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Plant Physiology 74:804-809 (1984) © 1984 American Society of Plant Biologists Helminthosporium maydis T Toxin Decreased Calcium Transport into Mitochondria of Susceptible Corn 1Botany Department, University of Kansas, Lawrence, Kansas 66045, Biochemistry Department, University of Kansas, Lawrence, Kansas 66045, Botany Department, University of Maryland, College Park, Maryland 20742
The effects of purified Helminthosporium maydis T (HmT) toxin on active Ca2+ transport into isolated mitochondria and microsomal vesicles were compared for a susceptible (T) and a resistant (N) strain of corn (Zea mays). ATP, malate, NADH, or succinate could drive 45Ca2+ transport into mitochondria of corn roots. Ca2+ uptake was dependent on the proton electrochemical gradient generated by the redox substrates or the reversible ATP synthetase, as oligomycin inhibited ATP-driven Ca2+ uptake while KCN inhibited transport driven by the redox substrates. Purified native HmT toxin completely inhibited Ca2+ transport into T mitochondria at 5 to 10 nanograms per milliliter while transport into N mitochondria was decreased slightly by 100 nanograms per milliliter toxin. Malate-driven Ca2+ transport in T mitochondria was frequently more inhibited by 5 nanograms per milliliter toxin than succinate or ATP-driven Ca2+ uptake. However, ATP-dependent Ca2+ uptake into microsomal vesicles from either N or T corn was not inhibited by 100 nanograms per milliliter toxin. Similarly, toxin had no effect on proton gradient formation ([14C]methylamine accumulation) in microsomal vesicles. These results show that mitochondrial and not microsomal membrane is a primary site of HmT toxin action. HmT toxin may inhibit formation of or dissipate the electrochemical proton gradient generated by substrate-driven electron transport or the mitochondrial ATPase, after interacting with a component(s) of the mitochondrial membrane in susceptible corn.
2 Present address: Department of Botany, University of Maryland, College Park, MD 20742. 1 Supported in part by the General Research Fund of the University of Kansas and by Department of Energy contract No. DE-AS05-82ER13015 to H. S. Scientific Article No. A-3563, Contribution No. 6638 of the Maryland Agricultural Experiment Station.
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