Добірка наукової літератури з теми "Ilex aquifolium L"
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Статті в журналах з теми "Ilex aquifolium L"
Majada, Juan Pedro, Ricardo Sánchez-Tamés, Maria Angeles Revilla, and Abelardo Casares. "Micropropagation of Ilex aquifolium L." In Vitro Cellular & Developmental Biology - Plant 36, no. 6 (November 2000): 521–26. http://dx.doi.org/10.1007/s11627-000-0093-4.
Повний текст джерелаKarlović, Ksenija, and Aleksandar Mešić. "Upotreba božikovine (Ilex aquifolium L.) u urbanom krajobrazu." Glasnik zaštite bilja 43, no. 6 (December 14, 2020): 4–10. http://dx.doi.org/10.31727/gzb.43.6.1.
Повний текст джерелаRuter, John M. "High-temperature-induced Electrolyte Leakage from Excised Leaves and Roots of Three Hollies." HortScience 28, no. 9 (September 1993): 927–28. http://dx.doi.org/10.21273/hortsci.28.9.927.
Повний текст джерелаWachendorf, M., M. Schloz, M. Küppers, A. Güney, and M. Veste. "Wintertime photosynthesis and spring recovery of Ilex aquifolium L." iForest - Biogeosciences and Forestry 12, no. 4 (August 31, 2019): 389–96. http://dx.doi.org/10.3832/ifor2983-012.
Повний текст джерелаNiemann, G. J. "Biosynthesis of pentacyclic triterpenoids in leaves of Ilex aquifolium L." Planta 166, no. 1 (1985): 51–56. http://dx.doi.org/10.1007/bf00397385.
Повний текст джерелаŠilić, Čedomil. "PRILOG POZNAVANJU SPONTANIH MUTACIJA NEKIH ŠUMSKIH VASKULARNIH BILJNIH VRSTA U BOSNI I HERCEGOVINI." Radovi Šumarskog fakulteta Univerziteta u Sarajevu 30, no. 1 (December 1, 2000): 1–6. http://dx.doi.org/10.54652/rsf.2000.v30.i1.234.
Повний текст джерелаNahrstedt, Adolf, and Victor Wray. "Structural revision of a putative cyanogenic glucoside from Ilex aquifolium." Phytochemistry 29, no. 12 (1990): 3934–36. http://dx.doi.org/10.1016/0031-9422(90)85364-l.
Повний текст джерелаPaluch, Emil, Piotr Okińczyc, Anna Zwyrzykowska-Wodzińska, Jakub Szperlik, Barbara Żarowska, Anna Duda-Madej, Przemysław Bąbelewski, et al. "Composition and Antimicrobial Activity of Ilex Leaves Water Extracts." Molecules 26, no. 24 (December 8, 2021): 7442. http://dx.doi.org/10.3390/molecules26247442.
Повний текст джерелаArrieta, Sagrario, and Francisco Suárez. "Germination and seed bank depletion of holly (Ilex aquifolium L.) in four microhabitat types." Seed Science Research 14, no. 3 (September 2004): 305–13. http://dx.doi.org/10.1079/ssr2004180.
Повний текст джерелаFjeld, T., N. A. Melberg, and W. R. Høgetveit. "ETHYLENE SENSITIVITY AND ETHYLENE PRODUCTION IN ENGLISH HOLLY (ILEX AQUIFOLIUM L.)." Acta Horticulturae, no. 405 (October 1995): 306–13. http://dx.doi.org/10.17660/actahortic.1995.405.40.
Повний текст джерелаДисертації з теми "Ilex aquifolium L"
Ranford, Jonathan J. "The impact of tropospheric ozone on Ilex aquifolium L., its leaf-miner (Phytomyza ilicis Curt.) and its parasites." Thesis, Staffordshire University, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.438085.
Повний текст джерелаPalu, Doreen. "Etude de la composition chimique d’extraits d’Ilex aquifolium Linné et de Calicotome villosa (Poiret) Link de Corse par RMN du carbone-13." Electronic Thesis or Diss., Corte, 2022. http://www.theses.fr/2022CORT0018.
Повний текст джерелаThe aim of this work was to determine chemical composition of wild growing corsican understudied plant species, with potential biological activities. This study was realized using the computerized NMR method developed over the past thirty years by the University of Corsica “Chimie et Biomasse” group, UMR CNRS “Sciences Pour l’environnement”. Identified secondary metabolites were then undertaken to evaluate their antimicrobial properties. As part of this study, we selected on the first place commun holly (Ilex aquifolium L.). After two successive column chromatography, hexane and dichloromethane leaves crude extracts and all chromatography fractions were analyzed by 13C NMR (GC(RI) and GC-MS sometimes) to allow the identification of eleven triterpens and α- and β-amyrin esters. Among identified compounds, ursolic acid and oleanolic acid were also quantified by 1H NMR in the dichloromethane crude extract using a reliable method developped and validated (accuracy, linearity precision of measurements). Ursolic acid accounted for 55.3% of the extract, followed by oleanolic acid, 20.8%. Evaluation of previous identified compounds antimicrobial activities has been performed in collaboration with « Biochimie et Biologie Moléculaire du Végétal » group (University of Corsica). Triterpen acids and chloramphenicol (reference antibiotic) displayed similar antibacterial activities against three Gram-positive bacteria, Staphylococcus aureus, Staphylococcus epidermidis and Bacillus cereus (MIC = 4 and 8 mg.L-1 vs. 2 and 4 mg.L-1). Moreover, dichloromethane and dichloromethane/ethyl acetate (50/50, v/v) berries extracts were submitted to successive column chromatography. Crude extracts and chromatography fractions 13C NMR spectra revealed presence of nine triterpens previously identidied, five phenolics derivatives, six monosaccharides and four lactones (menisdaurilide, aquilegiolide, dasycarponilide and 7-epi-griffonilide) were first time identified in berries holly extracts. On the second place, we determined chemical compositions of Calicotome villosa (Poir.) Link flowers and root extracts. 13C NMR analysis of dichloromethane and ethyl acetate flowers extracts and their chromatography fractions, allowed the identification of three flavonoids, five glycosyl flavonoids and four phenylpropanoids. We also studied chemical composition of a methanol root extract which has never been submitted to any chemical composition study. After successive column chromatography, eighteen compounds were identified by 13C NMR including sterols, flavonoids, a polyphenol and pterocarpans