Carbon Source For Polyhydroxyalkanoates Production Research Articles

Bacterial production of polyhydroxyalkanoates (PHAs) using various waste carbon sources.

Synthetic plastics are in great demand in society due to their diversified properties, but they cause environmental pollution due to their non-biodegradable nature. Therefore, synthetic plastics are in need to be replaced with biodegradable plastics. Polyhydroxyalkanoates (PHAs), bacterial biopolymers are natural alternative to synthetic plastics. These are present inside the bacterial cytoplasm in granular form. Presently, the production cost of PHA is high due to expensive carbon substrates used in its biosynthesis. Therefore, this study focuses on the cost-effective production of PHA using waste carbon sources. Rice bran and sugarcane molasses were used as the carbon source for PHA production from Bacillus subtilis, Bacillus cereus, Alcaligenes sp. and Pseudomonas aeruginosa. PHA production from these bacterial strains was confirmed through Sudan Black-B screening. With rice bran, as carbon source, the highest PHA yield obtained was for P. aeruginosa, which yielded 93.7% and lowest was 35.5% for B. cereus. Surprisingly, B. cereus produced the highest cell dry mass (0.045 g/L) but its extracted PHA contents were lowest being only 0.02 g/L. Alcaligenes sp. with 0.031 g/L CDM yielded 87.1% PHA. B. subtilis had a CDM 0.029 g/L, 0.02 g/L PHA content and a yield of 69.10%. In the case of sugarcane molasses, P. aeruginosa produced 95% PHA yield, 0.02 g/L CDM, and 0.019 g/L PHA content. Alcaligenes sp. yielded 90.9% PHA, 0.011 g/L CDM, and 0.01 g/L PHA content. B. subtilis produced 91.6% PHA yield, 0.012 g/L CDM, 0.011 g/L PHA content; B. cereus produced 80% PHA yield, 0.015 g/L CDM, 0.012 g/L PHA content at 37°C, pH 7. Higher concentrations of carbon sources increased the CDM and decreased the PHA yield. The maximum yield of PHA was obtained from sugarcane molasses. 24-48 h of incubation was optimal for B. subtilis and B. cereus, while for Alcaligenes and P. aeruginosa incubation time of 48-96 h was desirable for higher PHA yield. The extracted biopolymers were analyzed by Fourier transform infrared spectroscopy (FTIR), which identified the extracted biopolymers as poly-3-hydroxybutyrate P(3HB). The thermal properties of the extracted biopolymers, such as melting temperatures, were analyzed by differential scanning calorimetry (DSC), which confirmed the thermal stability.

Process integration for efficient conversion of cassava peel waste into polyhydroxyalkanoates

Polyhydroxyalkanoates (PHA) are biodegradable polyesters that can be produced from renewable resources. However, PHA biomanufacturing is costly compared to petrochemical-based plastics. A promising solution consists of using cassava (Manhiot esculenta) waste, abundant biomass in developing countries, as a carbon source for PHA production. This study involved characterising untreated and acid-hydrolysed cassava peel (CP) to confirm the degradation of polysaccharides into fermentable sugars after pre-treatment. A chemical and biological integrated process was developed, optimising the pre-treatment using a central composite design. The highest conversion of CP into reducing sugars was 97% (w/w) using 3 M H2SO4, 120 min and 90 ºC. The ability of Cupriavidus necator to grow on CP hydrolysate and produce PHA was screened resulting in up to OD600 15.8 and 1.5 g/L of PHA (31% (gPHA/gDCW)). Flow cytometry allowed rapid, simple, and high-throughput assessment of PHA content. These findings pave the way for developing a biorefinery platform for PHA production from cassava waste.

