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Microbiology 150 (2004), 1785-1796; DOI  10.1099/mic.0.26947-0
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Microbiology 150 (2004), 1785-1796; DOI  10.1099/mic.0.26947-0
© 2004 Society for General Microbiology

Diversity and distribution of Microcystis (Cyanobacteria) oligopeptide chemotypes from natural communities studied by single-colony mass spectrometry

Martin Welker1,{dagger}, Matthias Brunke2,{ddagger}, Karina Preussel1,3, Indra Lippert3 and Hans von Döhren1

1 Technische Universität Berlin, Inst. Chemie, AG Biochemie und molekulare Biologie, Franklinstrasse 29, 10587 Berlin, Germany
2 Institut für Gewässerökologie und Binnenfischerei, Müggelseedamm 301, 12587 Berlin, Germany
3 Humboldt-Universität Berlin, Inst. Biologie, Luisenstrasse 53, 10117 Berlin, Germany

Correspondence
Martin Welker
martin.welker{at}chem.tu-berlin.de

Microcystis sp. has been recognized in recent years as a producer of a high number of secondary metabolites. Among these, peptides that are produced by the non-ribosomal peptide synthetase pathway often show bioactivity or are toxic to humans. The production of particular peptides is specific for individual Microcystis clones, allowing their characterization as chemotypes by analysing the peptidome. The authors studied the in situ diversity of peptides and chemotypes in Microcystis communities from lakes in and around Berlin, Germany, by direct analysis of individual colonies by MALDI-TOF mass spectrometry. From 165 colonies analysed a total of 46 individual peptides could be identified, 21 of which have not been described previously. For six of the new peptides the structures could be elucidated from fragment patterns, while for others only a preliminary classification could be achieved. In most colonies, two to ten individual peptides were detected. In 19 colonies, 16 of which were identified as M. wesenbergii, no peptide metabolites could be detected. The peptide data of 146 colonies were subjected to an ordination (principal components analysis). The principal components were clearly formed by the microcystin variants Mcyst-LR, -RR and -YR, anabaenopeptins B and E/F, a putative microviridin, and a new cyanopeptolin. In the resulting ordination plots most colonies were grouped into five distinct groups, while 40 colonies scattered widely outside these groups. In some cases colonies from different lakes clustered closely, indicating the presence of similar chemotypes in the respective samples. With respect to colony morphology no clear correlation between a chemotype and a morphospecies could be established, but M. aeruginosa, for example, was found to produce predominantly microcystins. In contrast, M. ichthyoblabe colonies were mostly negative for microcystins and instead produced anabaenopeptins. The number of peptides detected in a limited number of samples and the various combinations of peptides in individual Microcystis colonies highlights the immense metabolic potential and diversity of this genus.


Abbreviations: CID, collision-induced dissociation; MALDI-TOF MS, matrix-associated laser desorption/ionization time of flight mass spectrometry; NRPS, non-ribosomal peptide synthetase; PCA, principal components analysis; PSD, post-source decay

{dagger}Present address: Institut Pasteur, Unité des Cyanobactéries, 28 rue du Dr Roux, 75724 Paris Cedex 15, France.

{ddagger}Present address: Landesamt für Natur und Umwelt, Hamburger Chaussee 25, 24220 Flintbek, Germany.




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