Related Experiment Video
Updated: Mar 7, 2026

Chromatographic Purification of Highly Active Yeast Ribosomes
Published on: October 24, 2011
Purification of cytochrome P450 from filamentous fungus Rhyzopus nigricans
Tomaž Makovec1, Katja Breskvar1
1Institute of Biochemistry, Faculty of Medicine, University of Ljubljana, Vrazov trg 2, Ljubljana, Slovenia, , , , , , SI.
Abstract:
It has been reported in our previous studies that steroid hydroxylation system of Rhizopus nigricans involves cytochrome P450 and NADPH-cytochrome P450 reductase in the electron transport system. Both enzymes are membrane bound and are located in the microsomal preparations of progesterone induced fungal mycelia. In order to identify and characterize the cytochrome P450 component of fungal monoxygenase system, microsomal proteins from induced mycelia were subjected to HIGH Q anion exchange and MONO P (FPLC) anion exchange chromatography. Four fractions containing cytochrome P450 have been resolved on MONO P column. They exhibit CO difference spectra and type II difference spectra with ketoconazole.

