Abstract
Background
Integrated metabolic engineering approaches that combine system and synthetic biology tools enable the efficient design of microbial cell factories for synthesizing high-value products. In this study, we utilized in silico design algorithms on the yeast genome-scale model to predict genomic modifications that could enhance the production of early-step Taxol® in engineered Saccharomyces cerevisiae cells.
Results
Using constraint-based reconstruction and analysis (COBRA) methods, we narrowed down the solution set of genomic modification candidates. We screened 17 genomic modifications, including nine gene deletions and eight gene overexpressions, through wet-lab studies to determine their impact on taxadiene production, the first metabolite in the Taxol® biosynthetic pathway. Under different cultivation conditions, most single genomic modifications resulted in increased taxadiene production. The strain named KM32, which contained four overexpressed genes (ILV2, TRR1, ADE13, and ECM31) involved in branched-chain amino acid biosynthesis, the thioredoxin system, de novo purine synthesis, and the pantothenate pathway, respectively, exhibited the best performance. KM32 achieved a 50% increase in taxadiene production, reaching 215 mg/L. Furthermore, KM32 produced the highest reported yields of taxa-4(20),11-dien-5α-ol (T5α-ol) at 43.65 mg/L and taxa-4(20),11-dien-5-α-yl acetate (T5αAc) at 26.2 mg/L among early-step Taxol® metabolites in S. cerevisiae.
Conclusions
This study highlights the effectiveness of computational and integrated approaches in identifying promising genomic modifications that can enhance the performance of yeast cell factories. By employing in silico design algorithms and wet-lab screening, we successfully improved taxadiene production in engineered S. cerevisiae strains. The best-performing strain, KM32, achieved substantial increases in taxadiene as well as production of T5α-ol and T5αAc. These findings emphasize the importance of using systematic and integrated strategies to develop efficient yeast cell factories, providing potential implications for the industrial production of high-value isoprenoids like Taxol®.
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Introduction
Microbial chassis have been extensively investigated for the sustainable and economically viable production of industrially important compounds, including pharmaceuticals [1], biofuels [2], enzymes [3] and polymers [4] in sustainable and economically attractive ways. Among these microbial hosts, Saccharomyces cerevisiae, commonly known as baker’s yeast, has emerged as the most widely studied eukaryotic synthetic biology chassis [5]. S. cerevisiae offers advantages such as high biomass production in cost-effective media [6] and efficient control and scalability of fermentation processes [7]. Furthermore, the development of numerous synthetic biology tools and well-characterized genetic parts have accelerated the design of engineered yeast strains with improved performance and reliability [8, 9].
S. cerevisiae has been harnessed as a platform to produce high-value biopharmaceuticals, ranging from recombinant therapeutic proteins to plant-derived natural products [10,11,12,13,14]. By integrating heterologous plant-derived genes, early-step precursors of Taxol® (paclitaxel), a leading anticancer drug with a market size over billions of USD [15], have been produced by yeast cell factories [16,17,18,19,20]. The biosynthesis of Taxol® initiates with the conversion of geranylgeranyl diphosphate (GGPP), a product of the yeast mevalonate pathway, into taxadiene (taxa-4(5),11(12)-diene) catalyzed by taxadiene synthase [21]. Subsequently, taxadiene undergoes hydroxylation by a class II cytochrome P450 hydroxylase, taxadiene-5α-hydroxylase (T5αOH) with the assistance of cytochrome P450 reductase (CPR), and an acylation catalyzed by taxadiene-5α-ol-O-acetyltransferase (TAT) [15]. Although these enzymes have been expressed, and their products have been successfully produced in yeast [22, 23], there is still room to improve their titers for economically feasible production of the subsequent Taxol® precursors. Figure 1 illustrates the biochemical reactions in the mevalonate and Taxol® pathways.
A The native biochemical reactions in the mevalonate pathway leading to the production of GGPP in yeast. B The Taxol® biosynthesis from GGPP in yew trees. HMG-CoA: hydroxymethylglutaryl-CoA, mevalonate-P: R-5-hosphomevalonate, mevalonate-PP: R-5 diphosphomevalonate, IPP: isopentenyl diphosphate, DMAPP: dimethylallyl diphosphate, GPP: geranyl diphosphate, FPP: farnesyl diphosphate, GGPP: geranylgeranyl diphosphate, T5α-ol: taxa-4(20),11-dien-5α-ol, T5αAc: taxa-4(20),11-dien-5-α-yl acetate. The dashed arrows represent naturally occurring multiple steps
As omics technologies are evolving and sequencing platforms are becoming more accessible, the reconstruction of genome-scale metabolic models (GEMs) for various organisms has gained momentum, enabling the conversion of integrated omics data into valuable system-level information [24]. Since the first yeast GEM was reconstructed in 2003, several iterations and enhancements of S. cerevisiae GEMs have been developed by adding and connecting more genes, reactions, and compartments [25,26,27]. The latest consensus yeast GEM, yeast 8 [27], serves as the basis for constructing more refined and up-to-date versions that better mimic yeast metabolism. Among the yeast 8 derivatives, yeast 8.5.0 comprises 4055 reactions, 2742 metabolites, and 1151 genes in 14 cellular compartments [28]. Leveraging yeast GEMs as a bottom-up systems biology tool, they have been employed in diverse applications, from designing yeast cell factories to optimizing culture conditions [29]. In recent years, the coupling of GEMs and constraint-based reconstruction and analysis (COBRA) methods [30] has found widespread usage in biological applications. COBRA is an integrative analysis framework that can be applied to biochemical systems to demonstrate and predict the connections from phenotype to genotype by imposing constraints considering factors such as physicochemical laws, environmental conditions, and genetic information [31, 32].
Several strain optimization algorithms and programs have been developed utilising COBRA methods and mathematical modelling [33]. For example, OptKnock [34] employs bilevel mixed-integer optimisation to predict gene deletions and elimination of reactions from the host's metabolism, thereby enhancing the production of target compounds. Another tool, OptGene [35], utilises genetic algorithms [36] to identify gene knockouts with the aim of improving bio-production yields. Leveraging bilevel programming, Ranganathan et al. (2010) introduced the OptForce framework to identify a set of reactions where fluxes need to be modified to achieve overproduction of the target compound [37]. These modifications can involve zeroing (deletion), decreasing (downregulation), or increasing (upregulation) of the fluxes associated with the target reactions, thus exploring all possible modifications [37].
Previously, we reported the production of early-step Taxol® precursors through the improved mevalonate pathway using our engineered yeast strains [22, 23]. In the present study, we used a combinatorial in silico system biology approach to further improve the flux towards GGPP in the mevalonate pathway to enhance the titers of the taxadiene and the next precursors in the Taxol® pathway. We utilised three strain design frameworks, namely OptKnock, OptGene and OptForce in conjunction with yeast GEM, to predict gene and reaction candidates for knockout or overexpression. The genomic modifications determined by in silico analyses were implemented using the CRISPR-based ACtivE toolkit [38] to design yeast strains. Overall, we tested the knockout of nine genes and the overexpression of eight genes, both individually and in various combinations. Following the screening of the strains, the best-performing one was also evaluated in 250 mL in a mini-scale bench-top bioreactor. We achieved a 50% increase in taxadiene yield compared to the parent strain when four reactions were upregulated by integrating an extra copy of ILV2, TRR1, ADE13 and ECM31 genes driven by a galactose-inducible promoter. Using a micro-scale high-throughput bioreactor platform, i.e. BioLector, we achieved the detection of 215 mg/L of taxadiene, 35.4 mg/L of T5α-ol and 26.2 mg/L of T5αAc in complete synthetic media (CSM). These are the highest titers reported until now in S. cerevisiae. Our findings highlight the applicability of the genomic modifications employed in this study to enhance the metabolic flux towards the yeast mevalonate pathway for the production of high-value terpenoids.
