Mass spectrometric characterization of the seco acid formed by cleavage of the macrolide ring of the algal metabolite goniodomin A.

Autor: Harris CM; Department of Chemistry, Vanderbilt University, Nashville, TN, 37235, USA., Hintze L; Alfred Wegener Institut-Helmholtz Zentrum für Polar- und Meeresforschung (AWI), 27570, Bremerhaven, Germany., Gaillard S; Department of Aquatic Health Sciences, Virginia Institute of Marine Science (VIMS), William & Mary, Gloucester Point, VA, 23062, USA., Tanniou S; Ifremer, PHYTOX, Laboratoire METALG, F-44000, Nantes, France., Small H; Department of Aquatic Health Sciences, Virginia Institute of Marine Science (VIMS), William & Mary, Gloucester Point, VA, 23062, USA., Reece KS; Department of Aquatic Health Sciences, Virginia Institute of Marine Science (VIMS), William & Mary, Gloucester Point, VA, 23062, USA., Tillmann U; Alfred Wegener Institut-Helmholtz Zentrum für Polar- und Meeresforschung (AWI), 27570, Bremerhaven, Germany., Krock B; Alfred Wegener Institut-Helmholtz Zentrum für Polar- und Meeresforschung (AWI), 27570, Bremerhaven, Germany., Harris TM; Department of Chemistry, Vanderbilt University, Nashville, TN, 37235, USA. Electronic address: thomas.m.harris@vanderbilt.edu.
Jazyk: angličtina
Zdroj: Toxicon : official journal of the International Society on Toxinology [Toxicon] 2023 Aug 01; Vol. 231, pp. 107159. Date of Electronic Publication: 2023 May 18.
DOI: 10.1016/j.toxicon.2023.107159
Abstrakt: Goniodomin A (GDA) is a polyketide macrolide produced by multiple species of the marine dinoflagellate genus Alexandrium. GDA is unusual in that it undergoes cleavage of the ester linkage under mild conditions to give mixtures of seco acids (GDA-sa). Ring-opening occurs even in pure water although the rate of cleavage accelerates with increasing pH. The seco acids exist as a dynamic mixture of structural and stereo isomers which is only partially separable by chromatography. Freshly prepared seco acids show only end absorption in the UV spectrum but a gradual bathochromic change occurs, which is consistent with formation of α,β-unsaturated ketones. Use of NMR and crystallography is precluded for structure elucidation. Nevertheless, structural assignments can be made by mass spectrometric techniques. Retro-Diels-Alder fragmentation has been of value for independently characterizing the head and tail regions of the seco acids. The chemical transformations of GDA revealed in the current studies help clarify observations made on laboratory cultures and in the natural environment. GDA has been found to reside mainly within the algal cells while the seco acids are mainly external with the transformation of GDA to the seco acids occurring largely outside the cells. This relationship, plus the fact that GDA is short-lived in growth medium whereas GDA-sa is long-lived, suggests that the toxicological properties of GDA-sa in its natural environment are more important for the survival of the Alexandrium spp. than those of GDA. The structural similarity of GDA-sa to that of monensin is noted. Monensin has strong antimicrobial properties, attributed to its ability to transport sodium ions across cell membranes. We propose that toxic properties of GDA may primarily be due to the ability of GDA-sa to mediate metal ion transport across cell membranes of predator organisms.
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
(Copyright © 2023 Elsevier Ltd. All rights reserved.)
Databáze: MEDLINE
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