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通过膜工程和两阶段培养对代谢工程改造的MG1655进行靛蓝生产强化

Enhancement of Indigo Production by a Metabolically Engineered MG1655 Using Membrane Engineering and Two-Stage Cultivation.

作者信息

Hu Heng, Li Zeyu, Chen Roulin, Lu Rui, Zhou Dingjie, Zhu Yingying, Mu Wanmeng

机构信息

State Key Laboratory of Food Science and Resources, School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu 214122, China.

Jiangsu Huacheng Biotechnology Co., Ltd., Wuxi, Jiangsu 214122, China.

出版信息

J Agric Food Chem. 2025 Apr 23;73(16):9782-9792. doi: 10.1021/acs.jafc.5c01400. Epub 2025 Apr 12.

Abstract

Indigo, a natural blue pigment extensively used in the food and textile industries, faces sustainability challenges due to toxic chemicals in its industrial synthesis. In this study, an efficient MG1655 system was developed for indigo biosynthesis. The strain was engineered by genomic integration and plasmid-based expression of flavin-containing monooxygenase (MaFMO) and endogenous tryptophanase (TnaA). To optimize metabolic flux toward indigo production, key competitive pathway genes were deleted, and membrane engineering genes were introduced to alleviate toxicity and improve product secretion. A two-stage fermentation strategy with controlled feeding of the tryptophan substrate and surfactants further optimized indigo production. The integrated approach achieved a maximum indigo titer of 3.9 g/L in 5 L of fed-batch fermentation. This study highlights the successful integration of genetic engineering and fermentation strategies to enhance microbial indigo production, offering a green alternative to chemical synthesis with potential applications in food-grade colorant production and the textile industries.

摘要

靛蓝是一种广泛应用于食品和纺织工业的天然蓝色颜料,由于其工业合成过程中使用有毒化学物质,面临可持续性挑战。在本研究中,开发了一种高效的MG1655系统用于靛蓝生物合成。该菌株通过基因组整合以及基于质粒表达含黄素单加氧酶(MaFMO)和内源性色氨酸酶(TnaA)进行工程改造。为了优化通向靛蓝生产的代谢通量,关键竞争途径基因被删除,并且引入了膜工程基因以减轻毒性并改善产物分泌。采用控制色氨酸底物和表面活性剂补料的两阶段发酵策略进一步优化了靛蓝生产。该综合方法在5 L补料分批发酵中实现了3.9 g/L的最大靛蓝滴度。本研究突出了基因工程与发酵策略成功整合以提高微生物靛蓝产量,为化学合成提供了一种绿色替代方案,在食品级色素生产和纺织工业中具有潜在应用。

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