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A genetic toolbox for metabolic engineering of Issatchenkia orientalis

机译:伊斯坦特尼奥奥斯塔利斯代谢工程的遗传工具箱

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摘要

The nonconventional yeast Issatchenkia orientalis can grow under highly acidic conditions and has been explored for production of various organic acids. However, its broader application is hampered by the lack of efficient genetic tools to enable sophisticated metabolic manipulations. We recently constructed an episomal plasmid based on the autonomously replicating sequence (ARS) from Saccharomyces cerevisiae (ScARS) in I. orientalis and developed a CRISPR/Cas9 system for multiplexed gene deletions. Here we report three additional genetic tools including: (1) identification of a 0.8 kb centromere-like (CEN-L) sequence from the I. orientalis genome by using bioinformatics and functional screening; (2) discovery and characterization of a set of constitutive promoters and terminators under different culture conditions by using RNA-Seq analysis and a fluorescent reporter; and (3) development of a rapid and efficient in vivo DNA assembly method in I. orientalis, which exhibited similar to 100% fidelity when assembling a 7 kb-plasmid from seven DNA fragments ranging from 0.7 kb to 1.7 kb. As proof of concept, we used these genetic tools to rapidly construct a functional xylose utilization pathway in I. orientalis.
机译:非共聚的酵母isatchenkia Orientalis可以在高度酸性条件下生长,并已探索生产各种有机酸。然而,由于缺乏有效的遗传工具,因此更广泛的应用程序阻碍了能够实现复杂的代谢操纵。我们最近基于I.Istidalis的自主复制序列(ARS)构建了一种基础质粒,其中I.iostalis中的酿酒酵母(Scars),并为多重基因缺失开发了一种CRISPR / CAS9系统。在这里,我们报告了三种额外的遗传工具,包括:(1)通过使用生物信息学和功能性筛选,从I. Orientalis基因组中鉴定0.8kb焦粒状(CEN-L)序列; (2)通过使用RNA-SEQ分析和荧光报告者在不同培养条件下发现和表征一组组成型启动子和终止子; (3)在I.irentalis中的体内DNA组装方法中的快速高效的发展,当从0.7kb至1.7kb的七个DNA片段组装7kb-质粒时,它表现出类似于100%的保真度。作为概念证明,我们使用这些遗传工具在I. Orientalis中迅速构建功能性木糖利用途径。

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