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Environmental and Stress Physiology

Heavy Metal-Activated Synthesis of Peptides in Chlamydomonas reinhardtii ¹

Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90024

In this study, we have addressed the capacity of the green alga Chlamydomonas reinhardtii to produce metal-binding peptides in response to stress induced by the heavy metals Cd²⁺, Hg²⁺, and Ag⁺. Cells cultured in the presence of sublethal concentrations of Cd²⁺ synthesized and accumulated oligopeptides consisting solely of glutamic acid, cysteine, and glycine in an average ratio of 3:3:1. Cadmium-induced peptides were isolated in their native form as higher molecular weight peptide-metal complexes with an apparent molecular weight of approximately 6.5 x 10³. The isolated complex bound cadmium (as evidenced by absorption spectroscopy) and sequestered (with a stoichiometry of 0.7 moles of cadmium per mole of cysteine) up to 70% of the total cadmium found in extracts of cadmium-treated cells. In Hg²⁺-treated cells, the principal thiol-containing compound induced by Hg²⁺ ions was glutathione. It is possible that glutathione functions in plant cells (as it does in animal cells) to detoxify heavy metals. Cells treated with Ag⁺ ions also synthesized a sulfur-containing component with a charge to mass ratio similar to Cd²⁺-induced peptides. But, in contrast to the results obtained using Cd²⁺ as an inducer, these molecules did not accumulate to significant levels in Ag⁺-treated cells. The presence of physiological concentrations of Cu²⁺ in the growth medium blocked the synthesis of the Ag⁺-inducible component(s) and rendered cells resistant to the toxic effects of Ag⁺, suggesting competition between Cu²⁺ and Ag⁺ ions, possibly at the level of metal uptake.

¹ This research was supported by a training grant (87-GRAD-9-0086) from the U.S. Department of Agriculture (G.H.), a U.S. Health and Human Services grant (GM42143), the Searle Scholars Foundation/Chicago Community Trust (S.M.), and a National Institutes of Health Biomedical Research Support Grant (RR07009-23) to UCLA.

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