10 Apr 2014:
The PLOS ONE Staff
Correction: Metabolic Engineering
Omega-3 long-chain (≥C20) polyunsaturated fatty acids (ω3 LC-PUFA) such as eicosapentaenoic acid (EPA) and docosapentaenoic acid (DHA) are critical for human health and development. Numerous studies have indicated that deficiencies in these fatty acids can increase the risk or severity of cardiovascular, inflammatory and other diseases or disorders. EPA and DHA are predominantly sourced from marine fish although the primary producers are microalgae. Much work has been done to engineer a sustainable land-based source of EPA and DHA to reduce pressure on fish stocks in meeting future demand, with previous studies describing the production of fish oil-like levels of DHA in the model plant species, Arabidopsis thaliana.
In this study we describe the production of fish oil-like levels (>12%) of DHA in the oilseed crop species Camelina sativa achieving a high ω3/ω6 ratio. The construct previously transformed in Arabidopsis as well as two modified construct versions designed to increase DHA production were used. DHA was found to be stable to at least the T5 generation and the EPA and DHA were found to be predominantly at the sn-1,3 positions of triacylglycerols. Transgenic and parental lines did not have different germination or seedling establishment rates.
DHA can be produced at fish oil-like levels in industrially-relevant oilseed crop species using multi-gene construct designs which are stable over multiple generations. This study has implications for the future of sustainable EPA and DHA production from land-based sources.
Citation: Petrie JR, Shrestha P, Belide S, Kennedy Y, Lester G, Liu Q, et al. (2014) Metabolic Engineering Camelina sativa with Fish Oil-Like Levels of DHA. PLoS ONE 9(1): e85061. doi:10.1371/journal.pone.0085061
Editor: Maeli Melotto, University of Texas, United States of America
Received: August 19, 2013; Accepted: November 21, 2013; Published: January 21, 2014
Copyright: © 2014 Petrie et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This research was funded by CSIRO Food Futures Flagship, Nuseed Pty Ltd and the Australian Grains Research and Development Corporation. The funders had no role in study design, data collection and analysis, or preparation of the manuscript. The authors were granted permission to publish the manuscript by the funders.
Competing interests: This study was partly funded by Nuseed Pty Ltd and the Australian Grains Research and Development Corporation (GRDC). Some of the data provided in this study may have been included in patent applications. CSIRO is in a commercial arrangement with GRDC and Nuseed to develop DHA land plants, although there is no product name as yet. There are no further patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors.
The omega-3 long-chain (≥C20) polyunsaturated fatty acids (ω3 LC-PUFA) EPA (eicosapentaenoic acid, 20∶5ω3) and DHA (docosahexaenoic acid, 22∶6ω3) are recognized for their strong health benefits. Developing an oilseed source of these fatty acids is desirable since these provide far stronger health benefits than the shorter chain terrestrial plant precursors of these fatty acids, α-linolenic acid (ALA, 18∶3ω3) and stearidonic acid (SDA, 18∶4ω3) . Moreover, the conversion of these precursor fatty acids to long-chain variants occurs at surprisingly low levels in humans . Importantly, studies have also found that high concentrations of ω6 fatty acids such as LA (linoleic acid, 18∶2ω6), GLA (γ-linolenic acid, 18∶3ω6) and ARA (arachidonic acid, 20∶4ω6) can decrease the bioconversion efficiency of C18 ω3 fatty acids to long-chain PUFA . The production of ω3 LC-PUFA in land plants as been a long-standing goal of bioengineers. The first demonstrations of LC-PUFA production were published in 2004 and showed EPA and ARA production in leaf  and seed . The first demonstrations of DHA production in seed were published soon after , . Subsequent work resulted in increasing levels of production, particularly for EPA –. The first report of production of fish oil-like levels of DHA in seed was published in 2012 . Progress has been extensively reviewed in recent years , .
Camelina sativa, also known as Gold of Pleasure and False Flax, is an ancient cultivated oilseed crop ,  with naturally high levels of the C18 ω3 ALA in seed oil. Commercial cultivation of the crop slowed significantly with the introduction of oilseed rape but has recently garnered significant attention as an underutilised species. Some C. sativa varieties have high oil content (in excess of 40%) and have strong agronomic performance on marginal lands  and approvals have recently been granted for C. sativa meal or oil use in food and animal feed applications in USA and Canada. In this article we describe the production of fish oil-like levels of DHA (12%) in C. sativa by the introduction of a transgenic Δ6-desaturase pathway (Figure 1) consisting of both yeast and microalgal genes to convert native OA (oleic acid, 18∶ω9), LA and ALA substrates to the beneficial ω3 LC-PUFA EPA and DHA.
