On the public citation graph

Tryptophan, thiamine and indole-3-acetic acid exchange between Chlorella sorokiniana and the plant growth-promoting bacterium Azospirillum brasilense

https://doi.org/10.1093/femsec/fiw077
0 signed · 161 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0470080124.ch3openalex-snapshot
Purification and Characterization
inferredcites →https://doi.org/10.1002/9781118297674.ch4openalex-snapshot
Microbial Interactions in the Rhizosphere
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/0-306-47615-0_331openalex-snapshot
Ultrastructure of Coimmobilization of the Microalga Chlorella vulgaris with the Plant Growth-Promoting Bacterium Azospirillum brasilense and with its Natural Associative Bacterium Phyllobacterium myrsinacearum in Alginate Beads
inferredcites →https://doi.org/10.1007/978-3-319-06542-7openalex-snapshot
Handbook for azospirillum : technical issues and protocols
inferredcites →https://doi.org/10.1007/978-3-319-06542-7_20openalex-snapshot
Interaction of Azospirillum spp. with Microalgae: A Basic Eukaryotic–Prokaryotic Model and Its Biotechnological Applications
inferredcites →https://doi.org/10.1007/978-3-319-20200-6_3openalex-snapshot
Microalgal Heterotrophic and Mixotrophic Culturing for Bio-refining: From Metabolic Routes to Techno-economics
inferredcites →https://doi.org/10.1007/978-3-540-75575-3_14openalex-snapshot
Effects of Root Exudates in Microbial Diversity and Activity in Rhizosphere Soils
inferredcites →https://doi.org/10.1007/978-94-009-0889-5_17openalex-snapshot
The phytohormonal interactions between Azospirillum and wheat
inferredcites →https://doi.org/10.1007/bf00446654openalex-snapshot
The cell content and secretion of water-soluble vitamins by several freshwater algae
inferredcites →https://doi.org/10.1007/bf02011424openalex-snapshot
Applicability of the fluorescein diacetate method of detecting active bacteria in freshwater
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/bf02226804openalex-snapshot
The phytohormonal interactions betweenAzospirillum and wheat
inferredcites →https://doi.org/10.1007/s00018-011-0649-yopenalex-snapshot
Using artificial systems to explore the ecology and evolution of symbioses
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/s00253-011-3585-8openalex-snapshot
Alginate beads provide a beneficial physical barrier against native microorganisms in wastewater treated with immobilized bacteria and microalgae
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/s00374-011-0653-2openalex-snapshot
Plant-borne flavonoids released into the rhizosphere: impact on soil bio-activities related to plant nutrition. A review
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/s10482-013-0095-yopenalex-snapshot
Indole-3-acetic acid in plant–microbe interactions
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/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/s10811-015-0697-zopenalex-snapshot
Enhancement of thiamine release during synthetic mutualism between Chlorella sorokiniana and Azospirillum brasilense growing under stress conditions
inferredcites →https://doi.org/10.1007/s11104-008-9814-yopenalex-snapshot
Plant-driven selection of microbes
inferredcites →https://doi.org/10.1007/s13213-014-0866-3openalex-snapshot
Activity of acetyl-CoA carboxylase is not directly linked to accumulation of lipids when Chlorella vulgaris is co-immobilised with Azospirillum brasilense in alginate under autotrophic and heterotrophic conditions
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.biortech.2009.09.043openalex-snapshot
Immobilized microalgae for removing pollutants: Review of practical aspects
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.femsle.2005.03.048openalex-snapshot
Growth and indole-3-acetic acid biosynthesis ofAzospirillum brasilenseSp245 is environmentally controlled
inferredcites →https://doi.org/10.1016/j.jbiotec.2014.02.014openalex-snapshot
Enhanced activity of ADP glucose pyrophosphorylase and formation of starch induced by Azospirillum brasilense in Chlorella vulgaris
inferredcites →https://doi.org/10.1016/j.resmic.2014.12.010openalex-snapshot
Involvement of indole-3-acetic acid produced by Azospirillum brasilense in accumulating intracellular ammonium in Chlorella vulgaris
inferredcites →https://doi.org/10.1016/j.resmic.2015.03.001openalex-snapshot
Accumulation of intra-cellular polyphosphate in Chlorella vulgaris cells is related to indole-3-acetic acid produced by Azospirillum brasilense
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.tplants.2014.11.005openalex-snapshot
Chlorella: 125 years of the green survivalist
inferredcites →https://doi.org/10.1016/j.watres.2003.09.022openalex-snapshot
Microalgae growth-promoting bacteria as “helpers” for microalgae: a novel approach for removing ammonium and phosphorus from municipal wastewater
inferredcites →https://doi.org/10.1016/s0021-9258(19)49609-9openalex-snapshot
Purification and characterization of indolepyruvate decarboxylase. A novel enzyme for indole-3-acetic acid biosynthesis in Enterobacter cloacae.
