Dependence of Ethanolic Fermentation, Cytoplasmic pH Regulation, and Viability on the Activity of Alcohol Dehydrogenase in Hypoxic Maize Root Tips.

We examined the role of alcohol dehydrogenase (ADH) in the metabolism and survival of hypoxic maize (Zea mays L.) root tips. The dependence of the rate of ethanolic fermentation, cytoplasmic pH, and viability on the activity of ADH in maize root tips during extreme hypoxia was determined. Maize lines with ADH activities differing over about a 200-fold range were studied. Effects of genetic background were controlled by comparing pairs of F4 progeny of crosses between mutant (low ADH activity) and reference inbred lines. The capacity of hypoxic root tips to perform ethanolic fermentation exhibited a dependence on ADH activity only at activities found in Adh 1 nulls. The ability of maize root tips to withstand prolonged and extreme hypoxia was like-wise independent of ADH activity, except at the lowest activities. Root tips that exhibited lower tolerance of hypoxia had more acidic cytoplasm during extreme hypoxia. We conclude that the activity of ADH in normal maize root tips does not limit the capacity for energy production via fermentation, and does not determine viability under extreme hypoxia. The significance of the induction of ADH activity in plants by hypoxia is discussed.

[1]  H. Holzhütter,et al.  Mathematical modelling of metabolic pathways affected by an enzyme deficiency. Energy and redox metabolism of glucose-6-phosphate-dehydrogenase-deficient erythrocytes. , 1989, European journal of biochemistry.

[2]  T. Kimmerer Alcohol Dehydrogenase and Pyruvate Decarboxylase Activity in Leaves and Roots of Eastern Cottonwood (Populus deltoides Bartr.) and Soybean (Glycine max L.). , 1987, Plant physiology.

[3]  H. Holzhütter,et al.  Mathematical modelling of metabolic pathways affected by an enzyme deficiency. A mathematical model of glycolysis in normal and pyruvate-kinase-deficient red blood cells. , 1985, European journal of biochemistry.

[4]  V. Walbot,et al.  Cytoplasmic acidosis as a determinant of flooding intolerance in plants. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[5]  V. Walbot,et al.  Mechanisms of cytoplasmic pH regulation in hypoxic maize root tips and its role in survival under hypoxia. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[6]  H. Kacser,et al.  Enzyme variation, metabolic flux and fitness: alcohol dehydrogenase in Drosophila melanogaster. , 1983, Genetics.

[7]  H. Beevers,et al.  Alcohol dehydrogenase and an inactivator from rice seedlings. , 1983, Plant physiology.

[8]  H. Kacser,et al.  MOlecular democracy: who shares the controls? , 1979, Biochemical Society transactions.

[9]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[10]  D. Schwartz An Example of Gene Fixation Resulting from Selective Advantage in Suboptimal Conditions , 1969, The American Naturalist.

[11]  T. Endo,et al.  Alcohol Dehydrogenase Polymorphism in Maize-simple and Compound Loci. , 1966, Genetics.

[12]  H. Holzhütter,et al.  Mathematical modelling of metabolic pathways affected by an enzyme deficiency. , 1990, Biomedica biochimica acta.

[13]  M. Drew,et al.  Metabolic Acclimation to Anoxia Induced by Low (2-4 kPa Partial Pressure) Oxygen Pretreatment (Hypoxia) in Root Tips of Zea mays. , 1988, Plant physiology.

[14]  J. K. Roberts,et al.  Cytoplasmic Acidosis and Flooding Tolerance in Crop Plants , 1988 .

[15]  M. Jackson,et al.  CHAPTER 3 – Effects of Flooding on Growth and Metabolism of Herbaceous Plants , 1984 .

[16]  H. Westerhoff,et al.  Modern theories of metabolic control and their applications , 1984, Bioscience reports.

[17]  H. Beevers Respiratory metabolism in plants , 1961 .