Cutin:cutin-acid endo-transacylase (CCT), a cuticle-remodelling enzyme activity in the plant epidermis. Issue 4 (26th February 2021)

• Record Type: Journal Article
• Authors: Xin, Anzhou; Fei, Yue; Molnar, Attila; Fry, Stephen C.
• Is Part Of: Biochemical journal. Volume 478:Issue 4(2021)
• Page Start: 777
• Page End: 798
• Publication Date: 2021-02-26
• Subjects: cell expansion -- cuticle -- cutin re-modelling -- pea epicotyl -- plant epidermis -- transacylase activity; Biochemistry -- Periodicals; 572
• DOI: 10.1042/BCJ20200835
• Languages: English
• ISSNs: 0264-6021

Abstract

Abstract : Cutin is a polyester matrix mainly composed of hydroxy-fatty acids that occurs in the cuticles of shoots and root-caps. The cuticle, of which cutin is a major component, protects the plant from biotic and abiotic stresses, and cutin has been postulated to constrain organ expansion. We propose that, to allow cutin restructuring, ester bonds in this net-like polymer can be transiently cleaved and then re-formed (transacylation). Here, using pea epicotyl epidermis as the main model, we first detected a cutin:cutin-fatty acid endo-transacylase (CCT) activity. In-situ assays used endogenous cutin as the donor substrate for endogenous enzymes; the exogenous acceptor substrate was a radiolabelled monomeric cutin-acid, 16-hydroxy-[ 3 H]hexadecanoic acid (HHA). High-molecular-weight cutin became ester-bonded to intact [ 3 H]HHA molecules, which thereby became unextractable except by ester-hydrolysing alkalis. In-situ CCT activity correlated with growth rate in Hylotelephium leaves and tomato fruits, suggesting a role in loosening the outer epidermal wall during organ growth. The only well-defined cutin transacylase in the apoplast, CUS1 (a tomato cutin synthase), when produced in transgenic tobacco, lacked CCT activity. This finding provides a reference for future CCT protein identification, which can adopt our sensitive enzyme assay to screen other CUS1-related enzymes.