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Cleavage of resveratrol in fungi: Characterization of the enzyme Rco1 from Ustilago maydis

https://doi.org/10.1016/j.fgb.2010.10.009
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cbic.200700724openalex-snapshot
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Cloning and disruption of a phenylalanine ammonia-lyase gene from Ustilago maydis
inferredcites →https://doi.org/10.1007/s00299-003-0728-0openalex-snapshot
Antifungal activity of stilbenes in in vitro bioassays and in transgenic Populus expressing a gene encoding pinosylvin synthase
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Cloning and characterisation of a maize carotenoid cleavage dioxygenase (ZmCCD1) and its involvement in the biosynthesis of apocarotenoids with various roles in mutualistic and parasitic interactions
inferredcites →https://doi.org/10.1007/s00438-003-0962-8openalex-snapshot
A PCR-based system for highly efficient generation of gene replacement mutants in Ustilago maydis
inferredcites →https://doi.org/10.1007/s00438-004-1047-zopenalex-snapshot
A reverse genetic approach for generating gene replacement mutants in Ustilago maydis
inferredcites →https://doi.org/10.1007/s00438-004-1067-8openalex-snapshot
A reverse genetic approach for generating gene replacement mutants in Ustilago maydis
inferredcites →https://doi.org/10.1007/s00438-007-0269-2openalex-snapshot
Identification of the gene responsible for torulene cleavage in the Neurospora carotenoid pathway
inferredcites →https://doi.org/10.1016/0092-8674(90)90744-yopenalex-snapshot
The b alleles of U. maydis, whose combinations program pathogenic development, code for polypeptides containing a homeodomain-related motif
inferredcites →https://doi.org/10.1016/0378-1119(87)90131-4openalex-snapshot
A ten-minute DNA preparation from yeast efficiently releases autonomous plasmids for transformaion of Escherichia coli
inferredcites →https://doi.org/10.1016/j.fgb.2007.07.008openalex-snapshot
Cleavage of β-carotene as the first step in sexual hormone synthesis in zygomycetes is mediated by a trisporic acid regulated β-carotene oxygenase
inferredcites →https://doi.org/10.1016/j.fgb.2008.04.007openalex-snapshot
Sending mixed signals: Redundancy vs. uniqueness of signaling components in the plant pathogen, Ustilago maydis
inferredcites →https://doi.org/10.1016/j.fgb.2008.05.007openalex-snapshot
Ustilago maydis secondary metabolism—From genomics to biochemistry
inferredcites →https://doi.org/10.1016/j.fgb.2008.09.001openalex-snapshot
Novel apocarotenoid intermediates in Neurospora crassa mutants imply a new biosynthetic reaction sequence leading to neurosporaxanthin formation
inferredcites →https://doi.org/10.1016/j.fgb.2009.06.011openalex-snapshot
Ustilago maydis accumulates β-carotene at levels determined by a retinal-forming carotenoid oxygenase
inferredcites →https://doi.org/10.1016/j.pbi.2006.03.005openalex-snapshot
Plant carotenoid cleavage oxygenases and their apocarotenoid products
inferredcites →https://doi.org/10.1016/j.phytochem.2007.06.032openalex-snapshot
Metabolite profiling of mycorrhizal roots of Medicago truncatula
inferredcites →https://doi.org/10.1016/j.tibtech.2007.11.002openalex-snapshot
Potential for metabolic engineering of resveratrol biosynthesis
inferredcites →https://doi.org/10.1016/j.tplants.2005.02.006openalex-snapshot
Related enzymes solve evolutionarily recurrent problems in the metabolism of carotenoids
inferredcites →https://doi.org/10.1016/j.tplants.2005.02.007openalex-snapshot
Oxidative tailoring of carotenoids: a prospect towards novel functions in plants
inferredcites →https://doi.org/10.1016/j.tplants.2007.03.009openalex-snapshot
Rhizosphere communication of plants, parasitic plants and AM fungi
inferredcites →https://doi.org/10.1016/s0021-9258(19)84072-3openalex-snapshot
Identification of Carotenoid Cleavage Dioxygenases from Nostoc sp. PCC 7120 with Different Cleavage Activities
inferredcites →https://doi.org/10.1016/s0065-2164(03)01010-4openalex-snapshot
The Fungal Genetics Stock Center: From Molds to Molecules
