Taste detection of the non-volatile isothiocyanate moringin results in deterrence to glucosinolate-adapted insect larvae
Müller C, van Loon J, Ruschioni S, de Nicola GR, Olsen CE, Iori R, Agerbirk N (2015)
Phytochemistry 118: 139-148.
Zeitschriftenaufsatz
| Veröffentlicht | Englisch
Download
Es wurden keine Dateien hochgeladen. Nur Publikationsnachweis!
Autor*in
Müller, CarolineUniBi;
van Loon, J;
Ruschioni, S;
de Nicola, GR;
Olsen, CE;
Iori, R;
Agerbirk, N
Einrichtung
Erscheinungsjahr
2015
Zeitschriftentitel
Phytochemistry
Band
118
Seite(n)
139-148
ISSN
0031-9422
Page URI
https://pub.uni-bielefeld.de/record/2777397
Zitieren
Müller C, van Loon J, Ruschioni S, et al. Taste detection of the non-volatile isothiocyanate moringin results in deterrence to glucosinolate-adapted insect larvae. Phytochemistry. 2015;118:139-148.
Müller, C., van Loon, J., Ruschioni, S., de Nicola, G. R., Olsen, C. E., Iori, R., & Agerbirk, N. (2015). Taste detection of the non-volatile isothiocyanate moringin results in deterrence to glucosinolate-adapted insect larvae. Phytochemistry, 118, 139-148. doi:10.1016/j.phytochem.2015.08.007
Müller, Caroline, van Loon, J, Ruschioni, S, de Nicola, GR, Olsen, CE, Iori, R, and Agerbirk, N. 2015. “Taste detection of the non-volatile isothiocyanate moringin results in deterrence to glucosinolate-adapted insect larvae”. Phytochemistry 118: 139-148.
Müller, C., van Loon, J., Ruschioni, S., de Nicola, G. R., Olsen, C. E., Iori, R., and Agerbirk, N. (2015). Taste detection of the non-volatile isothiocyanate moringin results in deterrence to glucosinolate-adapted insect larvae. Phytochemistry 118, 139-148.
Müller, C., et al., 2015. Taste detection of the non-volatile isothiocyanate moringin results in deterrence to glucosinolate-adapted insect larvae. Phytochemistry, 118, p 139-148.
C. Müller, et al., “Taste detection of the non-volatile isothiocyanate moringin results in deterrence to glucosinolate-adapted insect larvae”, Phytochemistry, vol. 118, 2015, pp. 139-148.
Müller, C., van Loon, J., Ruschioni, S., de Nicola, G.R., Olsen, C.E., Iori, R., Agerbirk, N.: Taste detection of the non-volatile isothiocyanate moringin results in deterrence to glucosinolate-adapted insect larvae. Phytochemistry. 118, 139-148 (2015).
Müller, Caroline, van Loon, J, Ruschioni, S, de Nicola, GR, Olsen, CE, Iori, R, and Agerbirk, N. “Taste detection of the non-volatile isothiocyanate moringin results in deterrence to glucosinolate-adapted insect larvae”. Phytochemistry 118 (2015): 139-148.
Daten bereitgestellt von European Bioinformatics Institute (EBI)
16 Zitationen in Europe PMC
Daten bereitgestellt von Europe PubMed Central.
Autofluorescence-Based Identification and Functional Validation of Antennal Gustatory Sensilla in a Specialist Leaf Beetle.
Pentzold S, Marion-Poll F, Grabe V, Burse A., Front Physiol 10(), 2019
PMID: 31001138
Pentzold S, Marion-Poll F, Grabe V, Burse A., Front Physiol 10(), 2019
PMID: 31001138
Moringin Induces Neural Differentiation in the Stem Cell of the Human Periodontal Ligament.
Romeo L, Diomede F, Gugliandolo A, Scionti D, Lo Giudice F, Lanza Cariccio V, Iori R, Bramanti P, Trubiani O, Mazzon E., Sci Rep 8(1), 2018
PMID: 29904155
Romeo L, Diomede F, Gugliandolo A, Scionti D, Lo Giudice F, Lanza Cariccio V, Iori R, Bramanti P, Trubiani O, Mazzon E., Sci Rep 8(1), 2018
PMID: 29904155
A Combined Approach of NMR and Mass Spectrometry Techniques Applied to the α-Cyclodextrin/Moringin Complex for a Novel Bioactive Formulation †.
