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Storage of Brewing Yeasts by Liquid Nitrogen Refrigeration

机译:液氮制冷储存啤酒酵母

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Many yeast strains are difficult to maintain in culture in a stable state, and long-term preservation by lyophilization, which has proved useful for other fungi, has given poor results with brewing yeasts. As an alternative to continuous subculture, which maximizes strain variability, various methods of cryogenic storage were investigated. Yeast strains were frozen with or without cryoprotectants (such as glycerol or inositol) and stored at -196 C. Recovery after warming was estimated from plate counts, and survivors were screened to detect changes in the frequency of morphological types, respiratory-deficient mutants, and glycerol-sensitive mutants. Strains varied in their sensitivity to freezing, and survival was modified by the growth medium, the freezing munstrua, and the freezing conditions. Suspension of cells in 10% (vol/vol) glycerol, cooled at 1 C/min, warmed rapidly and plated on malt-yeast extract-glucose-peptone agar produced the highest percentage of viable colonies with a minimal change in metabolic characteristics. In two of the strains tested, no significant increase in mutation rate was detected under any of the treatments; the strains were maintained in a stable state and were metabolically comparable to unfrozen strains. In one strain of Saccharomyces uvarum after some freezing treatments, the percentage of respiratory-deficient mutants increased markedly, the fermentation rate declined, and a loss of flocculation occurred. The freezing parameters which increased the level of respiratory-deficient cells should be avoided in maintaining this strain. Maintenance of cultures of brewing yeasts by cryogenic storage has several advantages over other preservation techniques: the method is simple and reproducible, the cultures have remained stable over a 3-year test period, and the viability is high.
机译:许多酵母菌株很难在培养物中保持稳定状态,而冻干的长期保存已被证明对其他真菌有用,而冻干的长期保存已证明酿造酵母的效果不佳。作为最大限度提高菌株变异性的连续传代培养的替代方法,研究了各种低温储存方法。酵母菌株在有或没有冷冻保护剂(例如甘油或肌醇)的情况下进行冷冻,并保存在-196°C。根据培养皿计数估算升温后的恢复率,并筛选幸存者以检测形态学类型,呼吸缺陷型突变体,和甘油敏感突变体。菌株对冷冻的敏感性各不相同,并且存活率因生长培养基,冷冻月经和冷冻条件而改变。将细胞悬浮于10%(vol / vol)的甘油中,以1 C / min的速度冷却,迅速升温并接种在麦芽酵母提取物-葡萄糖-内琼脂上,产生的活菌落百分比最高,代谢特性变化很小。在两种测试菌株中,在任何一种处理下均未检测到突变率的显着增加。这些菌株保持在稳定状态,并且在代谢上与未冷冻菌株相当。在经过一定程度的冷冻处理后,一株葡萄球菌的呼吸缺陷型突变体的百分比显着增加,发酵速率下降,并且发生了絮凝损失。为了维持这种应变,应避免增加呼吸缺陷细胞水平的冷冻参数。与其他保存技术相比,通过低温保存来维持酿造酵母的培养物具有多个优点:该方法简单且可重现,培养物在3年的测试期内保持稳定,并且具有很高的生存力。

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