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Flavonol–Aluminum Complex Formation: Enhancing Aluminum Accumulation in Tea Plants

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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/adfm.202008720openalex-snapshot
Copper Clusters: An Effective Antibacterial for Eradicating Multidrug‐Resistant Bacterial Infection In Vitro and In Vivo
inferredcites →https://doi.org/10.1002/jpln.201200311openalex-snapshot
Mechanisms of aluminum‐induced growth stimulation in tea (Camellia sinensis)
inferredcites →https://doi.org/10.1002/pei3.10028openalex-snapshot
Tissue ionome response to rhizosphere pH and aluminum in tea plants (Camellia sinensis L.), a species adapted to acidic soils
inferredcites →https://doi.org/10.1007/bf00009558openalex-snapshot
Global extent, development and economic impact of acid soils
inferredcites →https://doi.org/10.1007/s00299-019-02401-5openalex-snapshot
Transcriptomic and ionomic analysis provides new insight into the beneficial effect of Al on tea roots’ growth and nutrient uptake
inferredcites →https://doi.org/10.1007/s00425-017-2792-7openalex-snapshot
The contribution of cell wall composition in the expansion of Camellia sinensis seedlings roots in response to aluminum
inferredcites →https://doi.org/10.1007/s12010-016-2224-3openalex-snapshot
Essential and Beneficial Trace Elements in Plants, and Their Transport in Roots: a Review
inferredcites →https://doi.org/10.1016/j.envexpbot.2004.07.006openalex-snapshot
Aluminium-induced changes in the profiles of both organic acids and phenolic substances underlie Al tolerance in Rumex acetosa L.
inferredcites →https://doi.org/10.1016/j.envpol.2020.114230openalex-snapshot
Enhancement of polyphenolic metabolism as an adaptive response of lettuce (Lactuca sativa) roots to aluminum stress
inferredcites →https://doi.org/10.1016/j.foodchem.2005.11.038openalex-snapshot
Leaching and bioavailability of aluminium, copper and manganese from tea (Camellia sinensis)
inferredcites →https://doi.org/10.1016/j.foodchem.2007.03.019openalex-snapshot
Total content and speciation of aluminium in tea leaves and tea infusions
inferredcites →https://doi.org/10.1016/j.foodchem.2019.04.083openalex-snapshot
Metal ion interactions with methyl gallate characterized by UV spectroscopic and computational methods
inferredcites →https://doi.org/10.1016/j.foodchem.2019.125507openalex-snapshot
Evaluation of astringent taste of green tea through mass spectrometry-based targeted metabolic profiling of polyphenols
inferredcites →https://doi.org/10.1016/j.foodchem.2020.128368openalex-snapshot
Rapid measurement of total polyphenol content in tea by kinetic matching approach on microfluidic paper-based analytical devices
inferredcites →https://doi.org/10.1016/j.jchromb.2016.01.064openalex-snapshot
Quantification of flavonol glycosides in Camellia sinensis by MRM mode of UPLC-QQQ-MS/MS
inferredcites →https://doi.org/10.1016/j.jhazmat.2010.02.029openalex-snapshot
Effect of aluminium uptake on physiology, phenols and amino acids in Matricaria chamomilla plants
inferredcites →https://doi.org/10.1016/j.phytochem.2004.08.043openalex-snapshot
Chemical forms of aluminum in xylem sap of tea plants (Camellia sinensis L.)
