AG Genetik, Fachbereich Biologie/Chemie, Universität Osnabrück, Barbarastr. 11, D-49076 Osnabrück, Germany.
AG Zoologie, Fachbereich Biologie/Chemie, Universität Osnabrück, Barbarastr. 11, D-49076 Osnabrück, Germany.
Int J Mol Sci. 2023 Jan 17;24(3):1859. doi: 10.3390/ijms24031859.
is an ascomycetous yeast that frequently dominates the population in the first two days of wine fermentations. It contributes to the production of many beneficial as well as detrimental aroma compounds. While the genome sequence of the diploid type strain DSM 2768 has been largely elucidated, transformation by electroporation was only recently achieved. We here provide an elaborate toolset for the genetic manipulation of this yeast. A chromosomal replication origin was isolated and used for the construction of episomal, self-replicating cloning vectors. Moreover, homozygous auxotrophic deletion markers (, , , ) have been obtained in the diploid genome as future recipients and a proof of principle for the application of PCR-based one-step gene deletion strategies. Besides a hygromycin resistance cassette, a kanamycin resistance gene was established as a dominant marker for selection on G418. Recyclable deletion cassettes flanked by -sites and the corresponding Cre-recombinase expression vectors were tailored. Moreover, we report on a chemical transformation procedure with the use of freeze-competent cells. Together, these techniques and constructs pave the way for efficient and targeted manipulations of .
是一种子囊菌酵母,它通常在葡萄酒发酵的头两天主导种群。它有助于产生许多有益和有害的香气化合物。虽然二倍体型菌株 DSM 2768 的基因组序列已经基本阐明,但电穿孔转化直到最近才得以实现。我们在这里提供了一套用于该酵母遗传操作的精心设计的工具。分离出一个染色体复制起点,并用于构建附加型、自我复制的克隆载体。此外,在二倍体基因组中获得了纯合营养缺陷型缺失标记(、、、),作为未来的受体,并证明了基于 PCR 的一步基因缺失策略的应用原理。除了潮霉素抗性盒外,还建立了卡那霉素抗性基因作为在 G418 上选择的显性标记。定制了带有 - 位点的可回收缺失盒和相应的 Cre 重组酶表达载体。此外,我们还报告了使用冷冻敏感细胞的化学转化程序。总之,这些技术和构建体为的高效和靶向操作铺平了道路。