ORIGINAL RESEARCH article
Overexpression of Sedoheptulose-1,7-Bisphosphatase Enhances Photosynthesis in Chlamydomonas reinhardtii and Has No Effect on the Abundance of Other Calvin-Benson Cycle Enzymes
- 1Molecular Biotechnology & Systems Biology, TU Kaiserslautern, Kaiserslautern, Germany
- 2Computational Systems Biology, TU Kaiserslautern, Kaiserslautern, Germany
- 3Max Planck Institute of Molecular Plant Physiology, Potsdam, Germany
The productivity of plants and microalgae needs to be increased to feed the growing world population and to promote the development of a low-carbon economy. This goal can be achieved by improving photosynthesis via genetic engineering. In this study, we have employed the Modular Cloning strategy to overexpress the Calvin-Benson cycle (CBC) enzyme sedoheptulose-1,7-bisphosphatase (SBP1) up to threefold in the unicellular green alga Chlamydomonas reinhardtii. The protein derived from the nuclear transgene represented ∼0.3% of total cell protein. Photosynthetic rate and growth were significantly increased in SBP1-overexpressing lines under high-light and elevated CO2 conditions. Absolute quantification of the abundance of all other CBC enzymes by the QconCAT approach revealed no consistent differences between SBP1-overexpressing lines and the recipient strain. This analysis also revealed that the 11 CBC enzymes represent 11.9% of total cell protein in Chlamydomonas. Here, the range of concentrations of CBC enzymes turned out to be much larger than estimated earlier, with a 128-fold difference between the most abundant CBC protein (rbcL) and the least abundant (triose phosphate isomerase). Accordingly, the concentrations of the CBC intermediates are often but not always higher than the binding site concentrations of the enzymes for which they act as substrates. The enzymes with highest substrate to binding site ratios might represent good candidates for overexpression in subsequent engineering steps.
An increased productivity of plants and microalgae is required to feed the growing world population and to promote the development of a low-carbon economy. One way to increase plant and microalgal productivity is to improve photosynthesis by genetic engineering. Engineering efforts that have resulted in increased biomass are the rewiring of photorespiration (Kebeish et al., 2007; Nolke et al., 2014), the improvement of linear electron transport between the photosystems (Chida et al., 2007; Simkin et al., 2017b), or the overexpression of distinct Calvin-Benson cycle (CBC) enzymes [for recent reviews see Kubis and Bar-Even (2019) and Simkin et al. (2019)]. The rationale behind the latter approach is that the rising concentration of atmospheric CO2 caused by the burning of fossil fuels increases the velocity of the carboxylation reaction of Rubisco and inhibits the competing oxygenation reaction. This results in a shift in the limitation of photosynthesis away from carboxylation of ribulose 1,5-bisphosphate (RuBP) and toward RuBP regeneration. The CBC enzyme sedoheptulose-1,7-bisphosphatase (SBPase) has been shown to exert strong metabolic control over RuBP regeneration at light saturation, as the irreversible reaction that it catalyses is positioned at the branch point between regenerative (RuBP regeneration) and assimilatory (starch biosynthesis) portions of the CBC. SBPase catalyzes the irreversible dephosphorylation of sedoheptulose-1,7-bisphosphate (SBP) to sedoheptulose-7-phosphate (S7P). Accordingly, the overexpression of SBPase alone (Lefebvre et al., 2005; Tamoi et al., 2006; Feng et al., 2007; Rosenthal et al., 2011; Fang et al., 2012; Ding et al., 2016; Driever et al., 2017; Simkin et al., 2017a) or of the cyanobacterial bifunctional SBPase/FBPase (BiBPase) (Miyagawa et al., 2001; Yabuta et al., 2008; Ichikawa et al., 2010; Gong et al., 2015; Ogawa et al., 2015; Kohler et al., 2017; De Porcellinis et al., 2018) resulted in marked increases in photosynthesis and biomass yields in tobacco, lettuce, Arabidopsis thaliana, wheat, tomato, rice, soybean, in the cyanobacterium Synechococcus, and in the microalgae Euglena gracilis and Dunaliella bardawil.
Genetic engineering often is an iterative process essentially consisting of four steps: (i) the design and manufacturing of a gene construct, (ii) its transfection into the target organism and the recovery of transgenic lines, (iii) the screening for expressing transformants, and (iv) the readout of the trait to be altered, on which basis the gene construct for the next cycle is designed. The cloning steps used to be a time constraint, which was overcome by new cloning strategies like Gibson assembly or Modular Cloning (MoClo) for Synthetic Biology that allow the directed assembly of multiple genetic parts in a single reaction (Gibson et al., 2009; Weber et al., 2011). Still a major time constraint (months) in the genetic engineering of plants is the recovery of transfected plants and their propagation for reading out altered traits. This constraint can only be overcome by using plant models with short generation times, like microalgae.
A potential problem of genetic engineering are undesired side effects of the genetic engineering that can best be revealed by system-wide approaches. One way is to compare the proteomes of wild type and engineered lines by quantitative proteomics (Gillet et al., 2016). A more targeted approach is the use of quantification concatamers (QconCATs) (Beynon et al., 2005; Pratt et al., 2006). QconCATs are made of concatenated proteotypic peptides, an affinity tag allowing purification under denaturing conditions and, optionally, cysteine or tryptophan residues for easy quantification. The QconCAT protein is expressed in E. coli with a heavy isotope from a codon-optimized, synthetic gene. A known amount of the QconCAT protein is then added to the sample and, upon tryptic digestion, the heavy proteotypic peptides from the QconCAT protein are released together with the corresponding light peptides from the parent proteins. All QconCAT peptides are present in a strict 1:1 ratio at the concentration determined for the entire protein. After ionization, the pairs of heavy QconCAT peptides and light native peptides can be separated and quantified by mass spectrometry, with the heavy peptides serving as calibrators allowing absolute quantification of the target proteins in the sample. This method is limited to about 20 targets per QconCAT protein.
