Suzuki Takahito, Imanishi Yumi, Iwaguchi Shin-Ichi, Kamihara Teijiro
Department of Biological Science, Faculty of Science, Nara Women's University, Nara 630, Japan.
Department of Material Chemistry, Faculty of Engineering, Kyoto University, Kyoto 606-1, Japan.
Microbiology (Reading). 1998 Feb;144 ( Pt 2):403-410. doi: 10.1099/00221287-144-2-403.
Ethanol has been reported to cause mycelial growth in Candida tropicalis Pk233, and mycelial growth has also been shown to be abolished by concomitant addition of myo-inositol. In this study, the process of ethanol-induced mycelial growth in this organism was examined in combination with cytological characterization of actin localization. Cultivation with ethanol gave biphasic growth curves. During the first growth phase (doubling time 2.4 h), there was an accumulation of swollen spherical yeast cells, instead of the oblong ones observed in the control culture, followed by the appearance of spherical daughter cells in chains. Randomly-distributed actin patches were observed on these swollen yeast cells and the bud initiation sites of these cells appeared random. These observations suggested that ethanol caused depolarization of cell growth during the first phase. During the second growth phase (doubling time 7.4 h), pseudohyphal cells appeared, projecting from the swollen yeast cells. Activity of chitinase in the control culture rose during the exponential phase. In the ethanol culture the activity stayed at a low level throughout the growth phases. When pseudohyphal cells were transferred to fresh ethanol medium, yeast cells appeared from pseudohyphal filaments and changed their shape to spherical, and filamentation appeared to be inhibited during the first phase. From these observations, an initial effect of ethanol on C. tropicalis cells appeared to be depolarization of cell growth, and the resulting swollen cells grew as polar pseudohyphal cells. In the culture supplemented with both ethanol and inositol, or with both ethanol and sorbitol, the accumulation of swollen cells was not observed and single yeast cells with normal oblong shape were seen throughout the growth phases.
据报道,乙醇可导致热带假丝酵母Pk233出现菌丝体生长,并且同时添加肌醇可消除菌丝体生长。在本研究中,结合肌动蛋白定位的细胞学特征,对该生物体中乙醇诱导的菌丝体生长过程进行了研究。用乙醇培养得到双相生长曲线。在第一个生长阶段(倍增时间2.4小时),出现了肿胀的球形酵母细胞的积累,而不是在对照培养物中观察到的长方形细胞,随后出现了成链的球形子细胞。在这些肿胀的酵母细胞上观察到随机分布的肌动蛋白斑,并且这些细胞的芽起始位点似乎是随机的。这些观察结果表明,乙醇在第一阶段导致细胞生长去极化。在第二个生长阶段(倍增时间7.4小时),假菌丝细胞出现,从肿胀的酵母细胞伸出。对照培养物中的几丁质酶活性在指数生长期上升。在乙醇培养物中,该活性在整个生长阶段都保持在低水平。当将假菌丝细胞转移到新鲜的乙醇培养基中时,酵母细胞从假菌丝丝中出现并改变形状为球形,并且在第一阶段丝状化似乎受到抑制。从这些观察结果来看,乙醇对热带假丝酵母细胞的初始作用似乎是细胞生长去极化,并且由此产生的肿胀细胞作为极性假菌丝细胞生长。在同时添加乙醇和肌醇,或同时添加乙醇和山梨醇的培养物中,未观察到肿胀细胞的积累,并且在整个生长阶段都可以看到具有正常长方形形状的单个酵母细胞。