Evidence for differences in the metabolism of saxitoxin and C1+2 toxins in the freshwater cyanobacterium Cylindrospermopsis raciborskii T3

Biochim Biophys Acta. 2004 Sep 6;1674(1):60-7. doi: 10.1016/j.bbagen.2004.05.006.

Abstract

The activity of paralytic shellfish poisoning (PSP) toxins biosynthetic enzymes was assayed in the cyanobacterium Cylindrospermopsis raciborskii T3 after inhibiting protein synthesis with chloramphenicol (CAM). The production of C1+2 and saxitoxin (STX) was sensitive to CAM with STX levels decreasing by 70% after 24-h exposure to the antibiotic. PSP toxin production was strongly promoted by arginine supplementation, with a maximum 476% increase in intracellular STX concentrations after 24-h exposure to 10 mM of the amino acid. However, arginine had no stimulating effect on PSP toxin levels if supplemented in combination with CAM at 10 microg l(-1). Addition of agmatine and proline to C. raciborskii T3 cultures in the presence of 10 microg l(-1) CAM increased C1+2 toxins levels, while having a negative or no effect on STX accumulation. In vitro, PSP toxin levels increased naturally in cyanobacterial extracts, with CAM and arginine having no influence on either C1+2 or STX synthesis. The evidence presented in this study suggests a possible difference between the metabolism of STX and the C1+2 toxins and indicated a high turnover rate of STX biosynthetic enzymes in C. raciborskii T3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agmatine / metabolism
  • Animals
  • Bacterial Proteins / metabolism
  • Chloramphenicol / pharmacology
  • Cyanobacteria / drug effects
  • Cyanobacteria / metabolism*
  • Fresh Water
  • Marine Toxins / chemistry
  • Marine Toxins / metabolism*
  • Molecular Structure
  • Proline / metabolism
  • Protein Synthesis Inhibitors / pharmacology
  • Saxitoxin / chemistry
  • Saxitoxin / metabolism*

Substances

  • Bacterial Proteins
  • Marine Toxins
  • Protein Synthesis Inhibitors
  • Saxitoxin
  • Chloramphenicol
  • Agmatine
  • Proline