Purification and Immunochemical Characterization of NADP-Dependent Glyceraldehyde 3-Phosphate Dehydrogenase of Euglena gracilis

NADP-dependent glyceraldehyde 3-phosphate dehydrogenase fromEuglena gracilis (EC 1.2.1.13 [EC] ) was purified about 170-fold bya two-step procedure involving DEAE-SH cellulose chromatographyand affinity chromatography on ADP-Sepharose. The homogeneousenzyme from mildly sonicated cells contained equal amounts oftwo types of subunits with mol wts of 34,000 (A) and 38,000(B). The active enzyme had a mol wt 144,000 and is thereforean A₂B₂ tetramer. Enzyme from strongly sonicated Euglena cellscontained, in addition, a second allomer with a probable A₄structure. NADdependent glyceraldehyde 3-phosphate dehydrogenase,a tetramer with 36,000 mol wt subunits, was unrelated immunologicallyto the NADP-dependent enzyme although the latter also showedminor NAD-dependent activity. Both isoenzymes of the NADPlinkedglyceraldehyde 3-phosphate dehydrogenase, however, were immunologicallyidentical. ¹Dedicated, to Prof. Dr. O. H. Volk on his 80th birthday. (Received October 13, 1982; Accepted March 21, 1984)     

The Localization of Lead in the Lichen Ramalina duriaei (De Not.) Bagl.

In an attempt to ascertain whether the lichen Ramalina duriaei could be employed to biomonitor atmospheric lead pollution, specimens of this lichen were exposed to Pb (NO₃)₂ solutions and a buffered solution (tartaric acid/sodium bitartrate, pH 2.8) of sodium rhodizonate (C₆O₆Na₂) was used to locate lead in their thalli. The procedure entailed exposure of the lichen to 0, 5, 50 and 100 ppm Pb for 5 min and 1 h and the subsequent determination of the lead contents from photographs of the thalli. Distribution of lead in different parts of the thallus was assessed after exposure of the lichens to 2 ppm Pb (9 h or three d), 50 ppm (45 min) or 200 ppm (4d). Cross sections of vegetative parts of the thallus and of the apothecia revealed that lead penetrated into the cortical cells of the thallus but not into the algal cells of the phycobiont nor the ascospores or medullary cells. The observed massive penetration of lead into cortical cells supports the notion that Ramalina duriaei is sensitive to atmospheric lead pollution.