Functional expression and characterization of five wax ester synthases in Saccharomyces cerevisiae and their utility for biodiesel production
© Shi et al; licensee BioMed Central Ltd. 2012
Received: 2 November 2011
Accepted: 24 February 2012
Published: 24 February 2012
Wax ester synthases (WSs) can synthesize wax esters from alcohols and fatty acyl coenzyme A thioesters. The knowledge of the preferred substrates for each WS allows the use of yeast cells for the production of wax esters that are high-value materials and can be used in a variety of industrial applications. The products of WSs include fatty acid ethyl esters, which can be directly used as biodiesel.
Here, heterologous WSs derived from five different organisms were successfully expressed and evaluated for their substrate preference in Saccharomyces cerevisiae. We investigated the potential of the different WSs for biodiesel (that is, fatty acid ethyl esters) production in S. cerevisiae. All investigated WSs, from Acinetobacter baylyi ADP1, Marinobacter hydrocarbonoclasticus DSM 8798, Rhodococcus opacus PD630, Mus musculus C57BL/6 and Psychrobacter arcticus 273-4, have different substrate specificities, but they can all lead to the formation of biodiesel. The best biodiesel producing strain was found to be the one expressing WS from M. hydrocarbonoclasticus DSM 8798 that resulted in a biodiesel titer of 6.3 mg/L. To further enhance biodiesel production, acetyl coenzyme A carboxylase was up-regulated, which resulted in a 30% increase in biodiesel production.
Five WSs from different species were functionally expressed and their substrate preference characterized in S. cerevisiae, thus constructing cell factories for the production of specific kinds of wax ester. WS from M. hydrocarbonoclasticus showed the highest preference for ethanol compared to the other WSs, and could permit the engineered S. cerevisiae to produce biodiesel.
KeywordsBiodiesel fatty acid ethyl esters metabolic engineering Saccharomyces cerevisiae wax ester synthase
fatty acyl-coenzyme A
fatty acid ethyl ester
gas chromatography-mass spectrometry
human embryonic kidney cells
synthetic minimal dropout medium
wax ester synthase.
Natural wax esters are typically esters of long-chain fatty acids and long-chain alcohols ; due to their special properties, they have been widely used in lubricants, cosmetics, linoleum, printing inks, candles and polishes. For example, wax esters consisting of fatty acids with 20 carbon atoms (C20) and C20 alcohols are outstanding lubricants ; wax esters consisting of C14 to C20 fatty acids and a C2 alcohol represent good diesel fuels . Today, wax esters are harvested from plants and animal tissues, or generated by chemical synthesis using fossil sources, and this is considered to be the main limitation for their application due to the restricted availability and high costs of existing sources [2, 4]. Thus, there is a strong demand for the development of an alternative bioprocess to obtain cheap and sustainable wax esters.
Wax ester synthases (WSs) are promiscuous enzymes involved in wax ester synthesis from alcohols and acyl coenzyme As (CoAs) . Various WSs have different preferences for substrates with varied chain length and their unspecificity has been used in several biotechnological applications for ester production, for example, jojoba-like wax esters and fatty acid ethyl esters. In general, WSs naturally accept acyl groups with carbon chain lengths of C16 or C18 and linear alcohols with carbon chain lengths ranging from C12 to C20. Reported activities of WSs with short-chain alcohols were low . Depending on the substrate specificity of the WS, various mixtures of wax esters with specific chain-length composition can be generated, which have optimal chemical compositions for certain specialty markets. Designed wax ester mixtures that do not normally exist in nature can be generated by expressing mutant WSs or a combination of WSs. It has become feasible to produce biotechnological wax esters in bioreactors [2, 4, 5, 7–10]. The types of wax esters synthesized by a specific WS are determined by the WS substrate preference and available substrates provided through the host's metabolism.
One of the best characterized cell factories is the eukaryotic model organism, Saccharomyces cerevisiae. The well-studied industrial microorganism S. cerevisiae offers a number of advantages for producing fatty acid derived products (for example, wax esters) due to the ease of cultivation and genetic manipulation, its short generation time and extensive knowledge about its fatty acid metabolism [11–14]. The development of S. cerevisiae as a cell factory would represent a good choice for wax ester production.