Valorization of food waste derived anaerobic digestate into polyhydroxyalkanoate (PHA) using Thauera mechernichensis TL1

Polyhydroxyalkanoate (PHA) is a biopolymer that can be used as a bioplastic, offering a green alternative to petroleum-based plastics. In this study, we investigated PHA production using Thauera mechernichensis TL1. The optimal molar C/N ratio was determined to be 20 from among the ratios of 4, 20, 40, 80, and 200 and in the absence of nitrogen. Food waste anaerobic digestate, mainly comprised of acetate and propionate, was used as the carbon source for PHA production by T. mechernichensis TL1, resulting in a maximum PHA content of 23.98 ± 0.52 wt% (0.52 ± 0.02 g/L PHA) with a PHA productivity of 0.043 g/L-h PHA. In addition, when using acetate and propionate, T. mechernichensis TL1 produced PHA with a maximum PHA content of 57.43 ± 2.84 wt% (2.04 ± 0.11 g/L PHA) and 50.94 ± 1.61 wt% (2.62 ± 0.16 g/L PHA), with a PHA productivity of 0.092 g/L-h PHA and 0.070 g/L-h PHA, respectively. Proton nuclear magnetic resonance spectroscopy (1H NMR) confirmed polyhydroxybutyrate (PHB) production using acetate as a carbon source, and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) production using propionate or food waste anaerobic digestate as the carbon source. The whole-genome analysis of T. mechernichensis TL1 confirmed the existence of a PHA biosynthesis pathway, with the presence of phaA, phaB, phaC (Class I and Class II), and phaJ genes. This study was the first to demonstrate Thauera sp.’s ability to produce PHA from food waste anaerobic digestate, rendering it as a promising candidate for PHA-producing bacteria for the valorization of food waste.

Utilization of sugarcane molasses as the main carbon source for the production of polyhydroxyalkanoates from Enterobacter cloacae

Polyhydroxyalkanoates (PHAs) are biodegradable polymers that otherwise exhibit many properties similar to that of conventional, non-biodegradable plastics. Hence, they are considered as potential substitutes for non-biodegradable plastics. But industrial production and commercialization of PHA have been hindered greatly due to the high cost requirements, especially those involved in the provision of suitable carbon sources. In this study, sugarcane molasses was used as a cheap carbon source for PHA production using a wild strain of Enterobacter cloacae isolated from sugarcane extract. This isolate was selected for PHA production based on Sudan Black B staining, and it was subsequently identified by performing BLASTn using its 16S rRNA sequence (GenBank accession number: ON314993). The PHA yield was studied under varying conditions of initial pH, molasses concentration and inoculum concentration. The highest yield of 4.13 - 4.98 g/L or 48 - 56% PHA was obtained after 48-60 h incubation at initial pH 7, molasses concentration 4% and inoculum concentration 2%. After downstream processing, the extracted PHA was characterized by FTIR spectroscopy. It is concluded that E. cloacae has the potential to utilize sugarcane molasses as a cheap carbon source to yield impressive amounts of PHA, and that it should be considered a candidate for further studies and for the cheaper industrial production of PHA.

A comparative analysis of biopolymer production by microbial and bioelectrochemical technologies.

Production of biopolymers from renewable carbon sources provides a path towards a circular economy. This review compares several existing and emerging approaches for polyhydroxyalkanoate (PHA) production from soluble organic and gaseous carbon sources and considers technologies based on pure and mixed microbial cultures. While bioplastics are most often produced from soluble sources of organic carbon, the use of carbon dioxide (CO2) as the carbon source for PHA production is emerging as a sustainable approach that combines CO2 sequestration with the production of a value-added product. Techno-economic analysis suggests that the emerging approach of CO2 conversion to carboxylic acids by microbial electrosynthesis followed by microbial PHA production could lead to a novel cost-efficient technology for production of green biopolymers.

Optimization of Growth Conditions to Produce Sustainable Polyhydroxyalkanoate Bioplastic by Pseudomonas aeruginosa EO1.

