Soudier Paul, Larroude Macarena, Celińska Ewelina, Rossignol Tristan, Nicaud Jean-Marc
Micalis Institute, INRA, AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, France.
Department of Biotechnology and Food Microbiology, Poznan University of Life Sciences, Poznan, Poland.
Methods Mol Biol. 2019;1923:153-168. doi: 10.1007/978-1-4939-9024-5_6.
Yarrowia lipolytica has emerged as an alternative expression system for heterologous protein production and enzyme evolution. Several different expression systems dedicated for this species have been developed, ranging from the simple cloning of expression vectors to recently developed high-throughput methodologies using efficient cloning and assembly such as Gateway and Golden Gate strategies. The latter strategies, due to their modular character, enable multiple vector construction and the construction of expression cassettes containing different genes or a gene under different promoters of various strengths.Here, we present the Golden Gate cloning strategy for the construction of multiple expression cassettes, the transformation into Y. lipolytica, and the selection of efficient enzyme-producing strains using an insect alpha-amylase as a reporter detected via a thermal cycler-based microassay.
解脂耶氏酵母已成为用于异源蛋白生产和酶进化的替代表达系统。已经开发了几种专门用于该物种的不同表达系统,从简单的表达载体克隆到最近使用高效克隆和组装(如Gateway和Golden Gate策略)开发的高通量方法。后一种策略由于其模块化特性,能够进行多个载体构建以及构建包含不同基因或在不同强度启动子下的基因的表达盒。在此,我们展示了用于构建多个表达盒、转化解脂耶氏酵母以及使用昆虫α-淀粉酶作为报告基因通过基于热循环仪的微量测定法检测来选择高效产酶菌株的Golden Gate克隆策略。