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优化多拷贝染色体整合以获得稳定的高性能菌株。

Optimizing multicopy chromosomal integration for stable high-performing strains.

机构信息

School of Food Science and Pharmaceutical Engineering, Nanjing Normal University, Nanjing, China.

Research Institute of Intelligent Computing, Zhejiang Lab, Hangzhou, China.

出版信息

Nat Chem Biol. 2024 Dec;20(12):1670-1679. doi: 10.1038/s41589-024-01650-0. Epub 2024 Jun 10.

Abstract

The copy number of genes in chromosomes can be modified by chromosomal integration to construct efficient microbial cell factories but the resulting genetic systems are prone to failure or instability from triggering homologous recombination in repetitive DNA sequences. Finding the optimal copy number of each gene in a pathway is also time and labor intensive. To overcome these challenges, we applied a multiple nonrepetitive coding sequence calculator that generates sets of coding DNA sequence (CDS) variants. A machine learning method was developed to calculate the optimal copy number combination of genes in a pathway. We obtained an engineered Yarrowia lipolytica strain for eicosapentaenoic acid biosynthesis in 6 months, producing the highest titer of 27.5 g l in a 50-liter bioreactor. Moreover, the lycopene production in Escherichia coli was also greatly improved. Importantly, all engineered strains of Y. lipolytica, E. coli and Saccharomyces cerevisiae constructed with nonrepetitive CDSs maintained genetic stability.

摘要

染色体上基因的拷贝数可以通过染色体整合来修饰,从而构建高效的微生物细胞工厂,但由此产生的遗传系统容易因重复 DNA 序列的同源重组而失效或不稳定。找到途径中每个基因的最佳拷贝数也需要大量的时间和精力。为了克服这些挑战,我们应用了一种多重非重复编码序列计算器,该计算器可以生成编码 DNA 序列(CDS)变体集。开发了一种机器学习方法来计算途径中基因的最佳拷贝数组合。我们在 6 个月内获得了用于二十碳五烯酸生物合成的工程化解脂耶氏酵母菌株,在 50 升生物反应器中产生了 27.5g/L 的最高滴度。此外,大肠杆菌中的番茄红素产量也得到了极大提高。重要的是,用非重复 CDS 构建的所有工程化解脂耶氏酵母、大肠杆菌和酿酒酵母菌株都保持了遗传稳定性。

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