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迈向海洋蓝细菌中的遗传系统。

Toward a genetic system in the marine cyanobacterium .

作者信息

Laurenceau Raphaël, Bliem Christina, Osburne Marcia S, Becker Jamie W, Biller Steven J, Cubillos-Ruiz Andres, Chisholm Sallie W

机构信息

Department of Civil and Environmental Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.

Present address: Department of Molecular Biology and Microbiology Tufts University School of Medicine, Boston, MA, USA.

出版信息

Access Microbiol. 2020 Feb 19;2(4):acmi000107. doi: 10.1099/acmi.0.000107. eCollection 2020.

DOI:10.1099/acmi.0.000107
PMID:33005871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7523629/
Abstract

As the smallest and most abundant primary producer in the oceans, the cyanobacterium is of interest to diverse branches of science. For the past 30 years, research on this minimal phototroph has led to a growing understanding of biological organization across multiple scales, from the genome to the global ocean ecosystem. Progress in understanding drivers of its diversity and ecology, as well as molecular mechanisms underpinning its streamlined simplicity, has been hampered by the inability to manipulate these cells genetically. Multiple attempts have been made to develop an efficient genetic transformation method for over the years; all have been unsuccessful to date, despite some success with their close relative, . To avoid the pursuit of unproductive paths, we report here what has not worked in our hands, as well as our progress developing a method to screen the most efficient electroporation parameters for optimal DNA delivery into cells. We also report a novel protocol for obtaining axenic colonies and a new method for differentiating live and dead cells. The electroporation method can be used to optimize DNA delivery into any bacterium, making it a useful tool for advancing transformation systems in other genetically recalcitrant microorganisms.

摘要

作为海洋中最小且数量最多的初级生产者,蓝细菌受到了多个科学领域的关注。在过去30年里,对这种简单光合生物的研究使人们对从基因组到全球海洋生态系统等多个尺度的生物组织有了越来越深入的了解。然而,由于无法对这些细胞进行基因操作,在理解其多样性和生态驱动因素以及支撑其简化特性的分子机制方面的进展受到了阻碍。多年来,人们多次尝试为[具体蓝细菌名称]开发一种高效的遗传转化方法;尽管在其近亲[具体近亲名称]上取得了一些成功,但迄今为止所有尝试均未成功。为避免走无效的研究路径,我们在此报告我们尝试中未成功的方法,以及我们在开发一种筛选最有效电穿孔参数以将最佳DNA导入[具体蓝细菌名称]细胞方面取得的进展。我们还报告了一种获得无菌落的新方案以及一种区分活细胞和死细胞的新方法。这种电穿孔方法可用于优化将DNA导入任何细菌,使其成为推进其他遗传难处理微生物转化系统的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b52/7523629/ecde021d355f/acmi-2-107-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b52/7523629/9a1e279c8da3/acmi-2-107-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b52/7523629/fd9833097084/acmi-2-107-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b52/7523629/dfb393e1839b/acmi-2-107-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b52/7523629/ecde021d355f/acmi-2-107-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b52/7523629/9a1e279c8da3/acmi-2-107-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b52/7523629/fd9833097084/acmi-2-107-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b52/7523629/dfb393e1839b/acmi-2-107-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b52/7523629/ecde021d355f/acmi-2-107-g004.jpg

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