Skip to main content

Enzyme activity highlights the importance of the oxidative pentose phosphate pathway in lipid accumulation and growth of Phaeodactylum tricornutum under CO2 concentration



Rising CO2 concentration was reported to increase phytoplankton growth rate as well as lipid productivity. This has raised questions regarding the NADPH supply for high lipid synthesis as well as rapid growth of algal cells.


In this study, growth, lipid content, photosynthetic performance, the activity, and expression of key enzymes in Calvin cycle and oxidative pentose phosphate pathway (OPPP) were analyzed in the marine diatom Phaeodactylum tricornutum under three different CO2 concentrations (low CO2 (0.015 %), mid CO2 (atmospheric, 0.035 %) and high CO2 (0.15 %)). Both the growth rate and lipid content of P. tricornutum increased significantly under the high CO2 concentration. Enzyme activity and mRNA expression of three Calvin cycle-related enzymes (Rubisco, 3-phosphoglyceric phosphokinase (PGK), phosphoribulokinase (PRK)) were also increased under high CO2 cultivation, which suggested the enhancement of Calvin cycle activity. This may account for the observed rapid growth rate. In addition, high activity and mRNA expression of G6PDH and 6PGDH, which produce NADPH through OPPP, were observed in high CO2 cultured cells. These results indicate OPPP was enhanced and might play an important role in lipid synthesis under high CO2 concentration.


The oxidative pentose phosphate pathway may participate in the lipid accumulation in rapid-growth P. tricornutum cells in high CO2 concentration.


As a result of increased industrialization and human activities, global carbon dioxide (CO2) emission has increased dramatically and induces seawater acidification, which affects the growth and photosynthesis of marine phytoplankton [1]. Photosynthetic CO2 fixation by phytoplankton (e.g., eukaryotic microalga) mainly depends upon Calvin cycle, and ribulose-1, 5-bisphosphate carboxylase/oxygenase (Rubisco) catalyzes the initial step of CO2 fixing. The response of photosynthesis, metabolite including the Calvin cycle enzymes (especially Rubisco), and growth to elevated CO2 have been well studied in higher plants. It was shown that short-term CO2 elevating generally accelerates carbon fixation and leads to an increase of Rubisco activity followed by an enhancement of growth in C3 plants [26]. Yet, in the long-term, the photosynthesis decreased with increasing CO2, which is typically accompanied by a decline in the amount and activity of Rubisco and other enzymes in the Calvin cycle and a decrease of growth rates. Compared to high plants, the impacts of elevated CO2 concentration on microalgae and their response to CO2 levels, especially Calvin cycle enzyme (including Rubisco) activity and amount, have been learned much less extent and attentions mainly paid to photosynthesis and algal growth. Only in the study of Euglena gracilis Z, Nakano et al. focused on Rubisco and found Rubisco activity was higher in high CO2 conditions [7]. Whereas, elevated CO2 concentration increased the efficiency of photosynthetic carbon fixation and growth of phytoplankton was gradually known as general phenomenon [8, 9]. Kim et al. [10] reported that the growth of Skeletonema costatum enhanced at higher concentrations of CO2. Tortell et al. [11] also found that rising CO2 can enhance Chaetoceros spp. growth. In addition, various studies have shown that rising CO2 concentration increases lipid productivity as well as phytoplankton growth rate, such as in Phaeodactylum tricornutum [12], Nannochloropsis oculata [13], and Chlorella vulgaris [14], high levels of CO2 concentration enhanced both biomass production and lipid content, thus shedding light on the potential for biodiesel production from microalgae. To select microalgae for obtaining a higher lipid productivity, even higher concentrations of CO2 (10 % CO2 and flue gas) were used to cultivate Botryococcus braunii and Scenedesmus sp. [15]. At present, about 60 species of microalgae have been well domesticated with high concentration of CO2 for producing large biomass and achieving high biofuel yields [16]. However, most previous studies have only focused on microalgal growth rate, lipid content, and tolerance to high levels of CO2 [1720]. Little effort has been directed toward the analysis of the mechanism involved in lipid accumulation in microalgae and their simultaneous rapid growth rate.

Microalgal lipids, as a source of biofuel, are usually derived from long-chain fatty acids, which require NADPH for synthesis [21, 22]. For example, to produce an 18-carbon fatty acid, 16 NADPH molecules are required as electron donors. Therefore, enhanced lipid accumulation will surely increase metabolic demand in microalgae for NADPH. Microalgae have been demonstrated to grow rapidly in high CO2 concentrations. This suggests that quantity of NADPH, which is supplied by the light reaction, is required for photosynthetic carbon fixation which supplies substrates and energy for the synthesis of major constituents (proteins, nucleic acids, and carbohydrates) essential for algal growth. For effective CO2 fixation, ATP and NADPH produced by photosynthetic light reactions must be maintained at a molar ratio of 3:2 [23]. Once a large number of NADPH molecules are consumed, the ratio will be disrupted leading to a reduction in carbon fixation activity. An important question therefore remains about how NADPH is supplied for high fatty acid synthesis as well as rapid growth of algal cells cultured under high CO2 concentration. It is more likely that another pathway may contribute to providing this reductant.

In the present study, we evaluated the lipid content in the diatom P. tricornutum which was cultivated in three different CO2 conditions (0.015 %, atmospheric, and 0.15 %). Furthermore, we measured the activity of seven key enzymes and mRNA expression in P. tricornutum to explore the mechanism of rapid growth and the simultaneous increase in lipid accumulation in high-CO2 cultured algal cells. Our research showed that the pentose phosphate pathway may be incorporated in maintaining the NADPH supply under high CO2 concentrations.


