干酪乳杆菌
木聚糖酶
粘附
微生物学
乳酸菌
细胞壁
拉伤
单核细胞增生李斯特菌
化学
生物
细菌
食品科学
生物化学
酶
发酵
遗传学
有机化学
解剖
作者
Hsiang-Yun Hsueh,Bi Yu,Chi‐Te Liu,Je‐Ruei Liu
摘要
BACKGROUND Lactobacillus, which has great adhesion ability to intestinal mucosa and is able to hydrolyse plant cell walls, can be used more efficiently as a feed additive. To increase the adhesion ability and display a fungal xylanase on the cell surface of Lactobacillus casei, the Listeria monocytogenes cell-wall-anchoring protein gene, mub, was introduced into L. casei ATCC 393 cells and used as a fusion partner to display the rumen fungal xylanase XynCDBFV on the cell surface of the transformed strains. RESULTS The transformed strain L. casei pNZ-mub, which harboured mub gene, displayed recombinant Mub on its cell surface and showed greater adhesion ability to Caco-2 cells than the parental strain. The transformed strain L. casei pNZ-mub/xyn, which harboured mub-xynCDBFV fusion gene, acquired the capacity to break down oat spelt xylan and exhibited greater competition ability against the adhesion of L. monocytogenes to Caco-2 cells, in comparison with the parental strain. CONCLUSION Mub has a potential to be used as a fusion partner to display heterologous proteins on the cell surface of Lactobacillus. Moreover, this is the first report of the successful display of xylanase on the cell surface of Lactobacillus. © 2013 Society of Chemical Industry
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