inferredcites →https://doi.org/10.1016/j.phytochem.2007.06.007openalex-snapshot
Mechanism for the detoxification of aluminum in roots of tea plant (Camellia sinensis (L.) Kuntze)
inferredcites →https://doi.org/10.1016/j.plantsci.2018.02.009openalex-snapshot
CsMYB5a and CsMYB5e from Camellia sinensis differentially regulate anthocyanin and proanthocyanidin biosynthesis
inferredcites →https://doi.org/10.1016/j.plaphy.2017.09.002openalex-snapshot
Cell wall pectin methyl-esterification and organic acids of root tips involve in aluminum tolerance in Camellia sinensis
inferredcites →https://doi.org/10.1016/j.scienta.2017.03.018openalex-snapshot
Comparison of phenolic compound accumulation profiles in eight evergreen woody core eudicots indicating the diverse ecological adaptability of Camellia sinensis
inferredcites →https://doi.org/10.1016/j.xplc.2021.100182openalex-snapshot
Tease out the future: How tea research might enable crop breeding for acid soil tolerance
inferredcites →https://doi.org/10.1016/s0045-6535(03)00485-5openalex-snapshot
Fluoride and aluminium concentrations of tea plants and tea products from Sichuan Province, PR China
inferredcites →https://doi.org/10.1016/s0074-7696(00)00001-2openalex-snapshot
Cell biology of aluminum toxicity and tolerance in higher plants
inferredcites →https://doi.org/10.1016/s0074-7696(07)64005-4openalex-snapshot
Syndrome of Aluminum Toxicity and Diversity of Aluminum Resistance in Higher Plants
inferredcites →https://doi.org/10.1016/s0098-8472(02)00013-8openalex-snapshot
Fast root growth responses, root exudates, and internal detoxification as clues to the mechanisms of aluminium toxicity and resistance: a review
inferredcites →https://doi.org/10.1016/s0162-0134(02)00469-5openalex-snapshot
Spectroscopic and structural study of complexes of quercetin with Al(III)
inferredcites →https://doi.org/10.1016/s1360-1385(01)01961-6openalex-snapshot
Aluminium tolerance in plants and the complexing role of organic acids
inferredcites →https://doi.org/10.1016/s1386-1425(00)00412-1openalex-snapshot
Complexes of Al(III) with 3′4′-dihydroxy-flavone: characterization, theoretical and spectroscopic study
inferredcites →https://doi.org/10.1016/s1386-1425(99)00284-xopenalex-snapshot
Conformational and spectroscopic investigation of 3-hydroxyflavone–aluminium chelates
inferredcites →https://doi.org/10.1021/acs.jafc.0c01689openalex-snapshot
Proanthocyanidin–Aluminum Complexes Improve Aluminum Resistance and Detoxification of Camellia sinensis
inferredcites →https://doi.org/10.1021/acs.jafc.6b00331openalex-snapshot
Polyphenol–Aluminum Complex Formation: Implications for Aluminum Tolerance in Plants
inferredcites →https://doi.org/10.1021/jf4038437openalex-snapshot
Localization of Fluoride and Aluminum in Subcellular Fractions of Tea Leaves and Roots
inferredcites →https://doi.org/10.1021/jf902614nopenalex-snapshot
Investigation of the Site-Specific Accumulation of Catechins in the Tea Plant (Camellia sinensis (L.) O. Kuntze) via Vanillin−HCl Staining
inferredcites →https://doi.org/10.1038/s41438-021-00517-yopenalex-snapshot
The role of γ-aminobutyric acid in aluminum stress tolerance in a woody plant, Liriodendron chinense × tulipifera
inferredcites →https://doi.org/10.1038/srep08742openalex-snapshot
Analysis of accumulation patterns and preliminary study on the condensation mechanism of proanthocyanidins in the tea plant [Camellia sinensis]
inferredcites →https://doi.org/10.1046/j.1365-3040.1999.00467.xopenalex-snapshot
Accumulation of aluminium in the cell wall pectin in cultured tobacco (Nicotiana tabacum L.) cells treated with a combination of aluminium and iron
inferredcites →https://doi.org/10.1071/pp01012openalex-snapshot
Possible involvement of condensed tannins in aluminium tolerance of Lotus pedunculatus
inferredcites →https://doi.org/10.1080/00380768.2001.10408399openalex-snapshot
The plasma membrane strength of the root-tip cells and root phenolic compounds are correiated with Al tolerance in several common woody plants
inferredcites →https://doi.org/10.1080/00380768.2011.629176openalex-snapshot