Mathiron D, Iori R, Pilard S, Soundara Rajan T, Landy D, Mazzon E, Rollin P, Djedaïni-Pilard F., Molecules 23(7), 2018
PMID: 30011859
Mathiron D, Iori R, Pilard S, Soundara Rajan T, Landy D, Mazzon E, Rollin P, Djedaïni-Pilard F., Molecules 23(7), 2018
PMID: 30011859
Treatment of Periodontal Ligament Stem Cells with MOR and CBD Promotes Cell Survival and Neuronal Differentiation via the PI3K/Akt/mTOR Pathway.
Lanza Cariccio V, Scionti D, Raffa A, Iori R, Pollastro F, Diomede F, Bramanti P, Trubiani O, Mazzon E., Int J Mol Sci 19(8), 2018
PMID: 30096889
Lanza Cariccio V, Scionti D, Raffa A, Iori R, Pollastro F, Diomede F, Bramanti P, Trubiani O, Mazzon E., Int J Mol Sci 19(8), 2018
PMID: 30096889
The α-Cyclodextrin/Moringin Complex: A New Promising Antimicrobial Agent against Staphylococcus aureus.
Romeo L, Lanza Cariccio V, Iori R, Rollin P, Bramanti P, Mazzon E., Molecules 23(9), 2018
PMID: 30134562
Romeo L, Lanza Cariccio V, Iori R, Rollin P, Bramanti P, Mazzon E., Molecules 23(9), 2018
PMID: 30134562
A Combination of Moringin and Avenanthramide 2f Inhibits the Proliferation of Hep3B Liver Cancer Cells Inducing Intrinsic and Extrinsic Apoptosis.
Antonini E, Iori R, Ninfali P, Scarpa ES., Nutr Cancer 70(7), 2018
PMID: 30204484
Antonini E, Iori R, Ninfali P, Scarpa ES., Nutr Cancer 70(7), 2018
PMID: 30204484
The Role of the Glucosinolate-Myrosinase System in Mediating Greater Resistance of Barbarea verna than B. vulgaris to Mamestra brassicae Larvae.
Müller C, Schulz M, Pagnotta E, Ugolini L, Yang T, Matthes A, Lazzeri L, Agerbirk N., J Chem Ecol 44(12), 2018
PMID: 30218254
Müller C, Schulz M, Pagnotta E, Ugolini L, Yang T, Matthes A, Lazzeri L, Agerbirk N., J Chem Ecol 44(12), 2018
PMID: 30218254
Hydrogen Sulfide (H₂S) Releasing Capacity of Isothiocyanates from Moringa oleifera Lam.
Wang X, Liu Y, Liu X, Lin Y, Zheng X, Lu Y., Molecules 23(11), 2018
PMID: 30380667
Wang X, Liu Y, Liu X, Lin Y, Zheng X, Lu Y., Molecules 23(11), 2018
PMID: 30380667
The Isothiocyanate Isolated from Moringa oleifera Shows Potent Anti-Inflammatory Activity in the Treatment of Murine Subacute Parkinson's Disease.
Giacoppo S, Rajan TS, De Nicola GR, Iori R, Rollin P, Bramanti P, Mazzon E., Rejuvenation Res 20(1), 2017
PMID: 27245199
Giacoppo S, Rajan TS, De Nicola GR, Iori R, Rollin P, Bramanti P, Mazzon E., Rejuvenation Res 20(1), 2017
PMID: 27245199
Topical moringin-cream relieves neuropathic pain by suppression of inflammatory pathway and voltage-gated ion channels in murine model of multiple sclerosis.
Giacoppo S, Iori R, Bramanti P, Mazzon E., Mol Pain 13(), 2017
PMID: 28741431
Giacoppo S, Iori R, Bramanti P, Mazzon E., Mol Pain 13(), 2017
PMID: 28741431
The α-cyclodextrin complex of the Moringa isothiocyanate suppresses lipopolysaccharide-induced inflammation in RAW 264.7 macrophage cells through Akt and p38 inhibition.
Giacoppo S, Rajan TS, Iori R, Rollin P, Bramanti P, Mazzon E., Inflamm Res 66(6), 2017
PMID: 28289752
Giacoppo S, Rajan TS, Iori R, Rollin P, Bramanti P, Mazzon E., Inflamm Res 66(6), 2017
PMID: 28289752
Contact chemosensation of phytochemicals by insect herbivores.
Pentzold S, Burse A, Boland W., Nat Prod Rep 34(5), 2017
PMID: 28485430
Pentzold S, Burse A, Boland W., Nat Prod Rep 34(5), 2017
PMID: 28485430
Moringa isothiocyanate complexed with α-cyclodextrin: a new perspective in neuroblastoma treatment.