Algal growth, pH changes, and photosynthetic performance under low, mid, and high CO2 concentrations

When grown under low, mid, and high CO2 concentrations, the growth rate of P. tricornutum showed significant differences among the groups. The highest growth rate occurred under high CO2 concentration and was 0.20 at the beginning of treatment and 0.70 on the seventh day at the optical density (OD) of 730 nm, followed by mid CO2 concentration, and was 0.20 at the beginning of treatment and 0.41 on the seventh day at OD730 nm. No significant growth was observed in the low-CO2 cultured alga (Fig. 1a). This indicated that when nutrients were sufficient, the carbon source performs as the limiting factor which affected algal growth.

Fig. 1
figure 1

Effects of CO2 concentration on growth, medium pH, and photosynthetic performance of P. tricornutum. a Growth curve of P. tricornutum; b pH changes of all of the cultures; c The maximum quantum yield of PSII (F v/F m) in P. tricornutum; d The effective PSII quantum yield (YII) in P. tricornutum. Data are expressed as a mean ± SD (n = 3)

Figure 1b shows that the medium pH had a significant increase on day 1 under both mid-CO2 (from 8.83 to 9.41) and low-CO2 (from 8.83 to 9.45) conditions, and from day 2 to 7, the pH of mid-CO2 and low-CO2 cultures gradually increased, whereas the pH of algal culture bubbled with high level of CO2 strongly decreased on day 1 (from 8.83 to 7.07) and then gradually increased from 7.07 to 8.32. Faster growth and greater carbon fixation were observed in high-CO2 cultured P. tricornutum under the low pH and high CO2 condition. The consumption of NO3 during algal rapid growth may cause the increase of culture pH from day 2 to 7 under high CO2 concentration, and this increase of pH might correlate with algal growth rate and carbon fixation efficiency. Compared with high-CO2 culture, both mid- and low-CO2 cultures had an increase of culture pH values associated with a relative slow growth after bubbled with mid and low levels of CO2 from day 2 to 7.

As shown in Fig. 1c, d, both high-CO2 and mid-CO2 cells obtained high values of maximal photosynthesis system II (PSII) quantum yield (F v/F m) and effective PSII quantum yield (YII) during cultivation, and they all firstly represented a significant increase of F v/F m and Y (II) values and then gradually decreased. The high-CO2 cells consistently had the highest F v/F m and Y (II) values, followed by mid carbon cultured alga. Whereas, low CO2 cultivated alga had the lowest F v/F m and Y (II) values, which obviously decreased during cultivation. This suggested that the response to CO2 concentration in algal cells was also reflected in the changes in algal photosynthesis.

Lipid, fatty acid composition, total water-soluble proteins, chlorophyll a + c content and RNA concentration in algal cells measured under different CO2 concentrations

As described above, the concentration of CO2 had significant effects on P. tricornutum growth. To investigate the influence of CO2 concentrations on intracellular substances, we determined the lipid, total water-soluble proteins, and chlorophyll a + c content in P. tricornutum treated with different CO2 concentrations. Table 1 shows that when grown under the high CO2 condition, P. tricornutum had the highest lipid content (53.71 ± 2.41 %, w/w, % of dry cell weight (DCW)), followed by mid CO2 cultivated cells of 35.87 ± 1.72 %, and low CO2 cultured P. tricornutum had the lowest lipid content of 33.13 ± 1.21 %. As shown in Table 2, in low- and mid-CO2 cultured cells, 7.41 % (% of DCW) and 8.72 % (% of DCW) are longer-chain fatty acids (≥20C), respectively. Whereas, in high-CO2 cultured cells, the longer-chain fatty acids (≥20C) account in 16.41 % of dry cell weight. It was represented that a significant increase of longer-chain fatty acids content in high-CO2 cultured cells, compared to low- and mid-CO2 cultured cells. These results suggested that the high-CO2 cultured cells need much more cytosolic-generated reductant for lipids or longer-chain fatty acid synthesis.

Table 1 Dry weight and intracellular substances contents in three different CO2 concentrations cultivated P. tricornutum cells. Intracellular substances involved total water-soluble protein, lipids, chlorophyll a + c and RNA concentration. Data are expressed as a mean ± SD (n = 3)
Table 2 Fatty acid compositions of P. tricornutum under different CO2 concentration cultivation (w/w, % of DCW)

Table 1 exhibits the maximum water-soluble protein yield 16.29 ± 0.02 mg g−1FW in P. tricornutum also occurred in the high CO2 cultivated cells, while the mid-CO2, and low-CO2 cells had relatively lower soluble protein contents of 12.76 ± 0.04 and 7.63 ± 0.03 mg g−1 fresh weight (FW), respectively. Although high-CO2 P. tricornutum cells had high lipid and water-soluble protein contents, the concentration of chlorophyll a + c and RNA were lower than those in mid CO2 cultured cells (Table 1). Low-CO2 cultured cells had the lowest yield of intracellular substances, which may have been due to the limiting of carbon source.

Assays of the change in enzyme activities

P. tricornutum maintained in high CO2 concentration had the highest growth rate among the three experimental groups (Fig. 1). To investigate the mechanism underlying the different growth rates due to CO2 concentration, the activities of key enzymes in the Calvin cycle, including Rubisco, 3-phosphoglyceric phosphokinase (PGK), and phosphoribulokinase (PRK) were analyzed. As shown in Fig. 2, these enzymes showed maximum activity in P. tricornutum under the high CO2 concentration, followed by mid-CO2 cultured cells, which were slightly higher than low-CO2 cultured cells, but no significant difference was observed in the activity of PRK between mid-CO2 and low-CO2 cultured cells (P > 0.05). These results suggest that the activity of the Calvin cycle was enhanced under high CO2 cultivation, which was well matched with the high growth rate and photosynthetic performance of P. tricornutum in the high-CO2 concentration.

