André L, Hemming A, Adler L
Department of General and Marine Microbiology, University of Göteborg, Sweden.
FEBS Lett. 1991 Jul 29;286(1-2):13-7. doi: 10.1016/0014-5793(91)80930-2.
Production of glycerol and a key enzyme in glycerol production, glycerol 3-phosphate dehydrogenase (NAD+) (GPD), was studied in Saccharomyces cerevisiae cultured in basal media or media of high salinity, with glucose, raffinose or ethanol as the sole carbon source. At high salinity, glycerol production was stimulated with all carbon sources and glycerol was accumulated to high intracellular concentration in cells grown on glucose and raffinose. Cells grown on ethanol accumulated glycerol to a lower level but showed an increased content of trehalose at high salinity. However, the trehalose concentration corresponded only to about 20% of the glycerol level, and did not compensate for the shortfall in intracellular osmolyte content. Immunoblot analysis demonstrated an increased production of GPD at high salinity. This increase was osmotically mediated but was lower when glycerol was substituted for NaCl or sorbitol as the stress-solute. The enzyme also appeared to be subject to glucose repression; the specific activity of GPD was significantly lower in cells grown on glucose, than on raffinose or ethanol.
在以葡萄糖、棉子糖或乙醇作为唯一碳源,于基础培养基或高盐培养基中培养的酿酒酵母中,研究了甘油的产生以及甘油产生过程中的一种关键酶——甘油-3-磷酸脱氢酶(NAD⁺)(GPD)。在高盐条件下,所有碳源均能刺激甘油的产生,并且在以葡萄糖和棉子糖为碳源生长的细胞中,甘油积累至较高的细胞内浓度。以乙醇为碳源生长的细胞积累的甘油水平较低,但在高盐条件下海藻糖含量增加。然而,海藻糖浓度仅约为甘油水平的20%,无法弥补细胞内渗透溶质含量的不足。免疫印迹分析表明,在高盐条件下GPD的产量增加。这种增加是由渗透压介导的,但当用甘油替代NaCl或山梨醇作为应激溶质时,增加幅度较小。该酶似乎也受到葡萄糖阻遏作用的影响;在以葡萄糖为碳源生长的细胞中,GPD的比活性显著低于以棉子糖或乙醇为碳源生长的细胞。