Giacoppo S, Iori R, Rollin P, Bramanti P, Mazzon E., BMC Complement Altern Med 17(1), 2017
PMID: 28705212
Giacoppo S, Iori R, Rollin P, Bramanti P, Mazzon E., BMC Complement Altern Med 17(1), 2017
PMID: 28705212
The Chemopreventive Phytochemical Moringin Isolated from Moringa oleifera Seeds Inhibits JAK/STAT Signaling.
Michl C, Vivarelli F, Weigl J, De Nicola GR, Canistro D, Paolini M, Iori R, Rascle A., PLoS One 11(6), 2016
PMID: 27304884
Michl C, Vivarelli F, Weigl J, De Nicola GR, Canistro D, Paolini M, Iori R, Rascle A., PLoS One 11(6), 2016
PMID: 27304884
Glucosinolate diversity within a phylogenetic framework of the tribe Cardamineae (Brassicaceae) unraveled with HPLC-MS/MS and NMR-based analytical distinction of 70 desulfoglucosinolates.
Olsen CE, Huang XC, Hansen CIC, Cipollini D, Ørgaard M, Matthes A, Geu-Flores F, Koch MA, Agerbirk N., Phytochemistry 132(), 2016
PMID: 27743600
Olsen CE, Huang XC, Hansen CIC, Cipollini D, Ørgaard M, Matthes A, Geu-Flores F, Koch MA, Agerbirk N., Phytochemistry 132(), 2016
PMID: 27743600
Derivatization of isothiocyanates and their reactive adducts for chromatographic analysis.
Agerbirk N, De Nicola GR, Olsen CE, Müller C, Iori R., Phytochemistry 118(), 2015
PMID: 26342619
Agerbirk N, De Nicola GR, Olsen CE, Müller C, Iori R., Phytochemistry 118(), 2015
PMID: 26342619
67 References
Daten bereitgestellt von Europe PubMed Central.
Effects of indole glucosinolates on performance and sequestration by the sawfly Athalia rosae and consequences of feeding on the plant defense system
Abdalsamee, J. Chem. Ecol. 38(), 2013
Abdalsamee, J. Chem. Ecol. 38(), 2013
Rapid incorporation of glucosinolates as a strategy used by a herbivore to prevent activation by myrosinases.
Abdalsamee MK, Giampa M, Niehaus K, Muller C., Insect Biochem. Mol. Biol. 52(), 2014
PMID: 25017143
Abdalsamee MK, Giampa M, Niehaus K, Muller C., Insect Biochem. Mol. Biol. 52(), 2014
PMID: 25017143
Glucosinolate structures in evolution.
Agerbirk N, Olsen CE., Phytochemistry 77(), 2012
PMID: 22405332
Agerbirk N, Olsen CE., Phytochemistry 77(), 2012
PMID: 22405332
A common pathway for metabolism of 4-hydroxybenzylglucosinolate in Pieris and Anthocaris (Lepidoptera: Pieridae)
Agerbirk, Biochem. Syst. Ecol. 34(), 2006
Agerbirk, Biochem. Syst. Ecol. 34(), 2006
Host plant-dependent metabolism of 4-hydroxybenzylglucosinolate in Pieris rapae: substrate specificity and effects of genetic modification and plant nitrile hydratase.
Agerbirk N, Olsen CE, Topbjerg HB, Sorensen JC., Insect Biochem. Mol. Biol. 37(11), 2007
PMID: 17916498
Agerbirk N, Olsen CE, Topbjerg HB, Sorensen JC., Insect Biochem. Mol. Biol. 37(11), 2007
PMID: 17916498
Sinapis phylogeny and evolution of glucosinolates and specific nitrile degrading enzymes.
Agerbirk N, Warwick SI, Hansen PR, Olsen CE., Phytochemistry 69(17), 2008
PMID: 18995873
Agerbirk N, Warwick SI, Hansen PR, Olsen CE., Phytochemistry 69(17), 2008
PMID: 18995873
Variable glucosinolate profiles of Cardamine pratensis (Brassicaceae) with equal chromosome numbers.
Agerbirk N, Olsen CE, Chew FS, Orgaard M., J. Agric. Food Chem. 58(8), 2010
PMID: 20334382
Agerbirk N, Olsen CE, Chew FS, Orgaard M., J. Agric. Food Chem. 58(8), 2010
PMID: 20334382
Complex metabolism of aromatic glucosinolates in Pieris rapae caterpillars involving nitrile formation, hydroxylation, demethylation, sulfation, and host plant dependent carboxylic acid formation.