The aim of this work was to provide a proof of principle for a rapid metabolic engineering workflow to improve photosynthesis. We chose to overexpress SBPase via the MoClo strategy, the unicellular green alga Chlamydomonas as a chassis, and QconCAT-based absolute quantification as a tool for monitoring effects on other CBC enzymes.
Materials and Methods
Growth of Chlamydomonas Cells
Chlamydomonas reinhardtii UVM4 cells (Neupert et al., 2009) were grown in Tris-Acetate-Phosphate (TAP) medium (Kropat et al., 2011) on a rotatory shaker. For transformation, cells were grown at a light intensity of 100 μmol photons m–2 s–1 to a density of 5 × 106 cells/ml and collected by centrifugation at 4000 × g for 2 min. 5 × 107 cells were mixed with 1 μg DNA linearized with NotI and transformed by vortexing with glass beads (Kindle, 1990). Vortexed cells were diluted twofold with TAP and 2.5 × 107 cells were spread onto TAP agar plates containing 100 μg ml–1 spectinomycin. Plates were incubated over-night in the dark and then incubated at 30 μmol photons m–2 s–1 for about 10 days. For growth curves, cells were inoculated in 100 ml TAP medium and grown at 150 μmol photons m–2 s–1 to a density of about 8 × 106 cells/ml. 100 ml TAP or Hepes-Minimal-Phosphate (HMP) medium (5 mM Hepes-KOH instead of 20 mM Tris, no acetate) were then inoculated with 3 × 105 cells/ml in triplicates for each strain and growth was monitored by cell counting using the Z2 Coulter Particle Count and Size Analyzer (Beckmann). The culture volume is the summed cell volume of all cells in 1 ml medium. For mass spectrometry analyses, samples were harvested 22 h after inoculation (early log phase).
Measurement of Oxygen Evolution
Cells were inoculated in 50 ml TAP medium and grown overnight to early log phase. Oxygen measurements were performed in the Mini-PAM-II (Walz, Germany) device using the needle-type oxygen microsensor OXR-50 (Pyroscience, Germany). Before the measurements, the cell density was determined, and an aliquot was taken to determine the chlorophyll concentration. The PAM chamber was filled with 400 μl of Chlamydomonas culture and NaHCO3 was added to a final concentration of 30 mM. Cells were dark-adapted for 5 min and far-red light adapted for another 5 min. Then light with the intensities of 16, 29, 42, 58, 80, 122, 183, 269, 400, 525, 741, and 963 μmol photons m–2 s–1 was applied for 2 min each and oxygen evolution was monitored.
Cloning of the Chlamydomonas SBP1 Gene for MoClo
Our constructs are based on the Phytozome 12 annotation of the genomic version of the Chlamydomonas SBP1 gene (Cre03.g185550) with seven exons and six introns. However, we used the first ATG in the 5′ UTR as start codon instead of the third proposed by Phytozome. To domesticate a BsaI recognition site in the fifth exon (GAGACC → GAGACA), the SBP1 gene was PCR-amplified on total Chlamydomonas DNA in two fragments with primers 5′-TTGAAGACATAATGGCCGCTATGATGATGC-3′ and 5′-AC GAAGACGGGTTGTCTCCTTGACGTGC-3′ for fragment 1 (1257 bp) and with primers 5′-TTGAAGACGGCAACC CACATCGGTGAG-3′ and 5′-TTGAAGACTCCGAACCGGC AGCCACCTTCTCAGAG-3′ for fragment 2 (963 bp; BpiI sites are underlined). PCR was done with Q5 High-Fidelity Polymerase (NEB) following the manufacturer’s instructions and in the presence of 10% DMSO. The two PCR products were combined with destination vector pAGM1287 (Weber et al., 2011), digested with BpiI and directionally assembled by ligation into level 0 construct pMBS516. The latter was then combined with plasmids pCM0-020 (HSP70A-RBCS2 promoter + 5′UTR), pCM0-101 (MultiStop) or pCM0-100 (3xHA), and pCM0-119 (RPL23 3′UTR) from the Chlamydomonas MoClo kit (Crozet et al., 2018) as well as with destination vector pICH47742 (Weber et al., 2011), digested with BsaI and ligated to generate level 1 constructs pMBS517 (L1-SBP1-mStop) and pMBS518 (L1-SBP1-3xHA). Both level 1 constructs were then combined with pCM1-01 (level 1 construct with the aadA gene conferring resistance to spectinomycin flanked by the PSAD promoter and terminator) from the Chlamydomonas MoClo kit, with plasmid pICH41744 containing the proper end-linker, and with destination vector pAGM4673 (Weber et al., 2011), digested with BpiI, and ligated to yield level 2 constructs pMBS519 (aadA + SBP1-mstop) and pMBS520 (aadA + SBP1-3xHA). Correct cloning was verified by Sanger sequencing.
