Devi M K Akitha, Kumar Gyanendra, Giridhar P
Plant Cell Biotechnology Department, CSIR-Central Food Technological Research Institute, Mysore, Karnataka 570 020 India.
3 Biotech. 2020 Mar;10(3):98. doi: 10.1007/s13205-020-2065-1. Epub 2020 Feb 6.
The present investigation aimed to look at the effects of biotic and abiotic elicitors during Soybean seed development and cell suspension culture in isoflavones accumulation. The expression levels of four major genes viz., CHS7, CHS8, IFS2, and IFS1 involved on isoflavones biosynthesis during seed developmental stages from R5L-R7 was seen in both MAUS-2 and JS-335 Soybean varieties. The R7 stage showed 1.24-fold upregulation of IFS1transcript level and considered as the control for Soybean seed development. Both varieties during R6-R8 stages responded differently to the foliar application of 10 µM SA, 10 µM MJ and 0.1% . The transcripts were upregulated by SA at the R7 stage with 5.21- and 4.68-fold in JS-335 and MAUS-2, respectively. expression was significantly increased by treatment at R7 stage with 3.98- and 3.21-fold in MAUS-2 and JS-335, respectively. The expression of CHS7 and CHS8 by 10 μM SA at R7 level revealed maximum up-regulation of 0.51- and 1.01-fold in MAUS-2; 0.37- and 0.82-fold in JS-335, respectively. In the soybean callus suspension culture, biosynthetic genes were used to validate the effects of elicitor on isoflavones. Both biotic and abiotic treatments contribute to the upregulation of and expression, that in turn, leads to the accumulation of isoflavone in seed development as well as in suspension cultures. These data further suggested that the is the key gene responsible for the isoflavone accumulation during elicitor treatment.
本研究旨在探讨生物和非生物诱导子对大豆种子发育及细胞悬浮培养过程中异黄酮积累的影响。在MAUS - 2和JS - 335两个大豆品种的种子发育阶段(从R5L到R7),观察到参与异黄酮生物合成的四个主要基因CHS7、CHS8、IFS2和IFS1的表达水平。R7阶段显示IFS1转录水平上调1.24倍,被视为大豆种子发育的对照。在R6 - R8阶段,两个品种对10 μM水杨酸(SA)、10 μM茉莉酸甲酯(MJ)和0.1% [此处原文缺失具体物质] 的叶面喷施反应不同。在R7阶段,SA使转录本上调,在JS - 335和MAUS - 2中分别上调5.21倍和4.68倍。[此处原文缺失具体物质] 处理在R7阶段使表达显著增加,在MAUS - 2和JS - 335中分别增加3.98倍和3.21倍。10 μM SA在R7水平对CHS7和CHS8的表达显示,在MAUS - 2中最大上调0.51倍和1.01倍;在JS - 335中分别上调0.37倍和0.82倍。在大豆愈伤组织悬浮培养中,利用生物合成基因验证诱导子对异黄酮的影响。生物和非生物处理均有助于上调[此处原文缺失具体基因] 和[此处原文缺失具体基因] 的表达,进而导致种子发育和悬浮培养中异黄酮的积累。这些数据进一步表明,[此处原文缺失具体基因] 是诱导子处理期间异黄酮积累的关键基因。