Agerbirk N, Olsen CE, Poulsen E, Jacobsen N, Hansen PR., Insect Biochem. Mol. Biol. 40(2), 2010
PMID: 20079434
Agerbirk N, Olsen CE, Poulsen E, Jacobsen N, Hansen PR., Insect Biochem. Mol. Biol. 40(2), 2010
PMID: 20079434
Specific glucosinolate analysis reveals variable levels of epimeric glucobarbarins, dietary precursors of 5-phenyloxazolidine-2-thiones, in watercress types with contrasting chromosome numbers.
Agerbirk N, Olsen CE, Cipollini D, Orgaard M, Linde-Laursen I, Chew FS., J. Agric. Food Chem. 62(39), 2014
PMID: 25226408
Agerbirk N, Olsen CE, Cipollini D, Orgaard M, Linde-Laursen I, Chew FS., J. Agric. Food Chem. 62(39), 2014
PMID: 25226408
Multiple hydroxyphenethyl glucosinolate isomers and their tandem mass spectrometric distinction in a geographically structured polymorphism in the crucifer Barbarea vulgaris.
Agerbirk N, Olsen CE, Heimes C, Christensen S, Bak S, Hauser TP., Phytochemistry 115(), 2014
PMID: 25277803
Agerbirk N, Olsen CE, Heimes C, Christensen S, Bak S, Hauser TP., Phytochemistry 115(), 2014
PMID: 25277803
Derivatization of isothiocyanates and their reactive adducts for chromatographic analysis.
Agerbirk N, De Nicola GR, Olsen CE, Muller C, Iori R., Phytochemistry 118(), 2015
PMID: 26342619
Agerbirk N, De Nicola GR, Olsen CE, Muller C, Iori R., Phytochemistry 118(), 2015
PMID: 26342619
A role for isothiocyanates in plant resistance against the specialist herbivore Pieris rapae.
Agrawal AA, Kurashige NS., J. Chem. Ecol. 29(6), 2003
PMID: 12918924
Agrawal AA, Kurashige NS., J. Chem. Ecol. 29(6), 2003
PMID: 12918924
Identification of glucosinolate congeners able to form DNA adducts and to induce mutations upon activation by myrosinase.
Baasanjav-Gerber C, Monien BH, Mewis I, Schreiner M, Barillari J, Iori R, Glatt H., Mol Nutr Food Res 55(5), 2011
PMID: 21213326
Baasanjav-Gerber C, Monien BH, Mewis I, Schreiner M, Barillari J, Iori R, Glatt H., Mol Nutr Food Res 55(5), 2011
PMID: 21213326
Chemosensory and behavioural responses of the turnip sawfly, Athalia rosae, to glucosinolates and isothiocyanates
Barker, Chemoecology 16(), 2006
Barker, Chemoecology 16(), 2006
How novel are the chemical weapons of garlic mustard in North American forest understories
Barto EKathryn, Powell JeffR, Cipollini Don., Biol. Invasions 12(10), 2010
PMID: IND44429501
Barto EKathryn, Powell JeffR, Cipollini Don., Biol. Invasions 12(10), 2010
PMID: IND44429501
Varied response of Spodoptera littoralis against Arabidopsis thaliana with metabolically engineered glucosinolate profiles.
Bejai S, Fridborg I, Ekbom B., Plant Physiol. Biochem. 50(1), 2011
PMID: 21835629
Bejai S, Fridborg I, Ekbom B., Plant Physiol. Biochem. 50(1), 2011
PMID: 21835629
Profiling glucosinolates and phenolics in vegetative and reproductive tissues of the multi-purpose trees Moringa oleifera L. (horseradish tree) and Moringa stenopetala L.
Bennett RN, Mellon FA, Foidl N, Pratt JH, Dupont MS, Perkins L, Kroon PA., J. Agric. Food Chem. 51(12), 2003
PMID: 12769522
Bennett RN, Mellon FA, Foidl N, Pratt JH, Dupont MS, Perkins L, Kroon PA., J. Agric. Food Chem. 51(12), 2003
PMID: 12769522
Phyllotreta striolata flea beetles use host plant defense compounds to create their own glucosinolate-myrosinase system.
