Lactobacillus sporogenes에 의한 $\beta$-Galactosidase 생산에 관한 연구 -균체외 $\beta$-Galactosidase의 정제 -

Studies on Production of $\beta$-Galactosidase by Lactobacillus sporogenes - Purification of Extracellular $\beta$-Galactosidase -

  • 김영만 (일동제약㈜ 중앙연구소) ;
  • 이정치 (일동제약㈜ 중앙연구소) ;
  • 최용진 (고려대학교 유전공학과) ;
  • 양한철 (고려대학교 유전공학과)
  • 발행 : 1985.09.01

초록

L. sporogenes의 배양여액으로부터 균체외 $\beta$-galactosidase를 ammonium sulfate fractionation, Sephadex G-200 gel filtration, DEAE-Sephadex A-50 ion exchange chromatography와 hydroxyapatite adsorption chromatography등의 4단계 정제공정을 거쳐 순수하게 정제하였다. 정제효소는 347배 정제되어 비활성이 1,585 units/mg 이었으며 수율은 39.5%였다. Sephadex G-200 gel filtration에 의한 native enzyme의 분자량은 140,000이고 SDS-PAGE 에 의해서는 분자량이 72,000 한가지로 나타났으므로 L. sporogenes의 $\beta$-galactosidase는 동일한 subunit 2개로 구성된 dimer 효소이다.

Extracellular $\beta$-galactosidase from the culture broth of L. sporogenes was purified to apparent homogeniety by procedures including ammonium sulfate fractionation, Sephadex G-200 gel filtration, DEAE-Sephadex A-50 ion exchange chromatography, and Hydroxyapatite adsorption chromatography. The purifying procedures resulted in 347-fold purification with the overall yield of 39.5% The purified enzyme had a specific activity(using ONPG as a substrate) of about 1, 585 units per mg protein. The molecular weight of the enzyme protein was estimated to be 140, 000 by gel filtration on Sephadex G-200, and SDS-polyacrylamide gel electorphoresis showed that the enzyme consisted of two identical subunits with a molecular weight of 72, 000.

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