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Oleaginous microalgae have been emerging as the third-generation feedstocks for biofuel production. Genetic manipulation for improving triacylglycerol (TAG) accumulation represents a promising approach towards the economics of microalgal biofuels. Acetyl-CoA, the essential carbon precursor for de novo fatty acid biosynthesis, can be derived from pyruvate catalyzed by pyruvate dehydrogenase, which is negatively regulated by pyruvate dehydrogenase kinase (PDK). In the present study, we characterized a PDK gene (NsPDK) from Nannochloropsis salina. Subcellular localization assay assisted by green fluorescence protein (GFP) fusion indicated the localization of NsPDK in mitochondria of N. salina cells. NsPDK knockdown via RNA interference strategy attenuated NsPDK expression at the mRNA level and its enzymatic activity in vivo, leading to faster TAG accumulation without compromising cell growth under high light stress conditions. Interestingly, the TAG increase was accompanied by a decline in membrane polar lipids. NsPDK knockdown also altered fatty acid profile in N. salina. Furthermore, transcriptional analysis suggested that the carbon metabolic pathways might be influenced by NsPDK knockdown leading to diverted carbon flux towards TAG synthesis. Taken together, our results demonstrate the role of NsPDK in regulating TAG accumulation and provide valuable insights into future manipulation of oleaginous microalgae for improving biofuel production.
The increasing concerns about the shortage of fossil fuels and the burning-associated environmental problems have led to interest in developing sustainable and renewable biofuels in recent years1. Microalgae are considered as a promising feedstock for biofuels, in that they grow fast with high photosynthetic efficiency, have no competition with crops for arable lands, and can accumulate large quantities of triacylglycerols (TAGs), an ideal precursor for making biodiesel via transesterification2, 3. Although many advances have been achieved for microalgal biofuels, challenges remain to be addressed to bring down the production cost for commercial uses4. Efforts are being made to improve lipids, TAGs in particular, by rational genetic engineering based on the understanding of regulatory mechanisms involved in lipid metabolism5, 6.
TAG biosynthesis is believed to be mediated mainly via two pathways, acyl-CoA independent pathway and acyl-CoA dependent Kennedy pathway7. The latter pathway contributes largely to the TAG accumulation under abiotic stress conditions, which starts from glyceol-3-phosphate with three sequential acylation steps8. The acyls in TAG can be either from recycled membrane lipids or from de novo synthesized fatty acids (FAs), both with the primary precursor being acetyl-CoA. Li et al.9 found out that most of the genes involved in de novo FA synthesis were downregulated while total fatty acid accumulation was significantly enhanced in Nannochloropsis under nitrogen starvation. This could explain why previous attempts to increase lipid content by overexpressing acetyl-coA carboxylase or fatty acid synthase had limited success10–12. It has been speculated that provision of acetyl-CoA may be the rate-limiting step for TAG biosynthesis in Nannochloropsis. Pyruvate dehydrogenase complex (PDHC) is a multienzyme complex catalyzing the oxidative decarboxylation of pyruvate to yield acetyl-CoA and NAD(P)H13. PDHC contains three primary components: pyruvate dehydrogenase (E1), dihydrolipoyl acetyltransferase (E2) and dihydrolipoyl dehydrogenase (E3). Higher plants contain two distinct isoforms of PDHC, one located in mitochondria and the other in the plastid stroma14. Mitochondrial PDHC becomes inactive once Ser-phosphorylation occurs in the α-subunit of PDHC E1 component, which is catalyzed by pyruvate dehydrogenase kinase (PDK)13, 14. The characterization of PDK has been conducted in some higher plants as well as microalgae14–16. Overexpression of a PDK gene from Brassica napus in Arabidopsis resulted in a decrease in both the PDHC activity and seed oil content14. PDK knockdown, on the other hand, made Arabidopsis accumulate elevated oil levels in seeds17. Recently, it was reported that the antisense knockdown of PDK promoted neutral lipid accumulation in the diatom Phaeodactylum tricornutum, but with compromised cell growth15. Besides, only neutral lipids were analyzed based on Nile red staining in this study; the effects of PDK knockdown on TAG and polar lipids content remained unknown.
