Microcystin, a hepatotoxin produced by cyanobacteria
Microcystis species, is biosynthesized nonribosomally by a multifunctional enzyme complex. The enzyme is composed of peptide synthetase and polyketide synthase coded by the
mcy gene cluster. Especially,
mcyB and
mcyD are representative for microcystin biosynthesis genes of peptide synthetase and polyketide synthase, respectively. The effect of cell growth or cell cycle on the toxin biosynthesis of
Microcystis has not been clarified. The purpose of this study is to elucidate when the microcystins are synthesized and accumulated in the cell and how intracellular microcystins act in the cell. We examined the transcript levels of
mcyB and
mcyD under nitrate starved synchronous culture of axenic strain
Microcystis viridis NIES-102. Both the gene transcript levels could be observed with the proportion of the cells in S-phase. Then, microcystins were highly contained when the proportion of G
2/M-phase cells was the highest value in culture medium. Furthermore, it was indicated that pyrogallol, which was an allelopathic compound produced by macrophytes such a genus
Myriophyllom, inhibited the expression of the
mcyD genes in
M. viridis. These results suggested that the microcystin biosynthesis were closely correlated with the cell cycle in the toxin-producing cyanobacteria.
View full abstract