Hodgson J A, Berry D R, Johnston J R
J Gen Microbiol. 1985 Dec;131(12):3219-27. doi: 10.1099/00221287-131-12-3219.
The effects of elevated temperature and of digestion with a variety of proteinases on the flocforming ability of flocculent strains of Saccharomyces cerevisiae, both genetically defined (FLO1 and FLO5) laboratory and genetically undefined brewing strains, have been determined. This has permitted classification of the flocculent phenotypes of these strains according to criteria other than quantitative grading of flocculence. The flocculent phenotypes conferred by both the FLO1 and the FLO5 gene were irreversibly lost upon treatment with pronase, proteinase K, trypsin or 2-mercaptoethanol treatments. However, the floc-forming ability of cells of the FLO1 strain ABXL-1D was destroyed by chymotrypsin digestion and was stable to incubation at 70 degrees C, whereas the floc-forming ability of cells of the FLO5 strain ABXR-11A was resistant to the action of chymotrypsin and was heat labile. Tetrad analysis of a cross of these FLO1 and FLO5 strains indicated that the chymotrypsin and heat sensitivity phenotypes were FLO-gene determined. It appears that expression of the FLO1 and FLO5 genes leads to the production of different and characteristic cell-wall proteins underlying their respective flocculent phenotypes.
已经确定了高温以及用多种蛋白酶消化对酿酒酵母絮凝菌株絮凝能力的影响,这些菌株包括基因明确的(FLO1和FLO5)实验室菌株以及基因不明确的酿造菌株。这使得能够根据除絮凝定量分级之外的标准对这些菌株的絮凝表型进行分类。用链霉蛋白酶、蛋白酶K、胰蛋白酶或2-巯基乙醇处理后,FLO1和FLO5基因赋予的絮凝表型会不可逆地丧失。然而,FLO1菌株ABXL-1D的细胞絮凝能力在胰凝乳蛋白酶消化后被破坏,并且在70℃孵育时稳定,而FLO5菌株ABXR-11A的细胞絮凝能力对胰凝乳蛋白酶的作用具有抗性并且对热不稳定。对这些FLO1和FLO5菌株杂交的四分体分析表明,胰凝乳蛋白酶和热敏感性表型是由FLO基因决定的。看来FLO1和FLO5基因的表达导致产生不同的和具有特征性的细胞壁蛋白,这些蛋白是它们各自絮凝表型的基础。