Tien T. Dang, Tam T. T. Tran, Uyen N. P. Nguyen, Son H. Pham, Tuan H. N. Nguyen
{"title":"Characterization of Cyclotides via LC-MS/MS from the Vietnamese Plant Viola annamensis Bak.f.: Insights into Antimicrobial and Larvicidal Activities","authors":"Tien T. Dang, Tam T. T. Tran, Uyen N. P. Nguyen, Son H. Pham, Tuan H. N. Nguyen","doi":"10.1021/acs.jnatprod.6c00512","DOIUrl":null,"url":null,"abstract":"<p><em>Viola annamensis</em> Bak.f.,\r\na Vietnamese\r\nendemic species, is reported here for the first time as a source of\r\ncyclotides. LC–MS and LC - MS/MS analyses identified 11 cyclotides\r\n(3.1–3.8 kDa) bearing the conserved cyclic cystine knot (CCK)\r\nmotif, including four novel cyclotides designated Vian A, Vian B,\r\nVian C, and Vian D. Fraction M1 contained eight cyclotides, including\r\nVian A, whereas fractions M2 and M3 mainly contained Vian B/Vian C\r\nand Vian D, respectively. Vian D was successfully purified, sequenced,\r\nand evaluated for antimicrobial activity. The peptide mixtures M2\r\nand Vian D showed antibacterial activity against <em>Pseudomonas aeruginosa</em>, <em>Bacillus subtilis</em>, and <em>Listeria ivanovii</em>. Minimum inhibitory\r\nconcentration (MIC) values for M2 and Vian D ranged from 6.2 to 8.3\r\nmg/mL, confirming the contribution of these cyclotides to the antimicrobial\r\nproperties of <em>V.</em><em>annamensis</em>. Cytotoxicity assessment using the <em>Artemia salina</em> assay showed low toxicity for the salt-precipitated sample, with\r\nan LC<sub>50</sub> value of 1.042 mg/mL, whereas the purified peptide\r\nmixtures exhibited higher, concentration-dependent toxicity. Among\r\nthem, M1 demonstrated greater potency, with an LC<sub>50</sub> of\r\n0.049 mg/mL, followed by M2 with an LC<sub>50</sub> of 0.131 mg/mL.\r\nThis study identifies <em>V. annamensis</em> as a novel source of new cyclotides with potential antimicrobial\r\napplications.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":"89 8","pages":"2300–2313"},"PeriodicalIF":3.7000,"publicationDate":"2026-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Products ","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jnatprod.6c00512","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/8 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
Viola annamensis Bak.f.,
a Vietnamese
endemic species, is reported here for the first time as a source of
cyclotides. LC–MS and LC - MS/MS analyses identified 11 cyclotides
(3.1–3.8 kDa) bearing the conserved cyclic cystine knot (CCK)
motif, including four novel cyclotides designated Vian A, Vian B,
Vian C, and Vian D. Fraction M1 contained eight cyclotides, including
Vian A, whereas fractions M2 and M3 mainly contained Vian B/Vian C
and Vian D, respectively. Vian D was successfully purified, sequenced,
and evaluated for antimicrobial activity. The peptide mixtures M2
and Vian D showed antibacterial activity against Pseudomonas aeruginosa, Bacillus subtilis, and Listeria ivanovii. Minimum inhibitory
concentration (MIC) values for M2 and Vian D ranged from 6.2 to 8.3
mg/mL, confirming the contribution of these cyclotides to the antimicrobial
properties of V.annamensis. Cytotoxicity assessment using the Artemia salina assay showed low toxicity for the salt-precipitated sample, with
an LC50 value of 1.042 mg/mL, whereas the purified peptide
mixtures exhibited higher, concentration-dependent toxicity. Among
them, M1 demonstrated greater potency, with an LC50 of
0.049 mg/mL, followed by M2 with an LC50 of 0.131 mg/mL.
This study identifies V. annamensis as a novel source of new cyclotides with potential antimicrobial
applications.
期刊介绍:
The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
When new compounds are reported, manuscripts describing their biological activity are much preferred.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.