There are three unrelated families of WSs found in higher plants, mammals and bacteria . The first identified WS of plants, jojoba embryo wax ester synthase, did not show activity when heterologously expressed in S. cerevisiae . The second group of identified WSs was from bacteria identified by a homology search using the jojoba WS amino acid sequence. Some of the WSs from bacteria are bifunctional enzymes, that is, they functions as WS and as acyl-CoA:diacylglycerol acyltransferase (DGAT). The third group of WSs is from mammals, for example, WS from Mus musculus C57BL/6 . WSs from different organisms represent candidates for ester synthases with various substrate and product chain-length preferences. Some of these WSs have been expressed in Escherichia coli, but significant differences in substrate specificities were observed, depending on whether yeast or E. coli was used as the host for heterologous expression [9, 10].
We therefore decided to conduct a comparison of the substrate preferences of the representative WSs from bacteria and mammals in S. cerevisiae, where little information on WS expression and substrate preference is available. WS/DGAT from Acinetobacter baylyi ADP1 has been adopted in E. coli for ester production [4, 8, 16–18]. WS homologs are frequently found in the genomes of actinomycetes such as Rhodococcus [19, 20] or in the genome databases of several marine bacteria like Marinobacter [19, 21] and Psychrobacter . Few reports are available about WS from mammals. Recently, a study reported the isolation and characterization of a wax synthase enzyme from Mus musculus C57BL/6, which was expressed in human embryonic kidney (HEK) 293 cells . Therefore, five different WSs from A. baylyi ADP1, Marinobacter hydrocarbonoclasticus DSM 8798, Rhodococcus opacus PD630, M. musculus C57BL/6 and Psychrobacter arcticus 273-4 were chosen and characterized in S. cerevisiae, which is being considered as a platform for ester production. Apart from the A. baylyi WS, this is the first scientific study that has demonstrated WS activity from the other four species in S. cerevisiae. Variations in the substrate preferences of the WSs would lead to differences in the chain-length composition of products with various specialty applications.
A process that utilizes the promiscuous activity of WS is the biosynthesis of biodiesel. Biodiesel mixtures are composed of linear fatty acid methyl esters or fatty acid ethyl esters (FAEEs) ranging from C8 to C22, but are usually dominated by chain lengths from 16 to 18 carbons, for example, C16 to C18 methyl or ethyl esters . Biodiesel, currently derived from plant oil, is already produced in an increasing number of countries and has been considered as a clean and sustainable liquid fuel alternative to fossil fuels [22, 23]. However, the high costs and limited availability of plant oils are becoming a problem for large-scale commercial viability of biodiesel production, and different ways have been explored to address this problem [23, 24].
Results and discussion
Functional expression and characterization of five wax ester synthases in yeast
Low WS activity in crude cell extracts of S. cerevisiae has been reported. However, no formation of wax esters was detected in vivo . Only heterologous expression of the A. baylyi bifunctional WS/DGAT enzyme could result in the formation of detectable amounts of wax esters.
Several WSs have been identified in bacteria and mammals [5, 15, 19–21], out of which we selected five WSs for expression and characterization in S. cerevisiae CEN.PK 113-5D under control of the strong TEF1 promoter using plasmid pSP-GM2 . The selected five WSs are from A. baylyi ADP1, M. hydrocarbonoclasticus DSM 8798, R. opacus PD630, Mus musculus C57BL/6 and P. arcticus 273-4. In an effort to increase expression of the WSs, the gene sequences were codon optimized for expression in S. cerevisiae. Their transcription in S. cerevisiae CEN.PK 113-5D was initially confirmed by reverse transcription PCR (data not shown).
