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释放绿色生物制造潜力:利用T7整合过表达系统实现卓越的异源基因表达 于…… (原文此处不完整)

Unlocking Green Biomanufacturing Potential: Superior Heterologous Gene Expression with a T7 Integration Overexpression System in .

作者信息

Yao Zhi-Yuan, Yu Min-Jun, Li Qu-Quan, Gong Jin-Song, Zhang Peng, Jiang Jia-Yu, Su Chang, Xu Guoqiang, Jia Bing-Yi, Xu Zheng-Hong, Shi Jin-Song

机构信息

Key Laboratory of Carbohydrate Chemistry and Biotechnology of Ministry of Education, School of Life Sciences and Health Engineering, Jiangnan University, Wuxi 214122, PR China.

National Engineering Research Center for Cereal Fermentation and Food Biomanufacturing, School of Biotechnology, Jiangnan University, Wuxi 214122, PR China.

出版信息

ACS Synth Biol. 2024 Dec 24. doi: 10.1021/acssynbio.4c00694.

DOI:10.1021/acssynbio.4c00694
PMID:39718905
Abstract

Industrial biotechnology employs cells for producing valuable products and serving as biocatalysts sustainably, addressing resource, energy, and environmental issues. is a preferred host for creating microbial chassis cells and producing industrial enzymes and functional nutritional products. In this study, a dual-module T7 integration expression system in was established. The first module, driven by the T7 RNA polymerase, was integrated into the genome via the CRISPR/Cas9 system. Another module responsible for expression control was systematically integrated into 28 discrete chromosomal loci and the impact of different genomic positions on gene expression was explored, resulting in a high-intensity integrated expression system. Furthermore, by modifying the LacI repressor factor for biological regulation, we achieved a strong expression intensity without the inducer addition. This system was successfully used to express phospholipase D and hyaluronic acid lyase, resulting in extracellular enzyme activities of 339.12 U/mL and 2.60 × 10 U/mL, respectively. Additionally, by exclusively targeting the HA gene cluster for expression, a production yield of 6.86 g/L was achieved on a 5 L fermentation scale. The system eliminates the use of antibiotics and inducers, offering a controllable, efficient, and promising gene expression regulation tool in , enhancing its potential for biomanufacturing applications.

摘要

工业生物技术利用细胞可持续地生产有价值的产品并作为生物催化剂,解决资源、能源和环境问题。[具体生物名称]是创建微生物底盘细胞以及生产工业酶和功能性营养产品的首选宿主。在本研究中,在[具体生物名称]中建立了一个双模块T7整合表达系统。第一个模块由T7 RNA聚合酶驱动,通过CRISPR/Cas9系统整合到基因组中。另一个负责表达控制的模块被系统地整合到28个离散的染色体位点,并探索了不同基因组位置对基因表达的影响,从而得到一个高强度的整合表达系统。此外,通过修饰用于生物调控的LacI阻遏因子,我们在不添加诱导剂的情况下实现了较强的表达强度。该系统成功用于表达磷脂酶D和透明质酸裂解酶,胞外酶活性分别达到339.12 U/mL和2.60×10 U/mL。此外,通过专门靶向HA基因簇进行表达,在5 L发酵规模下实现了6.86 g/L的产量。该系统无需使用抗生素和诱导剂,为[具体生物名称]提供了一种可控、高效且有前景的基因表达调控工具,增强了其在生物制造应用中的潜力。

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