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/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/s0960-8524(97)00029-1openalex-snapshot
Efficiency of ammonia and phosphorus removal from a colombian agroindustrial wastewater by the microalgae Chlorella vulgaris and Scenedesmus dimorphus
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/10.1038/nature14488openalex-snapshot
Interaction and signalling between a cosmopolitan phytoplankton and associated bacteria
inferredcites →https://doi.org/10.1038/nrmicro1747openalex-snapshot
Microbial structuring of marine ecosystems
inferredcites →https://doi.org/10.1046/j.1432-1327.1999.00033.xopenalex-snapshot
Biosynthesis of indole‐3‐acetic acid in Azospirillum brasilense
inferredcites →https://doi.org/10.1080/02648725.1991.10647882openalex-snapshot
The Molecular Biology of Tryptophan Synthase: A Model for Protein-Protein Interaction
inferredcites →https://doi.org/10.1080/02648725.1991.10750004openalex-snapshot
7 The Molecular Biology of Tryptophan Synthase: A Model for Protein–Protein Interaction
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a028966openalex-snapshot
Indolepyruvate Pathway for Indole-3-Acetic Acid Biosynthesis in Bradyrhizobium elkanii
inferredcites →https://doi.org/10.1094/mpmi-19-0250openalex-snapshot
Organic Acids, Sugars, and l -Tryptophane in Exudates of Vegetables Growing on Stonewool and Their Effects on Activities of Rhizosphere Bacteria
inferredcites →https://doi.org/10.1094/mpmi-20-6-0619openalex-snapshot
Tryptophan-Dependent Production of Indole-3-Acetic Acid (IAA) Affects Level of Plant Growth Promotion by Bacillus amyloliquefaciens FZB42
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/10.1101/cshperspect.a001438openalex-snapshot
Auxin and Plant-Microbe Interactions
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/10.1105/tpc.3.4.345openalex-snapshot
Tryptophan mutants in Arabidopsis: the consequences of duplicated tryptophan synthase beta genes.
inferredcites →https://doi.org/10.1111/j.1472-765x.2006.01886.xopenalex-snapshot
Composition of the sheath produced by the green alga Chlorella sorokiniana
inferredcites →https://doi.org/10.1111/j.1529-8817.2008.00572.xopenalex-snapshot
ROLE OF GLUTAMATE DEHYDROGENASE AND GLUTAMINE SYNTHETASE IN CHLORELLA VULGARIS DURING ASSIMILATION OF AMMONIUM WHEN JOINTLY IMMOBILIZED WITH THE MICROALGAE‐GROWTH‐PROMOTING BACTERIUM AZOSPIRILLUM BRASILENSE1
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
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
inferredcites →https://doi.org/10.1128/aem.54.11.2833-2837.1988openalex-snapshot
Analysis of Indole-3-Acetic Acid and Related Indoles in Culture Medium from Azospirillum lipoferum and Azospirillum brasilense
inferredcites →https://doi.org/10.1128/aem.66.4.1527-1531.2000openalex-snapshot
Increased Growth of the Microalga Chlorella vulgaris when Coimmobilized and Cocultured in Alginate Beads with the Plant-Growth-Promoting Bacterium Azospirillum brasilense
inferredcites →https://doi.org/10.1128/aem.71.5.2365-2371.2005openalex-snapshot
Utilization of the Plant Hormone Indole-3-Acetic Acid for Growth by Pseudomonas putida Strain 1290
inferredcites →https://doi.org/10.1128/jb.00830-07openalex-snapshot
Characterization of Phenylpyruvate Decarboxylase, Involved in Auxin Production of Azospirillum brasilense
inferredcites →https://doi.org/10.1128/mmbr.00007-12openalex-snapshot
Interactions between Diatoms and Bacteria
inferredcites →https://doi.org/10.1139/cjm-46-7-653openalex-snapshot
Changes in the metabolism of the microalga Chlorella vulgaris when coimmobilized in alginate with the nitrogen-fixing Phyllobacterium myrsinacearum
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/w00-041openalex-snapshot
Changes in the metabolism of the microalga Chlorella vulgaris when coimmobilized in alginate with the nitrogen-fixing Phyllobacterium myrsinacearum
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/10.1139/w04-035openalex-snapshot
Azospirillum-plant relationships: physiological, molecular, agricultural, and environmental advances (1997-2003)
inferredcites →https://doi.org/10.1146/annurev.biochem.78.072407.102340openalex-snapshot
