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平衡EL222剂量与光照可改善法夫酵母中蛋白质生产的光遗传学诱导。

Balancing Doses of EL222 and Light Improves Optogenetic Induction of Protein Production in Komagataella phaffii.

作者信息

Hoffman Shannon M, Espinel-Ríos Sebastián, Kwartler Sarah K, Lalwani Makoto A, Avalos José L

机构信息

Department of Chemical and Biological Engineering, Hoyt Laboratory, Princeton University, Princeton, New Jersey, USA.

Department of Molecular Biology, Princeton University, Princeton, New Jersey, USA.

出版信息

Biotechnol Bioeng. 2025 Sep;122(9):2478-2498. doi: 10.1002/bit.29027. Epub 2025 May 24.

Abstract

Komagataella phaffii, also known as Pichia pastoris, is a powerful host for recombinant protein production, in part due to its exceptionally strong and tightly controlled P promoter. Most K. phaffii bioprocesses for recombinant protein production rely on P to achieve dynamic control in two-phase processes. Cells are first grown under conditions that repress P (growth phase), followed by methanol-induced recombinant protein expression (production phase). In this study, we propose a methanol-free approach for dynamic metabolic control in K. phaffii using optogenetics, which can help enhance input tunability and flexibility in process optimization and control. The light-responsive transcription factor EL222 from Erythrobacter litoralis is used to regulate protein production from the P promoter in K. phaffii with blue light. We used two system designs to explore the advantages and disadvantages of coupling or decoupling EL222 integration with that of the gene of interest. We investigate the relationship between EL222 gene copy number and light dosage to improve production efficiency for intracellular and secreted proteins. Experiments in lab-scale bioreactors demonstrate the feasibility of the outlined optogenetic systems as potential alternatives to conventional methanol-inducible bioprocesses using K. phaffii.

摘要

毕赤酵母(Komagataella phaffii),也被称为巴斯德毕赤酵母(Pichia pastoris),是用于重组蛋白生产的强大宿主,部分原因在于其异常强大且受到严格调控的P启动子。大多数用于重组蛋白生产的毕赤酵母生物过程依赖P启动子在两相过程中实现动态控制。细胞首先在抑制P启动子的条件下生长(生长阶段),随后通过甲醇诱导重组蛋白表达(生产阶段)。在本研究中,我们提出了一种利用光遗传学在毕赤酵母中进行无甲醇动态代谢控制的方法,这有助于提高过程优化和控制中的输入可调性和灵活性。来自嗜盐红细菌(Erythrobacter litoralis)的光响应转录因子EL222用于通过蓝光调节毕赤酵母中P启动子的蛋白生产。我们使用了两种系统设计来探索EL222整合与目的基因整合耦合或解耦的优缺点。我们研究了EL222基因拷贝数与光剂量之间的关系,以提高细胞内和分泌蛋白的生产效率。在实验室规模生物反应器中的实验证明了所概述的光遗传学系统作为使用毕赤酵母的传统甲醇诱导生物过程潜在替代方案的可行性。

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