Molecular cloning of phospho-$\beta$-galactosidase gene of lactobacillus casei in escherichia coli

Lactobacillus casei의 phospho-$\beta$-galactosidase 유전자의 대장균내 분자클로닝

  • 문경희 (숙명여자대학교 생물학과) ;
  • 박정희 (숙명여자대학교 생물학과) ;
  • 최순영 (숙명여자대학교 생물학과) ;
  • 이유미 (숙명여자대학교 생물학과) ;
  • 김태한 (일동제약㈜중앙연구실) ;
  • 김연수 (서울대학교 자연과학대학 미생물학과) ;
  • 민경희 (숙명여자대학교 생물학과)
  • Published : 1989.09.01

Abstract

Gene for lactose catabolism in Lactobacillus casei SW-M1 was encoded by a 60Kb metabolic plasmid. A derivative of only 10kb, pPlac 15 of recombinant plasmid, was constructed by introducing into pBR322 and was cloned into E. coli using restriction endonuclease Pst I. A 10kb insery DNA in plasmid pBR322 was identified as a gene encoded phospho-$\beta$-galactosidase by the determination of enzyme activity. Phospho-$\beta$-galactosidase was apparently expressed in E. coli. The enzyme activities of cell-free extract from transformant E. coli HB101 carrying pPLac 15 DNA were not different from that of L. casei as a donor strain on the basis of enzyme properites. However, specific activity of phospho-$\beta$-galactosidase in the cloned strain with Lac $Y^{-}$ phenotype of E. coli HB101 was lower than that in L. casei strain.

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