Raw starch conversion by Saccharomyces cerevisiae expressing Aspergillus tubingensis amylases
Biotechnology for Biofuels volume 6, Article number: 167 (2013)
Starch is one of the most abundant organic polysaccharides available for the production of bio-ethanol as an alternative transport fuel. Cost-effective utilisation of starch requires consolidated bioprocessing (CBP) where a single microorganism can produce the enzymes required for hydrolysis of starch, and also convert the glucose monomers to ethanol.
The Aspergillus tubingensis T8.4 α-amylase (amyA) and glucoamylase (glaA) genes were cloned and expressed in the laboratory strain Saccharomyces cerevisiae Y294 and the semi-industrial strain, S. cerevisiae Mnuα1. The recombinant AmyA and GlaA displayed protein sizes of 110–150 kDa and 90 kDa, respectively, suggesting significant glycosylation in S. cerevisiae. The Mnuα1[AmyA-GlaA] and Y294[AmyA-GlaA] strains were able to utilise 20 g l-1 raw corn starch as sole carbohydrate source, with ethanol titers of 9.03 and 6.67 g l-1 (0.038 and 0.028 g l-1 h-1), respectively, after 10 days. With a substrate load of 200 g l-1 raw corn starch, Mnuα1[AmyA-GlaA] yielded 70.07 g l-1 ethanol (0.58 g l-1 h-1) after 120 h of fermentation, whereas Y294[AmyA-GlaA] was less efficient at 43.33 g l-1 ethanol (0.36 g l-1 h-1).
In a semi-industrial amylolytic S. cerevisiae strain expressing the A. tubingensis α-amylase and glucoamylase genes, 200 g l-1 raw starch was completely hydrolysed (saccharified) in 120 hours with 74% converted to released sugars plus fermentation products and the remainder presumably to biomass. The single-step conversion of raw starch represents significant progress towards the realisation of CBP without the need for any heat pretreatment. Furthermore, the amylases were produced and secreted by the host strain, thus circumventing the need for exogenous amylases.
Declining oil reserves, political instability, climate change concerns and rising CO2 emissions have led to new interest in biofuels to supplement the growing demand for alternative and sustainable sources of transport fuels. Biofuels, which includes bio-ethanol, can be produced from renewable biomass resources that include dedicated crops (e.g. corn), by-products from agricultural processing activities (e.g. sugarcane bagasse) or even organic municipal waste. Although the positive environmental impact and sustainable nature of biofuels render it advantageous over fossil fuels , the cost-effective production of biofuels remains a challenge.
Starch, one of the most abundant polysaccharides in nature, has been used for commercial bio-ethanol production for a number of years, with a relatively mature technology developed for corn in the USA [2, 3]. The USA produced 52.6 billion litres of ethanol fuel in 2011, an increase from 49.2 billion litres in 2010 . However, the limitations of current starch-to-ethanol processes, in particular the energy-intensive liquefaction and substantial amounts of exogenous amylases required for the subsequent enzymatic hydrolysis to maltose and glucose, significantly impact the economic viability of raw starch as feedstock.
Starch consists of α-1,4 linked glucose units with α-1,6 branching points , which require a combination of α-amylases and glucoamylases for complete hydrolysis. The α-amylases (EC 184.108.40.206) hydrolyse the internal α-1,4-bonds of amylose and amylopectin at random, resulting in the production of short polymer chains (dextrins, 10 to 20 glucose units in length) as well as free glucose and maltose units . Glucoamylases (1,4-α-D-glucan glucohydrolase; EC 220.127.116.11) hydrolyse the terminal 1,4-linked α-D-glucopyranosyl units in an exo-fashion successively from the non-reducing end of starch chains to release β-D-glucose [7, 8]. When confronted with raw starch, α-amylase will contribute towards the liquefaction of the starch, whilst glucoamylase will predominantly be responsible for the saccharification of the polymers [9, 10].
Starch hydrolysing enzymes are abundant in the animal, microbial and plant kingdoms, but only a selected few are able to hydrolyse raw starch . Species of Aspergillus, Fusarium, Lipomycetes, Mucor, Penicillium, Rhizopus and Rhizomucor express α- and/or glucoamylases [3, 12, 13] and some Aspergillus and Rhizopus spp. have already been exploited for the commercial production of glucoamylases in the food industry [14, 15]. Raw starch degrading enzymes (RSDE) that can both liquefy and saccharify raw starch can significantly reduce the energy requirements and simplify the production of starch-based biofuels . However, only a few RSDE have been cloned and characterised, e.g. α-amylases from Lipomyces kononenkoae , Streptomyces bovis [18, 19], Cryptococcus and Bacillus , as well as glucoamylases from Rhizopus oryzae [18, 19] and Corticium rolfsii .