‘Des’ denotes desaturase and ‘elo’ denotes elongase. OA, oleic acid; LA, linoleic acid; GLA, γ-linolenic acid; DGLA, dihomo-γ-linolenic acid; ARA, arachidonic acid; DTA, docosatetraenoic acid; DPA6, ω6 docosapentaenoic acid; ALA, α-linolenic acid; SDA, stearidonic acid; ETA, eicosatetraenoic acid; EPA, eicosapentaenoic acid; DPA, ω3 docosapentaenoic acid.
Materials and Methods
Genes and expression vectors
Constructs mod-F and mod-G were made using a combination of DNA synthesis and restriction enzyme-based cloning starting with the previously described GA7 parent vector , Figure 2. Mod-F was made by replacing the SbfI-flanked Δ5-elongase expression cassette near the left border with a Δ6-elongase expression cassette. The original Δ6-desaturase expression cassette and the adjacent Δ6-elongase promoter and coding region were then excised with AscI + PmeI and replaced with the Cnl2:: Δ6-desaturase::NOS expression cassette plus the replacement Δ5-elongase promoter and coding region. The second Δ6-desaturase expression cassette was then added at the PmeI site as a PmeI-SwaI blunt-ended fragment to generate mod-F. Construct mod-G was generated by first replacing the original Δ6-desaturase expression cassette and the adjacent Δ6-elongase promoter and coding region (flanked by AscI + PmeI) with the new Δ5-elongase expression cassette and adjacent Δ6-elongase coding region. The original Δ5-elongase expression cassette adjacent to the left border (flanked by SbfI) was then replaced with the Δ6-desaturase expression cassette.
The box denotes the unchanged region. Abbreviations are: TER, terminator or polyadenylation region; PRO, promoter; NOS, Agrobacterium tumefaciens nopaline synthase terminator; FP1, Brassica napus truncated napin promoter; FAE1, Arabidopsis thaliana FAE1 promoter; Lectin, Glycine max lectin terminator; Cnl1 and Cnl2 denotes the Linum usitatissimum conlinin1 or conlinin2 promoter or terminator. MAR denotes the Rb7 matrix attachment region from Nicotiana tabacum and gene identities are given in the text and the Materials and Methods section.
Constructs were transformed in Agrobacterium tumefaciens strain AGL1 and cultured at 28°C on a rotary shaker to appropriate growth phase. C. sativa (“Celine”) was transformed by a floral dip method adapted from Liu et al. . Briefly, the freshly opened flower buds were dipped in A. tumefaciens solution for 15 s, wrapped in plastic film and left overnight in the dark at 24°C after which the plastic was removed.
Lipid fractionation and fatty acid profile analysis
Total lipid was extracted from seeds using chloroform: methanol: 0.1 M KCl (2∶1∶1 v/v/v as described in . Neutral lipid classes and polar lipid were fractionated from the total lipid on a TLC plate (Silica gel 60, MERCK) using a mixture of hexane: diethylether: acetic acid (70∶30∶1, v/v). The lipid bands were visualized under UV after spraying the plate with 0.001% primuline dissolved in acetone:water (80∶20 v/v). The individual lipid bands were identified on the basis of authentic lipid standards, which were run parallel to the seed lipid samples in the TLC, collected into separate glass vials and their fatty acid methyl esters (FAME) were prepared together with known amount of heptadecanoic acid as internal standard. FAMEs were analysed by GC as previously described  and individual lipids were quantified on the basis of the amounts of FAMEs produced from the known amount of internal standards used.
DHA levels in T5 seeds from 15 randomly selected homozygous plants grown in three glasshouses were analysed by One Way Analysis of Variance (ANOVA) using Sigmaplot (v12) by the Holm-Sidak method .