Polyhydroxyalkanoates (PHAs) are intracellularly synthesized by bacteria as carbonosomes that exhibit biodegradable thermoplastics and elastomeric properties. The use of cheaper edible oils as a source of carbon assists in the reduction of the production cost of such biopolyesters. In this work, different edible oils, such as groundnut oil (GNO), mustard oil, sesame oil, and soybean oil (SBO) were used to check their effect on PHA production from Pseudomonas aeruginosa EO1 (MK049902). Pseudomonas aeruginosa EO1 was used in a two-stage production system. In the first stage, bacterial growth was favored and, in the second, PHA was synthesized. GNO was found as the best carbon source for PHA production. The use of 2% (v/v) GNO, rich in saturated fatty acids, allowed PHA content of 58.41% and dry cell weight (DCW) of 10.5g/L at pH7 and temperature 35°C for 72h. Groundnut has a high potential for oil production and for the diversification of co-products with some potential of value aggregation. Such a perennial and sustainable species will almost certainly meet the criteria for becoming a significant commercial oilseed crop. Fourier transform infrared spectroscopy (FTIR) spectra showed strong characteristic bands at 1,282, 1,725, 2,935, 2,999, and 3,137cm−1 for the PHA polymer. Gas chromatography-mass spectrometry (GC-MS) detects the presence of PHA copolymers.

INVESTIGATION OF FERMENTATION CONDITION FOR PRODUCTION ENHANCEMENT OF POLYHYDROXYALKANOATE FROM CHEESE WHEY BY PSEUDOMONAS SP.

A newly acquired polyhydroxyalkanoate (PHA) producing Pseudomonas sp. was characterized based on 16S rRNA gene sequences (1,423 bp) and identified as P. Putida SS9. This strain P. putida SS9 was considered in respect of its potential for achieving maximum production of PHA under controlled volumetric oxygen transfer coefficient (kLa) using inexpensive substrate, cheese whey. The significant parameters such as pH, temperature, nitrogen source concentration were studied in shake flask. The influence of aeration and agitation on kLa and production of PHA was studied in stirred tank fermenter. Maximum PHA concentration of 5.98 and 4.33 g/l was obtained using cheese whey medium (CWM) and mineral salts medium (MSM) respectively. Further, the properties of PHA were analyzed by Differential scanning calorimetry, Thermal gravimetry analysis. The structure of the compound was elucidated by Fourier transform infrared and Nuclear magnetic resonance spectroscopy. The findings suggested that the cheese whey could be a most excellent alternative carbon source for PHA production using P. putida SS9 and thus it could effectively replace the synthetic mineral salts medium under optimum kLa. The nucleotide sequence proclaimed in this work will emerge in the GenBank nucleotide sequence database under accession number MF403057.

Statistical optimization and enhanced synthesis of polyhydroxyalkanoates from Ceiba pendantra oil as novel non-edible feedstock

Polyhydroxyalkanoates (PHA) are biopolymer synthesized as storage granules by microbes in the cell’s cytoplasm under excess carbon and limited nitrogen conditions. This study aims to examine the production and optimization of PHA from Ceiba pentandra oil, a non-edible feedstock, by Cupriavidus necator. Response surface methodology was used to optimize the concentrations of carbon, nitrogen, and inoculum for the production of PHA. To improve the physical, mechanical, and thermal properties of PHA, it was blended with polylactic acid (PLA) which possesses high bio-compatibility and bio-absorbability. Furthermore, batch mode cultivation of PHA in a 3-L bioreactor was performed under the optimized conditions (Ceiba pentandra oil—17.13 g/L, urea—1.34 g/L, and inoculum—53.42 mL/L), and 8.51 g/L (0.47 g PHA/g of Ceiba pentandra oil) of PHA product was obtained. The PHA was characterized by FTIR and the presence of functional groups such as C=O, OH, and CH were observed. 1H and 13C NMR spectroscopy revealed the existence of hydroxy valerate (HV) and hydroxybutyrate (HB), and maximal decomposition temperature was identified to be 217.7 °C from TGA analysis. Therefore, Ceiba pendantra oil appears to be an attractive alternate carbon source for PHA production.

