Production of Thermophilic α-Amylase Using Immobilized Transformed Escherichia coli by Addition of Glycine
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概要
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Efficient production of thermophilic α-amylase from Bacillus stearothermophilus was investigated using recombinant Escherichia coli HB101/pHI301 immobilized with κ-carrageenan by the addition of glycine. The effects of glycine, the concentrations of κ-carrageenan and KCl on the production of the enzyme as well as the stability of plasmid pHI301 were studied. In the absence of glycine, the enzyme was localized in the periplasmic space of the recombinant E. coli cells and a small amount of the enzyme was liberated in the culture broth. Although the addition of glycine was very effective for release of α-amylase from the periplasm of E. coli entrapped in gel beads, a majority of the enzyme accumulated in the gel matrix. (In this paper, production of the enzyme from recombinant cells to an ambient is expressed by the term "release", while diffusion-out from gel beads is referred to by the term "liberate".)Concentrations of KCl and immobilizing support significantly affected on the liberation of α-amylase to the culture broth. Mutants which produced smaller amounts of the enzyme emerged during a successive culture of recombinant E. coli, even under selective pressure, and they predominated in the later period of the passages. The population of plasmid-lost segregants increased with cultivation time. The stability of pHI301 for the free cells was increased by the addition of 2% KCl, which is a hardening agent for carrageenan. Although the viability of cells and α-amylase activity in the beads decreased with cultivation time during the successive sulture of the immobilized recombinant E. coli, the plasmid stability was increased successfully by immobilization. Efficient long-term production of α-amylase was attained by an iterative re-activation-liberation procedure using the immobilized recombinant cells. Although the viable cell number, plasmid stability and enzyme activity liberated in the glycine solution decreased at an early period in the cultivation cycles, the process attained steady state regardless of the addition of an antibiotic.
- 社団法人日本生物工学会の論文
- 1991-06-25
著者
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ARIGA OSAMU
Department of Fine Material Engineering, Faculty of Texile Science and Technology, Shinshu Universit
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SANO YOSHIKI
Department of Fine Material Engineering, Faculty of Texile Science and Technology, Shinshu Universit
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Ariga O
Shinshu Univ. Nagano Jpn
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Ariga Osamu
Department Of Fine Material Engineering Faculty Of Texile Science And Technology Shinshu University
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Sano Y
Shinshu Univ. Nagano Jpn
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Sano Y
Department Of Fine Material Engineering Faculty Of Texile Science And Technology Shinshu University
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Sano Yoshiki
Department Of Fine Material Engineering Faculty Of Texile Science And Technology Shinshu University
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ANDOH YASUYUKI
Department of Fine Materials Engineering, Faculty of Textile Science and Technology, Shinshu Univers
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FUJISHITA YOSHIYA
Department of Fine Materials Engineering, Faculty of Textile Science and Technology, Shinshu Univers
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WATARI TOHRU
Department of Fine Materials Engineering, Faculty of Textile Science and Technology, Shinshu Univers
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Watari Tohru
Department Of Fine Materials Engineering Faculty Of Textile Science And Technology Shinshu Universit
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Andoh Yasuyuki
Department Of Fine Materials Engineering Faculty Of Textile Science And Technology Shinshu Universit
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Fujishita Yoshiya
Department Of Fine Materials Engineering Faculty Of Textile Science And Technology Shinshu Universit
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ARIGA OSAMU
Department of Chemical Engineering, Faculty of Engineering, Nagoya University
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