Screening of SBP1 Overexpressing Lines
Transformants were grown in TAP medium until mid-log phase and harvested by centrifugation at 13,000 × g for 5 min at 25°C. Cells were resuspended in DTT-carbonate buffer (100 mM DTT; 100 mM Na2CO3), supplemented with SDS and sucrose at final concentrations of 2% and 12%, respectively, vortexed, heated to 95°C for 5 min, and centrifuged at 13,000 × g for 5 min at 25°C. The chlorophyll content was determined as described by Vernon (1960). Total proteins according to 1.5 μg total Chlamydomonas chlorophyll were loaded on a 12% SDS-polyacrylamide gel and analyzed by immunoblotting using a mouse anti-HA antibody (Sigma H9658, 1:10,000) for transformants with SBP1-3xHA or a rabbit anti-SBPase antibody (Agrisera AS15 2873, 1:2,500) for SBP1-mStop. Detection was done via enhanced chemiluminescence using the FUSION-FX7 device (Peqlab).
QconCAT Protein Expression and Purification
The coding sequence for the Calvin-Benson cycle QconCAT protein (CBC-Qprot) was codon-optimized for E. coli, synthesized by Biocat (Heidelberg) harboring BamHI/HindIII restriction sites, cloned into the pET-21b expression vector (Novagen), and transformed into E. coli ER2566 cells (New England Biolabs). Expression of CBC-Qprot as a 15N-labeled protein and purification via Co-NTA affinity chromatography and electroelution was performed as described previously for the photosynthesis QconCAT protein (PS-Qprot) (Hammel et al., 2018). The eluted protein was concentrated, and the buffer changed to 6 M urea, 40 mM NH4HCO3 using Amicon ultra-15 centrifugal filter units with 10,000 MWCO (Merck). The protein concentration was determined at 280 nm on a NanoDropTM spectrophotometer using the Lambert-Beer’s law, a molecular weight of the CBC-Qprot of 47,921 Da, and an extinction coefficient of 37,400 M–1 cm–1. The protein concentration was adjusted to 1 μg/μl. The protein was stored at −20°C.
In Solution Tryptic Digest and LC-MS/MS Analysis
Twenty micrograms of total Chlamydomonas protein, as determined by the Lowry assay (Lowry et al., 1951), were mixed with 12.5, 25, 50, and 100 ng CBC- and PS-Qprot for replicates 1–3, and with 25, 50, 100, and 200 ng CBC- and PS-Qprot for replicates 4–6. Proteins were then precipitated with ice-cold 80% acetone overnight, digested tryptically, and analyzed by LC-MS/MS (Eksigent nanoLC 425 coupled to a TripleTOF 6600, ABSciex) as described previously (Hammel et al., 2018). Extraction of ion chromatograms and the identification and quantification of labeled and unlabeled peptides was performed using the QConQuantifier software available at https://github.com/ZimmerD/qconquantifier. The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE (Perez-Riverol et al., 2019) partner repository with the dataset identifier PXD018833.
Construction of Chlamydomonas Strains Overexpressing Sedoheptulose-1,7-Bisphosphatase (SBP1)
The Chlamydomonas SBP1 gene encodes sedoheptulose-1,7-bisphosphatase of the CBC. We chose to use the genomic version of the gene including all seven exons and six introns to adapt it to the MoClo syntax (Weber et al., 2011; Patron et al., 2015). For this, we followed the protocol suggested previously (Schroda, 2019), which required two PCR amplifications to alter sequences around the start and stop codons and to remove an internal BpiI recognition site (Figure 1A). Using the Chlamydomonas MoClo toolkit (Crozet et al., 2018), the domesticated SBP1 gene was equipped with the strong constitutive HSP70A-RBCS2 fusion promoter [A(Δ-467)-R] (Lodha et al., 2008; Strenkert et al., 2013) and the RPL23 terminator (Lopez-Paz et al., 2017). We generated two variants, one encoding a 3xHA tag at the C-terminus (SBP1-3xHA), the other lacking any tags (SBP1-mStop) (Figure 1A). HA-tagged proteins are easy to screen for, because the anti-HA antibody used reacts strongly with the 3xHA tag and has little background on immunoblots with Chlamydomonas total proteins. This allows assessing the frequency and variance with which transformants express the transgenic protein, and whether it has the expected size. This information can then be used for the screening of transformants expressing the untagged transgenic protein, which is the preferable variant because the 3xHA tag might interfere with the protein’s function. After adding an aadA cassette to the constructs (Figure 1A), they were transformed into the Chlamydomonas UVM4 strain that expresses transgenes efficiently (Neupert et al., 2009). Of the 12 SBP1-3xHA transformants screened, three did not express the transgene and five expressed it to high levels (Figure 1B). A similar pattern was observed for the 12 SBP1-mStop transformants, of which three appeared not to express the transgene and three expressed it to high levels. The two best-expressing transformants of each construct were selected for further analyses.
Figure 1. Generation of Chlamydomonas lines overexpressing SBP1. (A) SBP1 construct used for transformation. The 2172 bp SBP1 ORF (exons shown as black boxes), interrupted by all native SBP1 introns (thin lines), was domesticated to generate a level 0 module for the MoClo strategy. Using MoClo, the SBP1 ORF was equipped with the HSP70A-RBCS2 promotor and the RPL23 terminator (pAR and tRPL23, respectively, white boxes) and with a 3xHA-tag or without a tag (mStop) (gray box), giving rise to two level 1 constructs. These were combined with another level 1 construct containing the aadA gene conferring resistance to spectinomycin (light gray box) to yield the final level 2 constructs for transformation. (B) Screening of transformants overexpressing SBP1. The UVM4 strain was transformed with the level 2 constructs shown in (A). Total cell proteins from 12 spectinomycin resistant transformants recovered with each construct were extracted and proteins corresponding to 1.5 μg chlorophyll were analyzed by immunoblotting using anti-HA or anti-SBPase antibodies. The transformant number is given on top of the lanes. Transformants exhibiting highest expression levels for SBP1-3HA or SBP1-mStop (red) were used for further analysis.
