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A supernumerary designer chromosome for modular

机译:模块化的叠加设计师染色体

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摘要

The construction of microbial cell factories for sustainable production of chemicals and pharmaceuticals requires extensive genome engineering. Using Saccharomyces cerevisiae, this study proposes synthetic neochromosomes as orthogonal expression platforms for rewiring native cellular processes and implementing new functionalities. Capitalizing the powerful homologous recombination capability of S. cerevisiae, modular neochromosomes of 50 and 100 kb were fully assembled de novo from up to 44 transcriptional-unit-sized fragments in a single transformation. These assemblies were remarkably efficient and faithful to their in silico design. Neochromosomes made of non-coding DNA were stably replicated and segregated irrespective of their size without affecting the physiology of their host. These non-coding neochromosomes were successfully used as landing pad and as exclusive expression platform for the essential glycolytic pathway. This work pushes the limit of DNA assembly in S. cerevisiae and paves the way for de novo designer chromosomes as modular genome engineering platforms in S. cerevisiae.
机译:用于可持续生产化学品和药品的微生物细胞工厂需要广泛的基因组工程。使用酿酒酵母酿酒酵母,本研究提出了合成的新核糖肌作为正交表达平台,用于重新加热天然细胞过程并实现新功能。利用S.Cerevisiae的强大同源重组能力,在单一转化中完全从多达44个转录单元大小的碎片完全组装50和100kb的模块化新染色体。这些组件非常有效,忠于他们的硅设计。不论其大小如何,不论其均尺寸无论在不影响其宿主的生理学的情况下如何稳定地复制和隔离。这些非编码的新荧光剂成功用作着陆垫和必需糖酵解途径的独占表达平台。这项工作推动了酿酒酵母DNA组装的极限,并为DE Novo设计师染色体铺平道路,作为酿酒酵母的模块化基因组工程平台。

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