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자료유형
학술저널
저자정보
저널정보
한국생물공학회 KSBB Journal KSBB Journal 제11권 제3호
발행연도
수록면
270 - 275 (6page)

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초록· 키워드

Heterologous expression of glucose oxidase gene using recombinant yeast has been carried out. Polymerase chain reaction was conducted to obtain the gene encoding glucose oxidase from Aspergillus niger and sequence comparison indicated the cloned 1.9kb DNA fragment appeared to be the glucose oxidase structural gene containing a signal sequence for extracellular location. Transforming shuttle vector was constructed with YEp352 to express the cloned glucose oxidase gene under the control of either GAL1 or GAL10 promoter. Plate assay of recombinant yeasts has shown that GAL1 promoter was more effective in yielding glucose oxidase than GAL10 promoter. Among the five different concentrations of galactose tried, 1% galactose showed the highest induction of glucose oxidase. Cellular localization experiment of recombinant enzyme using spheroplast revealed that most of enzymes(80%) were secreted into culture media in contrast to A. niger. There is no difference in heat-stability of recombinant enzyme up to 50°C compared to the glucose oxidase from A. niger. However, a dramatic reduction of enzyme activity was observed in both enzymes at 60°C.
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  1. ABSTRACT
  2. 서론
  3. 재료 및 방법
  4. 결과 및 고찰
  5. 요약
  6. 참고문헌

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UCI(KEPA) : I410-ECN-0101-2014-400-002850212