鲢抗菌肽Hepcidin的基因克隆和表达及抑菌活性分析

Cloning, expression and antimicrobial activity of Hepcidin from Hypophthalmichthys molitrix

  • 摘要: 利用同源克隆的方法从鲢(Hypophthalmichthys molitrix)的肝脏中克隆出抗菌肽Hepcidin cDNA(GenBank登入号KF312213)后,通过pET32a(+)构建含抗菌肽Hepcidin的重组质粒的pET-Hep/Rosetta菌株,在37 ℃、28 ℃和16 ℃下分别用0.5 mmol · L-1和1.0 mmol · L-1 IPTG诱导表达,产物用Ni SepharoseTM亲和层析柱纯化并进行体外抑菌试验。鲢Hepcidin cDNA总长度755 bp,ORF为282 bp,5′UTR为108 bp,3′UTR为365 bp,编码93氨基酸,信号肽24个氨基酸,前域42个氨基酸和成熟肽27个氨基酸。pET-Hep/Rosetta在28 ℃和16 ℃主要是可溶性表达,37 ℃主要是包涵体表达。纯化的产物经15% SDS-PAGE电泳验证为目的产物。目的产物、pET32/Rosetta产物以及氟苯尼考的体外抑菌试验表明,目的表达产物对无乳链球菌(Streptococcus agalactiae)、金黄色葡萄球菌(Staphylococcus aureus)、嗜水气单胞菌(Aeromonas hydrophila)等具有很好的抑菌效果。

     

    Abstract: The full-length Hepcidin cDNA sequence GenBank No.KF312213 was amplified from the liver of chub (Hypophthalmichthys molitrix) by semi-Nested PCR rapid amplification of cDNA ends (RACE).According to prodomain and mature peptide of the Hepcidin cDNA sequence, we designed an upstream primer with EcoR I restriction site and downstream primers with Sal I restriction site, and cloned the target gene into the expression vector pET-32a (+). The recombined plasmid was transformed into the expression stain-E .coliRosetta and expressed induciblely at different temperatures (37 ℃, 28 ℃ and 16 ℃) and of different IPTG concentrations (0.5 mmol · L-1 and 1.0 mmol · L-1). The protein was purified by Ni SepharoseTM affinity chromatography column. The full-length of the Hepcidin cDNA gene was 755 bp, which included a 282-bp ORF encoding a 93-amino acid prepropeptide. The prepropeptide contained a signal peptide (24 amino acids), a prodomain (42 amino acids) and a mature peptide (27 amino acids). The purified product displayed a single protein band through 15% SDS-PAGE electrophoresis. The purified production of pET-Hep/Rosetta had obvious antibacterial effect on Streptococcus agalactiae, Staphylococcus aureus and Aeromonas hydrophila, but the control group showed no inhibitory effect.

     

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