Materials & methods
in silico design and analyses
In three design algorithms, OptKnock, OptGene and OptForce, cytosolic acetyl-CoA and geranylgeranyl diphosphate (GGPP) were separately selected as target metabolites to increase production in glucose or galactose-containing media. During simulations, uptake routes for key molecules such as inorganic phosphate, sulphate, ammonia, and oxygen were unconstrained, while secretion routes for acetate, carbon dioxide, ethanol, glycolaldehyde, diphosphate, water, and glycerol and acetaldehyde were enabled. When galactose exchange was enabled, glucose exchange was constrained or vice versa. While S. cerevisiae cultivations (see below) used complete synthetic medium (CSM, Additional file 1: Table S6 and Table S7), it was decided not to allow for in silico amino acid uptake, due to the difficulties to provide realistic constraints for these nutrients.
The design algorithms underwent up to five iterative runs to generate a set of predictions, each containing a maximum of three candidates. Subsequently, we pooled all recommended genomic modification candidates and through various approaches we prioritized high-potential modifications from this collective pool, as described in the Additional file 1.
The COBRA Toolbox v3.0 [32, 39] was used in MATLAB R2019a for in silico studies, with Gurobi Optimizer (9.5.0) as the solver. Yeast GEM 8.5.0 [28] was used to represent yeast metabolism. The ECDF Linux Compute Cluster (Eddie), the University of Edinburgh’s research computing cluster, was employed to find to run OptForce. Escher [40] was used on the iMM904 yeast model to visualize the metabolic maps since Yeast 8 does not have a compatible Escher map.
Oligonucleotides and Reagents
All primers used in the study are listed in Additional file 1: Table S1 and Table S3. The primers were ordered from Integrated DNA Technologies (IDT) as standard DNA oligos. Synthetic gRNA cassettes (Additional file 1: Table S2) were ordered from Twist Bioscience. Phusion Flash High-Fidelity PCR Master Mix (Thermo Scientific™) and PrimeSTAR® GXL DNA Polymerase (TaKaRa) were used for PCR reactions to produce the DNA parts for genome modifications. GeneJET PCR Purification Kit (Thermo Scientific™) was used for PCR clean-up. DreamTaq Green PCR Master Mix (Thermo Scientific™) was used for colony PCR.
Strains and Media
The original S. cerevisiae strain used in this study is a CEN.PK2-1C-originated yeast strain, LRS6 (MATa, leu2-3, 112::HIS3MX6-GAL1p-ERG19/GAL10p-ERG8; ura3-52::URA3-GAL1p-MvaSA110G/GAL10p-MvaE; his3Δ1::hphMX4-GAL1p-ERG12/GAL10p-IDI1; trp1-289::TRP1_GAL1p-CrtE (X. dendrorhous)/GAL10p ERG20; YPRCdelta15::NatMX-GAL1p-CrtE/GAL10p-CrtE; ARS1014::GAL1p-TASY-GFP; ARS1622b::GAL1p-MBP-TASY-ERG20; ARS1114a::TDH3p-MBP-TASY-ERG20; ARS511b::GAL1p-T5αOH/GAL3-CPR; RKC3::GAL1-TAT) [23]. Briefly, the original strain contains additional copies of native and heterologous genes in the mevalonate pathway to improve GGPP production, along with codon-optimized heterologous genes encoding the enzymes responsible for early steps in Taxol® biosynthesis (Figs. 1, 3A). An additional GAL1 promoter-driven TAT gene was integrated to the RKC4 location into the LRS6 genome, which was used as the parent strain in the subsequent studies. The other strains derived from the parent strain are shown in Additional file 1: Table S4.
The workflow followed in this study from in silico design to lab bench scale production. Three design algorithms, OptKnock, OptGene and OptForce, were used on Yeast 8.5.0 to find gene candidates (Additional file 1: Table S5). 17 of these gene candidates were prioritised through further in silico predictions (Figs. 4, 5). After selecting the gene candidates, the yeast strains containing single genomic modifications were designed (Table 1). To engineer the yeast genome, the ACtivE Toolkit was used. The strains were then screened in deep-well plates to detect the good performance genomic modifications (Fig. 6). These modifications were then combined to design second-level yeast strains containing multiple genomic modifications (Table 2). The best-performing strains were then screened in the Biolector platform with real-time pH, DO and biomass monitoring (Fig. 7 and Fig. 8). Finally, the best-producer was used for the productions a lab bench scale bioreactor (Fig. 9)
Complete synthetic medium (CSM) consisting of 0.67% (w/v) yeast nitrogen base without amino acids (Alfa Aesar™), 0.08% (w/v) complete supplement mixture (MP Biomedicals™) and 2% (w/v) glucose (Alfa Aesar™) or 2% (w/v) galactose (ACROS Organics™) was used for the cultivations. The compositions of the yeast nitrogen base and the complete supplement mixture are given in Additional file 1: Table S6 and Table S7, respectively. Pre-cultures were grown in standard rich medium, YPD medium, 1% (w/v) yeast extract (Fisher BioReagents™), 2% (w/v) peptone (Merck, Millipore®), 2% (w/v) glucose. To select the positive transformants, selective media, CSM-URA, 0.67% (w/v) yeast nitrogen base without amino acids, 0.077% (w/v) complete supplement mixture without uracil, 2% glucose, 2% agar (ACROS Organics™) was used.
Yeast transformation and strain construction
The chemicals and reagents were obtained from Sigma-Aldrich unless otherwise stated. Transformations were carried out according to LiAc/PEG heat-shock method [41]. Briefly, fresh cultures were prepared to obtain the cells in the exponential phase following an overnight culture. The cells were then washed using sterile water and were pelleted by centrifugation. The transformation mix, 240 µL PEG (50%(w/v)), 36 µL 1.0 M lithium acetate (LiAc) and 50 µL single-stranded carrier DNA (2.0 mg/mL, herring sperm DNA, Promega), was added onto the cell pellet. Following this, DNA fragments and water were added until the volume was made up to 360 µL. After homogenous transformation mixes were obtained, the cells were incubated for 45 min at 42 °C. Finally, the transformation mix was removed, the cells were plated onto the selective media, and the plates were incubated for 2–3 days at 30 °C.
Genomic modifications, gene integrations or deletions, were carried out using the modular ACtivE toolkit and method that was recently developed by our group [38]. Additional file 1: Figure S1, S2 outline the overall working principle of the ACtivE method. Briefly, 50 fmol equivalent molarity of each plasmid module was used to assemble a single all-in-one CRISPR plasmid. Four plasmid modules, Cas9 cassette, selection marker (URA3), storage part (bacteria ORI and AmpR) and yeast origin of replication (2 µ) were combined with the corresponding gRNA cassettes according to the ACtivE method [38]. ARS209, ARS306, ARS727, ARS1531 and ARS1603 were used as integration sites for the genomic integrations [38]. 500 ng–1000 ng from each donor DNA part containing overlapping fragments with their neighbor parts was used. The upstream homology arm (UHA), promoter, coding sequence (with terminator) and downstream homology arm (DHA) were designed for integrations, whereas only UHA and DHA were used for deletions. The potential crRNA sequences on each region were scored using CRISPOR [42] (http://crispor.tefor.net), an online gRNA selection tool giving sequence-based scores using sequence prediction algorithms.