Comparison of acyl acceptor specificities of different wax ester synthases using palmitoyl coenzyme A as the acyl donor
Wax ester synthase activity (pmol/mg protein/min)
0.67 ± 0.15
4.6 ± 0.55
8.1 ± 1.87
2.7 ± 0.37
3.8 ± 0.51
5.9 ± 0.83
0.42 ± 0.21
10.8 ± 1.60
14.6 ± 1.75
6.8 ± 0.82
3.5 ± 0.53
4.2 ± 0.46
0.72 ± 0.20
17.3 ± 2.04
33.8 ± 3.77
16.1 ± 2.29
10.2 ± 1. 59
18.7 ± 2.19
0.83 ± 0.19
23.0 ± 2.39
45.7 ± 4.51
32.3 ± 3.84
22.3 ± 2.44
17.7 ± 1.67
0.75 ± 0.21
19.7 ± 3.11
41.1 ± 4.13
37.3 ± 3.90
33.5 ± 2.22
27.5 ± 2.50
0.78 ± 0.17
31.8 ± 3.48
48.4 ± 4.56
36.7 ± 3.78
44.2 ± 3.07
42.8 ± 3.11
0.81 ± 0.27
45.0 ± 4.72
49.7 ± 4.38
33.5 ± 3.66
35.1 ± 2.87
36.5 ± 3.03
0.90 ± 0.20
41.6 ± 2.21
49.0 ± 3.65
28.9 ± 3.29
35.5 ± 2.91
39.1 ± 2.72
0.77 ± 0.21
43.6 ± 2.21
40.1 ± 3.77
30.9 ± 3.12
39.5 ± 2.64
38.3 ± 2.32
WS from A. baylyi ADP1 exhibited a broad substrate range that included linear alcohols from C2 to C18 (Table 1). It showed the highest activity towards long-chain alcohols (C12 to C18) and the activity decreased gradually from C12 to C2. The WS activity on 1-hexadecanol was slightly lower than according to a previous study, where the same WS was expressed in S. cerevisiae H1246  using a different expression system, but here we were able to demonstrate its activity on an extended substrate range. The previous report showed that heterologous expression of WS from A. baylyi ADP1, which also has DGAT activity [4, 9], could confer neutral lipid (triacylglycerol (TAG) and wax ester) biosynthetic ability to the host strain, the quadruple mutant S. cerevisiae H1246 (dga1, lro1, are1, are2).
WS from M. hydrocarbonoclasticus DSM 8798 exhibited a lower specificity compared to the other WSs when expressed in S. cerevisiae (Table 1). It showed similar activity towards alcohols from C6 to C18, which is in accordance with a previous study that reported similar activity of the purified protein on C10 to C16 alcohols together with palmitoyl-CoA, albeit with a lower activity on octadecanol . Due to its broader activity, cell extracts from strains expressing this enzyme not only showed a higher performance with long- and medium-chain alcohols ranging from C6 to C18, but also with the short chain alcohols ethanol and butanol compared to strains expressing any of the other WSs, which makes this WS a good candidate for the production of fatty acid esters from short-chain alcohols.
WS from R. opacus PD630 showed a similar activity towards alcohols from C8 to C18, and there was a substantial drop in activity when the alcohol chain length was decreased from C8 to C6 (Table 1). This enzyme has also been expressed in E. coli and has shown low DGAT activity . However, no preference for specific acyl-CoA or alcohol substrates was reported in that study. In E. coli, the enzyme activity was measured using [1-14C] palmitoyl-CoA and 1-hexadecanol  and found to be 4.65 ± 0.04 pmol/mg protein/min, which is clearly lower than the activity found here in S. cerevisiae, which was 28.9 ± 3.29 pmol/mg protein/min (Table 1).
WS from M. musculus C57BL/6 also exhibited a broad substrate range (Table 1). It showed the highest activity towards long- and medium-chain length alcohols (C10 to C18), and the highest activity for C12 alcohol. This enzyme has been expressed in HEK 293 cells, which showed little or no DGAT activity and also showed greatest WS activity with alcohols from C10 to C18 . Here we have shown the successful construction of the mammalian wax esters biosynthetic pathway in a microorganism for the first time, which demonstrates the feasibility of adopting mammalian wax esters in industrial microorganisms.
