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The associative induction of succinic acid and hydrogen sulfide for high-producing biomass, astaxanthin and lipids in Haematococcus pluvialis

https://doi.org/10.1016/j.biortech.2022.127397
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What this work says

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

inferredcites →https://doi.org/10.1002/aocs.12230openalex-snapshot
The Discrepancy of Fatty Acid Composition of Astaxanthin Esters and Total Fatty Acids in Photoautotrophic and Heterotrophic Chlorella zofingiensis
inferredcites →https://doi.org/10.1002/jpln.200520560openalex-snapshot
Exogenous succinate increases resistance of maize plants to copper stress
inferredcites →https://doi.org/10.1007/s11676-017-0579-0openalex-snapshot
Exogenous application of succinic acid enhances tolerance of Larix olgensis seedling to lead stress
inferredcites →https://doi.org/10.1007/s11738-014-1648-zopenalex-snapshot
The response of rbcL, rbcS and rca genes in cucumber (Cucumis sativus L.) to growth and induction light intensity
inferredcites →https://doi.org/10.1007/s11802-016-2848-5openalex-snapshot
Changes in growth, carbon and nitrogen enzyme activity and mRNA accumulation in the halophilic microalga Dunaliella viridis in response to NaCl stress
inferredcites →https://doi.org/10.1007/s13399-021-01276-5openalex-snapshot
Simultaneous production of astaxanthin and lipids from Chlorella sorokiniana in the presence of reactive oxygen species: a biorefinery approach
inferredcites →https://doi.org/10.1016/j.algal.2015.08.024openalex-snapshot
Photosynthetic response to nitrogen starvation and high light in Haematococcus pluvialis
inferredcites →https://doi.org/10.1016/j.algal.2020.102089openalex-snapshot
Exogenous γ-aminobutyric acid promotes biomass and astaxanthin production in Haematococcus pluvialis
inferredcites →https://doi.org/10.1016/j.biortech.2012.07.002openalex-snapshot
Isolation of a novel strain of Monoraphidium sp. and characterization of its potential application as biodiesel feedstock
inferredcites →https://doi.org/10.1016/j.biortech.2017.09.133openalex-snapshot
Inhibition of autophagy modulates astaxanthin and total fatty acid biosynthesis in Chlorella zofingiensis under nitrogen starvation
inferredcites →https://doi.org/10.1016/j.biortech.2018.06.111openalex-snapshot
Butylated hydroxytoluene induces astaxanthin and lipid production in Haematococcus pluvialis under high-light and nitrogen-deficiency conditions
inferredcites →https://doi.org/10.1016/j.biortech.2018.12.030openalex-snapshot
Coupling of abiotic stresses and phytohormones for the production of lipids and high-value by-products by microalgae: A review
inferredcites →https://doi.org/10.1016/j.biortech.2019.122612openalex-snapshot
Disodium 2-oxoglutarate promotes carbon flux into astaxanthin and fatty acid biosynthesis pathways in Haematococcus
inferredcites →https://doi.org/10.1016/j.biortech.2019.122649openalex-snapshot
Enhancement of linoleic acid content stimulates astaxanthin esterification in Coelastrum sp.
