Rabe Kersten S, Spengler Mark, Erkelenz Michael, Müller Joachim, Gandubert Valerie J, Hayen Heiko, Niemeyer Christof M
Technische Universität Dortmund, Fakultät Chemie, Biologisch-Chemische Mikrostrukturtechnik, Otto-Hahn Strasse 6, Dortmund, Germany.
Chembiochem. 2009 Mar 2;10(4):751-7. doi: 10.1002/cbic.200800750.
Cytochrome P450 enzymes are known to catalyze a variety of reactions that are difficult to perform by standard organic synthesis, such as the oxidation of unactivated C--C bonds. Cytochrome P450 enzymes can also be used in artificial systems in which organic peroxides act as cosubstrates. To find substrates that are converted by a certain P450 catalyst in the presence of an organic peroxide, various screening assays have been established, however, most of them are limited to one or only a few specific substrates. Here, we report a simple and rapid screening assay that works independently of the nature of the substrate and utilizes a previously undescribed reactivity of catalase as reporter enzyme. In an initial demonstration of this assay, we screened 180 enzyme/peroxide/substrate combinations for potential bioconversions. As shown by subsequent verification of the screening results with liquid chromatography/multistage mass spectrometry (LC/MS(n)), we were able to identify three new substrates for the enzyme CYP152A1 and at least two previously undescribed conversions by the enzyme CYP119.
细胞色素P450酶已知可催化多种标准有机合成难以进行的反应,例如未活化的C-C键的氧化反应。细胞色素P450酶还可用于有机过氧化物作为共底物的人工体系中。为了找到在有机过氧化物存在下能被特定P450催化剂转化的底物,人们已经建立了各种筛选方法,然而,其中大多数方法仅限于一种或仅几种特定底物。在此,我们报道了一种简单快速的筛选方法,该方法独立于底物的性质,利用过氧化氢酶以前未描述的反应性作为报告酶。在该方法的初步验证中,我们筛选了180种酶/过氧化物/底物组合以寻找潜在的生物转化反应。通过随后用液相色谱/多级质谱(LC/MS(n))对筛选结果进行验证表明,我们能够鉴定出三种新的CYP152A1酶底物以及至少两种CYP119酶以前未描述的转化反应。