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Recombinant Expression of an Thermostable, Wide pH Spectrum, and Highly Active Xylanase from Paenibacillus sp. HPL-003

첫 페이지 보기
  • 발행기관
    한국생물공학회 바로가기
  • 간행물
    한국생물공학회 학술대회 바로가기
  • 통권
    2010 추계학술대회 및 국제심포지움 (2010.10)바로가기
  • 페이지
    pp.205-205
  • 저자
    No-Joong Park, Hee Kyung Lim, Ha Young Song, Soo Jin Cho, Ja Yeong Seo, Young Kyu Hwang, In Taek Hwang
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A129405

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원문정보

초록

영어
A new xylanase gene, KRICT PX3, isolated from Paenibacillus sp. HPL-003 (KCTC18179P), has been cloned and expressed in Escherichia coli. This gene encodes 540 amino acid residues (1,620bp) including 179 amino acid residues of a signal peptide, and the deduced amino acid sequence of KRICT PX3 showed 48% identity to endo-1,4-b-xylanase (YP_001817989) from Opitutus terrae PB90-1 among the xylanases of Glycosyl hydrolase 10 superfamily. Purified recombinant xylanase KRICT PX3 showed an thermostable, wide pH spectrum, and high activity on the different-origin of xylan. The specific activity of the purified xylanase KRICT PX3 at pH 7 and 50oC was 125 U, and exhibited Km and Vmax values of 0.2 mg/ml and 153.8 U/mg on birch wood xylan, respectively. This enzyme has a wide pH spectrum of pH 5 to pH 11. Optimum temperature was estimated at the range of 50~60oC and it was stable for 24 hrs at 50oC, however, easily lost the activity at 60oC after 20 min. Most salts did not significantly change the enzyme activity, and also ethylenediamine tetra-acetic acid, 2-mercaptoethanol, phenylmethanesulphonyl fluoride, and furfural were not influenced on the enzyme activity at 1 mM, however, Cu+2, Zn+2, Fe+2, and EDTA was slightly inhibited the enzyme activity. Thin layer chromatography analysis showed that the enzyme released a mixture of hydrolysis products including xylobiose, xylotriose and some of xylooligomers from birchwood xylan. Further research on the practical application will be necessary for the industrial usage.

키워드

Paenibacillus sp wide pH spectrum thermostability xylanase

저자

  • No-Joong Park [ BioRefinery Research Center, Korea Research Institute of Chemical Technology, Yuseong P.O. Box 107, Daejon 305-600. ]
  • Hee Kyung Lim [ BioRefinery Research Center, Korea Research Institute of Chemical Technology, Yuseong P.O. Box 107, Daejon 305-600. ]
  • Ha Young Song [ BioRefinery Research Center, Korea Research Institute of Chemical Technology, Yuseong P.O. Box 107, Daejon 305-600. ]
  • Soo Jin Cho [ BioRefinery Research Center, Korea Research Institute of Chemical Technology, Yuseong P.O. Box 107, Daejon 305-600. ]
  • Ja Yeong Seo [ BioRefinery Research Center, Korea Research Institute of Chemical Technology, Yuseong P.O. Box 107, Daejon 305-600. ]
  • Young Kyu Hwang [ BioRefinery Research Center, Korea Research Institute of Chemical Technology, Yuseong P.O. Box 107, Daejon 305-600. ]
  • In Taek Hwang [ BioRefinery Research Center, Korea Research Institute of Chemical Technology, Yuseong P.O. Box 107, Daejon 305-600. ]

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국생물공학회 [The Korean Society for Biotechnology and Bioengineering]
  • 설립연도
    1984
  • 분야
    공학>생물공학
  • 소개
    이 법인은 생물 공학의 발전과 보급에 이바지하고, 회원 상호 간의 연구 협력과 친목을 도모함을 목적으로 한다 1. 생물공학 분야의 발전을 위한 연구 협력 2. 생물공학의 실용화를 촉진시키기 위한 산학 협동 3. 학술연구 발표회, 강연회, 연수회 등 학술활동의 개최 4. 국,영문 학술지,소식지,학술회의 Proceedings 및 학술도서의 발간 5. 생물공학 발전을 위한 정책 건의 6. 기타 국제 교류 등 본 학회의 목적 달성을 위한 제반 활동

간행물

  • 간행물명
    한국생물공학회 학술대회
  • 간기
    반년간
  • 수록기간
    1985~2013
  • 십진분류
    KDC 476 DDC 576

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