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超越理性生物传感器引导的 100 株独立进化细菌株变体的分离及其基因组的比较分析。

Beyond rational-biosensor-guided isolation of 100 independently evolved bacterial strain variants and comparative analysis of their genomes.

机构信息

Institute of Bio- and Geosciences, Forschungszentrum Jülich, IBG-1: Biotechnology, 52425, Jülich, Germany.

Department I of Internal Medicine, University of Cologne, 50937, Cologne, Germany.

出版信息

BMC Biol. 2023 Sep 4;21(1):183. doi: 10.1186/s12915-023-01688-x.

Abstract

BACKGROUND

In contrast to modern rational metabolic engineering, classical strain development strongly relies on random mutagenesis and screening for the desired production phenotype. Nowadays, with the availability of biosensor-based FACS screening strategies, these random approaches are coming back into fashion. In this study, we employ this technology in combination with comparative genome analyses to identify novel mutations contributing to product formation in the genome of a Corynebacterium glutamicum L-histidine producer. Since all known genetic targets contributing to L-histidine production have been already rationally engineered in this strain, identification of novel beneficial mutations can be regarded as challenging, as they might not be intuitively linkable to L-histidine biosynthesis.

RESULTS

In order to identify 100 improved strain variants that had each arisen independently, we performed > 600 chemical mutagenesis experiments, > 200 biosensor-based FACS screenings, isolated > 50,000 variants with increased fluorescence, and characterized > 4500 variants with regard to biomass formation and L-histidine production. Based on comparative genome analyses of these 100 variants accumulating 10-80% more L-histidine, we discovered several beneficial mutations. Combination of selected genetic modifications allowed for the construction of a strain variant characterized by a doubled L-histidine titer (29 mM) and product yield (0.13 C-mol C-mol) in comparison to the starting variant.

CONCLUSIONS

This study may serve as a blueprint for the identification of novel beneficial mutations in microbial producers in a more systematic manner. This way, also previously unexplored genes or genes with previously unknown contribution to the respective production phenotype can be identified. We believe that this technology has a great potential to push industrial production strains towards maximum performance.

摘要

背景

与现代理性代谢工程相反,经典的菌株开发强烈依赖于随机诱变和筛选所需的生产表型。如今,随着基于生物传感器的 FACS 筛选策略的可用性,这些随机方法又重新流行起来。在这项研究中,我们结合比较基因组分析来识别导致 Corynebacterium glutamicum L-组氨酸生产菌株基因组中产物形成的新突变。由于该菌株中所有已知有助于 L-组氨酸生产的遗传靶标都已经被理性工程化,因此可以认为识别新的有益突变具有挑战性,因为它们可能与 L-组氨酸生物合成没有直观的联系。

结果

为了鉴定 100 个独立出现的改良菌株变体,我们进行了超过 600 次化学诱变实验、超过 200 次基于生物传感器的 FACS 筛选,分离出超过 50,000 个荧光增强的变体,并对超过 4500 个变体的生物量形成和 L-组氨酸生产进行了表征。基于对这 100 个累积 L-组氨酸 10-80%的变体的比较基因组分析,我们发现了一些有益的突变。通过组合选择的遗传修饰,构建了一个菌株变体,与起始变体相比,L-组氨酸产量提高了一倍(29 mM),产物产率提高了(0.13 C-mol C-mol)。

结论

这项研究可以为更系统地鉴定微生物生产菌株中的新有益突变提供蓝图。这样,也可以鉴定以前未探索的基因或以前未知的对相应生产表型有贡献的基因。我们相信这项技术具有将工业生产菌株推向最高性能的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7632/10478468/053ba63ebde7/12915_2023_1688_Fig1_HTML.jpg

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