inferredcites →https://doi.org/10.1016/j.biortech.2020.123069openalex-snapshot
Melatonin and calcium act synergistically to enhance the coproduction of astaxanthin and lipids in Haematococcus pluvialis under nitrogen deficiency and high light conditions
inferredcites →https://doi.org/10.1016/j.biortech.2020.124418openalex-snapshot
Gamma-aminobutyric acid facilitates the simultaneous production of biomass, astaxanthin and lipids in Haematococcus pluvialis under salinity and high-light stress conditions
inferredcites →https://doi.org/10.1016/j.biortech.2021.125648openalex-snapshot
A fed-batch feeding with succinic acid strategy for astaxanthin and lipid hyper-production in Haematococcus pluviualis
inferredcites →https://doi.org/10.1016/j.biortech.2021.125784openalex-snapshot
A joint strategy comprising melatonin and 3-methyladenine to concurrently stimulate biomass and astaxanthin hyperaccumulation by Haematococcus pluvialis
inferredcites →https://doi.org/10.1016/j.biortech.2021.126225openalex-snapshot
Enhancing astaxanthin and lipid coproduction in Haematococcus pluvialis by the combined induction of plant growth regulators and multiple stresses
inferredcites →https://doi.org/10.1016/j.ecoenv.2017.01.037openalex-snapshot
Role of two-sided crosstalk between NO and H 2 S on improvement of mineral homeostasis and antioxidative defense in Sesamum indicum under lead stress
inferredcites →https://doi.org/10.1016/j.enzmictec.2019.109487openalex-snapshot
Transcriptome analysis of Haematococcus pluvialis of multiple defensive systems against nitrogen starvation
inferredcites →https://doi.org/10.1016/j.fgb.2019.04.014openalex-snapshot
Hydrogen sulfide, a novel small molecule signalling agent, participates in the regulation of ganoderic acids biosynthesis induced by heat stress in Ganoderma lucidum
inferredcites →https://doi.org/10.1016/j.foodchem.2016.03.113openalex-snapshot
Involvement of energy metabolism to chilling tolerance induced by hydrogen sulfide in cold-stored banana fruit
inferredcites →https://doi.org/10.1016/j.fsi.2018.04.008openalex-snapshot
Dietary effects of succinic acid on the growth, digestive enzymes, immune response and resistance to ammonia stress of Litopenaeus vannamei
inferredcites →https://doi.org/10.1016/j.plaphy.2016.10.006openalex-snapshot
Hydrogen sulfide and proline cooperate to alleviate cadmium stress in foxtail millet seedlings
inferredcites →https://doi.org/10.1016/j.plaphy.2021.07.023openalex-snapshot
Hydrogen sulfide and nitric oxide are involved in melatonin-induced salt tolerance in cucumber
inferredcites →https://doi.org/10.1016/j.plaphy.2021.12.002openalex-snapshot
Hydrogen sulfide improves tall fescue photosynthesis response to low-light stress by regulating chlorophyll and carotenoid metabolisms
inferredcites →https://doi.org/10.1016/j.procbio.2005.02.014openalex-snapshot
Employment of reactive oxygen species to enhance astaxanthin formation in Chlorella zofingiensis in heterotrophic culture
inferredcites →https://doi.org/10.1016/j.renene.2021.03.051openalex-snapshot
Myo-inositol promotes lipid production and nutrients removal by microalga under molasses wastewater
inferredcites →https://doi.org/10.1016/j.scienta.2021.110366openalex-snapshot
H2S improves growth of tomato seedlings involving the MAPK signaling
inferredcites →https://doi.org/10.1016/s0032-9592(01)00246-1openalex-snapshot
Influence of stress on astaxanthin production in Haematococcus pluvialis grown under different culture conditions
inferredcites →https://doi.org/10.1016/s2095-3119(16)61358-8openalex-snapshot
Foliar application of sodium hydrosulfide (NaHS), a hydrogen sulfide (H2S) donor, can protect seedlings against heat stress in wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.1021/acs.analchem.9b04534openalex-snapshot
Autonomous Temporal Control of Hydrogen Sulfide Delivery
inferredcites →https://doi.org/10.1021/acs.jafc.2c00479openalex-snapshot
Supplementation with rac-GR24 Facilitates the Accumulation of Biomass and Astaxanthin in Two Successive Stages of Haematococcus pluvialis Cultivation
