| Literature DB >> 1367429 |
H J Woerdenbag1, N Pras, H W Frijlink, C F Lerk, T M Malingré.
Abstract
After complexation with beta-cyclodextrin, the phenolic steroid 17 beta-estradiol could be ortho-hydroxylated into a catechol, mainly 4-hydroxyestradiol, by a phenoloxidase from in vitro grown cells of Mucuna pruriens. By complexation with beta-cyclodextrin the solubility of the steroid increased from almost insoluble to 660 microM. The bioconversion efficiency after 72 hr increased in the following order: freely suspended cells (0%), immobilized cells (1%), cell homogenate (6%), phenoloxidase preparation (40%). Mushroom tyrosinase converted 17 beta-estradiol, as a complex with beta-cyclodextrin, solely into 2-hydroxyestradiol, with a maximal yield of 30% after 6-8 hr. Uncomplexed 17 beta-estradiol was not converted at all in any of these systems.Entities:
Mesh:
Substances:
Year: 1990 PMID: 1367429 DOI: 10.1016/0031-9422(90)80119-2
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072