Universität Osnabrück, Fachbereich Biologie/Chemie, AG Genetik, Osnabrück, Germany.
FEMS Yeast Res. 2010 May;10(3):333-42. doi: 10.1111/j.1567-1364.2009.00604.x.
A set of different marker deletions starting with a ura3 derivative of the Kluyveromyces lactis type strain CBS2359 was constructed. After a first cross to obtain a strain with the opposite mating type that also carried a leu2 allele, continuous back-crosses were used to obtain a congenic strain series with different marker combinations, including deletions in KlHIS3, KlADE2 and KlLAC4. Enzymes involved in carbohydrate metabolism were shown to behave very similarly to the original type strain and other K. lactis strains investigated previously. Moreover, a vector series of Saccharomyces cerevisiae genes flanked by loxP sites was constructed to be used as heterologous deletion cassettes in K. lactis, together with two plasmids for expression of Cre-recombinase for marker regeneration. To increase the frequency of homologous recombination, the Klku80 deletion was also introduced into the congenic strain series. A PCR-based method for determination of mating type is provided.
构建了一套以克鲁维酵母 CBS2359 型菌株的 ura3 衍生物为起点的不同标记缺失体。经过第一次杂交获得了具有相反交配型的菌株,该菌株还携带了 leu2 等位基因,然后连续回交获得了具有不同标记组合的同基因株系,包括 KlHIS3、KlADE2 和 KlLAC4 的缺失。参与碳水化合物代谢的酶的行为与原始类型菌株和之前研究过的其他克鲁维酵母菌株非常相似。此外,构建了一系列带有 loxP 位点的酿酒酵母基因载体,用作克鲁维酵母中的异源缺失盒,以及两个用于表达 Cre 重组酶进行标记再生的质粒。为了提高同源重组的频率,还将 Klku80 缺失引入同基因株系。提供了一种基于 PCR 的用于确定交配型的方法。