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通过组合代谢工程改造大肠杆菌以从未经处理的甘蔗糖蜜中高效生产L-苏氨酸。

Combinatorial metabolic engineering of Escherichia coli to efficiently produce L-threonine from untreated cane molasses.

作者信息

Jin Xin, Wang Sumeng, Gao Yaping, Qi Qingsheng, Liang Quanfeng

机构信息

State Key Laboratory of Microbial Technology, Shandong University, Qingdao 266237, China.

Qingdao Agricultural University, Qingdao 266100, China.

出版信息

Bioresour Technol. 2025 Mar;419:132058. doi: 10.1016/j.biortech.2025.132058. Epub 2025 Jan 10.

Abstract

BACKGROUND

The industrial production of L-threonine faces challenges because of high production costs, especially those of substrates, meaning new production methods are needed.

METHODS

Fur, a new global transcription factor related to L-threonine biosynthesis, was discovered in this study. Multidimensional regulation combined with global transcriptional machinery engineering was used to modify an Escherichia coli strain.

RESULTS

The most efficient mutant showed high titer (154.2 g/L), productivity (2.14 g/L/h), and yield (0.76 g/g) of L-threonine production. These three parameters indicated that these engineering strategies were economically feasible for developing high L-threonine-producing strains. We integrated the sucrose utilization gene cluster into the genome to further reduce the production cost of L-threonine. Using untreated cane molasses as the substrate, L-threonine was successfully produced with a titer of 92.46 g/L and a cost reduction of 48 %.

CONCLUSION

This research offers advantages for industrial scalability, and the resulting engineered bacterium holds significant industrial application potential.

摘要

背景

由于生产成本高昂,尤其是底物成本,L-苏氨酸的工业生产面临挑战,这意味着需要新的生产方法。

方法

本研究发现了一种与L-苏氨酸生物合成相关的新型全局转录因子Fur。采用多维调控与全局转录机器工程相结合的方法对大肠杆菌菌株进行改造。

结果

最有效的突变体显示出L-苏氨酸生产的高滴度(154.2 g/L)、生产率(2.14 g/L/h)和产量(0.76 g/g)。这三个参数表明,这些工程策略对于开发高产L-苏氨酸菌株在经济上是可行的。我们将蔗糖利用基因簇整合到基因组中,以进一步降低L-苏氨酸的生产成本。以未经处理的甘蔗糖蜜为底物,成功生产出L-苏氨酸,滴度为92.46 g/L,成本降低了48%。

结论

本研究为工业规模化提供了优势,所得工程菌具有显著的工业应用潜力。

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