Prospects for the Use of Whey for Polyhydroxyalkanoate (PHA) Production.

Plastic production and accumulation have devastating environmental effects, and consequently, the world is in need of environmentally friendly plastic substitutes. In this context, polyhydroxyalkanoates (PHAs) appear to be true alternatives to common plastics because they are biodegradable and biocompatible and can be biologically produced. Despite having comparable characteristics to common plastics, extensive PHA use is still hampered by its high production cost. PHAs are bacterial produced, and one of the major costs associated with their production derives from the carbon source used for bacterial fermentation. Thus, several industrial waste streams have been studied as candidate carbon sources for bacterial PHA production, including whey, an environmental contaminant by-product from the dairy industry. The use of whey for PHA production could transform PHA production into a less costly and more environmentally friendly process. However, the efficient use of whey as a carbon source for PHA production is still hindered by numerous issues, including whey pre-treatments and PHA producing strain choice. In this review, current knowledge on using whey for PHA production were summarized and new ways to overcome the challenges associated with this production process were proposed.

Use of bacteriostatic antibiotics for the optimization of new media in view of supplementing POME as an alternative carbon source for PHA production - a statistical approach

Abstract Polyhydroxyalkanoates (PHA) are among the available biodegradable plastics in the market today. However, production of biodegradable plastics cost twice as much as when compared with the production of petrochemical-based synthetic polymers due to the use of substrate costing more than 50% of the total production cost. To curb this problem, alternative renewable and cheap carbon sources are in need. The choice of renewable and cheap carbon source, in this study was palm oil mill effluent (POME). The ultimate aim of this research is to apply the use of bacteriostatic antibiotics for the optimization of new media in view of supplementing POME as an alternative carbon source for PHA production by applying statistical approach. Prior to this, isolated strains were screened for amylolytic, cellulolytic and PHA accumulation. Two potential strains selected for further optimization. The statistical software Design Expert, a new media composition was constructed which includes POME as the carbon source and Clindamycin as the metabolic inhibitor. Strain PHA-11 was able to accumulate the highest PHA concentration of 0.134 g/L under media composition of 1.2 mg/L of Clindamycin, 200 ml/L media of POME, 0.5 g/L of (NH4)2SO4 (N) and 1.5 g/L of K2HPO4-KH2PO4 mixture (P/K). On the contrary, strain PHA-17 was able to accumulate the highest PHA concentration of 0.138 g/L under media composition of 1.2 mg/ml of Clindamycin, 200 ml/L media of POME, 1.5 g/L of (NH4)2SO4 (N) and 1.5 g/L of K2HPO4-KH2PO4 mixture (P/K). The polymer content and the copolymer composition were further confirmed by HPLC analysis.

Polyhydroxyalkanoates (PHA) production in bacterial co‐culture using glucose and volatile fatty acids as carbon source

Mixed bacterial cultures are increasingly being used in the production of polyhydroxyalkanoates (PHAs), as they have the potential to be more cost effective than axenic pure cultures. The purpose of this study was to use pure cultures in combination to identify their potential of PHA production. In this work we used volatile fatty acids (VFAs) and glucose as carbon source to check the ability of selected strains ST2 (Pseudomonas sp.) and CS8 (Bacillus sp.) as co-culture. The production of PHA in pure co-cultures of bacteria was therefore investigated in order to understand the effect of combining cultures on PHA production parameters and material properties. Bacteria could use the feed in better way when mixed as compared to individual strain. In undertaking this analysis, model volatile fatty acids (i.e., acetic and propionic acids) were used alone and in combination with glucose as feedstock. The production by Pseudomonas was 34% while 24% by Bacillus. However when combined and mixed feed (glucose + propionic acid) was used, 35% PHA produced. Overall, it was found that the ability of the pure cultures to produce PHA was low but when selected cultures were mixed, their ability to produce PHA was enhanced. Copolymers were obtained instead of homopolymers with improved properties. This suggests that industrial wastewater rich in volatile fatty acids and carbohydrates can be a good carbon source for PHA production with variable properties.

