Twelve Australian marine algae from Sydney coastal waters, Ecklonia radiata, Hormosira banksii, a species of Sargassum, a species of Cystophora, Padinafraseri, Dictoyota dichotoma, Endarachne binghamiae, Splanchnidium rugosum, Colpomenia sinuosa and C. peregrina, Acinetospora crinata and a species of Zonaria were tested for alginate lyase and alginate epimerase activity. Easily soluble protein (ca 140 mg/kg wet algae) was prepared from acetone powders (3-15% of wet algae) at low temperatures (ca 0 °C) in tris(hydroxymethyl)aminomethane HC1 buffer (pH 7.8) containing 4% (w/v) polyvinylpyrolidone, 1.5 ΙΉΜ dithiothreitol and 200 mM NaCl. A species of Zonaria, Ecklonia radiata and Acinetospora crinata had highest lyase activity while the Zonaria species, the two Colpomenia species and A. crinata had highest epimerase activity. There were significant variations in enzyme activity between species, seasons and tissues. A 2 -8 fold purification was found for the epimerase from a single ammonium sulphate precipitation but the lyase gave only a l -3 fold improvement. Partial acid hydrolysis demonstrated that epimerised low mannuronic acid alginate gave ten to twenty per cent conversion to guluronic acid and the mannuronic/guluronic acid mixed segments showed the greatest degree of epimerisation.