Thomsson Elisabeth, Gustafsson Lena, Larsson Christer
Department of Chemistry and Bioscience, Molecular Biotechnology, Lundberg Laboratory, Chalmers University of Technology, Box 462, SE-405 30 Gothenburg, Sweden.
Appl Environ Microbiol. 2005 Jun;71(6):3007-13. doi: 10.1128/AEM.71.6.3007-3013.2005.
Anaerobic starvation conditions are frequent in industrial fermentation and can affect the performance of the cells. In this study, the anaerobic carbon or nitrogen starvation response of Saccharomyces cerevisiae was investigated for cells grown in anaerobic carbon or nitrogen-limited chemostat cultures at a dilution rate of 0.1 h(-1) at pH 3.25 or 5. Lactic or benzoic acid was present in the growth medium at different concentrations, resulting in 16 different growth conditions. At steady state, cells were harvested and then starved for either carbon or nitrogen for 24 h under anaerobic conditions. We measured fermentative capacity, glucose uptake capacity, intracellular ATP content, and reserve carbohydrates and found that the carbon, but not the nitrogen, starvation response was dependent upon the previous growth conditions. All cells subjected to nitrogen starvation retained a large portion of their initial fermentative capacity, independently of previous growth conditions. However, nitrogen-limited cells that were starved for carbon lost almost all their fermentative capacity, while carbon-limited cells managed to preserve a larger portion of their fermentative capacity during carbon starvation. There was a positive correlation between the amount of glycogen before carbon starvation and the fermentative capacity and ATP content of the cells after carbon starvation. Fermentative capacity and glucose uptake capacity were not correlated under any of the conditions tested. Thus, the successful adaptation to sudden carbon starvation requires energy and, under anaerobic conditions, fermentable endogenous resources. In an industrial setting, carbon starvation in anaerobic fermentations should be avoided to maintain a productive yeast population.
厌氧饥饿条件在工业发酵中很常见,并且会影响细胞的性能。在本研究中,对在pH 3.25或5、稀释率为0.1 h⁻¹的厌氧碳或氮限制恒化器培养中生长的酿酒酵母细胞的厌氧碳或氮饥饿反应进行了研究。生长培养基中存在不同浓度的乳酸或苯甲酸,从而产生16种不同的生长条件。在稳态下,收获细胞,然后在厌氧条件下使其碳或氮饥饿24小时。我们测量了发酵能力、葡萄糖摄取能力、细胞内ATP含量和储备碳水化合物,发现碳饥饿反应而非氮饥饿反应取决于先前的生长条件。所有经历氮饥饿的细胞都保留了其初始发酵能力的很大一部分,与先前的生长条件无关。然而,经历碳饥饿的氮限制细胞几乎丧失了所有发酵能力,而碳限制细胞在碳饥饿期间设法保留了较大部分的发酵能力。碳饥饿前糖原的量与碳饥饿后细胞的发酵能力和ATP含量之间存在正相关。在任何测试条件下,发酵能力和葡萄糖摄取能力均不相关。因此,成功适应突然的碳饥饿需要能量,并且在厌氧条件下需要可发酵的内源性资源。在工业环境中,应避免厌氧发酵中的碳饥饿,以维持高产的酵母群体。