代谢组
生物
酵母
样品制备
代谢组学
色谱法
代谢物
细胞内
甲醇
生物化学
生物信息学
化学
有机化学
作者
Silas G. Villas‐Bôas,Jesper Højer‐Pedersen,Mats Åkesson,Jørn Smedsgaard,Jens Nielsen
出处
期刊:Yeast
[Wiley]
日期:2005-10-21
卷期号:22 (14): 1155-1169
被引量:380
摘要
Abstract Sample preparation is considered one of the limiting steps in microbial metabolome analysis. Eukaryotes and prokaryotes behave very differently during the several steps of classical sample preparation methods for analysis of metabolites. Even within the eukaryote kingdom there is a vast diversity of cell structures that make it imprudent to blindly adopt protocols that were designed for a specific group of microorganisms. We have therefore reviewed and evaluated the whole sample preparation procedures for analysis of yeast metabolites. Our focus has been on the current needs in metabolome analysis, which is the analysis of a large number of metabolites with very diverse chemical and physical properties. This work reports the leakage of intracellular metabolites observed during quenching yeast cells with cold methanol solution, the efficacy of six different methods for the extraction of intracellular metabolites, and the losses noticed during sample concentration by lyophilization and solvent evaporation. A more reliable procedure is suggested for quenching yeast cells with cold methanol solution, followed by extraction of intracellular metabolites by pure methanol. The method can be combined with reduced pressure solvent evaporation and therefore represents an attractive sample preparation procedure for high‐throughput metabolome analysis of yeasts. Copyright © 2005 John Wiley & Sons, Ltd.
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