Torres N V, Meléndez-Hevia E
Departamento de Bioquímica y Biología Molecular, Facultad de Biología, Universidad de La laguna, Canary Islands, Spain.
Mol Cell Biochem. 1991 Feb 27;101(1):1-10. doi: 10.1007/BF00238432.
In this paper we give a general description of the 'shortening and enzyme titration method'. This method allows us to determine the Flux Control Coefficients of the different steps of a metabolic pathway in an in vitro experimental system. The system submitted to study is shortened in vitro by means of auxiliary enzymes, and the shortened pathway is titrated with extraneous enzymes. In this way we can modulate the activity of every enzyme of the system and thus every Flux Control Coefficient can be obtained. We criticize its different features in order to comment on the possibilities of its application to different types of systems. Our conclusion is that the method has a general applicability provided: a) that a correct definition of the metabolic pathway is given; b) that the system occurs in only one subcellular fraction and, c) that the dilution of the system by a given factor drives to the same reduction in every enzyme activity of the system.
在本文中,我们对“缩短和酶滴定法”进行了一般性描述。该方法使我们能够在体外实验系统中确定代谢途径不同步骤的通量控制系数。通过辅助酶在体外缩短用于研究的系统,并使用外源酶对缩短后的途径进行滴定。通过这种方式,我们可以调节系统中每种酶的活性,从而获得每个通量控制系数。我们对其不同特征进行了评判,以便评论其应用于不同类型系统的可能性。我们的结论是,该方法具有普遍适用性,条件如下:a)对代谢途径给出正确定义;b)系统仅存在于一个亚细胞组分中;c)系统按给定因子稀释会导致系统中每种酶活性产生相同程度的降低。