Nannochloropsis has been emerging as an oleaginous model alga to study TAG biosynthesis and regulation because of its fast growth, high TAG content, available genome sequence, and established genetic tools9, 18, 19. Nannochloropsis salina has been reported to be successfully transformed18. Here we report the characterization of a PDK gene (NsPDK) from Nannochloropsis salina. Assisted with the enhanced green fluorescence protein fusion, NsPDK was found to be positioned likely in mitochondria. NsPDK knockdown via RNA interference strategy not only promoted total lipid content and altered fatty acid profiles, but also enhanced TAG accumulation, while without slowing down cell growth. Transcriptional analysis suggested the possible gene regulatory network of PDK and its knockdown may bring more carbon precursors and reducing powers for de novo fatty acid synthesis thereby enhancing TAG accumulation. Our work helps understand the role of PDK in regulating carbons for lipid biosynthesis and provides insights into target genetic engineering of Nannochloropsis for trait improvement and production uses.
It has been reported that the genome of N. salina are highly identical to N. gaditana 19–21. Using the PDK sequence from N. gaditana as the reference, we successfully amplified NsPDK sequence (Supplementary Data 1). The phylogenetic analysis based on amino acid sequences revealed that the putative NsPDK was closely clustered with PDK from N. gaditana and N. oceanica IMET1 (Fig. 1). By analyzing with the software TargetP 1.1 (http://www.cbs.dtu.dk/services/TargetP/), NsPDK was predicted to have a transit peptide targeting to mitochondrion.
In order to examine the subcellular localization of NsPDK, we constructed the NsPDK-GFP fusion (Fig. 2a) and had it introduced into N. salina. With a confocal microscope, it was observed that the GFP fluorescence appeared as tubular structures next to, but not merged with the plastid, as indicated by the plastid autofluorescence (PAF) in red (Fig. 2b). By comparing a recent subcellular localization analysis in N. oceanica 22, NsPDK is likely positioned in mitochondria. These results further proved that NsPDK functioned as the regulator of mitochondrial PDHC.
The RNAi vector (Fig. 3a) was introduced into N. salina cells via electrotransformation. The zeocin-resistant colonies were selected and cultivated as putative transgenic lines. Genomic PCR was used to confirm the integration of the vector into the genome of transgenic lines. With the primers from both GUS linker and bleomycin coding region, the corresponding 464bp and 997bp PCR products were detected for NsPDK transgenic lines (Kd1-4 and Kd1-9) and the control line transformed with empty vector, but not in wild type. By contrast, with the primers crossing PDK and GUS sequence, the expected 1043bp and 1112bp bands were amplified from transgenic lines instead of wild type and control line (Fig. 3b). This proved the successful transformation of N. salina. The stress of high light (HL) was applied to induce lipid accumulation in transgenic N. salina. Two-stage cultivation strategy was employed with normal illumination (50μmol/m2·s) in the first stage followed by HL condition (250μmol/m2·s) in the second stage. N. salina showed an impaired cell growth with HL as compared to normal condition (Supplementary Fig. 2), indicating HL used in this study could be considered as stress condition. In order to evaluate the knockdown efficiency, quantitative real-time PCR was conducted. The results suggested that Kd1-4 and Kd1-9 exhibited a significant decrease in NsPDK expression under normal condition (by 25.6% and 51.3%, respectively) and HL condition (by 23.8% and 53.6%, respectively) as compared to the empty vector control line (Fig. 3c). The transgenic line Kd1-9 with a stronger knockdown efficiency was selected for further investigations. Kd1-9 showed a 53% decrease in NsPDK activity and a 33% increase in PDHC activity (Fig. 3d and e).
We examined the growth and photosynthetic parameters of transgenic N. salina lines. No significant difference in the cell density, chlorophyll a content or Fv/Fm was observed between Kd1-9 and empty vector control (Fig. 4), indicating that NsPDK knockdown had little effect on either growth or photosynthetic efficiency in N. salina.
