Molecular Tools for Leveraging the Potential of the Acid-Tolerant Yeast Zygosaccharomyces bailii as Cell Factory

  • Paola Branduardi*
  • , Liliane Barroso
  • , Laura Dato
  • , Edward J. Louis
  • , Danilo Porro
  • *Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

Abstract

Microorganisms offer a tremendous potential as cell factories, and they are indeed been used by humans since the previous centuries for biotransformations. Among them, yeasts combine the advantage of a unicellular state with a eukaryotic organization. Moreover, in the era of biorefineries, their biodiversity can offer solutions to specific process constraints. Zygosaccharomyces bailii, an ascomycete budding yeast, is widely known for its peculiar tolerance to different stresses, among which are organic acids. Moreover, the recent reclassification of the species, including diverse hybrids, is further expanding both fundamental and applied interests. It is therefore reasonable that despite the possibility to apply with this yeast some of the molecular tools and protocols routinely used to manipulate Saccharomyces cerevisiae, adjustments and optimizations are necessary. Here we describe in detail the methods for determining chromosome number, size, and aneuploidy, transformation, classical target gene disruption or gene integration, and designing of episomal expression plasmids helpful for engineering the yeast Z. bailii.

Original languageEnglish
Title of host publicationMethods in Molecular Biology
Number of pages26
PublisherHumana Press
Publication date2022
Pages179-204
DOIs
Publication statusPublished - 2022
SeriesMethods in Molecular Biology
Volume2513
ISSN1064-3745

Bibliographical note

Funding Information:
These works were partially supported by FAR (Fondo di Ateneo per la Ricerca) of the University of Milano-Bicocca to PB, by post-Doctoral fellowship to FM, and by YEASTDOC training network (People Programme (Marie Curie Actions) of the H2020-MSCA-ITN-2017 under REA grant agreement n 764927) to PB, LB, and EL.

Publisher Copyright:
© 2022, Springer Science+Business Media, LLC, part of Springer Nature.

Keywords

  • Contour-clamped homogeneous electric field (CHEF) gel electrophoresis
  • Plasmids
  • Promoters
  • Targeted gene deletion
  • Yeast transformation
  • Zygosaccharomyces bailii

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