RNA was extracted from developing seed taken from three plants of a high DHA line transformed with either GA7, mod-F or mod-G using RNeasy Plant Mini kit (Qiagen, Hilden, Germany). Total RNA (1 µg) was converted to cDNA using First-Strand cDNA synthesis mix (OriGene Inc., Australia). Diluted cDNA (0.2×) was used for quantitative real-time PCR by Bio-Rad CFX Real-Time System (BIO-RAD, USA) using iQSYBR Green Supermix (BIO-RAD). Reactions were carried with initial denaturation at 95°C for 3 min, followed by 35 cycles of 95°C for 10 sec, 58°C for 30 sec and 68°C for 30 sec. Target gene expression was normalized to the endogenous C. sativa HMG gene in the Bio-Rad CFX Manager software.
13C NMR analysis
A hexane-extracted oil (>99% TAG, confirmed by TLC-FID; results not shown) was obtained by sequential extraction of crushed seeds and prior to analysis was stored at -18°C. Samples were warmed to room temperature 1 h prior to NMR sample preparation. 100 mg oil was dissolved in deuteriochloroform containing 25 mM Tris(acetylacetonate) chromium(III) as a relaxation agent (0.6 mL). The solutions were transferred to 5 mm O.D. NMR tubes (New Era NE-UL5-7) and sealed with PTFE lids. Solutions for NMR spectroscopy were stored at 4°C until they were inserted into the magnet. Quantitative 13C NMR spectra were acquired on a Bruker BioSpin Av500 NMR spectrometer equipped with a 5 mm 1H-13C/15N triple-resonance inverse probe operating at 125.8 MHz for 13C. The data were acquired and processed in Bruker BioSpin TopSpin v3.2. The samples were maintained at 25°C during acquisition. 128 k data points were collected over a spectral width of 26.3 kHz summed over 46 k scans. Inverse-gated, bilevel adiabatic 1H-decoupling was employed with an acquisition time of 2.49 s and a recycle delay of 2.5 s. Data were processed to 128 k data points using a Gaussian multiplication with a Gaussian position factor of 0.12 and a line broadening of −0.15 Hz prior to Fourier transformation; a 5th-order polynomial baseline correction was applied to each spectrum. Spectra were referenced to the peak arising from C1 of 22∶6ω3 in the sn-2 position of TAG at 172.13 ppm  and the signals assigned using the published assignments . The raw data were processed in a similar fashion in triplicate and the mean and standard deviations calculated.
Results and Discussion
Construct design and manufacture
Use of construct pJP3416_GA7 (GA7) to generate DHA-containing seeds in A. thaliana has previously been described . Two GA7 construct variants, referred to here as mod-F and mod-G, were designed to improve the efficiency of the Δ6-desaturase and Δ6-elongase steps. The core GA7 sequence was left intact (Figure 2a) with only the terminal regions that contained the genes of interest modified. Specifically, the GA7 terminal FP1/NOS promoter/terminator pair was replaced with the Linum usitatissimum conlinin2 (Cnl2) promoter/terminator pair in both new variants. The mod-F changes consisted of the switching of the two elongase coding regions as well as the addition of a second Micromonas pusilla Δ6-desaturase coding region with different codon usage to the original GA7 version (Figure 2b). In addition to the conlinin2 cassette changes described above, the Δ6-desaturase and Δ5-elongase coding regions were also switched in mod-G (Figure 2c).
Conversion of ALA to SDA (Δ6-desaturation) had previously been identified as a bottleneck in DHA production in A. thaliana and in this study we tested both the effect of using different promoters (A. thaliana FAE1 and L. usitatissimum Cnl2) and the addition of a second expression cassette with different gene codon usage to avoid gene silencing. The changes made in mod-G also tested whether the expression cassette adjacent the right border was intrinsically compromised  by switching the Δ6-desaturation and Δ5-elongase cassettes. Similarly, the Δ5-elongase had previously been shown to have very high activity whilst the Δ6-elongase had lower activity. The changes in mod-F included switching the two elongase coding regions to test whether this was due to the expression cassette rather than the gene.
Camelina sativa transformation
Constructs were sequence confirmed and transformed in Agrobacterium strain AGL1 before floral dip of C. sativa. After the floral dip, plants were grown to maturity, seed harvested, and germinated in soil trays. Established seedlings (7–10 days) were sprayed with 0.1% BASTA herbicide (250 g/L glufosinate ammonium; Bayer Crop Science Pty Ltd, VIC Australia) to kill plants not expressing the selectable marker gene. The original GA7 construct was used to establish the C. sativa transformation protocol in the lab and was transformed before the mod-F and mod-G constructs.
