4.7 Article

Further Characterization of Glycine-Containing Microcystins from the McMurdo Dry Valleys of Antarctica

Journal

TOXINS
Volume 7, Issue 2, Pages 493-515

Publisher

MDPI
DOI: 10.3390/toxins7020493

Keywords

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Funding

  1. New Zealand Ministry of Business, Innovation and Employment [UOWX0505]
  2. Marsden Fund of the Royal Society of New Zealand [12-UOW-087]
  3. University of Waikato

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Microcystins are hepatotoxic cyclic peptides produced by several cyanobacterial genera worldwide. In 2008, our research group identified eight new glycine-containing microcystin congeners in two hydro-terrestrial mat samples from the McMurdo Dry Valleys of Eastern Antarctica. During the present study, high-resolution mass spectrometry, amino acid analysis and micro-scale thiol derivatization were used to further elucidate their structures. The Antarctic microcystin congeners contained the rare substitution of the position-1 d-alanine for glycine, as well as the acetyl desmethyl modification of the position-5 Adda moiety (3S-amino-9S-methoxy-2S,6,8S-trimethyl-10-phenyldeca-4E,6E-dienoic acid). Amino acid analysis was used to determine the stereochemistry of several of the amino acids and conclusively demonstrated the presence of glycine in the microcystins. A recently developed thiol derivatization technique showed that each microcystin contained dehydrobutyrine in position-7 instead of the commonly observed N-methyl dehydroalanine.

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