The effect of zinc on cell division, photosynthesis, ultrastructure, respiration, ATP levels, mitochondrial electron-transport chain (ETC)-activity, total thiols and glutathione in the marine diatom Nitzsehia elosterium (Ehrenberg) W. Smith was investigated. Although 65/~g Zn 1-a halved the cell division rate, photosynthesis and respiration were unaffected by zinc concentrations up to 500 pg Zn 1-1. Most of the zinc associated with the cells was bound at the cell surface, with only 3 to 4% of this extracellular zinc penetrating the cell membrane. Once inside the cell, zinc exerted its toxicity at a number of sites. Increased ATP production and ETC activity were observed in zinc-treated cells. Zinc also enhanced cellular thiols (SH) and total glutathione, and zinc toxicity was reversible by the addition of thiol compounds such as cysteine. Zinc-thiol binding may be a detoxification mechanism for the cell. It is suggested that increased ATP production may provide the energy required for increased glutathione synthesis at the expense of other energy-requiring processes including cell division. The mechanisms of toxicity of ionic zinc and copper to N. closterium were compared.synthesis (Gillan et al. 1983). Despite these studies, our understanding of the mechanism of ionic zinc toxicity to marine phytoplankton remains poor.In this paper we examine the effect of zinc on cell division, photosynthesis, ultrastructure, respiration, ATP levels, ETC activity, total thiols and glutathione in the marine diatom Nitzschia closterium (Ehrenberg) W. Smith. We also compare the mechanisms of zinc and copper toxicity to this species, and the reversal of toxicity by sulfhydryl compounds.
Materials and methods
Algae culturesThe unicellular marine diatom Nitzsehia closterium (Ehrenberg) W Smith (Hasle 1964) was cultured axenically in Mediumf(Guillard and Ryther 1962) with the trace elements and iron concentration halved. The culture was maintained on a 12 h light:12 h dark cycle (Philips TL 40 W fluorescent white, 6400 lux) at 21 °C. Cells in log-phase growth were used for all experiments.