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朝向细菌磁小体生物合成的“底盘”:通过多次缺失对食烷菌属进行基因组简化。

Towards a 'chassis' for bacterial magnetosome biosynthesis: genome streamlining of Magnetospirillum gryphiswaldense by multiple deletions.

机构信息

Department of Microbiology, University of Bayreuth, Bayreuth, Germany.

Institute of Bioengineering, Research Center of Biotechnology of the Russian Academy of Sciences, Moscow, Russia.

出版信息

Microb Cell Fact. 2021 Feb 4;20(1):35. doi: 10.1186/s12934-021-01517-2.

Abstract

BACKGROUND

Because of its tractability and straightforward cultivation, the magnetic bacterium Magnetospirillum gryphiswaldense has emerged as a model for the analysis of magnetosome biosynthesis and bioproduction. However, its future use as platform for synthetic biology and biotechnology will require methods for large-scale genome editing and streamlining.

RESULTS

We established an approach for combinatory genome reduction and generated a library of strains in which up to 16 regions including large gene clusters, mobile genetic elements and phage-related genes were sequentially removed, equivalent to ~ 227.6 kb and nearly 5.5% of the genome. Finally, the fragmented genomic magnetosome island was replaced by a compact cassette comprising all key magnetosome biosynthetic gene clusters. The prospective 'chassis' revealed wild type-like cell growth and magnetosome biosynthesis under optimal conditions, as well as slightly improved resilience and increased genetic stability.

CONCLUSION

We provide first proof-of-principle for the feasibility of multiple genome reduction and large-scale engineering of magnetotactic bacteria. The library of deletions will be valuable for turning M. gryphiswaldense into a microbial cell factory for synthetic biology and production of magnetic nanoparticles.

摘要

背景

由于其易于处理和直接的培养,磁性细菌 Magnetospirillum gryphiswaldense 已成为分析磁小体生物合成和生物生产的模型。然而,要将其未来用作合成生物学和生物技术的平台,就需要大规模基因组编辑和简化的方法。

结果

我们建立了一种组合基因组减少的方法,并生成了一个菌株文库,其中多达 16 个区域(包括大基因簇、移动遗传元件和噬菌体相关基因)依次被删除,相当于约 227.6 kb 和近基因组的 5.5%。最后,碎片化的基因组磁小体岛被一个包含所有关键磁小体生物合成基因簇的紧凑型盒取代。在最佳条件下,有前景的“底盘”显示出与野生型相似的细胞生长和磁小体生物合成,以及略高的弹性和更高的遗传稳定性。

结论

我们首次证明了对趋磁细菌进行多次基因组减少和大规模工程改造的可行性。缺失文库对于将 M. gryphiswaldense 转化为用于合成生物学和磁性纳米颗粒生产的微生物细胞工厂将非常有价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1c9/7860042/58b44d2ee235/12934_2021_1517_Fig1_HTML.jpg

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