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Screening of recombinant L. lactis strains expressing the fusion antimicrobial peptide BMAP18-BSN37. (A) Schematic diagram of the fusion protein BMAP18-BSN37 design. (B) Diagram of the construction of the recombinant expression vector pUBB. (C) PCR identification of the fusion antimicrobial peptide BMAP18-BSN37 (842 bp). M: DNA ladder (2000 bp); lanes 1 and 2: target gene; N: negative control. (D) Double digestion analysis of plasmid pUBB using <t>Hind</t> <t>III</t> and Nde I. M: DNA ladder (10,000 bp); lane 1: plasmid digested with HindIII and NdeI; lane 2: undigested plasmid. (E) Sequencing alignment of BMAP18-BSN37. (F) PCR screening of positive colonies transformed with pUBB. Lanes 1-91: Numbers of positive transformants identified. (G) Western blot screening of recombinant strains expressing BMAP18-BSN37. Lanes 1, 2, …, 74, 83: recombinant strains expressing BMAP18-BSN37.
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Screening of recombinant L. lactis strains expressing the fusion antimicrobial peptide BMAP18-BSN37. (A) Schematic diagram of the fusion protein BMAP18-BSN37 design. (B) Diagram of the construction of the recombinant expression vector pUBB. (C) PCR identification of the fusion antimicrobial peptide BMAP18-BSN37 (842 bp). M: DNA ladder (2000 bp); lanes 1 and 2: target gene; N: negative control. (D) Double digestion analysis of plasmid pUBB using <t>Hind</t> <t>III</t> and Nde I. M: DNA ladder (10,000 bp); lane 1: plasmid digested with HindIII and NdeI; lane 2: undigested plasmid. (E) Sequencing alignment of BMAP18-BSN37. (F) PCR screening of positive colonies transformed with pUBB. Lanes 1-91: Numbers of positive transformants identified. (G) Western blot screening of recombinant strains expressing BMAP18-BSN37. Lanes 1, 2, …, 74, 83: recombinant strains expressing BMAP18-BSN37.
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Screening of recombinant L. lactis strains expressing the fusion antimicrobial peptide BMAP18-BSN37. (A) Schematic diagram of the fusion protein BMAP18-BSN37 design. (B) Diagram of the construction of the recombinant expression vector pUBB. (C) PCR identification of the fusion antimicrobial peptide BMAP18-BSN37 (842 bp). M: DNA ladder (2000 bp); lanes 1 and 2: target gene; N: negative control. (D) Double digestion analysis of plasmid pUBB using <t>Hind</t> <t>III</t> and Nde I. M: DNA ladder (10,000 bp); lane 1: plasmid digested with HindIII and NdeI; lane 2: undigested plasmid. (E) Sequencing alignment of BMAP18-BSN37. (F) PCR screening of positive colonies transformed with pUBB. Lanes 1-91: Numbers of positive transformants identified. (G) Western blot screening of recombinant strains expressing BMAP18-BSN37. Lanes 1, 2, …, 74, 83: recombinant strains expressing BMAP18-BSN37.
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Screening of recombinant L. lactis strains expressing the fusion antimicrobial peptide BMAP18-BSN37. (A) Schematic diagram of the fusion protein BMAP18-BSN37 design. (B) Diagram of the construction of the recombinant expression vector pUBB. (C) PCR identification of the fusion antimicrobial peptide BMAP18-BSN37 (842 bp). M: DNA ladder (2000 bp); lanes 1 and 2: target gene; N: negative control. (D) Double digestion analysis of plasmid pUBB using <t>Hind</t> <t>III</t> and Nde I. M: DNA ladder (10,000 bp); lane 1: plasmid digested with HindIII and NdeI; lane 2: undigested plasmid. (E) Sequencing alignment of BMAP18-BSN37. (F) PCR screening of positive colonies transformed with pUBB. Lanes 1-91: Numbers of positive transformants identified. (G) Western blot screening of recombinant strains expressing BMAP18-BSN37. Lanes 1, 2, …, 74, 83: recombinant strains expressing BMAP18-BSN37.
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TaKaRa hindiii
Screening of recombinant L. lactis strains expressing the fusion antimicrobial peptide BMAP18-BSN37. (A) Schematic diagram of the fusion protein BMAP18-BSN37 design. (B) Diagram of the construction of the recombinant expression vector pUBB. (C) PCR identification of the fusion antimicrobial peptide BMAP18-BSN37 (842 bp). M: DNA ladder (2000 bp); lanes 1 and 2: target gene; N: negative control. (D) Double digestion analysis of plasmid pUBB using <t>Hind</t> <t>III</t> and Nde I. M: DNA ladder (10,000 bp); lane 1: plasmid digested with HindIII and NdeI; lane 2: undigested plasmid. (E) Sequencing alignment of BMAP18-BSN37. (F) PCR screening of positive colonies transformed with pUBB. Lanes 1-91: Numbers of positive transformants identified. (G) Western blot screening of recombinant strains expressing BMAP18-BSN37. Lanes 1, 2, …, 74, 83: recombinant strains expressing BMAP18-BSN37.
Hindiii, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Screening of recombinant L. lactis strains expressing the fusion antimicrobial peptide BMAP18-BSN37. (A) Schematic diagram of the fusion protein BMAP18-BSN37 design. (B) Diagram of the construction of the recombinant expression vector pUBB. (C) PCR identification of the fusion antimicrobial peptide BMAP18-BSN37 (842 bp). M: DNA ladder (2000 bp); lanes 1 and 2: target gene; N: negative control. (D) Double digestion analysis of plasmid pUBB using Hind III and Nde I. M: DNA ladder (10,000 bp); lane 1: plasmid digested with HindIII and NdeI; lane 2: undigested plasmid. (E) Sequencing alignment of BMAP18-BSN37. (F) PCR screening of positive colonies transformed with pUBB. Lanes 1-91: Numbers of positive transformants identified. (G) Western blot screening of recombinant strains expressing BMAP18-BSN37. Lanes 1, 2, …, 74, 83: recombinant strains expressing BMAP18-BSN37.

Journal: Poultry Science

Article Title: Probiotic and antibacterial properties of recombinant Lactococcus lactis expressing the fusion antimicrobial peptides BMAP18-BSN37 in mice and chickens

doi: 10.1016/j.psj.2026.106507

Figure Lengend Snippet: Screening of recombinant L. lactis strains expressing the fusion antimicrobial peptide BMAP18-BSN37. (A) Schematic diagram of the fusion protein BMAP18-BSN37 design. (B) Diagram of the construction of the recombinant expression vector pUBB. (C) PCR identification of the fusion antimicrobial peptide BMAP18-BSN37 (842 bp). M: DNA ladder (2000 bp); lanes 1 and 2: target gene; N: negative control. (D) Double digestion analysis of plasmid pUBB using Hind III and Nde I. M: DNA ladder (10,000 bp); lane 1: plasmid digested with HindIII and NdeI; lane 2: undigested plasmid. (E) Sequencing alignment of BMAP18-BSN37. (F) PCR screening of positive colonies transformed with pUBB. Lanes 1-91: Numbers of positive transformants identified. (G) Western blot screening of recombinant strains expressing BMAP18-BSN37. Lanes 1, 2, …, 74, 83: recombinant strains expressing BMAP18-BSN37.

Article Snippet: Plasmid pNZ8148 was double-digested with Nco I and Hind III (Takara, Japan), and the linearized pNZ8148 plasmid was recovered by gel extraction.

Techniques: Recombinant, Expressing, Plasmid Preparation, Negative Control, Sequencing, Transformation Assay, Western Blot