| Literature DB >> 35781206 |
Paola Branduardi1, Liliane Barroso2,3, Laura Dato2,4, Edward J Louis3, Danilo Porro2.
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 .Entities:
Keywords: Contour-clamped homogeneous electric field (CHEF) gel electrophoresis; Plasmids; Promoters; Targeted gene deletion; Yeast transformation; Zygosaccharomyces bailii
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Year: 2022 PMID: 35781206 DOI: 10.1007/978-1-0716-2399-2_11
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745