Engineering of benzoxazinoid biosynthesis in Arabidopsis thaliana: Metabolic and physiological challenges.
Arabidopsis thaliana (Brassicaceae)
Benzoxazinones
Bioengineering
Chemical defence
Indolinone
Metabolic stress
Pathway evolution
Phytotoxicity
Transgenic pathway
Zea mays (Poaceae)
Journal
Phytochemistry
ISSN: 1873-3700
Titre abrégé: Phytochemistry
Pays: England
ID NLM: 0151434
Informations de publication
Date de publication:
Dec 2021
Dec 2021
Historique:
received:
22
06
2021
revised:
29
08
2021
accepted:
07
09
2021
pubmed:
18
9
2021
medline:
16
11
2021
entrez:
17
9
2021
Statut:
ppublish
Résumé
Plant specialised metabolites constitute a layer of chemical defence. Classes of the defence compounds are often restricted to a certain taxon of plants, e.g. benzoxazinoids (BX) are characteristically detected in grasses. BXs confer wide-range defence by controlling herbivores and microbial pathogens and are allelopathic compounds. In the crops maize, wheat and rye high concentrations of BXs are synthesised at an early developmental stage. By transfer of six Bx-genes (Bx1 to Bx5 and Bx8) it was possible to establish the biosynthesis of 2,4-dihydroxy-1,4-benzoxazin-3-one glucoside (GDIBOA) in a concentration of up to 143 nmol/g dry weight in Arabidopsis thaliana. Our results indicate that inefficient channeling of substrates along the pathway and metabolisation of intermediates in host plants might be a general drawback for transgenic establishment of specialised metabolite biosynthesis pathways. As a consequence, BX levels required for defence are not obtained in Arabidopsis. We could show that indolin-2-one (ION), the first specific intermediate, is phytotoxic and is metabolised by hydroxylation and glycosylation by a wide spectrum of plants. In Arabidopsis, metabolic stress due to the enrichment of ION leads to elevated levels of salicylic acid (SA) and in addition to its intrinsic phytotoxicity, ION affects plant morphology indirectly via SA. We could show that Bx3 has a crucial role in the evolution of the pathway, first based on its impact on flux into the pathway and, second by C3-hydroxylation of the phytotoxic ION. Thereby BX3 interferes with a supposedly generic detoxification system towards the non-specific intermediate.
Identifiants
pubmed: 34534712
pii: S0031-9422(21)00296-X
doi: 10.1016/j.phytochem.2021.112947
pii:
doi:
Substances chimiques
Benzoxazines
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
112947Informations de copyright
Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.