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Yeast Cell Cycle During Fermentation and Beer Quality

机译:发酵过程中的酵母细胞周期和啤酒品质

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摘要

The yeast cell cycle is divided into four phases, G0/G1, S, G2, and M. Among them, G1 was thought to be the most important phase for fermentation performance because yeast cells undergo many critical preparations before budding. Therefore, it is advantageous to analyze the biochemical changes in the G1 phase to more precisely control the fermentation performance. However, the intracellular transition of yeast cells during the G1 phase has not been studied in detail because there was no method to simultaneously monitor the DNA and RNA contents in individual yeast cells. To solve this problem, we developed a new method for yeast cells by modifying the DNA/RNA double-staining method used for mammalian cells. DNA and RNA of yeast cells were stained with acridine orange under acidic conditions with ethylenediaminetetraacetic acid. The DNA and RNA contents in the yeast cells were measured using a flow cytome-ter. With this new method, we detected the amount of variation in the DNA and RNA. During the G1 phase, RNA was synthesized before the DNA synthesis that corresponded to yeast cell budding. The DNA/RNA synthesis during the G1 phase correlated with the fermentation performance and beer quality. It is worth noting that the DNA/RNA synthesis timing before the first budding significantly affects the final beer product quality.
机译:酵母细胞周期分为四个阶段:G0 / G1,S,G2和M。其中,G1被认为是发酵性能最重要的阶段,因为酵母细胞在出芽前需要经过许多关键的准备工作。因此,有利的是分析G1期中的生化变化以更精确地控制发酵性能。然而,由于没有方法可以同时监测单个酵母细胞中DNA和RNA的含量,因此尚未详细研究G1期酵母细胞的细胞内转变。为了解决这个问题,我们通过修改用于哺乳动物细胞的DNA / RNA双重染色方法,为酵母细胞开发了一种新方法。酵母细胞的DNA和RNA在酸性条件下用乙二胺四乙酸用a啶橙染色。使用流式细胞仪测量酵母细胞中的DNA和RNA含量。使用这种新方法,我们检测到了DNA和RNA的变异量。在G1阶段,与酵母细胞出芽相对应的DNA合成之前先合成RNA。 G1阶段的DNA / RNA合成与发酵性能和啤酒品质相关。值得注意的是,第一次萌芽前的DNA / RNA合成时间会显着影响最终啤酒产品的质量。

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