Thermostable Amylolytic Enzymes from a New Clostridium Isolate
- 1 July 1987
- journal article
- research article
- Published by American Society for Microbiology in Applied and Environmental Microbiology
- Vol. 53 (7) , 1661-1667
- https://doi.org/10.1128/aem.53.7.1661-1667.1987
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 Km 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.This publication has 24 references indexed in Scilit:
- Cloning of the pullulanase gene and overproduction of pullulanase in Escherichia coli and Klebsiella aerogenesApplied and Environmental Microbiology, 1985
- New Strains ofBacillus licheniformisandBacillus coagulansproducing Thermostable α-Amylase Active at Alkaline pHJournal of Applied Bacteriology, 1980
- Production of amylase(s) by Schwanniomyces castellii and Endomycopsis fibuligeraAntonie van Leeuwenhoek, 1980
- Glucoamylase ausEndomycopsis bispora I. Zur Produktion des Enzyms in SchüttelkulturJournal of Basic Microbiology, 1979
- [Regulation of alpha-amylase biosynthesis in Pichia burtonii B].1978
- Purification and some properties of alkaline pullulanase from a strain of Bacillus No. 202-1, an alkalophilic microorganismBiochimica et Biophysica Acta (BBA) - Enzymology, 1975
- A thermophilic extracellular α-amylase from Bacillus licheniformisArchives of Biochemistry and Biophysics, 1973
- Formation of isoamylase by Pseudomonas.1968
- Metabolism of the reserve polysaccharide of Streptococcus mitis. Some properties of a pullulanaseBiochemical Journal, 1968
- Pullulanase from aerobacter aerogenes; production in a cell-bound state. Purification and properties of the enzymeBiochemical and Biophysical Research Communications, 1966