Transgenic C. sativa can accumulate 12% DHA in seed oil
BASTA-resistant seedlings were grown to maturity before seed was harvested and analysed for fatty acid profile. Analysis of the fatty acid profile was also performed on single seeds from selected (higher pooled DHA) lines to rapidly get an indication of both maximum DHA production and locus number based on the segregation ratio of DHA-producing transgenic seeds to null seeds (Figure 3). The DHA level in single seeds from several independent events exceeded 12%. The transgenic:null ratio of these lines was found to be between approximately 3∶1 and 15∶1. Analysis of representative fatty acid profiles from the top DHA samples from each construct (Table 1) found only 1.2–1.4% GLA with no other new ω6 PUFA detected. In contrast, new ω3 PUFA (SDA) and new ω3 LC-PUFA (ETA, EPA, DPA, DHA) were found to accumulate to 18.5% (GA7), 25.8% (mod-F) and 21.9% (mod-G). The DHA levels in these lines were 9.6%, 12.4% and 11.5%, respectively.
The transgenic to null ratio is shown in parenthesis under the event number (note that not all zero DHA seeds were null). Open circles denote the DHA level in a pooled batch of 20 seeds (analysed separately).
Δ6-desaturation was found to be lower in the GA7 lines than the mod-F and mod-G lines (32% vs 47% and 43%) and this resulted in a reduction of ALA in the mod-F and mod-G lines relative to GA7. Another noteworthy difference was the accumulation of EPA in the mod-F seed (3.3% vs 0.8% in the other two transgenic lines) and this was reflected in the reduced Δ5-elongation observed in mod-F (80%) relative to the other lines (93% and 94%). There was a slight increase in Δ6-elongation in these lines (66% vs 60% and 61%) although the amount of SDA actually increased due to the slightly more active Δ6-desaturation.The distribution of DHA between the seed lipid fractions was also examined (Table 2). Polar lipids were found to comprise 3.0% of the total seed lipids and contained 3.7% DHA.
Whilst the focus of this study was the demonstration of DHA production in an oilseed crop species, the differences in gene activity noted above were also interesting from a construct design perspective. First, switching the Δ6- and Δ5-elongase coding region locations in mod-F resulted in the desired profile change with more EPA accumulated due to lower Δ5-elongation. A concomitant increase in Δ6-elongation was observed but this did not result in lower SDA levels. This was due to an increase in Δ6-desaturation in mod-F caused by adding an extra M. pusilla Δ6-desaturase expression cassette as well as by replacing the truncated napin promoter (FP1) with a more highly active L. usitatissimum Cnl2 promoter. The relatively moderate increase in Δ6-desaturation observed in mod-G was caused by capitalising on the highly expressed Δ5-elongase cassette in GA7. Switching the positions of the Δ6-desaturase and Δ5-elongase coding regions resulted in greater Δ6-desaturation. Δ5-elongase was not reduced in this instance due to the replacement of the FP1 promoter with the Cnl2 promoter. These functional changes were reflected in changes in the relative expression levels of the Δ6-desaturase, Δ6-elongase and Δ5-elongase genes in developing seeds from the three sample sets (Figure 4).
Error bars represent standard error. The data shown is for the Δ6-desaturase #1 for the mod-F construct (Figure 2) with the #2 desaturase found to have expression levels similar to the #1 gene across multiple events.
The DHA trait is stable over multiple generations
Seeds derived from the GA7 transgenic event with the highest DHA were sown out and subsequent generations established immediately to assess the trait stability over multiple generations. The maximum DHA levels observed was found to be stable to at least the fifth generation (Figure 5), although the pooled seed DHA level did not stabilise until T4 due to the presence of two transgenic loci. Interestingly, plants grown in one of the glasshouses contained significantly higher (P<0.001) levels of seed DHA than plants grown in other glasshouses (Figure 6). A more structured study is being performed to identify which environmental factors were responsible for this effect. T5 seed batches were also germinated on MS media alongside parental C. sativa seed with no obvious difference in germination rate or seedling vigour observed (Figure 7). The GA7 construct was transformed earlier than the modified versions and progressed through multi-generation characterisation rapidly. Similar multi-generation characterisation of mod-F and mod-G events is underway.
The T2 generation shows single seed DHA levels, whilst pooled seed results (20 seeds per batch) are shown for T3–5 (T4 and T5 are not segregating). Arrows denote lines which were progressed to form the next generation.
Events are colour-coded by glasshouse location (yellow, green and blue dots denote different glasshouses). The blue events were found to contain more DHA than the events in the other glasshouses (P<0.001).
