Cloning and Expression of $\beta$-Xylosidase Gene from Alkali-tolerant Bacillus sp. YA-14 in Escherichia coli

알카리 내성 Bacillus sp. YA-14의 $\beta$-Xylosidase 유전자의 Cloning 및 대장균에의 발현

  • 박덕철 (연세대학교 공과대학 식품공학과) ;
  • 김진만 (연세대학교 공과대학 식품공학과) ;
  • 정용준 (연세대학교 공과대학 식품공학과) ;
  • 공인수 (연세대학교 공과대학 식품공학과) ;
  • 배동훈 (연세대학교 공과대학 식품공학과) ;
  • 유주현 (연세대학교 공과대학 식품공학과)
  • Published : 1989.12.01

Abstract

Chromosomal DNA fragments of Bacillus sp. YA-14, isolated from soil as a potent $\beta$-xylosidase producing bacterium, were ligated to a vector plasmid pBR322 and used to transfer Escherichia coli HB101 cells. The recombinant plasmid pYXL22 was found to enable the transformants to produce $\beta$-xylosidase. pYXL22 was found to contain the 7.0 kb HindIII DNA fragment originated from the Bacillus sp. YA-14 chromosomal DNA by Southern hybridization. The optimum temperature for the reaction of $\beta$-xylosidase produced by E. coli HB101 (pYXL22) was appeared at 3$0^{\circ}C$. The enzyme was maintained stably up to 4$0^{\circ}C$ when stored 1hr at 4$0^{\circ}C$. The $\beta$-xylosidase was repressed completely by 0.4% (w/v) glucose concentration in E. coli HB101 (pYXL22). The optimum concentration of xylose for the $\beta$-xylosidase production in Bacillus sp. YA-14 was 0.2% (w/v).

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