Suppr超能文献

使用衰减全反射傅里叶变换红外光谱(ATR-FTIR)微光谱法监测基础酒中酿酒酵母细胞的自溶。

Use of ATR-FTIR microspectroscopy to monitor autolysis of Saccharomyces cerevisiae cells in a base wine.

机构信息

Dipartimento di Scienze, Tecnologie e Mercati della Vite e del Vino, Universita degli Studi di Verona, Via della Pieve 70, 37029 San Floriano, Verona, Italy.

出版信息

J Agric Food Chem. 2010 Jan 13;58(1):39-45. doi: 10.1021/jf902369s.

Abstract

In this study, we evaluated the potentialities of ATR-FTIR microspectroscopy coupled to PCA in monitoring the major biochemical changes that occur during the autolysis of yeasts used for sparkling wine production. For this purpose, mid-infrared measurements were made on cells of the model strain Saccharomyces cerevisiae EC1118 in the course of autolysis induced at 30 degrees C for five days in a model and in a base wine. By relating principal component loadings to the corresponding absorption bands, it was shown that they well describe compositional modifications induced by autolytic process on yeast cells, such as partial hydrolysis of proteins, increase of peptides, free nucleotides, lipids, mannans, and beta-1,3 glucans. The corresponding score-score plots allowed us to monitor the different kinetics and to distinguish among faster, intermediate, and slower processes. ATR-FTIR microspectroscopy coupled with PCA is proposed as a sensitive method that can provide useful information to select efficient yeast strains, capable of accelerated autolysis, to be used in the second fermentation and aging of sparkling wines.

摘要

在这项研究中,我们评估了 ATR-FTIR 微光谱结合 PCA 在监测用于起泡酒生产的酵母自溶过程中发生的主要生化变化方面的潜力。为此,在模型和基础酒中,于 30°C 下诱导自溶 5 天的过程中,对模型菌株酿酒酵母 EC1118 的细胞进行了中红外测量。通过将主成分载荷与相应的吸收带相关联,表明它们很好地描述了自溶过程对酵母细胞引起的组成变化,如蛋白质的部分水解、肽、游离核苷酸、脂类、甘露聚糖和β-1,3 葡聚糖的增加。相应的得分-得分图允许我们监测不同的动力学并区分更快、中等和更慢的过程。ATR-FTIR 微光谱结合 PCA 被提议作为一种敏感的方法,可以提供有用的信息来选择有效的酵母菌株,这些菌株能够加速自溶,用于起泡酒的二次发酵和陈酿。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验