Cost-effective conversion of raw starch to biofuels requires the expression of starch-hydrolysing enzymes in a fermenting yeast strain to achieve liquefaction, hydrolysis and fermentation (Consolidated Bioprocessing, CBP) by a single organism . The yeast Saccharomyces cerevisiae remains the preferred organism for ethanol production due to its high ethanol, osmo- and inhibitor tolerance in industrial processes, but it lacks starch degrading enzymes required for the efficient utilisation of starch . This could potentially be overcome with genetic engineering to allow heterologous expression of the enzymes required for the utilization of starch. Successful expression of recombinant cellulases and hemicellulases in S. cerevisiae demonstrated the potential of CBP for cellulolytic feedstock . This yeast is therefore the preferred candidate for the construction of an amylolytic yeast strain able to perform CBP of raw starch.
Co-expression of α-amylases and glucoamylases through extracellular secretion or tethering of enzymes on the cell surface of S. cerevisiae has previously been reported reviewed in . For example, secretion of the Aspergillus awamori GA1 and Debaryomyces occidentalis AMY in a polyploid S. cerevisiae was able to convert 98% of 200 g l-1 soluble starch to yield 80 g l-1 ethanol within 6 days . Although conversion of raw starch by yeast secreting or displaying α-amylases and glucoamylases was previously reported, it involved low substrate loads or conversion rates that will not be economically viable on industrial scale reviewed in . The challenge remains to construct an amylolytic yeast strain that is able to effectively liquefy and saccharify high concentrations of raw starch, as well as ferment the sugars to ethanol within a short time frame.
A screen for potential fungal candidates led to the isolation of an Aspergillus tubingensis strain that displayed significant extracellular amylase activity . Although the glucoamylase gene (glaA) was previously cloned and sequenced from an A. tubingensis (A. niger DSM 823) strain , no further characterisation of the protein has been reported. In this study, the α-amylase (amyA) and glucoamylase (glaA) coding regions were isolated from the A. tubingensis T8.4 strain and expressed in the laboratory strain S. cerevisiae Y294 as well as S. cerevisiae Mnuα1, a semi-industrial strain. The recombinant enzymes were partially characterised and the amylolytic yeast strains evaluated in terms of extracellular amylase activity and conversion of raw starch to ethanol (i.e. consolidated bioprocessing). The co-expressing strains, S. cerevisiae Y294[AmyA-GlaA] and S. cerevisiae Mnuα1[AmyA-GlaA], were also evaluated for their ability to hydrolyse and ferment raw starch at a high substrate loading (200 g l-1).
Results and discussion
Cloning and recombinant expression of amyA and glaA
Amplification of the A. tubingensis amyA cDNA yielded a 1 860 base pair (bp) fragment with 99.8% DNA sequence homology to the A. kawachii α-amylase gene [Genbank: AB008370]. Amplification of the A. tubingensis glaA cDNA yielded a 1 920 bp fragment with 99.3% DNA homology to the A. shirousami glucoamylase cDNA [Genbank: D10460 and E02366], as well as 100% homology over 1 917 bp with the A. tubingensis glucoamylase gene, glaA (GenBank: AY528665). The cDNA sequence of the A. tubingensis α-amylase gene (amyA) and predicted amino acid sequence were deposited [GenBank: JF809672].
The amyA and glaA genes were subcloned individually and combined in yBBH1-derived plasmids (Figure 1, Table 1) and transformed into the laboratory strain S. cerevisiae Y294. The S. cerevisiae strains expressing α-amylase (AmyA) developed clearing zones on solid SC-URA media containing 2% soluble starch (Figure 2), whilst zones were neither expected nor observed for strains expressing the exo-type glucoamylase. Similar results were obtained when the corresponding plasmids were transformed in S. cerevisiae Mnuα1 strain, a haploid strain derived from the industrial MH1000 strain (Table 1).
Characterisation of recombinant AmyA and GlaA
Maximum activities for the recombinant AmyA and GlaA in S. cerevisiae Y294 were observed at pH 4.0 and pH 4.5, respectively, with significant activity detected for both enzymes at pH 3 to 5 (Figure 3). These maxima compared well with those reported for other Aspergillus α-amylase and glucoamylases [3, 16, 29] and are aligned with the growth conditions of S. cerevisiae, which is desirable for a consolidated process . The temperature maxima (Figure 3) for the recombinant AmyA (60°C) and GlaA (70°C) were slightly higher than the 40 to 60°C generally reported for raw starch degrading α-amylases and glucoamylases [3, 16, 31].
Based on the deduced amino acid sequences, the predicted molecular weights of the unglycosylated AmyA and GlaA were 69.6 kDa and 68 kDa, respectively, which are in agreement with previous reports on similar proteins [25, 31, 32]. However, SDS-PAGE analysis of the supernatant indicated a large heterogeneous smear between 110 to 150 kDa for all four strains expressing amyA (Figure 3c), suggesting differentially glycosylated proteins. The putative recombinant GlaA was observed at approximately 90 kDa, which is within the range reported for fungal glucoamylases . This suggests glycosylation of GlaA, probably at one or more of the eight asparagine-linked glycosylation sites predicted for GlaA .