A) 0 days following 3 days imbibition in the dark at 4°C; B) 1 day at 24°C under light; C) 4 days.
It is also important to note that the segregation ratios observed (∼3∶1 to ∼15∶1) indicate that one or, at most, two transgenic loci are required to produce fish oil-like levels of DHA in C. sativa. This has important implications for the ease with which the transgenic trait can be bred as well as for transgene stability. It was encouraging to observe that the GA7 DHA trait was stable to at least the fifth generation.
EPA and DHA are located at sn-1/3 position in TAG
13C NMR regiospecificity analysis was performed on the transgenic C. sativa seed oil to determine the positional distribution of the ω3 LC-PUFA on TAG (Figure 8). An event with approximately equal EPA and DHA was selected to maximise response for these fatty acids and the ratio of sn-1,3 to sn-2 was found to be 0.75∶0.25 for EPA and 0.86∶0.14 for DHA where an unbiased distribution would be 0.66∶0.33. This indicated that both fatty acids were preferentially located on the sn-1,3 positions in C. sativa TAG although the preference for EPA was weaker than for DHA. The finding that DHA was predominantly found on sn-1,3 was similar to results previously reported in A. thaliana seed  although the preferential location of EPA at the sn-1,3 position is in contrast with earlier studies which did not see such preference in linseed with EPA  or Arabidopsis with ARA, another C20 fatty acid . It will be interesting to further identify positional distribution differences between host species.
This study demonstrated the production of fish oil-like levels of DHA (12%) in transgenic C. sativa seed with low levels of intermediate fatty acid production and very high ω3: ω6 ratios with no new long-chain (≥C20) ω6 products. New ω3 fatty acids were found to accumulate in excess of 25% of total seed lipid. EPA and DHA were found to be enriched at the sn-1,3 positions in seed TAG although the effect was less strong for EPA. DHA was also found in the polar lipid fraction with the implication that the lecithin meal fraction would be similarly enriched for feed applications. The study also showed the importance of strong construct design when engineering complex multi-gene pathways in a single construct. DHA production by these constructs was found to be stable to at least the fifth transgenic generation.
We thank Dawar Hussain, Lina Ma, Anne Mackenzie, Alexander D Miller, Nathalie Niesner, Lijun Tian and Adam White for their excellent technical assistance. We thank Malcolm Devine for helpful discussions.
Conceived and designed the experiments: JRP PDN SPS. Performed the experiments: PS SB YK GL UKD RJM MPM. Analyzed the data: PS QL RJM MPM PDN SPS. Contributed reagents/materials/analysis tools: RJM. Wrote the paper: JRP.
- 1. Turchini GM, Nichols PD, Barrow C, Sinclair AJ (2012) Jumping on the omega-3 bandwagon: distinguishing the role of long-chain and short-chain omega-3 fatty acids. Critical Reviews in Food Science and Nutrition 52: 795–803. doi: 10.1080/10408398.2010.509553
- 2. Brenna JT, Salem N, Sinclair AJ, Cunnane SC (2009) alpha-Linolenic acid supplementation and conversion to n-3 long-chain polyunsaturated fatty acids in humans. Prostaglandins Leukotrienes and Essential Fatty Acids 80: 85–91. doi: 10.1016/j.plefa.2009.01.004
- 3. Qi B, Fraser T, Mugford S, Dobson G, Sayanova O, et al. (2004) Production of very long chain polyunsaturated omega-3 and omega-6 fatty acids in plants. Nature Biotechnology 22: 739–45. doi: 10.1038/nbt972
- 4. Abbadi A, Domergue F, Bauer J, Napier JA, Welti R, et al. (2004) Biosynthesis of very-long-chain polyunsaturated fatty acids in transgenic oilseeds: constraints on their accumulation. The Plant Cell 16: 2734–48. doi: 10.1105/tpc.104.026070
- 5. Robert SS, Singh SP, Zhou X-R, Petrie JR, Blackburn SI, et al. (2005) Metabolic engineering of Arabidopsis to produce nutritionally important DHA in seed oil. Functional Plant Biology 32: 473–479. doi: 10.1071/fp05084
- 6. Wu G, Truksa M, Datla N, Vrinten P, Bauer J, et al. (2005) Stepwise engineering to produce high yields of very long-chain polyunsaturated fatty acids in plants. Nature Biotechnology 23: 1013–1017. doi: 10.1038/nbt1107
- 7. Cheng B, Wu G, Vrinten P, Falk K, Bauer J, et al. (2010) Towards the production of high levels of eicosapentaenoic acid in transgenic plants: the effects of different host species, genes and promoters. Transgenic Research 19: 221–229. doi: 10.1007/s11248-009-9302-z
- 8. Ruiz-López N, Haslam R, Venegas-Calerón M, Li T, Bauer J, et al.. (2012) Enhancing the accumulation of omega-3 long chain polyunsaturated fatty acids in transgenic Arabidopsis thaliana via iterative metabolic engineering and genetic crossing. Transgenic Research: 1–11.
