Walker Emma Jane Lougheed, Karas Bogumil Jacek
Biochemistry Department, Western University, London, Canada.
Bio Protoc. 2025 Jan 20;15(2):e5162. doi: 10.21769/BioProtoc.5162.
Chloroplast genomes present an alternative strategy for large-scale engineering of photosynthetic eukaryotes. Prior to our work, the chloroplast genomes of (204 kb) and (140 kb) had been cloned using bacterial and yeast artificial chromosome (BAC/YAC) libraries, respectively. These methods lack design flexibility as they are reliant upon the random capture of genomic fragments during BAC/YAC library creation; additionally, both demonstrated a low efficiency (≤ 10%) for correct assembly of the genome in yeast. With this in mind, we sought to create a highly flexible and efficient approach for assembling the 117 kb chloroplast genome of , a photosynthetic marine diatom. Our original article demonstrated a PCR-based approach for cloning the chloroplast genome that had 90%-100% efficiency when screening as few as 10 yeast colonies following assembly. In this article, we will discuss this approach in greater depth as we believe this technique could be extrapolated to other species, particularly those with a similar chloroplast genome size and architecture. Key features • Large fragments of the chloroplast genome can be readily amplified through PCR from total algal DNA isolate. • Assembly protocol can be completed within a day, and yeast colonies harboring chloroplast genomes can be obtained in as few as 4-5 days. • Cloned genomes isolated from yeast transformants can be moved to through electroporation.
叶绿体基因组为光合真核生物的大规模工程改造提供了另一种策略。在我们开展工作之前,莱茵衣藻(204 kb)和三角褐指藻(140 kb)的叶绿体基因组已分别使用细菌人工染色体(BAC)文库和酵母人工染色体(YAC)文库进行克隆。这些方法缺乏设计灵活性,因为它们依赖于BAC/YAC文库构建过程中基因组片段的随机捕获;此外,两者在酵母中基因组正确组装的效率都很低(≤10%)。考虑到这一点,我们试图创建一种高度灵活且高效的方法来组装光合海洋硅藻三角褐指藻117 kb的叶绿体基因组。我们最初的文章展示了一种基于PCR的方法来克隆三角褐指藻的叶绿体基因组,组装后筛选少至10个酵母菌落时,该方法的效率为90%-100%。在本文中,我们将更深入地讨论这种方法,因为我们认为该技术可以推广到其他物种,特别是那些具有相似叶绿体基因组大小和结构的物种。关键特性•叶绿体基因组的大片段可以通过PCR从分离的藻类总DNA中轻松扩增。•组装方案可以在一天内完成,并且在短短4-5天内就能获得含有叶绿体基因组的酵母菌落。•从酵母转化体中分离出的克隆基因组可以通过电穿孔转移到大肠杆菌中。