Anne Kakouridis, Spencer Diamond, Thomas Eng, Heath J Mills, Olivia Gámez Holzhaus, Michael L Summers, Ferran Garcia-Pichel, Aindrila Mukhopadhyay
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引用次数: 0
摘要
在太空旅行期间将生物系统作为货物进行有效运输是在外层空间使用合成生物学和生物制造的关键要求。利用微生物进行生物生产将推动在资源有限的环境中满足人类许多需求的程度。大量的生物部件和菌株储存库可以满足这一需求,但它们的现场可用性需要有效的运输。在这里,我们探索了一种方法,无需低温或低温储存,就能将 DNA 质粒这种无处不在的合成生物学部件安全地运送到国际空间站,然后再运回肯尼迪航天中心。我们的方法依赖于蓝藻 Nostoc punctiforme PC73102,它天然耐受长时间干燥。干燥后的穿刺藻能够将非本地的 pSCR119 质粒作为胞内货物安全地运往太空并返回。返回实验室后,提取的质粒没有出现 DNA 损伤或额外的突变,可以按原计划用于转化模式生物宿主大肠杆菌,以赋予其卡那霉素抗性。这项概念验证研究为在需要减少生物部件装载和储存设备和基础设施的环境中使用坚固耐用的 DNA 运输主机奠定了基础。
Desiccated Cyanobacteria Serve As Efficient Plasmid DNA Carriers in Space Flight.
Effective transport of biological systems as cargo during space travel is a critical requirement to use synthetic biology and biomanufacturing in outer space. Bioproduction using microbes will drive the extent to which many human needs can be met in environments with limited resources. Vast repositories of biological parts and strains are available to meet this need, but their on-site availability requires effective transport. Here, we explore an approach that allows DNA plasmids, ubiquitous synthetic biology parts, to be safely transported to the International Space Station and back to the Kennedy Space Center without low-temperature or cryogenic stowage. Our approach relied on the cyanobacterium Nostoc punctiforme PC73102, which is naturally tolerant to prolonged desiccation. Desiccated N. punctiforme was able to carry the non-native pSCR119 plasmid as intracellular cargo safely to space and back. Upon return to the laboratory, the extracted plasmid showed no DNA damage or additional mutations and could be used as intended to transform the model synbio host Escherichia coli to bestow kanamycin resistance. This proof-of-concept study provides the foundation for a ruggedized transport host for DNA to environments where there is a need to reduce equipment and infrastructure for biological parts stowage and storage.
期刊介绍:
The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism.
Topics may include, but are not limited to:
Design and optimization of genetic systems
Genetic circuit design and their principles for their organization into programs
Computational methods to aid the design of genetic systems
Experimental methods to quantify genetic parts, circuits, and metabolic fluxes
Genetic parts libraries: their creation, analysis, and ontological representation
Protein engineering including computational design
Metabolic engineering and cellular manufacturing, including biomass conversion
Natural product access, engineering, and production
Creative and innovative applications of cellular programming
Medical applications, tissue engineering, and the programming of therapeutic cells
Minimal cell design and construction
Genomics and genome replacement strategies
Viral engineering
Automated and robotic assembly platforms for synthetic biology
DNA synthesis methodologies
Metagenomics and synthetic metagenomic analysis
Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction
Gene optimization
Methods for genome-scale measurements of transcription and metabolomics
Systems biology and methods to integrate multiple data sources
in vitro and cell-free synthetic biology and molecular programming
Nucleic acid engineering.