• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于确定性筛选设计方法对DNA疫苗生产进行工艺表征

Process Characterization by Definitive Screening Design Approach on DNA Vaccine Production.

作者信息

Hocharoen Lalintip, Noppiboon Sarawuth, Kitsubun Panit

机构信息

Bioprocess Research and Innovation Centre (BRIC), National Biopharmaceutical Facility (NBF), King Mongkut's University of Technology Thonburi (KMUTT), Bangkok, Thailand.

Biochemical Engineering and System Biology Research Group (IBEG), National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency (NSTDA), Bangkok, Thailand.

出版信息

Front Bioeng Biotechnol. 2020 Oct 15;8:574809. doi: 10.3389/fbioe.2020.574809. eCollection 2020.

DOI:10.3389/fbioe.2020.574809
PMID:33178673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7593689/
Abstract

Plasmid DNA is a vital biological tool for molecular cloning and transgene expression of recombinant proteins; however, decades ago, it has become an exceptionally appealing as a potential biopharmaceutical product as genetic immunization for animal and human use. The demand for large-quantity production of DNA vaccines also increases. Thus, we, herein, presented a systematic approach for process characterization of fed-batch DH5α fermentation producing a porcine DNA vaccine. Design of Experiments (DoE) was employed to determine process parameters that have impacts on a critical quality attribute of the product, which is the active form of plasmid DNA referred as supercoiled plasmid DNA content, as well as the performance attributes, which are volumetric yield and specific yield from fermentation. The parameters of interest were temperature, pH, dissolved oxygen, cultivation time, and feed rate. Using the definitive-screening design, there were 16 runs, including 3 additional center points to create the predictive model, which then was used to simulate the operational ranges for capability analysis.

摘要

质粒DNA是分子克隆和重组蛋白转基因表达的重要生物工具;然而,几十年前,作为一种潜在的生物制药产品,用于动物和人类的基因免疫,它就已经变得极具吸引力。对DNA疫苗大量生产的需求也在增加。因此,我们在此提出了一种系统方法,用于表征生产猪DNA疫苗的分批补料DH5α发酵过程。采用实验设计(DoE)来确定对产品关键质量属性(即称为超螺旋质粒DNA含量的质粒DNA活性形式)以及性能属性(即发酵的体积产量和比产量)有影响的工艺参数。感兴趣的参数是温度、pH值、溶解氧、培养时间和进料速率。使用确定性筛选设计,进行了16次运行,包括3个额外的中心点以创建预测模型,然后该模型用于模拟操作范围以进行能力分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a63/7593689/f4666d9da445/fbioe-08-574809-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a63/7593689/759befd24fa5/fbioe-08-574809-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a63/7593689/c7150d3e8c12/fbioe-08-574809-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a63/7593689/9d8022151267/fbioe-08-574809-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a63/7593689/f4666d9da445/fbioe-08-574809-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a63/7593689/759befd24fa5/fbioe-08-574809-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a63/7593689/c7150d3e8c12/fbioe-08-574809-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a63/7593689/9d8022151267/fbioe-08-574809-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a63/7593689/f4666d9da445/fbioe-08-574809-g004.jpg

相似文献

1
Process Characterization by Definitive Screening Design Approach on DNA Vaccine Production.基于确定性筛选设计方法对DNA疫苗生产进行工艺表征
Front Bioeng Biotechnol. 2020 Oct 15;8:574809. doi: 10.3389/fbioe.2020.574809. eCollection 2020.
2
Automated fed-batch fermentation with feed-back controls based on dissolved oxygen (DO) and pH for production of DNA vaccines.基于溶解氧(DO)和pH值反馈控制的DNA疫苗生产自动补料分批发酵。
J Ind Microbiol Biotechnol. 1997 Jan;18(1):43-8. doi: 10.1038/sj.jim.2900355.
3
Toward QbD Process Understanding on DNA Vaccine Purification Using Design of Experiment.通过实验设计实现对DNA疫苗纯化的质量源于设计过程理解
Front Bioeng Biotechnol. 2021 May 12;9:657201. doi: 10.3389/fbioe.2021.657201. eCollection 2021.
4
[High-cell density cultivation of recombinant Escherichia coli for production of TRAIL by using a 2-stage feeding strategy].[采用两阶段补料策略进行重组大肠杆菌的高密度培养以生产肿瘤坏死因子相关凋亡诱导配体(TRAIL)]
Sheng Wu Gong Cheng Xue Bao. 2004 May;20(3):408-13.
5
Cultivation of E. coli carrying a plasmid-based Measles vaccine construct (4.2 kbp pcDNA3F) employing medium optimisation and pH-temperature induction techniques.采用培养基优化和 pH 值-温度诱导技术培养携带基于质粒的麻疹疫苗构建体(4.2 kbp pcDNA3F)的大肠杆菌。
Microb Cell Fact. 2011 Mar 5;10:16. doi: 10.1186/1475-2859-10-16.
6
Characterization of a Saccharomyces cerevisiae fermentation process for production of a therapeutic recombinant protein using a multivariate Bayesian approach.使用多元贝叶斯方法对酿酒酵母发酵生产治疗性重组蛋白过程的表征。
Biotechnol Prog. 2016 May;32(3):799-812. doi: 10.1002/btpr.2264. Epub 2016 Apr 20.
7
Upstream development of Escherichia coli fermentation process with PhoA promoter using design of experiments (DoE).利用设计实验(DoE)对带有 PhoA 启动子的大肠杆菌发酵过程进行上游开发。
J Ind Microbiol Biotechnol. 2020 Oct;47(9-10):789-799. doi: 10.1007/s10295-020-02302-7. Epub 2020 Aug 25.
8
Plasmid DNA production with Escherichia coli GALG20, a pgi-gene knockout strain: fermentation strategies and impact on downstream processing.利用大肠杆菌GALG20(一种pgi基因敲除菌株)生产质粒DNA:发酵策略及其对下游加工的影响。
J Biotechnol. 2014 Sep 30;186:119-27. doi: 10.1016/j.jbiotec.2014.06.008. Epub 2014 Jul 1.
9
The role of amino acids in the amplification and quality of DNA vectors for industrial applications.氨基酸在工业应用中扩增和提高 DNA 载体质量方面的作用。
Biotechnol Prog. 2019 Nov;35(6):e2883. doi: 10.1002/btpr.2883. Epub 2019 Aug 10.
10
Enhancement of plasmid DNA yields during fed-batch culture of a fruR-knockout Escherichia coli strain.在fruR基因敲除的大肠杆菌菌株分批补料培养过程中提高质粒DNA产量。
Biotechnol Appl Biochem. 2009 Jan;52(Pt 1):53-9. doi: 10.1042/BA20070260.