Monitoring SBP1-Overexpressing Lines for Improved Photosynthetic Rate and Growth
We first tested the four SBP1-overexpressing transformants for improved growth. As elevated SBPase activity has resulted in improved growth particularly under high light and high CO2 conditions (Miyagawa et al., 2001; Lefebvre et al., 2005; Tamoi et al., 2006; Ichikawa et al., 2010; Gong et al., 2015; Ogawa et al., 2015; Driever et al., 2017; De Porcellinis et al., 2018), we chose to grow the transformants under mixotrophic conditions with acetate in the medium at a light intensity of 150 μmol photons m–2 s–1 (our standard growth light intensity is 40 μmol photons m–2 s–1). Part of the acetate apparently is converted into CO2 by Krebs cycle activity in the mitochondria and available to Rubisco in the chloroplast (Johnson and Alric, 2012; Polukhina et al., 2016). As shown in Figure 2A, both SBP1-mStop transformants (St1 and St12) accumulated higher culture volumes (significant after 44 h and 52 h of growth, p < 0.001) and therefore reached stationary phase about 14 h earlier than the UVM4 recipient strain. Growth of the HA5 transformant did not differ from that of UVM4 and growth of HA11 even lagged behind that of UVM4. To test whether the enhanced growth rate of the SBP1-mStop transformants was due to an improved photosynthetic rate, we monitored the photosynthetic light response curves for UVM4 and the two SBP1-mStop lines. For this, we measured oxygen evolution as a function of applied light intensity under mixotrophic growth conditions (Figure 2B). Rates of oxygen evolution of the UVM4 strain were comparable with those measured earlier in another strain background (CC-125), with both strains exhibiting maximal oxygen evolution at 450 μmol photons m–2 s–1 (Wykoff et al., 1998). While UVM4 and the two transformants evolved oxygen with similar rates at light intensities of up to 183 μmol photons m–2 s–1, the SBP1-mStop lines started to evolve more oxygen at light intensities exceeding 183 μmol photons m–2 s–1 and this became significant (p < 0.05) at light intensities of 520 μmol photons m–2 s–1 and above. Under photoautotrophic growth conditions at a light intensity of 150 μmol photons m–2 s–1 we observed no difference in growth between all strains, presumably because they were CO2 limited (Figure 2C). We found no differences in chlorophyll content between the strains (t-test, p > 0.05, n = 3).
Figure 2. Growth and light response curves of SBP1-overexpressing lines versus the UVM4 recipient strain. (A) Growth curves under mixotrophic conditions. Cultures were inoculated in TAP medium at a density of 3 × 105 cells ml–1 and incubated on a rotatory shaker for 4 days at a light intensity of 150 μmol photons m–2 s–1. The culture volume (cell density × cell size) was determined with a Coulter counter. Values are the mean from three biological replicates, error bars indicate SD. Asterisks indicate significant differences to the UVM4 strain, p < 0.001 (one-way ANOVA with Dunnett’s multiple comparison test). (B) Light response curves. Cells were grown mixotrophically to mid-log phase and oxygen evolution at the indicated light intensities was measured on a Mini-PAM II with needle-type oxygen microsensor OXR-50. Values are the mean from three biological replicates, error bars indicate SD. Asterisks indicate significant differences to the UVM4 strain, p < 0.05 (one-way ANOVA with Dunnett’s multiple comparison test). (C) Growth curves under photoautotrophic conditions. Cultures were inoculated in HMP medium at a density of 3 × 105 cells ml–1 and incubated on a rotatory shaker for 10 days at a light intensity of 150 μmol photons m–2 s–1. The culture volume (cell density × cell size) was determined with a Coulter counter. Values are the mean from three biological replicates, error bars indicate SD.
Absolute Quantification of All CBC Enzymes in Chlamydomonas by the QconCAT Strategy
We observed improved growth for the SBP1-mStop transformants but not for the SBP1-3xHA transformants. We reasoned that this could have been due to higher SBP1 expression levels in the former, or due to a negative effect of the 3xHA tag on the protein’s function in the latter. To distinguish between these possibilities and to elucidate whether SBP1 overexpression affected the expression of the other 10 CBC enzymes, we quantified the absolute levels of all CBC enzymes in the UVM4 recipient strain and the four SBP1-overexpressing transformants with the QconCAT strategy. With this approach, using a single QconCAT protein (PS-Qprot), we already had determined the absolute cellular quantities of the complexes involved in the photosynthetic light reactions and of the Rubisco rbcL and RBCS subunits (Hammel et al., 2018). We designed a QconCAT protein (CBC-Qprot) that covered each of the missing 10 CBC enzymes with two or three proteotypic tryptic quantification (Q)-peptides (Supplementary Figure 1A and Supplementary Dataset 1). These Q-peptides have been detected by LC-MS/MS in earlier studies with good ion intensities and normal retention times. We had selected them before the d::pPop algorithm for predicting ionization propensities was available (Zimmer et al., 2018) and therefore some peptides are not the very best choice (see d::pPop ranks and scores in Table 1).
Table 1. Absolute quantification of Calvin-Benson cycle protein subunits in the Chlamydomonas UVM4 strain.
