Production of Thermostable α-Amylase, Pullulanase, and α-Glucosidase in Continuous Culture by a New Clostridium Isolate

Author:

Antranikian G.1,Herzberg C.1,Gottschalk G.1

Affiliation:

1. Institut für Mikrobiologie der Georg-August Universität Göttingen, 3400 Göttingen, Federal Republic of Germany

Abstract

The production of α-amylase, pullulanase, and α-glucosidase and the formation of fermentation products by the newly isolated thermophilic Clostridium sp. strain EM1 were investigated in continuous culture with a defined medium and an incubation temperature of 60°C. Enzyme production and excretion were greatly influenced by the dilution rate and the pH of the medium. The optimal values for the formation of starch-hydrolyzing enzymes were a pH of 5.9 and a dilution rate of 0.075 to 0.10 per h. Increase of the dilution rate from 0.1 to 0.3 per h caused a drastic drop in enzyme production. The ethanol concentration and optical density of the culture, however, remained almost constant. Growth limitation in the chemostat with 1% (wt/vol) starch was found optimal for enzyme production. Under these conditions 2,800 U of pullulanase per liter and 1,450 U of α-amylase per liter were produced; the amounts excreted were 70 and 55%, respectively.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference11 articles.

1. Changes in the cell envelope structure of Clostridium sp. strain EM1 during massive production of a-amylase and pullulanase;Antranikian G.;FEMS Microbiol. Lett.,1987

2. la.Bergmeyer H. U. K. Gawehn and M. Grabe. 1974. Enzyme als biochemische Reagentien p. 454-558. In H. U. Bergmeyer (ed.) Methoden der enzymatischen Analyse. Verlag Chemie Weinheim Federal Republic of Germany.

3. Bergmeyer H. U. and M. Grassi. 1983. Reagents for enzymatic analysis: enzymes-a-amylase p. 151-152. In H. U. Bergmeyer (ed.) Methods of enzymatic analysis 3rd ed. vol. 2. Verlag Chemie Weinheim Federal Republic of Germany.

4. Bergmeyer H. U. and M. Grassl. 1983. Reagents for enzymatic analysis: enzymes--glucosidase p. 205-206. In H. U. Bergmeyer (ed.) Methods of enzymatic analysis 3rd ed. vol. 2. Verlag Chemie Weinheim Federal Republic of Germany.

5. Derepression of hydrogenase during limitation of electron donors and derepression of ribulosebisphosphate carboxylase during carbon limitation of Alcaligenes eu- trophus;Friedrich C.;J. Bacteriol.,1982

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