Phenylpropanoid biosynthesis.

By T. Vogt. Molecular Plant, 2010

2,475 citations recorded by the source corpus.

Subfields: Biotechnology, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/f9b74855c033a62625fbd041116f3e5602a37f5e

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Citations in the corpus

Bioavailability of Dietary Polyphenols and Gut Microbiota Metabolism: Antimicrobial Properties (2015, background): “Both p-coumaric acid and p-coumaroyl-CoA are building blocks for hydroxycinnamic acids and flavonoids, respectively (Figure 1) [5].”
Current Approaches for Enhanced Expression of Secondary Metabolites as Bioactive Compounds in Plants for Agronomic and Human Health Purposes – a Review (2013, background): “The shikimate pathway is defi ned by seven metabolic steps beginning with the condensation of phosphoenolpyruvate (PEP) and erythrose 4-phosphate (E4P) and ending with the synthesis of chorismate [Vogt, 2010].”
The shikimate pathway and aromatic amino Acid biosynthesis in plants. (2012, background): “Phe is a common precursor of numerous phenolic compounds, which include flavonoids, condensed tannins, lignans, lignin, and phenylpropanoid/benzenoid volatiles (196).”
Comparative metabolomics and transcriptomics of plant response to Tomato yellow leaf curl virus infection in resistant and susceptible tomato cultivars (2014, background): “Differences between R and S plants were particularly pronounced in the phenylpropanoid pathway, a key component of the plant defense response (Vogt 2010), and in the SA biosynthesis pathway, one of the main defense signaling hormone mediating systemic acquired resistance (SAR).”
The cell biology of lignification in higher plants. (2015, background): “The phenylpropanoid pathway forms a crossroad whose branches lead to the synthesis of hormones, flavonoids, suberins and many different phenolic compounds such as (neo)lignans which derive from the same precursors as lignin (Vogt, 2010; Weng and Chapple, 2010).”
New insights into the shikimate and aromatic amino acids biosynthesis pathways in plants. (2010, background): “metabolites with multiple biological functions and biotechnological values (Bartel, 1997; Vogt, 2010).”
A specialist root herbivore reduces plant resistance and uses an induced plant volatile to aggregate in a density‐dependent manner (2012, background): “…example in response to the water-stress imposed by the root herbivore (Dunn & Frommelt 1998; Erb et al. 2011b), (ii) defence (D’Auria & Gershenzon 2005; Tzin & Galili 2010; Vogt 2010) or (iii) nitrogen transport away from the roots (Paine, Redak & Trumble 1993; Trumble, Kolodny-Hirsch & Ting 1993).”
An overview of lignin metabolism and its effect on biomass recalcitrance (2012, background): “abiotic and biotic stimuli, from mediating plant resistance towards pests to promoting a successful reproduction (Vogt 2010).”
Bioactive phenolic compounds, metabolism and properties: a review on valuable chemical compounds in Scots pine and Norway spruce (2019, background): “7) by dehydrogenation of 3-dehydroshikimic acid (Vogt 2010).”
High-Resolution Temporal Profiling of Transcripts during Arabidopsis Leaf Senescence Reveals a Distinct Chronology of Processes and Regulation[C][W][OA] (2011, background): “Specific members of the bZIP family have been shown to participate in defense against pathogens, development, stress treatments such as cold and drought, ABA signaling, and phenylpropanoid biosynthesis (Weisshaar and Jenkins, 1998; Jakoby et al., 2002).”
The Phenylpropanoid Pathway in Arabidopsis (2011, background): “…also gives rise to a host of other small molecules such as the flavonoids, coumarins, hydroxycinnamic acid conjugates, and lignans (D’Auria and Gershenzon, 2005; Vogt, 2010), many of which could be, and have been, the sole focus of review articles (e.g. Winkel-Shirley, 2001; Lepiniec et al., 2006).”