ArticleFrontiers in microbiology2016
Indole-3-Acetic Acid Is Produced by Emiliania huxleyi Coccolith-Bearing Cells and Triggers a Physiological Response in Bald Cells.
Article in Frontiers in microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.
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Who cites it
28 citing papers in PubMed, 101 citations in OpenAlex.
- The coccosphere of the heavy calcifying coccolithophore Coccolithus braarudii provides defense against bacteria.Communications biology · 2026Article
- Tryptophanol enhances nitrogen assimilation in marine diatoms.Nature communications · 2026Article
- Characterization and Phenolic Profiling of AnticandidalACS omega · 2025Article
- Bacteria induce an amoeboid phase in coccolithophores that persists after bloom collapse.Science advances · 2025Article
- Gut microbiota-derived indole-3-acetic acid ameliorates calcium oxalate renal stone formation via AHR/NF‑κB axis.Urolithiasis · 2025Article
- Preparation and characterization of immobilized indole-3-butyric acid on silver-cerium oxide nanoparticles for improving its stability and utilization in the study of plant root formation indices.Frontiers in plant science · 2025Article
- Article
- Origin and evolution of auxin-mediated acid growth.Proceedings of the National Academy of Sciences of the United States of America · 2024Article
- Widespread production of plant growth-promoting hormones among marine bacteria and their impacts on the growth of a marine diatom.Microbiome · 2024Article
- Genetic evidence for algal auxin production iniScience · 2024Article
- Comparative study between Salkowski reagent and chromatographic method for auxins quantification from bacterial production.Frontiers in plant science · 2024Article
- Performance of Plant-Growth-Promoting Rhizobacteria (PGPR) Isolated from Sandy Soil on Growth of Tomato (Plants (Basel, Switzerland) · 2023Article
- The birth of a giant: evolutionary insights into the origin of auxin responses in plants.The EMBO journal · 2023Review
- Review
- Plant Growth Promotion, Phytohormone Production and Genomics of the Rhizosphere-Associated Microalga,Plants (Basel, Switzerland) · 2023Article
- Indole-3-acetic acid as a cross-talking molecule in algal-bacterial interactions and a potential driving force in algal bloom formation.Frontiers in microbiology · 2023Review
- Resolving the Microalgal Gene Landscape at the Strain Level: a Novel Hybrid Transcriptome ofApplied and environmental microbiology · 2022Article
- Untargeted metabolite profiling to elucidate rhizosphere and leaf metabolome changes of wheat cultivars (Frontiers in microbiology · 2022Article
- Quorum sensing regulates 'swim-or-stick' lifestyle in the phycosphere.Environmental microbiology · 2020Article
- The Phylogeny of Class B Flavoprotein Monooxygenases and the Origin of the YUCCA Protein Family.Plants (Basel, Switzerland) · 2020Article
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Indole-3-acetic acid (IAA) is an auxin produced by terrestrial plants which influences development through a variety of cellular mechanisms, such as altering cell orientation, organ development, fertility, and cell elongation. IAA is also produced by bacterial pathogens and symbionts of plants and algae, allowing them to manipulate growth and development of their host. They do so by either producing excess exogenous IAA or hijacking the IAA biosynthesis pathway of their host. The endogenous production of IAA by algae remains contentious. Using Emiliania huxleyi, a globally abundant marine haptophyte, we investigated the presence and potential role of IAA in algae. Homologs of genes involved in several tryptophan-dependent IAA biosynthesis pathways were identified in E. huxleyi. This suggests that this haptophyte can synthesize IAA using various precursors derived from tryptophan. Addition of L-tryptophan to E. huxleyi stimulated IAA production, which could be detected using Salkowski's reagent and GC × GC-TOFMS in the C cell type (coccolith bearing), but not in the N cell type (bald). Various concentrations of IAA were exogenously added to these two cell types to identify a physiological response in E. huxleyi. The N cell type, which did not produce IAA, was more sensitive to it, showing an increased variation in cell size, membrane permeability, and a corresponding increase in the photosynthetic potential quantum yield of Photosystem II (PSII). A roseobacter (bacteria commonly associated with E. huxleyi) Ruegeria sp. R11, previously shown to produce IAA, was co-cultured with E. huxleyi C and N cells. IAA could not be detected from these co-cultures, and even when stimulated by addition of L-tryptophan, they produced less IAA than axenic C type culture similarly induced. This suggests that IAA plays a novel role signaling between different E. huxleyi cell types, rather than between a bacteria and its algal host.
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