Hauenstein Mareike, Hörtensteiner Stefan
Department of Plant and Microbial Biology, University of Zurich, Zurich, Switzerland.
Bio Protoc. 2017 Sep 20;7(18):e2561. doi: 10.21769/BioProtoc.2561.
Hydroxylation of chlorophyll catabolites at the so-called C3 position ( Hauenstein , 2016 ) is commonly found in all plant species analyzed to date. Here we describe an hydroxylation assay using chromoplast membranes as a source of the hydroxylating activity, which converts the substrate FCC ( Fluorescent Chlorophyll Catabolite) ( Mühlecker , 2000 ) to FCC-OH.
在迄今分析的所有植物物种中,叶绿素分解代谢产物在所谓的C3位置的羟基化作用(豪恩施泰因,2016年)普遍存在。在此,我们描述了一种羟基化测定方法,该方法使用有色体膜作为羟基化活性的来源,可将底物FCC(荧光叶绿素分解代谢产物)(米尔克,2000年)转化为FCC-OH。