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Isolation, Purification, and Characterization of Mitochondria from Chlamydomonas reinhardtii
Author(s) -
Mats Eriksson,
Per Gardeström,
Göran Samuelsson
Publication year - 1995
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.107.2.479
Subject(s) - salicylhydroxamic acid , chlamydomonas reinhardtii , chlamydomonas , oligomycin , alternative oxidase , biochemistry , mitochondrion , percoll , malate dehydrogenase , biology , organelle , antimycin a , centrifugation , enzyme , atpase , mutant , gene
Mitochondria were isolated from autotrophically grown Chlamydomonas reinhardtii cell-wall-less mutant CW 92. The cells were broken by vortexing with glass beads, and the mitochondria were collected by differential centrifugation and purified on a Percoll gradient. The isolated mitochondria oxidized malate, pyruvate, succinate, NADH, and [alpha]-ketoglutarate. Respiratory control was obtained with malate (2.0) and pyruvate (2.2) but not with the other substrates. From experiments with KCN and salicylhydroxamic acid, it was estimated that the capacity of the cytochrome pathway was at least 100 nmol O2 mg-1 protein min-1 and the capacity of the alternative oxidase was at least 50 nmol O2 mg-1 protein min-1. A low sensitivity to oligomycin indicates some difference in the properties of the mitochondrial ATPase from Chlamydomonas as compared to higher plants.

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