Variation of glucosinolate accumulation among different organs and developmental stages of Arabidopsis thaliana.

By P. Brown, J. Tokuhisa, M. Reichelt, J. Gershenzon. Phytochemistry, 2003

876 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/c1db549995369ffd09ab7eb08af8e3b3c258b200

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. Georg Jander
3. N. V. van Dam
4. S. Textor
5. B. Halkier
6. Islam Mostafa
7. J. Kirkegaard
8. C. Müller

In Plant Science

1. N. V. van Dam
2. J. Gershenzon
3. Georg Jander
4. S. Textor
5. B. Halkier
6. T. Tytgat
7. J. Kirkegaard
8. Martin Heil

Citations in the corpus

• Glucosinolate profiling of seeds and sprouts of B. oleracea varieties used for food (2007, background): “Glucosinolates are a group of allelochemicals characteristic to plants of the order Capparales that co-occur with myrosinase isoenzymes (E.C. 3.2.1.147) (Bellostas et al., 2003; Sørensen, 1990).”
• Glucosinolate Biosynthesis and the Glucosinolate–Myrosinase System in Plant Defense (2020, background): “The presence of 36 different glucosinolates in the reference plant, Arabidopsis thaliana [18,19], has inspired”
• Herbivore induction of the glucosinolate–myrosinase defense system: major trends, biochemical bases and ecological significance (2008, background): “The amounts observed vary depending on the organ, developmental stage, time of day and physical factors of the environment (Bellostas et al. 2007; Brown et al. 2003; Falk et al. 2007; Petersen et al. 2002; Rosa et al. 1994; Shelton 2005), but glucosinolates are usually present throughout the plant…”
• Indole glucosinolate breakdown and its biological effects (2008, background): “Due to the abundance of indole glucosinolates in the model plant Arabidopsis thaliana (Petersen et al. 2002; Brown et al. 2003 ), research on the biosynthesis and function of these secondary metabolites has greatly accelerated in recent years.”
• Specific and coordinated control of indolic and aliphatic glucosinolate biosynthesis by R2R3-MYB transcription factors in Arabidopsis thaliana (2008, background): “It can be concluded that HIG1/MYB51 is the key player in the regulation of indolic glucosinolate biosynthesis, at least in leaves which are the main sites on indolic glucosinolate biosynthesis and accumulation (Brown et al. 2003).”
• Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “GS are constitutively present in plant tissues of the order Capparales in different qualitative and quantitative composition (Brown et al., 2003) but their abundance can change following herbivore feeding in very species-specific ways and depending on the feeding pattern (Textor and Gershenzon, 2009”