When cultivated in double strength SC-URA medium with 20 g l-1 glucose under aerobic conditions, the extracellular α-amylase activities were similar for S. cerevisiae Y294[AmyA] and Mnuα1[AmyA] (Figure 4a). However, the glucoamylase activity in the supernatant from S. cerevisiae Mnuα1[GlaA] was significantly higher than that of S. cerevisiae Y294[GlaA] (Figure 4b), which could be ascribed to a potentially better secretion ability of S. cerevisiae Mnuα1. Furthermore, co-production of AmyA and GlaA resulted in lower levels of both activities compared to those observed for the individual enzymes. Similar results were observed for the separate and co-expression of a xylanase and xylosidase in S. cerevisiae Y294  and could be ascribed to a number of reasons that were not further investigated in this study.
During starch hydrolysis, α-amylases act first to hydrolyse the internal linkages of the starch molecules and thus provide opportunity for saccharification via the glucoamylases, suggesting that production of native α-amylases would precede that of glucoamylases. In the presence study, the activity of the recombinant α-amylase activity increased slightly faster than that of glucoamylase, which is in agreement with the findings of Yamada et al.  that the activity of the S. bovis α-amylase peaked before that of the R. oryzae glucoamylase when expressed in S. cerevisiae. The delay may be ascribed to the need for dimerization of the glucoamylase prior to its functioning on insoluble starch, as was described for the A. niger glucoamylase .
Fermentation of raw starch
After 10 days of cultivation on 20 g l-1 raw corn starch as sole carbohydrate source under fermentative conditions, simultaneous expression of the A. tubingensis α-amylase and glucoamylase in S. cerevisiae resulted in ethanol yields of 6.67 g l-1 and 9.03 g l-1 by S. cerevisiae Y294[AmyA-GlaA] and S. cerevisiae Mnuα1[AmyA-GlaA], respectively (Figure 5). The [AmyA] and [GlaA] strains converted less than 15% and 50% of the available carbon, respectively, whereas the [AmyA-GlaA] strains exceeded a 70% carbon conversion rate (Table 2). This confirmed that both the α-amylase and glucoamylase are required for efficient ethanol production from raw corn starch. Given the substrate loading of 20 g l-1 raw starch, a yield of 9.03 g l-1 ethanol for S. cerevisiae Mnuα1[AmyA-GlaA] translated into 83% carbon conversion and 80% of the theoretical ethanol yield (Table 2). This was statistically significantly higher than the ethanol yield from S. cerevisiae Y294[AmyA-GlaA] and represented a 4.76-fold improvement relative to the parental S. cerevisiae Mnuα1[BBH1] strain.
Towards the end of the fermentation, 0.31 g l-1 residual glucose was present in the Y294[AmyA-GlaA] culture, suggesting that fermentation could be rate-limiting for the Y294 strain. The S. cerevisiae Y294[AmyA] strain displayed some accumulation of maltose (0.42 and 0.69 g l-1 on day 5 and 8, respectively), whereas the Y294[AmyA-GlaA] metabolised the maltose much quicker (decreasing from 0.33 g l-1 on day 5 to 0.06 g l-1 on day 8) due to the presence of the glucoamylase. In contrast, the Mnuα1 strain has a native maltase, with no interim maltose accumulation observed for the any of the respective strains (data not shown). The recombinant S. cerevisiae Y294 strains produced more acetic acid and glycerol than the Mnuα1 strains, suggesting that the Y294 strains were coping less effectively with the starch fermentation conditions.
The CBP simulation was performed under fermentative conditions with S. cerevisiae Y294[AmyA-GlaA], S. cerevisiae Mnuα1[AmyA-GlaA] and the corresponding control strains using 200 g l-1 raw starch as well as 5 g l-1 glucose to provide an initial carbon source to the cells. The S. cerevisiae Y294[AmyA-GlaA] and Mnuα1[AmyA-GlaA] strains produced 43.33 and 70.07 g l-1 ethanol, respectively (corresponding to 37% and 61% of the theoretical yield) after 5 days of fermentation (Table 2). Although the ethanol concentration did not increase significantly after day 5, glucose accumulation in both strains indicated continued saccharification of the remaining starch (Figure 5). Glucose accumulation in the S. cerevisiae Mnuα1[AmyA-GlaA] fermentation (2.21 and 36.11 g l-1 after 5 and 10 days, respectively) suggested that the fermentation capability of the strain became the limiting factor. The glucose accumulation was less significant for S. cerevisiae Y294[AmyA-GlaA], with only 23.71 g l-1 glucose detected after 10 days. However, the activity of the recombinant GlaA in particular was significantly lower in the Y294 strain (Figure 4), which will reduce its saccharification ability relative to that of the S. cerevisiae Mnuα1[AmyA-GlaA] strain.