The 47.9-kDa CBC-Qprot was expressed as 15N-labeled protein in E. coli and purified via the tandem-hexa-histidine tag at its C-terminus [the labeling efficiency was 99.39 ± 0.37% (SD)]. The protein was further purified by preparative electrophoresis on an SDS-polyacrylamide gel, followed by electroelution from the excised gel band and spectroscopic quantification. Correct quantification and purity were verified by separating the CBC-Qprot next to a BSA standard on an SDS-polyacrylamide gel and staining with Coomassie blue (Supplementary Figure 1B). The CBC-Qprot was then tryptically digested and released peptides analyzed by LC-MS/MS on a short 6-min gradient (Supplementary Figure 1C). The latter shows that the Q-peptides separated with characteristic retention times and ion intensities. Despite the strict 1:1 stoichiometry of the peptides, the areas of the extracted ion chromatograms (XICs) varied by a factor of up to 370.
Four different amounts of the 15N-labeled PS-Qprot (Hammel et al., 2018) and the CBC-Qprot were mixed with 20 μg of (14N) whole-cell proteins extracted from samples of UVM4 and the four transformants taken 22 h after inoculation in the experiment shown in Figure 1A (early log phase). We employed only one preparation of the QconCAT proteins, but Chlamydomonas cells from 3 to 6 independent growth experiments. The proteins in the mixture were precipitated with acetone, digested tryptically in urea, and analyzed by LC-MS/MS on 45-min analytical gradients. The ion chromatograms of heavy Q-peptide and light native peptide pairs were extracted, XICs quantified, and ratios calculated (Supplementary Dataset 2).
Based on the Q-peptide to native peptide ratios and the known amounts of spiked-in QconCAT proteins, the abundances of the native peptides in the sample were calculated (in femtomoles per μg cell protein) (Supplementary Dataset 2). We determined that a Chlamydomonas UVM4 cell contains 27.6 ± 1.7 pg protein (SD, n = 6 biological replicates). This value allowed calculating the absolute amount of each peptide in attomol per cell (Table 1). We used the median of all quantification values of the 2–3 Q-peptides per protein (23 to 72 values) to get an estimate for the abundance of each CBC protein per cell (Table 1). Moreover, based on these median values and the molecular weight of the mature proteins, the fraction of each target protein in the whole-cell protein extract was estimated (Table 1), revealing that CBC enzymes represent ∼11.9% of total cell protein in Chlamydomonas (Supplementary Dataset 2). This procedure was repeated for all four SBP1-overexpressing transformants and the log2-fold change of the abundance of each CBC enzyme in the transformants versus the UVM4 strain was calculated (Figure 3 and Supplementary Dataset 2). It turned out that SBP1 was significantly (p < 0.01) overexpressed in all transformants (HA5: 1.6-fold; HA11: 1.7-fold; St1: 3-fold; St12: 2.2-fold). Except for the Rubisco subunits, levels of all other CBC enzymes were not significantly different between the SBP1-overexpressing transformants and the UVM4 strain. Compared to UVM4, transformant HA5 had significantly (p < 0.01) lower RBCS levels (but only by 8%), and transformant St12 had significantly (p < 0.01) lower levels of RBCS and rbcL (by about 40%).
Figure 3. Changes in abundance of CBC enzymes in SBP1-overexpressing lines versus the UVM4 recipient strain. The abundance of the CBC enzymes in transformants HA5 and HA11, generated with the SBP1-3xHA construct, and in transformants St1 and St12, generated with the SBP1-mStop construct, was determined using the QconCAT strategy. Abundances relative to those in the UVM4 recipient strain were log2 transformed and plotted. Asterisks designate significant differences between enzymes in the transformants versus the UVM4 strain (one-way ANOVA with Holm’s multiple comparison test, p < 0.01). PGK, phosphoglycerate kinase; GAP, glyceraldehyde-3-phosphate dehydrogenase; TPI, triose phosphate isomerase; FBA/SBA, fructose-1,6-bisphosphate aldolase/sedoheptulose-1,7-bisphosphate aldolase; FBP, fructose-1,6-bisphosphatase; TRK, transketolase; SBP, sedoheptulose-1,7-bisphosphatase; RPE, ribulose-5-phosphate 3-epimerase; RPI, ribose-5-phosphate isomerase; PRK, phosphoribulokinase; rbcL, ribulose bisphosphate carboxylase/oxygenase large subunit; RBCS, ribulose bisphosphate carboxylase/oxygenase small subunit.
Estimation of Substrate Binding Sites per CBC Enzyme
In a previous study, we had determined the levels of all CBC metabolites in Chlamydomonas cells during an increase in light intensity within the range where irradiance remains limiting for photosynthesis (Mettler et al., 2014). In that study, also the concentrations of the CBC enzymes in the chloroplast were estimated based on the empirical protein abundance index (emPAI) (Ishihama et al., 2005). These data sets allowed estimating the number of substrate binding sites per CBC enzyme 20 min after increasing the light intensity, when flux through the cycle was maximal (Mettler et al., 2014). To compare the emPAI-derived data with the QconCAT-derived data, we calculated the concentration of each CBC enzyme in the chloroplast based on the absolute quantities determined here and the assumption that a Chlamydomonas cell has a volume of 270 μm3, of which about half is occupied by the chloroplast (Weiss et al., 2000) (Table 2). While the concentration of rbcL determined by Mettler et al. (2014) matched that determined here with the QconCAT approach very well, the concentrations of all other CBC enzymes were strongly overestimated (between 8.8-fold for FBA3 and 34.5-fold for PRK1) (Table 2).
