Literature DB >> 25528221

Identification and expression of a stearoyl-ACP desaturase gene responsible for oleic acid accumulation in Xanthoceras sorbifolia seeds.

Na Zhao1, Yuan Zhang2, Qiuqi Li3, Rufang Li4, Xinli Xia5, Xiaowei Qin6, Huihong Guo7.   

Abstract

Xanthoceras sorbifolia Bunge is an oilseed tree that grows well on barren lands in dry climate. Its seeds contain a large amount of oil rich in oleic acid (18:1(Δ9)) and linoleic acid (18:2(Δ9, 12)). However, the molecular regulation of oil biosynthesis in X. sorbifolia seeds is poorly understood. Stearoyl-ACP desaturase (SAD, EC 1.14.99.6) is a plastid-localized soluble desaturase that catalyzes the conversion of stearic acid (18:0) to oleic acid, which plays a key role in determining the ratio of saturated to unsaturated fatty acids. In this study, a full-length cDNA of XsSAD was isolated from developing X. sorbifolia embryos. The XsSAD open reading frame had 1194-bp, encoding a polypeptide of 397 amino acids. XsSAD expression in Escherichia coli cells resulted in increased 18:1(Δ9) level, confirming the biological activity of the enzyme encoded by XsSAD. XsSAD expression in Arabidopsis ssi2 mutants partially restored the morphological phenotype and effectively increased the 18:1(Δ9) level. The levels of other unsaturated fatty acids synthesized with 18:1(Δ9) as the substrate also increased to some degree. XsSAD in X. sorbifolia had a much higher expression in embryos than in leaves and petals. XsSAD expression also correlated well with the oleic acid, unsaturated fatty acid, and total fatty acid levels in developing embryos. These data suggested that XsSAD determined the synthesis of oleic acid and contributed to the accumulation of unsaturated fatty acid and total oil in X. sorbifolia seeds. A preliminary tobacco rattle virus-based virus-induced gene silencing system established in X. sorbifolia can also be helpful for further analyzing the functions of XsSAD and other oil synthesis-related genes in woody plants.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Functional and expression analysis; Oleic acid; Seed oil; Stearoyl-ACP desaturase; Unsaturated fatty acid; Xanthoceras sorbifolia Bunge

Mesh:

Substances:

Year:  2014        PMID: 25528221     DOI: 10.1016/j.plaphy.2014.12.009

Source DB:  PubMed          Journal:  Plant Physiol Biochem        ISSN: 0981-9428            Impact factor:   4.270


  5 in total

1.  Improving Regulation of Enzymatic and Non-Enzymatic Antioxidants and Stress-Related Gene Stimulation in Cucumber mosaic cucumovirus-Infected Cucumber Plants Treated with Glycine Betaine, Chitosan and Combination.

Authors:  Ahmed R Sofy; Rehab A Dawoud; Mahmoud R Sofy; Heba I Mohamed; Ahmed A Hmed; Noha K El-Dougdoug
Journal:  Molecules       Date:  2020-05-17       Impact factor: 4.411

2.  Identification of genes associated with the biosynthesis of unsaturated fatty acid and oil accumulation in herbaceous peony 'Hangshao' (Paeonia lactiflora 'Hangshao') seeds based on transcriptome analysis.

Authors:  Jia-Song Meng; Yu-Han Tang; Jing Sun; Da-Qiu Zhao; Ke-Liang Zhang; Jun Tao
Journal:  BMC Genomics       Date:  2021-02-01       Impact factor: 3.969

3.  Transcriptome-based analysis of the effects of salicylic acid and high light on lipid and astaxanthin accumulation in Haematococcus pluvialis.

Authors:  Qunju Hu; Danqiong Huang; Anguo Li; Zhangli Hu; Zhengquan Gao; Yongli Yang; Chaogang Wang
Journal:  Biotechnol Biofuels       Date:  2021-04-01       Impact factor: 6.040

4.  Small RNA profiling for identification of microRNAs involved in regulation of seed development and lipid biosynthesis in yellowhorn.

Authors:  Li Wang; Chengjiang Ruan; Aomin Bao; He Li
Journal:  BMC Plant Biol       Date:  2021-10-12       Impact factor: 4.215

5.  Comparative RNA-Seq Analysis of High- and Low-Oil Yellow Horn During Embryonic Development.

Authors:  Li Wang; Chengjiang Ruan; Lingyue Liu; Wei Du; Aomin Bao
Journal:  Int J Mol Sci       Date:  2018-10-08       Impact factor: 5.923

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.