Immobilization of Exo-maltotetraohydrolase and Pullulanase
- 1 July 1989
- journal article
- research article
- Published by Oxford University Press (OUP) in Agricultural and Biological Chemistry
- Vol. 53 (7) , 1843-1848
- https://doi.org/10.1080/00021369.1989.10869562
Abstract
A dual enzyme system of exo-maltotetraohydrolase [EC 3.2.1.60] and pullulanase [EC 3.2.1.41] was studied for the continuous production of maltotetraose. Porous chitosan beads were selected from among many carriers as the best carrier to immobilize both enzymes. The properties of the immobilized enzymes were examined and compared with those of the native enzymes. For exo-maltotetraohydrolase, the optimum pH of the immobilized enzyme shifted slightly to the acidic side and the pH stability was improved on the alkaline side. The optimum temperature of the immobilized enzyme increased by about 15°C and thermostability was improved by about 10°C. As for pullulanase, very little difference in thermostability was observed. The effects of operating conditions on the continuous production of maltotetraose using exo- maltotetraohydrolase immobilized on the porous chitosan beads were examined. Porous chitosan beads were recognized to be superior to Diaion HP-50. The continuous production of maltotetraose was accomplished using the dual immobilized enzyme system. The dual enzyme system proved to be effective to increase the maltotetraose content in the product. A stable operation was successfully continued for more than 60 days.This publication has 7 references indexed in Scilit:
- Stability of immobilized maltotetraose-forming amylase fromPseudomonas stutzeriBiotechnology & Bioengineering, 1989
- Continuous production of maltotetraose using immobilized Pseudomonas stutzeri amylaseBiotechnology & Bioengineering, 1988
- Pullulanase-Amylase Complex Enzyme fromBacillus subtilisAgricultural and Biological Chemistry, 1987
- Action patterns of various exo-amylases and the anomeric configurations of their productsCarbohydrate Research, 1984
- Purification of α-Maltotetraose-formingexo-Amylase ofPseudomonas stutzeri—Two-forms of the Amylase and Their Enzymatic PropertiesAgricultural and Biological Chemistry, 1983
- Immobilization of the exo‐maltohexaohydrolase by the irradiation methodBiotechnology & Bioengineering, 1983
- Purification and Properties of an exo-α-Amylase fromPseudomonas stutzeriAgricultural and Biological Chemistry, 1982