Co-expression of the A. tubingensis amyA and glaA genes on episomal plasmids conveyed amylolytic activity to both a laboratory (Y294) and a semi-industrial strain (Mnuα1) of S. cerevisiae. The α-amylase and glucoamylase activities reached 1.51 and 1.16 U ml-1, respectively, in the Mnuα1[AmyA-GlaA] strain, which compare favourably with the 96–190 U ml-1 and 140–340 U ml-1 reported previously for α-amylase and glucoamylase expression in other haploid strains .
The recombinant S. cerevisiae Mnuα1[AmyA-GlaA] strain was superior in its ability to convert 83% of the available carbon in 20 g l-1 raw corn starch and produced 80% of the theoretical ethanol yield after 10 days. At a higher substrate loading of 200 g l-1 raw corn starch, 61% and 57% of the theoretical ethanol yield was achieved within 5 and 10 days, respectively. The starch was completely hydrolysed (saccharified) with 74% converted to released sugars plus fermentation products (mainly ethanol, glycerol and CO2) and the remainder presumably to yeast biomass. The lower ethanol and residual glucose levels for the S. cerevisiae Y294[AmyA-GlaA] fermentation suggested weaker saccharification by the recombinant S. cerevisiae Y294 strain, whereas fermentation capacity is the limiting factor for the S. cerevisiae Mnuα1[AmyA-GlaA] strain.
As different experimental procedures were used in other reports on raw starch-degrading yeasts, it is difficult to compare the results from the present study with those previously reported. The S. cerevisiae YF237 strain, displaying the Rhizopus oryzae glucoamylase and secreting the Streptococcus bovis α-amylase, was reported to produce 51 g l-1 of ethanol from 100 g l-1 of raw corn starch after 60 h of fermentation . A diploid strain displaying both these proteins on the cell surface, produced 46.5 g l-1 of ethanol from 200 g l-1 raw corn starch after 120 h of fermentation , i.e. an ethanol productivity of 0.43 g l-1 h-1. The S. cerevisiae Mnuα1[AmyA-GlaA] strain produced 70.07 g l-1 of ethanol from 200 g l-1 of raw corn starch after 120 h of fermentation (i.e. an ethanol productivity of 0.58 g l-1 h-1), which is significantly higher than that reported for the diploid strain mentioned above. Also, in contrast to the previously mentioned studies, the enzymes in this study were not tethered to the cell wall of precultured cells, but were both produced and secreted during cultivation on raw corn starch.
Bio-ethanol production from starch substrates has surpassed that of sugarcane in recent years and will still play a major role in years to come. Starch is much more readily degradable relative to cellulosic material, which is much more recalcitrant by nature. However, the production of ethanol from starch should not be seen as a “stand alone” option that could potentially threaten food security , but rather as part of an integrated bio-ethanol industry that utilise both starchy and cellulosic feedstocks. More cost-effective starch utilization processes could be implemented when it forms part of a biorefinery concept for whole plant utilisation, which will ultimately contribute to optimum biomass conversion and increased energy efficiency [39, 40]. The single-step conversion of raw starch to ethanol represents significant progress towards the realisation of consolidated bioprocessing without the need for heat pretreatment or exogenous enzymes. Taking into consideration that these were small-scale fermentation studies with no process optimisation, the current performance of the Mnuα1[AmyA-GlaA] strain warrants further development, including chromosomal integration of amyA and glaA in a yeast strain with a stronger fermentation capacity. Furthermore, repeated fermentations will most likely further improve the efficiency of the Mnuα1[AmyA-GlaA] strain, as was previously reported for other amylolytic strains that reached ethanol productivity and yield of 1.61 g l-1 h-1 and 76.6% after 23 cycles .
Strains and media
All strains and plasmids used in the study are listed in Table 1. The A. tubingensis T8.4 strain is protected under patent no. WO/2011/128712 and was deposited in the South African Plant Protection Research Institute’s culture collection [PPRI 13401].
All chemicals, media components and supplements were of analytical grade. Recombinant plasmids were constructed and amplified in Escherichia coli DH5α, cultivated aerobically at 37°C in Terrific Broth or on Luria Bertani agar , containing 100 μg/ml ampicillin when required.
The A. tubingensis T8.4 strain was maintained on MEA plates (50 g l-1 malt extract agar, Sigma-Aldrich) at 30°C. For cDNA preparation, A. tubingensis was cultivated in liquid synthetic complete (SC) medium (1.7 g l-1 yeast nitrogen base without amino acids, Difco Laboratories) with 2% raw corn starch (Sigma-Aldrich) in 125 ml Erlenmeyer flasks for 3 days at 100 rpm.
