Secondary metabolites and plant/environment interactions: a view through Arabidopsis thaliana tinged glasses

By Daniel J. Kliebenstein. 2004

412 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/2954c0ba198435020543623752b04d7b7b3fc7c2

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Citations in the corpus

Glucosinolates and other metabolites in the leaves of Arabidopsis thaliana from natural populations and their effects on a generalist and a specialist herbivore (2008, background): “Thus a mutation in one of the enzymes or a cross-pollination event could lead to a rapid glucosinolate profile shift from one generation to the next (Kliebenstein 2004).”
In vitro antifungal activity of brassinin, camalexin and two isothiocyanates against the crucifer pathogens Alternaria brassicicola and Alternaria brassicae (2007, background): “Glucosinolates constitute a group of sulphurcontaining glucosides that following tissue damage, are converted by the endogenous thioglucosidase myrosinase into breakdown products such as isothiocyanates (ITCs) and nitriles which exhibit toxicity towards bacteria, fungi and insects (Kliebenstein, 200”
Variation in natural plant products and the attraction of bodyguards involved in indirect plant defense (2010, background): “Phenylpropanoids have important functions in resistance against UV light because they absorb UV-B radiation (Kliebenstein 2004).”
Plant–soil feedbacks contribute to an intransitive competitive network that promotes both genetic and species diversity (2011, background): “While the toxic properties of glucosinolate breakdown products are well documented (Schreiner & Koide 1993; Kliebenstein 2004), the proximate mechanism by which the genetic differences in sinigrin expression in leaves caused the observed changes in soil microbial communities is not clear from this…”
Rapid Evolutionary Change and the Coexistence of Species (2011, background): “Sinigrin, a glucosinolate compound characteristic of many species in the mustard family, has shown toxicity to a broad range of organisms, including insects, microbes, and other plants (Kliebenstein 2004, Raybould & Moyes 2001).”
Network analysis of the MVA and MEP pathways for isoprenoid synthesis. (2013, background): “Production and accumulation of metabolites in a tissueand/or compartment-dependent manner enable their cost-effective utilization and channeling of resources to either growth or defense, thus increasing fitness and competitive ability (67).”
Regulation and accumulation of secondary metabolites in plant-fungus symbiotic system (2007, background): “Environmental factors including biotic and abiotic stimuli, carbon-nutrition balance, genotype and ontogenesis usually control and regulate the biosynthesis of secondary metabolites in plants (Kliebenstein, 2004; Laitinen et al., 2005; Lerdau, 2002; Mary Ann Lila, 2006).”
Ecological costs of biotrophic versus necrotrophic pathogen resistance, the hypersensitive response and signal transduction (2008, positive): “2 gene and genes associated with production of anti-microbial defense metabolites such as indole glucosinolates and the phytoalexin camalexin [65-67].”
Plant Phenolics – Secondary Metabolites with Diverse Functions (2009, background): “Therefore, they represent adaptive characters that have been subjected to natural selection during evolution (Hättenschwiler & Vitousek, 2000; Pichersky & Gang, 2000; Kutchan, 2001; Theis & Lerdau, 2003; Wink, 2003; Kliebenstein, 2004; Kutchan & Dixon, 2005; Memelink, 2005).”
Gene function beyond the single trait: natural variation, gene effects, and evolutionary ecology in Arabidopsis thaliana (2005, background): “Plant interactions with herbivores Secondary chemistry plays a key role in protection against herbivores and pathogens (Kliebenstein 2004).”
New insights into the shikimate and aromatic amino acids biosynthesis pathways in plants. (2010, background): “Extensive studies of the pad3 mutant led to the proposition that camalexin contributes to resistance against necrotrophic pathogens but not against biotrophs (Glazebrook, 2005; Kliebenstein, 2004).”
Flavonoids: biosynthesis, biological functions, and biotechnological applications (2012, background): “Thus, both plants and insect herbivores have evolved leading to the plant defense (i.e., plant secondary metabolites) and herbivore offense (i.e., detoxification ability) (Cornell and Hawkins, 2003; Kliebenstein, 2004; BidartBouzat and Imeh-Nathaniel, 2008).”
Differential accumulation of maysin and rhamnosylisoorientin in leaves of high‐altitude landraces of maize after UV‐B exposure (2005, background): “A number of phenylpropanoiddeficient mutants show increased sensitivity to UV-B, demonstrating that these molecules do have a major role in protection against UV-B (for a review, see Kliebenstein 2004).”
Light influences transpiration and calcium accumulation in fruit of kiwifruit plants (Actinidia deliciosa var. deliciosa) (2006, positive): “Here, we suggest a new working hypotheses to explain radiation induced Ca accumulation, taking into account the widely documented role of light in promoting the biosynthesis of phenolic compounds [40–42].”