Topology and enhanced toxicity of bound microcystins in Microcystis PCC 7806

F Jüttner1, H Lüthi

  • 1Limnological Station, Institute of Plant Biology, University of Zürich, 8802 Kilchberg, Switzerland. juttner@limnol.uzh.ch

Insights

Microcystis cyanobacteria produce toxins like microcystins, which bind to phycobilin proteins. This binding affects toxicity and analytical detection, potentially aiding toxin transport in grazers.

Area of Science:

  • Environmental Microbiology
  • Toxicology
  • Biochemistry

Background:

  • Microcystis is a major freshwater cyanobacterium responsible for harmful algal blooms and toxin production.
  • Microcystins and cyanopeptolins are potent toxins primarily stored intracellularly within Microcystis cells.
  • High intracellular concentrations of microcystins exceed their aqueous solubility, suggesting intracellular binding mechanisms.

Purpose of the Study:

  • To investigate the intracellular binding of microcystins and cyanopeptolins in Microcystis.
  • To identify the cellular components responsible for microcystin binding.
  • To understand the implications of this binding on toxin toxicity and analytical methods.

Main Methods:

  • Differential fractionation of Microcystis cell constituents.
  • Analysis of microcystin and cyanopeptolin association with protein fractions.
  • Toxicity assays using Thamnocephalus platyurus.
  • Investigation of microcystin binding to C18 cartridges.

Main Results:

  • Microcystins and cyanopeptolins were found bound to phycobilin proteins, not primarily in thylakoid membranes.
  • A molar ratio of approximately 6:1 (microcystin to phycobilin monomer) was observed.
  • Protein-bound microcystins exhibited altered toxicity and did not bind to C18 cartridges, unlike free microcystins.
  • Phycobilins may act as carrier molecules for microcystin transport in grazer guts.

Conclusions:

  • Phycobilins are likely the primary binding proteins for microcystins and cyanopeptolins in Microcystis.
  • The weak binding allows for rapid dissociation, potentially facilitating toxin uptake in grazers.
  • Protein binding explains analytical discrepancies and suggests released phycobilins can carry toxins in bloom collapse events.