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Impact of Glucose Concentration and NaCl Osmotic Stress on Yeast Cell Wall β- d -Glucan Formation during Anaerobic Fermentation Process

机译:厌氧发酵过程中葡萄糖浓度和NaCl渗透胁迫对酵母细胞壁β-d-葡聚糖形成的影响

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Yeast β-glucan polysaccharide is a proven immunostimulant molecule for human and animal health. In recent years, interest in β-glucan industrial production has been increasing. The yeast cell wall is modified during the fermentation process for biomass production. The impact of environmental conditions on cell wall remodelling has not been extensively investigated. The aim of this research work was to study the impact of glucose and NaCl stress on β-glucan formation in the yeast cell wall during alcoholic fermentation and the assessment of the optimum fermentation phase at which the highest β-glucan yield is obtained. VIN 13 Saccharomyces cerevisiae ( S. cerevisiae ) strain was pre-cultured for 24 h with 0% and 6% NaCl and inoculated in a medium consisting of 200, 300, or 400 g/L glucose. During fermentation, 50 mL of fermented medium were taken periodically for the determination of Optical Density (OD), cell count, cell viability, cell dry weight, β-glucan concentration and β-glucan yield. Next, dry yeast cell biomass was treated with lytic enzyme and sonication. At the early stationary phase, the highest β-glucan concentration and yield was observed for non-NaCl pre-cultured cells grown in a medium containing 200 g/L glucose; these cells, when treated with enzyme and sonication, appeared to be the most resistant. Stationary is the optimum phase for cell harvesting for β-glucan isolation. NaCl and glucose stress impact negatively on β-glucan formation during alcoholic fermentation. The results of this work could comprise a model study for yeast β-glucan production on an industrial scale and offer new perspectives on yeast physiology for the development of antifungal drugs.
机译:酵母β-葡聚糖多糖是一种公认​​的人类和动物健康的免疫刺激分子。近年来,对β-葡聚糖工业生产的兴趣一直在增加。酵母细胞壁在发酵过程中被修饰以产生生物质。环境条件对细胞壁重塑的影响尚未得到广泛研究。这项研究工作的目的是研究酒精发酵过程中葡萄糖和NaCl胁迫对酵母细胞壁中β-葡聚糖形成的影响,并评估获得最高β-葡聚糖产量的最佳发酵阶段。将VIN 13酿酒酵母(S. cerevisiae)菌株与0%和6%NaCl预培养24小时,然后接种在200、300或400 g / L葡萄糖组成的培养基中。在发酵过程中,定期取出50 mL发酵培养基,以测定光密度(OD),细胞计数,细胞活力,细胞干重,β-葡聚糖浓度和β-葡聚糖产量。接下来,将干酵母细胞生物质用裂解酶和超声处理。在静止初期,在含有200 g / L葡萄糖的培养基中生长的非NaCl预培养细胞观察到最高的β-葡聚糖浓度和产量。当用酶和超声处理时,这些细胞似乎是最有抵抗力的。平稳是用于β-葡聚糖分离的细胞收获的最佳阶段。 NaCl和葡萄糖胁迫对酒精发酵过程中β-葡聚糖的形成产生负面影响。这项工作的结果可能包括工业规模生产酵母β-葡聚糖的模型研究,并为开发抗真菌药物的酵母生理学提供新的观点。

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