The S. cerevisiae Y294 and Mnuα1 host strains were cultivated in YPD medium (10 g l-1 yeast extract, 20 g l-1 peptone and 20 g l-1 glucose). Yeast transformants were selected and maintained on SC medium supplemented with amino acids excluding uracil (SC-URA). Aerobic cultivation was performed in 125 ml Erlenmeyer flasks containing 20 ml SC-URA medium on a rotary shaker at 200 rpm at 30°C, unless stated otherwise.
For fermentation studies, pre-cultures were prepared in double strength SC-URA media and transferred to 120 ml glass serum bottles (in triplicate) containing double strength SC-URA media with 20 g l-1 raw corn starch as sole carbohydrate source. For the higher substrate loading, pre-cultures were transferred to 120 ml glass serum bottles (in triplicate) containing double strength SC-URA media with 200 g l-1 raw corn starch and 5 g l-1 glucose.
DNA amplification and sequence analyses
Table 3 lists the primers (Integrated DNA Technologies) used for PCR amplification of the respective genes. Primers AmyA-L + AmyA-R were based on the cDNA sequence of the Aspergillus kawachii amylase gene [GenBank: AB008370], while the GlaA-L + GlaA-R primers were based on the cDNA sequences of the Aspergillus shirousami glucoamylase gene [GenBank: D10460 and E02366]. The A. tubingensis species was verified with PCR amplification of the internal transcribed spacer (ITS) region of its genomic DNA using the universal ITS1 and ITS4 primers .
Total nucleic acid was isolated from A. tubingensis (grown in SC with 2% raw corn starch) using liquid nitrogen  and mRNA was retrieved with the FastTrack 2.0 mRNA Isolation Kit (Invitrogen Corporation, Carlsbad, CA, USA). First strand cDNA was obtained with the RevertAid™ H Minus First Strand cDNA Synthesis Kit (ThermoScientific, South Africa) and used for amplification of the complete cDNA copies of amyA and glaA using a Perkin Elmer Gene Amp® PCR System 2400 and TaKaRa Ex Taq™ (Takara Bio Inc, Japan) as per the manufacturer’s recommendations. The amyA and glaA cDNA fragments were blunt-end ligated into the pTZ57R/T vector (InsTAclone™ PCR Cloning Kit, ThermoScientific), thereafter designated pTZ-AmyA and pTZ-GlaA, respectively. Sequence analysis was done with the ABI PRISM™ 3100 Genetic Analyser, BLAST program (http://blast.ncbi.nlm.nih.gov/Blast.cgi) and DNAMAN (version 4.1) (Lynnon Biosoft).
Standard protocols were followed for DNA manipulation  with enzymes for restriction digests and ligations sourced from Roche Applied Science (Germany). Where applicable, DNA was eluted from agarose gels with the Zymoclean™ Gel Recovery Kit (Zymo Research). The glaA gene was subcloned as an Eco RI-Xho I fragment and the amyA gene as an Eco RI fragment into the corresponding sites of plasmid yBBH1, yielding plasmids yBBH1-AmyA and yBBH1-GlaA, respectively (Figure 1). The ENO1 P -GlaA-ENO1 T cassette was excised from yBBH1-GlaA as a Bam HI-Bgl II fragment and cloned into the Bgl II site on pBBH1-AmyA, generating pBBH1-AmyA-GlaA (Figure 1).
The host strains, S. cerevisiae Y294 and S. cerevisiae Mnuα1, were transformed with the recombinant plasmids using electroporation  with subsequent selection on SC-URA plates. The presence of the respective amylase genes was verified by PCR amplification with gene-specific primers (Table 3).
For qualitative assays, recombinant S. cerevisiae strains were cultured on SC-URA plates containing 2% soluble corn starch for 48 hours at 30°C. The plates were transferred to 4°C to allow precipitation of the residual starch, resulting in clear zones around colonies secreting α-amylases.
For quantitative assays, yeast transformants were cultured in 20 ml double-strength SC-URA medium in 125 ml Erlenmeyer flasks for 3 days with agitation at 200 rpm. The supernatant was harvested and enzyme activity levels were determined after 5 minutes with the reducing sugar assay  in citrate-phosphate buffer containing 0.2% soluble corn starch at 30°C and pH 5. For glucoamylase activity, 50 μl supernatant was incubated for 5 minutes with 450 μl of a 0.2% soluble corn starch solution (30°C, pH 5). The resulting glucose concentration was determined with the D-Glucose Assay Kit (Megazyme, Ireland). Enzyme activity was expressed as U ml-1 supernatant, with one unit defined as the amount of enzyme required to release 1 μmole of glucose per minute. The assays were repeated for S. cerevisiae Y294[AmyA] and Y294[GlaA] at different pH (pH 3, 4, 5, 6 and 7) and temperature values (30°C, 40°C, 50°C, 60°C, 70°C and 80°C).
