On the public citation graph
A novel intracellular nitrogen‐fixing symbiosis made by U stilago maydis and B acillus spp.
0 signed · 125 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00933493openalex-snapshot
Relationship between nitrogen fixation and mycorrhiza
inferredcites →https://doi.org/10.1007/bf02214561openalex-snapshot
Occurrence of nitrogen-fixing Azospirillum in vesicular-arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1007/s00203-002-0478-3openalex-snapshot
Different effectors of dimorphism in Yarrowia lipolytica
inferredcites →https://doi.org/10.1016/0304-4165(66)90383-7openalex-snapshot
Acetylene reduction by nitrogen-fixing preparations from Clostridium pasteurianum
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.femsec.2005.02.005openalex-snapshot
Effects of the inoculant strain Pseudomonas putida KT2442 (pNF142) and of naphthalene contamination on the soil bacterial community
inferredcites →https://doi.org/10.1016/j.fgb.2012.07.005openalex-snapshot
Metamorphosis of the Basidiomycota Ustilago maydis: Transformation of yeast-like cells into basidiocarps
inferredcites →https://doi.org/10.1016/j.funbio.2010.09.001openalex-snapshot
New evidence for nitrogen fixation within the Italian white truffle Tuber magnatum
inferredcites →https://doi.org/10.1016/j.ijantimicag.2008.06.007openalex-snapshot
Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures
inferredcites →https://doi.org/10.1016/s0167-7012(00)00152-4openalex-snapshot
Fluorescence in situ hybridization (FISH) for direct visualization of microorganisms
inferredcites →https://doi.org/10.1016/s0958-1669(00)00204-4openalex-snapshot
The identification of microorganisms by fluorescence in situ hybridisation
inferredcites →https://doi.org/10.1021/jf960017uopenalex-snapshot
Content of Free Amino Acids in Huitlacoche (Ustilago maydis)
inferredcites →https://doi.org/10.1023/a:1027336712748openalex-snapshot
Respiratory Protection of Nitrogenase Activity in Azotobacter vinelandii—Roles of the Terminal Oxidases
inferredcites →https://doi.org/10.1038/237102a0openalex-snapshot
Genetic Transfer of Nitrogen Fixation from Klebsiella pneumoniae to Escherichia coli
inferredcites →https://doi.org/10.1038/260268a0openalex-snapshot
Construction of a P plasmid carrying nitrogen fixation genes from Klebsiella pneumoniae
inferredcites →https://doi.org/10.1038/ismej.2012.119openalex-snapshot
Antagonism influences assembly of a Bacillus guild in a local community and is depicted as a food-chain network
inferredcites →https://doi.org/10.1038/nature05248openalex-snapshot
Insights from the genome of the biotrophic fungal plant pathogen Ustilago maydis
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03680.xopenalex-snapshot
Isolation and characterization from pathogenic fungi of genes encoding ammonium permeases and their roles in dimorphism
inferredcites →https://doi.org/10.1073/pnas.73.12.4570openalex-snapshot
Structure and transformation of chitin synthetase particles (chitosomes) during microfibril synthesis in vitro.
inferredcites →https://doi.org/10.1073/pnas.78.6.3496openalex-snapshot
Stable chromosomal integration of the entire nitrogen fixation gene cluster from Klebsiella pneumoniae in yeast.
inferredcites →https://doi.org/10.1073/pnas.86.15.5878openalex-snapshot
Different a alleles of Ustilago maydis are necessary for maintenance of filamentous growth but not for meiosis
inferredcites →https://doi.org/10.1073/pnas.86.3.978openalex-snapshot
Isolation of two alleles of the b locus of Ustilago maydis.
inferredcites →https://doi.org/10.1080/02648725.1984.10647781openalex-snapshot
Genetic Engineering and Nitrogen Fixation
inferredcites →https://doi.org/10.1093/molbev/mst197openalex-snapshot
MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040752openalex-snapshot
Estimation of the number of nucleotide substitutions when there are strong transition-transversion and G+C-content biases.
