A 44-residue hybrid peptide (CB (1-24)-Arg-Ser-Tyr-Tan (4-21)) incorporating 1-24 residues of cecropin B (CB) and 4-21 residues of thanatin (Tan) was designed and constructed. The CB-Tan gene was cloned into expressio...A 44-residue hybrid peptide (CB (1-24)-Arg-Ser-Tyr-Tan (4-21)) incorporating 1-24 residues of cecropin B (CB) and 4-21 residues of thanatin (Tan) was designed and constructed. The CB-Tan gene was cloned into expression plasmid pGEX-3X and expressed in E.coli BL21. The fusion protein was purified by affinity chromatography. After digested with enterokinase the gene product released with antibacterial activity and gave one band in Tricine-SDS-PAGE.展开更多
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 s...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.展开更多
文摘A 44-residue hybrid peptide (CB (1-24)-Arg-Ser-Tyr-Tan (4-21)) incorporating 1-24 residues of cecropin B (CB) and 4-21 residues of thanatin (Tan) was designed and constructed. The CB-Tan gene was cloned into expression plasmid pGEX-3X and expressed in E.coli BL21. The fusion protein was purified by affinity chromatography. After digested with enterokinase the gene product released with antibacterial activity and gave one band in Tricine-SDS-PAGE.
文摘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.