Beran F, Pauchet Y, Kunert G, Reichelt M, Wielsch N, Vogel H, Reinecke A, Svatos A, Mewis I, Schmid D, Ramasamy S, Ulrichs C, Hansson BS, Gershenzon J, Heckel DG., Proc. Natl. Acad. Sci. U.S.A. 111(20), 2014
PMID: 24799680
Beran F, Pauchet Y, Kunert G, Reichelt M, Wielsch N, Vogel H, Reinecke A, Svatos A, Mewis I, Schmid D, Ramasamy S, Ulrichs C, Hansson BS, Gershenzon J, Heckel DG., Proc. Natl. Acad. Sci. U.S.A. 111(20), 2014
PMID: 24799680
Altering glucosinolate profiles modulates disease resistance in plants
Brader, Plant J. 34(), 2006
Brader, Plant J. 34(), 2006
Biological targets of isothiocyanates.
Brown KK, Hampton MB., Biochim. Biophys. Acta 1810(9), 2011
PMID: 21704127
Brown KK, Hampton MB., Biochim. Biophys. Acta 1810(9), 2011
PMID: 21704127
The isothiocyanate produced from glucomoringin inhibits NF-kB and reduces myeloma growth in nude mice in vivo.
Brunelli D, Tavecchio M, Falcioni C, Frapolli R, Erba E, Iori R, Rollin P, Barillari J, Manzotti C, Morazzoni P, D'Incalci M., Biochem. Pharmacol. 79(8), 2009
PMID: 20006591
Brunelli D, Tavecchio M, Falcioni C, Frapolli R, Erba E, Iori R, Rollin P, Barillari J, Manzotti C, Morazzoni P, D'Incalci M., Biochem. Pharmacol. 79(8), 2009
PMID: 20006591
Supercritical fluid chromatography as a method of analysis for the determination of 4-hydroxybenzylglucosinolate degradation products.
Buskov S, Hasselstrom J, Olsen CE, Sorensen H, Sorensen JC, Sorensen S., J. Biochem. Biophys. Methods 43(1-3), 2000
PMID: 10869674
Buskov S, Hasselstrom J, Olsen CE, Sorensen H, Sorensen JC, Sorensen S., J. Biochem. Biophys. Methods 43(1-3), 2000
PMID: 10869674
Mustard oil glucosides as feeding stimulants for Pieris brassicae larvae in a semi-synthetic diet
David, Entomol. Exp. Appl. 9(), 1966
David, Entomol. Exp. Appl. 9(), 1966
Isolation and identification of 4-α-rhamnosyloxy benzyl glucosinolate in Noccaea caerulescens showing intraspecific variation.
de Graaf RM, Krosse S, Swolfs AE, te Brinke E, Prill N, Leimu R, van Galen PM, Wang Y, Aarts MG, van Dam NM., Phytochemistry 110(), 2014
PMID: 25482220
de Graaf RM, Krosse S, Swolfs AE, te Brinke E, Prill N, Leimu R, van Galen PM, Wang Y, Aarts MG, van Dam NM., Phytochemistry 110(), 2014
PMID: 25482220
Contact chemoreception of oviposition-stimulating glucosinolates and an oviposition-deterrent cardenolide in two subspecies of Pieris napi.
Du YJ, Loon JJAvon, Renwick JAA., Physiol. Entomol. 20(2), 1995
PMID: IND20482069
Du YJ, Loon JJAvon, Renwick JAA., Physiol. Entomol. 20(2), 1995
PMID: IND20482069
Development of a reliable extraction and quantification method for glucosinolates in Moringa oleifera.
Forster N, Ulrichs C, Schreiner M, Muller CT, Mewis I., Food Chem 166(), 2014
PMID: 25053080
Forster N, Ulrichs C, Schreiner M, Muller CT, Mewis I., Food Chem 166(), 2014
PMID: 25053080
Antibacterial activity of glucomoringin bioactivated with myrosinase against two important pathogens affecting the health of long-term patients in hospitals
Galuppo, Molecules 18(), 2013
Galuppo, Molecules 18(), 2013
4(α-l-rhamnosyloxy)-benzyl isothiocyanate, a bioactive phytochemical that attenuates secondary damage in an experimental model of spinal cord injury.
Giacoppo S, Galuppo M, De Nicola GR, Iori R, Bramanti P, Mazzon E., Bioorg. Med. Chem. 23(1), 2014
PMID: 25497964
Giacoppo S, Galuppo M, De Nicola GR, Iori R, Bramanti P, Mazzon E., Bioorg. Med. Chem. 23(1), 2014
PMID: 25497964
Near-silence of isothiocyanate carbon in (13)C NMR spectra: a case study of allyl isothiocyanate.
