作者
Karen Van Eunen, Jildau Bouwman, Pascale Daran‐Lapujade, Jarne Postmus, André B Canelas, Femke IC Mensonides, Rick Orij, Isil Tuzun, Joost Van Den Brink, Gertien J Smits, Walter M Van Gulik, Stanley Brul, Joseph J Heijnen, Johannes H De Winde, M Joost Teixeira de Mattos, Carsten Kettner, Jens Nielsen, Hans V Westerhoff, Barbara M Bakker
发表日期
2010/2
期刊
The FEBS journal
卷号
277
期号
3
页码范围
749-760
出版商
Blackwell Publishing Ltd
简介
Realistic quantitative models require data from many laboratories. Therefore, standardization of experimental systems and assay conditions is crucial. Moreover, standards should be representative of the in vivo conditions. However, most often, enzyme–kinetic parameters are measured under assay conditions that yield the maximum activity of each enzyme. In practice, this means that the kinetic parameters of different enzymes are measured in different buffers, at different pH values, with different ionic strengths, etc. In a joint effort of the Dutch Vertical Genomics Consortium, the European Yeast Systems Biology Network and the Standards for Reporting Enzymology Data Commission, we have developed a single assay medium for determining enzyme–kinetic parameters in yeast. The medium is as close as possible to the in vivo situation for the yeast Saccharomyces cerevisiae, and at the same time is …
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