Glucosinolate research in the Arabidopsis era.

By Ute Wittstock, B. Halkier. Trends in Plant Science, 2002

600 citations recorded by the source corpus.

Subfields: Molecular Biology, Organic Chemistry, Plant Science

View Paper: https://www.semanticscholar.org/paper/a7bea36b80efd06773d800edf7f0f6659fba74e2

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Molecular Biology

1. J. Gershenzon
2. Atle M. Bones
3. B. Halkier
4. Islam Mostafa
5. G. Xue
6. John Manners
7. Peer Schenk
8. Kemal Kazan

In Organic Chemistry

1. J. Gershenzon

In Plant Science

1. J. Gershenzon
2. Kemal Kazan
3. Atle M. Bones
4. B. Halkier
5. W. Boland
6. John Manners
7. I. Ahuja
8. Peer Schenk

Citations in the corpus

• MYC2 Differentially Modulates Diverse Jasmonate-Dependent Functions in Arabidopsis[W] (2007, background): “Intact IGs and glucosinolates, in general, are thought to be nontoxic, but their breakdown products, isothiocyanates and nitriles, can be toxic (reviewed in Wittstock and Halkier, 2002; Grubb and Abel, 2006).”
• Biology and biochemistry of glucosinolates. (2006, background): “It can, however, not be excluded that the in vitro activities of the recombinant CYP79s could differ from their in vivo activities, and that CYP79F1 can metabolize methionine, for example, or that CYP79A2 can convert homophenylalanine and possibly tyrosine, albeit at very low efficiency.”
• Defence mechanisms of Brassicaceae: implications for plant-insect interactions and potential for integrated pest management. A review (2010, background): “…sulphur atoms, one originating from cysteine, the other from phosphoadenosine phosphosulphate, possessing a β -D-glucopyranose moiety and a side chain derived from the amino acids methionine, tryptophan or phenylalanine (Fahey et al., 2001; Wittstock and Halkier, 2002; Rausch and Wachter, 2005).”
• Glucosinolate Biosynthesis and the Glucosinolate–Myrosinase System in Plant Defense (2020, background): “, by insect chewing), the contact of glucosinolates with myrosinases activates the rapid generation of an unstable aglycone—a thiohydroximate-O-sulfate intermediate which undergoes elimination of the sulfate group, leading to the formation of biologically active chemicals, including nitriles, epithi”
• Plant defense against herbivores: chemical aspects. (2012, background): “Besides cyanogenic glycosides, probably the best-known conjugated defense compounds are the glucosinolates (Figure 3) (19, 100, 116, 128), present in Brassicaceae, Capparidaceae, and Tropaeolaceae (Table 1).”
• Auxin Biosynthesis and Metabolism (2010, background): “P450 enzymes are involved in biosynthesis of a number of plant hormones (26) and secondary metabolites such as the glucosinolates, which are a class of amino acidderived plant defense compounds with anti-cancer properties ( 67 ).”