Glaser R, Hillebrand R, Wycoff W, Camasta C, Gates KS., J. Org. Chem. 80(9), 2015
PMID: 25882372
Glaser R, Hillebrand R, Wycoff W, Camasta C, Gates KS., J. Org. Chem. 80(9), 2015
PMID: 25882372
First synthesis of an O-glycosylated glucosinolate isolated from Moringa oleifera
Gueyrard, Tetrahedron Lett. 41(), 2000
Gueyrard, Tetrahedron Lett. 41(), 2000
Glucosinolate chemistry: synthesis of O-glycosylated derivatives of glucosinalbin
Gueyrard, Eur. J. Org. Chem. (), 2010
Gueyrard, Eur. J. Org. Chem. (), 2010
Characterization of products from the reaction of glucosinolate-derived isothiocyanates with cysteine and lysine derivatives formed in either model systems or broccoli sprouts.
Hanschen FS, Bruggemann N, Brodehl A, Mewis I, Schreiner M, Rohn S, Kroh LW., J. Agric. Food Chem. 60(31), 2012
PMID: 22794085
Hanschen FS, Bruggemann N, Brodehl A, Mewis I, Schreiner M, Rohn S, Kroh LW., J. Agric. Food Chem. 60(31), 2012
PMID: 22794085
Administration of isothiocyanates enhances heat tolerance in Arabidopsis thaliana
Hara, Plant Growth Regul. 69(), 2013
Hara, Plant Growth Regul. 69(), 2013
Isolation and structural elucidation of 4-(beta-D-glucopyranosyldisulfanyl)butyl glucosinolate from leaves of rocket salad (Eruca sativa L.) and its antioxidative activity.
Kim SJ, Jin S, Ishii G., Biosci. Biotechnol. Biochem. 68(12), 2004
PMID: 15618613
Kim SJ, Jin S, Ishii G., Biosci. Biotechnol. Biochem. 68(12), 2004
PMID: 15618613
Naturally derived isothiocyanates (mustard oils) and their parent glucosides
Kjær, Fortschr. Chem. Org. Naturst. 18(), 1960
Kjær, Fortschr. Chem. Org. Naturst. 18(), 1960
Isothiocyanates in myrosinase-treated seed extracts of Moringa peregrina
Kjær, Phytochemistry 18(), 1979
Kjær, Phytochemistry 18(), 1979
Feeding and growth of Plutella xylostella and Spodoptera eridania on Brassica juncea with varying glucosinolate concentrations and myrosinase activities
Li, J. Chem. Ecol. 26(), 2000
Li, J. Chem. Ecol. 26(), 2000
Behavioural and sensory responses to some neem compounds by Pieris brassicae larvae.
Lou LE, Loon JJAvan, Schoonhoven LM., Physiol. Entomol. 20(2), 1995
PMID: IND20482060
Lou LE, Loon JJAvan, Schoonhoven LM., Physiol. Entomol. 20(2), 1995
PMID: IND20482060
The mustard oil bomb – compartmentation of the myrosinase system
Matile, Biochem. Physiol. Pflanzen 175(), 1980
Matile, Biochem. Physiol. Pflanzen 175(), 1980
Physiology of the lateral galeal sensillum in red turnip beetle larvae (entomoscelis-American brown) – responses to NaCl, glucosinolates and other glycosides
Mitchell, J. Comp. Physiol. 144(), 1981
Mitchell, J. Comp. Physiol. 144(), 1981
Interactions between glucosinolate- and myrosinase-containing plants and the sawfly Athalia rosae
Müller, Phytochem. Rev. 8(), 2009
Müller, Phytochem. Rev. 8(), 2009
Analysis of a chemical defense in sawfly larvae: easy bleeding targets predatory wasps in late summer.
Muller C, Brakefield PM., J. Chem. Ecol. 29(12), 2003
PMID: 14969355
Muller C, Brakefield PM., J. Chem. Ecol. 29(12), 2003
PMID: 14969355
Effects of glucosinolate and myrosinase levels in Brassica juncea on a glucosinolate-sequestering herbivore – and vice versa
Müller, Chemoecology 16(), 2006
Müller, Chemoecology 16(), 2006
Sequestration of host plant glucosinolates in the defensive hemolymph of the sawfly Athalia rosae.
