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Volume 2013 (2013), Article ID 129268, 10 pages
Archaeal Production of Polyhydroxyalkanoate (PHA) Co- and Terpolyesters from Biodiesel Industry-Derived By-Products
1Institute of Biotechnology and Biochemical Engineering, Graz University of Technology, Petersgasse 12, 8010 Graz, Austria
2ARENA Arbeitsgemeinschaft für Ressourcenschonende und Nachhaltige Technologien, Inffeldgasse 23, 8010 Graz, Austria
3Institute of Chemistry, Karl-Franzens University of Graz, Heinrichstrasse 28, 8010 Graz, Austria
4Polymer Competence Center Leoben GmbH, c/o Petersgasse 12, 8010 Graz, Austria
5Institute for Chemistry and Technology of Materials, Graz University of Technology, Stremayrgasse 9, 8010 Graz, Austria
Received 16 August 2013; Accepted 30 September 2013
Academic Editor: F. Rodriguez-Valera
Copyright © 2013 Carmen Hermann-Krauss et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The archaeon Haloferax mediterranei was selected for production of PHA co- and terpolyesters using inexpensive crude glycerol phase (CGP) from biodiesel production as carbon source. CGP was assessed by comparison with the application of pure glycerol. Applying pure glycerol, a copolyester with a molar fraction of 3-hydroxybutyrate (3HB) of 0.90 mol/mol and 3-hydroxyvalerate (3HV) of 0.10 mol/mol, was produced at a volumetric productivity of 0.12 g/Lh and an intracellular PHA content of 75.4 wt.-% in the sum of biomass protein plus PHA. Application of CGP resulted in the same polyester composition and volumetric productivity, indicating the feasibility of applying CGP as feedstock. Analysis of molar mass distribution revealed a weight average molar mass of 150 kDa and polydispersity of 2.1 for pure glycerol and 253 kDa and 2.7 for CGP, respectively; melting temperatures ranged between 130 and 140°C in both setups. Supplying γ-butyrolactone as 4-hydroxybutyrate (4HB) precursor resulted in a poly[(R)-3-hydroxybutyrate-co-(R)-3-hydroxyvalerate-co-4-hydroxybutyrate] (PHBHV4HB) terpolyester containing 3HV (0.12 mol/mol) and 4HB (0.05 mol/mol) in the poly[(R)-3-hydroxybutyrate] (PHB) matrix; in addition, this process runs without sterilization of the bioreactor. The terpolyester displayed reduced melting (melting endotherms at 122 and 137°C) and glass transition temperature (2.5°C), increased molar mass (391 kDa), and a polydispersity similar to the copolyesters.
Polyhydroxyalkanoates (PHAs) attract increasing attention as biobased, biocompatible, and biodegradable “green plastics.” This is due to their promising material properties and sound integration of their life cycle into nature’s closed carbon balance; neither their production nor their application or degradation causes negative ecological impacts . These polyoxoesters of hydroxyalkanoic acids (HAs) constitute reserves for carbon and energy accumulated by various prokaryotic genera among eubacteria and archaea . Factors generally supporting intracellular PHA biosynthesis are, similar to the accumulation of other microbial storage compounds such as glycogen, a high intracellular energy charge, characterized by high pools of acetyl-CoA, ATP, or NAD(P)H. Such conditions result from a sufficient supply of carbon substrates together with suboptimal availability of growth-determining components such as nitrogen, phosphate, or growth-essential micronutrients .
Depending on the provided carbon source and the microbial production strain, the material properties of PHA resemble those of crystalline thermoplasts to flexible elastomers, latexes, and even high-performance, functional polymers; hence, they can be used for further processing towards vendible items. After their life span, PHAs are completely biodegradable to CO2 and water as the final products of mineralization . Their exact material properties highly depend on the composition on the monomeric level. Here, rather crystalline, thermoplastic short chain length PHAs (scl-PHAs), consisting of HAs with 3 to 5 carbon atoms, are distinguished from elastomeric medium chain length PHAs (mcl-PHAs) which constitute polyesters of HAs consisting of 6 to 14 carbon atoms. Hence, they exhibit the potential to replace various petrol-based competitors in several bulk and niche segments of the plastic market in the near future .
The implementation of “white biotechnology” for production of frequently used materials such as bioplastics can be regarded as really encouraging for sustainable industrial development, although, for a range of products, especially bulk materials, biotechnological production strategies still have not yet passed the threshold for economic feasibility. Particularly, the economics of PHA production is to a high extent, namely, up to 50% of the entire production costs, defined by costs met for the supply of raw materials, especially the carbon substrates. This can easily be understood considering the fact that PHA accumulation occurs under aerobic conditions, resulting in high losses of carbon substrate by intracellular respiration. Hence, mainly due to a considerable loss of carbon by CO2 formation and excretion of water soluble metabolites, only a maximum amount below half of the carbon source is directed towards cell biomass growth and PHA accumulation. Classically, PHAs are produced starting from prized substrates of high nutritional value, such as glucose, starch, or edible oils . Similar to the contemporary “fuel versus food” or “tank versus plate” controversy, this causes severe ethical conflicts considering the huge number of persons starving worldwide. Application of substrates of nutritional value for production of biopolymers or biofuels has an unquestioned impact on food prices, acting as a driving force for inflation, thus making food nearby unattainable for numerous people. As an outdoor, PHAs can be produced starting from inexpensive renewable resources as carbon feedstocks. For this purpose, pure saccharides, lipids, agroindustrial waste like hydrolysis products of (ligno)cellulosics, starch, crude glycerol phase (CGP) from biodiesel production or glycerol pitch from petrochemistry, lipids, whey lactose from dairy industry, alcohols like methanol, methane from anaerobic digestion of organic waste, and CO2 from industrial effluents are available at sufficient quantities [6–9]. The utilization of waste materials as feedstocks for PHA biosynthesis constitutes a viable strategy for cost-efficient biopolymer production and supports various agro-industrial branches to overcome the existing waste disposal problems.
