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Isolation and Characterization of [D-Leu(1)]microcystin-LY from Microcystis aeruginosa CPCC-464

[D-Leu(1)]MC-LY (1) ([M + H](+) m/z 1044.5673, Δ 2.0 ppm), a new microcystin, was isolated from Microcystis aeruginosa strain CPCC-464. The compound was characterized by (1)H and (13)C NMR spectroscopy, liquid chromatography–high resolution tandem mass spectrometry (LC–HRMS/MS) and UV spectroscopy....

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Detalles Bibliográficos
Autores principales: LeBlanc, Patricia, Merkley, Nadine, Thomas, Krista, Lewis, Nancy I., Békri, Khalida, Renaud, Susan LeBlanc, Pick, Frances R., McCarron, Pearse, Miles, Christopher O., Quilliam, Michael A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076857/
https://www.ncbi.nlm.nih.gov/pubmed/31979406
http://dx.doi.org/10.3390/toxins12020077
Descripción
Sumario:[D-Leu(1)]MC-LY (1) ([M + H](+) m/z 1044.5673, Δ 2.0 ppm), a new microcystin, was isolated from Microcystis aeruginosa strain CPCC-464. The compound was characterized by (1)H and (13)C NMR spectroscopy, liquid chromatography–high resolution tandem mass spectrometry (LC–HRMS/MS) and UV spectroscopy. A calibration reference material was produced after quantitation by (1)H NMR spectroscopy and LC with chemiluminescence nitrogen detection. The potency of 1 in a protein phosphatase 2A inhibition assay was essentially the same as for MC-LR (2). Related microcystins, [D-Leu(1)]MC-LR (3) ([M + H](+) m/z 1037.6041, Δ 1.0 ppm), [D-Leu(1)]MC-M(O)R (6) ([M + H](+) m/z 1071.5565, Δ 2.0 ppm) and [D-Leu(1)]MC-MR (7) ([M + H](+) m/z 1055.5617, Δ 2.2 ppm), were also identified in culture extracts, along with traces of [D-Leu(1)]MC-M(O(2))R (8) ([M + H](+) m/z 1087.5510, Δ 1.6 ppm), by a combination of chemical derivatization and LC–HRMS/MS experiments. The relative abundances of 1, 3, 6, 7 and 8 in a freshly extracted culture in the positive ionization mode LC–HRMS were ca. 84, 100, 3.0, 11 and 0.05, respectively. These and other results indicate that [D-Leu(1)]-containing MCs may be more common in cyanobacterial blooms than is generally appreciated but are easily overlooked with standard targeted LC–MS/MS screening methods.