Table 2. Comparison of CBC enzyme abundances and concentrations in Chlamydomonas determined in different studies by different methods.
To re-estimate the number of substrate binding sites per CBC enzyme, we used the concentrations of the CBC enzymes in the chloroplast determined here (Table 2) and the CBC metabolite data determined earlier 20 min after the light shift to 145 μmol photons m–2 s–1 (Mettler et al., 2014). Whilst most of the metabolites were directly measured, some like BPGA were calculated based on the equilibrium constants of the reactions in which they participate and the measured levels of other metabolites that participate in these reactions (see Mettler et al., 2014 for details). Although the growth conditions differed slightly between the two studies, metabolite levels do not vary greatly in Chlamydomonas in this irradiance range (Supplementary Figure 12 in Mettler et al., 2014). This re-analysis is shown in Figure 4 and compared with the earlier analysis in Supplementary Figure 2. It revealed that some CBC intermediates are indeed present at lower concentrations than the estimated binding site concentration of the enzymes for which they act as substrates (1,3-bisphosphoglycerate (BPGA) compared to PGK1 and GAP3; glyceraldehyde 3-phosphate (GAP) and erythrose 4-phosphate (E4P) compared to FBA3), some are at only slightly (<4.5-fold) higher concentrations than the respective binding site (GAP and E4P compared to TRK; ribulose-5-phosphate (Ru5P) compared to PRK1; fructose-1,6-bisphosphate (FBP) compared to FBA3). However, most of the other CBC intermediates are present at considerably higher concentrations than the respective estimated binding site concentration.
Figure 4. Substrate per binding site versus substrate concentration. Substrate per binding site values of CBC enzymes are plotted against their substrate concentrations. Binding site abundances of the eleven CBC enzymes (numbered) were calculated based on the QconCAT data (Table 2). Substrates of CBC reactions are presented by different colors. Substrate concentrations were determined via LC-MS/MS by Mettler et al. (2014) in Chlamydomonas cells harvested 20 min after the light intensity was increased from 41 to 145 μmol photons m–2 s–1, i.e., when flux through the CBC is maximal. For enzymes that catalyze readily reversible reactions (TPI, FBA/SBA, TRK, RPI, RPE) the relation to product level is also shown. To facilitate comparison, the same numbering and color code as used in Mettler et al. (2014) was adopted. The blue arrow shows the estimates for substrates per binding site for the SBP1 overexpressing lines St1 and St12 (encircled in red). The two values for Rubisco are based on the slightly different quantification values for the large and small subunits (Table 2). A comparison with the values calculated by Mettler et al. (2014) using the emPAI approach is shown in Supplementary Figure 2.
The Modularity of the MoClo Approach and the Use of Chlamydomonas as a Model Facilitate the Iterative Process of Genetic Engineering Toward Improving Plant Productivity
Here, we present a workflow for rapid and efficient metabolic engineering toward improving plant biomass production, with the overexpression of native Chlamydomonas SBPase (SBP1) in Chlamydomonas as a proof-of-concept. We used the Modular Cloning (MoClo) strategy for construct generation and employed the part library established recently (Weber et al., 2011; Crozet et al., 2018). The one-step, modular assembly of multiple genetic parts allowed generating complex constructs rapidly and with variations: one coding for SBP1 with a 3xHA tag and one lacking any tags. This double strategy was well chosen, as the variant with a C-terminal 3xHA tag did not result in enhanced photosynthetic rates and biomass production, while the variant lacking a tag did (Figures 2A,B). In the two transformant lines tested for each construct, tagged SBP1 was overexpressed 1.6 to 1.7-fold while the untagged form was overexpressed ∼2.2- and ∼3-fold (Figure 3). Therefore, it is possible that in Chlamydomonas SBPase must be expressed to levels higher than 1.7-fold to improve the photosynthetic rate. Alternatively, the C-terminal 3xHA tag interfered with SBP1 function. Although this issue can only be solved by measuring SBPase enzyme activity, we favor the latter explanation. This because SBPase overexpression giving rise to at most twofold increased activities already had positive effects on photosynthetic rates and biomass accumulation in tobacco (Lefebvre et al., 2005; Tamoi et al., 2006; Rosenthal et al., 2011), Dunaliella bardawil (Fang et al., 2012), and wheat (Driever et al., 2017). Like for these models, increased photosynthetic rates and biomass accumulation were observed in Chlamydomonas lines overexpressing SBP1 only if cells were grown at higher light intensities (150 μmol photons m–2 s–1) and elevated CO2 concentrations (in the presence of acetate) (Figure 2). Here it appears surprising that we observed elevated O2 evolution rates in SBP1-overexpressing lines only at light intensities above 183 μmol photons m–2 s–1 (Figure 2B). This discrepancy might be explained by differences in culture conditions, physiological state of the cells, or light quality between the experimental setups used for determining growth and O2 evolution. In any case, at high light intensities and elevated CO2 concentrations, SBPase levels represent a bottleneck in flux through the CBC in Chlamydomonas as in the other plant models. Therefore, the results obtained with Chlamydomonas readily apply to other alga and land plants.
SBP1 represents 0.15% of total cell protein in Chlamydomonas (Table 1), i.e., the transgenic protein in the best SBP1-overexpressing line makes up 0.3% of total cell protein. It is likely that the screening of more transformants would have allowed recovering lines with even higher expression levels. Furthermore, a SBP1 gene re-synthesized with optimal codon usage and the three RBCS2 introns probably would have allowed higher expression levels (Barahimipour et al., 2015; Schroda, 2019). Regarding the iterative process of genetic engineering it is important to recognize that by combining the MoClo strategy with Chlamydomonas as a model, a complete cycle of construct design and assembly, transformation, screening, and phenotype test can be achieved in as little as 8 weeks.