The colonies were first screened using colony PCR to detect the genomic modifications. Genomic DNAs of the positive transformants were extracted using Pierce Yeast DNA Extraction Reagent Kit (Thermo Scientific™). The target regions were confirmed by Sanger sequencing performed at GENEWIZ, Inc (Leipzig, Germany).
Before the cultivations, URA3 containing CRISPR plasmids were removed using the 5-Fluoroorotic Acid (5-FOA) (Thermo Fisher Scientific) counter-selection method with a synthetic defined medium supplemented with 0.1% (w/v) 5-FOA.
High-throughput strain screening
To determine the best producers of the Taxol® precursors, the strains containing single genomic modifications (integration or deletion) were screened using V-shaped, 24-deep well-plates (Axygen™). A 20% dodecane (ACROS Organics™) overlay was added to set a working volume of 2 ml in each well, and CSM with glucose or galactose was used for the cultivations. The initial OD600 was set to 1.0 for each well by diluting pre-cultures. The plates were incubated with shaking at 350 rpm at 30 °C for 72 h on thermomixers. Gas permeable adhesive plate seals (Thermo Scientific™) ensured oxygen transfer. The total biomass in each well was measured at 600 nm wavelength using the Nanodrop™ 2000c spectrophotometer (Thermo Scientific™).
In the second-level screening, the best performing strains with single genomic modifications and the strains containing multiple modifications were screened employing a BioLector Pro (mp2‐labs) microbioreactor‐screening platform. A flower-shaped, transparent bottom 48 well-plate (mp2‐labs) containing pH and dissolved oxygen (DO) optodotes was used for online monitoring of biomass, pH and DO. Similar to the first screening, glucose or galactose-containing CSM was used as the medium, the initial OD600 was set to 1.0, and a 20% dodecane overlay was used in 1 mL working volume. The plate was covered using a gas-permeable sealing foil with an evaporation reduction layer (mp2‐labs), and the temperature was maintained at 30 °C under the agitation of 1000 rpm. Biomass absorbance units were measured with the gain = 6.
After cultivations in the plates, dodecane layers were collected following a centrifuge step, and the taxane (taxadiene and derivatives) production was analysed via gas chromatography-mass spectrometry (GC–MS).
Bioreactor cultivation
MiniBio500 bioreactor (Applikon Biotechnology) was used for larger scale cultivation for the best producer strain. 250 mL total reaction volume containing a 20% dodecane layer was used for the cultivations. Similar to the other cultivations, the initial OD600 was adjusted to 1.0 by diluting overnight cultures. The same medium compositions as the previous experiments, galactose containing CSM, were used. To mitigate the foam formation, polypropylene glycol P2000 0.01% (v/v) (Alfa Aesar), was used in the medium as anti-foam. pH, DO, and temperature were measured online using the my‐control system (Applikon Biotechnology). Temperature was set to 30 °C. A setpoint 70% saturation of dissolved oxygen (DO) was applied, an air sparger was used automatically to maintain O2 level. pH was maintained in a particular range (5.0 < pH < 6.5) and 1 M of NaOH was added when the pH was below the threshold. Biomass was measured online using the Optura system with a BE2100 OD sensor (BugLab). Samples were taken daily for offline biomass measurement and quantification of the metabolite concentrations.
An inverted microscope (Leica Microsystems) was used following all cultures in this study to detect if there was microbial contamination. The cells were monitored under 100X lens with immersion oil (Nikon).
Metabolite identification and quantification
The dodecane layer collected at the end of the cultivations was analyzed by GC–MS as described previously [22]. A GC system, Trace™ 1300 Series (Thermo Scientific™), equipped with TraceGOLD™ TG-SQC GC column, was used. The mass spectra of 50–650 m/z were recorded on an ISQ™ Series Single Quadrupole MS (Thermo Scientific™) using EI ionization mode and a scan time of 0.204 s. The GC–MS data were processed using the Xcalibur™ software. Pure taxadiene provided by the Baran Lab (The Scripps Research Institute) and GGOH (Sigma Aldrich) were used as standards. The concentrations of the additional compounds were calculated relative to the taxadiene standard.
Statistical analysis
Strain screening experiments were conducted in at least three replicates. The well layouts in both 24-well plates and 48 well-plate were randomized to mitigate the plate effects and possible errors. The error bars represent the standard deviations of different experiments. The one-way analysis of variance (ANOVA) was used to determine if there was a statistically significant difference between the samples or experiments. The null hypothesis considered no significant difference between the samples/runs; the null hypothesis was rejected if the p-value ≤ 0.05.
Results & discussion
The main objective of the study was to improve metabolic fluxes towards the mevalonate pathway, thus, towards GGPP which is a common precursor of diterpenes [43], to enhance the production of the early step Taxol® precursors synthesized by our engineered yeast strains. To this end, computer-aided design was used to predict/identify potential genomic modifications that would be difficult to determine intuitively. Strain design algorithms were used on yeast GEM 8.5.0. The gene deletion or integration candidates were simulated using COBRA tools. The strains containing single genomic modifications were then designed using the ACtivE toolkit and were screened in V-shaped deep-well plates. The promising single genomic modifications and their combinations were tested in a BioLector microbioreactor system. Following this, the best producer was also tested in a lab bench bioreactor. Figure 2 demonstrates the whole process explained here.
in silico design
Our combinatorial approach benefited from three design algorithms, OptKnock, OptGene and OptForce on yeast GEM 8.5.0. Due to the incomplete knowledge on the Taxol biosynthetic pathway, including the exact reactions that are catalysed by its enzymes, we focused on acetyl-CoA and GGPP as production targets (after addition of their respective exchange reactions), which are the first and last metabolites in the mevalonate pathway, respectively (Fig. 3A).Since the S. cerevisiae strain used for genomic modifications employed inducible galactose promoters, the simulations were carried out with galactose or glucose as carbon source, separately. Nonessential reactions and genes were first determined for OptKnock and OptGene using flux balance analysis (FBA) [44]. Minimum growth rate was set to 50% of wild-type growth when targeting acetyl-CoA for OptKnock deletions, however, it was set to 20% for GGPP as OptKnock could not predict potential gene deletions in favour of GGPP maintaining higher growth rate. OptGene was run over 500 and 1000 generations, and all predictions were considered. The genomic modifications suggested by both the first “MUST set” and the second “MUST set” of OptForce runs [37] were considered. Since the design algorithms, OptKnock, OptGene and OptForce, used in this study prioritise growth-coupled solutions, all solutions taken into account were growth-coupled. Table 1 compiles the selected target genes and corresponding design algorithms.