Fig. 2
figure 2

Changes of Calvin cycle-related enzymes’ activities in P. tricornutum cells responded to different CO2 concentrations. a The activity of Rubisco in P. tricornutum; b The activity of PRK in P. tricornutum; c The activity of PGK in P. tricornutum. Data are expressed as a mean ± SD (n = 3)

In addition, alga cells grown under the high CO2 concentration had a maximum yield of lipids (Table 1). This prompted us to investigate probable pathways which supplied NADPH for lipid synthesis, as NADPH is essential for elongation of fatty acids. To the best of our knowledge, in the photosynthetic cells of plants, de novo biosynthesis of 16-carbon and 18-carbon fatty acids occurs in the chloroplast, where NADPH is produced via the light reactions of photosynthesis. The 16-carbon fatty acids (e.g., palmitate) are elongated to yield the 20-carbon and even longer-chain fatty acids in the cytosol, so these elongation steps are the only ones that require cytosolic-generated reductant [24].

The oxidative pentose phosphate pathway (OPPP) is the major resource of NADPH in the cytoplasm. To better understand the carbon flux and reductant source for lipid synthesis in P. tricornutum cells under three different CO2 concentrations, the activities of G6PDH and 6PGDH, two key enzymes in the OPPP, were evaluated. Figure 3 shows the activities of G6PDH and 6PGDH, and these results showed that G6PDH and 6PGDH activities were highest under high-CO2 cultivation, while algal cells maintained in mid- and low-CO2 showed lower and lowest activity, respectively. These findings indicate that the activity of the OPPP was enhanced in cells under high-CO2 cultivation and may have supplied NADPH for lengthening the fatty acids chain.

Fig. 3
figure 3

G6PDH and 6PGDH activities in P. tricornutum maintained with three different CO2 concentrations. Both G6PDH and 6PGDH had relatively high activities in high-CO2 cultivated P. tricornutum cells. a The activity of G6PDH in P. tricornutum; b The activity of 6PGDH in P. tricornutum. Data are expressed as a mean ± SD (n = 3)

As the OPPP is not the sole producer of NADPH, to verify whether the other sources for NADPH could contribute to cytosolic fatty acids elongation, two tricarboxylic acid (TCA) cycle enzymes activity were detected. Figure 4 shows that no significant differences were observed in the activity of MDH of three different CO2 concentration cultured P. tricornutum cells. Whereas, the activity of α-ketoglutarate dehydrogenase (α-KGDH) was peaked in high-CO2 cultivated P. tricornutum cells, followed by mid-CO2 cells, and the low-CO2 cultivated cells had the lowest α-KGDH activity. As α-KGDH is the rate-determining enzyme of the TCA cycle [25], the activity of α-KGDH was positively correlated with TCA cycle activity. High α-KGDH activity indicated a general enhancement of the TCA cycle under high CO2 concentration.

Fig. 4
figure 4

The activities of two TCA cycle enzymes in P. tricornutum cultured with different CO2 concentrations. a The activity of α-KGDH; b The activity of MDH. Data are expressed as a mean ± SD (n = 3)

Analysis of enzyme mRNA expression measured by qPCR

The results of real-time PCR showed that under high CO2 concentration, P. tricornutum had the highest relative expression level of Rubisco, PRK, PGK, G6PDH, and 6PGDH among the three treatments (Figs. 5 and 6). The expressions of Rubisco, PGK, and G6PDH in mid-CO2 cultivated P. tricornutum cells were higher than those of the low-CO2 cultured cells, but the expression of PRK and 6PGDH in mid -CO2 cultivated P. tricornutum was not significantly different to that found in low-CO2 cultured cells (P > 0.05) The mRNA expression level of these enzymes was consistent with the results of enzyme activity, which indicated that P. tricornutum under high CO2 cultivation not only had high enzyme activities but also high mRNA content. Higher enzyme activities and mRNA expression levels of Rubisco, PGK, and PRK suggested that, in Calvin cycle, the CO2 fixation, carbon reduction, and ribulose-1,5-bisphosphate (RuBP) regeneration were enhanced; in other words, the carbon fixation efficiency of Calvin cycle elevated and the production of carbon skeleton for biosynthesis increased. These might positively correlate with rapid growth of P. tricornutum under high CO2 concentration.

Fig. 5
figure 5

Three enzymes’ mRNA expression in different CO2 concentrations cultured P. tricornutum cells measured by qPCR. a Rubisco expression in P. tricornutum; b PRK expression in P. tricornutum; c PGK expression in P. tricornutum. Data are expressed as a mean ± SD (n = 3)

Fig. 6
figure 6

The expressions of G6PDH and 6PGDH in P. tricornutum cultured with different CO2 concentration. a The relative expression level of G6PDH; b The relative expression level of 6PGDH. Data are expressed as a mean ± SD (n = 3)


As described in Fig. 1, P. tricornutum can tolerate relatively high levels of CO2 and has a rapid growth rate when cultivated in high CO2 concentration, which was consistent with the finding that rising CO2 concentration increased phytoplankton growth rate [1, 8, 9, 12, 26]. Moreover, Rubisco activity and mRNA expression were increased (Figs. 2 and 5) under high CO2 concentration. As the rate-limiting and key regulatory enzyme of the Calvin cycle, the level of Rubisco monitors the carbon flux through this pathway [27]. In addition to high Rubisco activity, the activities of PRK and PGK were high in high CO2 concentration cultured cells and significantly higher than Rubisco activity. Rubisco acts as a CO2 receptor and takes part in the carbon fixation stage of the Calvin cycle, and PGK participates in the reduction stage of the Calvin cycle, whereas PRK is incorporated in the regeneration phase in the Calvin cycle; high activities of Rubisco, PGK, and PRK in high CO2 cultured cells indicated that the Calvin cycle activity was enhanced and was operating effectively in algal cells under high CO2 cultivation. This may account for the rapid growth rate observed. However, when P. tricornutum was grown under low CO2 concentration, the activities of the Calvin cycle-related enzymes were weaker, which suggested that substrates and energy required for algal growth were deficient. This might be the major reason why no significant growth under the low CO2 concentration of algal cells was observed. These results indicated elevated CO2 concentration provided plenty of carbon resource for photosynthetic carbon fixation and then induced an enhancement of algal photosynthetic carbon fixation and growth rate which were consistent with numerous previous studies that higher levels of CO2 support higher growth rates.

