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Plant J. 2019 Dec 9. doi: 10.1111/tpj.14642. [Epub ahead of print]

A genetically validated approach for detecting inorganic polyphosphates in plants.

Author information

1
Structural Plant Biology Laboratory, Department of Botany and Plant Biology, University of Geneva, 30 Quai E. Ansermet, Geneva, 1211, Switzerland.
2
Department of Botany and Plant Biology, University of Geneva, 30 Quai E. Ansermet, Geneva, 1211, Switzerland.
3
Max-Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, Potsdam-Golm, 14476, Germany.
4
Center of Plant System Biology and Biotechnology, Ruski Blvd. 139, Plovdiv, 4000, Bulgaria.
5
Center for Self-assembly and Complexity, IBS and Department of Chemistry, POSTECH, 50, Jigok-ro 127beon-gil, Nam-gu, Pohang-si, Gyeongsangbuk-do, Pohang, 37673, Republic of Korea.

Abstract

Inorganic polyphosphates (polyPs) are linear polymers of orthophosphate units linked by phosphoanhydride bonds. Polyphosphates represent important stores of phosphate and energy, and are abundant in many pro- and eukaryotic organisms. In plants, the existence of polyPs has been established using microscopy and biochemical extraction methods that are now known to produce artifacts. Here we use a polyP-specific dye and a polyP-binding domain to detect polyPs in plant and algal cells. To develop the staining protocol, we induced polyP granules in Nicotiana benthamiana and Arabidopsis cells by heterologous expression of Escherichia coli polyphosphate kinase 1 (PPK1). Over-expression of PPK1 but not of a catalytically impaired version of the enzyme leads to severe growth phenotypes, suggesting that ATP-dependent synthesis and accumulation of polyPs in the plant cytosol is toxic. We next crossed stable PPK1-expressing Arabidopsis lines with plants expressing the polyP-binding domain of E. coli exopolyphosphatase (PPX1c), which co-localized with PPK1-generated polyP granules. These granules were stained by the polyP-specific dye JC-D7 and appeared as electron-dense structures in transmission electron microscopy sections. Using the polyP staining protocol derived from these experiments, we screened for polyP stores in different organs and tissues of both mono- and dicotyledonous plants. While we could not detect polyP granules in higher plants, we could visualize the polyP-rich acidocalcisomes in the green alga Chlamydomonas reinhardtii.

KEYWORDS:

Chlamydomonas ; Arabidopsis; energy metabolism; inorganic polyphosphate; polyphosphate kinase; polyphosphate phosphatase

PMID:
31816134
DOI:
10.1111/tpj.14642

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