The pathways, genes and reactions modified in this study. A) The mevalonate pathway. The additional copies of native genes (blue shaded) and the heterologous genes (orange shaded) integrated in a previous study to construct the parent strain LRS6 [23] are highlighted. B Fatty acid biosynthesis in mitochondria C Glyoxylate cycle D Connected pathways; branched-chain amino acid biosynthesis (from two pyruvate molecules to L-valine or L-leucine), pantothenate pathway (from 3-methyl-2-oxobutanoate a 5,10-methylenetetrahydrofolate to pantothenate) and the spermidine biosynthesis (from S-adenosyl-L-methionine to spermidine) E de novo purine biosynthesis. The red crosses indicate corresponding gene deletions suggested by the design algorithms; thick arrows highlighted with green colour indicate the corresponding overexpressed genes suggested by the design algorithms. The arrows show the direction of the fluxes. Dashed arrows indicate multiple reactions. A-CoA: acetyl-CoA, AA-CoA: acetoacetyl-CoA, HMG-CoA: hydroxymethylglutaryl-CoA, MEV: mevalonate, MEV-P: R-5 phosphomevalonate, MEV-PP: R-5-diphosphomevalonate, IPP: isopentenyl diphosphate, DMAPP: dimethylallyl diphosphate, GPP: geranyl diphosphate, FPP: farnesyl diphosphate, FOH: farnesol, GGPP: geranylgeranyl diphosphate, TXN: taxadiene, T5α-ol: taxa-4(20),11-dien-5α-ol, T5αAc: taxa-4(20),11-dien-5-α-yl acetate, Mal-CoA: malonyl-CoA, Mal-ACP: malonyl-ACP, 3-KA-ACP: 3-ketoacyl-ACP, 3-hydroxyacyl-ACP, t2-E-ACP: trans-2-enoyl-ACP, OAA: oxaloacetic acid, 2-A-Lac: 2-acetolactate, diOH-M-B: 2,3-dihydroxy-3 methylbutanoate, 3MOB: 3-methyl-2-oxobutanoate, 2-DHP: 2-dehydropantoate, Pnto: R-pantothenate, P-Pan: R- 4’ phosphopantothenate, P-Pan-Cys: R- 4’ phosphopantothenoyl-L-cysteine, Pan-4P: 4’-phosphopantetheine, DP-CoA: 3’-dephospho-CoA, PRPP: 5-Phospho-alpha-D-ribose 1-diphosphate, PRAm: 5-Phospho-beta-D-ribosylamine, GAR: N1-(5-Phospho-D-ribosyl) glycinamide, FGAm: N2-Formyl-N1-(5-phospho-D-ribosyl) glycinamide, FPRAm: 2-(Formamido)-N1-(5-phospho-D-ribosyl) acetamidine, AIR: 5-amino-1-(5-phospho-D-ribosyl)imidazole, 5AIZC: 5-amino-1-(5-phospho-D-ribosyl) imidazole-4-carboxylate, 25AICS: (S)-2-[5-Amino-1-(5-phospho-D-ribosyl) imidazole-4-carboxamido]succinate, AICar: 5-Amino-1-(5-Phospho-D-ribosyl)imidazole-4-carboxamide, FPRICa: 5-Formamido-1-(5-phospho-D-ribosyl)imidazole-4-carboxamide
Using different conditions and design algorithms as highlighted above, various gene and reaction candidates were found for either acetyl-CoA or GGPP overproduction. We intended to use these in silico predicted targets to implement in vivo by constructing relatively simple single-mutation strains. To therefore prioritize the most promising ones among the predicted genomic modifications (Additional file 1: Table S5), we employed in silico simulations to validate their effect. In these simulations, the lower bound of the biomass function was set to a value of 0.1, to ensure that the optimised model would still have active fluxes toward the biomass reaction. Then, by going through one candidate reaction at a time, initial flux of these reactions were first fixed to an arbitrary value of 0.01 in an initial simulation, while in a subsequent simulation of a mutant strain the fluxes were fixed to either 0 or 0.02 to mimic deletion (reaction knock-out) and overexpression (gene integration), respectively. Then, in each of the model variants, the maximum production fluxes of acetyl-CoA, GGPP and biomass were determined, and the effect of the genomic modification relative to the initial simulation was plotted (Fig. 4). The genes that showed the largest increase in maximum flux values were prioritized for further analysis and wet-lab experiments.
Although clear increases were found with approximately two-fold overproduction in acetyl-CoA when particular genes were overexpressed in silico, the overproduction rates were relatively low in gene deletions except for DPP1, OAR1 and MDH3 that showed ~ 40% increase (Fig. 4). To understand the lower increases better, metabolite interaction maps were constructed for the gene deletions including ACH1, MLS1, DIT1, LPP1, ISC1 and DTR1 to investigate the effects of these gene knock-outs. First, wild-type and knock-out models were optimised by FBA in glucose or galactose containing media, then the metabolite interactions in the mevalonate pathway were determined with their fluxes, as shown in Fig. 5. The acetyl-CoA-centered and GGPP-centered interactions were also investigated from this map (Additional file 1: Figure S3–S9), and flux differences between the wild-type and knock-out models were compared (Fig. 5). We could not detect flux increase towards GGPP in any of the knock-out models even though the objective functions were removed, as explained in the methodology section. Therefore, only acetyl-CoA increases were considered. The gene deletions that were predicted to increase the possible maximum fluxes (Fig. 4A & B) and in metabolite interaction maps (Fig. 5, Additional file 1: Figure S3–S9) were selected for the strain construction.
Comparison of maximum in silico fluxes for corresponding objectives, acetyl-CoA, GGPP and biomass reactions. For simplicity, the initial state (flux value was 0.01) was referred to as wild-type, while the final state (flux value is 0.00 for deletion and 0.02 for integration) was referred to as modification. A, C were simulated in galactose containing CSM, B, D were simulated in glucose-containing CSM. ∆; gene deletion,:; gene integration
For overexpressions, only the reactions that increased the fluxes towards acetyl-CoA production were considered (Table 1). This was because OptForce suggested to upregulate particular reactions in the mevalonate pathway (Additional file 1: Table S5) for GGPP overproduction, and these were already improved in our engineered strain, LRS6. Therefore, the initial metabolic state in the parent strain was as if OptForce’s predictions were implemented in the mevalonate pathway. OptForce did not find upregulation of early step reactions (the reactions of ERG10 and ERG13 genes) useful in the mevalonate pathway; the possible maximum flux of the GGPP production did not change compared to the initial state. It was a consistent result found by in silico simulations as a previous experimental study reported that early step mevalonate pathway genes of S. cerevisiae did not show efficient production of mevalonate compared to bacterial-sourced equivalents [47]. OptForce did not suggest any reaction in other pathways to be upregulated to enhance GGPP production.
Strain construction and screening of the single genomic modifications
As our engineered yeast strains contained additional genes (Fig. 3) driven by galactose-inducible promoters, the parent strain KM1 (Additional file 1: Table S4), was not able to induce the integrated mevalonate pathway genes using glucose as sole carbon source. Therefore, we first deleted the GAL80 gene yielding with EJ1 strain (Additional file 1: Table S4) to allow glucose utilization as Gal80 protein inhibits the transcription of the galactose-inducible genes in the absence of galactose [48]. These two strains were then designed to incorporate the genomic modifications, single-gene deletion or integration (overexpression), predicted by the design algorithms. When the additional copies of native yeast genes were integrated for overexpression, native promoters were simply changed with GAL1 promoter using the ACtivE method (Additional file 1: Figure S2) [38] to enhance their expression rates [22, 49]. Additional copies were integrated into an intergenic region close to the autonomously replication sequence (ARS) 1603 [38] in each strain to screen the effect of single gene overexpression.
