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三种酰基辅酶 A 还原酶(BdFAR1、BdFAR2 和 BdFAR3)参与了拟南芥角质层蜡初级醇生物合成。

Three Fatty Acyl-Coenzyme A Reductases, BdFAR1, BdFAR2 and BdFAR3, are Involved in Cuticular Wax Primary Alcohol Biosynthesis in Brachypodium distachyon.

机构信息

College of Agronomy, Northwest A&F University, Yangling 712100, Shaanxi, China.

State Key Laboratory of Crop Stress Biology for Arid Areas, Northwest A&F University, Yangling 712100, Shaanxi, China.

出版信息

Plant Cell Physiol. 2018 Mar 1;59(3):527-543. doi: 10.1093/pcp/pcx211.

Abstract

Plant cuticular wax is a heterogeneous mixture of very long chain fatty acids (VLCFAs) and their derivatives. Primary alcohols are the dominant wax components throughout leaf development of Brachypodium distachyon (Brachypodium). However, the genes involved in primary alcohol biosynthesis have not been investigated and their exact biological function remains unclear in Brachypodium to date. Here, we monitored the leaf wax profile and crystal morphology during Brachypodium leaf morphogenesis, and isolated three Brachypodium fatty acyl-CoA reductase (FAR) genes, named BdFAR1, BdFAR2 and BdFAR3, then analyzed their biochemical activities, substrate specificities, expression patterns, subcellular localization and stress induction. Transgenic expression of BdFAR genes in yeast (Saccharomyces cerevisiae), tomato (Solanum lycopersicum), Arabidopsis (Arabidopsis thaliana) and Brachypodium increased the production of primary alcohols. The three BdFAR genes were preferentially expressed in Brachypodium aerial tissues, consistent with known sites of wax primary alcohol deposition, and localized in the endoplasmic reticulum (ER) in Arabidopsis protoplasts. Finally, expression of the BdFAR genes was induced by drought, cold and ABA treatments, and drought stress significantly increased cuticular wax accumulation in Brachypodium. Taken together, these results indicate that the three BdFAR genes encode active FARs involved in the biosynthesis of Brachypodium wax primary alcohols and respond to abiotic stresses.

摘要

植物角质层蜡是非常长链脂肪酸(VLCFAs)及其衍生物的不均匀混合物。在拟南芥(Brachypodium)叶片发育的整个过程中,伯醇是蜡的主要成分。然而,迄今为止,尚未研究参与伯醇生物合成的基因,其确切的生物学功能在拟南芥中仍不清楚。在这里,我们监测了拟南芥叶片形态发生过程中的叶蜡轮廓和晶体形态,并分离出三个拟南芥脂肪酸辅酶 A 还原酶(FAR)基因,命名为 BdFAR1、BdFAR2 和 BdFAR3,然后分析了它们的生化活性、底物特异性、表达模式、亚细胞定位和胁迫诱导。BdFAR 基因在酵母(酿酒酵母)、番茄(番茄)、拟南芥(拟南芥)和拟南芥中的过表达增加了伯醇的产量。这三个 BdFAR 基因在拟南芥气生组织中优先表达,与已知的蜡伯醇沉积部位一致,并在拟南芥原生质体中定位于内质网(ER)。最后,BdFAR 基因的表达受到干旱、寒冷和 ABA 处理的诱导,干旱胁迫显著增加了拟南芥的角质层蜡积累。综上所述,这些结果表明,这三个 BdFAR 基因编码参与拟南芥蜡伯醇生物合成的活性 FAR,并对非生物胁迫作出响应。

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