Yan Chunyan, Wang Jue, Duan Guoyan, Yu Rongmin
Department of Natural Medicinal Chemistry, College of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China.
Pharmacogn Mag. 2012 Apr;8(30):124-8. doi: 10.4103/0973-1296.96555.
Transgenic plant suspension cultures could be used as an effective tool for the biotransformation of exogenous compounds.
To investigate the biotransformation of furannoligularenone (1) by transgenic crown galls of Panax quinquefolium.
Compound 1 was administered into the crown gall cultures and co-cultured for 6 days. The cultures were dried and extracted with methanol for HPLC analyses. The extract was separated on column chromatography, and biotransformation products' structures were elucidated by the physicochemical properties and the data of NMR and MS. Moreover, three flasks were randomly chosen each day to establish time-course during the period for co-culturing.
Co-culturing compound 1 with crown galls yielded two compounds, 3-oxo-eremophila-1,7(11)-dien-12,8-olide (2) and 3-oxo-8-hydroxy-eremophila-1,7(11)-dien-12,8-olide (3), which were obtained by biotransformation using P. quinquefolium crown galls for the first time. Time-course investigation revealed that the mole conversion ratio reached the highest level of 45.5% and 33.9% on fourth and fifth day after substrate administration, respectively. Furthermore, a proposal biosynthesis pathway was given from compound 1 to compounds 2 and 3.
This was the first example of compound 1 being successfully converted into compounds 2 and 3 by transgenic crown galls of P. quinquefolium.
转基因植物悬浮培养物可作为外源化合物生物转化的有效工具。
研究西洋参转基因冠瘿对呋喃愈创木烯酮(1)的生物转化。
将化合物1加入冠瘿培养物中,共培养6天。培养物干燥后用甲醇提取,进行高效液相色谱分析。提取物经柱色谱分离,通过物理化学性质以及核磁共振和质谱数据阐明生物转化产物的结构。此外,在共培养期间每天随机选取三个烧瓶以建立时间进程。
化合物1与冠瘿共培养产生了两种化合物,3-氧代-艾里莫芬-1,7(11)-二烯-12,8-内酯(2)和3-氧代-8-羟基-艾里莫芬-1,7(11)-二烯-12,8-内酯(3),这是首次利用西洋参冠瘿通过生物转化获得的。时间进程研究表明,底物加入后第4天和第5天摩尔转化率分别达到最高水平,为45.5%和33.9%。此外,给出了从化合物1到化合物2和3的推测生物合成途径。
这是化合物1首次被西洋参转基因冠瘿成功转化为化合物2和3的实例。