inferredcites →https://doi.org/10.1016/s0065-2660(06)57001-4openalex-snapshot
Genetics of Morphogenesis and Pathogenic Development of Ustilago maydis
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inferredcites →https://doi.org/10.1021/jf011429sopenalex-snapshot
Phytoalexins from the Vitaceae: Biosynthesis, Phytoalexin Gene Expression in Transgenic Plants, Antifungal Activity, and Metabolism
inferredcites →https://doi.org/10.1023/b:joec.0000006444.79951.75openalex-snapshot
Biological Activity of Resveratrol, a Stilbenic Compound from Grapevines, Against Botrytis cinerea, the Causal Agent for Gray Mold
inferredcites →https://doi.org/10.1038/nature05248openalex-snapshot
Insights from the genome of the biotrophic fungal plant pathogen Ustilago maydis
inferredcites →https://doi.org/10.1038/nature07271openalex-snapshot
Strigolactone inhibition of shoot branching
inferredcites →https://doi.org/10.1038/nature07272openalex-snapshot
Inhibition of shoot branching by new terpenoid plant hormones
inferredcites →https://doi.org/10.1042/bj20060592openalex-snapshot
Retinal is formed from apo-carotenoids in Nostoc sp. PCC7120: in vitro characterization of an apo-carotenoid oxygenase
inferredcites →https://doi.org/10.1042/bj20080568openalex-snapshot
Carotenoid oxygenases involved in plant branching catalyse a highly specific conserved apocarotenoid cleavage reaction
inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02424.xopenalex-snapshot
A homologue of the transcriptional repressor Ssn6p antagonizes cAMP signalling in Ustilago maydis
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.02801.xopenalex-snapshot
Resveratrol acts as a natural profungicide and induces self‐intoxication by a specific laccase
inferredcites →https://doi.org/10.1074/jbc.m409004200openalex-snapshot
The Biochemical Characterization of Two Carotenoid Cleavage Enzymes from Arabidopsis Indicates That a Carotenoid-derived Compound Inhibits Lateral Branching
inferredcites →https://doi.org/10.1091/mbc.e02-08-0513openalex-snapshot
Microtubule Organization Requires Cell Cycle-dependent Nucleation at Dispersed Cytoplasmic Sites: Polar and Perinuclear Microtubule Organizing Centers in the Plant Pathogen Ustilago maydis
inferredcites →https://doi.org/10.1091/mbc.e05-03-0176openalex-snapshot
Microtubules Are Dispensable for the Initial Pathogenic Development but Required for Long-Distance Hyphal Growth in the Corn Smut FungusUstilago maydis
inferredcites →https://doi.org/10.1093/emboj/19.9.1974openalex-snapshot
A putative endosomal t‐SNARE links exo‐ and endocytosis in the phytopathogenic fungus Ustilago maydis
inferredcites →https://doi.org/10.1093/jn/130.8.1996openalex-snapshot
β-Carotene Is Converted Primarily to Retinoids in Rats In Vivo
inferredcites →https://doi.org/10.1094/mpmi-18-0075openalex-snapshot
Identification of cis-Active Elements in Ustilago maydis mig2 Promoters Conferring High-Level Activity During Pathogenic Growth in Maize
inferredcites →https://doi.org/10.1104/pp.108.125062openalex-snapshot
RNA Interference-Mediated Repression of MtCCD1 in Mycorrhizal Roots of Medicago truncatula Causes Accumulation of C27 Apocarotenoids, Shedding Light on the Functional Role of CCD1
inferredcites →https://doi.org/10.1105/tpc.7.7.1085openalex-snapshot
Stress-Induced Phenylpropanoid Metabolism
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04460.xopenalex-snapshot
Retinal biosynthesis in Eubacteria: in vitro characterization of a novel carotenoid oxygenase from Synechocystis sp. PCC 6803
inferredcites →https://doi.org/10.1111/j.1365-2958.2005.04952.xopenalex-snapshot
Rac1 and Cdc42 regulate hyphal growth and cytokinesis in the dimorphic fungus Ustilago maydis
inferredcites →https://doi.org/10.1111/j.1365-2958.2007.05665.xopenalex-snapshot
Identification and biochemical characterization of a novel carotenoid oxygenase: elucidation of the cleavage step in the Fusarium carotenoid pathway
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06349.xopenalex-snapshot
