重组人乳头瘤病毒 52 型 L1 蛋白在养甲酵母 Hansenula polymorpha 中的表达和放大生产

IF 3.5 Q3 Biochemistry, Genetics and Molecular Biology Journal of Genetic Engineering and Biotechnology Pub Date : 2024-02-12 DOI:10.1016/j.jgeb.2023.100342
Sheila Chairunnisa , Apon Zaenal Mustopa , Budiman Bela , Moh Egy Rahman Firdaus , Shasmita Irawan , Rosyida Khusniatul Arifah , Herman Irawan , Maritsa Nurfatwa , Rifqiyah Nur Umami , Nurlaili Ekawati , Ai Hertati , Nurhasni Hasan
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引用次数: 0

摘要

背景人乳头瘤病毒(HPV)疫苗接种是重要的国家疫苗接种计划之一,旨在降低与人乳头瘤病毒感染相关的疾病的发病率,这些疾病继续构成全球健康问题。然而,HPV 疫苗的分配存在很大差异,尤其是在中低收入国家,HPV 疫苗的费用成为了主要障碍。因此,确保提供经济上可行的人乳头瘤病毒疫苗至关重要,必须立即努力提高疫苗生产的成本效益。本研究旨在利用养甲酵母Hansenula polymorpha表达系统开发一种高效的重组HPV 52型L1蛋白生产系统,作为HPV疫苗材料。受 MOX 启动子调控的 pHIPX4 质粒能产生表达目标蛋白的稳定克隆。采用合成培养基 SYN6(10),并控制其参数(如温度、pH 值、进料策略和通气)培养,可产生 0.15 µg/mL 的 HPV 52 型 L1 蛋白,这表明有可能扩大到更高的生产水平。
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Expression and scale-up production of recombinant human papillomavirus type 52 L1 protein in methylotrophic yeast Hansenula polymorpha

Background

Human papillomavirus (HPV) vaccination is one of the crucial national vaccination programs aimed at reducing the prevalence of the diseases associated with HPV infections, which continue to pose a global health concern. However, a significant disparity exists in the distribution of HPV vaccine, particularly in low-middle income countries where the cost of HPV vaccine becomes a major obstacle. Thus, it is essential to ensure the availability of an economically feasible HPV vaccine, necessitating immediate efforts to enhance the cost-effectiveness of vaccine production. This study aimed to develop an efficient production system for the recombinant HPV type 52 L1 protein as HPV vaccine material using methylotrophic yeast Hansenula polymorpha expression system.

Results

This study presents an in-depth examination of the expression and scale-up production of HPV type 52 L1 protein using DASGIP® parallel bioreactor system. The pHIPX4 plasmid, which is regulated by the MOX promoter, generates stable clones that express the target protein. Cultivation employing the synthetic medium SYN6(10) with controlled parameters (e.g. temperature, pH, feeding strategy, and aeration) produces 0.15 µg/mL of HPV type 52 L1 protein, suggesting a possibility for scaling up to a higher production level.

Conclusion

The scale-up production of HPV type 52 L1 protein using Hansenula polymorpha expression system described in this study provides an opportunity for an economical manufacturing platform for the development of the HPV vaccine.

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来源期刊
Journal of Genetic Engineering and Biotechnology
Journal of Genetic Engineering and Biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
5.70
自引率
5.70%
发文量
159
审稿时长
16 weeks
期刊介绍: Journal of genetic engineering and biotechnology is devoted to rapid publication of full-length research papers that leads to significant contribution in advancing knowledge in genetic engineering and biotechnology and provide novel perspectives in this research area. JGEB includes all major themes related to genetic engineering and recombinant DNA. The area of interest of JGEB includes but not restricted to: •Plant genetics •Animal genetics •Bacterial enzymes •Agricultural Biotechnology, •Biochemistry, •Biophysics, •Bioinformatics, •Environmental Biotechnology, •Industrial Biotechnology, •Microbial biotechnology, •Medical Biotechnology, •Bioenergy, Biosafety, •Biosecurity, •Bioethics, •GMOS, •Genomic, •Proteomic JGEB accepts
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