In the last years, a considerable increase in the production of biodiesel has caused a sharp decrease in the cost of glycerol, the main by-product of biodiesel manufacturing; about 10% of glycerol accrues considering the quantity of lipids used as feedstock [10, 11]. As a result, glycerol has become a very attractive substrate for “white biotechnology.” Additionally, because carbon atoms in glycerol are higher reduced than in carbohydrates, cells using glycerol are in a more reduced physiological state, favoring intracellular polymer synthesis. In general, glycerol can be regarded as one of the most favorable substrates for generation of the PHB precursor acetyl-CoA. CGP from the biodiesel production contains up to 60% of glycerol and various impurities such as water, methanol, hydroxide residues, salts, fatty acids, and esters . As methanol constitutes a severe cell toxin for many microbial strains, the selection of an adequate production strain that tolerates a certain concentration of this alcohol is desired. This is the case for Methylomonas extorquens, an organism that, if cultivated in CGP, first converts methanol before utilizing glycerol as carbon substrate, as previously reported by Braunegg and colleagues .
The use of glycerol for microbial PHA synthesis has been analyzed in natural PHA producers, such as, among others, Methylobacterium rhodesianum and Ralstonia eutropha , Methylomonas extorquens , Azohydromonas lata DSM 1124 , several Pseudomonas strains like Ps. putida KT2442 , the recently described Zobellella denitrificans , Cupriavidus necator [17, 18], Novosphingobium capsulatum , and Bacillus sp. . Glycerol has also been investigated as a substrate for PHB synthesis in recombinant E. coli carrying the PHB biosynthetic genes from Streptomyces aureofaciens , Burkholderia cepacia ATCC 17759 , the archaea Haloarcula sp. IRU1 , Halomonas sp. KM-1 , and Haloferax mediterranei DSM 1411 .
Beside a convenient inexpensive raw material, efficient PHA production requires stable, robust, and fast-growing microbial production strains. The archaeon Haloferax mediterranei was isolated at the Mediterranean coast and first exhaustively described as PHA producer by Rodriguez-Valera and Lillo . Within the phylum of the Euryarchaeota, the organism belongs to the class of halobacteria, the extremely halophile branch of the domain Archaea. This strain not only tolerates high salinity, but even requires 2–5 M NaCl for growth. The genus Haloferax is of special interest due to the faster growth compared to related organisms, its high PHA-productivity, the high quality of PHA produced by the strain, and features a broader substrate spectrum; it is known to convert several mono-, di-, and polysaccharides [26, 27], inter alia whey-derived sugars, and several starch-rich feedstocks [28, 29]. In addition to biopolyesters, the strain is reported to produce a high-value extracellular polysaccharide (EPS) that might by applied in food technology due to its xanthan-like properties [2, 25]. This is well visible by the mucous character of H. mediterranei colonies growing on solid media; due to the high content in bacterioruberins, a group of C50 carotenoides, these colonies are pinkish to reddish shaded . EPS production negatively impacts PHA biosynthesis due to the partial shift of carbon towards EPS instead of biopolyester production. Recently, it was demonstrated how to overcome this problem by knocking out part of the gene cluster responsible for EPS biosynthesis; compared to the wild type strain, this novel-engineered H. mediterranei strain featured enhanced PHA biosynthesis rate of about 20%. . Only recently, the complete sequence of the H. mediterranei genome was deciphered and reported .
1.1. Aim of the Study
Based on the first reproducible results for archaeal PHA production on CGP , the presented work compares PHA copolyester biosynthesis on pure glycerol and CGP to biosynthesis of PHA terpolyesters using CGP together with the 4-hydroxybutyrate (4HB) precursor γ-butyrolactone (GBL). Haloferax mediterranei was selected as robust archaeal production strain. The work encompasses kinetic process analysis and a detailed characterization of the obtained material properties regarding thermoanalysis and molar mass distribution. The elaborated data are discussed in comparison with literature data for PHA production by H. mediterranei on glucose, whey, and starch-based materials and shall be further used for designing a pilot-scale production plant for semi-industrial archaeal PHA production from CGP.
2. Materials and Methods
2.1. Production Strain
A lyophilized culture of Haloferax mediterranei DSM 1411 was purchased from DSMZ culture collection (Braunschweig, Germany).
2.2. Raw Material
CGP from tallow-base biodiesel production was obtained from Argent Energy (UK) Limited, UK.