As expected, a significant increase in lipid content was also found in the high CO2 cultivated rapid-growth P. tricornutum cells. As we know, microalgal lipid production typically begins at the onset of nitrogen depletion as the C/N ratio (carbon to nitrogen ratio) in algal cells increased, which lead to most of the fixed carbon divert into nitrogen deficient compounds such as lipids [28]. In this research, P. tricornutum were maintained in nitrogen repletion cultures, which might not trigger lipid accumulation. Yet we observed 1.5-fold increase of lipid content in high-CO2 cultured cells, compared to mid-CO2 cultured cells. We thought that maybe because of a higher C/N ratio in algal cells that caused by high CO2 concentration. This is supported by the conclusion that the elemental stoichiometry (carbon to nitrogen ratio) was raised under high CO2 conditions in both nitrogen limited and nitrogen replete conditions in P. tricornutum according to Li et al. [29].

Lipids, especially triacylglycerol (TAG), primarily serve as a storage form of carbon and energy in algal cells [30], which require numerous NADPH molecules for biosynthesis in the cytoplasm. During rapid growth of algal cells, ATP and NADPH generated by the light reaction are mainly supplied for the maintenance of algal growth. Therefore, under high CO2 cultivation, the key problem in the rapid growth of algal cells is how the additional NADPH required for lipid synthesis comes from. NADPH can be primarily generated from the OPPP or TCA cycle. The first two steps of the OPPP, catalyzed by G6PDH and 6PGDH respectively, are the major source of NADPH. As shown in Fig. 6, with a high level of CO2 concentration, enhanced activity and mRNA expression of G6PDH and 6PGDH were observed, except for increased lipid accumulation, which indicated that OPPP activity was enhanced. In a study of Chlorella, Xiong et al. [31] found that NADPH supplied through OPPP increased under nitrogen limited condition when lipid synthesis increased, and they speculated that NADPH from the mitochondrial TCA cycle was difficult to be trapped for lipid metabolism in the cytoplasm. The enhancement of TCA cycle might contribute to two possibilities: (i) to provide ATP for lipid synthesis; (ii) to produce quantity of intermediates (e.g., malic acid) to offer substrate or carbon skeleton for fatty acid synthesis [32]. Thus, G6PDH together with 6PGDH that are of great importance in the synthesis of the reductant NADPH through the OPPP [33], may play an important role in elongation of fatty acids under high CO2 concentration.


In this study, growth, lipid content, photosynthetic performance, the activity, and expression of key enzymes in Calvin cycle and OPPP were analyzed in the marine diatom P. tricornutum under three different CO2 concentrations. Both the growth rate and lipid content of P. tricornutum increased significantly under the high CO2 concentration. Enzyme activity and mRNA expression of three Calvin cycle-related enzymes (Rubisco, PGK, PRK) were also increased under high CO2 cultivation, which suggested the enhancement of the Calvin cycle activity. This may account for the observed rapid growth rate. In addition, high activity and mRNA expression of G6PDH and 6PGDH, which produce NADPH through OPPP, were observed in high CO2 cultured cells. These results indicate OPPP was enhanced and might play an important role in elongation of fatty acids or lipid synthesis under high CO2 concentration.


Alga strain cultivation

P. tricornutum was screened from the East China Sea and confirmed unialgal as previously described by Wu et al. [34]. The alga strain was cultivated in sterilized carbon source deprived artificial seawater enriched with f/2-Si medium [35] and grown at 20 ± 1 °C under a constant light intensity of 100 μmol m−2 s−1 with a 14:10 h light-dark (L/D) cycle.

CO2 treatment

The alga culture was maintained with aeration and cultivated in 2-L flasks containing 1.5-L medium. Three different CO2 concentrations in the bubbling aeration system were tested: low CO2 (0.015 %), mid CO2 (atmospheric, 0.035 %), and high CO2 (0.15 %). The handheld indoor air quality testing detector Telaire 7001 CO2 Monitor (USA), which can be able to display CO2 readings in less than 30 s, was used to measure CO2 concentration in this study. Each treatment included three replicates. The pH of algal culture bubbled with different CO2 concentration was daily measured using a Switzerland Mettler Toledo Delta 320 pH meter.

Growth and photosynthetic determination

Algal growth was measured daily by cell number and the OD value at the optical wavelength for P. tricornutum (730 nm) using a spectrophotometer (UV-1800). A hemocytometer was used to count algal cells.

To investigate the photosynthetic performance of P. tricornutum in response to CO2 concentration, the chlorophyll fluorescence of PSII was measured by a Dual-PAM-100 fluorometer (Heinz Walz, Effeltrich, Germany) which was conducted with a PC using the WinControl software (Heinz Walz). Two parameters, the maximum quantum yield of PSII (F v/F m) and the effective PSII quantum yield (YII), were evaluated using the pulse-amplitude modulated method as described by Lin et al. [36] with some modifications. To ensure the consistency of cell density for PAM fluorescence measurement, the growing algal samples were adjusted to 0.6 at OD730 nm before detected. The minimum fluorescence (F 0) and maximum fluorescence (F m) were determined after the samples were incubated in darkness for 5 min. Variable fluorescence (F v) was calculated according to formula F v = F mF 0. The maximal PSII quantum yield was calculated as F v/F m. The effective quantum yield of PSII (Y (II)) was calculated as (F m F)/F m , where F m was the maximal fluorescence detected under photosynthetic active radiation (PAR) of 58 μmol m−2 s−1 and F is the real-time fluorescence yield under illumination.

