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Genetic Manipulation of a Lipolytic Yeast Candida aaseri SH14 Using CRISPR-Cas9 System

机译:使用CRISPR-CAS9系统脂溶性酵母Candida Aaseri SH14的遗传操作

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摘要

A lipolytic yeast Candida aaseri SH14 that can utilise long-chain fatty acids as the sole carbon source was isolated from oil palm compost. To develop this strain as a platform yeast for the production of bio-based chemicals from renewable plant oils, a genetic manipulation system using CRISPR-Cas9 was developed. Episomal vectors for expression of Cas9 and sgRNA were constructed using an autonomously replicating sequence isolated from C. aaseri SH14. This system guaranteed temporal expression of Cas9 for genetic manipulation and rapid curing of the vector from transformed strains. A β-oxidation mutant was directly constructed by simultaneous disruption of six copies of acyl-CoA oxidases genes (AOX2, AOX4 and AOX5) in diploid cells using a single sgRNA with 70% efficiency and the Cas9 vector was efficiently removed. Blocking of β-oxidation in the triple AOX mutant was confirmed by the accumulation of dodecanedioic acid from dodecane. Targeted integration of the expression cassette for C. aaseri lipase2 was demonstrated with 60% efficiency using this CRISPR-Cas9 system. This genome engineering tool could accelerate industrial application of C. aaseri SH14 for production of bio-based chemicals from renewable oils.
机译:脂肪酵母念珠菌Asaseri Sh14可以利用长链脂肪酸作为唯一的碳源,从油棕榈堆肥中分离。为了将这种菌株作为平台酵母,用于生产来自可再生植物油的生物基化学品,开发了使用CRISPR-CAS9的遗传操作系统。使用从C.Aaseri SH14中分离的自主复制序列构建CAS9和SGRNA表达的蜕皮载体。该系统保证CAS9的时间表达用于遗传操作和转化菌株的载体的快速固化。通过使用单个SGRNA在二倍体中同时破坏六份酰基-CoA氧化酶基因(AOX2,AOX4和AXOX5)使用具有70%效率的单个SGRNA的酰基-COA氧化酶基因(AOX2,AOX4和AOX5)直接构建β-氧化突变体。通过从十二烷的十二烷基甲酸的积累来证实三重氧化氢突变体中的β-氧化的阻断。使用该CRISPR-CAS9系统,对C.Aaseri脂肪酶2的表达盒的靶向整合。该基因组工程可以加速C. Aaseri SH14的工业应用,以生产来自可再生油的生物基化学品。

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