2.3. Media Composition and Cultivation Conditions
The strain was cultivated in a 10 L bioreactor (L 1523, BIOENGINEERING, Wald, Switzerland) for production of poly[(R)3-(hydroxybutyrate-co-(R)-3-hydroxyvalerate) (PHBHV) copolyesters or poly[(R)-3-hydroxybutyrate-co-(R)-3-hydroxyvalerate-co-4-hydroxybutyrate) (P(HBHV4HB).
The basic saline medium was composed as follows (g/L): NaCl, 150; MgCl2*6H2O, 13.0; KCl, 4.00; CaCl2*2H2O, 13.0; FeCl3, 0.0025; trace element solution SL6 , 1; MgSO4*7H2O, 20.0; NaHCO3, 0.20; NaBr, 0.50; complex nitrogen source (yeast extract/casein peptone, 1 : 1), 5.0; carbon source (glycerol or CGP, resp.), 10 g/L. In the case of P(HBHV4HB) production (fermentation F3), γ-butyrolactone (GBL) was added stepwise by addition of a total of 14 small portions during the phase of predominant PHA biosynthesis in order to keep the actual GBL concentration in a range of approximately 0.5 g/L (starting from 58 h until 168 h of cultivation; entire addition of GBL: 60.5 mL).
Inoculum cultures were prepared in 1 L baffled shaking flasks containing 250 mL saline medium, starting with 10 g/L glycerol as sole carbon source and 5 g/L complex nitrogen source. The pH value was adjusted to 7.0, and the cultures were continuously shaken for 48 h at 37°C. Bioreactor fermentations were started with 10 g/L carbon source (pure glycerol or CGP) in the case of fermentations F1 and F2 and 2 g/L in the case of fermentation F3; 5 g/L complex nitrogen source (yeast extract/casein peptone [1 : 1]) for each fermentation setup. In order to achieve phosphate limiting conditions as the most efficient factor provoking PHA synthesis in H. mediterranei , the only phosphate source derived from phosphate content presents in yeast extract. Further additions of substrates were done when necessary to keep the concentration of glycerol in a range between 10 and 20 g/L. The experiments were carried out under controlled conditions at a pH value of 7.0, a temperature of 37°C, and oxygen tension of about 20% of air saturation controlled by the agitation speed of the stirrer and the aeration rate.
2.4. Determination of Glycerol and GBL
A HPLC equipment consisting of a thermostated Aminex HPX 87H column (80°C), a HP 7673 Controller, a JASCO 880-PU intelligent HPLC pump, and a BISCHOFF RI-Detector 8110 were used. The elution solvent was 0.005 M H2SO4, with a flow of 0.60 mL min−1. Pure glycerol and GBL were used as external standards.
2.5. Determination of PHA
PHA content in cells was analyzed by acidic methanolysis according to Braunegg’s method . The gas chromatographic analysis was performed with a 6850 Network GC System (Agilent Technologies), equipped with a 25 m × 0.32 mm × 0.52 μm HP5 capillary column and a flame ionization detector (FID). Helium (Linde; purity = 4.6) was used as carrier gas with a split ratio of 1 : 5, hydrogen (Linde; purity = 5.0) and synthetic air (Linde; purity = “free of hydrocarbons”) as detector gases, and nitrogen (Linde; purity = 5.0) as auxiliary gas.
The following protocol was used: initial temperature: 50°C; rate 1: 15°C/min; final temperature 1: 60°C; rate 2: 2°C/min; final temperature 2: 80°C; final temperature 3: 300°C; final time 3: 5 min. mcl-PHA were determined as follows: initial temperature: 50°C; rate 1: 15°C/min; final temperature 1: 200°C; final time 1 : 10 min; rate 2 : 15°C/min; final temperature 2: 240°C; final time 2: 4 min final temperature 3: 300°C; final time 3: 5 min. The determination of all samples was done in duplicate. Methyl esters of PHA-building blocks were analyzed using a flame ionization detector (FID). Helium acted as carrier gas, the applied split ratio amounted to 1:5, 2 µL were used as injection volume.
As reference materials, poly[(R)-3HB-co-15.6%-(R)-3HV] (BIOPOL, ICI, UK) and poly[(R)-3HB-co-11.2%-4HB] (GreenBioTM, Tianjin Green Bioscience & DSM, PR China) were used as PHA references; hexanoic acid acted as internal standard.
2.6. PHA Extraction
After the stop of the bioreactor cultivations, cells were in situ pasteurized, centrifuged, frozen, and lyophilized for 24 hours. Biomass was degreased overnight by a Soxhlet extraction with ethanol, air-dried, and subsequently Soxhlet extracted overnight with CHCl3; extracted polymer and remaining biomass were finally analyzed by GC to determine the purity and the completeness of the extraction.
2.7. Determination of Molar Mass Distribution and Thermal Analysis Characterization
Molar masses, expressed as weight average molar mass and number average molar mass , were measured on a Jasco PU-1580 HPLC connected to a Jasco 830-RI detector and equipped with two PLgel 5 μm mixed C columns, with CHCl3 as solvent at a flow rate of 1.0 mL/min. Monodisperse polystyrene was used as external standard. Polydispersity was defined as the ratio of to .