Lipid analysis

Algal cultures were harvested after 7-day cultivation by centrifugation at 5000g, and the algal cells were quickly frozen in liquid nitrogen. A freeze dryer was used to dry the frozen algal cells. Lipids were extracted from 50 mg dryness algal powder using a modified chloroform-methanol system as described by Bligh and Dyer [37]. Crude samples were dried with N2 flow until a constant weight was obtained. Gravimetric means, a conventional lipid quantification method, was used for total lipid analysis. The fatty acid compositions of different CO2 concentration cultivated P. tricornutum were determined by gas chromatography [38].

Enzyme assays

Harvested algal cells were washed twice with 0.01 M PBS buffer (pH 7.4) and were ground into fine powder using a pre-chilled mortar and pestle with liquid N2. Crude enzyme extracts were prepared from the algal powder in three times the volume of ice-cold extraction buffer. Enzyme activities were determined spectrophotometrically using a UV-1800 spectrophotometer by measuring at 340 nm in total volumes of 0.4 mL and in triplicate. The change in absorbance was recorded for 5 min. Results were expressed as μmol NAD (P) H oxidation or NAD (P) + reduction min −1 g −1 AFDW, as we had standardized the correlation between fresh weight and ash-free dry weight of different CO2 cultured P. tricornutum. The compositions of the extract and assay medium for the respective enzymes are detailed below. All chemicals and enzymes used for enzyme assays were purchased from Sigma-Aldrich (Sigma-Aldrich Co. LLC., USA).

Rubisco (ribulose-1, 5-bisphosphate carboxylase/oxygenase), which controls the initial step in photosynthetic carbon fixation via the Calvin cycle, is one of the most abundant proteins in both higher plants and algae [39]. The carboxylase activity of Rubisco relative to photosynthetic rates has been reported in many previous studies of macroalgae and microalgae [27]. Rubisco (EC activity was measured using a modification of the basic procedure according to Gerard and Driscoll [27]. 300 μL of chilled extraction buffer (40 mM Tris-HC1, 0.25 mM EDTA, 10 mM MgCl2, 5 mM glutathione, at pH 7.6) was added per 100-mg fresh algal powder. The mixture was stirred for 2 min to homogeneity, and centrifuged at 13,000g for 10 min. The supernatants were incubated on ice for further enzyme assays. The reaction mixture contained 0.1 M Tris-HCl (pH 7.8), 0.2 mM NaHCO3, 12 mM MgCl2, 5 mM NADH, 50 mM ATP, 50 mM phosphocreatine, 160 units per milliliter of creatine phosphokinase (EC, and PGK (EC, and 25 mM RuBP was added to initiate the reaction.

For measurement of PRK (EC and PGK activities in crude extracts, the method described by Rao and Terry [40] was used. Frozen fresh algal cells were extracted in three times the volume of extraction buffer (100 mM Hepes-NaOH (pH 8.0), 10 mM MgCl2, 0.4 mM EDTA, 1 % polyvinypyrrolidone, 100 mM Na-ascorbate, 0.1 % BSA at 0–4 °C) and then stirred for 2 min with a vortex at a maximum speed. Crude homogenates were then centrifuged at 13,000g for 10 min. The supernatants were prepared for further assays. For the assay of PRK, pre-chilled 30 mM Hepes-NaOH (pH 8.0), containing 10 mM MgCl2, 5 mM DL-Dithiothreitol (DTT), 2 mM ATP, 2 mM phosphoenolpyruvic acid, 0.4 mM ribose-5-phosphate, 0.3 mM NADH, 2 units per mL of ribose-5-phosphate isomerase (EC, lactic dehydrogenase (EC, and pyruvate kinase (EC was used as the assay media; the reaction was initiated by adding the algal extract. The activity of PGK (EC was assayed in 30 mM Hepes-KOH (pH 7.8), 5 mM MgCl2, 1 mM NaF, 1 mM KH2PO4, 5 mM DTT, 2 mM ATP, 4 mM phosphoglycerate, 0.3 mM NADH, and 4 units per mL of NAD-glyceraldehyde-3-phosphate dehydrogenase (EC and triose phosphate isomerase (EC; the reaction was initiated by adding ATP.

The oxidation pentose phosphate pathway is the major resource of cytosolic-generated NADPH, which is catalyzed by G6PDH and 6PGDH. G6PDH, the rate-limiting and key regulatory enzyme of the OPPP, controls the flow of carbon through this pathway and produces reductant to meet the cellular needs for reductive biosynthesis. To determine the activities of G6PDH (EC and 6PGDH (EC, the method described by Fahrendorf et al. [41] was used with some modifications. Algal cells prepared as described above were extracted in 50 mM Tris-HC1 pH 8.0, 300 mM NaC1, 0.1 mM benzamidine, and 0.1 mM phenylmethylsulfonyl fluoride (PMSF). G6PDH activity was measured in a continuous assay at 30 °C, including 0.1 M Tris-HC1 pH 8.0, 0.4 mM NADP+, and 3 mM glucose-6-phosphate. 6PGDH activity was measured at 30 °C in 0.1 M Hepes pH 7.5, 0.4 mM NADP+, and 3 mM 6-phosphogluconate. Reactions were started by the addition of algal extracts. Reduction of NADP+ at 340 nm was used to monitor G6PDH and 6PGDH activities.