inferredcites →https://doi.org/10.1094/mpmi-19-0827openalex-snapshot
Bacterial Endophytes and Their Interactions with Hosts
inferredcites →https://doi.org/10.1097/00010694-197605000-00012openalex-snapshot
The Biology of Nitrogen Fixation
inferredcites →https://doi.org/10.1099/00207713-34-4-451openalex-snapshot
Bacillus azotofixans sp. nov., a Nitrogen-Fixing Species from Brazilian Soils and Grass Roots
inferredcites →https://doi.org/10.1099/00221287-148-8-2293openalex-snapshot
Evidence for protection of nitrogenase from O2 by colony structure in the aerobic diazotroph Gluconacetobacter diazotrophicus
inferredcites →https://doi.org/10.1099/13500872-141-3-695openalex-snapshot
Yeast-mycelial dimorphism of haploid and diploid strains of Ustilago maydis
inferredcites →https://doi.org/10.1099/ijs.0.02382-0openalex-snapshot
‘Candidatus Glomeribacter gigasporarum’ gen. nov., sp. nov., an endosymbiont of arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1099/mic.0.055954-0openalex-snapshot
Phenotypic comparison of samdc and spe mutants reveals complex relationships of polyamine metabolism in Ustilago maydis
inferredcites →https://doi.org/10.1104/pp.43.8.1185openalex-snapshot
The Acetylene-Ethylene Assay for N 2 Fixation: Laboratory and Field Evaluation
inferredcites →https://doi.org/10.1111/j.1758-2229.2011.00260.xopenalex-snapshot
Ultra‐deep pyrosequencing of pmoA amplicons confirms the prevalence of Methylomonas and Methylocystis in Sphagnum mosses from a Dutch peat bog
inferredcites →https://doi.org/10.1126/science.1173036openalex-snapshot
Symbiotic Nitrogen Fixation in the Fungus Gardens of Leaf-Cutter Ants
inferredcites →https://doi.org/10.1128/aem.62.8.3005-3010.1996openalex-snapshot
An obligately endosymbiotic mycorrhizal fungus itself harbors obligately intracellular bacteria
inferredcites →https://doi.org/10.1128/aem.63.8.3233-3241.1997openalex-snapshot
Analysis of actinomycete communities by specific amplification of genes encoding 16S rRNA and gel-electrophoretic separation in denaturing gradients
inferredcites →https://doi.org/10.1128/aem.64.8.3052-3058.1998openalex-snapshot
Whole-Cell Immunolocalization of Nitrogenase in Marine Diazotrophic Cyanobacteria, Trichodesmium spp
inferredcites →https://doi.org/10.1128/aem.67.2.725-732.2001openalex-snapshot
Nitrogen Fixation Genes in an Endosymbiotic Burkholderia Strain
inferredcites →https://doi.org/10.1128/aem.67.6.2790-2798.2001openalex-snapshot
Burkholderia , a Genus Rich in Plant-Associated Nitrogen Fixers with Wide Environmental and Geographic Distribution
inferredcites →https://doi.org/10.1128/aem.68.11.5342-5350.2002openalex-snapshot
Ethylene Production byBotrytis cinereaIn Vitro and in Tomatoes
inferredcites →https://doi.org/10.1128/jb.186.20.6876-6884.2004openalex-snapshot
Isolation, Free-Living Capacities, and Genome Structure of “ Candidatus Glomeribacter gigasporarum,” the Endocellular Bacterium of the Mycorrhizal Fungus Gigaspora margarita
inferredcites →https://doi.org/10.1146/annurev-genet-110410-132549openalex-snapshot
The Rules of Engagement in the Legume-Rhizobial Symbiosis
inferredcites →https://doi.org/10.1146/annurev.biochem.78.070907.103812openalex-snapshot
Mechanism of Mo-Dependent Nitrogenase
inferredcites →https://doi.org/10.1146/annurev.ge.20.120186.003031openalex-snapshot
REGULATION OF NITROGEN FIXATION GENES
inferredcites →https://doi.org/10.1146/annurev.pp.17.060166.001103openalex-snapshot
Biological Nitrogen Fixation
inferredcites →https://doi.org/10.1186/1471-2148-7-55openalex-snapshot
Nitrogen fixation in eukaryotes – New models for symbiosis
inferredcites →https://doi.org/10.1371/journal.pone.0086527openalex-snapshot
Transcriptional Profiling of Nitrogen Fixation and the Role of NifA in the Diazotrophic Endophyte Azoarcus sp. Strain BH72
inferredcites →https://doi.org/10.5053/ejobios.2010.4.0.5openalex-snapshot
Isolation and characterization of salt-tolerant nitrogen-fixing microorganisms from food