Although PDK knockdown showed no effect on lipid accumulation when cells grew under normal illumination conditions (Supplementary Fig. 3), it affected lipid synthesis significantly when cells were cultured under HL stress conditions. For example, the lipid accumulation was enhanced in Kd1-4 and Kd1-9 on day 2 (by 21.6 and 30.1%, respectively) as compared to the control (Fig. 5a). Accordingly, the total fatty acid (TFA) synthesis was significantly enhanced in Kd1-9 during the first two days (Fig. 5b and c). We further studied the effect of NsPDK knockdown on total fatty acid profile (Fig. 5d). C14:0, C16:0, C16:1 and C20:5 were the main fatty acids and together accounted for about 80% of total fatty acids in both the control and Kd1-9. The fatty acid profile was altered following the downregulated PDK expression, with an increase in the relative content of C16:0 and a decline in C14:0 and polyunsaturated fatty acids (C18:2, C18:3, C20:4 and C20:5). The knockdown of NsPDK promoted the TAG accumulation by 100% (per cell) and 86% (per dry weight) in Kd1-9 on day 2 (Fig. 5e and f). However, TAG content showed no difference between Kd1-9 and control on day 4. C16:0 was the major fatty acid in TAG derived fatty acids, followed by C16:1 and C14:0. But NsPDK knockdown had little effect on the fatty acid profile of TAG (Fig. 5g). Noteworthily, NsPDK knockdown led to differential changes in in membrane polar lipids: a considerable decrease in monogalactosyl diacylglycerol (MGDG), digalactosyl diacylglycerol (DGDG), phosphatidylglycerol (PG) and phophatidylinositol (PI), while no change in diacylglycerol-N,N,N-trimethylhomoserine (DGTS), phosphatidylethanolamine (PE) and sulfoquinovosyldiacylglycerol (SQDG), (Fig. 5h). Interestingly, NsPDK knockdown showed little effect on lipid content under nitrogen deficiency conditions (Supplementary Fig. 4), a commonly used stress for inducing lipid accumulation in microalgae18.
Protein and carbohydrate are the major macromolecules synthesized in microalgal cells. The total protein content decreased slightly in Kd1-9, which was 10% lower than control (Fig. 6a). The carbohydrate content, on the other hand, was not significantly affected by NsPDK knockdown (Fig. 6b).
The transcript abundance of key genes was analyzed by qPCR (Fig. 7). NsPDK knockdown led to elevated PDHC E1 component (PDHCe1) expression level (~2.2 fold). The mRNA abundance of PDHC E2 component (PDHCe2) in transgenic line was upregulated following NsPDK knockdown. The TCA cycle involved key genes: citrate synthase (CS) and isocitrate dehydrogenase (ICDH) were downregulated in Kd1-9 by 30% and 31%, respectively. Malic enzyme (ME), catalyzing the provision of NADPH as reductant for de novo fatty acid synthesis23, was upregulated. Glucose-6-phosphate dehydrogenase (G6PDH), involved in pentose phosphate pathway, is considered to be an ancillary means of producing NADPH in oleaginous microorganisms23. However, G6PDH was not influenced in N. salina by the NsPDK knockdown. Pyruvate can also be converted to acetate by a pyruvate decarboxylase (PDC) and an aldehyde dehydrogenase (ALDH), which is called “PDHC bypass” to produce acetyl-CoA9. There was no change in either PDC or ALDH expression level. The transcriptional abundance of acetyl-CoA synthase (ACS) was not influenced by NsPDK knockdown.
Nannochloropsis represents a genus of marine microalgae with high photosynthetic efficiency and can convert carbon dioxide to storage lipids mainly in the form of TAGs24. It has been reported that total lipid accumulation in Nannochloropsis can be largely enhanced (up to 60% dry weight) by stress conditions, such as nitrogen deficiency and excess light, indicative of the potential of this alga for biofuels applications18, 25, 26. The reported successful genetic manipulation of Nannochloropsis 20, 27–29 points to new directions for trait improvement.