Muller C, Agerbirk N, Olsen CE, Boeve JL, Schaffner U, Brakefield PM., J. Chem. Ecol. 27(12), 2001
PMID: 11789955
Muller C, Agerbirk N, Olsen CE, Boeve JL, Schaffner U, Brakefield PM., J. Chem. Ecol. 27(12), 2001
PMID: 11789955
Host plant derived feeding deterrence towards ants in the turnip sawfly Athalia rosae
Muller C, Boeve J, Brakefield PM., Entomol. Exp. Appl. 104(1), 2002
PMID: IND23321180
Muller C, Boeve J, Brakefield PM., Entomol. Exp. Appl. 104(1), 2002
PMID: IND23321180
Covalent modification of lysine residues by allyl isothiocyanate in physiological conditions: plausible transformation of isothiocyanate from thiol to amine.
Nakamura T, Kawai Y, Kitamoto N, Osawa T, Kato Y., Chem. Res. Toxicol. 22(3), 2009
PMID: 19216492
Nakamura T, Kawai Y, Kitamoto N, Osawa T, Kato Y., Chem. Res. Toxicol. 22(3), 2009
PMID: 19216492
Behavioral and electrophysiological responses of Aphids to host and nonhost plant volatiles.
Nottingham SF, Hardie J, Dawson GW, Hick AJ, Pickett JA, Wadhams LJ, Woodcock CM., J. Chem. Ecol. 17(6), 1991
PMID: 24259180
Nottingham SF, Hardie J, Dawson GW, Hick AJ, Pickett JA, Wadhams LJ, Woodcock CM., J. Chem. Ecol. 17(6), 1991
PMID: 24259180
Isolation of glucosinolates and the identification of o-(α-l-rhamnopyranosyloxy)benzylglucosinolate from Reseda odorata
Olsen, Phytochemistry 18(), 1979
Olsen, Phytochemistry 18(), 1979
Glucosinolates in Sesamoides canescens and S. pygmaea: identification of 2-α-l-arabinopyranosyloxy)-2-phenylethylglucosinolate
Olsen, Phytochemistry 20(), 1981
Olsen, Phytochemistry 20(), 1981
Desulfation followed by sulfation: metabolism of benzylglucosinolate in Athalia rosae (Hymenoptera: Tenthredinidae).
Opitz SE, Mix A, Winde IB, Muller C., Chembiochem 12(8), 2011
PMID: 21506231
Opitz SE, Mix A, Winde IB, Muller C., Chembiochem 12(8), 2011
PMID: 21506231
Inhibition of lipopolysaccharide-induced cyclooxygenase-2 and inducible nitric oxide synthase expression by 4-[(2'-O-acetyl-α-L-rhamnosyloxy)benzyl]isothiocyanate from Moringa oleifera.
Park EJ, Cheenpracha S, Chang LC, Kondratyuk TP, Pezzuto JM., Nutr Cancer 63(6), 2011
PMID: 21774591
Park EJ, Cheenpracha S, Chang LC, Kondratyuk TP, Pezzuto JM., Nutr Cancer 63(6), 2011
PMID: 21774591
Sinalexin, a phytoalexin from white mustard elicited by destruxin B and Alternaria brassicae
Pedras, Phytochemistry 46(), 1997
Pedras, Phytochemistry 46(), 1997
The multiple strategies of an insect herbivore to overcome plant cyanogenic glucoside defence.
Pentzold S, Zagrobelny M, Roelsgaard PS, Moller BL, Bak S., PLoS ONE 9(3), 2014
PMID: 24625698
Pentzold S, Zagrobelny M, Roelsgaard PS, Moller BL, Bak S., PLoS ONE 9(3), 2014
PMID: 24625698
A recycling pathway for cyanogenic glycosides evidenced by the comparative metabolic profiling in three cyanogenic plant species.
Picmanova M, Neilson EH, Motawia MS, Olsen CE, Agerbirk N, Gray CJ, Flitsch S, Meier S, Silvestro D, Jorgensen K, Sanchez-Perez R, Moller BL, Bjarnholt N., Biochem. J. 469(3), 2015
PMID: 26205491
Picmanova M, Neilson EH, Motawia MS, Olsen CE, Agerbirk N, Gray CJ, Flitsch S, Meier S, Silvestro D, Jorgensen K, Sanchez-Perez R, Moller BL, Bjarnholt N., Biochem. J. 469(3), 2015
PMID: 26205491
Chemoreception and feeding behaviour in a caterpillar: towards a model of brain functioning in insects.