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.4784983openalex-extracted
Distribution and Functional of Brevundimonas-Related Endobacteria within Verticillium Dahliae
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0699openalex-snapshot
Phytobiomes, the Reason Why Microbiologists and Botanists Should Work Together
inferred← citeshttps://doi.org/10.1002/jobm.201600660openalex-snapshot
Transcriptional analysis of the adaptation ofUstilago maydisduring growth under nitrogen fixation conditions
inferred← citeshttps://doi.org/10.1007/978-3-030-41870-0_1openalex-snapshot
Fungal Epigenetic Engineering
inferred← citeshttps://doi.org/10.1007/978-3-030-71206-8_18openalex-snapshot
Perspectives on Nitrogen-Fixing Bacillus Species
inferred← citeshttps://doi.org/10.1007/978-3-032-16045-4_4openalex-snapshot
Unraveling the Role of Yeasts and Potential Endosymbionts in Plant Growth Promotion: Insights from Rhodotorula mucilaginosa
inferred← citeshttps://doi.org/10.1007/978-981-13-9349-5_2openalex-snapshot
The Developmental History of Ustilago maydis: A Saprophytic Yeast, a Mycelial Fungus, Mushroom-Like, and a Smut
inferred← citeshttps://doi.org/10.1007/978-981-15-6953-1_7openalex-snapshot
Nitrogen and Phosphorus Use Efficiency in Agroecosystems
inferred← citeshttps://doi.org/10.1007/978-981-16-8770-9_2openalex-snapshot
Intermicrobial Interactions in the Pedosphere and Their Importance
inferred← citeshttps://doi.org/10.1007/s00203-017-1388-8openalex-snapshot
Lipid droplets accumulation and other biochemical changes induced in the fungal pathogen Ustilago maydis under nitrogen-starvation
inferred← citeshttps://doi.org/10.1007/s10123-019-00100-5openalex-snapshot
The signaling mechanisms involved in the dimorphic phenomenon of the Basidiomycota fungus Ustilago maydis
inferred← citeshttps://doi.org/10.1007/s11104-024-07161-0openalex-snapshot
Intricate Russian dolls relationships between plants, fungi and bacteria
inferred← citeshttps://doi.org/10.1007/s13199-020-00682-zopenalex-snapshot
Alterations in the sap-associated microbiota of Carica papaya in response to drought stress
inferred← citeshttps://doi.org/10.1007/s44154-022-00046-1openalex-snapshot
Bacterial-fungal interactions under agricultural settings: from physical to chemical interactions
inferred← citeshttps://doi.org/10.1016/b978-0-12-819990-9.00038-xopenalex-snapshot
Proteomics in Mycorrhizal and Plant Pathogenic Fungi
inferred← citeshttps://doi.org/10.1016/j.crmicr.2026.100617openalex-snapshot
Endogenous hydrogen sulfide reprograms mitochondrial respiration and modulates pathogenicity in Ustilago maydis
inferred← citeshttps://doi.org/10.1016/j.fbr.2018.08.003openalex-snapshot
Endohyphal bacteria; the prokaryotic modulators of host fungal biology
inferred← citeshttps://doi.org/10.1016/j.funbio.2021.04.010openalex-snapshot
Role for nitrate assimilatory genes in virulence of Ustilago maydis
inferred← citeshttps://doi.org/10.1016/j.funeco.2018.08.008openalex-snapshot
Context-dependent and variable effects of endohyphal bacteria on interactions between fungi and seeds
inferred← citeshttps://doi.org/10.1016/j.isci.2025.112253openalex-snapshot
Genomic evidence of symbiotic adaptations in fungus-associated bacteria
inferred← citeshttps://doi.org/10.1016/j.jenvman.2024.120886openalex-snapshot
Intercropping improves maize yield and nitrogen uptake by regulating nitrogen transformation and functional microbial abundance in rhizosphere soil
inferred← citeshttps://doi.org/10.1016/j.mib.2024.102496openalex-snapshot
Symbioses between fungi and bacteria: from mechanisms to impacts on biodiversity
inferred← citeshttps://doi.org/10.1016/j.micres.2025.128361openalex-snapshot
Endofungal bacteria: Emerging paradigms and future directions
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.10.010openalex-snapshot
Symbiotic bacteria of plant-associated fungi: friends or foes?
