Plasma membrane phylloquinone biosynthesis in nonphotosynthetic parasitic plants

Author:

Gu Xi1,Chen Ing-Gin2,Harding Scott A234ORCID,Nyamdari Batbayar234,Ortega Maria A234ORCID,Clermont Kristen5ORCID,Westwood James H5,Tsai Chung-Jui1234ORCID

Affiliation:

1. Institute of Bioinformatics, University of Georgia, Athens, GA 30602, USA

2. School of Forestry and Natural Resources, University of Georgia, Athens, GA 30602, USA

3. Department of Genetics, University of Georgia, Athens, GA 30602, USA

4. Department of Plant Biology, University of Georgia, Athens, GA 30602, USA

5. School of Plant and Environmental Sciences, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA

Abstract

Abstract Nonphotosynthetic holoparasites exploit flexible targeting of phylloquinone biosynthesis to facilitate plasma membrane redox signaling. Phylloquinone is a lipophilic naphthoquinone found predominantly in chloroplasts and best known for its function in photosystem I electron transport and disulfide bridge formation of photosystem II subunits. Phylloquinone has also been detected in plasma membrane (PM) preparations of heterotrophic tissues with potential transmembrane redox function, but the molecular basis for this noncanonical pathway is unknown. Here, we provide evidence of PM phylloquinone biosynthesis in a nonphotosynthetic holoparasite Phelipanche aegyptiaca. A nonphotosynthetic and nonplastidial role for phylloquinone is supported by transcription of phylloquinone biosynthetic genes during seed germination and haustorium development, by PM-localization of alternative terminal enzymes, and by detection of phylloquinone in germinated seeds. Comparative gene network analysis with photosynthetically competent parasites revealed a bias of P. aegyptiaca phylloquinone genes toward coexpression with oxidoreductases involved in PM electron transport. Genes encoding the PM phylloquinone pathway are also present in several photoautotrophic taxa of Asterids, suggesting an ancient origin of multifunctionality. Our findings suggest that nonphotosynthetic holoparasites exploit alternative targeting of phylloquinone for transmembrane redox signaling associated with parasitism.

Funder

Georgia Research Alliance-Hank Haynes Forest Biotechnology Endowment

National Science Foundation

National Institute of Food and Agriculture

University of Georgia Graduate School’s Innovative and Interdisciplinary Research Grant

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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