» Articles » PMID: 25417743

Modifying the Lipid Content and Composition of Plant Seeds: Engineering the Production of LC-PUFA

Overview
Date 2014 Nov 25
PMID 25417743
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Omega-3 fatty acids are characterized by a double bond at the third carbon atom from the end of the carbon chain. Latterly, long chain polyunsaturated omega-3 fatty acids such as eicosapentaenoic acid (EPA; 20:5Δ5,8,11,14,17) and docosahexanoic acid (DHA; 22:6 Δ4,7,10,13,16,19), which typically only enter the human diet via the consumption of oily fish, have attracted much attention. The health benefits of the omega-3 LC-PUFAs EPA and DHA are now well established. Given the desire for a sustainable supply of omega-LC-PUFA, efforts have focused on enhancing the composition of vegetable oils to include these important fatty acids. Specifically, EPA and DHA have been the focus of much study, with the ultimate goal of producing a terrestrial plant-based source of these so-called fish oils. Over the last decade, many genes encoding the primary LC-PUFA biosynthetic activities have been identified and characterized. This has allowed the reconstitution of the LC-PUFA biosynthetic pathway in oilseed crops, producing transgenic plants engineered to accumulate omega-3 LC-PUFA to levels similar to that found in fish oil. In this review, we will describe the most recent developments in this field and the challenges of overwriting endogenous seed lipid metabolism to maximize the accumulation of these important fatty acids.

Citing Articles

Phosphorus starvation induces the synthesis of novel lipid class diacylglyceryl glucuronide and diacylglyceryl-N,N,N-trimethylhomoserine in two species of cold-adapted microalgae Raphidonema (Chlorophyta).

Suzuki H, Cuine S, Legeret B, Wijffels R, Hulatt C, Li-Beisson Y Plant J. 2025; 121(2):e17227.

PMID: 39868466 PMC: 11771548. DOI: 10.1111/tpj.17227.


Improving Undernutrition with Microalgae.

Panchal S, Heimann K, Brown L Nutrients. 2024; 16(18).

PMID: 39339823 PMC: 11435262. DOI: 10.3390/nu16183223.


ω-6 and ω-3 Polyunsaturated Fatty Acids: Inflammation, Obesity and Foods of Animal Resources.

Jeong H, Moon Y, Cho K Food Sci Anim Resour. 2024; 44(5):988-1010.

PMID: 39246544 PMC: 11377208. DOI: 10.5851/kosfa.2024.e65.


Understanding the Role of Polyunsaturated Fatty Acids in the Development and Prevention of Cancer.

Akbar S, Rahman A, Ahmad N, Imran M, Hafeez Z Cancer Treat Res. 2024; 191:57-93.

PMID: 39133404 DOI: 10.1007/978-3-031-55622-7_3.


Biotechnological production of omega-3 fatty acids: current status and future perspectives.

Qin J, Kurt E, LBassi T, Sa L, Xie D Front Microbiol. 2023; 14:1280296.

PMID: 38029217 PMC: 10662050. DOI: 10.3389/fmicb.2023.1280296.


References
1.
Metz J, Roessler P, Facciotti D, Levering C, Dittrich F, Lassner M . Production of polyunsaturated fatty acids by polyketide synthases in both prokaryotes and eukaryotes. Science. 2001; 293(5528):290-3. DOI: 10.1126/science.1059593. View

2.
Hoffmann M, Wagner M, Abbadi A, Fulda M, Feussner I . Metabolic engineering of omega3-very long chain polyunsaturated fatty acid production by an exclusively acyl-CoA-dependent pathway. J Biol Chem. 2008; 283(33):22352-62. DOI: 10.1074/jbc.M802377200. View

3.
Zank T, Zahringer U, Beckmann C, Pohnert G, Boland W, Holtorf H . Cloning and functional characterisation of an enzyme involved in the elongation of Delta6-polyunsaturated fatty acids from the moss Physcomitrella patens. Plant J. 2002; 31(3):255-68. DOI: 10.1046/j.1365-313x.2002.01354.x. View

4.
Sayanova O, Beaudoin F, Libisch B, Castel A, Shewry P, Napier J . Mutagenesis and heterologous expression in yeast of a plant Delta6-fatty acid desaturase. J Exp Bot. 2001; 52(360):1581-5. DOI: 10.1093/jexbot/52.360.1581. View

5.
Ruiz-Lopez N, Sayanova O, Napier J, Haslam R . Metabolic engineering of the omega-3 long chain polyunsaturated fatty acid biosynthetic pathway into transgenic plants. J Exp Bot. 2012; 63(7):2397-410. DOI: 10.1093/jxb/err454. View