inferredcites →https://doi.org/10.1021/acssuschemeng.9b06748openalex-snapshot
Hydrogen Sulfide Improves Lipid Accumulation in Nannochloropsis oceanica through Metabolic Regulation of Carbon Allocation and Energy Supply
inferredcites →https://doi.org/10.1080/00318884.2019.1670012openalex-snapshot
Linoleic-acid-enhanced astaxanthin content of Chlorella sorokiniana (Chlorophyta) under normal and light shock conditions
inferredcites →https://doi.org/10.1093/jxb/eru206openalex-snapshot
Comparative analyses of lipidomes and transcriptomes reveal a concerted action of multiple defensive systems against photooxidative stress in Haematococcus pluvialis
inferredcites →https://doi.org/10.1111/tpj.12713openalex-snapshot
Molecular mechanisms of the coordination between astaxanthin and fatty acid biosynthesis in Haematococcus pluvialis (Chlorophyceae)
inferredcites →https://doi.org/10.1186/s13068-021-01933-xopenalex-snapshot
Transcriptome-based analysis of the effects of salicylic acid and high light on lipid and astaxanthin accumulation in Haematococcus pluvialis
inferredcites →https://doi.org/10.3389/fpls.2016.00930openalex-snapshot
The Significance of Hydrogen Sulfide for Arabidopsis Seed Germination
inferredcites →https://doi.org/10.3389/fpls.2019.00743openalex-snapshot
Atmospheric H2S: Impact on Plant Functioning
inferredcites →https://doi.org/10.3389/fpls.2020.00108openalex-snapshot
Improving Photosynthetic Capacity, Alleviating Photosynthetic Inhibition and Oxidative Stress Under Low Temperature Stress With Exogenous Hydrogen Sulfide in Blueberry Seedlings
inferredcites →https://doi.org/10.3389/fpls.2020.01105openalex-snapshot
Hydrogen Sulfide Signaling Protects Chlamydomonas reinhardtii Against Allelopathic Damage From Cyanobacterial Toxin Microcystin-LR
inferredcites →https://doi.org/10.3390/antiox9090825openalex-snapshot
An Integrated Strategy for Nutraceuticals from Haematoccus pluvialis: From Cultivation to Extraction
inferredcites →https://doi.org/10.3390/ijms17010103openalex-snapshot
Free Radical Scavenging and Cellular Antioxidant Properties of Astaxanthin
inferredcites →https://doi.org/10.3390/ijms21010118openalex-snapshot
Comparative Proteomic Analysis Reveals the Regulatory Effects of H2S on Salt Tolerance of Mangrove Plant Kandelia obovata
inferredcites →https://doi.org/10.3390/ijms22179326openalex-snapshot
Regulation of Reactive Oxygen Species and Antioxidant Defense in Plants under Salinity
inferredcites →https://doi.org/10.3390/md20010001openalex-snapshot
Transcriptomic and Proteomic Characterizations of the Molecular Response to Blue Light and Salicylic Acid in Haematococcus pluvialis

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.4632160openalex-extracted
Synchronous Enhancement of Astaxanthin and Lipid Accumulation in Haematococcus Pluvialis Through Co-Mutation of Ethanol and Artp: An Exploration of Characteristics and Underlying Mechanisms
inferred← citeshttps://doi.org/10.1007/978-981-95-7234-2_6openalex-snapshot
Astaxanthin from Haematococcus pluvialis: A Natural Key to Future Therapeutics and Functional Foods
inferred← citeshttps://doi.org/10.1007/978-981-95-8593-9_17openalex-snapshot
Succinic Acid: A Metabolic Enhancer for Plants Under Stress
inferred← citeshttps://doi.org/10.1007/s00449-026-03351-5openalex-snapshot
β-cyclodextrin and succinic acid–driven metabolic enhancement of lipid, phycobiliprotein, and exopolysaccharide production in Porphyridium purpureum
inferred← citeshttps://doi.org/10.1007/s00709-025-02105-6openalex-snapshot
Humic acid induced astaxanthin accumulation by changing GABA, polyamines, and H2O2 levels in Haematococcus lacustris at the stationary growth phase
inferred← citeshttps://doi.org/10.1007/s11101-023-09906-8openalex-snapshot
From present to prosperity: assessing the current status and envisioning opportunities in the industrial-scale cultivation of Haematococcus pluvialis for astaxanthin production
inferred← citeshttps://doi.org/10.1007/s43393-026-00547-4openalex-snapshot
Next-generation microalgae biorefinery: innovations in sustainable astaxanthin, biofuel, and aquafeed production
