Volume 6, Issue 1 pp. 19-23
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Carbon Nutrition and Metabolism of Polytomella caeca*

DONALD L. WISE

DONALD L. WISE

Department of Biology, University College, New York University, New York 53, N. Y.

Department of Biology, The College of Wooster, Wooster, Ohio.

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First published: February 1959
Citations: 38

From a dissertation presented in partial fulfillment of the requirements for the Ph.D. in biology at New York University.

Abstract

SYNOPSIS. Polytomella caeca utilizes as sole carbon sources in chemically defined media: acetate, propionate, butyrate, valerate, pyruvate, succinate, ethyl, butyl, amyl, and hexyl alcohols. Glyceraldehyde and α-ketoglutarate sustain very small populations. Caproate, caprylate, fumarate, malate, propyl, heptyl, and octyl alcohols and the iso-compounds iso-butyrate, iso-butyl and iso-hexyl alcohols are inadequate.

Acetate is not assimilated <pH 5.0, propionate and butyrate <pH 6.0, and valerate <pH 7.0. Optimum for utilization of succinate is pH 3.0, for pyruvate pH 4.0, utilized also at pH 2.0 Fatty acids are utilized dissociated; succinate and pyruvate are utilized undissociated. Alcohols are assimilated throughout pH 4.0–7.4, except hexanol at pH 7.4. Alcohol availability is proportional to molecular length-1.

pH after growth of fatty acid media is 8.4 ± 0.4; stable in pH 2.0 pyruvate and pH 3.0 succinate media; 3.5 ± 0.3 in alcohol media with initial pH <6.0. Longer alcohols cause less pH decrease during growth.

Acetate concentrations <0.2% do not support maximum populations; concentrations of 0.2–1.0% do. pH after growth increases in these media to pH 8.5 with maximum populations.

Malate, fumarate, α-ketoglutarate, and lactate seem not to penetrate the cell, but are metabolized by homogenates. Methylene blue reduction by homogenates indicates the presence of lactic, malic, succinic and α-ketoglutaric dehydrogenases, fumarase and glutamic transaminase. Extracts contain Embden-Meyerhof phosphate esters, ATP, and ADP.

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