首页> 外文OA文献 >BBF RFC 94: Type IIS Assembly for Bacterial Transcriptional Units: A Standardized Assembly Method for Building Bacterial Transcriptional Units Using the Type IIS Restriction Enzymes BsaI and BbsI
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BBF RFC 94: Type IIS Assembly for Bacterial Transcriptional Units: A Standardized Assembly Method for Building Bacterial Transcriptional Units Using the Type IIS Restriction Enzymes BsaI and BbsI

机译:BBF RFC 94:用于细菌转录单位的IIs组装:使用IIs限制酶BsaI和BbsI构建细菌转录单位的标准化组装方法

摘要

This RFC94 describes an assembly standard based on the Type IIS restriction enzymes BsaI and BbsI (also called BpiI). This assembly standard is based upon the Modular Cloning (MoClo) assembly strategy, which was introduced in 2011 by Weber et al. [1] and is based upon Golden Gate cloning [2].In this RFC, we describe our proposed MoClo standard for generating a library of bacterial DNA parts for generating four-part transcriptional units (promoter : 5’UTR : CDS : 3’UTR). In this work, we define 5’UTRs as including ribosomal binding sites (RBS) and bi-cistronic design elements (BCDs) [3], and 3’UTRs as transcriptional terminators. The 2012-2014 BostonU iGEM teams completed this work and a more compact library has also been created based on this work [4].
机译:该RFC94描述了基于IIS型限制酶BsaI和BbsI(也称为BpiI)的组装标准。此组装标准基于模块化克隆(MoClo)组装策略,该策略于2011年由Weber等人引入。 [1]并基于Golden Gate克隆[2]。在此RFC中,我们描述了拟议的MoClo标准,该标准用于生成细菌DNA部分的文库,用于生成四部分转录单位(启动子:5'UTR:CDS:3' UTR)。在这项工作中,我们将5'UTR定义为包括核糖体结合位点(RBS)和双顺反子设计元件(BCD)[3],并将3'UTR定义为转录终止子。 2012-2014年BostonU iGEM团队完成了这项工作,并且基于此工作还创建了一个更紧凑的库[4]。

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