The Structural and Biochemical Foundations of Thiamin Biosynthesis
inferredcites →https://doi.org/10.1371/journal.pone.0089680openalex-snapshot
A Selected Core Microbiome Drives the Early Stages of Three Popular Italian Cheese Manufactures
inferredcites →https://doi.org/10.1371/journal.pone.0098162openalex-snapshot
Evaluation of Reference Genes for Gene Expression Analysis Using Quantitative RT-PCR in Azospirillum brasilense
inferredcites →https://doi.org/10.1373/clinchem.2008.112797openalex-snapshot
The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments
inferredcites →https://doi.org/10.2307/1540052openalex-snapshot
CHEMOTACTIC AND GROWTH RESPONSES OF MARINE BACTERIA TO ALGAL EXTRACELLULAR PRODUCTS
inferredcites →https://doi.org/10.2331/suisan.45.199openalex-snapshot
Production of vitamin B12, thiamine, and biotin by freshwater phytoplankton.
inferredcites →https://doi.org/10.3109/1040841x.2012.716819openalex-snapshot
Activity, distribution and function of indole-3-acetic acid biosynthetic pathways in bacteria

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4675641openalex-extracted
Microalgae-Bacteria Nexus for Environmental Remediation and Renewable Energy Resources: Advances, Mechanisms and Biotechnological Applications
inferred← citeshttps://doi.org/10.1002/9781119724995.ch10openalex-snapshot
Azospirillum: A Salient Source for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1002/bit.27172openalex-snapshot
Algal photosynthetic aeration increases the capacity of bacteria to degrade organics in wastewater
inferred← citeshttps://doi.org/10.1007/978-3-030-52395-4_7openalex-snapshot
Biodegradation of Hydrocarbons in Marine Environment
inferred← citeshttps://doi.org/10.1007/978-3-032-09222-9_15openalex-snapshot
Interaction of Azospirillum with Microalgae
inferred← citeshttps://doi.org/10.1007/978-981-96-8054-2_11openalex-snapshot
Environmental and Economic Benefits of Algal-Microbial Remediation
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/s00248-018-1282-1openalex-snapshot
Early Changes in Nutritional Conditions Affect Formation of Synthetic Mutualism Between Chlorella sorokiniana and the Bacterium Azospirillum brasilense
inferred← citeshttps://doi.org/10.1007/s00248-021-01772-1openalex-snapshot
Extracellular Polymeric Substances Drive Symbiotic Interactions in Bacterial‒Microalgal Consortia
inferred← citeshttps://doi.org/10.1007/s00248-022-02026-4openalex-snapshot
Differences in Exudates Between Strains of Chlorella sorokiniana Affect the Interaction with the Microalga Growth-Promoting Bacteria Azospirillum brasilense
inferred← citeshttps://doi.org/10.1007/s00284-024-03805-7openalex-snapshot
The Role of PGPB-Microalgae interaction in Alleviating Salt Stress in Plants
inferred← citeshttps://doi.org/10.1007/s00284-025-04534-1openalex-snapshot
Polyhydroxybutyrates Production by Azospirillum brasilense as a Microalgal Growth Promotion Trait During CO2 Fixation from Biogas
inferred← citeshttps://doi.org/10.1007/s00299-024-03194-yopenalex-snapshot
The role of microbial partners in heavy metal metabolism in plants: a review
inferred← citeshttps://doi.org/10.1007/s10725-023-01019-8openalex-snapshot
Potential benefit of microalgae and their interaction with bacteria to sustainable crop production
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/s10811-019-02007-0openalex-snapshot
Bacterial abundance and diversity in Microchloropsis salina (formerly Nannochloropsis salina) cultures in response to the presence of ammonium, nitrate and glycerol
inferred← citeshttps://doi.org/10.1007/s10811-022-02891-zopenalex-snapshot
Growth and metabolism enhancement in microalgae co-cultured in suspension with the bacterium Azospirillum brasilense under heterotrophic conditions
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/s11756-026-02149-wopenalex-snapshot
Symbiotic interactions between Chlorella vulgaris C1 and growth-promoting bacteria: a pathway to enhanced microalgal cultivation
inferred← citeshttps://doi.org/10.1007/s12155-022-10411-7openalex-snapshot
Chemical and Physical Affinity of Microalga–Azospirillum Consortium Co-cultured in Suspension During CO2 Fixation from Biogas
