Affiliation:
1. Institut für Mikrobiologie der Georg-August Universität Göttingen, 3400 Göttingen, Federal Republic of Germany, and Department of Food Science and Technology, School of Agriculture, Nagoya University, Chikusa, Nagoya 464 Japan2
Abstract
A new
Clostridium
strain was isolated on starch at 60°C. Starch, pullulan, maltotriose, and maltose induced the synthesis of α-amylase and pullulanase, while glucose, ribose, fructose, and lactose did not. The formation of the amylolytic enzymes was dependent on growth and occurred predominantly in the exponential phase. The enzymes were largely cell bound during growth of the organism with 0.5% starch, but an increase of the starch concentration in the growth medium was accompanied by the excretion of α-amylase and pullulanase into the culture broth; but also by a decrease of total activity. α-Amylase, pullulanase, and α-glucosidase were active in a broad temperature range (40 to 85°C) and displayed temperature optima for activity at 60 to 70°C. During incubation with starch under aerobic conditions at 75°C for 2 h, the activity of both enzymes decreased to only 90 or 80%. The apparent
K
m
values of α-amylase, pullulanase, and α-glucosidase for their corresponding substrates, starch, pullulan, and maltose were 0.35 mg/ml, 0.63 mg/ml, and 25 mM, respectively.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Reference32 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. Untersuchungen an Pullulan. II. Spezifischer Abbau durch ein bakterielles Enzym;Bender H.;Biochem. Z.,1961
3. Pullulanase (an amylopectin and glycogen debranching enzyme) from Aerobacter aerogenes;Bender H.;Methods Enzymol.,1966
4. 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 GmbH Weinheim Federal Republic of Germany.
5. Bergmeyer H. U. and M. Grassl. 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 GmbH Weinheim Federal Republic of Germany.
Cited by
71 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Thermostable Amylopullulanases: Sources and Applications;Industrial Biotechnology;2024-05-09
2. Industrial applications of thermophilic/hyperthermophilic enzymes;Developments and Applications of Enzymes from Thermophilic Microorganisms;2023
3. Industrial Enzyme Technology;Biotechnology;2019
4. Industrial Enzyme Technology;Research Advancements in Pharmaceutical, Nutritional, and Industrial Enzymology;2018
5. Thermoanaerobacterium;Bergey's Manual of Systematics of Archaea and Bacteria;2015-09-14