Publikationen von Daniel Giddings Vassão
Alle Typen
Zeitschriftenartikel (44)
2007
Zeitschriftenartikel
465 (1), S. 209 - 218 (2007)
A pinoresinol–lariciresinol reductase homologue from the creosote bush (Larrea tridentata) catalyzes the efficient in vitro conversion of p-coumaryl/coniferyl alcohol esters into the allylphenols chavicol/eugenol, but not the propenylphenols p-anol/isoeugenol. Archives of Biochemistry and Biophysics 2006
Zeitschriftenartikel
4 (14), S. 2733 - 2744 (2006)
Chavicol formation in sweet basil (Ocimum basilicum): cleavage of an esterified C9 hydroxyl group with NAD(P)H-dependent reduction. Organic & Biomolecular Chemistry
Zeitschriftenartikel
: Eugenol and isoeugenol, characteristic aromatic constituents of spices, are biosynthesized via reduction of a coniferyl alcohol ester. Proceedings of the National Academy of Sciences of the United States of America 103 (26), S. 10128 - 10133 (2006)
2004
Zeitschriftenartikel
66 (18), S. 2238 - 2247 (2004)
Biflavonoids from Brazilian pine Araucaria angustifolia as potentials protective agents against DNA damage and lipoperoxidation. Phytochemistry Preprint (1)
2024
Preprint
Influence of plant defense signaling and innate insect metabolic differences to the overall performance of fall armyworm (Spodoptera frugiperda) corn and rice strains on maize as a host. bioRxiv: the preprint server for biology (2024)
Buchkapitel (5)
2016
Buchkapitel
80, S. 199 - 245 (Hg. Kopriva, S.). Academic Press, London, Oxford, Boston, New York und San Diego (2016)
Insect detoxification of glucosinolates and their hydrolysis products. In: Advances in Botanical Research: Glucosinolates, Bd. 2015
Buchkapitel
45, S. 163 - 194 (Hg. Jetter, R.). Springer International Publishing, Switzerland (2015)
Metabolism of glucosinolates and their hydrolysis products in insect herbivores. In: Recent Advances Phytochemistry: The formation, structure and activity of phytochemicals, Bd. 2010
Buchkapitel
1, S. 815 - 928 (Hg. Mander, L.; Townsend, C. A.). Elsevier, Amsterdam [u.a.] (2010)
Lignans (neolignans) and allyl/propenyl phenols: Biogenesis, structural biology, and biological/human health considerations. In: Natural products structural diversity-I. Secondary metabolites: organization and biosynthesis, Bd.
Buchkapitel
3, S. 1173 - 1296 (Hg. Liu, H.-W. (.; Mander, L.). Elsevier, Oxford, UK (2010)
Trees: A remarkable biochemical bounty. In: Comprehensive Natural Products II - Chemistry and Biology, Bd. 2008
Buchkapitel
1, S. 385 - 428 (Hg. Bohnert, H. J.; Nguyen, H.; Lewis, N. G.). Elsevier, Oxford, UK (2008)
Metabolic engineering of plant allyl/propenyl phenol and lignin pathways: Future potential for biofuels/bioenergy, polymer intermediates and specialty chemicals? In: Bioengineering and Molecular Biology of Plant Pathways, Bd. Patent (1)
2008
Patent
Genes encoding chavicol/eugenol synthase from the creosote bush Larrea tridentata. US20100031398 (2008)