Plant Tissue Culture and Genetic Engineering, National Agri-Food Biotechnology Institute (NABI), Mohali, 140306, Punjab, India.
Department of Life sciences, Sant Baba Bhag Singh University, Khiala, Padhiana, Jalandhar, 144030, Punjab, India.
Phytochemistry. 2020 Aug;176:112405. doi: 10.1016/j.phytochem.2020.112405. Epub 2020 May 27.
Elevating the lipid content in high-biomass forage crops has emerged as a new research platform for increasing energy density and improving livestock production efficiency associated with improved human health beneficial meat and milk quality. To gain insights of triacylglycerol (TAG) biosynthesis in forage sorghum, two type-1 diacylglycerol acyltransferase (designated as SbDGAT1-1 and SbDGAT1-2) were characterized for its in vivo function. SbDGAT1-2 is more abundantly expressed in embryo and bran during the early stage of the grain development in comparison to SbDGAT1-1. Heterologous expression of SbDGAT1 genes in TAG deficient H1246 strain restored the TAG accumulation capability with high substrate predilection towards 16:0, 16:1 and 18:1 fatty acids (FA). In parallel, we have identified N-terminal intrinsically disordered region (IDR) in SbDGAT1 proteins. To test the efficacy of the N-terminal region, truncated variants of SbDGAT1-1 (designated as SbDGAT1-1 and SbDGAT1-1) were generated and expressed in yeast H1246 strain. Deletion in the N-terminal region resulted in decreased accumulation of TAG and FA (16:0 and 18:0) when compared to the SbDGAT1-1 variant expressed in yeast H1246 strain. The present study provides significant insight in forage sorghum DGAT1 gene function, useful for enhancing the green-forage TAG content through metabolic engineering.
提高高生物量饲料作物的脂质含量已成为一个新的研究平台,可用于提高能量密度,并改善与改善肉质和牛奶质量相关的牲畜生产效率。为了深入了解饲料高粱中的三酰基甘油(TAG)生物合成,对两种 1 型二酰基甘油酰基转移酶(分别命名为 SbDGAT1-1 和 SbDGAT1-2)进行了体内功能表征。与 SbDGAT1-1 相比,SbDGAT1-2 在胚胎和谷粒发育早期的麸皮中表达更为丰富。SbDGAT1 基因在 TAG 缺陷型 H1246 菌株中的异源表达恢复了 TAG 积累能力,对 16:0、16:1 和 18:1 脂肪酸(FA)具有很高的底物偏好性。同时,我们已经鉴定了 SbDGAT1 蛋白中的 N 端无规卷曲结构域(IDR)。为了测试 N 端区域的功效,生成了 SbDGAT1-1 的截短变体(命名为 SbDGAT1-1 和 SbDGAT1-1)并在酵母 H1246 菌株中表达。与在酵母 H1246 菌株中表达的 SbDGAT1-1 变体相比,N 端区域缺失导致 TAG 和 FA(16:0 和 18:0)的积累减少。本研究为饲料高粱 DGAT1 基因功能提供了重要的见解,有助于通过代谢工程提高绿色饲料的 TAG 含量。