WS from P. arcticus 273-4 has 50.4% identity to the WS from A. baylyi ADP1 , and has not been characterized before. In this study, its WS activity was confirmed in S. cerevisiae for the first time. Activity with alcohols from C12 to C18 was relatively high, with a drop in activity when the alcohol chain length decreased to 10 carbons. However, whether this enzyme exhibits DGAT activity remains to be elucidated. P. arcticus 273-4 has remarkable activity levels in low temperatures, even at temperatures below 0°C . It has been reported that lowering the growth temperature of batch cultures of S. cerevisiae results in increased levels of lipids  and this enzyme may be useful in this context.
All expressed WSs displayed a general preference for long-chain alcohols and a lower activity for short-chain alcohols, and the specific substrate preference varied among different WSs. Our findings have clearly shown the chain-length specificities and the broad substrate range of the different WSs. It will be possible to harness WS diversity for biotechnological production of individual esters and/or mixtures of esters with a particular combination of chain-length distribution that do not normally occur in nature in a single species. These rationally designed wax ester biosynthetic pathways can then be introduced into S. cerevisiae for industrial production of specific wax esters.
Application of wax ester synthases for biodiesel production
Biodiesel, the primary renewable alternative to petroleum-based diesel fuel, is composed of fatty acid methyl and ethyl esters. The substrate profiles in Table 1 show that all WSs are able to catalyze the esterification of a fatty acid to ethanol to synthesize FAEEs (such as biodiesel). S. cerevisiae is already a good ethanol producer and produces fatty acids with a chain length of mainly 16 or 18 carbon atoms , indicating its ability to provide the required two substrates for WS. As described above, the WSs have the capability to accept ethanol as a substrate, resulting in the formation of FAEEs. Therefore, a de novo biodiesel (FAEEs) biosynthesis process can be established by introducing WS in S. cerevisiae .
Physiological features and biodiesel production in the wax ester synthase-expressing and reference strains
Specific growth rate (/h)
0.44 ± 0.01
0.32 ± 0.01
0.36 ± 0.02
0.34 ± 0.01
0.37 ± 0.01
0.33 ± 0.02
43 ± 3
28 ± 3
40 ± 4
38 ± 3
36 ± 4
38 ± 4
6.9 ± 0.2
5.9 ± 0.2
6.6 ± 0.3
6.5 ± 0.2
6.2 ± 0.3
4.9 ± 0.2
5.0 ± 0.8
6.3 ± 1.2
2.1 ± 0.3
1.3 ± 0.2
2.3 ± 0.4
In the first part of this study, it was demonstrated that WSs have varied activity for a broad range of linear fatty alcohols, including ethanol. The information on specificities of different WSs suggests that the WS from M. hydrocarbonoclasticus, which has the highest relative activity towards ethanol in vitro, would also result in the highest biodiesel production. This was confirmed by the results of the FAEE production. As expected, S. cerevisiae CB2 expressing WS from M. hydrocarbonoclasticus DSM 8798 could produce FAEEs (biodiesel) at a titer of 6.3 mg/L, which is higher than that of any of the other WS-expressing yeast strains (Table 2). The WS from M. hydrocarbonoclasticus should therefore be the choice for constructing a biodiesel producing yeast. Additionally, for most of the WS enzymes, DGAT activity has been observed, which results in the formation of TAG, the predominant storage lipid. A previous report showed that WS from M. hydrocarbonoclasticus DSM 8798 does not have DGAT activity . This property makes it even more suitable for producing biodiesel as it avoids direction of fatty acyl-CoAs towards TAG biosynthesis.
Growth of WS-expressing strains was performed in SD medium lacking uracil and some physiological features are listed in Table 2. The shake-flask experiments proved that all WS-expressing strains displayed the normal diauxic growth pattern. Initially, glucose was consumed, and once the glucose was exhausted, respiration of ethanol resulted in yet another phase of biomass formation. During the growth on glucose, ethanol is accumulated at a high concentration and hence biodiesel production is not limited by ethanol supply; it is most likely that the supply of fatty acyl-CoAs naturally occurring in S. cerevisiae is not sufficient to support biodiesel production at significant amounts.