- 9. Ruiz-Lopez N, Haslam RP, Usher SL, Napier JA, Sayanova O (2013) Reconstitution of EPA and DHA biosynthesis in arabidopsis: iterative metabolic engineering for the synthesis of n-3 LC-PUFAs in transgenic plants. Metabolic Engineering 17: 30–41. doi: 10.1016/j.ymben.2013.03.001
- 10. Petrie JR, Shrestha P, Zhou X-R, Mansour MP, Liu Q, et al. (2012) Metabolic engineering plant seeds with fish oil-like levels of DHA. PLOS One 7: e49165. doi: 10.1371/journal.pone.0049165
- 11. Petrie JR, Singh SP (2011) Expanding the docosahexaenoic acid food web for sustainable production: engineering lower plant pathways into higher plants. AOB Plants doi: 10.1093/aobpla/plr011.
- 12. Ruiz-López N, Sayanova O, Napier JA, Haslam RP (2012) Metabolic engineering of the omega-3 long chain polyunsaturated fatty acid biosynthetic pathway into transgenic plants. Journal of Experimental Botany 63: 2397–2410. doi: 10.1093/jxb/err454
- 13. Putnam D, Budin J, Field L, Breene W (1993) Camelina: a promising low-input oilseed. New Crops (Janick J and Simon JE, eds) New YorkWiley314322.
- 14. Zubr J (1997) Oil-seed crop: Camelina sativa. Industrial Crops and Products 6: 113–119. doi: 10.1016/s0926-6690(96)00203-8
- 15. Vollmanna J, Moritza T, Kargla C, Baumgartnerb S, Wagentristla H (2007) Agronomic evaluation of camelina genotypes selected for seed quality characteristics. Industrial Crops and Products 26: 270–277. doi: 10.1016/j.indcrop.2007.03.017
- 16. Liu X, Brost J, Hutcheon C, Guilfoil R, Wilson AK, et al. (2012) Transformation of the oilseed crop Camelina sativa by Agrobacterium-mediated floral dip and simple large-scale screening of transformants. In Vitro Cellular & Developmental Biology – Plant 48: 462–468. doi: 10.1007/s11627-012-9459-7
- 17. Vanhercke T, El Tahchy A, Shrestha P, Zhou X-R, Singh S, et al. (2013) Synergistic effect of WRI1 and DGAT1 coexpression on triacylglycerol biosynthesis in plants. FEBS Letters 587: 364–369. doi: 10.1016/j.febslet.2012.12.018
- 18. Zar JH (2010) Biostatistical Analysis, 5th Edn.Upper Saddle RiverNJPrentice-Hall.
- 19. Standal IB, Axelson DE, Aursand M (2009) Differentiation of fish oils according to species by 13C-NMR regiospecific analyses of triacyglycerols. Journal of the American Oil Chemists' Society 86: 401–407. doi: 10.1007/s11746-009-1370-y
- 20. Aursand M, Jørgensen L, Grasdalen H (1995) Positional distribution of ω3 Fatty acids in marine lipid triacylglycerols by high-resolution 13C nuclear magnetic resonance spectroscopy. Journal of the American Oil Chemists' Society 72: 293–297. doi: 10.1007/bf02541085
- 21. Breyne P, Gheysen G, Jacobs A, Van Montagu M, Depicker A (1992) Effect of T-DNA configuration on transgene expression. Molecular and General Genetics 235: 389–396. doi: 10.1007/bf00279385
- 22. Petrie JR, Shrestha P, Belide S, Mansour MP, Liu Q, et al. (2012) Transgenic production of arachidonic acid in oilseeds. Transgenic Research 21: 139–147. doi: 10.1007/s11248-011-9517-7