极端微生物基因组编辑与CRISPR/Cas系统及其应用

S. Panicker
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引用次数: 0

摘要

极端微生物将成为下一代工业生物技术(NGIB)的选择,因为它们已知具有抗污染能力,但对它们的基因组进行工程设计一直是一项困难且耗时的任务。因此可以采用CRISPR /Cas (clustered regularly interspaced short palindromic repeat and CRISPR associated proteins)系统。编辑了一种工业上重要的嗜盐菌(即盐单胞菌)的基因组,以研究四种不同基因对葡萄糖分解和聚(3-羟基丁酸酯-co-3-羟基戊酸酯)生产的综合影响。这种编辑使3HV增加了16倍,并且由CRIPR/Cas系统产生的突变体在合成PHBV方面效果显著。不幸的是,这个系统并不总是有效,特别是在嗜极微生物中,因为Cas9或Cpf1来自嗜中温细菌。因此,可以选择使用内源性CRISPR/Cas系统来编辑这些生物的基因组。此次对极端微生物进行基因组编辑,将为开发下一代工业生物技术(NGIB)打开大门。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genome Editing and CRISPR/Cas System of Extremophiles and Its Applications
Extremophiles will be the choice of next generation industrial biotechnology (NGIB) as they are known to be contaminant resistant, but engineering their genomes has always been difficult and time consuming task. CRIPR/Cas (clustered regularly interspaced short palindromic repeat and CRISPR associated proteins) system can be employed for this reason. The genome of an industrially important halophile (i.e., Halomonas) was edited to study a combined effect of four different genes on glucose breakdown and production of poly (3-hydroxybutyrate-co-3-hydroxyvalerate). This editing has resulted in 16-fold increase of 3HV, and the mutants generated by CRIPR/Cas system were significantly effective in synthesizing PHBV. Unfortunately, this system does not always work, specifically in extremophilic microorganisms because Cas9 or Cpf1 are from mesophilic bacteria. Therefore, alternatively, the endogenous CRISPR/Cas system is used for editing the genomes of such organisms. This genome editing of extremophiles will open the doors for developing next generation industrial biotechnology (NGIB).
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