TCA cycle is another major resource of NADPH, via isocitrate dehydrogenase. To verify whether this process contributes reductant to fatty acid elongation, the activity of two TCA cycle enzymes, α-KGDH and MDH was measured following the method as described by Peng L and Shimizu K [42]. Algal cells were extracted in 100 mM Tris-HCl (pH 7.0) containing 20 mM KCl, 5 mM MnSO4, 2 mM DTT, and 0.1 mM EDTA. The assay conditions were as follows: α-KGDH 0.2 M phosphate buffer (pH 7.2), 1 mM CoASH, 0.1 M cysteine-HCl (pH 7.2), 10 mM NAD+ (pH 7.2), 3 mM a-ketoglutarate. Malate dehydrogenase, 0.1 M Tris-HCl (pH 8.8), 0.1 mM sodium malate, 10 mM NAD+, and reactions were started by the addition of algal extracts.

Real-time PCR analysis

Total RNA was extracted from frozen algal powder using the Plant RNA kit (OMEGA, Norcross, USA) following the manufacturer’s instructions which included the first step of genomic DNA digestion. The concentrations of RNA extracts were measured using a NanoDrop 1000 Spectrophotometer (Thermo, Wilmington, Delaware, USA).

For single strand cDNA synthesis, the PrimeScript RT regent Kit with gDNA Eraser (TaKaRa Biotech Co., Dalian, China) was used to perform the reverse transcription reaction according to the user’s manual. In this protocol, further genomic DNA removal was performed to purify the RNA extracts. All tests were performed on ice. PCR was performed to confirm the absence of genomic DNA contamination.

Real-time PCR was performed with the cDNA template from the reverse transcription reaction and five pairs of specific primers (Table 3). Primers were designed based on the alignment of the deduced amino-acid sequences, which were obtained from the National Center for Biotechnology Information (NCBI) web site (, using the Primer Premier 5.0 software. Levels of specific mRNA transcripts were quantified by the Bio-Rad iQ5 Multicolor Real-Time PCR Reaction system (Bio-Rad, Hercules, CA, USA). The real-time PCR amplifications were performed with the reagents from the Fast Essential DNA Green Master (Roche, Germany). The cycling parameters for real-time PCR were 95 °C for 10 min (denaturation), followed by 40 cycles at 94 °C for 10 s (denaturation), 58 °C for 20 s (primer annealing), and (c) 72 °C for 10 s (elongation). To ensure only the single specific DNA fragment was amplified, melting curve analyses were performed on all PCR products. Triplicate qPCRs were performed for each sample. Data derived from the PCR program were analyzed with the Bio-Rad optical system software.

Table 3 List of primers used in the real-time PCR analysis

Chlorophyll estimations

For P. tricornutum, the chlorophyll a and c1 + c2 content was estimated by a 90 % acetone extraction system. Fifty-milligram fresh algal powder ground from frozen algal cells in liquid N2 was added in 5 mL 90 % acetone and thereafter read the fluorescence emission of the centrifuged extracts at 664 and 630 nm which were obtained as described by Jeffrey and Humphrey [43].

Total water-soluble proteins preparations

P. tricornutum water-soluble proteins were prepared using the method according to Wang et al. [44] with some modifications. Algal water-soluble proteins were extracted in fivefold volume of pre-chilled extract buffer, containing 50 mM Tris-HCl buffer (pH 8.0), 3 mMDTT, 5 mM MgCl2, 10 % glycerol, 0.5 % polyvinylpyrrolidone (PVP), 5 mM Na2-EDTA, 1 mM PMSF, 5 mM benzimidin, 5 mM Acoproicand, 1 % (v/v) plant protease inhibitor cocktail (Sigma). Crude extracts were centrifuged at 15,000g for 30 min at 4 °C, and the supernatants were used for proteins determination. The Coomassie Brilliant Blue G-250 assay was used for protein quantitation in the study [45].

Statistical analysis

All data are expressed as the mean ± standard deviation (SD) of three independent experiments. All statistical analyses were conducted using SPSS, and t test was used to identify data of any significance within the treatments at P value ≤ 0.05.



Oxidative pentose phosphate pathway


Ribulose-1, 5-bisphosphate carboxylase oxygenase


3-phosphoglyceric phosphokinase




Glucose-6-phosphate dehydrogenase


6-phosphogluconate dehydrogenase




Photosynthesis system II




Fresh weight


Dry cell weight


Ash-free dry weight

TCA cycle:

Tricarboxylic acid cycle


α-ketoglutarate dehydrogenase


Malate dehydrogenase


  1. Wu Y, Gao K, Riebesell U. CO2-induced seawater acidification affects physiological performance of the marine diatom Phaeodactylum tricornutum. Biogeosciences. 2010;7:2915–23.

    Article  CAS  Google Scholar 

  2. Gunderson CA, Wullschleger SD. Photosynthetic acclimation in trees to rising atmospheric CO2—a broader perspective. Photosynthesis Res. 1994;39:369–88.

    Article  CAS  Google Scholar 

  3. Faria T, Wilkins D, Besford RT, Vaz M, Pereira JS, Chaves MM. Growth at elevated CO2 leads to down-regulation of photosynthesis and altered response to high temperature in Quercus suber L. seedlings. J Exp Bot. 1996;47:1755–61.

    Article  CAS  Google Scholar 

  4. Cheng SH, Moore BD, Seemann JR. Effects of short- and long-term elevated CO2 on the expression of ribulose-1,5-bisphosphate carboxylase/oxygenase genes and carbohydrate accumulation in leaves of Arabidopsis thaliana (L.) Heynh. Plant Physiol. 1998;116:715–23.

