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基于质粒的毕赤酵母基因敲除策略及后续标记回收。

Plasmid-Based Gene Knockout Strategy with Subsequent Marker Recycling in Pichia pastoris.

机构信息

Graz Institute of Molecular Biotechnology, University of Technology, Graz, Austria.

Austrian Centre of Industrial Biotechnology (ACIB), Graz, Austria.

出版信息

Methods Mol Biol. 2022;2513:135-151. doi: 10.1007/978-1-0716-2399-2_9.

Abstract

Gene knockout is a key technology in the development of cell factories and basic research alike. The methylotrophic yeast Pichia pastoris is typically employed as a producer of proteins and of fine chemicals, due to its ability to accumulate high cell densities in conjunction with a set of strong inducible promoters. However, protocols for genome engineering in this host are still cumbersome and time-consuming. Moreover, extensive genome engineering raises the need for a multitude of selection markers, which are limited in P. pastoris. In this chapter, we describe a fast and efficient method for gene disruption in P. pastoris that utilizes marker recycling to enable repetitive genome engineering cycles. A set of ready-to-use knockout vectors simplifies cloning procedures and facilitates quick knockout generation.

摘要

基因敲除是细胞工厂开发和基础研究的关键技术。甲醇营养酵母巴斯德毕赤酵母通常被用作蛋白质和精细化学品的生产者,因为它能够在一系列强诱导启动子的作用下积累高细胞密度。然而,该宿主的基因组工程仍然繁琐且耗时。此外,广泛的基因组工程需要大量的选择标记,而这些标记在巴斯德毕赤酵母中是有限的。在本章中,我们描述了一种在巴斯德毕赤酵母中进行基因敲除的快速有效的方法,该方法利用标记回收来实现重复的基因组工程循环。一组即用型敲除载体简化了克隆程序,加快了敲除的生成。

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