
Auxin formation by rhizosphere bacteria as a factor of root growth
inferredcites →https://doi.org/10.1007/s002849900012openalex-snapshot
Isolation and Characterization of Mutants of the Plant Growth-Promoting Rhizobacterium Pseudomonas putida GR12-2 That Overproduce Indoleacetic Acid
inferredcites →https://doi.org/10.1016/0014-5793(86)80436-7openalex-snapshot
Agrobacterium T‐DNA gene 1 codes for tryptophan 2‐monooxygenase activity in tobacco crown gall cells
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(93)90225-zopenalex-snapshot
Growth promotion of blackcurrant softwood cuttings by recombinant strain Pseudomonas fluorescens BSP53a synthesizing an increased amount of indole-3-acetic acid
inferredcites →https://doi.org/10.1016/0167-4838(94)90191-0openalex-snapshot
Involvement of l-tryptophan aminotransferase in indole-3-acetic acid biosynthesis in Enterobacter cloacae
inferredcites →https://doi.org/10.1016/0167-4838(95)00011-iopenalex-snapshot
Structure and function of indolepyruvate decarboxylase, a key enzyme in indole-3-acetic acid biosynthesis
inferredcites →https://doi.org/10.1016/0167-7799(92)90283-2openalex-snapshot
Enzymatic synthesis of acrylamide: a success story not yet over
inferredcites →https://doi.org/10.1016/0378-1097(94)90474-xopenalex-snapshot
Versatile nitrilases: Nitrile-hydrolysing enzymes
inferredcites →https://doi.org/10.1016/0885-5765(91)90001-xopenalex-snapshot
Indole-3-acetic acid biosynthetic pathways in Erwinia herbicola in relation to pathogenicity on Gypsophila paniculata
inferredcites →https://doi.org/10.1016/0923-2508(93)90216-oopenalex-snapshot
Effect on wheat root development of inoculation with an Azospirillum brasilense mutant with altered indole-3-acetic acid production
inferredcites →https://doi.org/10.1016/0962-8924(94)90122-8openalex-snapshot
Approaches to understanding auxin action
inferredcites →https://doi.org/10.1016/s0021-9258(18)50276-3openalex-snapshot
A new metabolic pathway of tryptophan initiated by tryptophan side chain oxidase.
inferredcites →https://doi.org/10.1016/s0021-9258(18)68787-3openalex-snapshot
Purification and properties of a nitrilase specific for the herbicide bromoxynil and corresponding nucleotide sequence analysis of the bxn gene.
inferredcites →https://doi.org/10.1016/s0021-9258(18)88968-2openalex-snapshot
Regulation of 3-indoleacetic acid production in Pseudomonas syringae pv. savastanoi. Purification and properties of tryptophan 2-monooxygenase.
inferredcites →https://doi.org/10.1016/s0277-5387(97)00068-5openalex-snapshot
Mössbauer spectroscopic evidence for the reduction of iron(III) by anthranilic acid in aqueous solution
inferredcites →https://doi.org/10.1016/s0944-5013(11)80108-4openalex-snapshot
Effects of pH and glucose on auxin production of phosphate-solubilizing rhizobacteria in vitro
inferredcites →https://doi.org/10.1016/s0944-5013(11)80132-1openalex-snapshot
Biosynthesis of auxins by phosphate-solubilizing rhizobacteria from wheat (Triticum aestivum and rye (Secale cereale)
inferredcites →https://doi.org/10.1038/364161a0openalex-snapshot
Arabidopsis auxin-resistance gene AXR1 encodes a protein related to ubiquitin-activating enzyme E1
inferredcites →https://doi.org/10.1042/bj1000169openalex-snapshot
The production of tryptamine from tryptophan by Bacillus cereus (KVT)
inferredcites →https://doi.org/10.1073/pnas.79.9.2812openalex-snapshot
Agrobacterium Ti plasmid indoleacetic acid gene is required for crown gall oncogenesis
inferredcites →https://doi.org/10.1073/pnas.81.16.5071openalex-snapshot
Crown gall oncogenesis: evidence that a T-DNA gene from the Agrobacterium Ti plasmid pTiA6 encodes an enzyme that catalyzes synthesis of indoleacetic acid.
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/10.1073/pnas.82.19.6522openalex-snapshot
Nucleotide sequences of the Pseudomonas savastanoi indoleacetic acid genes show homology with Agrobacterium tumefaciens T-DNA
inferredcites →https://doi.org/10.1073/pnas.90.1.247openalex-snapshot
Nitrilase in biosynthesis of the plant hormone indole-3-acetic acid from indole-3-acetonitrile: cloning of the Alcaligenes gene and site-directed mutagenesis of cysteine residues.
inferredcites →https://doi.org/10.1073/pnas.90.2.442openalex-snapshot
The conserved lysine of the catalytic domain of protein kinases is actively involved in the phosphotransfer reaction and not required for anchoring ATP.
inferredcites →https://doi.org/10.1073/pnas.90.21.10355openalex-snapshot
Arabidopsis thaliana auxotrophs reveal a tryptophan-independent biosynthetic pathway for indole-3-acetic acid.
inferredcites →https://doi.org/10.1073/pnas.90.24.11442openalex-snapshot
Cellular signaling: new insights into the action of the plant growth hormone auxin.