The ylo‐1 gene encodes an aldehyde dehydrogenase responsible for the last reaction in the Neurospora carotenoid pathway
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03590.xopenalex-snapshot
Reprogramming a maize plant: transcriptional and metabolic changes induced by the fungal biotroph Ustilago maydis
inferredcites →https://doi.org/10.1111/j.1467-7652.2008.00377.xopenalex-snapshot
Molecular engineering of resveratrol in plants
inferredcites →https://doi.org/10.1111/j.1541-4337.2006.00001.xopenalex-snapshot
Bioactivity of Resveratrol
inferredcites →https://doi.org/10.1111/j.1574-6968.2008.01173.xopenalex-snapshot
Dimorphism in fungal plant pathogens
inferredcites →https://doi.org/10.1111/j.1742-4658.2008.06820.xopenalex-snapshot
Characterization of the rice carotenoid cleavage dioxygenase 1 reveals a novel route for geranial biosynthesis
inferredcites →https://doi.org/10.1128/ec.00392-06openalex-snapshot
Retinal Biosynthesis in Fungi: Characterization of the Carotenoid Oxygenase CarX fromFusarium fujikuroi
inferredcites →https://doi.org/10.1146/annurev-phyto-080508-081923openalex-snapshot
Ustilago maydis as a Pathogen
inferredcites →https://doi.org/10.1271/bbb.57.926openalex-snapshot
Cloning, Expression, and Sequence Analysis of a Lignostilbene-α,β-dioxygenase Gene fromPseudomonas paucimobilisTMY1009
inferredcites →https://doi.org/10.1271/bbb.67.1394openalex-snapshot
A Common Structure of Substrate Shared by Lignostilbenedioxygenase Isozymes fromSphingomonas paucimobilisTMY1009
inferredcites →https://doi.org/10.1271/bbb.70023openalex-snapshot
Chemical Identification and Functional Analysis of Apocarotenoids Involved in the Development of Arbuscular Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.4161/cc.7.8.5740openalex-snapshot
Resveratrol: A multitargeted agent for age-associated chronic diseases

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/open.201800259openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00775-018-1586-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10529-014-1651-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.mie.2021.10.020openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.abb.2015.02.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbalip.2019.158590openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.enzmictec.2024.110425openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fbr.2017.01.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fgb.2015.12.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jbc.2021.100758openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jbiotec.2024.09.020openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.biochem.7b00251openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00031openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacsau.5c00456openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c8cy01885eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0np00030bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1073/pnas.1608917113openalex-snapshot
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inferred← citeshttps://doi.org/10.1074/jbc.m115.696799openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/10408398.2022.2048352openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/are.15670openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/j.1365-2958.2011.07805.xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1111/mec.14943openalex-snapshot
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inferred← citeshttps://doi.org/10.1128/aem.00104-18openalex-snapshot
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inferred← citeshttps://doi.org/10.1128/ec.00084-13openalex-snapshot
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inferred← citeshttps://doi.org/10.1194/jlr.m057919openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fmicb.2022.1010332openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2019.01168openalex-snapshot
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inferred← citeshttps://doi.org/10.5114/bta.2019.87583openalex-snapshot
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