Acc1p catalyzes the formation of malonyl-CoA, which is the first and crucial step for fatty acid biosynthesis , and it has previously been shown that overexpression results in improved production of malonyl-CoA derived products [11, 12, 28]. The sources of malonyl-CoA are generally supposed to be limited, impeding its utility for overproducing fatty acids [12, 28]. We therefore overexpressed Acc1p to enhance the supply of malonyl-CoA in S. cerevisiae CB2. As a result, the level of biodiesel produced increased about 30%, resulting in a biodiesel titer of 8.2 ± 1.1 mg/L. This clearly shows that it is possible to direct more flux towards biodiesel in yeast expressing WS and this provides interesting prospects for future metabolic engineering of lipid metabolism in order to further enhance biodiesel production through yeast-based fermentation.
We have functionally expressed and characterized five WSs from different species in S. cerevisiae thus constructing cell factories for production of wax esters. The preferred in vitro substrates for the five WS enzyme were identified, and this can be used as a guide to generate specific ester-producing cell factories. Besides the adopted WS, the chain-length compositions of the produced esters are also governed by substrate availability. Additional enzymes and corresponding genes might therefore have to be introduced to ensure de novo synthesis of the required substrates. For example, since S. cerevisiae is not capable of providing long-chain fatty alcohols as substrates, the conversion of fatty acids to fatty alcohols catalyzed by alcohol-forming fatty acyl reductases is required to form de novo wax esters with long-chain alcohols and long-chain acyl-CoAs.
We have used the information of substrate preferences of WSs to produce biodiesel (FAEEs), which requires a WS with activity on ethanol and long-chain fatty acids. WS from M. hydrocarbonoclasticus showed the highest preference for ethanol compared to the other WSs, and could permit the engineered S. cerevisiae to produce biodiesel to a concentration of 6.3 mg/L. We over-expressed acetyl-CoA carboxylase to further enhance biodiesel production, and this resulted in a 30% increase of the titer. Clearly much more work is needed in order to reach commercial targets of biodiesel, but we are confident that our work provides the basis for advancing towards microbial-based production of biodiesel.
Strains and plasmids
List of strains used in this study and their genotypes
E. coli strains
E. coli DH5α
supE44 lacU169 (ϕ80lacZ ΔM15) hsdR17 recA1 endA1 gyrA96 thi-1 relA1
S. cerevisiae strains
MATa MAL2-8c SUC2 ura3-52
P. Kötter, University of Frankfurt, Germany
pSP-GM2 carrying WS gene from A. baylyi ADP1
pSP-GM2 carrying WS gene from M. hydrocarbonoclasticus DSM 8798
pSP-GM2 carrying WS gene from R. opacus PD630
pSP-GM2 carrying WS gene from Mus musculus C57BL/6
pSP-GM2 carrying WS gene from P. arcticus 273-4
pSP-GM2 carrying WS gene from M. hydrocarbonoclasticus DSM 8798 and ACC1
List of primers used in this study
Primer sequence 5'→3'
Wax ester synthase from A. baylyi ADP1 [GenBank: AF529086]
Wax ester synthase from M. hydrocarbonoclasticus DSM 8798 (EF219377)
Wax ester synthase from R. opacus PD630 (GQ923886)
Wax ester synthase from Mus musculus C57BL/6 (AY611032)
Wax ester synthase from P. arcticus 273-4 (YP_263530)
Acetyl-CoA carboxylase [GenBank: NM_001183193] from S. cerevisiae
E. coli recombinant cells were grown in Luria-Bertani medium in the presence of ampicillin (100 mg/L) at 37°C.
Recombinant strains of S. cerevisiae were cultured in 500 mL shake flasks containing 100 mL SD medium lacking uracil and 2% (w/v) glucose at 30°C with reciprocal shaking at 120 rpm, which were inoculated to an optical density at 600 nm of 0.02 from pre-cultures.