Tea plant ( Camellia sinensis L.) roots secrete oxalic acid and caffeine into medium containing aluminum
inferredcites →https://doi.org/10.1080/02773819809349576openalex-snapshot
Effects of the Hydroxylation Patterns and Degrees of Polymerization of Condensed Tannins on their Metal-Chelating Capacity
inferredcites →https://doi.org/10.1080/07352689.2011.615706openalex-snapshot
Cell Wall Modifying Proteins Mediate Plant Acclimatization to Biotic and Abiotic Stresses
inferredcites →https://doi.org/10.1080/07388551.2021.1874282openalex-snapshot
Aluminum toxicity and aluminum stress-induced physiological tolerance responses in higher plants
inferredcites →https://doi.org/10.1093/jxb/erx370openalex-snapshot
Genome-wide analysis of MATE transporters and molecular characterization of aluminum resistance in Populus
inferredcites →https://doi.org/10.1093/pcp/41.4.383openalex-snapshot
Role of Organic Acids in Detoxification of Aluminum in Higher Plants
inferredcites →https://doi.org/10.1093/pcp/pch060openalex-snapshot
Aluminum Targets Elongating Cells by Reducing Cell Wall Extensibility in Wheat Roots
inferredcites →https://doi.org/10.1104/pp.110.166967openalex-snapshot
Transient Proliferation of Proanthocyanidin-Accumulating Cells on the Epidermal Apex Contributes to Highly Aluminum-Resistant Root Elongation in Camphor Tree
inferredcites →https://doi.org/10.1104/pp.113.219147openalex-snapshot
Coordination between Apoplastic and Symplastic Detoxification Confers Plant Aluminum Resistance
inferredcites →https://doi.org/10.1104/pp.113.222885openalex-snapshot
Identification of a Hydrolyzable Tannin, Oenothein B, as an Aluminum-Detoxifying Ligand in a Highly Aluminum-Resistant Tree, Eucalyptus camaldulensis
inferredcites →https://doi.org/10.1104/pp.114.243790openalex-snapshot
Xyloglucan Endotransglucosylase-Hydrolase17 Interacts with Xyloglucan Endotransglucosylase-Hydrolase31 to Confer Xyloglucan Endotransglucosylase Action and Affect Aluminum Sensitivity in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.117.3.753openalex-snapshot
High Aluminum Resistance in Buckwheat1
inferredcites →https://doi.org/10.1111/j.1399-3054.2010.01347.xopenalex-snapshot
Interactive intoxicating and ameliorating effects of tannic acid, aluminum (Al3+), copper (Cu2+), and selenate (SeO42−) in wheat roots: a descriptive and mathematical assessment
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03288.xopenalex-snapshot
Oxalate exudation into the root‐tip water free space confers protection from aluminum toxicity and allows aluminum accumulation in the symplast in buckwheat (Fagopyrum esculentum)
inferredcites →https://doi.org/10.1111/jipb.12942openalex-snapshot
Aluminium is essential for root growth and development of tea plants ( Camellia sinensis )
inferredcites →https://doi.org/10.1111/nph.14420openalex-snapshot
Loss‐of‐function mutation of the calcium sensor CBL 1 increases aluminum sensitivity in Arabidopsis
inferredcites →https://doi.org/10.1111/pce.13150openalex-snapshot
Two citrate transporters coordinately regulate citrate secretion from rice bean root tip under aluminum stress
inferredcites →https://doi.org/10.1111/pce.13658openalex-snapshot
A multidrug and toxic compound extrusion (MATE) transporter modulates auxin levels in root to regulate root development and promotes aluminium tolerance
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112156openalex-snapshot
Metal Hyperaccumulation in Plants
inferredcites →https://doi.org/10.1146/annurev-arplant-043014-114822openalex-snapshot
Plant Adaptation to Acid Soils: The Molecular Basis for Crop Aluminum Resistance
inferredcites →https://doi.org/10.1146/annurev.arplant.55.031903.141655openalex-snapshot
HOW DO CROP PLANTS TOLERATE ACID SOILS? MECHANISMS OF ALUMINUM TOLERANCE AND PHOSPHOROUS EFFICIENCY
inferredcites →https://doi.org/10.1371/journal.pone.0062315openalex-snapshot
Tissue-Specific, Development-Dependent Phenolic Compounds Accumulation Profile and Gene Expression Pattern in Tea Plant [Camellia sinensis]
inferredcites →https://doi.org/10.1663/0006-8101(2002)068[0235:ahiaar]2.0.co;2openalex-snapshot