Polyhydroxyalkanoates (PHA) production from phenol in an acclimated consortium: Batch study and impacts of operational conditions

Microbial intracellular biopolymer PHA was synthesized from toxic pollutant phenol by an acclimated consortium. Various operational conditions were experimented for their effects on biomass growth and PHA accumulation. Carbon to nitrogen ratios from 5 to 40 (w/w) showed little impact, as did the levels of Fe, Ca and Mg in a short term. Acidic pH inhibited both growth and PHA synthesis, and an optimal dissolved oxygen level of 1–4 mg L−1 was identified. Low temperature (7 °C) significantly slowed but did not totally repress microbial activities. A 2% NaCl shock retarded reactions and 4% NaCl caused irreversible damage. Various initial phenol (S0) and biomass concentrations (X0) were combined to study the effect of food to microbe (F/M) ratio. High S0 and F/M exerted toxicity, reducing reaction rates but generating higher ultimate PHA wt% in biomass. Increasing X0 alleviated phenol inhibition and improved productivity and carbon conversion from phenol. A pseudo-optimized F/M ratio of 0.2–0.4 and a maximum PHA% rate of 1.15% min−1 were identified under medium S0/high X0. This study is the first to systematically investigate the feasibility of toxic industrial waste as the carbon source for PHA production, and likely the only one indicating potential for scaling-up and industrialization.

The Molecular Level Characterization of Biodegradable Polymers Originated from Polyethylene Using Non-Oxygenated Polyethylene Wax as a Carbon Source for Polyhydroxyalkanoate Production.

There is an increasing demand for bio-based polymers that are developed from recycled materials. The production of biodegradable polymers can include bio-technological (utilizing microorganisms or enzymes) or chemical synthesis procedures. This report demonstrates the corroboration of the molecular structure of polyhydroxyalkanoates (PHAs) obtained by the conversion of waste polyethylene (PE) via non-oxygenated PE wax (N-PEW) as an additional carbon source for a bacterial species. The N-PEW, obtained from a PE pyrolysis reaction, has been found to be a beneficial carbon source for PHA production with Cupriavidus necator H16. The production of the N-PEW is an alternative to oxidized polyethylene wax (O-PEW) (that has been used as a carbon source previously) as it is less time consuming to manufacture and offers fewer industrial applications. A range of molecular structural analytical techniques were performed on the PHAs obtained; which included nuclear magnetic resonance (NMR) and electrospray ionisation tandem mass spectrometry (ESI-MS/MS). Our study showed that the PHA formed from N-PEW contained 3-hydroxybutyrate (HB) with 11 mol% of 3-hydroxyvalerate (HV) units.

Oxidized Polyethylene Wax as a Potential Carbon Source for PHA Production.

We report on the ability of bacteria to produce biodegradable polyhydroxyalkanoates (PHA) using oxidized polyethylene wax (O-PEW) as a novel carbon source. The O-PEW was obtained in a process that used air or oxygen as an oxidizing agent. R. eutropha H16 was grown for 48 h in either tryptone soya broth (TSB) or basal salts medium (BSM) supplemented with O-PEW and monitored by viable counting. Study revealed that biomass and PHA production was higher in TSB supplemented with O-PEW compared with TSB only. The biopolymers obtained were preliminary characterized by nuclear magnetic resonance (NMR), gel permeation chromatography (GPC), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The detailed structural evaluation at the molecular level was performed by electrospray ionization tandem mass spectrometry (ESI-MS/MS). The study revealed that, when TSB was supplemented with O-PEW, bacteria produced PHA which contained 3-hydroxybutyrate and up to 3 mol % of 3-hydroxyvalerate and 3-hydroxyhexanoate co-monomeric units. The ESI-MS/MS enabled the PHA characterization when the content of 3-hydroxybutyrate was high and the appearance of other PHA repeating units was very low.

