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Developing a piggyBac Transposon System and Compatible Selection Markers for Insertional Mutagenesis and Genome Engineering in Yarrowia lipolytica
Author(s) -
Wagner James M.,
Williams Eden V.,
Alper Hal S.
Publication year - 2018
Publication title -
biotechnology journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.144
H-Index - 84
eISSN - 1860-7314
pISSN - 1860-6768
DOI - 10.1002/biot.201800022
Subject(s) - yarrowia , biology , insertional mutagenesis , transposable element , mutagenesis , genome , genetics , genome engineering , forward genetics , metabolic engineering , synthetic biology , transposon mutagenesis , computational biology , genome editing , mutant , yeast , gene
Yarrowia lipolytica is a non‐conventional yeast of interest to the biotechnology industry. However, the physiology, metabolism, and genetic regulation of Y. lipolytica diverge significantly from more well‐studied and characterized yeasts such as Saccharomyces cerevisiae . To develop additional genetic tools for this industrially relevant host, the piggyBac transposon system to enable efficient generation of genome‐wide insertional mutagenesis libraries and introduction of scarless, footprint‐free genomic modifications in Y. lipolytica . Specifically, we demonstrate piggyBac transposition in Y. lipolytica , and then use the approach to screen transposon insertion libraries for rapid isolation of mutations that confer altered canavanine resistance, pigment formation, and neutral lipid accumulation. We also develop a variety of piggyBac compatible selection markers for footprint‐free genome engineering, including a novel dominant marker cassette ( Escherichia coli guaB ) for effective Y. lipolytica selection using mycophenolic acid. We utilize these marker cassettes to construct a piggyBac vector set that allows for auxotrophic selection (uracil or tryptophan biosynthesis) or dominant selection (hygromycin, nourseothricin, chlorimuron ethyl, or mycophenolic acid resistance) and subsequent marker excision. These new genetic tools and techniques will help to facilitate and accelerate the engineering of Y. lipolytica strains for efficient and sustainable production of a wide variety of small molecules and proteins.