Multigene Engineering by GoldenBraid Cloning: From Plants to Filamentous Fungi and Beyond
Marta Vazquez-Vilar, Mónica Gandía, Victor García-Carpintero, Eric Marqués, Alejandro Sarrion-Perdigones, Lynne Yenush, Julio Polaina, Paloma Manzanares, Jose F. Marcos, Diego Orzaez
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Abstract
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
利用金辫克隆进行多基因工程:从植物到丝状真菌及其他
许多合成生物学家在克隆过程中采用了基于IIS型限制性内切酶和金门技术的方法,因为这些方法可以按照标准规则以非常有效的方式组合模块元素。GoldenBraid (GB)是一个基于Golden gate的模块化克隆系统,此外,由于其迭代克隆方案,它有助于大型多基因构建的工程设计和DNA部分的交换。GB最初是专门为植物合成生物学开发的,随后通过将许多宿主特异性特征纳入其基本方案,扩展并适应于其他生物,如酿酒酵母菌、丝状真菌和人类细胞。本文描述了GB的一般克隆程序,并提供了其适应丝状真菌的详细方案-一种被称为FungalBraid的GB变体。还显示了通过同源重组进行基因破坏的盒式磁带的组装,这是GB实用程序的真菌特异性扩展。FungalBraid的开发相对简单,因为植物和真菌都可以通过农杆菌介导的转化使用相同的二元质粒进行工程设计。我们还描述了在GB网站上提供的一组基于web的工具的使用,这些工具可以帮助用户进行所有克隆过程。GB的植物和真菌版本的可用性将促进这些工业相关生物的基因工程。©2020 by John Wiley &基本方案1:软件辅助的两个基因表达盒的模块化DNA组装与gb2:农杆菌介导的丝状真菌的转化;基本方案3:软件辅助的基因破坏盒的模块化DNA组装使用gb4:获得破坏转化体
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