Abstract

Cyclotides are disulfide-rich macrocyclic peptides that display a wide range of bioactivities and represent an important group of plant defense peptide biologics. A few linear variants of cyclotides have recently been identified. They share a high sequence homology with cyclotides but are biosynthetically unable to cyclize from their precursors. All hitherto reported cyclotides and their acyclic variants were isolated from dicot plants of the Rubiaceae, Violaceae, Cucurbitaceae, and recently the Fabaceae and Solanaceae families. Although several cyclotide-like genes in the Poaceae family were known from the data mining of the National Center for Biotechnology Information (NCBI) nucleotide database, their expression at the protein level has yet to be proven. Here, we report the discovery and characterization of nine novel linear cyclotides, designated as panitides L1-9, from the Panicum laxum of the Poaceae family and provide the first evidence of linear cyclotides at the protein level in a monocot plant. Disulfide mapping of panitide L3 showed that it possesses a cystine knot arrangement similar to cyclotides. Several panitides were shown to be active against Escherichia coli and cytotoxic to HeLa cells. They also displayed a high stability against heat and proteolytic degradation. Oxidative folding of the disulfide-reduced panitide L1 showed that it can fold efficiently into its native form. The presence of linear cyclotides in both dicots and monocots suggests their ancient origin and existence before the divergence of these two groups of flowering plants. Moreover, the Poaceae family contains many important food crops, and our discovery may open up new avenues of research using cyclotides and their acyclic variants in crop protection.

Highlights

  • Cyclotides are biologically active, plant-derived macrocyclic peptides

  • All tested plant species were found to express peptides around the cyclotide mass range of 2.5– 4 kDa (Fig. 1) with six Cys after S-reduction and S-alkylation. To show that they are cyclotide-like peptides, P. laxum was selected as a model species for further investigation. ϳ0.5 g of aerial tissues of P. laxum was extracted with 3 ml of water and semipurified on a C18 solid phase extraction column

  • In this study, we have analyzed six species belonging to the Poaceae family and provided the first evidence at the protein level for the expression of linear cyclotides in a monocot plant

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Summary

Background

Cyclotides are biologically active, plant-derived macrocyclic peptides. All cyclotides and their acyclic variants have been isolated from dicots. Additional linear cyclotides have been identified from various plants, including hedyotide B2 from Hedyotis biflora [21], chassatide C7 and C8 from Chassalia chartacea [18], psyle C from Psychotria leptothyrsa [23], kalata B20-lin from O. affinis [24], and Phyb M from Petunia hybrida [15] Analysis of their genetic structures revealed that they contain, at the mature cyclotide domain, either a truncated precursor sequence without the essential C-terminal Asn residue and the CTPP or a mutation to a stop codon prior to the CTPP. Our study confirms their presence in monocots and contributes to our understanding of cyclotides and their acyclic variants in the Poaceae family

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