Thermal analysis characterization was performed on a Mettler TA 4000 System instrument consisting of DSC-30 Differential Scanning Calorimeter, TGA-50 furnace with M3 microbalance, and TA72 GraphWare software. Measurements were carried out at 80 mL min−1 nitrogen of flow rate according to the following protocol: first, second, and third heating from −30 to 200°C at 10°C min−1 first cooling (quenching after the first heating) from 200 to −30°C at 100°C min−1, and the second cooling from 200 to −30°C at 10°C min−1.
2.8. Determination of Proteins
After disrupting cells by ultrasonic treatment, proteins were monitored according to Lowry’s method .
3. Results and Discussion
3.1. F1: Production of P(HBHV) from Pure Glycerol
As single carbon source pure glycerol (10 g/L) was used, yeast extract/casein [1 : 1] (5 g/L) acted as complex nitrogen and phosphate source. Preexperiments performed by the authors of this study demonstrated that an exceeding of the substrate concentration beyond 20 g/L does not show any negative impact due to the high osmophilicity of the organism. Glycerol concentration during the fermentation therefore was kept between 10 and approximately 20 g/L. The time courses of glycerol as well as the concentrations of PHA and residual biomass (expressed as protein) are illustrated by the fermentation pattern in Figure 1. At the end of the fermentation, a maximum PHA concentration of 15.2 g/L and a protein concentration of 5.0 g/L were reached, corresponding to a maximum content of PHA in biomass (expressed as sum of protein and PHA) of 75%. Kinetic data are shown in Table 1, comparing the results of fermentation F1 with the other accomplished experiments and data from the literature using different main carbon sources. Due to the fact that specific production rate in the early production phase clearly differs from in the late production phase, and were introduced to describe this phenomenon. Here, amounted to 0.03 g/gh, whereas was calculated with 0.02 g/gh, respectively.
The volumetric productivity for PHA amounted to 0.12 g/Lh for the entire process that is drastically lower than reports on glucose  but higher than the valued reported for whey-stemming substrates [33, 36]. The highest productivity was observed between and 80 h (0.21 g/Lh). Until the end of the process ( h), productivity significantly decreased to 0.06 g/Lh. The yield for conversion of glycerol towards PHA amounted to 0.37 g/g that is very similar to data for semi-industrial eubacterial PHA production from hydrolyzed cane sugar (0.33 g/g)  and significantly higher if compared to reported PHA production on glucose and inorganic nitrogen and phosphate sources (0.26 g/g) .
The investigated organism is able to directly produce 3-hydroxyvalerate (3HV) units from glycerol, resulting in the accumulation of PHBHV containing about 10 mol-% of 3HV. In most cases, 3HV production requires the application of structurally related precursor substrates like propionic acid or valeric acid; these precursors significantly raise the production costs. In the case of H. mediterranei, the percentage of 3-HV in the polyester remained at a constant level of 10 mol-% during the production phase. This rare copolyester production from unrelated substrates can be explained by the particularities of the gene cluster (phaECHme) encoding H. mediterranei PHA synthase. Lu and colleagues revealed that in H. mediterranei a novel member of the class III PHA synthases, composed of PhaCHme and PhaEHme, accounts for PHBHV synthesis . More recently, Han and colleagues discovered that strain uses multiple pathways for propionyl-CoA biosynthesis as precursor for 3HV biosynthesis, including the citramalate/2-oxobutyrate pathway, the aspartate/2-oxobutyrate pathway, the methylmalonyl-CoA pathway, and a novel 3-hydroxypropionate pathway . The metabolic pathways supplying the required intracellular precursors for PHBHV production by H. mediterranei were first investigated and described in detail by Feng and coworkers . Additional investigation by whole-genome analysis has revealed eight potential β-ketothiolase genes in H. mediterranei, among which the PHBV-specific BktB and PhaA were identified by gene knockout and complementation analysis .
For most applications, a 3-HV share of at least 10 to more than 20 mol-% is necessary in order to sufficiently lower crystallinity of the product  and thus facilitate polyester processing. The formation of considerable shares of 3HV without the need for precursor substrates contributes to lowering the production costs of high-quality biopolyesters.
Molar mass distribution was determined at the end of the fermentation with a weight average molecular weight kD and a polydispersity index of of 2.1. The received molar mass is lower than reported molar masses for polyesters produced, for example, from carbohydrates like glucose  or whey lactose . Madden and coworkers have proven that substances like glycerol or glycols cause a termination of chain propagation by covalent linking at the carboxyl terminus of PHA “endcapping effect”, resulting in lower molar masses . Thermoanalysis of the polymer revealed a glass transition temperature of 4.3°C, a cold crystallization point at 67.2°C, and two melting endotherms and at 130.2 and 140.6°C. The appearance of multiple melting endotherms is a typical finding for H. mediterranei PHA and is also reported for PHA production on other carbon substrates like whey or glucose [25, 28]. By fractionation using chloroform/acetone, Don and colleagues revealed that the produced PHBHV consists of two copolymers of different composition, different melting points, and different molar masses .
3.2. F2: Production of PHBHV from Glycerol Liquid Phase (CGP) from Biodiesel Production
In this case, pure glycerol was replaced by CGP as sole carbon source. Figure 2 shows the fermentation pattern, including time curves for glycerol, PHA, and protein.