Characterization of polyhydroxyalkanoates extracted from wastewater sludge under different environmental conditions

Polyhydroxyalkanoates (PHAs) are bioplastics that naturally accumulate in the microbial cells while performing organic substrate metabolism. PHAs bioconversion in microbial cells is affected by both growth environments (aerobic and anaerobic) and feeding systems (carbon and nutrient limitations). Sequential batch reactors (SBRs) were used in this research for producing PHAs; studies showed on an average 42% with a maximum of 63% PHAs yield under anaerobic–oxic conditions quantified by gas chromatography. Produced PHAs from phase 4 were thermally and physically characterized. Fourier transform infrared spectroscopy showed strong presence of carbonyl peaks at 1720cm−1 in all PHAs. Gel permeation chromatography reported polydipersity index values in range of 2.4–3.6 showing non-uniformity of molecular weights in the slice of PHAs and differential scanning calorimetry reported melting point temperatures of 146–154°C, confirming usefulness of produced PHAs in industrial applications. X-Ray Diffraction confirmed crystal structure in all PHAs with the most crystalline from SBR3. Thermogravimetric analysis further confirmed highest thermal degradation temperature of 283°C for PHAs from SBR3. Different blends of wastewater fed to mixed sodium acetate acclimatized biomass further showed the importance of substrate carbon source for PHAs production in various growth environments.

Characterization of Polyhydroxyalkanoates Produced by Contaminated Soil Bacteria using Wastewater and Glucose as Carbon Sources

Purpose: To isolate polyhydroxyalkanoates (PHA)-producing bacterial strains from contaminated soil using industrial wastewater and glucose as carbon soured by Macrogen sequencing. Two different sources, namely, glucose and wastewater were used to ces.Methods: The strains were isolated and identified as Pseudomonas, Bacillus, Enterobacter, Exiguobacterium and Stenotrophomonas using biochemical tests and further confirmevaluate and compare the use of wastewater as a carbon source for PHA production. The biomass obtained was analyzed by Fourier transform infra-red (FTIR) to identify the presence of PHA in it. Afterwards, PHA extraction was carried out and then gas chromatography (GC) performed to identify PHA monomers.Results: Utilization of glucose resulted in the production of PHB, while wastewater yielded copolymers poly-3 hydroxybutyrate-co-3hydroxyvalerate P(3HB-co-3HV) due to its content of volatile fatty acids such as acetic acid, propionic acid and butyric acid, which led to the production of different types of polymers. The maximum PHA production was 41 ± 0.22 % obtained for Stenotrophomonas (SM03) using 2 % glucose as carbon source while for wastewater, maximum production was achieved by the Pseudomonas strain (SM01).Conclusion: Wastewater is produced in large quantities daily during various activities and therefore can be used as a cheap carbon source for the production of valuable products such as PHA.Keywords: Polyhydroxyalkanoates, Wastewater, Glucose, Pseudomonas strain, Stenotrophomonas