The previous report on transcriptomes in Nannochloropsis has indicated that the key enzymes involved in de novo FA biosynthesis may be present in excess, and the provision of carbon precursor could be more crucial for FA production9. Acetyl-CoA is the vital carbon precursor for de novo fatty acid synthesis. PDHC catalyzes the generation of acetyl-CoA, and the activity is primarily regulated by phosphorylation by PDK. Consequently, PDK is considered to play a key role in the regulation of FA biosynthesis. The genetic manipulation of PDK in higher plants and microalga has suggested the vital role of PDK in lipid accumulation14, 15. Here we engineered a N. salina strain with lowered NsPDK expression level, with the aim to channel carbon precursors into fatty acid synthesis.
The predicted NsPDK in the present study is likely localized in the mitochondria (Fig. 2), in line with the previous studies in P. tricornutum and higher plants15, 16. The mitochondrial PDHC expression is responsive to light13, and the stress of high light can stimulate TAG accumulation in Nannochloropsis species 24, 30. In the present study, both the transcriptional abundance and the enzymatic activity of PDK were lowered in the transgenic line Kd1-9 as compared to control under HL stress conditions (Fig. 3c and d). The knockdown efficiency in the present study was similar to the reported investigations in P. tricornutum 15. In line with the previous reports24, 31, HL led to decreased chlorophyll content and Fv/Fm. Unlike in P. tricornutum 15, NsPDK knockdown showed little effect on cell growth and photosynthetic activity in N. salina (Fig. 4).
Enhanced total lipid content and slightly decreased protein content in transgenic cells might be due to the carbon reallocation between lipid and protein components (Figs 5a and and6a).6a). NsPDK knockdown significantly accelerated the biosynthesis of TFA and TAG in N. salina in the first two days with high light (Fig. 5b, c, e and f). The doubled TAG content was accompanied by a considerable decrease in membrane lipid content (Fig. 5e and h), which may be due to the involvement of membrane lipid turnover for TAG assembly. The altered fatty acid profile was observed in transgenic line with a higher C16:0 proportion and a reduced C20:5 proportion (Fig. 5d). This might be caused by augmented TAG synthesis in Kd1-9 because TAG had a considerably higher percentage of saturated/monounsaturated fatty acids and a lower proportion of polyunsaturated fatty acids (Fig. 5g). It was different in the diatom P. tricornutum that antisense knockdown of PDK did not have much impact on fatty acid profile15. These biochemical results altogether indicated that TAG biosynthesis was promoted by NsPDK knockdown in N. salina without compromising cell growth.
The proposed working model for TAG accumulation induced by NsPDK knockdown in N. salina was depicted in Fig. 8. PDK attenuation could result in the activation of PDHC enzyme, and might alter the regulation of PDHC expression. An expected higher PDHC activity may be attributed to a lower phosphorylation status of PDHCe1 following NsPDK knockdown and the marked elevation of mitochondrial PDHC expression. Consequently, an increase in the production of acetyl-CoA in NsPDK knockdown line may occur, which can be channeled to chloroplast for de novo fatty acid synthesis25, 32–34. Nannochloropsis tends to produce large amounts of TAGs in response to high light stress3. ME may be activated and produces more NADPH to support the enhanced de novo fatty acid synthesis, therefore contributing to elevated TAG accumulation. More malate may be catalyzed to provide NADPH and less malate participates in TCA cycle in mitochondria, which attenuates TCA cycle in NsPDK knockdown line. This hypothesis was partly supported by the downregulated expression of CS and ICDH. It has been reported that the suppression of CS via RNAi affected the carbon flux channeling and increased the TAG content in Chlamydomonas reinhardtii 35. However, we didn’t observe the expected upregulation of “PDHC bypass” pathway, which may be explained by the involvement of post-transcriptional regulation. Taken all together, NsPDK knockdown in N. salina is likely to divert more carbon flux towards TAG synthesis and activate NADPH supplying pathway, leading to an overall enhanced TAG accumulation.