A comparison of the results with the previous fermentation F1 reveals a specific growth rate of 0.06 h−1, significantly lower than on pure glycerol (0.10 h−1). This might be due to inhibiting compounds in GGP remaining from the transesterification process, such as methanol or lipid residues. Moreover, specific production rate in the early production phase was slightly lower than that on pure glycerol, whereas specific production rates in the late production phase were equal (see Table 1). The yield for PHA conversion towards PHA (0.19 g/g) was lower than that for pure glycerol (0.37 g/g). Looking at the final concentration for protein (5.5 g/L versus 5.0 g/L) and PHA (16.2 g/L versus 13.4 g/L), significantly higher concentrations was obtained using CGP than in the case of pure glycerol; volumetric productivity for the entire process were identical for both processes(0.12 g/Lh; Table 1). The highest productivities were observed between and 147 h (0.16 g/Lh); until the end of the process, productivity decreased to 0.03 g/Lh.
The composition of the copolyester produced from CGP was similar to the one produced from pure glycerol (F1) and to the literature data for glucose  and whey lactose . Also here, the strain was able to produce 3-HV units for P(HBHV) copolyester synthesis with a molar 3-HV fraction in the copolyester of 0.10. Molar mass and molar mass distribution were determined at the end of the fermentation with kDa and . Similar to the values for the F1 polyester, thermoanalysis of the polymer showed a glass transition temperature of 7.0°C, a cold crystallization point at 64.5°C, and two melting endotherms and at 128.7 and 138.8°C (see Table 1).
3.3. F3: Production of P(HBHV4HB) from CGP and GBL
In order to further improve the thermomechanical polyester properties, it was intended to produce a PHBHV4HB terpolyester consisting of the building blocks 3HB, 3HV, and 4HB. CGP was used as main carbon source for production of biomass, 3HB and 3HV, and GBL acted as precursor for 4HB production. This is a similar approach to the, until today, only reported archaeal terpolyester production by H. mediterranei on hydrolyzed whey lactose plus GBL . According to literature reports, PHA terpolyesters harboring 4HB building blocks display advantageous properties if compared to PHBHV copolyesters, especially in terms of reduced secondary crystallization (typical of PHB and PHBHV) and increased elongation to break and tensile strength [45, 46]. GBL was added stepwise as cosubstrate after the end of the exponential growth phase (after 58 hours of cultivation; see Materials and Methods) to reach approximately 5% 4-HB in the polymer; finally, a terpolyester poly-[(R)-3HB-co-10%-(R)-3HV-co-5%-4HB) was obtained. Furthermore, this fermentation was run at reduced sterility precautions (no sterilization of the bioreactor equipment; only media components were heat sterilized in autoclaves) to demonstrate the high robustness of the applied production strain against contamination by microbial competitors. During the entire fermentation period, the culture maintained monoseptic, as surveyed microscopically. This is due to the high salinity of the cultivation medium counteracting the growth of most microbes. Considering the fact that microbial contamination is one of the major technical risks for continuous biotechnological processes, H. mediterranei appears especially suitable for such process mode, as already suggested previously .
The initial concentration of glycerol was 2 g/L; additional CGP was added by feed pulses in order to maintain this concentration. After the stop of growth phase (48 h), the glycerol concentration was increased up to 15 g/L (see Figure 3). Yeast extract and casein hydrolysate (in a 1 : 1 ratio) were added after 6, 18, 26, 31.5, 35.5, 42.5, 52, 68, and 76.5 hours.
Figure 3 illustrates the glycerol concentration, protein production, cell dry mass (expressed as sum of protein and PHA), and polymer production. After a quite short lag phase, the exponential growth started after 6 hours. After 24 hours a protein content of 1.5 g/L was obtained; subsequently, the time curve of protein became linear. During the phase of exponential growth, a max. specific growth rate of 0.20 h−1 was observed that constitutes the highest value of the investigated setups. This indicates that low starting concentrations of glycerol are beneficial for a short lag phase and fast cell growth. After the final addition of complex nitrogen and phosphate source after 76.5 hours, protein concentration increased again. Polymer production and the percentage of polymer in CDM started to increase at an early stage after 12 hours, reaching a level of 68.5% PHA in CDM after 68 hours, and maintained this amount until the end. A final protein concentration of 5.6 g/L was obtained at the end of fermentation (191 h), while the final polymer concentration amounted to 11.1 g/L. The volumetric productivity was calculated with 0.10 g/Lh considering the entire fermentation process which is slightly lower if compared to the prior PHBHV productions and terpolyester production from whey and GBL . The highest productivity was observed between 58 and 191 h of cultivation; during the early stage of the fermentation ( to 58 h), only low productivity was observed (0.07 g/Lh) due to the restricted supply with carbon source during this phase that favored protein formation. The yield amounted to 0.16 g/g lower than it was the case for copolyester production and literature reports (see Table 1).
GBL was first added continuously in order to obtain a homogenous distribution of 4HB in the terpolyester; GBL addition was accomplished from 58 hours until the end of the process. At the end of fermentation after 191 hours, the concentrations of produced HA-building blocks amounted to 9.3 g/L 3HB, 1.3 g/L 3HV, and 0.5 g/L 4HB, respectively; Figure 4 reflects the composition of the polymer during fermentation. The molar fraction of 3HV in PHA reached a stable value of 0.09–0.12 mol/mol. 4HB building blocks were detected immediately after the start of GBL feeding; the molar share increased steadily to reach a final value of 0.05 mol/mol at the end of fermentation, almost identical to the value in the whey-stemming terpolyester .