inferredcites →https://doi.org/10.1073/pnas.91.13.6021openalex-snapshot
Molecular characterization of two cloned nitrilases from Arabidopsis thaliana: key enzymes in biosynthesis of the plant hormone indole-3-acetic acid.
inferredcites →https://doi.org/10.1073/pnas.91.14.6649openalex-snapshot
Differential regulation of an auxin-producing nitrilase gene family in Arabidopsis thaliana.
inferredcites →https://doi.org/10.1073/pnas.92.3.714openalex-snapshot
Occurrence of enzymes involved in biosynthesis of indole-3-acetic acid from indole-3-acetonitrile in plant-associated bacteria, Agrobacterium and Rhizobium.
inferredcites →https://doi.org/10.1080/00021369.1991.10870678openalex-snapshot
IAA Biosynthetic Pathway from TryptophanviaIndole-3-pyruvic Acid inEnterobacter cloacae
inferredcites →https://doi.org/10.1080/15324988709381135openalex-snapshot
The effect ofAzospirillum brasilenseand auxin on root morphology in seedlings ofSorghum bicolor × Sorghum sudanense
inferredcites →https://doi.org/10.1093/nar/17.15.6400openalex-snapshot
Nucleotide sequence of a gene for indole-3-acetamide hydrolase fromBradyrhizobium japonicum
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a077574openalex-snapshot
Detection of the IAA Biosynthetic Pathway from Tryptophan via Indole-3-Acetamide in Bradyrhizobium spp.
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078385openalex-snapshot
Presence of a Pathway for the Biosynthesis of Auxin via Indole-3-Acetamide in Trifoliata Orange
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078391openalex-snapshot
The Identification of Indole-3-Acetic Acid and Indole-3-Acetamide in the Hypocotyls of Japanese Cherry
inferredcites →https://doi.org/10.1094/mpmi-4-207openalex-snapshot
Research NotesCloning of the Genes for Indoleacetic Acid Synthesis fromPseudomonas syringaepv.syringae
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/10.1094/phyto-76-386openalex-snapshot
Influence of Bacterial Sources of Indole-3-acetic Acid on Root Elongation of Sugar Beet
inferredcites →https://doi.org/10.1094/phyto-83-234openalex-snapshot
Cloning and Characterization ofiaaMandiaaHfromErwinia herbicolapathovargypsophilae
inferredcites →https://doi.org/10.1099/00221287-128-9-2157openalex-snapshot
Relation of Plasmid DNA to Indoleacetic Acid Production in Different Strains of Pseudomonas syringae pv. savastanoi
inferredcites →https://doi.org/10.1099/00221287-137-10-2273openalex-snapshot
Indole-3-acetic acid (IAA) synthesis in the biocontrol strain CHA0 of Pseudomonas fluorescens: role of tryptophan side chain oxidase
inferredcites →https://doi.org/10.1099/00221287-72-2-211openalex-snapshot
Tryptophan and Indoleacetic Acid Transport in the Olive and Oleander Knot Organism Pseudomonas savastanoi (E. F. Smith) Stevens
inferredcites →https://doi.org/10.1104/pp.102.2.409openalex-snapshot
Evidence for Two Indoleacetic Acid-Induced Growth Responses in the Avena Straight-Growth Indoleacetic Acid Assay
inferredcites →https://doi.org/10.1104/pp.68.6.1424openalex-snapshot
Evidence That IAA Conjugates Are Slow-Release Sources of Free IAA in Plant Tissues
inferredcites →https://doi.org/10.1104/pp.83.1.33openalex-snapshot
Effect on Root Growth of Endogenous and Applied IAA and ABA
inferredcites →https://doi.org/10.1104/pp.99.3.1062openalex-snapshot
Transgenic Tobacco Plants Coexpressing the Agrobacterium tumefaciens iaaM and iaaH Genes Display Altered Growth and Indoleacetic Acid Metabolism
inferredcites →https://doi.org/10.1105/tpc.3.11.1187openalex-snapshot
Control of ethylene synthesis by expression of a bacterial enzyme in transgenic tomato plants.
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Effects on Plant Growth Produced by Azotobacter paspali Related to Synthesis of Plant Growth Regulating Substances
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Indole-3-butyric acid in plants: occurrence, synthesis, metabolism and transport
inferredcites →https://doi.org/10.1111/j.1432-1033.1984.tb07927.xopenalex-snapshot
The T‐region of Ti plasmids codes for an enzyme synthesizing indole‐3‐acetic acid
inferredcites →https://doi.org/10.1111/j.1432-1033.1987.tb10692.xopenalex-snapshot
Nitrile hydratase of Pseudomonas chlororaphis B23
inferredcites →https://doi.org/10.1111/j.1432-1033.1990.tb19467.xopenalex-snapshot
A novel nitrilase, arylacetonitrilase, of Alcaligenes faecalis JM3
inferredcites →https://doi.org/10.1111/j.1438-8677.1995.tb00764.xopenalex-snapshot
Multiple hormonal control in plants
inferredcites →https://doi.org/10.1111/j.1574-6941.1997.tb00384.xopenalex-snapshot
Production of auxin and other indolic and phenolic compounds by Paenibacillus polymyxa strains isolated from different proximity to plant roots
inferredcites →https://doi.org/10.1111/j.1574-6968.1986.tb01672.xopenalex-snapshot
Wheat inoculation withAzospirillum brasilenseSp6 and some mutants altered in nitrogen fixation and indole-3-acetic acid production
inferredcites →https://doi.org/10.1126/science.3511528openalex-snapshot
Molecular Basis for the Auxin-Independent Phenotype of Crown Gall Tumor Tissues
inferredcites →https://doi.org/10.1128/aem.37.5.1016-1024.1979openalex-snapshot
Plant Growth Substances Produced by Azospirillum brasilense and Their Effect on the Growth of Pearl Millet ( Pennisetum americanum L.)
