Should I stay or should I go: are chlorogenic acids mobilized towards lignin biosynthesis?

• Published in: Phytochemistry (Oxford) 2019-10, Vol.166, p.112063-112063, Article 112063
• Main Authors: Volpi e Silva, Nathalia, Mazzafera, Paulo, Cesarino, Igor
• Format: Article
• Language: English
• Subjects: Caffeoyl shikimate esterase; Chlorogenic acids; Hydroxycinnamoyl CoA:shikimate/quinate hydroxycinnamoyl transferase; Lignin; Phenylpropanoids; Quinate; Shikimate
• ISSN: 0031-9422; 1873-3700
• DOI: 10.1016/j.phytochem.2019.112063

Chlorogenic acids (CGAs) and the biopolymer lignin are both products of the phenylpropanoid pathway. Whereas CGAs have been reported to play a role during stress responses, lignin is a major component of secondary cell walls, providing physical strength and hydrophobicity to supportive and water-conducting tissues. Because the chemical structure of CGAs largely resembles those of some lignin intermediates and because CGAs can be converted back to hydroxycinnamoyl-CoAs in vitro, CGAs have been considered authentic intermediates of the lignin biosynthetic pathway. However, it is still unclear whether and how the CGA pool can be channeled towards the production of lignin monomers in response to developmental or environmental signals. Comprehensive studies on the catalytic activity of recombinant enzymes together with functional characterizations in planta have been very useful in understanding the potential interdependence between these two metabolic routes. Here we present the current understanding on CGA metabolism and discuss the biochemical and molecular evidence of the metabolic re-routing of CGAs towards lignin. [Display omitted] •Chlorogenic acids (CGAs) and lignin are products of the phenylpropanoid pathway.•The chemical structure of CGAs largely resembles those of some lignin intermediates.•It is still unclear whether and how CGAs are channeled towards lignin biosynthesis.•Caffeoyl shikimate esterase might be the missing link between CGAs and lignin.