Molar mass ( kDa; the highest value of the three described setups) and molar mass distribution (; similar to the values for the copolyesters produced in F1 and F2) were determined at the end of the fermentation. Thermoanalysis of the terpolyester by DSC revealed a glass transition temperature of 2.5°C, a cold crystallization point at 64.3°C, and two melting endotherms and at 122.4 and 137.1°C. The start of polymer decomposition was 285°C. This is similar to the value obtained for the copolyester in F2 but significantly higher than that for the copolyester obtained from pure glycerol in the setup F1 (about 240°C). Comparing the data with the copolyesters from F1 and F2, the terpolyester showed a lower glass transition temperature and a decomposition point about 5°C higher.
The presented experimental results demonstrate that expensive carbon sources for archaeal PHA production can be replaced by the inexpensive surplus product CGP from the biodiesel production process. Comparing CGP to pure glycerol phase does not reveal any negative effect in terms of productivity or polyester properties. The applied production strain H. mediterranei features the advantage to utilize inexpensive surplus products of industrial origin, lower energy requirements due to negligible sterility precautions, and the production of 3HV-containing copolyesters from unrelated carbon sources like glycerol. Further, similar to the application of sugars from hydrolyzed whey as main carbon source, the organism is able to accumulate PHBHV4HB terpolyesters when provided with adequate 4HB precursors.
Future work should focus on the production of the presented polymers on a larger scale for detailed assessment of their biodegradability, processability, and applicability for production of biobased blends and composites with other biocompatible materials. In addition, simple and convenient methods for recovery of PHA from the archaeal biomass have to be optimized for large-scale application; here, one can profit from the high intracellular pressure of H. mediterranei cells, disrupting them by exposure to hypotonic media (deionized water), releasing the biopolyester granules into the aqueous media. Regarding the process design, continuous production mode should be assessed based on first attempts described in the literature using this organism. Continuous mode should result in increased productivities during extended time periods and constant and reproducible product qualities. Especially, the tailored distribution of 4HB building blocks in PHBHV4HB can be facilitated by an optimized continuous feeding strategy. Finally, the presented results from laboratory scale are considered for planning and dimensioning the facilities and unit operations for semi-industrial archaeal PHA production from CGP waste stream of the biodiesel production. In order to save expenses for transportation of the raw material CGP, this production plant should be directly integrated into the existing production lines for biodiesel, where CGP directly accrues.
|CGP:||Crude glycerol phase|
|mcl-PHA:||Medium chain length PHA|
|:||Weight average molar mass|
|:||Number average molar mass|
|:||Maximum specific growth rate|
|:||Maximum specific product formation rate|
|scl-PHA:||Short chain length PHA|
|:||Cold crystallization temperature|
|:||Onset temperature of decomposition|
|:||Yield for conversion of substrate to PHA|
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
This work was supported by BIODIEPRO EU-Project NNE5/2001/832 and ANIMPOL EU-FP7 Project (Grant no. 245084). The authors thank the industrial partner Argent Energy UK Unlimited for providing the feedstock CGP.
- T. Keshavarz and I. Roy, “Polyhydroxyalkanoates: bioplastics with a green agenda,” Current Opinion in Microbiology, vol. 13, no. 3, pp. 321–326, 2010.
- A. Poli, P. Di Donato, G. R. Abbamondi, and B. Nicolaus, “Synthesis, production, and biotechnological applications of exopolysaccharides and polyhydroxyalkanoates by Archaea,” Archaea, vol. 2011, Article ID 693253, 13 pages, 2011.
- G. Q. Chen, “Plastics completely synthesized by bacteria: polyhydroxyalkanoates,” Plastics from Bacteria: Natural Functions and Applications, vol. 14, pp. 17–38, 2010.
- M. Zinn, B. Witholt, and T. Egli, “Occurrence, synthesis and medical application of bacterial polyhydroxyalkanoate,” Advanced Drug Delivery Reviews, vol. 53, no. 1, pp. 5–21, 2001.
- J. G. C. Gomez, B. S. Méndez, P. I. Nikel, M. J. Pettinari, M. A. Prieto, and L. F. Silva, “Making green polymers even greener: towards sustainable production of polyhydroxyalkanoates from agroindustrial by-products,” in Advances in Applied Biotechnology, 2012.
- S. Y. Lee, “Plastic bacteria? Progress and prospects for polyhydroxyalkanoate production in bacteria,” Trends in Biotechnology, vol. 14, no. 11, pp. 431–438, 1996.
- M. Koller, A. Salerno, M. D. S. Dias, A. Reiterer, and G. Braunegg, “Modern biotechnological polymer synthesis: a review,” Food Technology and Biotechnology, vol. 48, no. 3, pp. 255–269, 2010.
- K. Sudesh, K. Bhubalan, J. A. Chuah et al., “Synthesis of polyhydroxyalkanoate from palm oil and some new applications,” Applied Microbiology and Biotechnology, vol. 89, no. 5, pp. 1373–1386, 2011.
- M. Titz, K. H. Kettl, K. Shahzad, M. Koller, H. Schnitzer, and M. Narodoslawsky, “Process optimization for efficient biomediated PHA production from animal-based waste streams,” Clean Technologies and Environmental Policy, vol. 14, no. 3, pp. 495–503, 2012.