inferred← citeshttps://doi.org/10.1007/s12649-018-00577-7openalex-snapshot
Effects of Tryptophan Along with Sodium Pyruvate and Sodium Thiosulfate on Chlorella vulgaris Growth
inferred← citeshttps://doi.org/10.1007/s13762-023-05069-3openalex-snapshot
Microalgae-based wastewater treatment system: current state, antibiotic resistant bacteria and antibiotic resistance genes reduction potentials
inferred← citeshttps://doi.org/10.1007/s42770-025-01693-yopenalex-snapshot
Effects of lichen symbiotic bacteria-derived indole-3-acetic acid on the stress responses of an algal–fungal symbiont
inferred← citeshttps://doi.org/10.1016/b978-0-12-817941-3.00012-7openalex-snapshot
Bioconversion of Agricultural Wastes From the Livestock Industry for Biofuel and Feed Production
inferred← citeshttps://doi.org/10.1016/b978-0-12-823355-9.00014-6openalex-snapshot
Medicinal plants associated microflora as an unexplored niche of biopesticide
inferred← citeshttps://doi.org/10.1016/j.aca.2020.11.008openalex-snapshot
Polydopamine/graphene/MnO2 composite-based electrochemical sensor for in situ determination of free tryptophan in plants
inferred← citeshttps://doi.org/10.1016/j.algal.2018.05.019openalex-snapshot
Impact of thiamine metabolites and spent medium from Chlorella sorokiniana on metabolism in the green algae Auxenochlorella prototheciodes
inferred← citeshttps://doi.org/10.1016/j.algal.2018.101390openalex-snapshot
Genome-wide exploration of Escherichia coli genes to promote Chlorella vulgaris growth
inferred← citeshttps://doi.org/10.1016/j.algal.2019.101547openalex-snapshot
Effects of an auxin-producing symbiotic bacterium on cell growth of the microalga Haematococcus pluvialis: Elevation of cell density and prolongation of exponential stage
inferred← citeshttps://doi.org/10.1016/j.algal.2019.101696openalex-snapshot
Riboflavin and lumichrome exuded by the bacterium Azospirillum brasilense promote growth and changes in metabolites in Chlorella sorokiniana under autotrophic conditions
inferred← citeshttps://doi.org/10.1016/j.algal.2020.102156openalex-snapshot
Comparison of algae growth and symbiotic mechanisms in the presence of plant growth promoting bacteria and non-plant growth promoting bacteria
inferred← citeshttps://doi.org/10.1016/j.algal.2021.102585openalex-snapshot
Microalga Growth-Promoting Bacteria (MGPB): A formal term proposed for beneficial bacteria involved in microalgal–bacterial interactions
inferred← citeshttps://doi.org/10.1016/j.algal.2023.103198openalex-snapshot
Microalga-bacteria interaction mitigates adverse effects on microalga produced by ZnO nanoparticles
inferred← citeshttps://doi.org/10.1016/j.algal.2025.103967openalex-snapshot
Discerning promotion mechanisms of fungi Clonostachys rosea on growth of freshwater microalga Chlorella sp. by non-contact culture
inferred← citeshttps://doi.org/10.1016/j.algal.2025.104163openalex-snapshot
Scale-up study of enhancing algal growth through bioaugmentation with the indole-3-acetic acid producing bacteria Azospirillum brasilense
inferred← citeshttps://doi.org/10.1016/j.apsoil.2025.106684openalex-snapshot
Combined application of microalgae and plant growth-promoting rhizobacteria: Synergistic effects in improving soil health and crop root disease resistance
inferred← citeshttps://doi.org/10.1016/j.biortech.2019.122445openalex-snapshot
Anaerobic microbial communities can influence algal growth and nutrient removal from anaerobic digestate
inferred← citeshttps://doi.org/10.1016/j.biortech.2022.126732openalex-snapshot
Co-culture of microalga Chlorella sorokiniana with syntrophic Streptomyces thermocarboxydus in cassava wastewater for wastewater treatment and biodiesel production
inferred← citeshttps://doi.org/10.1016/j.biortech.2024.130607openalex-snapshot
Unlocking synergies: Harnessing the potential of biological methane sequestration through metabolic coupling between Methylomicrobium alcaliphilum 20Z and Chlorella sp. HS2
inferred← citeshttps://doi.org/10.1016/j.biortech.2025.133310openalex-snapshot
Enhancement of microalgal carbon fixation via synergistic interactions with a facultative autotrophic bacterium Cytobacillus KQ-2
inferred← citeshttps://doi.org/10.1016/j.biosx.2021.100086openalex-snapshot
