Sequential regiospecific gem-diprenylation of tetrahydroxyxanthone by prenyltransferases from Hypericum sp

© 2018 The Authors. New Phytologist © 2018 New Phytologist Trust.

Détails bibliographiques
Publié dans:The New phytologist. - 1984. - 222(2019), 1 vom: 01. Apr., Seite 318-334
Auteur principal: Nagia, Mohamed (Auteur)
Autres auteurs: Gaid, Mariam, Biedermann, Eline, Fiesel, Tobias, El-Awaad, Islam, Hänsch, Robert, Wittstock, Ute, Beerhues, Ludger
Format: Article en ligne
Langue:English
Publié: 2019
Accès à la collection:The New phytologist
Sujets:Journal Article 8-prenylxanthone Hypericum species aromatic gem-diprenylation chloroplast envelope coexpression patulone reporter fusions xanthones 1,3,6,7-tetrahydroxyxanthone plus... Plant Proteins RNA, Messenger Xanthones Dimethylallyltranstransferase EC 2.5.1.1
Description
Résumé:© 2018 The Authors. New Phytologist © 2018 New Phytologist Trust.
Polyprenylated acylphloroglucinol derivatives, such as xanthones, are natural plant products with interesting pharmacological properties. They are difficult to synthesize chemically. Biotechnological production is desirable but it requires an understanding of the biosynthetic pathways. cDNAs encoding membrane-bound aromatic prenyltransferase (aPT) enzymes from Hypericum sampsonii seedlings (HsPT8px and HsPTpat) and Hypericum calycinum cell cultures (HcPT8px and HcPTpat) were cloned and expressed in Saccharomyces cerevisiae and Nicotiana benthamiana, respectively. Microsomes and chloroplasts were used for functional analysis. The enzymes catalyzed the prenylation of 1,3,6,7-tetrahydroxyxanthone (1367THX) and/or 1,3,6,7-tetrahydroxy-8-prenylxanthone (8PX) and discriminated nine additionally tested acylphloroglucinol derivatives. The transient expression of the two aPT genes preceded the accumulation of the products in elicitor-treated H. calycinum cell cultures. C-terminal yellow fluorescent protein fusions of the two enzymes were localized to the envelope of chloroplasts in N. benthamiana leaves. Based on the kinetic properties of HsPT8px and HsPTpat, the enzymes catalyze sequential rather than parallel addition of two prenyl groups to the carbon atom 8 of 1367THX, yielding gem-diprenylated patulone under loss of aromaticity of the gem-dialkylated ring. Coexpression in yeast significantly increased product formation. The patulone biosynthetic pathway involves multiple subcellular compartments. The aPTs studied here and related enzymes may be promising tools for plant/microbe metabolic pathway engineering
Description:Date Completed 27.02.2020
Date Revised 30.09.2020
published: Print-Electronic
GENBANK: MH461100, MH461101, MH461102, MH461103
Citation Status MEDLINE
ISSN:1469-8137
DOI:10.1111/nph.15611