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Screening for Cyclotides in Sri Lankan Medicinal Plants: Discovery, Characterization, and Bioactivity Screening of Cyclotides from Geophila repens
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Pharmaceutical Biosciences. Department of Chemistry, Faculty of Science, University of Colombo, Thurstan Road, Colombo 00300, Sri Lanka.. (Farmakognosi)ORCID iD: 0000-0002-7351-805X
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Pharmaceutical Biosciences. W. Szafer Institute of Botany of the Polish Academy of Sciences, 46 Lubicz, 31-512 Cracow, Poland.. (Farmakognosi)ORCID iD: 0000-0002-4143-6543
Univ Colombo, Fac Sci, Dept Chem, Colombo 00300, Sri Lanka..
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Pharmaceutical Biosciences. (Farmakognosi)
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2023 (English)In: Journal of Natural Products, ISSN 0163-3864, E-ISSN 1520-6025, Vol. 86, no 1, p. 52-65Article in journal (Refereed) Published
Abstract [en]

Cyclotides are an intriguing class of structurally stable circular miniproteins of plant origin with numerous potential pharmaceutical and agricultural applications. To investigate the occurrence of cyclotides in Sri Lankan flora, 50 medicinal plants were screened, leading to the identification of a suite of new cyclotides from Geophila repens of the family Rubiaceae. Cycloviolacin O2-like (cyO2-like) gere 1 and the known cyclotide kalata B7 (kB7) were among the cyclotides characterized at the peptide and/or transcript level together with several putative enzymes, likely involved in cyclotide biosynthesis. Five of the most abundant cyclotides were isolated, sequenced, structurally characterized, and screened in antimicrobial and cytotoxicity assays. All gere cyclotides showed cytotoxicity (IC50 of 2.0-10.2 mu M), but only gere 1 inhibited standard microbial strains at a minimum inhibitory concentration of 4-16 mu M. As shown by immunohistochemistry, large quantities of the cyclotides were localized in the epidermis of the leaves and petioles of G. repens. Taken together with the cytotoxicity and membrane permeabilizing activities, this implicates gere cyclotides as potential plant defense molecules. The presence of cyO2-like gere 1 in a plant in the Rubiaceae supports the notion that phylogenetically distant plants may have coevolved to express similar cytotoxic cyclotides for a specific functional role, most likely involving host defense.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2023. Vol. 86, no 1, p. 52-65
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Botany Pharmaceutical Sciences
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URN: urn:nbn:se:uu:diva-501761DOI: 10.1021/acs.jnatprod.2c00674ISI: 000903277100001PubMedID: 36525646OAI: oai:DiVA.org:uu-501761DiVA, id: diva2:1756645
Funder
Swedish Research Council, 2013-06672Lars Hierta Memorial Foundation, FO2011-0639Lars Hierta Memorial Foundation, FO2016-0618Available from: 2023-05-12 Created: 2023-05-12 Last updated: 2023-05-12Bibliographically approved

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Slazak, BlazejMuhammad, TajStrömstedt, Adam A.Göransson, UlfGunasekera, Sunithi

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Rajendran, SanjeevanSlazak, BlazejMuhammad, TajStrömstedt, Adam A.Göransson, UlfGunasekera, Sunithi
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