Schoonhoven LM, Blom F., Entomol. Exp. Appl. 49(1/2), 1988
PMID: IND89020076
Schoonhoven LM, Blom F., Entomol. Exp. Appl. 49(1/2), 1988
PMID: IND89020076
An inventory of taste in caterpillars: each species its own key
Schoonhoven, Acta Zool. Acad. Sci. Hung. 48(), 2002
Schoonhoven, Acta Zool. Acad. Sci. Hung. 48(), 2002
Schoonhoven, 2005
Turning the 'mustard oil bomb' into a 'cyanide bomb': aromatic glucosinolate metabolism in a specialist insect herbivore.
Stauber EJ, Kuczka P, van Ohlen M, Vogt B, Janowitz T, Piotrowski M, Beuerle T, Wittstock U., PLoS ONE 7(4), 2012
PMID: 22536404
Stauber EJ, Kuczka P, van Ohlen M, Vogt B, Janowitz T, Piotrowski M, Beuerle T, Wittstock U., PLoS ONE 7(4), 2012
PMID: 22536404
Specialist deterrent chemoreceptors enable Pieris caterpillars to discriminate between chemically different deterrents.
Loon JJAvan, Schoonhoven LM., Entomol. Exp. Appl. 91(1), 1999
PMID: IND22014170
Loon JJAvan, Schoonhoven LM., Entomol. Exp. Appl. 91(1), 1999
PMID: IND22014170
Flavonoids from cabbage are feeding stimulants for diamondback moth larvae additional to glucosinolates: Chemoreception and behaviour
van Loon JJA, Wang CZ, Nielsen JK, Gols R, Qiu YT., Entomol. Exp. Appl. 104(1), 2002
PMID: IND23321149
van Loon JJA, Wang CZ, Nielsen JK, Gols R, Qiu YT., Entomol. Exp. Appl. 104(1), 2002
PMID: IND23321149
Differential sensory perception of plant compounds by insects
Visser, ACS Symp. Ser. 208(), 1983
Visser, ACS Symp. Ser. 208(), 1983
Olfactory antennal responses to plant volatiles in apterous virginoparae of the vetch aphid Megoura viciae.
Visser JH, Piron PGM., Entomol. Exp. Appl. 77(1), 1995
PMID: IND20531972
Visser JH, Piron PGM., Entomol. Exp. Appl. 77(1), 1995
PMID: IND20531972
Stable, water extractable isothiocyanates from Moringa oleifera leaves attenuate inflammation in vitro.
Waterman C, Cheng DM, Rojas-Silva P, Poulev A, Dreifus J, Lila MA, Raskin I., Phytochemistry 103(), 2014
PMID: 24731259
Waterman C, Cheng DM, Rojas-Silva P, Poulev A, Dreifus J, Lila MA, Raskin I., Phytochemistry 103(), 2014
PMID: 24731259
Insect herbivore counteradaptations to the plant glucosinolate-myrosinase system.
Winde I, Wittstock U., Phytochemistry 72(13), 2011
PMID: 21316065
Winde I, Wittstock U., Phytochemistry 72(13), 2011
PMID: 21316065
Constitutive plant toxins and their role in defense against herbivores and pathogens
Wittstock, Curr. Opin. Plant Biol. 5(), 2002
Wittstock, Curr. Opin. Plant Biol. 5(), 2002
Successful herbivore attack due to metabolic diversion of a plant chemical defense.
Wittstock U, Agerbirk N, Stauber EJ, Olsen CE, Hippler M, Mitchell-Olds T, Gershenzon J, Vogel H., Proc. Natl. Acad. Sci. U.S.A. 101(14), 2004
PMID: 15051878
Wittstock U, Agerbirk N, Stauber EJ, Olsen CE, Hippler M, Mitchell-Olds T, Gershenzon J, Vogel H., Proc. Natl. Acad. Sci. U.S.A. 101(14), 2004
PMID: 15051878
Chemosensory basis of behavioural plasticity in response to deterrent plant chemicals in the larva of the Small Cabbage White butterfly Pieris rapae.
Zhou DS, Wang CZ, van Loon JJ., J. Insect Physiol. 55(9), 2009
PMID: 19414011
Zhou DS, Wang CZ, van Loon JJ., J. Insect Physiol. 55(9), 2009
PMID: 19414011
Export
Markieren/ Markierung löschen
Markierte Publikationen
Web of Science
Dieser Datensatz im Web of Science®Quellen
PMID: 26318325
PubMed | Europe PMC
Suchen in