Ethanol Production by a New Method of Alginate-Immobilization

새로운 Alginate 고정화 방법에 의한 에탄올 생산

  • Kim, Eun-Young (Institute of Genetic Engineering, The University of Suwon) ;
  • Kim, Seung-Wook (Institute of Genetic Engineering, The University of Suwon) ;
  • Kim, Keun (Institute of Genetic Engineering, The University of Suwon)
  • 김은영 (수원대학교 유전공학연구소) ;
  • 김승욱 (수원대학교 유전공학연구소) ;
  • 김근 (수원대학교 유전공학연구소)
  • Published : 1993.08.01

Abstract

When the cells of yeast K35 were immobilized in Ca-alginate gel, cell concentration and viability decreased as alginate concentration increased. Considering the results, 2% (w/v) Ca-alginate concentration would be suitable. Among various concentrations of additives and cross-lin-king agent, the addition of 1.67% (w/v) of bentonite together with 0.33% (v/v) of glutaraldehyde (ABG bead) resulted in the highest ethanol production of 1.8%(w/v), using YPD medium containing 2% glucose. ABG bead seemed to be more resistant to phosphate ion than Ca-alginate bead. 0.33%(w/v) of phosphate was a proper concentration for the ethanol production by ABG bead. Scanning electron microscopic observation depicted that the immobilized cells on the bead surface were coated by alginate gel and that the cells in the internal bead were cross-linked with alginate matrix. When repeated-batch culture was performed with ABG bead for 40 days in a packed-bed reactor, ethanol concentration of about 90~110 g/l-gel was maintained. Cell viability was maintained around 70%, and outgrowing cell concentration was below 6.3% of total cell concentration. Consequently, the results showed that ABG head was a potential carrier for continuous production of ethanol compared to conventional Ca-alginate bead.

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