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The Azospirillum brasilense type VI secretion system promotes cell aggregation, biocontrol protection against phytopathogens and attachment to the microalgae Chlorella sorokiniana

https://doi.org/10.1111/1462-2920.15749
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Outgoing claims: the papers this work cites, builds on, or argues with.

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The Agrobacterium Type VI Secretion System: A Contractile Nanomachine for Interbacterial Competition
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Interaction of Azospirillum spp. with Microalgae: A Basic Eukaryotic–Prokaryotic Model and Its Biotechnological Applications
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Active attachment of Azospirillum brasilense to root surface of non-cereal plants and to sand particles
inferredcites →https://doi.org/10.1007/bf02187438openalex-snapshot
Active attachment ofAzospirillum brasilense to root surface of non-cereal plants and to sand particles
inferredcites →https://doi.org/10.1007/bf02220698openalex-snapshot
Aggregation inAzospirillum brasilense Cd: Conditions and factors involved in cell-to-cell adhesion
inferredcites →https://doi.org/10.1007/bf02220714openalex-snapshot
Ultrastructural localization and identification ofAzospirillum brasilense Cd on and within wheat root by immuno-gold labeling
inferredcites →https://doi.org/10.1007/s00114-014-1223-xopenalex-snapshot
Accumulation fatty acids of in Chlorella vulgaris under heterotrophic conditions in relation to activity of acetyl-CoA carboxylase, temperature, and co-immobilization with Azospirillum brasilense
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/s00248-018-1282-1openalex-snapshot
Early Changes in Nutritional Conditions Affect Formation of Synthetic Mutualism Between Chlorella sorokiniana and the Bacterium Azospirillum brasilense
inferredcites →https://doi.org/10.1007/s002849900302openalex-snapshot
Cell-Surface Lectins of Azospirillum spp.
inferredcites →https://doi.org/10.1007/s00374-005-0025-xopenalex-snapshot
Increase in auxiliary photoprotective photosynthetic pigments in wheat seedlings induced by Azospirillum brasilense
inferredcites →https://doi.org/10.1007/s00374-011-0555-3openalex-snapshot
Development of two culture media for mass cultivation of Azospirillum spp. and for production of inoculants to enhance plant growth
inferredcites →https://doi.org/10.1007/s00374-020-01463-yopenalex-snapshot
Everything you must know about Azospirillum and its impact on agriculture and beyond
inferredcites →https://doi.org/10.1007/s10482-013-0095-yopenalex-snapshot
Indole-3-acetic acid in plant–microbe interactions
inferredcites →https://doi.org/10.1007/s10811-015-0571-zopenalex-snapshot
Chlorella sorokiniana (formerly C. vulgaris) UTEX 2714, a non-thermotolerant microalga useful for biotechnological applications and as a reference strain
inferredcites →https://doi.org/10.1007/s11104-015-2778-9openalex-snapshot
Assessment of affinity and specificity of Azospirillum for plants
inferredcites →https://doi.org/10.1007/s12275-015-5055-yopenalex-snapshot
Against friend and foe: Type 6 effectors in plant-associated bacteria
inferredcites →https://doi.org/10.1016/0003-2697(63)90094-0openalex-snapshot
Microdetermination of lipids and serum total fatty acids
inferredcites →https://doi.org/10.1016/0038-0717(86)90105-7openalex-snapshot
Adsorption of Azospirillum brasilense to corn roots
inferredcites →https://doi.org/10.1016/0147-619x(89)90058-9openalex-snapshot
Plasmid localization and mapping of two Azospirillum brasilense loci that affect exopolysaccharide synthesis
inferredcites →https://doi.org/10.1016/0147-619x(91)90048-2openalex-snapshot
Identification and mapping of loci involved in motility, adsorption to wheat roots, colony morphology, and growth in minimal medium on the Azospirillum brasilense Sp7 90-MDa plasmid
inferredcites →https://doi.org/10.1016/0167-7799(87)90037-0openalex-snapshot
Microalgae biotechnology
inferredcites →https://doi.org/10.1016/0378-1119(94)90324-7openalex-snapshot
Small mobilizable multi-purpose cloning vectors derived from the Escherichia coli plasmids pK18 and pK19: selection of defined deletions in the chromosome of Corynebacterium glutamicum
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Carbohydrate analysis by a phenol–sulfuric acid method in microplate format
inferredcites →https://doi.org/10.1016/j.algal.2016.02.019openalex-snapshot
