Effects of aluminium on ATP pools and utilization in the cyanobacterium Anabaena cylindrica: a model for the in vivo toxicity

ATP pools extracted from the cyanobacterium Anabaena cylindrica , grown in the absence or presence of AlCl₃, were measured using the luciferin-luciferase assay. Addition of low concentrations of AlCl₃ (3.6–36 μ M ) increased the ATP pool 20–40% within 24 h, the effect being more marked with time. When using the Tris-EDTA boiling technique for extraction of cellular ATP, the ATP from aluminium-exposed cells appeared more stable during the extraction than the ATP from untreated cells. The higher ATP pools in aluminium-exposed cells were also evident after dark treatment and addition of the phosphorylating inhibitors carbonylcyanide m -chloro-phenylhydrazone (CCCP) and N,N-dicyclohexylcarbodiimide (DCCD). The formation of elevated ATP pools in cells exposed to aluminium was curtailed by high concentrations of cellular phosphate and postincubation at high pH (>8). These results favour the hypothesis that intracellular aluminium binds to ATP by competing with Mg²⁺ and, as a consequence, the stable Al³⁺-ATP complex formed is no longer available for cellular metabolism. The cyanobacterium is assumed to compensate by increasing the total pool of ATP. At high AlCl₃-concentrations, and in particular at low phosphate: aluminium molar ratios (<1), aluminium apparently also interferes with the membranes in A. cylindrica as indicated by inhibited O₂ production, reduced ATP production and cell lysis.