메뉴 건너뛰기
.. 내서재 .. 알림
소속 기관/학교 인증
인증하면 논문, 학술자료 등을  무료로 열람할 수 있어요.
한국대학교, 누리자동차, 시립도서관 등 나의 기관을 확인해보세요
(국내 대학 90% 이상 구독 중)
로그인 회원가입 고객센터 ENG
주제분류

추천
검색

논문 기본 정보

자료유형
학술저널
저자정보
저널정보
한국미생물생명공학회 Journal of Microbiology and Biotechnology Journal of Microbiology and Biotechnology 제24권 제4호
발행연도
2014.1
수록면
431 - 439 (9page)

이용수

표지
📌
연구주제
📖
연구배경
🔬
연구방법
🏆
연구결과
AI에게 요청하기
추천
검색

초록· 키워드

오류제보하기
We report the construction of two Bacillus subtilis expression vectors, pBNS1/pBNS2. Bothvectors are based on the strong promoter P43 and the ampicillin resistance gene expressioncassette. Additionally, a fragment with the Shine-Dalgarno sequence and a multiple cloningsite (BamHI, SalI, SacI, XhoI, PstI, SphI) were inserted. The coding region for the amyQ(encoding an amylase) signal peptide was fused to the promoter P43 of pBNS1 to construct thesecreted expression vector pBNS2. The applicability of vectors was tested by first generatingthe expression vectors pBNS1-GFP/pBNS2-GFP and then detecting for green fluorescentprotein gene expression. Next, the mannanase gene from B. pumilus Nsic-2 was fused to vectorpBNS2 and we measured the mannanase activity in the supernatant. The mannanase totalenzyme activity was 8.65 U/ml, which was 6 times higher than that of the parent strain. Ourwork provides a feasible way to achieve an effective transformation system for geneexpression in B. subtilis and is the first report to achieve B. pumilus mannanase secretoryexpression in B. subtilis.

목차

등록된 정보가 없습니다.

참고문헌 (18)

참고문헌 신청

이 논문의 저자 정보

최근 본 자료

전체보기

댓글(0)

0