Biology and biochemistry of glucosinolates.

By B. Halkier, J. Gershenzon. Annual Review of Plant Biology, 2006

2,201 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/0380fcfdb540c54702632fae7c6d287927d5d228

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Citations in the corpus

Metabolism and Plant Hormone Action During Clubroot Disease (2009, background): “Glucosinolates can be divided into three groups according to their core structure (Halkier and Gershenzon 2006).”
The ‘mustard oil bomb’: not so easy to assemble?! Localization, expression and distribution of the components of the myrosinase enzyme system (2008, background): “Although one may think that most is known about glucosinolate metabolism, new genes/proteins involved in the biosynthesis (Hansen et al. 2007) and hydrolysis (Burow et al. 2007a) of glucosinolates and the regulation (Gigolashvili et al. 2007a, b) of the system have only been recently identified…”
Specific and coordinated control of indolic and aliphatic glucosinolate biosynthesis by R2R3-MYB transcription factors in Arabidopsis thaliana (2008, background): “Glucosinolates encompass the amino acid-derived class of sulfur and nitrogen containing secondary metabolites, characteristic of the order Brassicales, which include brassica vegetables, oilseed rape and the model plant Arabidopsis thaliana (Grubb and Abel 2006; Halkier and Gershenzon 2006 ).”
Plant Defense against Insect Herbivores (2013, methodology): “More information on GSL can be found in the reviews by Halkier and Gershenzon [235], and Hopkins et al.”
Plant-mediated effects in the Brassicaceae on the performance and behaviour of parasitoids (2008, background): “At present, the elucidation of pathways involved in the biosynthesis of GS, especially aliphatic GS, relies substantially on research with Arabidopsis (Halkier and Gershenzon 2006).”
Chemical ecology in coupled human and natural systems: people, manioc, multitrophic interactions and global change (2010, background): “The latter is not only a degradative product of glucosinolates (Halkier and Gershenzon 2006) but is also produced by the reaction by which many organisms, including many plants, use the enzyme rhodanese to detoxify cyanide (Beesley et al. 1985), generated by a geographically widespread class of…”
Phytochemical diversity: The sounds of silent metabolism (2009, neutral): “It is reminiscent of binary systems where enzymes and substrates are spatially separated in different cell types or layers, such as glucosinolates and cyanogenic glycosides [48].”
Callose deposition: a multifaceted plant defense response. (2011, background): “Given the toxic nature of glucosinolate break-down products (Halkier and Gershenzon 2006), their function in callose deposition may be explained as part of a cellular detoxification response, which mediates secretion of these defense metabolites into the apoplast, in which they are captured in…”
Herbivore induction of the glucosinolate–myrosinase defense system: major trends, biochemical bases and ecological significance (2008, background): “Their basic skeleton consists of a b-D-glucose residue linked via a sulfur atom to a (Z)-N-hydroximinosulfate ester and a variable side chain (Halkier and Gershenzon 2006) (Fig.”
The Brassica oleracea genome reveals the asymmetrical evolution of polyploid genomes (2014, neutral): “CYP81F1 [1, 2, 4] CYP81F2 [1, 3, 3] CYP81F3 [1, 1, 1]”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “Especially the isothiocyanates act toxic to many organisms including nematodes (Zasada and Ferris, 2003; Halkier and Gershenzon 2006).”