Our present study demonstrated that RNAi knockdown of NsPDK significantly promoted TAG accumulation in N. salina. The transgenic cells exhibited similar growth, reduced NsPDK expression and inhibited PDK activity as compared to empty vector control. Consequently, both the total fatty acid and TAG content were significantly enhanced following NsPDK knockdown, accompanied by an obvious decline in membrane lipids. The fatty acid composition was also altered in knockdown mutant. The transcriptional analysis of key genes involved in fatty acid synthesis indicated the channeling of carbon flux into TAG synthesis may occur. These attempts provide sights into genetic manipulation of microalgae as feedstocks for biofuel production.
N. salina (CCMP 537) was obtained from the National Center for Marine Algae and Microbiota (NCMA, USA). The medium used in this study was modified f/2 medium (Guillard and Ryther, 1962) which contains (per liter): 375mg NaNO3, 5.65mg NaH2PO4·2H2O, 3.15mg FeCl3·6H2O, 4.36mg Na2EDTA·2H2O, 0.01mg CoCl2·6H2O, 0.18mg MnCl2·4H2O, 22μg ZnSO4·7H2O, 6.3μg Na2MoO4·2H2O, 9.8μg CuSO4·5H2O and 20g sea salts (Sigma-Aldrich, USA). The exponentially growing cells was inoculated at a cell density of 2×106/mL (Day 0) into 250-mL flasks containing 100mL medium. Cells cultivated with normal illumination (50μmol/m2·s) for 6 days were collected (by centrifugation at 5,000rpm for 10min) and then resuspended in the fresh medium illuminated with a light intensity of 250μmol/m2·s (high light, HL). The experiments were conducted at 25±1°C with continuous shaking at 110rpm in a thermostatic shaker.
The putative N. salina PDK sequence (NsPDK) was amplified based on the PDK gene of N. gaditana (Genbank accession number XM_005855411). N. salina cells were harvested by centrifugation at 5,000rpm for 10min, and the total RNA was extracted with a RNeasy Plant Mini Kit (QIAGEN, Germany) according to the manufacturer’s instructions. The reverse transcription was performed with SuperScript III First-strand Synthesis System (Invitrogen, USA) for cDNA synthesis. All the primers were shown in Supplementary Table 1. Amino acid sequence alignment and similarity among species were determined by MEGA6 using sequences from NCBI (http://blast.ncbi.nlm.nih.gov/Blast.cgi) and QIBEBT EnergyAlgae DB (http://www.bioenergychina.org:8989/). The phylogenetic tree of protein clusters was constructed by MEGA6 using the neighbor-joining method.
The pPha-VCP vector containing the bidirectional VCP2 promoter (from N. oceanica) and VCP1 3’UTR terminator (from N. oceanica) as well as sh ble resistance gene was constructed22, 36. The enhanced green fluorescent protein (eGFP) fragment was amplified by PCR from the pPhaT1-eGFP vector36 using the primers eGFP_ KpnI_f and eGFP_XbaI_r and ligated into the pPha-VCP vector (between the KpnI and XbaI sites), and was named as pPha-VCP-eGFP. For the localization analysis of PDK, a construct was generated to express C-terminal GFP fusion proteins in N. salina. The ORF of PDK was amplified by PCR from the cDNA using the primers PDK_KpnI_f and PDK_KpnI_r. The PCR products were inserted into the KpnI sites, which reside immediately upstream of the eGFP sequence within the pPha-VCP-eGFP vector. The vector was introduced into wild-type N. salina by electroporation using Bio-Rad GenePulser Xcell apparatus (Bio-Rad, USA) at 12,000V/cm, 50 µFD and 600 Ω. Zeocin (Invitrogen, USA) at the final concentration of 2μg/ml (agar medium) and 1μg/ml (liquid medium) was used for selecting transgenic cells. GFP positive cells were observed using a Leica TCS SP8 laser scanning confocal microscope.