Recombinant S. cerevisiae strains were cultivated in 20 ml SC-URA medium for 3 days. Two micrograms of lyophilised supernatant were resuspended in 20 μl distilled water, loading buffer was added and the samples denatured by boiling for 3 minutes. The recombinant enzymes were separated on an 8% SDS-polyacrylamide gel using a 5% stacking gel and Tris-glycine buffer . Electrophoresis was carried out at 100 V for ± 90 minutes at ambient temperature and protein species were visualised with the silver staining method .
The precultures were inoculated into double strength SC-URA media with the appropriate carbon sources to a final concentration of 1×106 cells ml-1. Ampicillin (100 μg ml-1) and streptomycin (15 μg ml-1) were added to inhibit bacterial contamination. Agitation and incubation were performed on a magnetic multi-stirrer at 30°C, with regular sampling through a syringe needle pierced through the rubber stopper. Fermentation with high substrate loading was performed similarly, but the double strength SC-URA media containing 200 g l-1 raw corn starch and 5 g l-1 glucose, was inoculated with a 50 g l-1 inoculum (wet weight). The wet cell weight was determined by weighing a cell pellet obtained from centrifugation of the pre-culture at 3 000 × g for 5 minutes.
Ethanol, glycerol, acetic acid, maltose and glucose concentrations were quantified with HPLC, using a Surveyor Plus liquid chromatograph (Thermo Scientific) consisting of a liquid chromatography pump, autosampler and Refractive Index Detector. The compounds were separated on a Rezex RHM Monosaccharide 7.8 × 300 mm column (00H0132-K0, Phenomenex) at 60°C with 5 mM H2SO4 as mobile phase at a flow rate of 0.6 ml min-1. The theoretical CO2 yields were calculated based on the ethanol concentrations.
Raw starch degrading enzymes
Malt extract agar
Synthetic complete lacking uracil
Yeast extract, peptone, dextrose
Polymerase chain reaction
Internal transcribed spacer
Sodium dodecyl sulphate polyacrylamide gel electrophoresis
Basic local alignment search tool
High performance liquid chromatography
Hofvendahl K, Hahn-Hägerdal B: Factors affecting the fermentative lactic acid production from renewable resources. Enzyme Microb Technol 2000, 26: 87-107. 10.1016/S0141-0229(99)00155-6
Gray KA, Zhao L, Emptage M: Bioethanol. Curr Opin Chem Biol 2006, 10: 141-146. 10.1016/j.cbpa.2006.02.035
Sun H, Zhao P, Ge X, Xia Y, Hao Z, Liu J, Peng M: Recent advances in microbial raw starch degrading enzymes. Appl Biochem Biotechnol 2010, 160: 998-1003.
Renewable Fuels Association: Accelerating industry innovation. Washington: 2012 Ethanol industry outlook; 2012.
Tester RF, Karkalas J, Qi X: Starch – composition, fine structure and architecture. J Cereal Sci 2004, 39: 151-165. 10.1016/j.jcs.2003.12.001
Kennedy JF, Cabral JMS, Sá-Correira I, White CA: Starch biomass: a chemical feedstock for enzyme and fermentation processes. In Starch: properties and potential. Edited by: Galliard T. New York: John Wiley & Sons; 1987:115-148.
Belshaw NJ, Williamson G: Specificity of the binding domain of glucoamylase 1. Eur J Biochem 1993, 211: 717-724. 10.1111/j.1432-1033.1993.tb17601.x
Sauer J, Sigurskjold BW, Christensen U, Frandsen TP, Mirgorodskaye E, Harrison M, Roepstorff P, Svensson B: Glucoamylase: structure/function relationship, and protein engineering. Biochem Biophys J 2000, 1543: 275-293. 10.1016/S0167-4838(00)00232-6
Nielsen JE, Borchett TV: Protein engineering of bacterical α-amylases. Biochim Biophys Acta 2000, 1543: 253-274. 10.1016/S0167-4838(00)00240-5
Soni SK, Kaur A, Gupta JK: A solid state fermentation based bacterial α-amylase and fungal glucoamylase system and its suitability for the hydrolysis of wheat starch. Process Biochem 2003, 39: 185-192. 10.1016/S0032-9592(03)00058-X
Van Zyl WH, Bloom M, Viktor MJ: Engineering yeasts for raw starch conversion. Appl Microbiol Biotechnol 2012, 95: 1377-1388. 10.1007/s00253-012-4248-0
Mukerjea R, Slocum G, Mukerjea R, Robyt JF: Significant differences in the activities of α-amylases in the absence and presence of polyethylene glycol assayed on eight starches solubilised by two methods. Carbohydr Res 2006, 341: 2049-2054. 10.1016/j.carres.2006.05.009