inferred← citeshttps://doi.org/10.1016/j.biortech.2022.128030openalex-snapshot
Recent advancements in astaxanthin production from microalgae: A review
inferred← citeshttps://doi.org/10.1016/j.biortech.2023.130232openalex-snapshot
Mechanism of enhanced microalgal biomass and lipid accumulation through symbiosis between a highly succinic acid-producing strain of Escherichia coli SUC and Aurantiochytrium sp. SW1
inferred← citeshttps://doi.org/10.1016/j.biortech.2024.130305openalex-snapshot
Synchronous enhancement of astaxanthin and lipid accumulation in Haematococcus lacustris through co-mutation of ethanol and atmospheric and room temperature plasma: Exploration of characteristics and underlying mechanisms
inferred← citeshttps://doi.org/10.1016/j.cej.2026.183014openalex-snapshot
Methanol serves as both carbon donor and chemical signal to enhance growth and astaxanthin accumulation in two-stage cultivation of Haematococcus lacustris
inferred← citeshttps://doi.org/10.1016/j.fbio.2026.110222openalex-snapshot
Enhanced astaxanthin production by immobilized Haematococcus pluvialis in calcium alginate hydrogel beads with pore size distribution modulated by polyethylene glycol
inferred← citeshttps://doi.org/10.1016/j.foodchem.2025.145406openalex-snapshot
Regulation of astaxanthin accumulation in Phaffia rhodozyma under titanium dioxide and rapeseed oil stress by amino acid metabolism
inferred← citeshttps://doi.org/10.1016/j.jenvman.2024.123982openalex-snapshot
Construction and transcriptomic analysis of salinity-induced lipid-rich flocculent microalgae
inferred← citeshttps://doi.org/10.1016/j.procbio.2026.09.001openalex-snapshot
A comprehensive analysis of succinic acid production from diverse feedstock
inferred← citeshttps://doi.org/10.1016/j.rsma.2023.103245openalex-snapshot
Physio-biochemical and metabolomic analyses of the agarophyte Gracilaria salicornia indicates its tolerance to elevated pCO2 levels
inferred← citeshttps://doi.org/10.1016/j.sjbs.2023.103681openalex-snapshot
Phenol phycoremediation by Haematococcus pluvialis coupled with enhanced astaxanthin and lipid production under rac-GR24 supplementation for enhanced biodiesel production
inferred← citeshttps://doi.org/10.1016/j.tifs.2023.04.014openalex-snapshot
Chemical inducers regulate ROS signalling to stimulate astaxanthin production in Haematococcus pluvialis under environmental stresses: A review
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c00199openalex-snapshot
Candida glycerinogenes-Promoted α-Pinene and Squalene Co-production Strategy Based on α-Pinene Stress
inferred← citeshttps://doi.org/10.1080/07388551.2025.2537816openalex-snapshot
Astaxanthin: nature’s multifunctional molecule, natural sources, health benefits, and process advancements
inferred← citeshttps://doi.org/10.1186/s12934-023-02256-2openalex-snapshot
Enhancement of phycocyanin productivity and thermostability from Arthrospira platensis using organic acids
inferred← citeshttps://doi.org/10.1186/s13068-024-02527-zopenalex-snapshot
Synergistic and stepwise treatment of resveratrol and catechol in Haematococcus pluvialis for the overproduction of biomass and astaxanthin
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3557352/v1openalex-snapshot
Effect of organic carbon sources on the growth of Chaetoceros muelleri
inferred← citeshttps://doi.org/10.3390/life14010029openalex-snapshot
Effects of Four Organic Carbon Sources on the Growth and Astaxanthin Accumulation of Haematococcus lacustris
inferred← citeshttps://doi.org/10.3390/md21100514openalex-snapshot
Astaxanthin: Past, Present, and Future
inferred← citeshttps://doi.org/10.34172/bi.32651openalex-snapshot
Current advancements and future prospects in the biorefinery and hyper-production of astaxanthin from Haematococcus pluvialis
inferred← citeshttps://doi.org/10.6084/m9.figshare.26043662openalex-snapshot
Additional file 1 of Synergistic and stepwise treatment of resveratrol and catechol in Haematococcus pluvialis for the overproduction of biomass and astaxanthin
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