The backbone vector pGreenII 000037 was generously offered by Singapore-Peking University Research Centre. The target sequence was synthesized based on a 198-bp fragment of NsPDK. A 1026-bp GUS sequence was chosen as the loop structure linking sense and antisense fragments. The endogenous promoter β-tubulin29 was used to drive the expression of both a bleomycin resistance gene and target sequence. The foreign terminator ribulose-1,5-bisphosphate carboxylase/oxygenase small subunit (RbcS1) from Dunaliella tertiolecta (GenBank accession AY530155) was used here. For nuclear transformation, plasmid was linearized with HpaI and transformed into N. salina via electroporation using Bio-Rad GenePulser Xcell apparatus (Bio-Rad, USA) at 12,000V/cm, 50 µFD and 600 Ω. After electroporation, cells were incubated in 10mL medium without antibiotics for 24h, before they were transferred to f/2 plates. Zeocin (Invitrogen, USA) at the final concentration of 4μg/ml (agar medium) and 1μg/ml (liquid medium) was used for selecting transgenic cells.
Ten mL culture (about 400 billion cells) was harvested by centrifugation (5,000rpm, 10min at 4°C). The cell pellet was washed twice, then suspended in 0.5mL extraction buffer (2% SDS, 400mM NaCl, 40mM EDTA, 100mM Tris-HCl, pH 8.0) at 65°C for 30min. The genomic DNA was extracted by addition of 0.5mL phenol/chloroform/isoamyl alcohol mixture (25:24:1, Sigma-Aldrich, USA), followed by centrifugation (13,000rpm, 30min at 4°C). The aqueous phase was mixed with equivalent volume isopropanol, inverted and centrifuged (12,000rpm, 20min at 4°C). The DNA pellet was washed with 75% ethanol twice and dried for 2h. PCR was performed with primers of GUS, the bleomycin resistance region, fragments crossing sense/GUS sequence and fragment crossing GUS/antisense sequence (Supplementary Table 1).
Quantitative real time PCR was performed in a BioRad CFX96 Real-Time System (BioRad, USA) in the presence of SYBR Premix (Thermo Scientific, USA). The profile was 50°C for 2min, then 95°C for 10min followed by 40 cycles of 95°C for 15s and 60°C for 1min, finally 65°C for 5s and 95°C for 5s. Data was collected at the end of each extension step. The relative quantitative of gene expressions in the treatment groups was analyzed by the 2−ΔΔCt method, where the Ct was the cycle number at which the fluorescent signal statistically above the background. The actin amplification product was used as an internal standard.
Twenty mL culture (about 400 billion cells) was harvested by centrifugation (12,000rpm, 5min at 4°C). The cell pellet was washed twice, frozen with liquid nitrogen and pulverized with pestle and mortar. After extraction with extraction buffer (containing 100mM KH2PO4/KOH (pH 7.5), 20% (v/v) glycerol, 1mM benzamidine·HCl and 1mM DTT) and centrifugation (12,000rpm, 10min at 4°C), the supernatant was collected as a crude extract for enzymatic reactions. PDK activity was assayed with PDK Activity Elisa Kit (R&D system, USA) following the manufacturer’s instructions. PDH Activity Assay Kit (Sigma-Aldrich, USA) was used for determination of PDH activity, with pyruvate as substrate and NADH standard for quantification. One unit (U) of enzyme activity was defined as that amount of enzyme catalyzing the formation of 1μmol of each enzymatic reaction product per min under the above-mentioned conditions. Soluble protein was measured with BCA Protein Assay Kit (Cwbio Biotechnology, China).
Cell number was calculated by counting under microscope using a hemocytometer.
Chlorophyll a in fresh algal cells (5mL culture, centrifugation 12,000rpm for 10min) was extracted with 5mL methanol for 5h at 4°C. By measuring the optical density respectively at 665nm, 652nm, 480nm and 750nm with a spectrophotometer U-3900H (Hitachi, Japan), the concentration was calculated with the following equation, and absorbances at 652nm, 665nm and 480nm were corrected by subtracting absorbency at 750nm (Ritchie, 2006).
[Chlorophyll a] mg/L=16.5169×A665−8.0962×A652
Fv/Fm (the variable/maximum fluorescence ratio) indicates the maximum photochemical quantum yield of PSII reaction centers, reflecting the photosynthetic light energy conversion efficiency. The cells were kept in the dark for 15min, then exposed to a saturating light pulse while the chlorophyll fluorescence intensities were measured with a OS5p chlorophyll fluorimeter (Opti-Sciences, US) following the manufacture’s recommendations.
