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Immobilization of Aspergillus oryzae ${eta}$-Galactosidase on Low-pressure Plasma-modified Cellulose Acetate Membrane Using Polyethyleneimine for Production of Galactooligosaccharide
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  • Immobilization of Aspergillus oryzae ${eta}$-Galactosidase on Low-pressure Plasma-modified Cellulose Acetate Membrane Using Polyethyleneimine for Production of Galactooligosaccharide
  • Immobilization of Aspergillus oryzae ${eta}$-Galactosidase on Low-pressure Plasma-modified Cellulose Acetate Membrane Using Polyethyleneimine for Production of Galactooligosaccharide
저자명
Gulec. Hac Ali,Gurdas. Sevim,Albayrak. Nedim,Mutlu. Mehmet
간행물명
Biotechnology and bioprocess engineering
권/호정보
2010년|15권 6호|pp.1006-1015 (10 pages)
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한국생물공학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

The aim of this study was to produce galactooligosaccharides (GOS) from lactose using ${eta}$-galactosidase from Aspergillus oryzae immobilized on a low-pressure plasma-modified cellulose acetate (CA) membrane. Specifically, a novel method was developed for multilayer enzyme immobilization involving polyethyleneimine (PEI)-enzyme aggregate formation and growth on a CA membrane. A large amount of enzyme (997 ${mu}g/cm^2$ membrane) was immobilized with 66% efficiency. The $K_m$ value for the immobilized enzyme was estimated to be 48 mM, which indicates decreased affinity for the substrate, whereas the Vmax value was smaller. The immobilized enzyme showed good storage and operational stability. The half-life of the immobilized enzyme on the membrane was about 1 month at $30^{circ}C$ and ~ 60 h at $60^{circ}C$. Maximum GOS production of 27% (w/w) was achieved with 70% lactose conversion from 320 g/L of lactose at pH 4.5 and $60^{circ}C$. Trisaccharides were the major types of GOS formed and accounted for about 75% of the total GOS produced. Based on these results, immobilized enzyme technology could be applied to GOS production from lactose.