- G. P. da Silva, M. Mack, and J. Contiero, “Glycerol: a promising and abundant carbon source for industrial microbiology,” Biotechnology Advances, vol. 27, no. 1, pp. 30–39, 2009.
- D. K. Y. Solaiman, R. D. Ashby, T. A. Foglia, and W. N. Marmer, “Conversion of agricultural feedstock and coproducts into poly(hydroxyalkanoates),” Applied Microbiology and Biotechnology, vol. 71, no. 6, pp. 783–789, 2006.
- M. Hájek and F. Skopal, “Treatment of glycerol phase formed by biodiesel production,” Bioresource Technology, vol. 101, no. 9, pp. 3242–3245, 2010.
- G. Braunegg, K. Genser, R. Bona, G. Haage, F. Schellauf, and E. Winkler, “Production of PHAs from agricultural waste material,” Macromolecular Symposia, vol. 144, no. 1, pp. 375–383, 1999.
- E. J. Bormann and M. Roth, “The production of polyhydroxybutyrate by Methylobacterium rhodesianum and Ralstonia eutropha in media containing glycerol and casein hydrolysates,” Biotechnology Letters, vol. 21, no. 12, pp. 1059–1063, 1999.
- G. Haage, E. Wallner, R. Bona, F. Schellauf, and G. Braunegg, “Production of poly-3-hydroxybutyrate-co-3-hydroxy-valerate with Alcaligenes latus DSM, 1124 on various carbon sources,” in Biorelated Polymers, pp. 147–155, Springer, New York, NY, USA, 2001.
- M. H. A. Ibrahim and A. Steinbüchel, “Poly(3-hydroxybutyrate) production from glycerol by Zobellella denitrificans MW1 via high-cell-density fed-batch fermentation and simplified solvent extraction,” Applied and Environmental Microbiology, vol. 75, no. 19, pp. 6222–6231, 2009.
- J. M. B. T. Cavalheiro, M. C. M. D. de Almeida, C. Grandfils, and M. M. R. da Fonseca, “Poly(3-hydroxybutyrate) production by Cupriavidus necator using waste glycerol,” Process Biochemistry, vol. 44, no. 5, pp. 509–515, 2009.
- I. V. Špoljarić, M. Lopar, M. Koller et al., “Mathematical modeling of poly[-(R)-3-hydroxyalkanoate] synthesis by Cupriavidus necator DSM 545 on substrates stemming from biodiesel production,” Bioresource Technology, vol. 133, pp. 482–494, 2013.
- J. Teeka, T. Imai, A. Reungsang et al., “Characterization of polyhydroxyalkanoates (PHAs) biosynthesis by isolated Novosphingobium sp. THA_AIK7 using crude glycerol,” Journal of Industrial Microbiology and Biotechnology, vol. 39, no. 5, pp. 749–758, 2012.
- S. V. Reddy, M. Thirumala, and S. K. Mahmood, “A novel Bacillus sp. accumulating poly (3-hydroxybutyrate-co-3-hydroxyvalerate) from a single carbon substrate,” Journal of Industrial Microbiology and Biotechnology, vol. 36, no. 6, pp. 837–843, 2009.
- L. H. Mahishi, G. Tripathi, and S. K. Rawal, “Poly(3-hydroxybutyrate) (PHB) synthesis by recombinant Escherichia coli harbouring Streptomyces aureofaciens PHB biosynthesis genes: effect of various carbon and nitrogen sources,” Microbiological Research, vol. 158, no. 1, pp. 19–27, 2003.
- C. Zhu, C. T. Nomura, J. A. Perrotta, A. J. Stipanovic, and J. P. Nakas, “Production and characterization of poly-3-hydroxybutyrate from biodiesel-glycerol by Burkholderia cepacia ATCC 17759,” Biotechnology Progress, vol. 26, no. 2, pp. 424–430, 2010.
- M. Taran, E. Azizi, S. Taran, and N. Asadi, “Archaeal poly (3-hydroxybutyrate) polymer production from glycerol: optimization by Taguchi methodology,” Journal of Polymers and the Environment, vol. 19, no. 3, pp. 750–754, 2011.
- Y. Kawata and S. I. Aiba, “Poly(3-hydroxybutyrate) production by isolated Halomonas sp. KM-1 using waste glycerol,” Bioscience, Biotechnology and Biochemistry, vol. 74, no. 1, pp. 175–177, 2010.
- M. Koller, R. Bona, G. Braunegg et al., “Production of polyhydroxyalkanoates from agricultural waste and surplus materials,” Biomacromolecules, vol. 6, no. 2, pp. 561–565, 2005.
- F. Rodriguez-Valera and J. A. G. Lillo, “Halobacteria as producers of polyhydroxyalkanoates,” FEMS Microbiology Reviews, vol. 103, no. 2–4, pp. 181–186, 1992.
- M. Koller, A. Salerno, A. Reiterer et al., “Sugar cane as feedstock for biomediated polymer production,” in Sugarcane: Production, Cultivation and Uses, pp. 105–136, 2012.
- C. W. Chen, T. M. Don, and H. F. Yen, “Enzymatic extruded starch as a carbon source for the production of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) by Haloferax mediterranei,” Process Biochemistry, vol. 41, no. 11, pp. 2289–2296, 2006.