In this study, nine gene knock-outs and eight gene overexpressions were tested to determine whether these modifications affect biomass and the production of early steps Taxol® precursors, taxadiene, taxa-4(20),11-dien-5α-ol (T5α-ol), and taxa-4(20),11-dien-5-α-yl acetate (T5αAc), via the mevalonate pathway. To screen single genomic modifications, the strains containing single gene deletions or integrations were cultured for three days in galactose or glucose-containing CSM media as simulated previously. In addition to the Taxol® precursors, some side compounds such as verticillene, iso-taxadiene, geranylgeraniol (GGOH), 5(12)-oxa-3(11)-cyclotaxane (OCT), iso-OCT, and additional diterpenes were also detected by GC/MS analyses as previously reported in more detail [23]. Among them, GGOH and OCT were also quantified to compare the production of these side products. Two Taxol® precursors (taxadiene and T5α-ol), two side-products (GGOH and OCT) and biomass were considered in a micro-scale screening in 2 mL cultures to characterize the modified strains. Figure 6 shows the comparison of the production of these metabolites and biomass between the parent strains and designed strains.
Comparison of biomass and production of early step Taxol® precursors and side products. A KM1-derived strains in the galactose-containing CSM. B EJ1-derived strains in the glucose-containing CSM. Relative values are shown considering 100% baseline (dashed line) of the parent strains, KM1 or EJ1. Error bars indicate standard deviations between three replicates. ∆; gene deletion, gene integration
Differences in production between galactose-containing (CSM w/ galactose) and glucose-containing (CSM w/glucose) media were detected. Taxadien-5α-ol productions varying from ~ 4 mg/L to ~ 8 mg/L were observed in galactose-containing media with KM1-derived strains; however, only weak peaks were seen in the gas chromatogram for T5α-ol when the glucose-containing media was used with EJ1-derived strains that did not contain the GAL80 gene. This was most probably because the expression rates of the galactose-inducible promoters were still higher in galactose-containing media, even though EJ1-derived strains could produce taxadiene under glucose only conditions (Fig. 6). Additional regulatory elements might have had an impact on the activation of galactose-inducible promoters in the presence of glucose. In the galactose-containing CSM media, mainly integrations increased the downstream production from GGPP, whereas most of the deletions and integrations showed positive impacts on the production of the precursors in glucose-containing media.
DPP1 and LPP1 genes, encode two Mg+2-independent phosphatidate phosphatases found in yeast [50]. Deletion of these genes might result in higher farnesyl diphosphate (FPP) and GGPP titers as these enzymes are also responsible for converting FPP to farnesol (Fig. 3A). However, in the galactose-containing medium, both single deletions showed a similar pattern with lower average (p > 0.05) taxadiene production (Fig. 6A). On the other hand, a ~ 20% increase (p < 0.05) in taxadiene production with DPP1 deletion was observed in the glucose-containing medium (Fig. 6B), while LPP1 deletion resulted in almost the same taxadiene production (p > 0.05). No significant growth phenotype was observed in any condition (Fig. 6). in silico simulations suggested that DPP1 deletion could lead to acetyl-CoA overproduction in a glucose-containing medium (Table 1 and Fig. 4B), and experimental results (Fig. 6B) supported this.
The protein encoded by OAR1 is an NADPH-dependent 3-oxoacyl-(acyl-carrier-protein) reductase, which is involved in fatty acid biosynthesis in yeast [51, 52] (as illustrated in Fig. 3B). OAR1 deficient yeast strains could survive on fermentable carbon sources like glucose but not on non-fermentable carbon sources such as glycerol [51, 52]. Approximately 30% reduction in biomass was observed in the glucose-containing and the galactose-containing CSMs (Fig. 6). Also, the production rate of the Taxol® precursors obtained from KM12 was less than 40% of the parent strain. In contrast, more than 40% increase was noted in glucose-containing CSM using KMJR12 (Fig. 6B).
Both OptKnock and OptForce found MDH3 as a good target to increase acetyl-CoA (Table 1). MDH3 encodes a peroxisomal malate dehydrogenase [53] responsible for the interconversion of malate and oxaloacetate using NAD+ or NADH depending on the reaction in the glyoxylate cycle (Fig. 3C) [54, 55]. OptKnock also suggested deleting the MLS1 gene that encodes another enzyme, malate synthase, involved in the glyoxylate cycle [54]. Malate synthase catalyses the formation of malate from glyoxylate and acetyl-CoA in either cytosol or peroxisome, depending on the carbon source (Fig. 3C) [56]. Cytosolic and peroxisomal acetyl-CoA is an essential compound in the glyoxylate cycle. However, the glyoxylate cycle is activated when two-carbon compounds such as ethanol and acetate are used as the sole carbon sources or β-oxidation of fatty acids is enabled [56]. Although we used only six-carbon sources, galactose or glucose, we detected significant effects of MDH3 or MLS1 deletions in our study, as shown in Fig. 6. MLS1 deleted strain KMRJ15 produced less biomass, ~ 60% of the reference strain, in glucose-containing CSM. A similar growth trend was previously reported [57]. On the other hand, KM13 (MDH3∆) showed a significant increase with ~ 40% in taxadiene production when galactose was used as carbon source even though it was unexpected as MDH3 might not be functional in the galactose-containing medium. In contrast, MLS1 deletion resulted in ~ 30% lower taxadiene in KM15. These results might indicate that the glyoxylate cycle genes might still be functional under different carbon sources, and that blocking particular reactions in this cycle can affect cytosolic acetyl-CoA synthesis even if the carbon source is not a two-carbon compound or fatty acid.
In mitochondria, acetyl-CoA hydrolase (Ach1) encoded by ACH1 can catalyse the conversion of acetyl-CoA into acetate and CoA. Ach1 can also reversibly transfer CoA from succinyl-CoA to acetate [58]. OptKnock and OptGene proposed ACH1 deletion to increase acetyl-CoA concentration in glucose-containing media. Although we detected significantly lower biomass (p < 0.05) in both KM14 and KMRJ14 strains (Fig. 6), taxadiene concentrations were comparable with the reference strains, indicating that production of Taxol® precursors was improved per OD with ACH1 deletion even if the total production could not be enhanced.
Perhaps, the most surprising findings of OptGene were the deletions of DIT1 and DTR1 genes that take part in the sporulation process [59, 60]. Dit1 plays a role in forming the dityrosine layer of the spore wall, and its expression rate increases during spore wall maturation [61]. Dit1 expression might be active in vegetative cells; yet, its cellular activities of are not fully elucidated [62]. DTR1 is a member of the gene network controlling the assembly of the spore wall [63]. Dtr1 protein can also increase the resistance against some growth inhibitors in vegetative yeast cells [60]. The deletions of these genes did not show a significant decrease in biomass in either glucose-containing or galactose-containing CSM (Fig. 6). However, DIT1 deletion in KM16 caused a dramatically lower production of the Taxol precursors in the galactose-containing medium. In contrast, DTR1 deletion increased taxadiene concentration in the glucose-containing medium. It is very likely that deletion of these sporulation-specific genes directly makes an impact on GGPP concentration, as it was reported that geranylgeranyl diphosphate synthase has a critical role in the sporulation process in fission yeast, and related genes have functional similarity with S. cerevisiae [64].
ISC1 encodes inositol phosphosphingolipase C that hydrolyses sphingolipids to produce ceramide, a compound involved in regulations of cell growth, death and stress response [65]. There is no direct relation between ISC1 and acetyl-CoA or GGPP, and it was shown that ISC1 deletion might lead to a higher budding pattern than the wild-type strains [66]. Consistently, ISC1 deletions resulted in higher average biomass in galactose or glucose-containing media (Fig. 6). OptGene suggested ISC1 deletion to increase acetyl-CoA concentration in a galactose-containing CSM. Parallel to this, we obtained a higher average production for the target metabolites with a ~ 6% increase in average in taxadiene and T5α-ol in the galactose-containing medium, although it was not statistically significant (p > 0.05).
