Joint universal modular plasmids (JUMP): a flexible vector platform for synthetic biology.

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS
Synthetic biology (Oxford, England) Pub Date : 2021-02-02 eCollection Date: 2021-01-01 DOI:10.1093/synbio/ysab003
Marcos Valenzuela-Ortega, Christopher French
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引用次数: 13

Abstract

Generation of new DNA constructs is an essential process in modern life science and biotechnology. Modular cloning systems based on Golden Gate cloning, using Type IIS restriction endonucleases, allow assembly of complex multipart constructs from reusable basic DNA parts in a rapid, reliable and automation-friendly way. Many such toolkits are available, with varying degrees of compatibility, most of which are aimed at specific host organisms. Here, we present a vector design which allows simple vector modification by using modular cloning to assemble and add new functions in secondary sites flanking the main insertion site (used for conventional modular cloning). Assembly in all sites is compatible with the PhytoBricks standard, and vectors are compatible with the Standard European Vector Architecture (SEVA) as well as BioBricks. We demonstrate that this facilitates the construction of vectors with tailored functions and simplifies the workflow for generating libraries of constructs with common elements. We have made available a collection of vectors with 10 different microbial replication origins, varying in copy number and host range, and allowing chromosomal integration, as well as a selection of commonly used basic parts. This design expands the range of hosts which can be easily modified by modular cloning and acts as a toolkit which can be used to facilitate the generation of new toolkits with specific functions required for targeting further hosts.

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联合通用模块质粒(JUMP):一个灵活的合成生物学载体平台。
新DNA结构的生成是现代生命科学和生物技术的一个重要过程。基于金门克隆的模块化克隆系统,使用IIS型限制性内切酶,允许从可重复使用的基本DNA部分以快速,可靠和自动化友好的方式组装复杂的多部分结构。有许多这样的工具包,具有不同程度的兼容性,其中大多数针对特定的宿主生物。在这里,我们提出了一种载体设计,它允许简单的载体修改,通过使用模块化克隆在主插入位点侧翼的次要位点上组装和添加新的功能(用于传统的模块化克隆)。所有站点的组装都与PhytoBricks标准兼容,载体与欧洲标准载体架构(SEVA)以及BioBricks兼容。我们证明,这有助于构造具有定制函数的向量,并简化了生成具有公共元素的构造库的工作流程。我们已经收集了10种不同微生物复制起点的载体,这些载体在拷贝数和宿主范围上有所不同,并允许染色体整合,以及选择常用的基本部分。这种设计扩大了宿主的范围,可以通过模块化克隆轻松修改,并作为一个工具包,可以用来促进生成具有特定功能的新工具包,以针对更多的宿主。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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