首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >Genetic Engineering of an Unconventional Yeast for Renewable Biofuel and Biochemical Production
【2h】

Genetic Engineering of an Unconventional Yeast for Renewable Biofuel and Biochemical Production

机译:用于可再生生物燃料和生化生产的非常规酵母的基因工程

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Yarrowia lipolytica is a non-pathogenic, dimorphic and strictly aerobic yeast species. Owing to its distinctive physiological features and metabolic characteristics, this unconventional yeast is not only a good model for the study of the fundamental nature of fungal differentiation but is also a promising microbial platform for biochemical production and various biotechnological applications, which require extensive genetic manipulations. However, genetic manipulations of Y. lipolytica have been limited due to the lack of an efficient and stable genetic transformation system as well as very high rates of non-homologous recombination that can be mainly attributed to the KU70 gene. Here, we report an easy and rapid protocol for the efficient genetic transformation and for gene deletion in Y. lipolytica Po1g. First, a protocol for the efficient transformation of exogenous DNA into Y. lipolytica Po1g was established. Second, to achieve the enhanced double-crossover homologous recombination rate for further deletion of target genes, the KU70 gene was deleted by transforming a disruption cassette carrying 1 kb homology arms. Third, to demonstrate the enhanced gene deletion efficiency after deletion of the KU70 gene, we individually deleted 11 target genes encoding alcohol dehydrogenase and alcohol oxidase using the same procedures on the KU70 knockout platform strain. It was observed that the rate of precise homologous recombination increased substantially from less than 0.5% for deletionof the KU70 gene in Po1g to 33%-71% for the single gene deletion of the 11 target genes in Po1g KU70Δ. A replicative plasmid carrying the hygromycin B resistance marker and the Cre/LoxP system was constructed, and the selection marker gene in the yeast knockout strains was eventually removed by expression of Cre recombinase to facilitate multiple rounds of targeted genetic manipulations. The resulting single-gene deletion mutants have potential applications in biofuel and biochemical production.
机译:解脂耶氏酵母是一种非致病性,二态性和严格需氧的酵母菌种。由于其独特的生理特性和代谢特性,这种非常规酵母不仅是研究真菌分化基本特性的良好模型,而且还是生化生产和各种生物技术应用的有希望的微生物平台,需要广泛的基因操作。然而,解脂耶氏酵母的基因操作受到限制,原因是缺乏有效和稳定的遗传转化系统以及非同源重组的比率很高,这主要归因于KU70基因。在这里,我们报告了一个简单而快速的协议,用于解脂耶氏酵母Po1g中的有效遗传转化和基因缺失。首先,建立了将外源DNA有效转化为解脂耶氏酵母Po1g的方案。其次,为了实现进一步的靶基因缺失的双交换同源重组率的提高,通过转化带有1kb同源臂的破坏盒来缺失KU70基因。第三,为了证明在删除KU70基因后增强的基因删除效率,我们在KU70基因敲除平台菌株上使用相同的程序分别删除了11个编码醇脱氢酶和醇氧化酶的靶基因。观察到,精确同源重组的比率从缺失Po1g中的KU70基因的小于0.5%显着增加到缺失Po1gKU70Δ中的11个靶基因的单基因的33%-71%。构建了带有潮霉素B抗性标记和Cre / LoxP系统的复制质粒,并最终通过表达Cre重组酶去除了酵母敲除菌株中的选择标记基因,以促进多轮靶向遗传操作。所得的单基因缺失突变体在生物燃料和生化生产中具有潜在的应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号