inferredcites →https://doi.org/10.1128/aem.42.3.497-501.1981openalex-snapshot
Enzymatic Basis for Overproduction of Tryptophan and Its Metabolites in Hansenula polymorpha Mutants
inferredcites →https://doi.org/10.1128/aem.53.8.1839-1845.1987openalex-snapshot
Auxin Production by Plant-Pathogenic Pseudomonads and Xanthomonads
inferredcites →https://doi.org/10.1128/jb.143.2.950-957.1980openalex-snapshot
Involvement of plasmid deoxyribonucleic acid in indoleacetic acid synthesis in Pseudomonas savastanoi
inferredcites →https://doi.org/10.1128/jb.149.1.40-46.1982openalex-snapshot
Cloning characterization of iaaM, a virulence determinant of Pseudomonas savastanoi.
inferredcites →https://doi.org/10.1128/jb.154.3.1162-1167.1983openalex-snapshot
Transposable element that causes mutations in a plant pathogenic Pseudomonas sp
inferredcites →https://doi.org/10.1128/jb.166.2.598-603.1986openalex-snapshot
Cloning of the gene for indoleacetic acid-lysine synthetase from Pseudomonas syringae subsp. savastanoi
inferredcites →https://doi.org/10.1128/jb.170.5.2367-2373.1988openalex-snapshot
Role of indoleacetic acid-lysine synthetase in regulation of indoleacetic acid pool size and virulence of Pseudomonas syringae subsp. savastanoi
inferredcites →https://doi.org/10.1128/jb.171.3.1718-1724.1989openalex-snapshot
Molecular cloning of a gene for indole-3-acetamide hydrolase from Bradyrhizobium japonicum
inferredcites →https://doi.org/10.1128/jb.172.10.5593-5601.1990openalex-snapshot
Indoleacetic acid operon of Pseudomonas syringae subsp. savastanoi: transcription analysis and promoter identification
inferredcites →https://doi.org/10.1128/jb.172.10.5742-5749.1990openalex-snapshot
Inhibition by Agrobacterium tumefaciens and Pseudomonas savastanoi of development of the hypersensitive response elicited by Pseudomonas syringae pv. phaseolicola
inferredcites →https://doi.org/10.1128/jb.176.5.1374-1382.1994openalex-snapshot
A mutation in the indole-3-acetic acid biosynthesis pathway of Pseudomonas syringae pv. syringae affects growth in Phaseolus vulgaris and syringomycin production
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/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/m95-015openalex-snapshot
The enhancement of plant growth by free-living bacteria
inferredcites →https://doi.org/10.1146/annurev.arplant.37.1.407openalex-snapshot
Rapid Gene Regulation by Auxin
inferredcites →https://doi.org/10.1146/annurev.pp.37.060186.002203openalex-snapshot
Rapid Gene Regulation by Auxin
inferredcites →https://doi.org/10.1271/bbb.57.1323openalex-snapshot
Characterization of Nitrile Hydratase Genes Cloned by DNA Screeing fromRhodococcus erythropolis
inferredcites →https://doi.org/10.2323/jgam.16.3_191openalex-snapshot
ROLE OF AMINOTRANSFERASE AND INDOLE-3-PYRUVIC ACID IN THE SYNTHESIS OF INDOLE-3-ACETIC ACID IN PSEUDOMONAS SAVASTANOI
inferredcites →https://doi.org/10.3109/10408419509113531openalex-snapshot
Synthesis of Phytohormones by Plant-Associated Bacteria
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Bacterial Mixtures, the Future Generation of Inoculants for Sustainable Crop Production
inferred← citeshttps://doi.org/10.1007/978-3-030-35947-8_12openalex-snapshot
Role of Biofertilizer in Biological Management of Fungal Diseases of Pigeon Pea [(Cajanus cajan) (L.) Millsp.]