For protein determination, 10mg lyophilized algal biomass was hydrolyzed in 200μL 1M sodium hydroxide (NaOH) and then incubated in a water bath at 80°C for 10min. Then 1.8mL H2O was added to the hydrolysate to bring the volume to 2mL. The mixture was centrifuged at 12,000rpm for 30min and the supernatant was transferred to a new tube. This extraction procedure was repeated twice, and all the resulting supernatants were pooled together. Then the protein concentration was measured by the BCA Protein assay kit (Cwbio Biotechnology, China) with bovine serum albumin as the standard. For carbohydrate determination, 10mg lyophilized algal biomass was incubated with 0.5mL acetic acid at 80°C for 20min before 10mL acetone was added, followed by centrifugation at 3500g for 10min. The pellet was resuspended in 2.5mL 4M trifluoroacetic acid and then boiled for 4h to release reducing sugars. The suspension was cooled and centrifuged at 10,000rpm for 5minutes, and then 20μL supernatant was mixed with 900μL sulfuric acid:H2O:phenol (300:150:3, v/v/w) and boiled for 20min prior to reading the optical density at 490nm. Glucose was used to establish the standard curve for the quantification of total carbohydrate content.
Total lipids were extracted from lyophilized algal cells in a chloroform-methanol-water (4:2:1.5, by vol) system38. The chloroform layer was evaporated under nitrogen gas and dried at 60°C for 2h in a vacuum oven. The lipids were then weighed for quantification. Total fatty acids were obtained via transesterification of total lipids and quantified by GC-MS.
TAG was separated on a TLC plate coated with silica gel 60 (Merck, USA) using a mixture of hexane/diethyl ether/acetic acid (70:30:1, by vol) as the mobile phase, while polar lipids were separated on a TLC plate using a mixture of chloroform/methanol/acetic acid/water (25/4/0.7/0.3, by vol) as the mobile phase. For quantification, lipids on TLC plate were visualized with iodine vapor, recovered, transesterified and analyzed by GC-MS.
Lipid transesterification was performed in 1% (by vol) sulfuric acid in methanol at 85°C water bath for 2.5h. Heptadecanoic acid (C17:0, Sigma-Aldrich, USA) was used as the internal standard. After extracting with hexane, the fatty acid methyl esters (FAMEs) were analyzed by using a GC-MS-QP 2010 SE (Electron Ionization type) gas chromatograph-mass spectrometer (Shimadzu, Japan) and a Stabilwax-DA capillary column (30m×0.25 mm×0.25μm) (Shimadzu, Japan). Helium was used as the carrier gas. The injection temperature, ion temperature and interface temperature were set at 250°C, 200°C and 260°C, respectively. The initial column temperature was set at 150°C. The column temperature subsequently rose to 200°C at 10°C/min and then to 250°C at 15°C/min, followed by a hold at 250°C for 3min. FAMEs were identified using the NIST 11 mass spectral library (NIST/EPA/NIH mass spectral library, 2011 edition).
All data were obtained by using at least three biological samples to ensure the reproducibility of the results. The statistical significance of the results was evaluated by independent samples t-test and one-way ANOVA Turkey’s HSD tests (p<0.05) using the SPSS version 16.
All data generated or analyzed during this study are included in this published article and its Supplementary Information files.
We wish to thank Dr Huixin Lin for providing us the pGreenII 0000 vector. We greatly thank Dr Hanhua Hu and Dr Yufang Pan for assisting us with the localization analyses. We also greatly acknowledge support from National Natural Science Foundation of China (Project No.: 31471717 and Project No.: 31571807), the 863 Plan of Ministry of Science and Technology of China (2012AA02A707), and the Singapore-Peking University Research Centre for a Sustainable Low-carbon Future.
X.N.M., J.L. and F.C. conceived the study and performed the manuscript. L.N.Y. performed the PCR analysis. B.Y. performed fatty acid data analysis by GC-MS. Y.K.L. contributed with the provision of study materials and valuable discussions.
The authors declare that they have no competing interests.
Electronic supplementary material
Supplementary information accompanies this paper at 10.1038/s41598-017-11932-4.
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