Aluminum Hyperaccumulation in Angiosperms: A Review of Its Phylogenetic Significance
inferredcites →https://doi.org/10.32604/phyton.2015.84.086openalex-snapshot
Localization and compartmentation of Al in the leaves and roots of tea plants
inferredcites →https://doi.org/10.3390/ijms20071551openalex-snapshot
Molecular Mechanisms for Coping with Al Toxicity in Plants
inferredcites →https://doi.org/10.3390/su13041782openalex-snapshot
Recent Advances in Understanding Mechanisms of Plant Tolerance and Response to Aluminum Toxicity

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.4494935openalex-extracted
Effects of Metal Ions on the Binding Reaction of (-)-Epigallocatechin Gallate with Bovine Serum Albumin in Vitro
inferred← citeshttps://doi.org/10.1007/s42773-023-00220-2openalex-snapshot
Biochar addition to tea garden soils: effects on tea fluoride uptake and accumulation
inferred← citeshttps://doi.org/10.1007/s44281-025-00074-7openalex-snapshot
Physiological insights into the responses of tea plants to aluminum through an integrated transcriptomic and metabolomic analysis
inferred← citeshttps://doi.org/10.1016/j.foodchem.2023.137000openalex-snapshot
Analysis of differences in the accumulation of tea compounds under various processing techniques, geographical origins, and harvesting seasons
inferred← citeshttps://doi.org/10.1016/j.foodchem.2025.146826openalex-snapshot
Paper-based sensing of cinnamic ortho-diphenols in food samples using photoluminescent laser-induced aluminum nanostructures
inferred← citeshttps://doi.org/10.1016/j.hpj.2024.12.008openalex-snapshot
Aluminum-tolerant, growth-promoting rhizosphere bacteria improve growth and alleviate aluminum stress in tea plants
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.122352openalex-snapshot
Aluminum induced flavonols in root exudates: Orchestrating rhizosphere bacteria to fuel tea plant growth
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112676openalex-snapshot
Root-specific CsATs enhances acylated flavonol-glycoside accumulation to promote aluminum tolerance in tea roots
inferred← citeshttps://doi.org/10.1016/j.scienta.2025.114460openalex-snapshot
Translational regulation of ion transporters modules mineral homestasis in tea roots under phosphate aluminum interaction
inferred← citeshttps://doi.org/10.1016/j.tifs.2026.105897openalex-snapshot
Schaftoside as a multifunctional food ingredient: Resources, bioactivities, disposition and applications enabled by synthetic biology and precision delivery
inferred← citeshttps://doi.org/10.1021/acs.jchemed.3c01223openalex-snapshot
Dyeing Cloth Green Using Red Onion Skin: A pH-Responsive Dye and Aluminum-Ion Complex
inferred← citeshttps://doi.org/10.1093/jxb/erag435openalex-snapshot
The transcription factor CsART1 activates the aluminum transporter CsALS3s to promote the absorption and tolerance of aluminum in tea plants
inferred← citeshttps://doi.org/10.1111/pce.15372openalex-snapshot
Crucial Role of Aluminium‐Regulated Flavonol Glycosides (F2‐Type) Biosynthesis in Lateral Root Formation of Camellia sinensis
inferred← citeshttps://doi.org/10.47352/bioactivities.2963-654x.457openalex-snapshot
A Comparative Study on Bioactivities of Aqueous Extracts from Various Parts of Moringa Oleifera
inferred← citeshttps://doi.org/10.48130/bpr-0024-0006openalex-snapshot
Accumulation patterns of flavonoids during multiple development stages of tea seedlings
inferred← citeshttps://doi.org/10.48130/bpr-0024-0010openalex-snapshot
Critical review of fluoride in tea plants (Camellia sinensis): absorption, transportation, tolerance mechanisms, and defluorination measures
inferred← citeshttps://doi.org/10.48130/bpr-0024-0013openalex-snapshot
Exogenous hydrogen sulfide enhanced Al stress tolerance in tea plant Camellia sinensis
inferred← citeshttps://doi.org/10.48130/bpr-0025-0009openalex-snapshot
Exploration of the biosynthesis of galloylated catechins in tea plants
inferred← citeshttps://doi.org/10.48130/bpr-2023-0018openalex-snapshot
Research advances in aluminum tolerance and accumulation in tea plant (Camellia sinensis)
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