inferred← citeshttps://doi.org/10.1016/j.procbio.2023.06.008openalex-snapshot
A new bacterial endosymbiotic relationship in Kluyveromyces marxianus isolated from the mezcal fermentation process
inferred← citeshttps://doi.org/10.1016/j.soilbio.2020.108060openalex-snapshot
Feremycorrhizal symbiosis confers growth and nutritional benefits to mycorrhizal and non-mycorrhizal crops
inferred← citeshttps://doi.org/10.1080/15592324.2020.1855016openalex-snapshot
Wide distribution of the Ustilago maydis -bacterium endosymbiosis in naturally infected maize plants
inferred← citeshttps://doi.org/10.1093/dnares/dsy044openalex-snapshot
A unique life-strategy of an endophytic yeast Rhodotorula mucilaginosa JGTA-S1—a comparative genomics viewpoint
inferred← citeshttps://doi.org/10.1093/femsle/fnz108openalex-snapshot
Autophagosomes accumulation in the vacuoles of the fungus Ustilago maydis and the role of proteases in their digestion
inferred← citeshttps://doi.org/10.1093/femsre/fuy008openalex-snapshot
Bacterial–fungal interactions: ecology, mechanisms and challenges
inferred← citeshttps://doi.org/10.1093/ismejo/wraf128openalex-snapshot
Endofungal bacteria as hidden facilitators of biotic interactions
inferred← citeshttps://doi.org/10.1093/ismejo/wraf260openalex-snapshot
In situ degradation of 2-methylnaphthalene by a soil Penicillium strain associated with fungal–bacterial interactions
inferred← citeshttps://doi.org/10.1094/pbiomes-02-23-0012-popenalex-snapshot
Predictive Ecology and Management of Phyllosphere Microbial Communities Through Cross-Scale Synthesis
inferred← citeshttps://doi.org/10.1094/pbiomes-12-24-0117-mrvwopenalex-snapshot
A Plant Health View on Endohyphal Bacteria and Their Fungal Hosts
inferred← citeshttps://doi.org/10.1099/mgen.0.000101openalex-snapshot
Absence of genome reduction in diverse, facultative endohyphal bacteria
inferred← citeshttps://doi.org/10.1101/2022.09.29.510055openalex-snapshot
Atmospheric nitrogen fixation by eukaryotes: Should we reconsider the nitrogen cycle in nature?
inferred← citeshttps://doi.org/10.1101/2023.09.14.557762openalex-snapshot
Genome analysis and hyphal movement characterization of the hitchhiker endohyphal Enterobacter sp. from Rhizoctonia solani
inferred← citeshttps://doi.org/10.1101/2025.02.11.633654openalex-snapshot
Crusty-Pinky: A Novel Polyextremotolerant Fungus and its Methylobacterium Symbionts Could be an Essential Symbiosis for the Biological Soil Crust Consortium
inferred← citeshttps://doi.org/10.1105/tpc.19.00385openalex-snapshot
A Tripartite Interaction among the Basidiomycete Rhodotorula mucilaginosa , N 2 -Fixing Endobacteria, and Rice Improves Plant Nitrogen Nutrition
inferred← citeshttps://doi.org/10.1111/1462-2920.13669openalex-snapshot
Comparative genomics of Mortierella elongata and its bacterial endosymbiont Mycoavidus cysteinexigens
inferred← citeshttps://doi.org/10.1111/1462-2920.13731openalex-snapshot
The fungal holobiont: Evidence from early diverging fungi
inferred← citeshttps://doi.org/10.1111/mec.13250openalex-snapshot
Molecular evolution patterns reveal life history features of mycoplasma‐related endobacteria associated with arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1111/nph.13895openalex-snapshot
An interdomain network: the endobacterium of a mycorrhizal fungus promotes antioxidative responses in both fungal and plant hosts
inferred← citeshttps://doi.org/10.1128/aem.00660-18openalex-snapshot
Unveiling Concealed Functions of Endosymbiotic Bacteria Harbored in the Ascomycete Stachylidium bicolor
inferred← citeshttps://doi.org/10.1128/aem.02245-23openalex-snapshot
Genome analysis and hyphal movement characterization of the hitchhiker endohyphal Enterobacter sp. from Rhizoctonia solani
inferred← citeshttps://doi.org/10.1134/s0026261719020127openalex-snapshot
Rhizobacteria Strain from a Hypersaline Environment Promotes Plant Growth of Kengyilia thoroldiana
inferred← citeshttps://doi.org/10.1186/s12866-022-02580-4openalex-snapshot
Community composition, bacterial symbionts, antibacterial and antioxidant activities of honeybee-associated fungi
inferred← citeshttps://doi.org/10.1186/s13568-023-01618-8openalex-snapshot
Klebsiella michiganensis: a nitrogen-fixing endohyphal bacterium from Ustilago maydis
inferred← citeshttps://doi.org/10.1186/s40168-018-0445-0openalex-snapshot
Microbial interactions within the plant holobiont
inferred← citeshttps://doi.org/10.1186/s40168-023-01484-3openalex-snapshot
Microbiota and functional analyses of nitrogen-fixing bacteria in root-knot nematode parasitism of plants
inferred← citeshttps://doi.org/10.1201/9781315119496-40openalex-snapshot
Chapter 39 Ecology and Evolution of Fungal-Bacterial Interactions
inferred← citeshttps://doi.org/10.1264/jsme2.me17138openalex-snapshot
Comparative Genomic Insights into Endofungal Lifestyles of Two Bacterial Endosymbionts, Mycoavidus cysteinexigens and Burkholderia rhizoxinica
inferred← citeshttps://doi.org/10.18297/etd/2322openalex-snapshot
Atmospheric nitrogen assimilation in Ustilago maydis.
