Ahlawat Seema, Saxena Parul, Ali Athar, Khan Shazia, Abdin Malik Z
Department of Biotechnology, Faculty of Science, Centre for Transgenic Plant Development, Jamia Hamdard, New Delhi 110062, India.
Department of Biotechnology, Faculty of Science, Centre for Transgenic Plant Development, Jamia Hamdard, New Delhi 110062, India.
Plant Physiol Biochem. 2017 May;114:19-28. doi: 10.1016/j.plaphy.2017.02.013. Epub 2017 Feb 17.
Ashwagandha (Withania somnifera) is one of the most reputed medicinal plants in the traditional medicinal system. In this study, cell suspension culture of W. somnifera was elicited with cell homogenates of fungi (A. alternata, F. solani, V. dahliae and P. indica) in shake flask and the major withanolides like withanolide A, withaferin A and withanone were analysed. Simultaneously expression levels of key pathway genes from withanolides biosynthetic pathways were also checked via quantitative PCR in shake flask as well as in bioreactor. The results show that highest gene expression of 10.8, 5.8, 4.9, and 3.3 folds were observed with HMGR among all the expressed genes in cell suspension cultures with cell homogenates of 3% P. indica, 5% V. dahliae, 3% A. alternata and 3% F. solani, respectively, in comparison to the control in shake flask. Optimized concentration of cell homogenate of P. indica (3% v/v) was added to the growing culture in 5.0-l bioreactor under optimized up-scaling conditions and harvested after 22 days. The genes of MVA, MEP and withanolides biosynthetic pathways like HMGR, SS, SE, CAS, FPPS, DXR and DXS were up-regulated by 12.5, 4.9, 2.18, 4.65, 2.34, 1.89 and 1.4 folds, respectively in bioreactor. The enhancement of biomass (1.13 fold) and withanolides [withanolide A (1.7), withaferin A (1.5), and withanone (1.5) folds] in bioreactor in comparison to shake flask was also found to be in line with the up-regulation of genes of withanolide biosynthetic pathways.
印度人参(Withania somnifera)是传统医学体系中最负盛名的药用植物之一。在本研究中,在摇瓶中用真菌(链格孢菌、茄腐镰刀菌、大丽轮枝菌和印度梨形孢)的细胞匀浆对印度人参进行细胞悬浮培养,并分析了主要的睡茄内酯,如睡茄内酯A、睡茄素A和睡茄酮。同时,还通过定量PCR在摇瓶和生物反应器中检测了睡茄内酯生物合成途径关键途径基因的表达水平。结果表明,与摇瓶中的对照相比,在细胞悬浮培养物中,分别用3%印度梨形孢、5%大丽轮枝菌、3%链格孢菌和3%茄腐镰刀菌的细胞匀浆处理后,所有表达基因中HMGR的基因表达最高,分别为10.8、5.8、4.9和3.3倍。在优化的放大条件下,将优化浓度的印度梨形孢细胞匀浆(3% v/v)添加到5.0升生物反应器中的生长培养物中,并在22天后收获。在生物反应器中,MVA、MEP和睡茄内酯生物合成途径的基因,如HMGR、SS、SE、CAS、FPPS、DXR和DXS分别上调了12.5、4.9、2.18、4.65、2.34、1.89和1.4倍。与摇瓶相比,生物反应器中生物量(1.13倍)和睡茄内酯[睡茄内酯A(1.7)、睡茄素A(1.5)和睡茄酮(1.5)倍]的增加也与睡茄内酯生物合成途径基因的上调一致。