Ghasemi Younes, Rasoul-Amini Sara, Morowvat Mohammad Hossein, Raee Mohammad Javad, Ghoshoon Mohammad Bagher, Nouri Fatemeh, Negintaji Narges, Parvizi Rezvan, Mosavi-Azam Seyed Bagher
Department of Pharmacognosy and Pharmaceutical Sciences, Research Center, Faculty of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
Molecules. 2008 Oct 31;13(10):2416-25. doi: 10.3390/molecules13102416.
A unicellular microalga, Chlamydomonas reinhardtii, was isolated from rice paddy-field soil and water samples and used in the biotransformation of hydrocortisone (1). This strain has not been previously tested for steroid bioconversion. Fermentation was carried out in BG-11 medium supplemented with 0.05% substrate at 25 degrees C for 14 days of incubation. The products obtained were chromatographically purified and characterized using spectroscopic methods. 11b,17 beta-Dihydroxyandrost-4-en-3-one (2), 11 beta-hydroxyandrost-4-en-3,17-dione (3), 11 beta,17 alpha,20 beta,21-tetrahydroxypregn-4-en-3-one (4) and prednisolone (5) were the main products of the bioconversion. The observed bioreaction features were the side chain degradation of the substrate to give compounds 2 and 3 and the 20-ketone reduction and 1,2-dehydrogenation affording compounds 4 and 5, respectively. A time course study showed the accumulation of product 2 from the second day of the fermentation and of compounds 3, 4 and 5 from the third day. All the metabolites reached their maximum concentration in seven days. Microalgal 18S rRNA gene was also amplified by PCR. PCR products were sequenced to confirm their authenticity as 18S rRNA gene of microalgae. The result of PCR blasted with other sequenced microalgae in NCBI showed 100% homology to the 18S small subunit rRNA of two Chlamydomonas reinhardtii spp.
从稻田土壤和水样中分离出一种单细胞微藻莱茵衣藻,并将其用于氢化可的松的生物转化(1)。该菌株此前尚未进行过甾体生物转化测试。在补充有0.05%底物的BG-11培养基中于25℃进行发酵,培养14天。对获得的产物进行色谱纯化,并使用光谱方法进行表征。11β,17β-二羟基雄甾-4-烯-3-酮(2)、11β-羟基雄甾-4-烯-3,17-二酮(3)、11β,17α,20β,21-四羟基孕甾-4-烯-3-酮(4)和泼尼松龙(5)是生物转化的主要产物。观察到的生物反应特征是底物的侧链降解生成化合物2和3,以及20-酮还原和1,2-脱氢分别生成化合物4和5。时间进程研究表明,发酵第二天开始积累产物2,第三天开始积累化合物3、4和5。所有代谢物在七天内达到最大浓度。还通过PCR扩增了微藻的18S rRNA基因。对PCR产物进行测序以确认其作为微藻18S rRNA基因的真实性。在NCBI中与其他已测序微藻进行比对的PCR结果显示,与两种莱茵衣藻的18S小亚基rRNA具有100%的同源性。