In vivo detection of L-tryptophan in tomatoes using multi-walled carbon nanotubes and poly (sulfosalicylic acid) film modified graphite rod electrode
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2025.108591openalex-snapshot
Bacteria-microalgae interactions from an evolutionary perspective and their biotechnological significance
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2022.136183openalex-snapshot
Latest eco-friendly approaches for pesticides decontamination using microorganisms and consortia microalgae: A comprehensive insights, challenges, and perspectives
inferred← citeshttps://doi.org/10.1016/j.cjac.2022.100169openalex-snapshot
In vivo detection of L-tryptophan in cucumbers using poly (9-Aminoacridine) film modified pencil graphite electrode
inferred← citeshttps://doi.org/10.1016/j.envpol.2021.116723openalex-snapshot
Pollutants affect algae-bacteria interactions: A critical review
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e31170openalex-snapshot
Microalgae-bacteria nexus for environmental remediation and renewable energy resources: Advances, mechanisms and biotechnological applications
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e36503openalex-snapshot
Diverse interactions between bacteria and microalgae: A review for enhancing harmful algal bloom mitigation and biomass processing efficiency
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2022.03.007openalex-snapshot
Isolation of indole-3-acetic acid-producing Azospirillum brasilense from Vietnamese wet rice: Co-immobilization of isolate and microalgae as a sustainable biorefinery
inferred← citeshttps://doi.org/10.1016/j.jece.2025.116383openalex-snapshot
Interaction mechanism of organic toxicity removal by hydrolytic bacteria-Tetradesmus obliquus symbiotic system in anaerobic hydrolysate medium of toxic sludge
inferred← citeshttps://doi.org/10.1016/j.jenvman.2024.121226openalex-snapshot
Role of microalgae-bacterial consortium in wastewater treatment: A review
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2018.11.039openalex-snapshot
The collaborative effect of Chlorella vulgaris-Bacillus licheniformis consortia on the treatment of municipal water
inferred← citeshttps://doi.org/10.1016/j.micres.2024.127813openalex-snapshot
Microalgae growth-promoting bacteria for cultivation strategies: Recent updates and progress
inferred← citeshttps://doi.org/10.1016/j.mimet.2017.02.005openalex-snapshot
Immobilization of microalgae cells in alginate facilitates isolation of DNA and RNA
inferred← citeshttps://doi.org/10.1016/j.pbi.2018.03.004openalex-snapshot
Sniffing bacterial volatile compounds for healthier plants
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2025.179961openalex-snapshot
Mineral UV filters and their effects on Pocillopora damicornis metabolome
inferred← citeshttps://doi.org/10.1016/j.tim.2022.06.004openalex-snapshot
Synergy between microalgae and microbiome in polluted waters
inferred← citeshttps://doi.org/10.1016/j.watres.2024.122595openalex-snapshot
Removal of sulfamethoxazole in an algal-bacterial membrane aerated biofilm reactor: Microbial responses and antibiotic resistance genes
inferred← citeshttps://doi.org/10.1038/s41467-023-42663-yopenalex-snapshot
Coral endosymbiont growth is enhanced by metabolic interactions with bacteria
inferred← citeshttps://doi.org/10.1038/s43705-023-00311-yopenalex-snapshot
Abundant Sulfitobacter marine bacteria protect Emiliania huxleyi algae from pathogenic bacteria
inferred← citeshttps://doi.org/10.1080/07388551.2019.1654972openalex-snapshot
Soil microalgae and cyanobacteria: the biotechnological potential in the maintenance of soil fertility and health
inferred← citeshttps://doi.org/10.1093/femsec/fiw167openalex-snapshot
Editorial: Special thematic issue on microbe-assisted crop production
inferred← citeshttps://doi.org/10.1111/1462-2920.15749openalex-snapshot
The Azospirillum brasilense type VI secretion system promotes cell aggregation, biocontrol protection against phytopathogens and attachment to the microalgae Chlorella sorokiniana
inferred← citeshttps://doi.org/10.1111/are.13722openalex-snapshot
Growth and potential purification ability of Nitzschia sp. benthic diatoms in sea cucumber aquaculture wastewater
