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作 者:黄音[1] 刘飞鹏[2] 周天鸿[2] 朱嘉明[2]
机构地区:[1]上海复旦大学遗传所 [2]暨南大学生物工程系,广州510632
出 处:《生物工程学报》2001年第2期207-210,共4页Chinese Journal of Biotechnology
基 金:广东省自然科学基金!资助 (970 6 36 )
摘 要:A hybrid peptide gene was designed and synthesized. Its encoding peptide is constructed from residues 3~14 of magainin and residues 1~13 of melittin. The MA E gene was cloned into plasmids pUC18 and pBV220. By DNA sequencing, the whole sequences of this gene is confirmed to be correct. The recombinant plasmid pBMA\|E was expressed in \%E.coli\% DH5α. A gene product band can be seen with Tricine\|SDS\|PAGE. The MA E hybrid peptide was purified by immobilized metal affinity chromatography. Bioactivity assay was carried out in liquid turbidity method. The bactericide value to \%E.coli\% K 12 D 31 is 0.182.A hybrid peptide gene was designed and synthesized. Its encoding peptide is constructed from residues 3~14 of magainin and residues 1~13 of melittin. The MA E gene was cloned into plasmids pUC18 and pBV220. By DNA sequencing, the whole sequences of this gene is confirmed to be correct. The recombinant plasmid pBMA\|E was expressed in \%E.coli\% DH5α. A gene product band can be seen with Tricine\|SDS\|PAGE. The MA E hybrid peptide was purified by immobilized metal affinity chromatography. Bioactivity assay was carried out in liquid turbidity method. The bactericide value to \%E.coli\% K 12 D 31 is 0.182.
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