Majority of the OptForce predictions were involved in the biosynthesis of metabolic precursors in yeast. ILV2 encodes acetolactate synthase that catalyses the conversion of two pyruvate molecules to 2-acetolactate in isoleucine and valine biosynthesis pathways [67]. From 3-methyl-2-oxobutanoate produced in valine biosynthesis, coenzyme-A precursors are produced in the phosphopantothenate biosynthetic pathway, where ECM31 and CAB1 catalyse the first and fourth steps, respectively [68]. The product of SPE2 plays a critical role in spermidine biosynthesis [69]. Although, these genes and pathways might look irrelevant and independent from each other, connecting the intermediate or final products in these pathways (as shown in Fig. 3D) reveals their direct impacts on CoA production and possibly enhanced acetyl-CoA production. ADE4, ADE5,7 and ADE13 are responsible for five reactions in de novo purine synthesis as shown in Fig. 3E [70]. while TRR1 regulates the thioredoxin system, protecting yeast against oxidative stress [71].
Integration of ADE5,7 encoding a bifunctional protein responsible for the second and fifth reaction in de novo purine synthesis pathway resulted in lower taxediene production (~ 23% decrease, p < 0.05) in galactose-containing CSM with strain KM24. In contrast, taxediene production was significantly higher in the glucose-containing medium. Apart from this, overexpression of the CAB1 gene could not increase the production even though an increased flux in the phosphopantothenate pathway could potentially increase acetyl-CoA concentration. Olzhausen et al. (2021) reported that the native CAB1 is relatively inefficient for the production of coenzyme A compared to other phosphopantothenate pathway genes, and the researchers dramatically increased coenzyme A titer using mutant CAB1 W331R [72]. This might be the reason behind non-effective taxane production when CAB1 was overexpressed. OptForce suggested upregulation of early-stage and mid-stage reactions in de novo purine synthesis that have relatively lower fluxes than the late-stage reactions, as shown in Additional file 1: Figure S11 that seems like an effective strategy to enhance the flux towards the downstream part of the pathway. Still, the relation of de novo purine synthesis pathway and thioredoxin system with acetyl-CoA should be further investigated as increased fluxes in these systems can potentially increase acetyl-CoA concentration or the fluxes in the mevalonate pathway towards GGPP.
In Fig. 3, we have highlighted genomic modifications spanning various metabolic pathways. While certain modifications, such as the deletions of the LPP1 and DPP1 genes, may appear intuitively predictable, it is important to note that a significant portion of these genomic alterations, including those not depicted in Fig. 3, such as DTR1 and DIT1 deletions, or TRR1 overexpression, are considerably challenging to anticipate. These findings show that mathematical modelling and optimization of the microbial systems can be beneficial in finding useful genomic modifications that are very difficult to be intuitively predicted. Indeed, detecting small changes using a relatively low number of replicates is quite challenging as the noise deviations can make the screening and evaluations harder. Nevertheless, statistically significant impacts of the genomic alterations were detected when single modifications were tested. Here, we coupled the native genes with strong galactose-inducible promoters. Therefore, alternative approaches such as protein engineering or integrating heterologous genes encoding higher performance enzymes for the target reaction could also be used to enhance the fluxes in the pathways of interest.
Next level screening using high-throughput microscale bioreactor system
To investigate the impact of multiple modifications on taxane production, we incorporated the empirical findings from the first screening experiments and strategically combined the most promising modifications to engineer next-level strains. For galactose-containing CSM, five genomic integrations and one gene deletion were combined to construct different combinations of KM1-derived strains, while three gene deletions and two genomic integrations were used to produce EJ1-derived strains to be used in glucose-containing CSM, as shown in Table 2.
The first-level strain screening revealed promising genomic modifications enhancing GGPP and taxadiene productions, as discussed above. However, the next compound, T5α-ol, in the Taxol® pathway could not be effectively detected, and only KM25 and KM28 showed a significant increase (p-value < 0.05) in T5α-ol titer compared to the parent strain (Fig. 6). In addition, KMRJ strains could not form a clear T5α-ol peak in the GC chromatogram when they were used in glucose-containing media. The reason behind it was probably the limited agitation and air transfer in deep-well plates because of the shape of the wells and the shaking frequency (350 rpm) as it was proven that oxygen supply is critical for oxygenation reactions for T5α-ol synthesis [23]. Therefore, in the second-level screening, the BioLector Pro microbioreactor‐screening platform was utilized with a flower-shaped plate and a higher shaking frequency of 1000 rpm to ensure sufficient oxygen transfer since the flower shape geometry can provide a better oxygen supply [73].
To this end, we primarily considered taxadiene yields, as it is the direct product derived from GGPP. In contrast, T5α-ol titers were significantly lower, reaching a maximum of only 8 mg/L compared to taxadiene, which reached a maximum of 95 mg/L. For the galactose-containing medium, the three best taxadiene producer strains containing single modifications (KM21, KM25 and KM13) and four strains containing multiple modifications (KM31, KM32, KM33 and KM34) were screened while biomass, pH and DO were monitored in real-time using the BioLector. Interestingly, all multiple modification strains resulted in higher biomass compared to the parent strain, KM1, after three days. It seems increasing fluxes in particular reactions and pathways ended in favor of biomass rather than a metabolic burden on the cell although overexpression of ILV2 (KM21) or deletion of MDH3 (KM13) led to lower biomass compared to the parent strain KM1. Most of the strains showed a similar pattern for pH change during three days of cultivation. The initial pH between 5.50 and 5.75 dropped to ~ 5.0 and slightly increased to around 5.25, as shown in Fig. 7B. S. cerevisiae tends to acidify the culture pH [74], therefore it was an expected behavior. However, KM31 containing overexpressed ILV2 and TRR1 genes showed a higher pH between 20 and 50 h of culture. To further elucidate the reason behind this, the pH pattern of KM22 cultures should also be tested.
Although KM21, KM25 and KM13 strains increased taxadiene production by 35%–40% in the deep well-plates compared to KM1 (Fig. 6A), taxadiene concentration was only enhanced by ~ 15% (p-value < 0.05) by these strains in the BioLector (Fig. 7C). However, the highest taxadiene concentration was ~ 110 mg/L in deep-well plates and it was doubled in the BioLector system as ~ 215 mg/L production was recorded with KM32. This is a remarkable improvement as approximately 1.6-fold higher production was achieved than the previously reported maximum, which was 137 mg/L in S. cerevisiae cell factories [23]. It is worth noting that previous studies on taxadiene synthesis used richer media, which likely contributed to higher production yields. In this study, complete synthetic defined media were used, as all in silico illustrations were conducted using defined media. While E. coli achieved higher taxadiene production at 1 g/L in a previous attempt [75], the expression of the next step enzymes, T5αOH and CPR, completely abolished taxadiene synthesis in E. coli [75]. In contrast, KM32 increased taxadiene production while also expressing the downstream genes responsible for the second and third steps, namely T5αOH, CPR, and TAT.