    Article  CAS  Google Scholar 

  5. Stitt M, Krapp A. The interaction between elevated carbon dioxide and nitrogen nutrition: the physiological and molecular background. Plant Cell Environ. 1999;22:583–621.

    Article  CAS  Google Scholar 

  6. Bloom AJ, Smart DR, Nguyen DT, Searles PS. Nitrogen assimilation and growth of wheat under elevated carbon dioxide. Proc Natl Acad Sci U S A. 2002;99:1730–5.

    Article  CAS  Google Scholar 

  7. Nakano Y, Miyatake K, Okuno H, Hamazaki K, Takenaka S, Honami N, et al. Growth of photosynthetic algae euglena in high CO2 conditions and its photosynthetic characteristics. Acta Horticult (Wageningen). 1996;440:49–54.

    Google Scholar 

  8. Riebesell U, Wolfgladrow DA, Smetacek V. Carbon-dioxide limitation of marine phytoplankton growth rates. Nature. 1993;361:249–51.

    Article  CAS  Google Scholar 

  9. Hein M, SandJensen K. CO2 increases oceanic primary production. Nature. 1997;388:526–7.

    Article  CAS  Google Scholar 

  10. Kim JM, Lee K, Shin K, Kang JH, Lee HW, Kim M, et al. The effect of seawater CO2 concentration on growth of a natural phytoplankton assemblage in a controlled mesocosm experiment. Limnol Oceanogr. 2006;51:1629–36.

    Article  CAS  Google Scholar 

  11. Tortell PD, Payne CD, Li YY, Trimborn S, Rost B, Smith WO, et al. CO2 sensitivity of southern ocean phytoplankton. Geophys Res Lett. 2008;35.

  12. Yongmanitchai W, Ward OP. Growth of and omega-3-fatty-acid production by Phaeodactylum tricornutum under different culture conditions. Appl Environ Microbiol. 1991;57:419–25.

    CAS  Google Scholar 

  13. Chiu S-Y, Kao C-Y, Tsai M-T, Ong S-C, Chen C-H, Lin C-S. Lipid accumulation and CO2 utilization of Nannochloropsis oculata in response to CO2 aeration. Bioresour Technol. 2009;100:833–8.

    Article  CAS  Google Scholar 

  14. Tsuzuki M, Ohnuma E, Sato N, Takaku T, Kawaguchi A. Effects of CO2 concentration during growth on fatty-acid composition in microalgae. Plant Physiol. 1990;93:851–6.

    Article  CAS  Google Scholar 

  15. Yoo C, Jun SY, Lee JY, Ahn CY, Oh HM. Selection of microalgae for lipid production under high levels carbon dioxide. Bioresour Technol. 2010;101:S71–4.

    Article  CAS  Google Scholar 

  16. Chisti Y. Biodiesel from microalgae. Biotechnol Adv. 2007;25:294–306.

    Article  CAS  Google Scholar 

  17. Matsuda Y, Hara T, Colman B. Regulation of the induction of bicarbonate uptake by dissolved CO2 in the marine diatom. Phaeodactylum tricornutum Plant Cell Environ. 2001;24:611–20.

    Article  CAS  Google Scholar 

  18. Hyun B, Jang PG, Lee WJ, Shin K. Effects of increased CO2 and temperature on the growth of four diatom species (Chaetoceros debilis, Chaetoceros didymus, Skeletonema costatum and Thalassiosira nordenskioeldii) in laboratory experiments. J Environ Sci Int. 2014;23:1003–12.

    Article  Google Scholar 

  19. Schippers P, Lurling M, Scheffer M. Increase of atmospheric CO2 promotes phytoplankton productivity. Ecol Lett. 2004;7:446–51.

    Article  Google Scholar 

  20. Bermúdez M Jr (2010) Effect of CO2 on elemental composition and fatty acids of diatoms and concomitant effects on copepods. Master thesis. Christian-Albrechts-Universität zu Kiel, Faculty of Mathematics and Natural Sciences; 2010.

  21. Guschina IA, Harwood JL. Lipids and lipid metabolism in eukaryotic algae. Prog Lipid Res. 2006;45:160–86.

    Article  CAS  Google Scholar 

  22. Harwood JL, Guschina IA. The versatility of algae and their lipid metabolism. Biochimie. 2009;91:679–84.

    Article  CAS  Google Scholar 

  23. Allen JF. Photosynthesis of ATP— electrons, proton pumps, rotors, and poise. Cell. 2002;110:273–6.

    Article  CAS  Google Scholar 

  24. Leninger A, Nelson DL, Cox MM. Principles of biochemistry. New York: Worth Publishers; 1993.

    Google Scholar 

  25. Li M, Ho PY, Yao SJ, Shimizu K. Effect of lpda gene knockout on the metabolism in Escherichia coli based on enzyme activities, intracellular metabolite concentrations and metabolic flux analysis by 13C-labeling experiments. J Biotechnol. 2006;122:254–66.

    Article  CAS  Google Scholar 

  26. Araujo SD, Garcia VMT. Growth and biochemical composition of the diatom Chaetoceros cf. wighamii brightwell under different temperature, salinity and carbon dioxide levels. I. Protein, carbohydrates and lipids. Aquaculture. 2005;246:405–12.

    Article  Google Scholar 

  27. Gerard VA, Driscoll T. A spectrophotometric assay for rubisco activity: application to the kelp Laminaria saccharina and implications for radiometric assays. J Phycol. 1996;32:880–4.

    Article  CAS  Google Scholar 

  28. Cescut J, Fillaudeau L, Molina-Jouve C, Uribelarrea J-L. Carbon accumulation in Rhodotorula glutinis induced by nitrogen limitation. Biotechnol Biofuels. 2014;7:164.

