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Natural Product Discovery with LC-MS/MS Diagnostic Fragmentation Filtering: Application for Microcystin Analysis
Published on: May 31, 2019
Topology and enhanced toxicity of bound microcystins in Microcystis PCC 7806
1Limnological Station, Institute of Plant Biology, University of Zürich, 8802 Kilchberg, Switzerland. juttner@limnol.uzh.ch
Abstract:
The cyanobacterium Microcystis is a potent producer of microcystins and cyanopeptolins and causes most of the toxicity outbreaks in freshwaters worldwide. Microcystins are mainly stored in the cells and little is found in the water. The intracellular concentration of microcystins in Microcystis PCC 7806 was at least 0.9 mM, although the solubility of microcystins in water was only about 10 microM. This low solubility does not allow the solubilisation of such high amounts of microcystins in the cytosol of Microcystis. Differential fractionation of cell constituents showed that microcystins and cyanopeptolins were bound to a protein fraction primarily composed of phycobilins. The percentage of microcystins and cyanopeptolins found in the thylakoid membranes was very low. Phycobilins may be the major proteins that have binding sites for these oligopeptides. A molar ratio near to 6 was observed for microcystins to the phycobilin (alphabeta) monomer. The binding of the microcystins to the protein was rather weak and allowed rapid dissociation of microcystins from the protein-matrix. Toxicity assays with Thamnocephalus platyurus showed that native microcystin when still bound to cyanobacterial protein was more toxic than an equivalent amount that has been desorbed from the protein by treatment with methanol. It is suggested that phycobilins serve in the gut of grazers as carrier molecules for the rapid transport of microcystin from lysed cells of Microcystis to the epithelium where the uptake of microcystins occurs. Because protein-bound microcystin does not bind to C18 cartridges, this behaviour can be the cause of many analytical discrepancies observed. The blue-coloured water observed upon the collapse of Microcystis blooms may be extremely toxic because the released phycobilins may carry the major fraction of microcystins.
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.
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