QconCAT-Based Quantitative Proteomics Allows Monitoring Effects of SBP1 Overexpression on the Accumulation of Other CBC Enzymes
Increased activities of SBPase by overexpressing SBPase alone or BiBPase from cyanobacteria had no effect on the levels or activities of selected other CBC enzymes in tobacco (Miyagawa et al., 2001; Lefebvre et al., 2005; Rosenthal et al., 2011), lettuce (Ichikawa et al., 2010) or wheat (Driever et al., 2017). In contrast, overexpression of BiBPase from Synechocystis in Synechococcus resulted in increased activities of Rubisco (2.4-fold) and aldolase (1.6-fold) as well as increased protein levels of rbcL (∼3-fold), TPI (1.5-fold) and RPI (1.4-fold) (De Porcellinis et al., 2018). Similarly, overexpressing SBPase leading to up to 1.85-fold higher SBPase activity in Arabidopsis resulted in elevated FBPA activity and protein levels (Simkin et al., 2017a). We employed the QconCAT approach to determine absolute quantities of all other 10 CBC enzymes and found no consistent changes between wild type and the four SBP1-overexpressing lines (Figure 3). Only the St12 line with ∼2.2-fold higher SBP1 expression had a significant ∼40% reduction of both Rubisco subunits rbcL and RBCS. Since both Rubisco subunits were unaffected in line St1 with ∼3-fold higher SBP1 levels, SBP1 overexpression cannot be the cause for the reduced accumulation of Rubisco in line St12. More likely, a gene required for Rubisco expression, assembly or stability was destroyed by the integration of the SBP1 expression vector. It is surprising that photosynthetic rate and biomass accumulation was increased to a similar extent in lines St1 and St12 despite the reduced Rubisco levels in line St12 (Figure 2). This indicates that Rubisco levels are not limiting CBC flux in Chlamydomonas, in line with previous observations in Chlamydomonas that reducing Rubisco to almost 50% of wild-type levels enabled full photosynthetic growth (Johnson, 2011).
CBC Enzymes Exhibit a Larger Abundance Range Than Estimated Earlier
In addition to looking at possible effects of SBP1-overexpression on the expression of other CBC enzymes, the QconCAT approach allowed for the quantification of absolute levels of CBC enzymes in Chlamydomonas cells. With this strategy, we had already determined absolute quantities of rbcL and RBCS in another cell wall-deficient strain background (CC-1883) (Hammel et al., 2018). There, absolute amounts of rbcL and RBCS were ∼1.4-fold lower than in UVM4 cells. However, CC-1883 cells also had a ∼1.3-fold lower protein content than UVM4 cells, such that the fraction of rbcL and RBCS in total cell protein are about comparable (6.6% and 1.3% in CC-1883 versus 6.88% and 1.45% in UVM4, respectively).
The abundance of all CBC enzymes in Chlamydomonas cells has been estimated earlier. One study used “Mass Western,” which is based on the spiking-in of known amounts of heavy isotope-labeled Q-peptides into tryptic digests of whole-cell proteins followed by LC-MS/MS analysis (Wienkoop et al., 2010). The other studies used the emPAI (empirical protein abundance index) and iBAQ (intensity-based absolute quantification) approaches on quantitative shotgun proteomics datasets (Mettler et al., 2014; Schroda et al., 2015).
The iBAQ-based ranking of protein abundances exactly reflects the quantities of the more abundant CBC enzymes determined here by the QconCAT approach (Table 2). Only the low-abundance CBC enzymes RPE1, RPI1 and TPI1 were ranked by iBAQ in the opposite order of their abundance determined by the QconCAT method. Most likely, this is due to the impaired accuracy of the iBAQ approach for less-abundant proteins (Soufi et al., 2015).
The absolute quantities determined by Mass Western roughly matched those determined with the QconCAT approach, except for RBCS, PGK1, and SBP1, which were 24.6-fold, 7.7-fold, and 13.3-fold lower (Table 2). As suggested earlier (Hammel et al., 2018), this discrepancy can be explained by an incomplete extraction of some proteins from whole-cell homogenates with the extraction protocol employed (Wienkoop et al., 2010).
In the study by Mettler et al. (2014), the cellular abundance of rbcL was estimated by densitometry on Coomassie-stained SDS-gels and was used to normalize the emPAI-derived quantification values of the other CBC enzymes. The estimated abundance of rbcL matches that determined here via the QconCAT approach (Table 2). However, the emPAI-derived values for the other CBC enzymes are much higher than those determined by QconCAT (up to 34.5-fold higher for PRK1). A likely cause for this strong overestimation is that proteins of very high abundance tend to exhibit a saturated emPAI signal (Ishihama et al., 2008). Consequently, the range of concentrations of CBC enzymes is much larger than estimated earlier. For example, the difference between the most abundant CBC protein rbcL and the least abundant TPI1 is 128-fold rather than only 7-fold (Table 2).
The strong overestimation of many CBC enzymes by the emPAI approach challenges the conclusion that many CBC intermediates are present at concentrations that are far lower than the estimated binding site concentration of the enzymes for which they act as substrates (Mettler et al., 2014). For example, the concentration of sedoheptulose-1,7-bisphosphate (SBP) is ∼106-fold higher than that of SBP1 rather than only ∼6-fold as estimated previously (Figure 4 and Supplementary Figure 2). Moreover, comparisons of the in vivo SBP concentration and the modeled in vivo Km for SBP1 indicate that SBP1 is likely to be near-saturated in vivo (Mettler et al., 2014). Hence, flux at SBPase is likely restricted by the degree of post-translational activation of SBP1 and SBP1 abundance. This explains better why an increase in CBC flux can be achieved by increasing SBP1 protein concentrations.