    Article  Google Scholar 

  29. Li W, Gao KS, Beardall J. Interactive effects of ocean acidification and nitrogen-limitation on the diatom Phaeodactylum tricornutum. Plos One. 2012;7.

  30. Hu Q, Sommerfeld M, Jarvis E, Ghirardi M, Posewitz M, Seibert M, et al. Microalgal triacylglycerols as feedstocks for biofuel production: perspectives and advances. Plant J. 2008;54:621–39.

    Article  CAS  Google Scholar 

  31. Xiong W, Liu LX, Wu C, Yang C, Wu QY. 13C-tracer and gas chromatography-mass spectrometry analyses reveal metabolic flux distribution in the oleaginous microalga Chlorella protothecoides. Plant Physiol. 2010;154:1001–11.

    Article  CAS  Google Scholar 

  32. Recht L, Toepfer N, Batushansky A, Sikron N, Gibon Y, Fait A, et al. Metabolite profiling and integrative modeling reveal metabolic constraints for carbon partitioning under nitrogen starvation in the green algae Haematococcus pluvialis. J Biol Chem. 2014;289:30387–403.

    Article  CAS  Google Scholar 

  33. Kletzien RF, Harris PKW, Foellmi LA. Glucose-6-phosphate-dehydrogenase—a housekeeping enzyme subject to tissue-specific regulation by hormones, nutrients, and oxidant stress. FASEB J. 1994;8:174–81.

    CAS  Google Scholar 

  34. Wu S, Zhang B, Huang A, Huan L, He L, Lin A, et al. Detection of intracellular neutral lipid content in the marine microalgae Prorocentrum micans and Phaeodactylum tricornutum using Nile red and BODIPY 505/515. J Appl Phycol. 2014;26:1659–68.

    Article  CAS  Google Scholar 

  35. Guillard RR, Ryther JH. Studies of marine planktonic diatoms.1. Cyclotella nana Hustedt, and Detonula confervacea (Cleve) Gran. Can J Microbiol. 1962;8:229–39.

    Article  CAS  Google Scholar 

  36. Lin AP, Wang GC, Yang F, Pan GH. Photosynthetic parameters of sexually different parts of Porphyra katadai var. hemiphylla (Bangiales, Rhodophyta) during dehydration and re-hydration. Planta. 2009;229:803–10.

    Article  CAS  Google Scholar 

  37. Bligh E, Dyer WJ. A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959;37:911–7.

    Article  CAS  Google Scholar 

  38. Li W-q, Li Q, Liao Q-b, Chen Q-h. Effect of temperature on fatty acid composition of four species of marine microalgae. J Oceanogr Taiwan Strai. 2003;22:9–13.

    Google Scholar 

  39. Wang C, Fan XL, Wang GC, Niu JF, Zhou BC. Differential expression of Rubisco in sporophytes and gametophytes of some marine macroalgae. Plos One. 2011;6.

  40. Rao IM, Terry N. Leaf phosphate status, photosynthesis, and carbon partitioning in sugar-beet. I. Changes in growth, gas-exchange, and calvin cycle enzymes. Plant Physiol. 1989;90:814–9.

    Article  CAS  Google Scholar 

  41. Fahrendorf T, Ni WT, Shorrosh BS, Dixon RA. Stress responses in alfalfa (Medicago sativa L.). XIX. Transcriptional activation of oxidative pentose-phosphate pathway genes at the onset of the isoflavonoid phytoalexin response. Plant Mol Biol. 1995;28:885–900.

    Article  CAS  Google Scholar 

  42. Peng L, Shimizu K. Global metabolic regulation analysis for Escherichia coli K12 based on protein expression by 2-dimensional electrophoresis and enzyme activity measurement. Appl Microbiol Biotechnol. 2003;61:163–78.

    Article  CAS  Google Scholar 

  43. Jeffrey SW, Humphrey GF. New spectrophotometric equations for determining chlorophylls a, b, c1 and c2 in higher-plants, algae and natural phytoplankton. BPP. 1975;167:191–4.

    CAS  Google Scholar 

  44. Wang SB, Hu Q, Sommerfeld M, Chen F. An optimized protocol for isolation of soluble proteins from microalgae for two-dimensional gel electrophoresis analysis. J Appl Phycol. 2003;15:485–96.

    Article  CAS  Google Scholar 

  45. Bradford MM. Rapid and sensitive method for quantitation of microgram quantities of protein utilizing principle of protein-dye binding. Anal Biochem. 1976;72:248–54.

    Article  CAS  Google Scholar 

Download references


This work was supported by International Science & Technology Cooperation Program of China (ISTCP, 2015DFG32160), Ministry of Science and Technology of the PRC fundamental research work (NO. 2012FY112900-01), the National Natural Science Foundation of China (41406169), the Science and Technology Strategic Pilot of the Chinese Academy of Sciences (XDA05030401), and Tianjin Natural Science foundation (12JCZDJC22200).

Author information

Authors and Affiliations


Corresponding author

Correspondence to Guangce Wang.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

SW, AH, and GW designed the experiments. SW and AH carried out the cultivation and analysis of lipid contents, enzyme activity, and mRNA expressions of P. tricornutum. BZ, LH, and PZ participated in the design of the primer used in the study. AL participated in the analysis of the photosynthetic performance of P. tricornutum. SW and GW drafted the manuscript. GW and AH revised the manuscript. GW conceived of the study. All authors read and approved the final manuscript.

Songcui Wu and Aiyou Huang contributed equally to this work.

Rights and permissions

Open Access  This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made.

The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.

To view a copy of this licence, visit

The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wu, S., Huang, A., Zhang, B. et al. Enzyme activity highlights the importance of the oxidative pentose phosphate pathway in lipid accumulation and growth of Phaeodactylum tricornutum under CO2 concentration. Biotechnol Biofuels 8, 78 (2015).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: