| Literature DB >> 35781204 |
Simon Kobalter1,2, Astrid Radkohl1, Helmut Schwab1,2, Anita Emmerstorfer-Augustin1,2, Harald Pichler3,4.
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.Entities:
Keywords: Gene disruption; Homologous recombination; Knockout plasmids; Marker recycling; Pichia pastoris
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Year: 2022 PMID: 35781204 DOI: 10.1007/978-1-0716-2399-2_9
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745