Dissolved oxygen (DO) was maintained between 75%–100% for all the strains used in the BioLector system (Additional file 1: Figure S12 and S13). Accordingly, greater T5α-ol was synthesized by all KM1-derived strains with at least 23 mg/L concentration in KM33 (Fig. 7C). This production was almost three-fold higher than the maximum T5α-ol production observed in deep-well plates, proving that oxygen supply was the critical factor for T5α-ol production. Also, the acetylated precursor, T5αAc, was detected in all KM1-derived strains with concentrations ranging from 15 to 26 mg/L. Nevertheless, all multi-modification strains KM31, KM32, KM33 and KM34, produced less T5αAc (p-value < 0.05) than the parent strain as shown in Fig. 7C even though a significant increase (p-value < 0.05) was observed in taxadiene production in KM32, KM33 and KM34 and single-modification strains (KM21, KM25, KM13). This indicates that to enhance the yield of T5α-ol and the following compound, T5αAc, further improvement in the second reaction catalyzed by T5αOH and CPR is a necessity. KM25 was the best producer of T5α-ol and T5αAc with 35.4 mg/L and 26.2 mg/L, respectively. Yet, no statistically significant difference (p-value > 0.05) was observed for T5αAc titer between KM1, KM21, KM25 and KM13. In addition to taxadiene, these are the highest yields for T5α-ol and T5αAc production reported so far using S. cerevisiae as a cell factory. It is noteworthy that the previous study conducted in E. coli achieved a T5α-ol production of 23 mg/L without the expression of the subsequent gene, TAT, in the pathway [75]. In addition, this E. coli strain was unable to accumulate taxadiene, as mentioned earlier. Taking these findings into account, it is anticipated that further enhancements will lead to an increased metabolic flux towards T5αAc in our S. cerevisiae strains.
In the glucose-containing CSM, KMRJ12, KMRJ19 and KMRJ24 strains were used with multi-modification strains KMRJ31, KMRJ32, KMRJ33, and KMRJ34 (Table 2) in the BioLector platform. In parallel to the deep-well plates, all strains with the OAR1Δ genotype produced less biomass in the BioLector system as shown in Fig. 8A. A correlation was also observed between pH change and biomass and/or OAR1Δ (Fig. 8B). Like in the galactose-containing medium, after a sharp drop, the pH reached around 5.25 for the strains expressing the OAR1 gene (EJ1, KMRJ19, KMRJ24). The pH stabilised at around 5.0 for the other strains, this might be because of lower biomass or the OAR1 deletion.
Another interesting finding with OAR1 deletion was the dramatic reductions in the titers of the oxygenated product, T5α-ol, and naturally, the next product T5αAc as seen in Fig. 8C. Also, GGOH production dropped at least twofold in all OAR1-deleted strains. GGOH is indeed a valuable compound that can be used in the pharmaceutical and cosmetic industries. Metabolic engineering studies have been carried out to improve GGOH production in S. cerevisiae [76, 77]. Although the GGOH synthesis is not fully identified in yeast, native phosphatases are thought to be involved in GGOH synthesis from GGPP. Considering its chemical structure, oxygenation reactions should also take a part in GGOH synthesis [78]. Taking the reductions in T5α-ol and GGOH into consideration, it is likely that OAR1 deletion affected the oxygenation capability of S. cerevisiae, and it might also be one of the reasons behind the decrease in cell fitness. On the other hand, still, the strains with the OAR1Δ genotype showed greater taxadiene production than the reference strain (Fig. 8C), meaning that OAR1 deletion led to the highest taxadiene production per OD. However, it should be also noted that GGOH reduction might have improved the taxadiene concentration.
The combination of OAR1Δ and DTR1Δ in KMRJ31 resulted in the maximum taxadiene production of 128 mg/L, which is still a remarkable titer for taxadiene considering the similar studies reported previously [22, 79]. On the other hand, even if OAR1Δ genotypes were excluded, KMRJ strains produced ~ 7 mg/L of T5α-ol from each 100 mg/L taxadiene on average (7% yield), whereas this amount was ~ 18 mg/L for KM strains (18% yield). This is probably because the galactose-inducible promoters could not express T5αOH in glucose-containing CSM as efficiently as in galactose-containing CSM, even though the GAL80 was deleted.
In addition to Taxol® precursors, KMRJ19 with DTR1 deletion produced the highest GGOH with 221 mg/L among all the strains used in this study, it was followed by KMRJ24 and KM31in the galactose-containing medium with the 219 mg/L (p-value > 0.05). These production yields of GGOH are comparable with those in similar studies [76, 77]. For this reason, the related modifications, DTR1 deletion, ADE 5,7 overexpression or simultaneous overexpression of ILV2 and TRR1, are promising genomic modifications to increase GGOH production.
While we have tested three single modifications in the Biolector platform, there are several other promising candidates, such as KM28, KM26, and KM23, which warrant further investigation in well-controlled conditions. Specifically, understanding the impact of overexpressing the SPE2, ECM31, and ADE4 genes is crucial to gain deeper insights into their potential contributions to the overall process. Therefore, future experiments focusing on these candidates could provide valuable data to complement and enrich our current findings.
Scale-up of the production of the Taxol ® precursors using the best strain
Finally, the production was scaled-up using the best taxadiene producer, KM32, in a 2% (w/v) galactose-containing CSM medium in 250 mL reaction volume in a mini-scale bioreactor. To maintain similar conditions as in the BioLector system and to mimic the in silico simulations where the oxygen was not a limiting factor, the minimum %DO was set to 75% and O2 was supplied with air when it was below the threshold. Yet, it is important to note that in an industrial-scale setting, the availability of oxygen can potentially act as a limiting factor that may impact production yields. Likewise, the pH was set to 6.0 as it is a suitable pH considering both yeast growth and the enzymatic activities in the Taxol® pathway [23]. A 1 M NaOH was added as needed when the pH was less than 6.0. Figure 9 shows the reactor parameters and the production of Taxol® precursors during the five days of cultivation.
Considering the first three days, the growth showed a similar pattern as a decrease was observed towards the third day and then dramatically dropped down (Fig. 9A). Although this decrease was expected, the sharp drop between 72nd and 80th hours was probably a temporary a sensor problem. On the other hand, the production yield was relatively low for the Taxol® precursors in the first three days. In 72 h, 182.5 mg/L taxadiene, 35.8 mg/L of T5α-ol and 19.2 mg/L of T5αAc were produced. These reached to 236.7, 47.1 and 31.2 mg/L, respectively on the fifth day (Fig. 9B). Although the total titers of the target molecules were higher at the end of cultivation, on the fifth day, the yield on the third day was lower compared to the BioLector system.
In contrast, the concentration of GGOH was significantly higher than that of taxadiene (Fig. 9B). The accumulation of GGOH is primarily attributed to the promiscuous activity of TASY enzymes, as previously reported [19]. While adjusting the media composition and conditions can reduce the synthesis of this undesired side product [19], it appears necessary to engineer the TASY enzymes to enhance their specificity in order to mitigate GGOH accumulation and improve taxadiene titer.
pH and DO showed more fluctuations in the bioreactor-scale. This might be the reason behind the decrease in production yield. Consequently, optimising the bioprocess conditions and implementing better pH and DO control measures may further enhance the titers of Taxol® precursors on larger scales.
