Permeability Properties of the Inner Membrane of Mung Bean Mitochondria and Changes during Energization

S C Huber1, D E Moreland

  • 1United States Department of Agriculture, Science and Education Administration, Agricultural Research, Departments of Crop Science and Botany, North Carolina State University, Raleigh, North Carolina 27650.

Plant Physiology
|July 1, 1979
PubMed

Insights

Mung bean mitochondria possess an active phosphate/hydroxyl antiporter, sensitive to sulfhydryl reagents. Energization enhances the activity of a low-activity (Na+) K+/H+ antiporter in the inner mitochondrial membrane.

Area of Science:

  • Mitochondrial physiology
  • Membrane transport

Background:

  • The inner mitochondrial membrane regulates metabolite transport, crucial for cellular energy production.
  • Understanding anion and cation transport mechanisms is key to deciphering mitochondrial function.

Purpose of the Study:

  • To investigate the permeability properties of the mung bean mitochondrial inner membrane.
  • To identify and characterize specific transporters, including phosphate and cation antiporters.

Main Methods:

  • Osmotic swelling techniques were employed to assess membrane permeability.
  • The effects of various solutes (ammonium salts, potassium salts) and inhibitors (sulfhydryl reagents, tributyltin, uncouplers) were evaluated.
  • Oxygen uptake measurements were used to correlate transport with electron transport chain activity.

Main Results:

  • Active phosphate/hydroxyl antiporter identified, inhibited by sulfhydryl reagents.
  • Phosphate transport is distinct from dicarboxylic acid transport.
  • Chloride, sulfate, and phosphate anions show higher permeability than acetate.
  • A low-activity (Na+) K+/H+ antiporter is present, with activity enhanced by energization and NADH.
  • Contraction phase, coupled to pH gradient, showed increased oxygen uptake.

Conclusions:

  • The inner mitochondrial membrane of mung bean exhibits specific anion and cation transport systems.
  • Phosphate transport is mediated by an active antiporter, separate from dicarboxylate carriers.
  • Mitochondrial energization significantly modulates the activity of the (Na+) K+/H+ antiporter.

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