inferred← citeshttps://doi.org/10.1111/gcbb.70036openalex-snapshot
Rhizosphere Microbiome Diversity Potentially Supports Robust Nature of Field Pennycress (Thlaspi arvense L.) in Dryland Cropping Systems of Eastern Washington
inferred← citeshttps://doi.org/10.1111/jam.15509openalex-snapshot
Active indole-3-acetic acid biosynthesis by the bacterium Azospirillum brasilense cultured under a biogas atmosphere enables its beneficial association with microalgae
inferred← citeshttps://doi.org/10.1159/000513167openalex-snapshot
Complete Genomes of the Anaerobic Degradation Specialists Aromatoleum petrolei ToN1T and Aromatoleum bremense PbN1T
inferred← citeshttps://doi.org/10.1186/s12934-019-1233-7openalex-snapshot
Simultaneous and sequential based co-fermentations of Trichoderma asperellum GDFS1009 and Bacillus amyloliquefaciens 1841: a strategy to enhance the gene expression and metabolites to improve the bio-control and plant growth promoting activity
inferred← citeshttps://doi.org/10.1186/s40168-024-01899-6openalex-snapshot
Widespread production of plant growth-promoting hormones among marine bacteria and their impacts on the growth of a marine diatom
inferred← citeshttps://doi.org/10.1186/s44314-024-00005-2openalex-snapshot
Bacterial–microalgal consortia for bioremediation of textile industry wastewater and resource recovery for circular economy
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011587openalex-snapshot
Ethylene signals through an ethylene receptor to modulate biofilm formation and root colonization in a beneficial plant-associated bacterium
inferred← citeshttps://doi.org/10.1371/journal.pone.0192618openalex-snapshot
Genome mining of Streptomyces scabrisporus NF3 reveals symbiotic features including genes related to plant interactions
inferred← citeshttps://doi.org/10.1371/journal.pone.0276305openalex-snapshot
Specific bacterial microbiome enhances the sexual reproduction and auxospore production of the marine diatom, Odontella
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/10.2166/wst.2018.155openalex-snapshot
Exploiting symbiotic interactions between Chlorella protothecoides and Brevundimonas diminuta for an efficient single-step urban wastewater treatment
inferred← citeshttps://doi.org/10.22267/rcia.213802.162openalex-snapshot
Detection of auxinic compounds in germinating seedlings
inferred← citeshttps://doi.org/10.26508/lsa.202000878openalex-snapshot
Fungal mycelia and bacterial thiamine establish a mutualistic growth mechanism
inferred← citeshttps://doi.org/10.3389/fmicb.2019.00385openalex-snapshot
The Phytoplankton Taxon-Dependent Oil Response and Its Microbiome: Correlation but Not Causation
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1540274openalex-snapshot
Symbiotic microalgae and microbes: a new frontier in saline agriculture
inferred← citeshttps://doi.org/10.3390/biology10040282openalex-snapshot
Toward the Enhancement of Microalgal Metabolite Production through Microalgae–Bacteria Consortia
inferred← citeshttps://doi.org/10.3390/microorganisms7090275openalex-snapshot
Plant Tissue Localization and Morphological Conversion of Azospirillum brasilense upon Initial Interaction with Allium cepa L.
inferred← citeshttps://doi.org/10.3390/phycology6030089openalex-snapshot
Growth Promotion of Chlamydomonas reinhardtii by Cupriavidus oxalaticus MEYA8
inferred← citeshttps://doi.org/10.3390/plants12040788openalex-snapshot
Chlamydomonas reinhardtii, a Reference Organism to Study Algal–Microbial Interactions: Why Can’t They Be Friends?
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/pr13072177openalex-snapshot
Transcriptomic Response of Azospirillum brasilense Co-Cultured with Green Microalgae Chlorella sp. and Scenedesmus sp. During CO2 Biogas Fixation
inferred← citeshttps://doi.org/10.3390/su11030707openalex-snapshot
Symbiotic Co-Culture of Scenedesmus sp. and Azospirillum brasilense on N-Deficient Media with Biomass Production for Biofuels
inferred← citeshttps://doi.org/10.3390/w16182561openalex-snapshot
Microalgal–Bacteria Biofilm in Wastewater Treatment: Advantages, Principles, and Establishment
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.