Yoon S, Fulton DB, Robyt JF: Formation of covalent β-linked carbohydrate-enzyme intermediates during the reactions catalyzed by α-amylases. Carbohydr Res 2007, 342: 55-64. 10.1016/j.carres.2006.10.028
Jin B, van Leeuwen HJ, Patel B, Doelle HW, Yu Q: Production of fungal protein and glucoamylase by Rhizopus oligosporus from starch processing wastewater. Process Biochem 1999, 34: 59-65. 10.1016/S0032-9592(98)00069-7
Koutinas AA, Wang R, Kookos IK, Webb C: Kinetic parameters of Aspergillus awamori in submerged cultivations on whole wheat flour under oxygen limiting conditions. Biochem Eng J 2003, 16: 23-34. 10.1016/S1369-703X(03)00018-4
Robertson GH, Wong DWS, Lee CC, Wagschal K, Smith MR, Orts WJ: Native or raw starch digestion: a key step in energy efficient biorefining of grain. J Agric Food Chem 2006, 54: 353-365. 10.1021/jf051883m
Ramachandran N, Joubert L, Gundlapalli SB, Cordero Otero PR, Pretorius IS: The effect of flocculation on the efficiency of raw-starch fermentation by Saccharomyces cerevisiae producing the Lipomyces kononenkoae LKA1 -encoded α-amylase. Ann Microbiol 2008, 58: 99-108. 10.1007/BF03179452
Yamada R, Bito Y, Adachi T, Tanaka T, Ogino C, Fukuda H, Kondo A: Efficient production of ethanol from raw starch by a mated diploid Saccharomyces cerevisiae with integrated α-amylase and glucoamylase genes. Enzyme Microb Technol 2009, 44: 344-349. 10.1016/j.enzmictec.2009.01.001
Yamada R, Tanaka T, Ogino C, Fukuda H, Kondo A: Novel strategy for yeast construction using δ-integration and cell fusion to efficiently produce ethanol from raw starch. Appl Microbiol Biotechnol 2010, 85: 1491-1498. 10.1007/s00253-009-2198-y
Lin LL, Ma YJ, Chien HR, Hsu WH: Construction of an amylolytic yeast by multiple integration of the Aspergillus awamori glucoamylase gene into a Saccharomyces cerevisiae chromosome. Enzyme Microb Technol 1998, 23: 360-365. 10.1016/S0141-0229(98)00058-1
Van Zyl WH, Lynd LR, den Haan R, McBride ME: Consolidated bioprocessing for bioethanol production using Saccharomyces cerevisiae . Adv Biochem Eng Biotechnol 2007, 108: 205-235.
Kim HR, Im YK, Ko HM, Chin JE, Kim IC, Lee HB, Bai S: Raw starch fermentation to ethanol by an industrial distiller’s yeast strain of Saccharomyces cerevisiae expressing glucoamylase and α-amylase genes. Biotechnol Lett 2011, 33: 1643-1648. 10.1007/s10529-011-0613-9
Den Haan R, Kroukamp H, Mert MJ, Bloom M, Gorgens JF, van Zyl WH: Engineering Saccharomyces cerevisiae for next generation ethanol production. J Chem Technol Biotechnol 2013, 88: 983-991. 10.1002/jctb.4068
Viktor MJ: The expression of fungal enzymes in Saccharomyces cerevisiae for bio-ethanol production from raw corn starch. MSc thesis: University of Stellenbosch, Department Microbioloyg; 2011.
Manger-Jacob F, Muller T, Janssen M, Hofer M, Holker U: Isolation and sequencing of a new glucoamylase gene from an Aspergillus niger aggregate strain (DSM 823) molecularly classified as Aspergillus tubingensis . Antonie Van Leeuwenhoek 2005, 88: 267-275. 10.1007/s10482-005-3989-5
Sambrook J, Fritsch EF, Maniatis T: Molecular cloning: A laboratory manual. Cold Spring Harbor, New York: Cold Spring Harbor Laboratory Press; 1989:34.
Van Zyl JM, van Rensburg E, van Zyl WH, Harms TM, Lynd LR: A kinetic model for simultaneous saccharification and fermentation of Avicel with Saccharomyces cerevisiae . Biotechnol Bioeng 2011, 108: 924-933. 10.1002/bit.23000
Sadie CJ, Rose SH, den Haan R, van Zyl WH: Co-expression of a cellobiose phosphorylase and lactose permease enables intracellular cellobiose utilisation by Saccharomyces cerevisiae . Appl Microb Biotechnol 2011, 90: 1373-1380. 10.1007/s00253-011-3164-z
Solomon B: Starch hydrolysis by immobilized enzymes/industrial applications. In Advances in biochemical engineering. Edited by: Ghose TK, Fiechter A, Blakebrough N. New York: Springer-Verlag; 1978:131-177.
Murai T, Yoshino T, Ueda M, Haranoya I, Ashikari T, Yoshizumi H, Tanaka A: Evaluation of the function of arming yeast displaying glucoamylase on its cell surface by direct fermentation of corn to ethanol. J Ferment Bioeng 1998, 6: 569-572.
