ArticlePlanta2017
Structural and functional characterisation of a class I endochitinase of the carnivorous sundew (Drosera rotundifolia L.).
Article in Planta, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 22 citations in OpenAlex.
- Structural and functional characterization of chitinase from carnivorous plant Drosera adelae.FEBS open bio · 2025Article
- Complex transcription regulation of acidic chitinase suggests fine-tuning of digestive processes in Drosera binata.Planta · 2025Article
- An acidophilic fungus promotes prey digestion in a carnivorous plant.Nature microbiology · 2024Article
- Comparative Transcriptome Analysis Reveals the Molecular Basis ofPlants (Basel, Switzerland) · 2023Article
- Water Cannot Activate Traps of the Carnivorous Sundew PlantPlants (Basel, Switzerland) · 2023Article
- Expression and Refolding of the Plant Chitinase FromFrontiers in bioengineering and biotechnology · 2021Article
- Expression of Drosera rotundifolia Chitinase in Transgenic Tobacco Plants Enhanced Their Antifungal Potential.Molecular biotechnology · 2019Article
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- Coprophagous features in carnivorous Nepenthes plants: a task for ureases.Scientific reports · 2017Article
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Authors and funding
6 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
MAIN
conclusionChitinase gene from the carnivorous plant, Drosera rotundifolia , was cloned and functionally characterised. Plant chitinases are believed to play an important role in the developmental and physiological processes and in responses to biotic and abiotic stress. In addition, there is growing evidence that carnivorous plants can use them to digest insect prey. In this study, a full-length genomic clone consisting of the 1665-bp chitinase gene (gDrChit) and adjacent promoter region of the 698 bp in length were isolated from Drosera rotundifolia L. using degenerate PCR and a genome-walking approach. The corresponding coding sequence of chitinase gene (DrChit) was obtained following RNA isolation from the leaves of aseptically grown in vitro plants, cDNA synthesis with a gene-specific primer and PCR amplification. The open reading frame of cDNA clone consisted of 978 nucleotides and encoded 325 amino acid residues. Sequence analysis indicated that DrChit belongs to the class I group of plant chitinases. Phylogenetic analysis within the Caryophyllales class I chitinases demonstrated a significant evolutionary relatedness of DrChit with clade Ib, which contains the extracellular orthologues that play a role in carnivory. Comparative expression analysis revealed that the DrChit is expressed predominantly in tentacles and is up-regulated by treatment with inducers that mimick insect prey. Enzymatic activity of rDrChit protein expressed in Escherichia coli was confirmed and purified protein exhibited a long oligomer-specific endochitinase activity on glycol-chitin and FITC-chitin. The isolation and expression profile of a chitinase gene from D. rotundifolia has not been reported so far. The obtained results support the role of specific chitinases in digestive processes in carnivorous plant species.
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