inferred← citeshttps://doi.org/10.20710/dojo.87.4_254openalex-snapshot
土壌微生物が創る共生の世界―その先端的研究事例と農業への応用的研究展開 4．糸状菌に共生する細菌その機能と生態―
inferred← citeshttps://doi.org/10.21640/ns.v7i15.278openalex-snapshot
Reprogramación celular de embriones de Anthurium andraeanum por fitohormonas para micropropagación masiva
inferred← citeshttps://doi.org/10.33073/pjm-2023-007openalex-snapshot
Characterization of a Plant Growth-Promoting Endohyphal Bacillus subtilis in Fusarium acuminatum from Spiranthes sinensis
inferred← citeshttps://doi.org/10.3389/fmicb.2017.00350openalex-snapshot
An Endohyphal Bacterium (Chitinophaga, Bacteroidetes) Alters Carbon Source Use by Fusarium keratoplasticum (F. solani Species Complex, Nectriaceae)
inferred← citeshttps://doi.org/10.3389/fmicb.2022.855399openalex-snapshot
Plant Growth-Promoting Ability of Mycorrhizal Fusarium Strain KB-3 Enhanced by Its IAA Producing Endohyphal Bacterium, Klebsiella aerogenes
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1349447openalex-snapshot
Endosymbiotic bacteria within the nematode-trapping fungus Arthrobotrys musiformis and their potential roles in nitrogen cycling
inferred← citeshttps://doi.org/10.3389/fmicb.2026.1864871openalex-snapshot
Endosymbiotic interactions in the fungal kingdom: a framework for progressive endosymbiosis
inferred← citeshttps://doi.org/10.3390/jof11110813openalex-snapshot
Endobacteria Have a Negative Effect on the Virulence of Metarhizium
inferred← citeshttps://doi.org/10.3390/jof9020204openalex-snapshot
Phenotypic and Genomic Difference among Four Botryosphaeria Pathogens in Chinese Hickory Trunk Canker
inferred← citeshttps://doi.org/10.6084/m9.figshare.20168022openalex-snapshot
Additional file 1 of Community composition, bacterial symbionts, antibacterial and antioxidant activities of honeybee-associated fungi
inferred← citeshttps://doi.org/10.6084/m9.figshare.20168025openalex-snapshot
Additional file 2 of Community composition, bacterial symbionts, antibacterial and antioxidant activities of honeybee-associated fungi
inferred← citeshttps://doi.org/10.6084/m9.figshare.22625861openalex-snapshot
Additional file 1 of Microbiota and functional analyses of nitrogen-fixing bacteria in root-knot nematode parasitism of plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.22625864openalex-snapshot
Additional file 2 of Microbiota and functional analyses of nitrogen-fixing bacteria in root-knot nematode parasitism of plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.22625867openalex-snapshot
Additional file 3 of Microbiota and functional analyses of nitrogen-fixing bacteria in root-knot nematode parasitism of plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.22625870openalex-snapshot
Additional file 4 of Microbiota and functional analyses of nitrogen-fixing bacteria in root-knot nematode parasitism of plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.22625873openalex-snapshot
Additional file 5 of Microbiota and functional analyses of nitrogen-fixing bacteria in root-knot nematode parasitism of plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.22625876openalex-snapshot
Additional file 6 of Microbiota and functional analyses of nitrogen-fixing bacteria in root-knot nematode parasitism of plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.22625879openalex-snapshot
Additional file 7 of Microbiota and functional analyses of nitrogen-fixing bacteria in root-knot nematode parasitism of plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.22625882openalex-snapshot
Additional file 8 of Microbiota and functional analyses of nitrogen-fixing bacteria in root-knot nematode parasitism of plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.26656489openalex-snapshot
Additional file 1 of Klebsiella michiganensis: a nitrogen-fixing endohyphal bacterium from Ustilago maydis
inferred← citeshttps://doi.org/10.64898/2026.06.18.733246openalex-snapshot
An endosymbiotic Paenibacillus sp. modulates disease severity caused by the common watermelon pathogen, Fusarium oxysporum f sp. niveum
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.