Rouwenhorst R J, van der Baan A A, Scheffers W A, Van Dijken J P
Department of Microbiology and Enzymology, Kluyver Laboratory of Biotechnology, Delft University of Technology, The Netherlands.
Appl Environ Microbiol. 1991 Feb;57(2):557-62. doi: 10.1128/aem.57.2.557-562.1991.
In synchronized continuous cultures of Saccharomyces cerevisiae CBS 8066, the production of the extracellular invertase (EC 3.2.1.26) showed a cyclic behavior that coincided with the budding cycle. The invertase activity increased during bud development and ceased at bud maturation and cell scission. The cyclic changes in invertase production resulted in cyclic changes in amounts of invertase localized in the cell wall. However, the amount of enzyme invertase present in the culture liquid remained constant throughout the budding cycle. Also, in asynchronous continuous cultures of S. cerevisiae, the production and localization of invertase showed significant fluctuation. The overall invertase production in an asynchronous culture was two to three times higher than in synchronous cultures. This could be due to more-severe invertase-repressive conditions in a synchronous chemostat culture. Both the intracellular glucose-6-phosphate concentration and residual glucose concentration were significantly higher in synchronous chemostat cultures than in asynchronous chemostat cultures. In the asynchronous and synchronous continuous cultures of S. cerevisiae, about 40% of the invertase was released into the culture liquid; it has generally been believed that S. cerevisiae releases only about 5% of its invertase. In contrast to invertase production and localization in the chemostat cultures of S. cerevisiae, no significant changes in inulinase (EC 3.2.1.7) production and localization were observed in chemostat cultures of Kluyveromyces maxianus CBS 6556. In cultures of K. marxianus about 50% of the inulinase was present in the culture liquid.
在酿酒酵母CBS 8066的同步连续培养中,胞外转化酶(EC 3.2.1.26)的产生呈现出与出芽周期一致的循环行为。转化酶活性在芽发育过程中增加,并在芽成熟和细胞分裂时停止。转化酶产生的循环变化导致了细胞壁中转化酶含量的循环变化。然而,培养液中存在的转化酶量在整个出芽周期中保持恒定。此外,在酿酒酵母的异步连续培养中,转化酶的产生和定位也表现出显著波动。异步培养中转化酶的总体产量比同步培养高两到三倍。这可能是由于同步恒化器培养中存在更严重的转化酶抑制条件。同步恒化器培养中的细胞内6-磷酸葡萄糖浓度和残余葡萄糖浓度均显著高于异步恒化器培养。在酿酒酵母的异步和同步连续培养中,约40%的转化酶释放到培养液中;一般认为酿酒酵母仅释放约5%的转化酶。与酿酒酵母恒化器培养中转化酶的产生和定位不同,在马克斯克鲁维酵母CBS 6556的恒化器培养中,未观察到菊粉酶(EC 3.2.1.7)的产生和定位有显著变化。在马克斯克鲁维酵母培养物中,约50%的菊粉酶存在于培养液中。