Expression of Escherichia coli heat-labile enterotoxin B subunit (LTB) in Saccharomyces cerevisiae

被引:0
作者
Rezaee, MA
Rezaee, A
Moazzeni, SM
Salmanian, AH
Yasuda, Y
Tochikubo, K
Pirayeh, SN
Arzanlou, M
机构
[1] Tarbiat Modarres Univ, Fac Med Sci, Tehran, Iran
[2] NIGEB, Tehran, Iran
[3] Nagoya City Univ, Sch Med, Dept Microbiol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
关键词
enterotoxigenic Escherichia coli; LTB; Saccharomyces cerevisiae; gene expression; immunoblotting;
D O I
暂无
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Heat-labile enterotoxin B subunit (LTB) of enterotoxigenie Escherichia coli (ETEC) is both a strong mucosal adjuvant and immunogen. It is a subunit vaccine candidate to be used against ETEC-induced diarrhea. It has already been expressed in several bacterial and plant systems. In order to construct yeast expressing vector for the LTB protein, the eltB gene encoding LTB was amplified from a human origin enterotoxigenic E. coli DNA by PCR. The expression plasmid pLTB83 was constructed by inserting the eltB gene into the pYES2 shuttle vector immediately downstream of the GAL] promoter. The recombinant vector was transformed into S. cerevisiae and was then induced by galactose. The LTB protein was detected in the total soluble protein of the yeast by SDS-PAGE analysis. Quantitative ELISA showed that the maximum amount of LTB protein expressed in the yeast was approximately 1.9% of the total soluble protein. Immunoblotting analysis showed the yeast-derived LTB protein was antigenically indistinguishable from bacterial LTB protein. Since the whole-recombinant yeast has been introduced as a new vaccine formulation the expression of LTB in S. cerevisiae can offer an inexpensive yet effective strategy to protect against ETEC, especially in developing countries where it is needed most.
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页码:354 / 360
页数:7
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