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通过原生质体融合改建酵母细胞的研究——Ⅴ.酿酒酵母与糖化酵母种间融合杂种的遗传分析 被引量:4

Studies of Reform of Yeast Cell by Protoplast Fusion V. Geaetic Analysis of the Interspecific Fusion Hybrid Between Saccharomyces cerevisiae and 5. diaslaticas
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摘要 HU-KDP-185菌株是由单倍体糖化酵母与二倍体椭圆酿酒酵母经原生质体融合而获得的种间三倍体融合杂种。遗传分析表明,该杂种在遗传上是稳定的;在一般情况下,其产孢率为13.54%;但在特定预培养条件下,可提高到38.61%,即使在只含0.98%醋酸钾和0.186%KCl的HU-Li简易产孢培养基上,其产孢率也可达33.23%。用显微操作器解剖了202个4孢子子囊,得到376个四分子单孢株,其孢子成活率达46.53%;四分子的交配型出现A、a、AA、aa4种类型,没有发现有AAa交配型存在。四分子发酵可溶性淀粉的能力为1:2(发酵:不发酵);而遗传标记的分离比为野生型:营养缺陷型(包括hisˉ,argˉ,hisˉargˉ)约为1:1。 The strain HU-KDF-185 tested is an interspecific triploid hybrid obtained by protoplast fusion of a diploid Saccharomyces cerevisiae and a haploid S. diastaticus. The following aspects were shown in the genetic analysis: (1) The strain HU-KDF-185 was a stable hybrid genetically in terms of the genetic markers. (2) The sporulation rate (Le. ascus forming rate) of the hybrid was 13.54% in general conditions, but it could increase to 38.61% in special condition of pre-sporulation culture, and in the case of presporulation culture it also could reach 33.23% even when the hybrid cells were cultured in a simple HU-Li sporulation medium containing only 0.98% potassium acetate and 0.186% KC1 and 2% purified agar. 202 asci were dissected and there were only 376 single spore clones, which means that spore viability was about 46.53%. (3) The genotype of these spore clones were determined Mating type of tetrads from the hybtld HU-KDF-185 contained four types: a, α, 2α, and aa, but no aaα maing type. Fermentability of the tetrads for soluble starch was about 1:2 (fermenter: non-fermenter), Genetic markers of the tetrads showed that the prototroph: auxotroph was 1:1.
机构地区 杭州大学生物系
出处 《Acta Genetica Sinica》 SCIE CAS CSCD 1992年第5期467-474,共8页
基金 国家自然科学基金 浙江省自然科学基金~~
关键词 遗传分析 原生质体融合 酵母 Interspecific fused hybrid, Saccharomyccs diastaticus, Genetic analysis
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参考文献9

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二级参考文献3

  • 1Brian L. Holaway,Donna J. Lehman,Donald A. Primerano,P. T. Magee,Mary J. Clancy. Sporulation-regulated genes ofSaccharomyces cerevisiae[J] 1985,Current Genetics(3):163~169
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