The growth was measured by optical density at 600 nm and samples were taken in the early stationary phase. The dry cell weight was determined by filtering 5 ml of the cell culture through a 0.45 μm pore-size nitrocellulose filter (Sartorius Stedim, Göttingen, Germany) and measuring the increased weight of the dry filter. The exponential growth rate was calculated by log-linear regression analysis of the biomass versus cultivation time. The concentrations of residual glucose and external metabolites were analyzed using the Dionex Ultimate 3000 HPLC system (Dionex Softron GmbH, Germering, Germany) with an Aminex HPX-87H column (Bio-Rad, CA, USA) using 5 mM H2SO4 as the mobile phase.
Lipid extraction and thin-layer chromatography
The harvested cells were washed twice with distilled water and freeze-dried for about three days or until they appeared dry. Lipids were extracted from the lyophilized cell pellets using the previously reported method ; 25 μL of heptadecanoic acid ethyl ester was used as the internal standard. FAEEs in the total lipid extracts were purified by preparative TLC  using TLC Silica gel 60 F254plates (Merck, Darmstadt, Germany) and the solvent system of heptane, 2-propanol and acetic acid in the ratio 95:5:1 (v/v/v). Lipids were visualized by being sprayed with 0.05% 2,7-dichlorofluoresceine in ethanol. Heptadecanoic acid, glyceryl triheptadecanoate, cholesteryl palmitate and heptadecanoic acid ethyl ester (Sigma-Aldrich, St. Louis, MO, USA) were used as reference substances for free fatty acids, TAGs, sterol esters and FAEEs, respectively. The spots corresponding to FAEEs were scraped from the TLC plate using a razor-blade and transferred to 12-mL Teflon-lined screw-capped tubes. FAEEs were extracted from the scraped TLC powder with 7 mL of a hexane, methanol and water mixture (3:2:2). After centrifuging for 5 min at 3000 relative centrifugal force, an aliquot of the upper phase was transferred to a GC-vial and used for GC-MS analysis.
Gas chromatography-mass spectrometry analysis of fatty acid ethyl esters
The FAEEs were separated and quantified using a Focus GC DSQ II single quadruple GC-MS (Thermo Fisher Scientific, Waltham, MA, USA). The separation was performed on a Zebron (ZB-WAX) GC column (30 m × 0.25 mm internal diameter, 0.25 μm film thickness; Phenomenex, Macclesfield, UK). A 1-μL portion of the organic phase was injected into the GC-MS using splitless injection (1 μL at 250°C); helium was used as a carrier gas (1 μL/min). The chromatographic separation was initially set at 50°C (1.5 min), then the temperature was increased to 180°C (25°C per min), and finally the temperature was increased to 250°C (10°C per min) and held for 3 min. The mass transfer line and ion source were at 250°C and 200°C, respectively. The FAEEs were detected with electron ionization (70 eV) in scan mode (50 to 650 m/z) and selected ion monitoring mode at m/z 88 and 55 (for quantitative analysis).
The identification of unknown FAEEs was achieved by comparison of their retention times and mass spectrum profiles with known standards (Cayman Chemical, Ann Arbor, MI, USA). The standards used in this study were lauric acid ethyl ester, myristic acid ethyl ester, palmitic acid ethyl ester, palmitoleic acid ethyl ester, heptadecanoic acid ethyl ester, stearic acid ethyl ester and oleic acid ethyl ester. The quantification of FAEEs was performed using the QuanBrowser function in Xcalibur software version 2.0 (Thermo Fisher Scientific).
Enzyme activity assay
Cell-free extracts were prepared using a previously reported fast preparation method for enzyme analysis . WS activities in the extracts were measured in vitro using [1-14C] palmitoyl-CoA and alcohols with varied chain length (C2 to C16) as substrates .
This work was supported by the Chalmers Foundation, Knut and Alice Wallenberg Foundation, the European Research Council and the Mexican National Council of Science and Technology.
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