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细菌传递给多种真菌的高级接合质粒

Superior Conjugative Plasmids Delivered by Bacteria to Diverse Fungi.

作者信息

Cochrane Ryan R, Shrestha Arina, Severo de Almeida Mariana M, Agyare-Tabbi Michelle, Brumwell Stephanie L, Hamadache Samir, Meaney Jordyn S, Nucifora Daniel P, Say Henry Heng, Sharma Jehoshua, Soltysiak Maximillian P M, Tong Cheryl, Van Belois Katherine, Walker Emma J L, Lachance Marc-André, Gloor Gregory B, Edgell David R, Shapiro Rebecca S, Karas Bogumil J

机构信息

Department of Biochemistry, Schulich School of Medicine and Dentistry, The University of Western Ontario, London, ON, Canada, N6A 5C1.

Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada, N1G 2W1.

出版信息

Biodes Res. 2022 Aug 19;2022:9802168. doi: 10.34133/2022/9802168. eCollection 2022.

DOI:10.34133/2022/9802168
PMID:37850145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10521675/
Abstract

Fungi are nature's recyclers, allowing for ecological nutrient cycling and, in turn, the continuation of life on Earth. Some fungi inhabit the human microbiome where they can provide health benefits, while others are opportunistic pathogens that can cause disease. Yeasts, members of the fungal kingdom, have been domesticated by humans for the production of beer, bread, and, recently, medicine and chemicals. Still, the great untapped potential exists within the diverse fungal kingdom. However, many yeasts are intractable, preventing their use in biotechnology or in the development of novel treatments for pathogenic fungi. Therefore, as a first step for the domestication of new fungi, an efficient DNA delivery method needs to be developed. Here, we report the creation of superior conjugative plasmids and demonstrate their transfer via conjugation from bacteria to 7 diverse yeast species including the emerging pathogen . To create our superior plasmids, derivatives of the 57 kb conjugative plasmid pTA-Mob 2.0 were built using designed gene deletions and insertions, as well as some unintentional mutations. Specifically, a cluster mutation in the promoter of the conjugative gene had the most significant effect on improving conjugation to yeasts. In addition, we created Golden Gate assembly-compatible plasmid derivatives that allow for the generation of custom plasmids to enable the rapid insertion of designer genetic cassettes. Finally, we demonstrated that designer conjugative plasmids harboring engineered restriction endonucleases can be used as a novel antifungal agent, with important applications for the development of next-generation antifungal therapeutics.

摘要

真菌是大自然的分解者,促进生态养分循环,进而维持地球上生命的延续。一些真菌存在于人类微生物群中,对健康有益,而另一些则是机会致病菌,可导致疾病。酵母属于真菌界,已被人类驯化用于生产啤酒、面包,最近还用于生产药品和化学品。然而,真菌界仍存在巨大的未开发潜力。然而,许多酵母难以处理,阻碍了它们在生物技术中的应用或用于开发针对致病真菌的新疗法。因此,作为驯化新真菌的第一步,需要开发一种高效的DNA递送方法。在此,我们报告了优质接合质粒的创建,并展示了它们通过接合作用从细菌转移到7种不同酵母物种,包括新兴病原体。为了创建我们的优质质粒,我们利用设计的基因缺失和插入以及一些无意的突变构建了57 kb接合质粒pTA-Mob 2.0的衍生物。具体而言,接合基因启动子中的簇突变对改善与酵母的接合作用影响最为显著。此外,我们创建了与金门组装兼容的质粒衍生物,可用于生成定制质粒,以便快速插入设计的遗传盒。最后,我们证明携带工程化限制内切酶的设计接合质粒可作为一种新型抗真菌剂,在下一代抗真菌治疗药物的开发中具有重要应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/b8fcd36cbd33/9802168.fig.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/d414e4355d35/9802168.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/f014f1f8b50f/9802168.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/20f74a83f917/9802168.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/08892b6a74c4/9802168.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/b7bc51e7791a/9802168.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/cebe594a8e42/9802168.fig.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/b8fcd36cbd33/9802168.fig.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/d414e4355d35/9802168.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/f014f1f8b50f/9802168.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/20f74a83f917/9802168.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/08892b6a74c4/9802168.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/b7bc51e7791a/9802168.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/cebe594a8e42/9802168.fig.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6266/10521675/b8fcd36cbd33/9802168.fig.007.jpg

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