Abstract

Key messageTurnover rates have implications for understanding cyclotide biology and improving plant cell culture-based production systems.Cyclotides are a family of polypeptides recognized for a broad spectrum of bioactivities. The cyclic, cystine knot structural motif imparts these peptides with resistance to temperature, chemicals and proteolysis. Cyclotides are found widely distributed across the Violaceae and in five other plant families, where their presumed biological role is host defense. Violets produce mixtures of different cyclotides that vary depending on the organ, tissue or influence of environmental factors. In the present study, we investigated the biosynthesis and turnover of cyclotides in plant cells. Viola uliginosa suspension cultures were grown in media where all nitrogen containing salts were replaced with their 15N counterparts. This approach combined with LC–MS analysis allowed to separately observe the production of 15N-labelled peptides and decomposition of 14N cyclotides present in the cells when switching the media. Additionally, we investigated changes in cyclotide content in V. odorata germinating seeds. In the suspension cultures, the degradation rates varied for individual cyclotides and the highest was noted for cyO13. Rapid increase in production of 15N peptides was observed until day 19 and subsequently, a plateau of production, indicating an equilibrium between biosynthesis and turnover. The developing seedling appeared to consume cyclotides present in the seed endosperm. We show that degradation processes shape the cyclotide pattern present in different tissues and environments. The results indicate that individual cyclotides play different roles—some in defense and others as storage proteins. The turnover of cyclotides should be accounted to improve cell culture production systems.

Highlights

  • Cyclotides are a family of plant peptides with unique features

  • We investigated the cyclotide biosynthesis in V. uliginosa cell suspension cultures using 15N growth media allowing for introduction of 15N isotopes into the peptides

  • LC–Murashige and Skoog (MS) analysis of the extracts showed that the main cyclotides produced were cyO13 and 3097; small quantities of cyO3, cyO8 and mram8 were detected (Fig. 1)

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Summary

Introduction

Cyclotides are a family of plant peptides with unique features. As the name suggests, peptides belonging to this family have a macrocyclic amino acid backbone, which is completed through a peptide bond between the N- and C-termini. Different quantities of particular peptides are found in the same species, depending on the location or season (Trabi et al 2004; Simonsen et al 2005) This is apparently caused by changes in cyclotide gene expression levels but decomposition rates may contribute in shaping the final suite of peptides. In Murashige and Skoog (MS) medium, nitrogen is supplied in the form of two salts: ammonium nitrate and potassium nitrate (Murashige and Skoog 1962) The replacement of these two salts with ones containing 15N isotopes results in isotope labelling of amino acids and, in consequence, peptides and proteins (Kim et al 2005; Schaff et al 2008). The current work investigated the biosynthesis and turnover of cyclotides in V. uliginosa cell suspension cultures using 15N-labeling and in germinating V. odorata seeds

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