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Statistical optimization of medium composition and culture condition for the production of recombinant anti-lipopolysaccharide factor of Eriocheir sinensis in Escherichia coli

机译:在大肠杆菌中生产重组中华绒螯蟹抗脂多糖因子的培养基组成和培养条件的统计优化

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摘要

Anti-lipopolysaccharide factors (ALFs) are important antimicrobial peptides that are isolated from some aquatic species. In a previous study, we isolated ALF genes from Chinese mitten crab, Eriocheir sinensis. In this study, we optimized the production of a recombinant ALF by expressing E. sinensis ALF genes in Escherichia coli maintained in shake-flasks. In particular, we focused on optimization of both the medium composition and the culture condition. Various medium components were analyzed by the Plackett-Burman design, and two significant screened factors, (NH4)2SO4 and KH2PO4, were further optimized via the central composite design (CCD). Based on the CCD analysis, we investigated the induction start-up time, the isopropylthio-D-galactoside (IPTG) concentration, the post-induction time, and the temperature by response surface methodology. We found that the highest level of ALF fusion protein was achieved in the medium containing 1.89 g/L (NH4)2SO4 and 3.18 g/L KH2PO4, with a cell optical density of 0.8 at 600 nm before induction, an IPTG concentration of 0.5 mmol/L, a post-induction temperature of 32.7°C, and a post-induction time of 4 h. Applying the whole optimization strategy using all optimal factors improved the target protein content from 6.1% (without optimization) to 13.2%. We further applied the optimized medium and conditions in high cell density cultivation, and determined that the soluble target protein constituted 10.5% of the total protein. Our identification of the economic medium composition, optimal culture conditions, and details of the fermentation process should facilitate the potential application of ALF for further research.
机译:抗脂多糖因子(ALF)是从某些水生物种中分离出来的重要抗菌肽。在先前的研究中,我们从中华绒螯蟹中华绒螯蟹中分离了ALF基因。在这项研究中,我们通过在摇瓶中维持的大肠杆菌中表达中华绒螯蟹ALF基因来优化重组ALF的生产。特别是,我们专注于培养基组成和培养条件的优化。通过Plackett-Burman设计分析各种培养基成分,并进一步优化(NH4 )2 SO4 和KH2 PO4 的两个重要筛选因子通过中央复合设计(CCD)。基于CCD分析,我们通过响应面方法研究了诱导启动时间,异丙硫基-D-半乳糖苷(IPTG)浓度,诱导后时间和温度。我们发现,在含有1.89 g / L(NH4 )2 SO4 和3.18 g / L KH2 PO4 的培养基中,ALF融合蛋白水平最高。 sub>,诱导前600 nm的细胞光密度为0.8,IPTG浓度为0.5 mmol / L,诱导后温度为32.7°C,诱导后时间为4 h。使用所有最佳因素应用整个优化策略,可将目标蛋白质含量从6.1%(无优化)提高到13.2%。我们在高细胞密度培养中进一步应用了优化的培养基和条件,并确定可溶性靶蛋白占总蛋白的10.5%。我们对经济培养基组成,最佳培养条件和发酵过程细节的鉴定应有助于ALF在进一步研究中的潜在应用。

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