- T. Y. Huang, K. J. Duan, S. Y. Huang, and C. W. Chen, “Production of polyhydroxyalkanoates from inexpensive extruded rice bran and starch by Haloferax mediterranei,” Journal of Industrial Microbiology and Biotechnology, vol. 33, no. 8, pp. 701–706, 2006.
- F. Rodriguez-Valera, G. Juez, and D. J. Kushner, “Halobacterium mediterranei spec, nov., a new carbohydrate-utilizing extreme halophile,” Systematic and Applied Microbiology, vol. 4, no. 3, pp. 369–381, 1983.
- D. Zhao, L. Cai, J. Wu et al., “Improving polyhydroxyalkanoate production by knocking out the genes involved in exopolysaccharide biosynthesis in Haloferax mediterranei,” Applied Microbiology and Biotechnology, vol. 97, no. 7, pp. 3027–3036, 2013.
- J. Han, F. Zhang, J. Hou et al., “Complete genome sequence of the metabolically versatile halophilic archaeon Haloferax mediterranei, a poly (3-hydroxybutyrate-co-3-hydroxyvalerate) producer,” Journal of Bacteriology, vol. 194, no. 16, pp. 4463–4464, 2012.
- M. Koller, P. Hesse, R. Bona, C. Kutschera, A. Atlić, and G. Braunegg, “Biosynthesis of high quality polyhydroxyalkanoate co- and terpolyesters for potential medical application by the archaeon Haloferax mediterranei,” Macromolecular Symposia, vol. 253, pp. 33–39, 2007.
- G. Braunegg, B. Sonnleitner, and R. M. Lafferty, “A rapid gas chromatographic method for the determination of poly β hydroxybutyric acid in microbial biomass,” European Journal of Applied Microbiology and Biotechnology, vol. 6, no. 1, pp. 29–37, 1978.
- O. H. Lowry, N. J. Rosebrough, A. L. Farr, and R. J. Randall, “Protein measurement with the Folin phenol reagent,” The Journal of Biological Chemistry, vol. 193, no. 1, pp. 265–275, 1951.
- M. Koller, H. Niebelschütz, and G. Braunegg, “Strategies for recovery and purification of poly [(R)-3-hydroxyalkanoates](PHA) biopolyesters from surrounding biomass,” Engineering in Life Sciences, vol. 35, no. 7, pp. 1023–1028, 2013.
- R. V. Nonato, P. E. Mantelatto, and C. E. V. Rossell, “Integrated production of biodegradable plastic, sugar and ethanol,” Applied Microbiology and Biotechnology, vol. 57, no. 1-2, pp. 1–5, 2001.
- Q. Lu, J. Han, L. Zhou, J. Zhou, and H. Xiang, “Genetic and biochemical characterization of the poly(3-hydroxybutyrate-co-3-hydroxyvalerate) synthase in Haloferax mediterranei,” Journal of Bacteriology, vol. 190, no. 12, pp. 4173–4180, 2008.
- J. Han, J. Hou, F. Zhang et al., “Multiple propionyl coenzyme A-supplying pathways for production of the bioplastic poly(3-hydroxybutyrate-co-3-hydroxyvalerate) in Haloferax mediterranei,” Applied and Environmental Microbiology, vol. 79, no. 9, pp. 2922–2931, 2013.
- B. Feng, S. Cai, J. Han, H. Liu, J. Zhou, and H. Xiang, “Identification of the phaB genes and analysis of the PHBV precursor supplying pathway in Haloferax mediterranei,” Acta Microbiologica Sinica, vol. 50, no. 10, pp. 1305–1312, 2010.
- J. Hou, B. Feng, J. Han et al., “Haloarchaeal type β-ketothiolases involved in poly(3-hydroxybutyrate-co-3-hydroxyvalerate) synthesis in Haloferax mediterranei,” Applied and Environmental Microbiology, 2013.
- S. Y. Lee, “Bacterial polyhydroxyalkanoates,” Biotechnology and Bioengineering, vol. 49, no. 1, pp. 1–14, 1996.
- L. A. Madden, A. J. Anderson, D. T. Shah, and J. Asrar, “Chain termination in polyhydroxyalkanoate synthesis: involvement of exogenous hydroxy-compounds as chain transfer agents,” International Journal of Biological Macromolecules, vol. 25, no. 1–3, pp. 43–53, 1999.
- T. M. Don, C. W. Chen, and T. H. Chan, “Preparation and characterization of poly(hydroxyalkanoate) from the fermentation of Haloferax mediterranei,” Journal of Biomaterials Science, Polymer Edition, vol. 17, no. 12, pp. 1425–1438, 2006.
- L. A. Madden, A. J. Anderson, J. Asrar, and P. Berger, “Production and characterization of poly(3-hydroxybutyrate-co-3-hydroxyvalerate-co-4-hydroxybutyrate) synthesized by Ralstonia eutropha in fed-batch cultures,” Polymer, vol. 41, no. 10, pp. 3499–3505, 2000.
- D. P. Martin and S. F. Williams, “Medical applications of poly-4-hydroxybutyrate: a strong flexible absorbable biomaterial,” Biochemical Engineering Journal, vol. 16, no. 2, pp. 97–105, 2003.