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Effects of Fermentation Parameters and Cell Wall Properties on Yeast Flocculation

机译:发酵参数和细胞壁特性对酵母絮凝的影响

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Industrial wort was fermented with a NewFlo phenotype ale yeast in lab-scale cylindrical fermenters. The effects of various fermentation parameters and yeast cell wall properties on yeast flocculation were studied during 120 h fermentation. The evaluation of the cell volume during the fermentation revealed a non-normal distribution (p < 0.05) at most fermentation times. Overall yeast cell size initially decreased during the first 24 h of fermentation then increased during the 24-60 h fermentation period. Cell size subsequently declined until the end of fermentation presumably due to floc settling. While yeast flocculation began after 24 h fermentation, most floes remained in suspension until 60 h when the average turbulent shear rate caused by CO_2 evolution declined to below 8 s~(-1). Both the Helm's floccu-lence and cell surface hydrophobicity values rapidly increased to high numbers from 24 h onward. Changes in the orthokinetic capture coefficient (α_0) value with fermentation time, measured in fermenting worts, indicated a significant increase (p < 0.001) after 24 h of fermentation. Presumably, this change was due to increases in ethanol and the decline in sugar concentration with time. Although a significant positive correlation (p < 0.05) was observed between zymolectin densities and cell surface areas, the total zymolectin level on yeast cell walls did not change significantly with fermentation time (p > 0.05). Interestingly, no significant difference existed in Helm's flocculation values of suspended and settled yeast cells (p > 0.05). The flocculation rate of LCC125 was readily inhibited by addition of glucose or maltose. Results suggest that fermentable sugar levels and shear force exert major influences on yeast flocculation during beer fermentations.
机译:在实验室规模的圆柱形发酵罐中,用NewFlo表型强麦酒酵母发酵工业麦芽汁。研究了120 h发酵过程中各种发酵参数和酵母细胞壁特性对酵母絮凝的影响。发酵过程中细胞体积的评估表明,在大多数发酵时间中,细胞分布均呈非正态分布(p <0.05)。总体酵母细胞大小最初在发酵的前24小时减小,然后在24-60 h的发酵期间增加。随后细胞大小下降,直到发酵结束,大概是由于絮凝沉淀所致。发酵24 h后开始絮凝,大部分絮凝物保持悬浮状态,直至60 h,CO_2释放引起的平均湍流剪切速率降至8 s〜(-1)以下。从24小时起,Helm的絮凝度和细胞表面疏水性值均迅速增加至较高数值。在发酵麦芽汁中测得的随时间变化的原动力捕获系数(α_0)值表明发酵24小时后显着增加(p <0.001)。据推测,这种变化是由于乙醇的增加和糖浓度随时间的下降而引起的。尽管观察到zymolectin密度与细胞表面积之间存在显着的正相关性(p <0.05),但酵母细胞壁上的总zymolectin水平并未随发酵时间而显着变化(p> 0.05)。有趣的是,悬浮和沉淀酵母细胞的Helm絮凝值没有显着差异(p> 0.05)。加入葡萄糖或麦芽糖很容易抑制LCC125的絮凝速率。结果表明,啤酒发酵过程中可发酵糖水平和剪切力对酵母絮凝有重要影响。

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