Establishment of stable synthetic mutualism without co-evolution between microalgae and bacteria demonstrated by mutual transfer of metabolites (NanoSIMS isotopic imaging) and persistent physical association (Fluorescent in situ hybridization)
inferredcites →https://doi.org/10.1016/j.algal.2020.101845openalex-snapshot
Indole-3-acetic acid from Azosprillum brasilense promotes growth in green algae at the expense of energy storage products
inferredcites →https://doi.org/10.1016/j.bbamcr.2014.03.018openalex-snapshot
Architecture and assembly of the Type VI secretion system
inferredcites →https://doi.org/10.1016/j.biortech.2009.09.043openalex-snapshot
Immobilized microalgae for removing pollutants: Review of practical aspects
inferredcites →https://doi.org/10.1016/j.chom.2009.12.007openalex-snapshot
A Type VI Secretion System of Pseudomonas aeruginosa Targets a Toxin to Bacteria
inferredcites →https://doi.org/10.1016/j.chom.2010.06.012openalex-snapshot
Type VI Secretion: Not Just for Pathogenesis Anymore
inferredcites →https://doi.org/10.1016/j.chom.2014.06.002openalex-snapshot
Agrobacterium tumefaciens Deploys a Superfamily of Type VI Secretion DNase Effectors as Weapons for Interbacterial Competition In Planta
inferredcites →https://doi.org/10.1016/j.chom.2017.05.004openalex-snapshot
Shigella sonnei Encodes a Functional T6SS Used for Interbacterial Competition and Niche Occupancy
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.2008.08.004openalex-snapshot
Growth promotion of the freshwater microalga Chlorella vulgaris by the nitrogen-fixing, plant growth-promoting bacterium Bacillus pumilus from arid zone soils
inferredcites →https://doi.org/10.1016/j.enzmictec.2012.07.012openalex-snapshot
Enhanced accumulation of starch and total carbohydrates in alginate-immobilized Chlorella spp. induced by Azospirillum brasilense: II. Heterotrophic conditions
inferredcites →https://doi.org/10.1016/j.enzmictec.2012.07.013openalex-snapshot
Enhanced accumulation of starch and total carbohydrates in alginate-immobilized Chlorella spp. induced by Azospirillum brasilense: I. Autotrophic conditions
inferredcites →https://doi.org/10.1016/j.mib.2008.01.006openalex-snapshot
Type VI secretion: a beginner's guide
inferredcites →https://doi.org/10.1016/j.resmic.2016.02.005openalex-snapshot
Influence of tryptophan and indole-3-acetic acid on starch accumulation in the synthetic mutualistic Chlorella sorokiniana–Azospirillum brasilense system under heterotrophic conditions
inferredcites →https://doi.org/10.1016/j.tcb.2017.05.003openalex-snapshot
Using Force to Punch Holes: Mechanics of Contractile Nanomachines
inferredcites →https://doi.org/10.1016/j.tim.2014.06.004openalex-snapshot
VgrG, Tae, Tle, and beyond: the versatile arsenal of Type VI secretion effectors
inferredcites →https://doi.org/10.1016/j.tim.2018.01.006openalex-snapshot
Antibacterial Weapons: Targeted Destruction in the Microbiota
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Microalgae growth-promoting bacteria as “helpers” for microalgae: a novel approach for removing ammonium and phosphorus from municipal wastewater
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How the Plant Growth-Promoting Bacterium Azospirillum Promotes Plant Growth—A Critical Assessment
inferredcites →https://doi.org/10.1016/s0168-6496(00)00034-9openalex-snapshot
Starvation-induced changes in the cell surface of Azospirillum lipoferum
inferredcites →https://doi.org/10.1016/s0168-6496(99)00023-9openalex-snapshot
Root-surface colonization of black mangrove seedlings by Azospirillum halopraeferens and Azospirillum brasilense in seawater
inferredcites →https://doi.org/10.1016/s0378-1097(04)00003-5openalex-snapshot
Disruption of dTDP-rhamnose biosynthesis modifies lipopolysaccharide core, exopolysaccharide production, and root colonization inAzospirillum brasilense
inferredcites →https://doi.org/10.1021/ac60111a017openalex-snapshot
Colorimetric Method for Determination of Sugars and Related Substances
inferredcites →https://doi.org/10.1038/embor.2008.131openalex-snapshot
The type VI secretion toolkit
inferredcites →https://doi.org/10.1038/ismej.2016.169openalex-snapshot
The Pseudomonas putida T6SS is a plant warden against phytopathogens
inferredcites →https://doi.org/10.1038/nbt1183-784openalex-snapshot
A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative Bacteria
inferredcites →https://doi.org/10.1038/nrmicro3185openalex-snapshot
Type VI secretion system effectors: poisons with a purpose
