Vaccine Research and Development Center, National Health Research Institutes, Zhunan, Miaoli County, Taiwan.
Appl Microbiol Biotechnol. 2012 Feb;93(4):1539-52. doi: 10.1007/s00253-011-3516-8. Epub 2011 Aug 6.
Bacterial lipoproteins are crucial antigens for protective immunity against bacterial pathogens. Expression of exogenous lipoproteins in Escherichia coli at high levels is thought to be an extremely difficult endeavor because it frequently results in incomplete or absent lipid modification. Previously, we identified a fusion sequence (D1) from a Neisseria meningitidis lipoprotein that induced a non-lipidated protein, E3 (the domain III of the dengue virus envelope protein), to become lipidated. However, without optimizing the growth conditions, some of the D1-fusion proteins were not lipidated. Here, we report the influence of medium components on the expression of recombinant lipoproteins in E. coli. For high-level expression of mature lipoproteins in the C43 (DE3) strain, M9 medium was better than M63 and the rich medium. Furthermore, we analyzed the influence of other media factors (including nitrogen and carbon sources, phosphate, ferrous ions, calcium, magnesium, and pH) on the levels of lipoprotein expression. The results showed that excess nitrogen sources and phosphate in M9 medium could increase the amount of immature lipoproteins, and glucose was a better carbon source than glycerol for expressing mature lipoproteins. We also found that lipoproteins tended to be completely processed in the alkaline environment, even in the nutrient-rich medium. Additional constructs expressing different immunogens or lipid signal peptides as targets were also utilized, demonstrating that these targets could be expressed as completely mature lipoproteins in the M9 medium but not in the rich medium. Our results provide the useful information for expressing mature exogenous lipoproteins in E. coli.
细菌脂蛋白是针对细菌病原体的保护性免疫的关键抗原。在大肠杆菌中高水平表达外源脂蛋白被认为是一项极其困难的任务,因为它经常导致不完全或不存在脂质修饰。以前,我们从脑膜炎奈瑟菌脂蛋白中鉴定出一个融合序列 (D1),该融合序列可诱导非脂化蛋白 E3(登革热病毒包膜蛋白的结构域 III)发生脂化。然而,如果不优化生长条件,一些 D1 融合蛋白就无法脂化。在这里,我们报告了培养基成分对大肠杆菌中重组脂蛋白表达的影响。为了在 C43 (DE3) 菌株中高水平表达成熟脂蛋白,M9 培养基优于 M63 和丰富培养基。此外,我们分析了其他培养基因素(包括氮源和碳源、磷酸盐、亚铁离子、钙、镁和 pH)对脂蛋白表达水平的影响。结果表明,M9 培养基中的过量氮源和磷酸盐会增加不成熟脂蛋白的数量,而葡萄糖是表达成熟脂蛋白比甘油更好的碳源。我们还发现,在碱性环境中,脂蛋白倾向于完全加工,即使在营养丰富的培养基中也是如此。还利用了表达不同免疫原或脂质信号肽作为靶标的其他构建体,结果表明这些靶标可以在 M9 培养基中完全成熟的脂蛋白表达,但不能在丰富的培养基中表达。我们的研究结果为在大肠杆菌中表达成熟的外源脂蛋白提供了有用的信息。