Instituto de Biología Molecular y Celular de Plantas (IBMCP), Universitat Politècnica de València-Consejo Superior de Investigaciones Científicas (CSIC), Valencia, Spain.
Department of Food Biotechnology, Instituto de Agroquímica y Tecnología de Alimentos (IATA), Consejo Superior de Investigaciones Científicas (CSIC), Valencia, Spain.
Curr Protoc Mol Biol. 2020 Mar;130(1):e116. doi: 10.1002/cpmb.116.
Many synthetic biologists have adopted methods based on Type IIS restriction enzymes and Golden Gate technology in their cloning procedures, as these enable the combinatorial assembly of modular elements in a very efficient way following standard rules. GoldenBraid (GB) is a Golden Gate-based modular cloning system that, in addition, facilitates the engineering of large multigene constructs and the exchange of DNA parts as result of its iterative cloning scheme. GB was initially developed specifically for plant synthetic biology, and it has been subsequently extended and adapted to other organisms such as Saccharomyces cerevisiae, filamentous fungi, and human cells by incorporating a number of host-specific features into its basic scheme. Here we describe the general GB cloning procedure and provide detailed protocols for its adaptation to filamentous fungi-a GB variant known as FungalBraid. The assembly of a cassette for gene disruption by homologous recombination, a fungal-specific extension of the GB utility, is also shown. Development of FungalBraid was relatively straightforward, as both plants and fungi can be engineered using the same binary plasmids via Agrobacterium-mediated transformation. We also describe the use of a set of web-based tools available at the GB website that assist users in all cloning procedures. The availability of plant and fungal versions of GB will facilitate genetic engineering in these industrially relevant organisms. © 2020 by John Wiley & Sons, Inc. Basic Protocol 1: Software-assisted modular DNA assembly of a two gene expression-cassette with GB Basic Protocol 2: Agrobacterium tumefaciens-mediated transformation of filamentous fungi Basic Protocol 3: Software-assisted modular DNA assembly of a gene disruption-cassette using GB Basic Protocol 4: Obtaining disruption transformants.
许多合成生物学家在其克隆程序中采用了基于 Type IIS 限制酶和 Golden Gate 技术的方法,因为这些方法可以按照标准规则非常有效地组合模块化元件。GoldenBraid (GB) 是一种基于 Golden Gate 的模块化克隆系统,除了其迭代克隆方案外,它还可以方便地构建大型多基因构建体和交换 DNA 片段,从而促进工程设计。GB 最初是专门为植物合成生物学开发的,后来通过将一些宿主特异性特征纳入其基本方案,已被扩展并适应于其他生物体,如酿酒酵母、丝状真菌和人类细胞。在这里,我们描述了一般的 GB 克隆程序,并提供了将其适应丝状真菌的详细方案,即称为 FungalBraid 的 GB 变体。还展示了通过同源重组进行基因敲除的盒的组装,这是 GB 功能的真菌特异性扩展。FungalBraid 的开发相对简单,因为可以通过根癌农杆菌介导的转化,使用相同的二元质粒对植物和真菌进行工程设计。我们还描述了在 GB 网站上提供的一组基于网络的工具的使用,这些工具可以在所有克隆程序中为用户提供帮助。植物和真菌版本的 GB 的可用性将促进这些工业相关生物体的遗传工程。 © 2020 年 John Wiley & Sons, Inc. 基本方案 1:使用 GB 进行两个基因表达盒的软件辅助模块化 DNA 组装 基本方案 2:利用农杆菌介导的丝状真菌转化 基本方案 3:使用 GB 进行基因敲除盒的软件辅助模块化 DNA 组装 基本方案 4:获得敲除转化体。