Miki B L, Poon N H, Seligy V L
J Bacteriol. 1982 May;150(2):890-9. doi: 10.1128/jb.150.2.890-899.1982.
The biological control of flocculation interactions by factors related to growth under different conditions of aeration was documented with a new assay for flocculence. The degree of flocculence expressed in a genetically defined Saccharomyces cerevisiae strain (FLO1/FLO1 ade1/ade1) remained constant during aerobic growth but varied with aeration. Flocculence was repressed in anaerobically growing cells but was induced in stationary cells or cells returned to aerobic growth. Repression was correlated with the selective inactivation of cell surface lectin-like components. The changes in flocculence were accompanied by changes in 16 extractable proteins separated by electrophoresis; however, a clear correlation between specific protein bands and flocculence could not be established. The study clearly demonstrated that the phenotypic expression of FLO1 could be reproducibly manipulated for experimental purposes by aeration alone.
通过一种新的絮凝测定法,记录了在不同曝气条件下与生长相关的因素对絮凝相互作用的生物控制。在一个基因定义的酿酒酵母菌株(FLO1/FLO1 ade1/ade1)中表达的絮凝程度在有氧生长期间保持恒定,但随曝气而变化。絮凝在厌氧生长的细胞中受到抑制,但在静止细胞或恢复有氧生长的细胞中被诱导。抑制与细胞表面凝集素样成分的选择性失活相关。絮凝的变化伴随着通过电泳分离的16种可提取蛋白质的变化;然而,无法确定特定蛋白条带与絮凝之间的明确相关性。该研究清楚地表明,仅通过曝气就可以为实验目的可重复地操纵FLO1的表型表达。