inferred← citeshttps://doi.org/10.1007/978-3-030-35947-8_2openalex-snapshot
Exploration of Secondary Metabolites for Management of Chickpea Diseases
inferred← citeshttps://doi.org/10.1007/978-3-030-44368-9_1openalex-snapshot
Introduction to Plant Growth-Promoting Bacteria
inferred← citeshttps://doi.org/10.1007/978-3-030-44368-9_5openalex-snapshot
Modulating Phytohormone Levels
inferred← citeshttps://doi.org/10.1007/978-3-030-61153-8_18openalex-snapshot
PGPR-Assisted Bioremediation and Plant Growth: A Sustainable Approach for Crop Production Using Polluted Soils
inferred← citeshttps://doi.org/10.1007/978-3-030-73161-8_8openalex-snapshot
Sustainable Development of Microbial Community in Some Localities in the Desert Soil of Egypt
inferred← citeshttps://doi.org/10.1007/978-3-030-73507-4_2openalex-snapshot
Microbes Associated with Crops: Functional Attributes for Crop Productivity
inferred← citeshttps://doi.org/10.1007/978-3-030-95365-2_14openalex-snapshot
Plant–Microbe Interactions in Combating Abiotic Stresses
inferred← citeshttps://doi.org/10.1007/978-3-030-95365-2_19openalex-snapshot
Potential of Plant Growth Promoting Rhizobacteria for Enhancement of Plant Growth and Its Role in Improving Soil Health Under Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-3-031-04805-0_1openalex-snapshot
Potential of Streptomyces and Its Secondary Metabolites for Biocontrol of Fungal Plant Pathogens
inferred← citeshttps://doi.org/10.1007/978-3-031-07559-9_3openalex-snapshot
The Role of PGPR-Secondary Metabolites on Plant Photosynthesis
inferred← citeshttps://doi.org/10.1007/978-3-031-28307-9_3openalex-snapshot
Rhizosphere Mycobiome: Roles, Diversity, and Dynamics
inferred← citeshttps://doi.org/10.1007/978-3-031-71844-1_2openalex-snapshot
Soil Microbial Products: Specific Roles in Green Vegetations
inferred← citeshttps://doi.org/10.1007/978-3-031-71844-1_3openalex-snapshot
Interaction Between Soil Microbiomes and Plants
inferred← citeshttps://doi.org/10.1007/978-3-031-91114-9_20openalex-snapshot
Plant Microbe Interaction for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-211-99753-6_16openalex-snapshot
Role of Azospirillum in the Improvement of Legumes
inferred← citeshttps://doi.org/10.1007/978-3-211-99753-6_19openalex-snapshot
Plant Growth Promoting Rhizobacteria Improving the Legume–Rhizobia Symbiosis
inferred← citeshttps://doi.org/10.1007/978-3-211-99753-6_9openalex-snapshot
Growth Promotion of Legumes by Inoculation of Rhizosphere Bacteria
inferred← citeshttps://doi.org/10.1007/978-3-319-06542-7_16openalex-snapshot
Methods to Study 1-Aminocyclopropane-1-carboxylate (ACC) Deaminase in Plant Growth-Promoting Bacteria
inferred← citeshttps://doi.org/10.1007/978-3-319-08216-5_2openalex-snapshot
Mechanism of Phosphate Solubilization and Physiological Functions of Phosphate-Solubilizing Microorganisms
inferred← citeshttps://doi.org/10.1007/978-3-319-10969-5_9openalex-snapshot
Phytoremediation Using Rhizobia
inferred← citeshttps://doi.org/10.1007/978-3-319-12910-5_1openalex-snapshot
Coastal Sand Dunes: A Potential Goldmine of Bioresources
inferred← citeshttps://doi.org/10.1007/978-3-319-13401-7_6openalex-snapshot
Plant Growth-Promoting Rhizobacteria (PGPR): Emergence and Future Facets in Medicinal Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-13921-0_1openalex-snapshot
Introduction to Plant Growth-promoting Bacteria
inferred← citeshttps://doi.org/10.1007/978-3-319-13921-0_3openalex-snapshot
Modulating Phytohormone Levels
inferred← citeshttps://doi.org/10.1007/978-3-319-23075-7_4openalex-snapshot
Developing Disease-Suppressive Soil Through Agronomic Management
inferred← citeshttps://doi.org/10.1007/978-3-319-24654-3_11openalex-snapshot
Exploitation of Phytohormone-Producing PGPR in Development of Multispecies Bioinoculant Formulation
inferred← citeshttps://doi.org/10.1007/978-3-319-24654-3_5openalex-snapshot
Soil Bacteria and Phytohormones for Sustainable Crop Production
inferred← citeshttps://doi.org/10.1007/978-3-319-24654-3_7openalex-snapshot
Phytohormone-Producing PGPR for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-319-24654-3_8openalex-snapshot
Indole-3-Acetic Acid and 1-Aminocyclopropane-1-Carboxylate Deaminase: Bacterial Traits Required in Rhizosphere, Rhizoplane and/or Endophytic Competence by Beneficial Bacteria
inferred← citeshttps://doi.org/10.1007/978-3-319-24654-3_9openalex-snapshot
Role of Abscisic Acid Producing PGPR in Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-319-27093-7_24openalex-snapshot
Plant Growth Promoting Rhizobacteria Associated to Halophytes: Potential Applications in Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-319-27312-9_3openalex-snapshot
Eco Friendly Management of Damping-off of Solanaceous Crops Caused by Pythium Species
inferred← citeshttps://doi.org/10.1007/978-3-319-27455-3_10openalex-snapshot
Plant Growth-Promoting Rhizobacteria: An Eco-friendly Approach for Sustainable Agroecosystem
inferred← citeshttps://doi.org/10.1007/978-3-319-28899-4_12openalex-snapshot
Plant–Rhizobacteria Interaction and Drought Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-40148-5_18openalex-snapshot
Potential Promising Set of Plant–Microbe Interactions for the Revegetation of Open-Pit Mining and Smelting Areas in Brazil
inferred← citeshttps://doi.org/10.1007/978-3-319-43107-9_12openalex-snapshot
The Importance of Horticultural Growing Media and Biochemical Processes
inferred← citeshttps://doi.org/10.1007/978-3-319-43107-9_9openalex-snapshot
Transformations of Organic Matter in Soils Under Shelterbelts of Different Ages in Agricultural Landscape
inferred← citeshttps://doi.org/10.1007/978-3-319-44409-3_12openalex-snapshot
Expanding the Horizons for the Use of Paenibacillus Species as PGPR for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-319-48257-6_6openalex-snapshot
Plant Growth-Promoting Bacteria: An Emerging Tool for Sustainable Crop Production Under Salt Stress
inferred← citeshttps://doi.org/10.1007/978-3-319-49727-3_8openalex-snapshot
Role of Rhizospheric Microbes in Heavy Metal Uptake by Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-54401-4_6openalex-snapshot
Perspectives of Plant Growth Promoting Rhizobacteria in Growth Enhancement and Sustainable Production of Tomato
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/10.1007/978-3-319-64982-5_6openalex-snapshot
Rhizobium in Rice Yield and Growth Enhancement
inferred← citeshttps://doi.org/10.1007/978-3-319-64982-5_7openalex-snapshot
Plant Growth-Promoting Rhizobium: Mechanisms and Biotechnological Prospective
inferred← citeshttps://doi.org/10.1007/978-3-319-75910-4_12openalex-snapshot
Perspectives of Rhizobacteria with ACC Deaminase Activity in Plant Growth Under Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-3-540-74004-9_4openalex-snapshot
Biotic Interactions in the Rhizosphere: Effects on Plant Growth and Herbivore Development
inferred← citeshttps://doi.org/10.1007/978-3-540-74051-3_8openalex-snapshot
The Use of ACC Deaminase-Containing Plant Growth-Promoting Bacteria to Protect Plants Against the Deleterious Effects of Ethylene
inferred← citeshttps://doi.org/10.1007/978-3-540-74231-9_15openalex-snapshot
Endophytes and Rhizosphere Bacteria of Plants Growing in Heavy Metal-Containing Soils
inferred← citeshttps://doi.org/10.1007/978-3-540-75575-3openalex-snapshot
Molecular Mechanisms of Plant and Microbe Coexistence
inferred← citeshttps://doi.org/10.1007/978-3-540-75575-3_12openalex-snapshot
Signals in the Underground: Microbial Signaling and Plant Productivity
inferred← citeshttps://doi.org/10.1007/978-3-642-01979-1openalex-snapshot
Microbial Strategies for Crop Improvement
inferred← citeshttps://doi.org/10.1007/978-3-642-01979-1_1openalex-snapshot
The Use of Microorganisms to Facilitate the Growth of Plants in Saline Soils
inferred← citeshttps://doi.org/10.1007/978-3-642-01979-1_7openalex-snapshot
Plant Growth Promoting Rhizobacteria and Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-642-02167-1_8openalex-snapshot
The Role of Auxin in Root-Symbiont and Root-Pathogen Interactions: From Development to Defense
inferred← citeshttps://doi.org/10.1007/978-3-642-13612-2_15openalex-snapshot
Bacillus and Paenibacillus spp.: Potential PGPR for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-642-13612-2_3openalex-snapshot
Potential of PGPR in Agricultural Innovations
inferred← citeshttps://doi.org/10.1007/978-3-642-18357-7openalex-snapshot
Bacteria in Agrobiology: Crop Ecosystems
inferred← citeshttps://doi.org/10.1007/978-3-642-18357-7_11openalex-snapshot
Plant Growth-Promoting Bacteria: Fundamentals and Exploitation
inferred← citeshttps://doi.org/10.1007/978-3-642-18357-7_2openalex-snapshot
Bacillus as PGPR in Crop Ecosystem
inferred← citeshttps://doi.org/10.1007/978-3-642-18357-7_8openalex-snapshot
Use of Plant Growth Promoting Rhizobacteria in Horticultural Crops
inferred← citeshttps://doi.org/10.1007/978-3-642-20332-9openalex-snapshot
Bacteria in Agrobiology: Plant Growth Responses
inferred← citeshttps://doi.org/10.1007/978-3-642-20332-9_1openalex-snapshot
Genetic and Phenotypic Diversity of Plant Growth Promoting Bacilli
inferred← citeshttps://doi.org/10.1007/978-3-642-20332-9_11openalex-snapshot
Bacteria Associated with Orchid Roots
inferred← citeshttps://doi.org/10.1007/978-3-642-20332-9_13openalex-snapshot
Actinobacteria–Plant Interactions: A Boon to Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-642-21061-7_2openalex-snapshot
Mechanisms Used by Plant Growth-Promoting Bacteria
inferred← citeshttps://doi.org/10.1007/978-3-642-21061-7_7openalex-snapshot
Basic and Technological Aspects of Phytohormone Production by Microorganisms: Azospirillum sp. as a Model of Plant Growth Promoting Rhizobacteria
inferred← citeshttps://doi.org/10.1007/978-3-642-23465-1_8openalex-snapshot
Microbial ACC-Deaminase Biotechnology: Perspectives and Applications in Stress Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-642-27515-9_17openalex-snapshot
Contribution of N2 Fixation for the World Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-642-30194-0_19openalex-snapshot
Bacteriocyte-Associated Endosymbionts of Insects
inferred← citeshttps://doi.org/10.1007/978-3-642-32653-0_15openalex-snapshot
Enhancement of Plant Drought Tolerance by Microbes
inferred← citeshttps://doi.org/10.1007/978-3-642-35564-6_7openalex-snapshot
Use of Wetland Plants in Bioaccumulation of Heavy Metals
inferred← citeshttps://doi.org/10.1007/978-3-642-37241-4_1openalex-snapshot
Endophytic Bacteria: A Biotechnological Potential in Agrobiology System
inferred← citeshttps://doi.org/10.1007/978-3-642-37241-4_4openalex-snapshot
Rhizosphere Bacteria from Coastal Sand Dunes and Their Applications in Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-662-08818-0_7openalex-snapshot
Increased Plant Fitness by Rhizobacteria
inferred← citeshttps://doi.org/10.1007/978-3-662-10378-4_9openalex-snapshot
Biosynthesis, Biological Role and Application of Fungal Phytohormones
inferred← citeshttps://doi.org/10.1007/978-3-7091-0730-0_10openalex-snapshot
Role of Plant-Growth-Promoting Rhizobacteria in the Management of Cadmium-Contaminated Soil
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8openalex-snapshot
Auxin and Its Role in Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_13openalex-snapshot
Evolutionary Aspects of Auxin Signalling
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_18openalex-snapshot
Auxin and the Interaction Between Plants and Microorganisms
inferred← citeshttps://doi.org/10.1007/978-81-322-0810-5_33openalex-snapshot
Evaluation of Pseudomonas sp. VSMKU-4046 for Suppression of Sheath Blight (ShB) of Rice in Detached Leaf Assay
inferred← citeshttps://doi.org/10.1007/978-81-322-1087-0_8openalex-snapshot
Characterization of Groundnut Rhizosphere Pseudomonas sp. VSMKU 2013 for Control of Phytopathogens
inferred← citeshttps://doi.org/10.1007/978-81-322-1287-4_5openalex-snapshot
Soil Rhizobacteria Regulating the Uptake of Nutrients and Undesirable Elements by Plants
inferred← citeshttps://doi.org/10.1007/978-81-322-2068-8_1openalex-snapshot
Rhizosphere Bacteria for Crop Production and Improvement of Stress Tolerance: Mechanisms of Action, Applications, and Future Prospects
inferred← citeshttps://doi.org/10.1007/978-81-322-2068-8_18openalex-snapshot
Role of Plant Growth-Promoting Rhizobacteria and Their Formulation in Biocontrol of Plant Diseases
inferred← citeshttps://doi.org/10.1007/978-81-322-2259-0_4openalex-snapshot
Agricultural Applications of Microbes
inferred← citeshttps://doi.org/10.1007/978-81-322-2647-5_1openalex-snapshot
Strategies for Characterization of Agriculturally Important Bacteria
inferred← citeshttps://doi.org/10.1007/978-94-007-1914-9_3openalex-snapshot
Bioremediation: New Approaches and Trends
inferred← citeshttps://doi.org/10.1007/978-94-007-3913-0openalex-snapshot
The Plant Family Brassicaceae
inferred← citeshttps://doi.org/10.1007/978-94-007-3913-0_8openalex-snapshot
The Role of Plant Growth-Promoting Rhizosphere Bacteria in Toxic Metal Extraction by Brassica spp.
inferred← citeshttps://doi.org/10.1007/978-94-007-4116-4_5openalex-snapshot
The American Halophyte Prosopis strombulifera, a New Potential Source to Confer Salt Tolerance to Crops
inferred← citeshttps://doi.org/10.1007/978-94-011-4453-7_54openalex-snapshot
ACC Deaminase is Central to the Functioning of Plant Growth Promoting Rhizobacteria
inferred← citeshttps://doi.org/10.1007/978-94-017-0776-3_12openalex-snapshot
Hormonal Balance in Plants During Colonization by Mycorrhizal Fungi
inferred← citeshttps://doi.org/10.1007/978-94-017-1601-7_21openalex-snapshot
A possible role for phenyl acetic acid (PAA) on Alnus glutinosa nodulation by Frankia
inferred← citeshttps://doi.org/10.1007/978-94-017-7752-0_6openalex-snapshot
Pesticide Toxicity to Microorganisms: Exposure, Toxicity and Risk Assessment Methodologies
inferred← citeshttps://doi.org/10.1007/978-981-10-0707-1_3openalex-snapshot
Enhancing Soil Health and Plant Growth Promotion by Actinomycetes
inferred← citeshttps://doi.org/10.1007/978-981-10-0707-1_9openalex-snapshot
Role of Endophytic Actinomycetes in Crop Protection: Plant Growth Promotion and Biological Control
inferred← citeshttps://doi.org/10.1007/978-981-10-2854-0_22openalex-snapshot
Plant Growth-Promoting Rhizobacteria Play a Role as Phytostimulators for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-10-2854-0_3openalex-snapshot
Applications and Mechanisms of Plant Growth-Stimulating Rhizobacteria
inferred← citeshttps://doi.org/10.1007/978-981-10-3084-0_1openalex-snapshot
Phytoremediation: A Multidimensional and Ecologically Viable Practice for the Cleanup of Environmental Contaminants
inferred← citeshttps://doi.org/10.1007/978-981-10-3473-2_21openalex-snapshot
PGPR: Current Vogue in Sustainable Crop Production
inferred← citeshttps://doi.org/10.1007/978-981-10-4059-7_6openalex-snapshot
Soil Microbiome and Their Effects on Nutrient Management for Plants
inferred← citeshttps://doi.org/10.1007/978-981-10-4247-8_5openalex-snapshot
Impact Assessment of Bio-inoculants on Growth of Litchi [Litchi chinensis (Gaertn.) Sonn.] Plants
inferred← citeshttps://doi.org/10.1007/978-981-10-4862-3_3openalex-snapshot
Pseudomonadaceae: From Biocontrol to Plant Growth Promotion
inferred← citeshttps://doi.org/10.1007/978-981-10-5514-0_6openalex-snapshot
Role of Secondary Metabolites from Plant Growth-Promoting Rhizobacteria in Combating Salinity Stress
inferred← citeshttps://doi.org/10.1007/978-981-10-5813-4_12openalex-snapshot
Endophytic and Epiphytic Modes of Microbial Interactions and Benefits
inferred← citeshttps://doi.org/10.1007/978-981-10-5813-4_26openalex-snapshot
Beneficial Bacteria for Disease Suppression and Plant Growth Promotion
inferred← citeshttps://doi.org/10.1007/978-981-10-6241-4_19openalex-snapshot
Rhizosphere Microorganisms: Application of Plant Beneficial Microbes in Biological Control of Weeds
inferred← citeshttps://doi.org/10.1007/978-981-10-6593-4_11openalex-snapshot
Green Input in Agriculture: An Overview
inferred← citeshttps://doi.org/10.1007/978-981-10-6593-4_16openalex-snapshot
Beneficial Microbes for Disease Suppression and Plant Growth Promotion
inferred← citeshttps://doi.org/10.1007/978-981-10-6593-4_19openalex-snapshot
Potential of Beneficial Bacteria as Eco-friendly Options for Chemical-Free Alternative Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-10-6593-4_29openalex-snapshot
Belowground Microbial Crosstalk and Rhizosphere Biology
inferred← citeshttps://doi.org/10.1007/978-981-10-6647-4_8openalex-snapshot
Plant Growth–Promoting Microbes: A Boon for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-10-7284-0_7openalex-snapshot
Plausible Role of Plant Growth-Promoting Rhizobacteria in Future Climatic Scenario
inferred← citeshttps://doi.org/10.1007/978-981-10-7380-9_4openalex-snapshot
Plant Growth-Promoting Rhizobacteria for Abiotic Stress Alleviation in Crops
inferred← citeshttps://doi.org/10.1007/978-981-10-8402-7_1openalex-snapshot
Rhizospheric Microbes for Sustainable Agriculture: An Overview
inferred← citeshttps://doi.org/10.1007/978-981-10-8402-7_13openalex-snapshot
Bioherbicidal Potential of Rhizosphere Microorganisms for Ecofriendly Weed Management
inferred← citeshttps://doi.org/10.1007/978-981-13-0044-8_9openalex-snapshot
Role of PGPR in Sustainable Agriculture: Molecular Approach Toward Disease Suppression and Growth Promotion
inferred← citeshttps://doi.org/10.1007/978-981-13-0393-7_7openalex-snapshot
Fungal Endophytes: Role in Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-13-1861-0_10openalex-snapshot
Plant-Associated Microbial Interactions in the Soil Environment: Role of Endophytes in Imparting Abiotic Stress Tolerance to Crops
inferred← citeshttps://doi.org/10.1007/978-981-13-6040-4_3openalex-snapshot
Biofilmed Biofertilizer for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-13-6040-4_9openalex-snapshot
Potential Role of Plant Growth Promoting Rhizobacteria in Alleviation of Biotic Stress
inferred← citeshttps://doi.org/10.1007/978-981-13-6986-5_5openalex-snapshot
Amelioration of Biotic Stress by Application of Rhizobacteria for Agriculture Sustainability
inferred← citeshttps://doi.org/10.1007/978-981-13-8383-0_7openalex-snapshot
Plant Growth-Promoting Rhizobacteria (PGPRs): Functions and Benefits
inferred← citeshttps://doi.org/10.1007/978-981-13-8383-0_8openalex-snapshot
Functional Diversity of Plant Growth-Promoting Rhizobacteria: Recent Progress and Future Prospects
inferred← citeshttps://doi.org/10.1007/978-981-13-8391-5_6openalex-snapshot
Interactions in Soil-Microbe-Plant System: Adaptation to Stressed Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-13-8487-5_3openalex-snapshot
Soil Microbiota and Sustainable Jhum Agroecosystem
inferred← citeshttps://doi.org/10.1007/978-981-13-8495-0_22openalex-snapshot
Metagenomic Approach in Relation to Microbe–Microbe and Plant–Microbiome Interactions
inferred← citeshttps://doi.org/10.1007/978-981-13-8495-0_5openalex-snapshot
Applications of Beneficial Microbe in Arid and Semiarid Agroecosystem: IAA-Producing Bacteria
inferred← citeshttps://doi.org/10.1007/978-981-15-2576-6_6openalex-snapshot
Isolation and Screening of Inorganic Phosphate Solubilizing Pseudomonas Strains from the Lotus creticus Rhizosphere Soil from the Northwest of Morocco
inferred← citeshttps://doi.org/10.1007/978-981-15-3204-7_2openalex-snapshot
Potassium Solubilization and Mobilization: Functional Impact on Plant Growth for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-15-4439-2_2openalex-snapshot
Microbial Biofertilizers and Biopesticides: Nature’s Assets Fostering Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-15-6125-2_10openalex-snapshot
Rhizosphere Plant–Microbe Interactions Under Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-981-15-6125-2_13openalex-snapshot
Inter-Organismal Signaling in the Rhizosphere
inferred← citeshttps://doi.org/10.1007/978-981-15-6949-4_1openalex-snapshot
Soil Microbiomes for Healthy Nutrient Recycling
inferred← citeshttps://doi.org/10.1007/978-981-15-7094-0_15openalex-snapshot
Bacterial Antagonists Effective Against Soil Borne and Foliar Pathogens
inferred← citeshttps://doi.org/10.1007/978-981-16-1350-0_18openalex-snapshot
Rhizobacters as Remedy of Stress Tolerance in Potato
inferred← citeshttps://doi.org/10.1007/978-981-16-3840-4_26openalex-snapshot
Harnessing the Rhizomicrobiome Interactions for Plant Growth Promotion and Sustainable Agriculture: Mechanisms, Applications and Recent Advances
inferred← citeshttps://doi.org/10.1007/978-981-16-7759-5_12openalex-snapshot
IAA Biosynthesis in Bacteria and Its Role in Plant-Microbe Interaction for Drought Stress Management
inferred← citeshttps://doi.org/10.1007/978-981-19-3696-8_16openalex-snapshot
Rhizobacteriome: Plant Growth-Promoting Traits and Its Functional Mechanism in Plant Growth, Development, and Defenses
inferred← citeshttps://doi.org/10.1007/978-981-19-4101-6_13openalex-snapshot
Exploration of Plant Growth-Promoting Rhizobacteria (PGPR) for Improving Productivity and Soil Fertility Under Sustainable Agricultural Practices
inferred← citeshttps://doi.org/10.1007/978-981-19-5029-2_3openalex-snapshot
The Role of the Root Microbiome in the Utilization of Functional Traits for Increasing Plant Productivity
inferred← citeshttps://doi.org/10.1007/978-981-19-9570-5_5openalex-snapshot
Phytohormonal Role of Microorganisms Involved in Bioinoculants
inferred← citeshttps://doi.org/10.1007/978-981-32-9084-6_12openalex-snapshot
Influence of Endophytic Bacteria on Growth Promotion and Protection against Diseases in Associated Plants
inferred← citeshttps://doi.org/10.1007/978-981-32-9084-6_14openalex-snapshot
Perspectives of Plant Growth-Promoting Rhizobacteria in Conferring Salinity Tolerance in Crops
inferred← citeshttps://doi.org/10.1007/978-981-32-9084-6_5openalex-snapshot
Plant Growth-Promoting Rhizobacteria (PGPRs): A Fruitful Resource
inferred← citeshttps://doi.org/10.1007/978-981-95-7844-3openalex-snapshot
Sustainable Crop Production
inferred← citeshttps://doi.org/10.1007/978-981-95-9849-6_15openalex-snapshot
Agricultural Application of Marine Actinobacteria: A 10-Year Overview
inferred← citeshttps://doi.org/10.1007/978-981-96-0169-1_15openalex-snapshot
Microbial Biostimulants Involved in Vegetable Crop Production and Quality Improvement
inferred← citeshttps://doi.org/10.1007/978-981-96-9622-2_13openalex-snapshot
Auxin-Induced Arsenic Regulation in Plants: New Insight
inferred← citeshttps://doi.org/10.1007/978-981-97-3473-3_3openalex-snapshot
Nitrogen-Fixing Bradyrhizobium spp. as Plant Growth-Promoting Bacteria to Improve Soil Quality and Plant Tolerance to Biotic and Abiotic Stresses
inferred← citeshttps://doi.org/10.1007/978-981-97-3473-3_4openalex-snapshot
Potential of Plant Growth-Promoting Rhizobacteria for Ensuring Soil Fertility and Plant Health
inferred← citeshttps://doi.org/10.1007/978-981-99-0030-5_10openalex-snapshot
Plant–Endophyte Interactions: A Driving Phenomenon for Boosting Plant Health under Climate Change Conditions
inferred← citeshttps://doi.org/10.1007/978-981-99-3947-3_3openalex-snapshot
Molecular Events and Defence Mechanism Against Biotic Stress Induced by Bio-Priming of Beneficial Microbes
inferred← citeshttps://doi.org/10.1007/978-981-99-4480-4_15openalex-snapshot
Regulation of PGPR-Related Genes in Medicinal Plants in Adverse Conditions
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