引用本文的文献

1
Optimization of an Ultra-Sonication Extraction Method for Major Compounds Found in Using Design of Experiment.采用实验设计优化超声提取法提取中的主要化合物。
Molecules. 2022 Apr 29;27(9):2836. doi: 10.3390/molecules27092836.
2
Toward QbD Process Understanding on DNA Vaccine Purification Using Design of Experiment.通过实验设计实现对DNA疫苗纯化的质量源于设计过程理解
Front Bioeng Biotechnol. 2021 May 12;9:657201. doi: 10.3389/fbioe.2021.657201. eCollection 2021.

本文引用的文献

1
Therapeutic DNA Vaccines for Human Papillomavirus and Associated Diseases.治疗性 HPV 疫苗及其相关疾病的 DNA 疫苗。
Hum Gene Ther. 2018 Sep;29(9):971-996. doi: 10.1089/hum.2017.197. Epub 2018 Mar 16.
2
Model selection for dynamical systems via sparse regression and information criteria.通过稀疏回归和信息准则进行动态系统的模型选择
Proc Math Phys Eng Sci. 2017 Aug;473(2204):20170009. doi: 10.1098/rspa.2017.0009. Epub 2017 Aug 30.
3
Efficient high-throughput biological process characterization: Definitive screening design with the ambr250 bioreactor system.
高效高通量生物过程表征:使用安捷伦250生物反应器系统的析因筛选设计
Biotechnol Prog. 2015 Sep-Oct;31(5):1388-95. doi: 10.1002/btpr.2142. Epub 2015 Jul 15.
4
Efficient biological process characterization by definitive-screening designs: the formaldehyde treatment of a therapeutic protein as a case study.通过明确筛选设计进行高效的生物工艺表征:以治疗性蛋白的甲醛处理为例。
Biotechnol Lett. 2013 Mar;35(3):323-9. doi: 10.1007/s10529-012-1089-y. Epub 2012 Nov 18.
5
NIH Image to ImageJ: 25 years of image analysis.NIH 图像到 ImageJ:25 年的图像分析。
Nat Methods. 2012 Jul;9(7):671-5. doi: 10.1038/nmeth.2089.
6
DNA vaccines for targeting bacterial infections.用于靶向细菌感染的 DNA 疫苗。
Expert Rev Vaccines. 2010 Jul;9(7):747-63. doi: 10.1586/erv.10.57.
7
Defining process design space for monoclonal antibody cell culture.定义单克隆抗体细胞培养的工艺设计空间。
Biotechnol Bioeng. 2010 Aug 15;106(6):894-905. doi: 10.1002/bit.22764.
8
Clinical and immunological responses in metastatic melanoma patients vaccinated with a high-dose poly-epitope vaccine.高剂量多表位疫苗接种转移性黑色素瘤患者的临床和免疫反应。
Cancer Immunol Immunother. 2010 Jun;59(6):863-73. doi: 10.1007/s00262-009-0811-7. Epub 2009 Dec 31.
9
Bioprocess optimization using design-of-experiments methodology.使用实验设计方法进行生物过程优化。
Biotechnol Prog. 2008 Nov-Dec;24(6):1191-203. doi: 10.1002/btpr.67.
10
Growth hormone-releasing hormone plasmid treatment by electroporation decreases offspring mortality over three pregnancies.通过电穿孔法进行生长激素释放激素质粒治疗可降低三次妊娠子代的死亡率。
Mol Ther. 2008 Nov;16(11):1891-7. doi: 10.1038/mt.2008.178. Epub 2008 Aug 19.