Lehrstuhl für Pharmazeutische Biologie, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg, Staudtstr. 5, D-91058 Erlangen, Germany.
Steroids. 2012 Nov;77(13):1373-80. doi: 10.1016/j.steroids.2012.07.016. Epub 2012 Aug 11.
Cell cultures of Digitalis species are known to accept exogenous substrates for biotransformation reactions. We here report the biotransformation of 21-O-acetyl-deoxycorticosterone (1) by cell suspension cultures of Digitalis lanata strain W.1.4. Nine derivatives of 1 were obtained and their chemical structures determined by spectroscopic methods. 2β-Hydroxylation and C-21-glucosylation of the steroidal nucleus were described for the first time in suspension-cultured plant cells. Steroid 5α- and 5β-reduction products were also observed. Among the compounds isolated and structures elucidated were 2β,3β,21-trihydroxy-4-pregnen-20-one, 2β,3α,21-trihydroxy-4-pregnen-20-one and 3β,21-dihydroxy-5α-pregnan-20-one-3β-O-β-glucoside.
已知洋地黄属植物的细胞培养物能够接受外源底物进行生物转化反应。我们在此报告了毛地黄细胞悬浮培养物 W.1.4 对 21-O-乙酰去氧皮质酮(1)的生物转化。得到了 9 种 1 的衍生物,并通过光谱方法确定了它们的化学结构。在悬浮培养植物细胞中首次描述了甾体核的 2β-羟化和 C-21-葡糖苷化。还观察到了甾体 5α-和 5β-还原产物。分离得到的化合物和阐明的结构包括 2β,3β,21-三羟基-4-孕烯-20-酮、2β,3α,21-三羟基-4-孕烯-20-酮和 3β,21-二羟基-5α-孕烷-20-酮-3β-O-β-葡糖苷。