The complexity of intercellular localisation of alkaloids revealed by single-cell metabolomics.

Catharanthus roseus Apocynaceae Imaging MS alkaloid idioblast cell laticifer cell secondary metabolism single-cell MS

Journal

The New phytologist
ISSN: 1469-8137
Titre abrégé: New Phytol
Pays: England
ID NLM: 9882884

Informations de publication

Date de publication:
10 2019
Historique:
received: 15 01 2019
accepted: 19 06 2019
pubmed: 23 8 2019
medline: 12 5 2020
entrez: 23 8 2019
Statut: ppublish

Résumé

Catharanthus roseus is a medicinal plant well known for producing bioactive compounds such as vinblastine and vincristine, which are classified as terpenoid indole alkaloids (TIAs). Although the leaves of this plant are the main source of these antitumour drugs, much remains unknown on how TIAs are biosynthesised from a central precursor, strictosidine, to various TIAs in planta. Here, we have succeeded in showing, for the first time in leaf tissue of C. roseus, cell-specific TIAs localisation and accumulation with 10 μm spatial resolution Imaging mass spectrometry (Imaging MS) and live single-cell mass spectrometry (single-cell MS). These metabolomic studies revealed that most TIA precursors (iridoids) are localised in the epidermal cells, but major TIAs including serpentine and vindoline are localised instead in idioblast cells. Interestingly, the central TIA intermediate strictosidine also accumulates in both epidermal and idioblast cells of C. roseus. Moreover, we also found that vindoline accumulation increases in laticifer cells as the leaf expands. These discoveries highlight the complexity of intercellular localisation in plant specialised metabolism.

Identifiants

pubmed: 31436868
doi: 10.1111/nph.16138
doi:

Substances chimiques

Secologanin Tryptamine Alkaloids 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

848-859

Informations de copyright

© 2019 The Authors. New Phytologist © 2019 New Phytologist Trust.

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Auteurs

Kotaro Yamamoto (K)

Department of Biology, Graduate School of Science, Kobe University, Kobe, Hyogo, 657-8501, Japan.
Department of Biological Chemistry, John Innes Centre, Norwich Research Park, Norwich, NR4 7UH, UK.

Katsutoshi Takahashi (K)

Biotechnology Research Institute for Drug Discovery, National Institute of Advanced Industrial Science and Technology (AIST), Koutou-ku, Tokyo, 135-0064, Japan.

Lorenzo Caputi (L)

Department of Biological Chemistry, John Innes Centre, Norwich Research Park, Norwich, NR4 7UH, UK.

Hajime Mizuno (H)

Laboratory of Analytical and Bio-Analytical Chemistry, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Shizuoka, 422-8526, Japan.

Carlos E Rodriguez-Lopez (CE)

Department of Biological Chemistry, John Innes Centre, Norwich Research Park, Norwich, NR4 7UH, UK.

Tetsushi Iwasaki (T)

Department of Biology, Graduate School of Science, Kobe University, Kobe, Hyogo, 657-8501, Japan.

Kimitsune Ishizaki (K)

Department of Biology, Graduate School of Science, Kobe University, Kobe, Hyogo, 657-8501, Japan.

Hidehiro Fukaki (H)

Department of Biology, Graduate School of Science, Kobe University, Kobe, Hyogo, 657-8501, Japan.

Miwa Ohnishi (M)

Department of Biology, Graduate School of Science, Kobe University, Kobe, Hyogo, 657-8501, Japan.

Mami Yamazaki (M)

Graduate School of Pharmaceutical Sciences, Chiba University, Chiba, Chiba, 263-8522, Japan.

Tsutomu Masujima (T)

Quantitative Biology Centre (QBiC), RIKEN, Suita, Osaka, 565-0874, Japan.

Sarah E O'Connor (SE)

Department of Biological Chemistry, John Innes Centre, Norwich Research Park, Norwich, NR4 7UH, UK.

Tetsuro Mimura (T)

Department of Biology, Graduate School of Science, Kobe University, Kobe, Hyogo, 657-8501, Japan.

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