Characterization of Xylanase from an Hybird between Aspergillus oryzae var. oryzae and Aspergillus Nidulans 514 by Nuclear Transfer

핵전이에 의한 Aspergillus oryzae var. Oryzae와 Aspergillus nidulans 514의 잡종으로부터 생산된 Xylanase의 특성

  • Yang, Young-Ki (Department of Genetic Engineering, College of Natural Science, Chosun University) ;
  • Moon, Myeng-Nim (Department of Genetic Engineering, College of Natural Science, Chosun University) ;
  • Park, Hyung-Nam (Department of Genetic Engineering, College of Natural Science, Chosun University) ;
  • Lim, Chae-Young (Department of Genetic Engineering, College of Natural Science, Chosun University)
  • 양영기 (조선대학교 자연과학대학 유전공학과) ;
  • 문명님 (조선대학교 자연과학대학 유전공학과) ;
  • 박형남 (조선대학교 자연과학대학 유전공학과) ;
  • 임채영 (조선대학교 자연과학대학 유전공학과)
  • Published : 1996.02.01

Abstract

Interspecific hybrids between Aspergillus oryzae var oryzae and A. nidulans 514 were obtained by nuclear transfer technique. Several autotrophic mutants isolated from conidiospores of the two strains were mutagenized with ultraviolet and N-methyl-N-nitrosoguanidine. Optimal conditions for formation of intergeneric hybrids were investigated. Frequencies of hybrid formation by nuclear transfer were $3{\times}10^{-5}{\sim}1{\times}10^{-5}$. From observation of genetic stability, conidial size, DNA content, and nuclear stain, it was suggested that their karyptypes are aneuploid. The hybrids showed 1.1~1.4 fold higher xylanase activities than parental strains did. The xylanase of Aspergiilus sp. TAVD514-3 was purified and some of it's enzymatc characteristics were investigated. The enzyme was purified about 85 fold with an overall yield of 17% from the culture medium by ammonium sulfate fractionation, Sephadex G-75 gel permeation chromatography, and CM-sephadex A-50 ion exchange chromatography. The purified enzyme functions optimally at pH 9.0 and 80$^{\circ}C$. The enzymatic activity was increased by the presence of $Mg^{2+}$ and $Mn^2$ ions.

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