Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/71457
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dc.contributor.authorTran, Thi Hong-
dc.contributor.authorTon, That Huu Dat-
dc.contributor.authorNguyen, Phuong Hoa-
dc.contributor.authorPham, Viet Cuong-
dc.contributor.authorNguyen, Thi Kim Cuc-
dc.date.accessioned2021-12-28T02:33:53Z-
dc.date.available2021-12-28T02:33:53Z-
dc.date.issued2018-
dc.identifier.issn2615-9023-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/71457-
dc.description.abstractMarine sponge is known as a “gold mine” of natural products from marine environment. Many novel bioactive compounds have been isolated from marine sponges and sponge-associated microorganisms such as antibiotics, anti-cancer compounds, protease inhibitors, etc. In this study, we selected a gene encoding protease inhibitor from metagenome of a sponge collected in Quang Tri to express in Escherichia coli (E. coli) BL21(DE3). The gene PI-DN9encoding protease inhibitor (1.3 kb) was cutoff cloning vector pUC57/PI-DN9 containing gene PI-DN9and inserted into expression vector pET-32a(+), the recombinant vector pET-32a(+)/PI-DN9 then was transformed and expressed in the E. coli strain BL21(DE3). Results showed that recombinant protein (50kDa) was expressed successfully at 25°C, 1 mM of IPTG in 5 hours. The recombinant protein was purified using Ni-NTA affinity chromatography column. Western blot assay and bioactive assay showed good activity of the purified protein.vi_VN
dc.language.isoenvi_VN
dc.relation.ispartofseriesAcademia journal of biology;Vol. 40, No. 04 .- P.77-84-
dc.subjectEscherichia colivi_VN
dc.subjectExpression vectorvi_VN
dc.subjectProtease inhibitorvi_VN
dc.subjectRecombinant proteinvi_VN
dc.subjectSpongevi_VN
dc.titleExpression of a novel gene encoding protease inhibitor from metagenome of sponge in Vietnamvi_VN
dc.typeArticlevi_VN
Appears in Collections:Academia journal of biology

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