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基于LuxI/R元件的新型枯草芽孢杆菌自诱导细胞外表达系统的开发与构建。

Development and construction of a novel Bacillus subtilis autoinducible extracellular expression system based on a LuxI/R device.

作者信息

Wang Bin, Wang Keyi, Zhao Xiuyue, Fang Zemin, Zhao Yanyan, Fang Yulu, Xiao Yazhong, Yao Dongbang

机构信息

School of Life Sciences, Anhui University, Hefei, 230601, China.

Anhui Key Laboratory of Biocatalysis and Modern Biomanufacturing, Hefei, 230601, China.

出版信息

Microb Cell Fact. 2025 Apr 19;24(1):86. doi: 10.1186/s12934-025-02719-8.

Abstract

BACKGROUND

Microbial chassis expression systems are valuable tools in biotechnology and synthetic biology, and Bacillus subtilis is an important industrial microbial chassis. Quorum sensing (QS)-based dynamic regulation is widely used to automatically activate gene expression in response to changes in cell density. The main bottleneck currently limiting the use of exogenous QS systems in B. subtilis for efficient autoinducible extracellular expression of recombinant proteins is their low level of autoinducible expression.

RESULTS

A novel B. subtilis autoinducible extracellular expression system based on the LuxI/R-type QS system (lux system) of Vibrio fischeri was developed in which the autoinducible expression of the lux system was enhanced by engineering the sensing module and response module promoters. By engineering the sensing module promoter SP core region (- 10 and - 35 elements) and critical region (UP and spacer elements), and the response module promoter RP core region and lux box copy number in the original LuxI/R device (S0-R0), the high-expression Sc-R2 construct was obtained. After shake flask and 3-L fermenter fermentation, the extracellular amylase activity obtained with Sc-R2 was 2.7- and 3.1-fold greater, respectively, than that obtained with the well-characterized promoter P. Sc-R2 achieved 2.6-fold greater extracellular activity than S0-R0 when either levansucrase or invertase was used as a reporter protein. Overall, the B. subtilis autoinducible extracellular expression system developed in this study showed good generalizability and application potential for industrial-scale fermentation.

CONCLUSIONS

To our knowledge, this is the first study to report enhanced autoinducible expression of the lux system in B. subtilis by engineering the sensing module promoter SP sequence and the lux box copy number of the response module promoter RP. This study further expands the application potential of the B. subtilis expression system in synthetic biology.

摘要

背景

微生物底盘表达系统是生物技术和合成生物学中的重要工具,枯草芽孢杆菌是一种重要的工业微生物底盘。基于群体感应(QS)的动态调控被广泛用于根据细胞密度变化自动激活基因表达。目前限制在枯草芽孢杆菌中使用外源QS系统进行重组蛋白高效自诱导细胞外表达的主要瓶颈是其自诱导表达水平较低。

结果

开发了一种基于费氏弧菌LuxI/R型QS系统(lux系统)的新型枯草芽孢杆菌自诱导细胞外表达系统,其中通过对感应模块和响应模块启动子进行工程改造来增强lux系统的自诱导表达。通过对原始LuxI/R装置(S0-R0)中的感应模块启动子SP核心区域(-10和-35元件)和关键区域(UP和间隔元件)以及响应模块启动子RP核心区域和lux框拷贝数进行工程改造,获得了高表达的Sc-R2构建体。经过摇瓶和3-L发酵罐发酵后,Sc-R2获得的细胞外淀粉酶活性分别比具有良好表征的启动子P获得的活性高2.7倍和3.1倍。当使用蔗糖酶或转化酶作为报告蛋白时,Sc-R2的细胞外活性比S0-R0高2.6倍。总体而言,本研究开发的枯草芽孢杆菌自诱导细胞外表达系统在工业规模发酵中显示出良好的通用性和应用潜力。

结论

据我们所知,这是第一项通过对感应模块启动子SP序列和响应模块启动子RP的lux框拷贝数进行工程改造来报道枯草芽孢杆菌中lux系统自诱导表达增强的研究。本研究进一步扩展了枯草芽孢杆菌表达系统在合成生物学中的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8645/12008979/d997d7cae797/12934_2025_2719_Fig1_HTML.jpg

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