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通过酵母转化相关重组合成满头部包装噬菌体

Synthesis of Headful Packaging Phages Through Yeast Transformation-Associated Recombination.

作者信息

Lu Cheng, He Lan, Guo Yangyijun, Wang Tingting, Ye Yanrui, Lin Zhanglin

机构信息

School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China.

School of Biomedicine, Guangdong University of Technology, Guangzhou 510006, China.

出版信息

Viruses. 2024 Dec 31;17(1):45. doi: 10.3390/v17010045.

Abstract

De novo synthesis of phage genomes enables flexible genome modification and simplification. This study explores the synthetic genome assembly of phage vB_PaeS_SCUT-S4 (S4), a 42,932 bp headful packaging phage, which encapsidates a terminally redundant, double-stranded DNA genome exceeding unit length. We demonstrate that using the yeast TAR approach, the S4 genome can be assembled and rebooted from a unit-length genome plus a minimal 60 bp terminal redundant sequence. Furthermore, we show that S4 can be synthesized from arbitrary starting nucleotides and modified with a red fluorescent protein as a reporter. Additionally, we successfully designed and assembled synthetic S4 phages with reduced genomes, knocking out up to 10 of the 24 hypothetical genes simultaneously, with a combined length of 2883 bp, representing 6.7% of the unit-length genome. This work highlights the potential for engineering simplified, customizable headful packaging phage genomes, providing a foundation for future studies of these phages for potential clinical applications.

摘要

噬菌体基因组的从头合成能够实现灵活的基因组修饰和简化。本研究探索了噬菌体vB_PaeS_SCUT-S4(S4)的合成基因组组装,S4是一种42,932 bp的末端冗余包装噬菌体,其包裹着一个超过单位长度的末端冗余双链DNA基因组。我们证明,使用酵母TAR方法,可以从单位长度基因组加上最少60 bp的末端冗余序列组装并重启S4基因组。此外,我们表明S4可以从任意起始核苷酸合成,并用红色荧光蛋白作为报告基因进行修饰。此外,我们成功设计并组装了基因组简化的合成S4噬菌体,同时敲除了24个假定基因中的多达10个,总长度为2883 bp,占单位长度基因组的6.7%。这项工作突出了工程化简化、可定制的末端冗余包装噬菌体基因组的潜力,为这些噬菌体未来潜在临床应用的研究奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2acd/11769102/ae8de7d7ca40/viruses-17-00045-g001.jpg

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