Comparison of the in silico predictions and wet-lab results
The genome-scale model utilised in this study, yeast 8.5.0, represents a significant advancement in S. cerevisiae S288C's metabolic understanding [27]. While it is important to acknowledge that certain discrepancies may arise due to the specific genotype of the parent strain employed in our research, we observed enhancements in taxadiene production, and by extension, the likely increase in GGPP production, meaning that our wet-lab validations clearly demonstrated the potency of mathematical models and computational frameworks in identifying valuable targets that may elude intuitive prediction. Considering Table 1, Fig. 4, and the experimental results, however, there are also exceptions. OAR1 deletion was predicted to increase GGPP concentration in the galactose-containing CSM, and MDH3 deletion was suggested to increase acetyl-CoA production in the cytosol in the glucose-containing medium. Nevertheless, these deletions showed higher productions in the opposite carbon source (Fig. 6). According to the in silico predictions, MLS1 deletion should have increased the acetyl-CoA production in the galactose-containing medium, but in contrast, this deletion decreased GGPP concentration and probably acetyl-CoA concentration in the galactose-containing medium and could not make any difference in glucose-containing CSM (Fig. 6). The other deletions showed either predicted results with overproductions or similar production yields to the reference strains (p-value > 0.05). It is also possible that more replicates could have given more precise results and could have mitigated the analytic measurement deviations.
Based on these findings, the in silico predictions provided a refined set of solutions, taking into account the comprehensive genomic context of the host organism. We further refined our selection process by detecting the possible maximum fluxes in conjunction with metabolite interaction maps, enabling us to prioritize single genomic modifications from an initial pool of over 60 predictions (Additional file 1: Table S5). It is worth to notion that the three algorithms are able to predict sets of genomic modifications that together have a beneficial effect. Both in silico and experimental validation of single genomic modifications from these sets can therefore lead to somewhat false negatives, as some of these modifications are only beneficial in combination with others. Regardless, this strategy was designed to match our desire to experimentally validate single genomic modifications, and this prioritization strategy indeed resulted in a strain with improved taxadiene productions.
Conclusion
Computational tools, in silico design frameworks and genome-scale models were used to rationally design yeast cell factories in a way that intuitive estimations are very difficult. In specific, in this study, a combinatorial design approach was used with three in silico algorithms, OptKnock, OptGene and OptForce, on the yeast-GEM 8.5.0. A set of 17 genomic modifications were predicted by the simulations (nine gene knock-outs, eight gene overexpressions and their combinations via extra copies and strong promoters) and tested for the increased production of Taxol® precursors, through GGPP overproduction. Therefore, this study is one of the most comprehensive studies reported until now in terms of the amount and the variability of the genomic manipulations. Without a doubt, the ACtivE toolkit and method facilitated this process with an accelerated genome editing process. The findings of this work showed that simultaneous overexpression of four genes, ILV2, TRR1, ADE13 and ECM31, related to upregulations in the pantothenate pathway, branched-amino acid biosynthesis pathways and de novo purine synthesis pathway, could enhance taxadiene production by ~ 50% through GGPP overproduction. Also, single modifications could increase taxadiene yield from 15 to 40% depending on the cultivation conditions and carbon source. As the oxygen supply is crucial for the second step in the Taxol® biosynthesis pathway, higher yields in T5α-ol and T5αAc productions were reported with the conditions allowing better oxygen access. Using the best-performing strain KM32 containing additional copies of the above-mentioned four genes, we achieved 215 mg/L of taxadiene, 43.65 mg/L of T5α-ol and 26.2 mg/L of T5αAc titers that are the highest production yields reported until now in S. cerevisiae. The genomic modifications reporting higher GGPP synthesis can be also used to increase the production of other high-value isoprenoids through the same precursor. In addition to the mevalonate pathway, similar integrated approaches combining different design algorithms, genome engineering and bioprocessing studies can be used for enhancing metabolic fluxes towards the target native or heterologous pathways in S. cerevisiae. Developing alternative in silico prediction and design tools, constructing more accurate genome-scale models would improve the efficiency of this process.
Availability of data and materials
MATLAB scripts are available on https://github.com/kmalci/yeast_modelling. Plasmids and other data will be made available on request.
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Acknowledgements
We would like to thank Mr Stuart Martin, Mr Mark Lauchlan and Miss Katalin Kis at the School of Engineering, University of Edinburgh, UK for their technical support with GC-MS analysis and laboratory operations. We would like to thank Dr David Gomez-Cabeza at the School of Engineering, University of Edinburgh, UK for their kind assistance with the inverted microscope.
This work was supported by the YLSY program of the Ministry of National Education of Turkey, the Mexican government’s dependence CONACyT (Mexican National Council for Science and Technology) CVU:675492 and CVU: 537962, Novo Nordisk Foundation (Grant Number NNF20CC0035580), the Engineering and Physical Sciences Research Council (Grant number EP/R513209/1), the Royal Society (Grant Number RSG\R1\180345) and the British Council (Grant Number: 527429894).
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KM: Conceptualization, Methodology, Software, Formal Analysis, Investigation, Writing—Original Draft. RS: Methodology, Software, Writing—Reviewing and Editing. NJ-B: Investigation, Resources. JS-G: Investigation. EJK: Supervision, Writing—Reviewing and Editing. LR-S: Conceptualization, Supervision, Writing—Reviewing and Editing, Project administration.
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Additional file 1: Table S1.
The primer list used to produce the donor DNA parts for the gene deletions. Table S2. crRNA sequences used to target the corresponding genes for deletions. Table S3. The primer list used to produce the donor DNA parts for the genomic integrations. Table S4. The yeast strains used in the study. Table S5. The gene candidates predicted by the design algorithms. Table S6. The components of the yeast nitrogen base used in the study. Table S7. The components of the complete supplement mixture used in the study. Figure S1. The ACtivE method for gene deletion. Figure S2. The ACtivE method for genomic integration. Figure S3. Acetyl-CoA-centred sub-metabolite interaction map of the wild-type model. Figure S4. Acetyl-CoA-centred sub-metabolite interaction map of DTR1 deleted model. Figure S5. Acetyl-CoA-centred sub-metabolite interaction map of ACH1 deleted model. Figure S6. Acetyl-CoA-centred sub-metabolite interaction map of MLS1 deleted model. Figure S7. Acetyl-CoA-centred sub-metabolite interaction map of DIT1 deleted model. Figure S8. Acetyl-CoA-centred sub-metabolite interaction map of LPP1 deleted model. Figure S9. Acetyl-CoA-centred sub-metabolite interaction map of ISC1 deleted model. Figure S10. de novo purine nucleotide biosynthesis pathway. Figure S11. Phosphopantothenate biosynthesis pathway. Figure S12. Dissolved oxygen (DO) concentrations of three-day cultures of KM1-derived strains measured by the BioLector microbioreactor system in the galactose-containing CSM. Figure S13. Dissolved oxygen (DO) concentrations of three-day cultures of EJ1-derived strains measured by the BioLector microbioreactor system in the glucose-containing CSM. Figure S14. Gas chromatography shows the compounds’ peaks produced by KM32 and the mass spectrum of taxadiene. Figure S15. Gas chromatography shows the compounds’ peaks produced by KM32 and the mass spectrum of T5α-ol. The retention time of the T5α-ol peak was at 8.20th minutes. Figure S16. Gas chromatography shows the compounds’ peaks produced by KM32 and the mass spectrum of T5αAc. The retention time of the T5αAc peak was at 8.61st minutes.
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Malcı, K., Santibáñez, R., Jonguitud-Borrego, N. et al. Improved production of Taxol® precursors in S. cerevisiae using combinatorial in silico design and metabolic engineering. Microb Cell Fact 22, 243 (2023). https://doi.org/10.1186/s12934-023-02251-7
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DOI: https://doi.org/10.1186/s12934-023-02251-7