Still correct is that the concentration of GAP is below or slightly above the concentration of substrate binding sites of FBA3 and TRK1 (0.4-fold and 2.2-fold, respectively), as is E4P compared to FBA3 and TRK1 (0.5-fold and 2.7-fold, respectively). Furthermore, ribulose-5-phosphate (Ru5P) is only 4.3-fold above the binding site concentration of PRK, indicating that increased flux in the regeneration phase of the CBC to increase Ru5P levels will aid increased RuBP formation and fixation of CO2. The low concentration of these key CBC intermediates relative to their enzyme binding sites, together with the low concentration of these and further CBC intermediates relative to the likely in vivo Km values of CBC enzymes (Mettler et al., 2014), explains how RuBP regeneration speeds up when rising light intensity drives faster conversion of 3-phosphoglycerate to GAP.
The lower abundance of CBC enzymes reported here does not affect the analyses of the relationship between metabolite concentrations and the estimated in vivo Km values of CBC enzymes in Mettler et al. (2014). These estimations were based on the simplifying assumption that the measured metabolites reflect the free concentrations. This assumption is even more justified by the generally lower protein abundances as determined here by the QconCAT approach. Mettler et al. (2014) concluded that some of the CBC enzymes are near-saturated in vivo (Rubisco, PGK, FBPase, SBPase) whilst the remainder operate at low substrate saturation. For the former, increased flux will depend on allosteric or post-translational regulation, or on increasing protein abundance (as explained above for SBPase). For the latter, only a fraction of the enzyme active sites will be occupied by substrate at a given time and occupancy will increase in conditions where the substrate concentration rises, leading to an increase in flux at that enzyme. This will serve to increase overall flux around the CBC when there is a general increase in metabolite levels, and to rebalance flux at different sites in the CBC when there is an increase in the concentration of the substrate of one or a subset of the CBC enzymes.
The next step would be to stack multiple transgenes for the overexpression of CBC enzymes that in SBP1-overexpressing lines potentially become new bottlenecks for flux through the cycle. Indicative for this scenario is the finding that SBPase overexpression in Arabidopsis entailed an overexpression of FBPA (Simkin et al., 2017a). Moreover, overexpression of BiBPase in Synechococcus came along with an increase in levels of RPI and TPI (De Porcellinis et al., 2018), which are the CBC enzymes of lowest abundance in Chlamydomonas (Tables 1, 2). More candidates for multigene stacking might be PGK1, TRK1, TPI1, and FBP1, whose substrates are in largest excess of the substrate binding sites (Figure 4). To our knowledge, there are yet no reports on the overexpression of PGK, RPI, and TPI (Simkin et al., 2019). Two studies report no or even negative effects upon TRK overexpression in rice and tobacco, respectively (Khozaei et al., 2015; Suzuki et al., 2017). Positive effects of FBPase overexpression on photosynthetic rates and biomass accumulation were reported for numerous plant models – except for Chlamydomonas where FBP1 overexpression in the chloroplast had negative effects (Dejtisakdi and Miller, 2016). Apparently, the highly complex regulation of the CBC and its central role in cellular metabolism make predictions difficult. This is highlighted by recent work, indicating that the balance between different steps in the CBC varies from species to species (Arrivault et al., 2019; Borghi et al., 2019). Therefore, experimental test is the route of choice that with the combination of MoClo and Chlamydomonas can be pursued readily.
Data Availability Statement
The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PXD018833.
AH performed all experiments. FS designed the QconCAT protein and performed the LC-MS/MS analyses. AH and DZ analyzed the data and were supervised by TM, MSt, and MSc. MSc conceived and supervised the work. MSc wrote the manuscript with contributions from all other authors. All authors contributed to the article and approved the submitted version.
This work was funded by the Deutsche Forschungsgemeinschaft (TRR 175, projects C02 and D02) and the Landesforschungssc- hwerpunkt BioComp.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We are grateful to Karin Gries for technical help. This manuscript has been released as a pre-print at bioRxiv (Hammel et al., 2020).
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2020.00868/full#supplementary-material
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Keywords: mass spectrometry, proteotypic peptide, QconCAT, Synthetic Biology, Modular Cloning, photosynthesis, Chlamydomonas reinhardtii
Citation: Hammel A, Sommer F, Zimmer D, Stitt M, Mühlhaus T and Schroda M (2020) Overexpression of Sedoheptulose-1,7-Bisphosphatase Enhances Photosynthesis in Chlamydomonas reinhardtii and Has No Effect on the Abundance of Other Calvin-Benson Cycle Enzymes. Front. Plant Sci. 11:868. doi: 10.3389/fpls.2020.00868
Received: 14 February 2020; Accepted: 27 May 2020;
Published: 23 June 2020.
Edited by:Dimitris Petroutsos, UMR 5168 Laboratoire de Physiologie Cellulaire Vegetale (LPCV), France
Reviewed by:Christine Anne Raines, University of Essex, United Kingdom
Paolo Trost, University of Bologna, Italy
Copyright © 2020 Hammel, Sommer, Zimmer, Stitt, Mühlhaus and Schroda. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Michael Schroda, email@example.com