inferredcites →https://doi.org/10.1038/nrmicro3456openalex-snapshot
Secretion systems in Gram-negative bacteria: structural and mechanistic insights
inferredcites →https://doi.org/10.1038/s41598-021-85218-1openalex-snapshot
Pseudomonas fluorescens F113 type VI secretion systems mediate bacterial killing and adaption to the rhizosphere microbiome
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Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways: a genetic analysis
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A hierarchical quorum‐sensing system in Yersinia pseudotuberculosis is involved in the regulation of motility and clumping
inferredcites →https://doi.org/10.1073/pnas.1525637113openalex-snapshot
Human symbionts inject and neutralize antibacterial toxins to persist in the gut
inferredcites →https://doi.org/10.1073/pnas.1608858113openalex-snapshot
Salmonella Typhimurium utilizes a T6SS-mediated antibacterial weapon to establish in the host gut
inferredcites →https://doi.org/10.1093/femsec/fiw077openalex-snapshot
Tryptophan, thiamine and indole-3-acetic acid exchange between Chlorella sorokiniana and the plant growth-promoting bacterium Azospirillum brasilense
inferredcites →https://doi.org/10.1093/femsre/fuab033openalex-snapshot
The ecological impact of a bacterial weapon: microbial interactions and the Type VI secretion system
inferredcites →https://doi.org/10.1093/nar/gkaa899openalex-snapshot
BastionHub: a universal platform for integrating and analyzing substrates secreted by Gram-negative bacteria
inferredcites →https://doi.org/10.1093/nar/gkr988openalex-snapshot
KEGG for integration and interpretation of large-scale molecular data sets
inferredcites →https://doi.org/10.1093/plankt/18.12.2377openalex-snapshot
Determination of chlorophylls and carotenoids of marine phytoplankton: separation of chlorophyll a from divinylchlorophyll a and zeaxanthin from lutein
inferredcites →https://doi.org/10.1094/mpmi-01-19-0021-ropenalex-snapshot
Plant-Pathogenic Agrobacterium tumefaciens Strains Have Diverse Type VI Effector-Immunity Pairs and Vary in In-Planta Competitiveness
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A Rhizobium leguminosarum Biovar trifolii Locus Not Localized on the Sym Plasmid Hinders Effective Nodulation on Plants of the Pea Cross-Inoculation Group
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A Transcriptional Regulator of the LuxR-UhpA Family, FlcA, Controls Flocculation and Wheat Root Surface Colonization by Azospirillum brasilense Sp7
inferredcites →https://doi.org/10.1094/mpmi.2003.16.1.53openalex-snapshot
Infection-Blocking Genes of a Symbiotic Rhizobium leguminosarum Strain That Are Involved in Temperature-Dependent Protein Secretion
inferredcites →https://doi.org/10.1094/mpmi.2003.16.7.634openalex-snapshot
GacS Sensor Domains Pertinent to the Regulation of Exoproduct Formation and to the Biocontrol Potential of Pseudomonas fluorescens CHA0
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Type VI secretion system: secretion by a contractile nanomachine
inferredcites →https://doi.org/10.1099/00221287-132-11-3069openalex-snapshot
Evidence for a Weak Active External Adsorption of Azospirillum brasilense Cd to Wheat Roots
inferredcites →https://doi.org/10.1099/00221287-133-12-3473openalex-snapshot
Horizontal and Vertical Movement of Azospirillum brasilense Cd in the Soil and along the Rhizosphere of Wheat and Weeds in Controlled and Field Environments
inferredcites →https://doi.org/10.1099/00221287-134-8-2269openalex-snapshot
Active Attachment of Azospirillum brasilense Cd to Quartz Sand and to a Light-textured Soil by Protein Bridging
inferredcites →https://doi.org/10.1099/00221287-137-1-187openalex-snapshot
Root surface colonization of non-cereal crop plants by pleomorphic Azospirillum brasilense Cd
inferredcites →https://doi.org/10.1099/00221287-144-7-1989openalex-snapshot
Aggregation in Azospirillum brasilense: effects of chemical and physical factors and involvement of extracellular components
inferredcites →https://doi.org/10.1099/mic.0.000789openalex-snapshot
The Type VI secretion system: a versatile bacterial weapon
inferredcites →https://doi.org/10.1099/mic.0.031807-0openalex-snapshot
The Azospirillum brasilense Sp7 noeJ and noeL genes are involved in extracellular polysaccharide biosynthesis
inferredcites →https://doi.org/10.1101/cshperspect.a001438openalex-snapshot
Auxin and Plant-Microbe Interactions
inferredcites →https://doi.org/10.1111/1462-2920.12794openalex-snapshot
SecReT6 : a web‐based resource for type VI secretion systems found in bacteria
inferredcites →https://doi.org/10.1111/1462-2920.13956openalex-snapshot
Type VI secretion systems in plant‐associated bacteria
inferredcites →https://doi.org/10.1111/1462-2920.15457openalex-snapshot
Plant holobiont interactions mediated by the type VI secretion system and the membrane vesicles: promising tools for a greener agriculture
inferredcites →https://doi.org/10.1111/cmi.13153openalex-snapshot
Causalities of war: The connection between type VI secretion system and microbiota
inferredcites →https://doi.org/10.1111/cmi.13241openalex-snapshot
Type VI secretion system effector proteins: Effective weapons for bacterial competitiveness
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INVOLVEMENT OF INDOLE‐3‐ACETIC ACID PRODUCED BY THE GROWTH‐PROMOTING BACTERIUM AZOSPIRILLUM SPP. IN PROMOTING GROWTH OF CHLORELLA VULGARIS1
inferredcites →https://doi.org/10.1111/j.1529-8817.2011.01062.xopenalex-snapshot
CELL‐CELL INTERACTION IN THE EUKARYOTE‐PROKARYOTE MODEL OF THE MICROALGAE CHLORELLA VULGARIS AND THE BACTERIUM AZOSPIRILLUM BRASILENSE IMMOBILIZED IN POLYMER BEADS1
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Construction of an artificial symbiotic community using a Chlorella–symbiont association as a model
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Extracellular biology ofMyxococcus xanthus
inferredcites →https://doi.org/10.1111/jam.14080openalex-snapshot
New insights into indole-3-acetic acid metabolism inAzospirillum brasilense
inferredcites →https://doi.org/10.1111/mmi.14648openalex-snapshot
Activity, delivery, and diversity of Type VI secretion effectors
inferredcites →https://doi.org/10.1128/aem.00518-08openalex-snapshot
Joint Immobilization of Plant Growth-Promoting Bacteria and Green Microalgae in Alginate Beads as an Experimental Model for Studying Plant-Bacterium Interactions
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Transposon Mutagenesis of Azospirillum brasilense and Azospirillum lipoferum : Physical Analysis of Tn 5 and Tn 5 -Mob Insertion Mutants
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Root-to-Root Travel of the Beneficial Bacterium Azospirillum brasilense
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A critical examination of the specificity of the salkowski reagent for indolic compounds produced by phytopathogenic bacteria
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In Situ Localization of Azospirillum brasilense in the Rhizosphere of Wheat with Fluorescently Labeled, rRNA-Targeted Oligonucleotide Probes and Scanning Confocal Laser Microscopy
inferredcites →https://doi.org/10.1128/aem.66.5.2175-2184.2000openalex-snapshot
Mutants with Enhanced Nitrogenase Activity in HydroponicAzospirillum brasilense-Wheat Associations
inferredcites →https://doi.org/10.1128/genomea.00683-14openalex-snapshot
Complete Genome Sequence of the Model Rhizosphere Strain Azospirillum brasilense Az39, Successfully Applied in Agriculture
inferredcites →https://doi.org/10.1128/iai.00531-10openalex-snapshot
The Type VI Secretion System Plays a Role in Type 1 Fimbria Expression and Pathogenesis of an Avian Pathogenic Escherichia coli Strain
inferredcites →https://doi.org/10.1128/jb.00310-12openalex-snapshot
The Azospirillum brasilense Che1 Chemotaxis Pathway Controls Swimming Velocity, Which Affects Transient Cell-to-Cell Clumping
inferredcites →https://doi.org/10.1128/jb.00945-08openalex-snapshot
SciN Is an Outer Membrane Lipoprotein Required for Type VI Secretion in EnteroaggregativeEscherichia coli
inferredcites →https://doi.org/10.1128/jb.182.21.6042-6048.2000openalex-snapshot
Energy Taxis Is the Dominant Behavior in Azospirillum brasilense
inferredcites →https://doi.org/10.1128/jb.186.19.6595-6604.2004openalex-snapshot
An Energy Taxis Transducer Promotes Root Colonization byAzospirillum brasilense
inferredcites →https://doi.org/10.1128/jb.188.4.1451-1461.2006openalex-snapshot
Quorum Sensing inYersinia enterocoliticaControls Swimming and Swarming Motility
inferredcites →https://doi.org/10.1128/microbiolspec.psib-0031-2019openalex-snapshot
Structure and Activity of the Type VI Secretion System
inferredcites →https://doi.org/10.1139/b89-312openalex-snapshot
Contribution of Azospirillum brasilense Cd to growth of tomato seedlings is not through nitrogen fixation
inferredcites →https://doi.org/10.1139/cjm-47-1-1openalex-snapshot
Ultrastructure of interaction in alginate beads between the microalga Chlorella vulgaris with its natural associative bacterium Phyllobacterium myrsinacearum and with the plant growth-promoting bacterium Azospirillum brasilense
inferredcites →https://doi.org/10.1139/m83-243openalex-snapshot
Swarming of Azospirillum brasilense on solid media
inferredcites →https://doi.org/10.1139/o59-099openalex-snapshot
A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION
inferredcites →https://doi.org/10.1139/w02-051openalex-snapshot
Increased pigment and lipid content, lipid variety, and cell and population size of the microalgae Chlorella spp. when co-immobilized in alginate beads with the microalgae-growth-promoting bacterium Azospirillum brasilense
inferredcites →https://doi.org/10.1186/1471-2164-9-75openalex-snapshot
The RAST Server: Rapid Annotations using Subsystems Technology
inferredcites →https://doi.org/10.1186/s12866-015-0405-9openalex-snapshot
A Pseudomonas fluorescens type 6 secretion system is related to mucoidy, motility and bacterial competition
inferredcites →https://doi.org/10.1201/b15251-10openalex-snapshot
Bacterial Protein Secretion Systems
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/10.1371/journal.pgen.1005545openalex-snapshot
The Type VI Secretion TssEFGK-VgrG Phage-Like Baseplate Is Recruited to the TssJLM Membrane Complex via Multiple Contacts and Serves As Assembly Platform for Tail Tube/Sheath Polymerization
inferredcites →https://doi.org/10.1371/journal.pgen.1009682openalex-snapshot
Diverse LXG toxin and antitoxin systems specifically mediate intraspecies competition in Bacillus subtilis biofilms
inferredcites →https://doi.org/10.1371/journal.pone.0089411openalex-snapshot
A Type VI Secretion System Is Involved in Pseudomonas fluorescens Bacterial Competition
inferredcites →https://doi.org/10.1371/journal.pone.0114435openalex-snapshot
Cellular Responses during Morphological Transformation in Azospirillum brasilense and Its flcA Knockout Mutant
inferredcites →https://doi.org/10.1371/journal.pone.0170770openalex-snapshot
Contribution of the Pseudomonas fluorescens MFE01 Type VI Secretion System to Biofilm Formation
inferredcites →https://doi.org/10.3389/fcimb.2020.587948openalex-snapshot
From Welfare to Warfare: The Arbitration of Host-Microbiota Interplay by the Type VI Secretion System
inferredcites →https://doi.org/10.3390/jof5020050openalex-snapshot
A New Front in Microbial Warfare—Delivery of Antifungal Effectors by the Type VI Secretion System
inferredcites →https://doi.org/10.3390/microorganisms8050622openalex-snapshot
Crosstalk between the Type VI Secretion System and the Expression of Class IV Flagellar Genes in the Pseudomonas fluorescens MFE01 Strain
inferredcites →https://doi.org/10.3390/toxins11050262openalex-snapshot
Toxin–Antitoxin Systems in Bacillus subtilis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Environmental and Economic Benefits of Algal-Microbial Remediation
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The role of the type VI secretion system in the stress resistance of plant-associated bacteria
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Microalgae-bacteria nexus for environmental remediation and renewable energy resources: Advances, mechanisms and biotechnological applications
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inferred← citeshttps://doi.org/10.1016/j.mib.2023.102297openalex-snapshot
Rhizosphere bacterial interactions and impact on plant health
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.rhisph.2023.100721openalex-snapshot
A unique small RNA, sSp_p4 governs nutrition stress response and plant-growth promoting traits in Azospirillum baldaniorum Sp245
inferred← citeshttps://doi.org/10.1038/s42003-026-09863-wopenalex-snapshot
Tke5 is a Pseudomonas putida toxin that kills plant pathogens by depolarising membranes
inferred← citeshttps://doi.org/10.1093/ismeco/ycaf158openalex-snapshot
The Pseudomonas putida type VI secretion systems shape the tomato rhizosphere microbiota
inferred← citeshttps://doi.org/10.1093/jambio/lxad071openalex-snapshot
UnravelingAzospirillum’s colonization ability through microbiological and molecular evidence
inferred← citeshttps://doi.org/10.1094/pdis-11-25-2379-reopenalex-snapshot
Biocontrol Potential of a Novel Bacillus velezensis Strain Against Major Soft Rot Bacteria Pectobacterium and Dickeya
inferred← citeshttps://doi.org/10.1099/ijsem.0.005475openalex-snapshot
Genome-based reclassification of Azospirillum brasilense Az39 as the type strain of Azospirillum argentinense sp. nov.
inferred← citeshttps://doi.org/10.1111/1462-2920.16100openalex-snapshot
An antibacterial T6SS in Pantoea agglomerans pv. betae delivers a lysozyme‐like effector to antagonize competitors
inferred← citeshttps://doi.org/10.1111/1462-2920.16195openalex-snapshot
Azospirillum baldaniorum Sp245 exploits Pseudomonas fluorescens A506 biofilm to overgrow in dual‐species macrocolonies
inferred← citeshttps://doi.org/10.1111/1462-2920.16492openalex-snapshot
Pseudomonas fluorescens MFE01 delivers a putative type VI secretion amidase that confers biocontrol against the soft‐rot pathogen Pectobacterium atrosepticum
inferred← citeshttps://doi.org/10.1111/1751-7915.14235openalex-snapshot
The emerging role of auxins as bacterial signal molecules: Potential biotechnological applications
inferred← citeshttps://doi.org/10.1111/1751-7915.14420openalex-snapshot
Potential of the quorum‐quenching and plant‐growth promoting halotolerant Bacillus toyonensis AA1EC1 as biocontrol agent
inferred← citeshttps://doi.org/10.1111/mpp.13412openalex-snapshot
The type VI secretion system of Stenotrophomonas rhizophila CFBP13503 limits the transmission of Xanthomonas campestris pv. campestris 8004 from radish seeds to seedlings
inferred← citeshttps://doi.org/10.1126/sciadv.abo2431openalex-snapshot
High-resolution spatial and genomic characterization of coral-associated microbial aggregates in the coral Stylophora pistillata
inferred← citeshttps://doi.org/10.1128/aem.00828-24openalex-snapshot
Identification and functional characterization of a fructose-inducible phosphotransferase system in Azospirillum brasilense Sp7
inferred← citeshttps://doi.org/10.1128/aem.02384-24openalex-snapshot
Indole-3-acetic acid (IAA) protects Azospirillum brasilense from indole-induced stress
inferred← citeshttps://doi.org/10.20944/preprints202305.1461.v1openalex-snapshot
Microalgal and Nitrogen-Fixing Bacterial Consortia: From Interaction to Biotechnological Potential
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1169809openalex-snapshot
From salty to thriving: plant growth promoting bacteria as nature’s allies in overcoming salinity stress in plants
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1355750openalex-snapshot
Secretory molecules from secretion systems fine-tune the host-beneficial bacteria (PGPRs) interaction
inferred← citeshttps://doi.org/10.3390/f16050758openalex-snapshot
Comparative Analysis of Endophytic Bacterial Microbiomes in Healthy and Phytoplasma-Infected European Blueberry Plants
inferred← citeshttps://doi.org/10.3390/horticulturae12070780openalex-snapshot
A Simplified Synthetic Community of Indigenous Rhizobacteria Enhances Tomato Growth, Fruit Yield and Quality, and Suppresses Bacterial Wilt Under Continuous Cropping in Northwest China
inferred← citeshttps://doi.org/10.3390/plants12132476openalex-snapshot
Microalgal and Nitrogen-Fixing Bacterial Consortia: From Interaction to Biotechnological Potential
inferred← citeshttps://doi.org/10.3390/plants13060829openalex-snapshot
Exchange or Eliminate: The Secrets of Algal-Bacterial Relationships
inferred← citeshttps://doi.org/10.3390/plants14203230openalex-snapshot
Effects on Soil Fertility and Crop Productivity Under Residual Agricultural Gypsum and Azospirillum brasilense in Cover Crops in a Consolidated No-Tillage System
inferred← citeshttps://doi.org/10.3390/su17157104openalex-snapshot
Harnessing an Algae–Bacteria Symbiosis System: Innovative Strategies for Enhancing Complex Wastewater Matrices Treatment
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