Gupta R, Gigras P, Mohapatra H, Goswami VK, Chauhan B: Microbial α-amylases: a biotechnological perspective. Process Biochem 2003, 38: 1599-1616. 10.1016/S0032-9592(03)00053-0
Kaneko A, Sudo S, Takayasu-Sakamoto Y, Tamura G, Ishikawa T, Oba T: Molecular cloning and determination of the nucleotide sequence of a gene encoding an acid-stable α-amylase from Aspergillus kawachii . J Fermen Bioeng 1996, 81: 292-298. 10.1016/0922-338X(96)80579-4
Suresh C, Dubey AK, Srikanta S, Kumar US: Characterization of starch hydrolyzing enzyme of Aspergillus niger . Appl Microbiol Biotechnol 1999, 51: 673-675. 10.1007/s002530051450
La Grange DC, Claeyssens IM, Pretorius IS, van Zyl WH: Degradation of xylan to D -xylose by recombinant Saccharomyces cerevisiae co-expressing the Aspergillus niger β-xylosidase ( xlnD ) and the Trichoderma reesei xylanase II ( xyn2 ) genes. Appl Environ Microbiol 2001, 67: 5512-5519. 10.1128/AEM.67.12.5512-5519.2001
Jørgensen AD, Nøhr J, Kastrup JS, Gajhede M, Sigurskjold BW, Sauer J, Svergun DI, Svensson B, Vestergaard B: Small angle X-ray studies reveal that Aspergillus niger glucoamylase has a defined extended conformation and can form dimers in solution. J Biol Chem 2008, 283: 14772-14780. 10.1074/jbc.M801709200
Khaw TS, Katakura Y, Koh J, Kondo A, Ueda M, Shioya S: Evaluation of performance of different surface-engineered yeast strains for direct ethanol production from raw starch. Appl Microbiol Biotechnol 2006, 70: 573-579. 10.1007/s00253-005-0101-z
Yamakawa S, Yamada R, Tanaka T, Ogino C, Kondo A: Repeated fermentation from raw starch using Saccharomyces cerevisiae displaying both glucoamylase and α-amylase. Enzyme Microb Technol 2012, 50: 343-347. 10.1016/j.enzmictec.2012.03.005
Srinivasan S: The food v. Fuel debate: a nuanced view of incentive structures. Renewable Energy; 2009:950-954.
Gallezot P: Direct routes from biomass to end-products. Catal Today 2011, 167: 31-36. 10.1016/j.cattod.2010.11.054
Hatti-Kaul R: Biorefineries – a path to sustainability? Crop Sci 2010, 50: S152.
White TJ, Bruns T, Lee S, Taylor J: Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In PCR protocols. Edited by: Innis A, Gelfand DH, Sninsky JJ. San Diego: Academic Press; 1990:315-322.
La Grange DC, Pretorius IS, van Zyl WH: Expression of a Trichoderma reesei beta-xylanase gene ( XYN2 ) in Saccharomyces cerevisiae . Appl Environ Microbiol 1996, 62: 1036-1044.
Cho KM, Yoo YJ, Kang HS: δ-Integration of endo/exoglucanase and β-glucosidase genes into the yeast chromosomes for direct conversion of cellulose to ethanol. Enzyme Microb Technol 1999, 25: 23-30. 10.1016/S0141-0229(99)00011-3
Miller GL: Use of dinitrosalicyclic acid reagent for determination of reducing sugars. Anal Chem 1959, 31: 426-428. 10.1021/ac60147a030
O'Connell K, Stults JT: Identification of mouse liver proteins on two-dimensional electrophoresis gels by matrix-assisted laser desorption/ionization mass spectrometry of in situ enzymatic digests. Electrophoresis 1997, 18: 349-359. 10.1002/elps.1150180309
The authors would like to thank the South African National Energy Research Institute (SANERI), the Department of Science and Technology (DST) and the National Research Foundation (NRF) for financial support to the Chair of Energy Research: Biofuels and other clean alternative fuels. This work is based on the research supported in part by the National Research Foundation of South Africa (numbers 61170, 76597 to MVB and 68955 to WHvZ).
The authors declare that they have no competing interests.
MJV participated in the design of the study, performed the experimental work and analyses related to the cloning and characterisation in Y294, and drafted the manuscript. SHR performed the experimental work and analyses related to subcloning and expression in Mnuα1, participated in the design of the study and revised the manuscript. WHVZ and MVB participated in the design of the study and revised the manuscript. All authors read and approved the final manuscript.
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Viktor, M.J., Rose, S.H., van Zyl, W.H. et al. Raw starch conversion by Saccharomyces cerevisiae expressing Aspergillus tubingensis amylases. Biotechnol Biofuels 6, 167 (2013). https://doi.org/10.1186/1754-6834-6-167