Softwood hydrolysate as a carbon source for polyhydroxyalkanoate production

BACKGROUND Forest biomass represents a potential low-cost feedstock for polyhydroxyalkanoate (PHA) production. Softwoods, such as Pinus radiata (D.Don) are difficult to digest and require special pretreatments to expose polysaccharides for enzymatic saccharification. Different pretreatments can lead to inhibitor formation that may adversely affect PHA synthesis. RESULTS Pinus radiata wood chips were subjected to high-temperature mechanical pre-treatment (HTMP) or steam explosion in the presence of sulphur dioxide (SEW) before being enzymatically treated to produce corresponding hydrolysates. Two PHA-producing bacteria Novosphingobium nitrogenifigens Y88T and Sphingobium scionense WP01T were grown on these hydrolysates. The highest content of PHA was produced by WP01 grown on HTMP hydrolysate (32% w/w PHA, YPHA/glucose = 0.22 and theoretical maximum yield of 46%). Gas chromatography and proton nuclear magnetic resonance spectroscopy indicated that the PHA produced was made up of polyhydroxybutyrate (PHB) with molecular weights ranging from 50–1600 kDa and polydispersities between 4.6 and 8.4. The melting temperature was close to that of pure PHB with percentage crystallinity ranging from 44–64%. CONCLUSION This is the first report on the production of PHA from softwood hydrolysates derived from enzymatically saccharified pretreated Pinus radiata pulps. © 2013 Society of Chemical Industry

Comparison of ecological footprint for biobased PHA production from animal residues utilizing different energy resources

Realizing a sustainable development of our planet requires a reduction of waste production, harmful emissions, and higher energy efficiency as well as utilization of renewable energy sources. One pathway to this end is the design of sustainable biorefinery concepts. Utilizing waste streams as raw material is gaining great importance in this respect. This reduces environmental burden and may at the same time contribute to economic performance of biorefineries. This paper investigates the utilization of slaughtering waste to produce biodegradable polyesters, polyhydroxyalkanoates (PHA), via bioconversion. PHA are the target product while production of high quality biodiesel along with meat and bone meal (MBM) as by-products improves the economic performance of the process. The paper focuses on ecological comparison of different production scenarios and the effect of geographical location of production plants taking different energy production technologies and resources into account; ecological footprint evaluation using Sustainable Process Index methodology was applied. Keeping in mind that the carbon source for PHA production is produced from waste by energy intensive rendering process, the effect of available energy mixes in different countries becomes significant. Ecological footprint results from the current study show a bandwidth from 372,950 to 956,060 m2/t PHA production, depending on the energy mix used in the process which is compared to 2,508,409 m2/t for low density polyethylene.

Influence of Substrate Load on Polyhydroxyalkanoates (Pha) Accumulation by Unenriched Mixed Cultures from Excess Sludge Fermentation Liquid

To reduce the production cost of polyhydroxyalkanoates (PHA) and disposal amount of excess sludge simultaneously, volatile fatty acids (VFAs) from alkaline excess sludge fermentation was used as carbon sources to synthesize PHA by unenriched mixed cultures. Released phosphorus and residual ammonium in the fermentative VFAs was controlled by adding magnesium to form struvite precipitation. Four VFAs liquids obtained was used to test the influence of initial carbon load and carbon to nitrogen ratio (C:N ratio) on the VFAs uptake rate, PHA storage rate and biomass growth rate. Results show that higher initial carbon substrate load results in relatively higher VFAs uptake rate and higher PHA storage rate, while higher initial C:N ratio results in relatively lower biomass growth rate from VFAs. VFAs generated from thermophilic alkaline sludge fermentation were a suitable carbon source for PHA production by mixed cultures.

Influence of Substrate Load on Polyhydroxyalkanoates (Pha) Accumulation by Unenriched Mixed Cultures from Excess Sludge Fermentation Liquid

To reduce the production cost of polyhydroxyalkanoates (PHA) and disposal amount of excess sludge simultaneously, volatile fatty acids (VFAs) from alkaline excess sludge fermentation was used as carbon sources to synthesize PHA by unenriched mixed cultures. Released phosphorus and residual ammonium in the fermentative VFAs was controlled by adding magnesium to form struvite precipitation. Four VFAs liquids obtained was used to test the influence of initial carbon load and carbon to nitrogen ratio (C:N ratio) on the VFAs uptake rate, PHA storage rate and biomass growth rate. Results show that higher initial carbon substrate load results in relatively higher VFAs uptake rate and higher PHA storage rate, while higher initial C:N ratio results in relatively lower biomass growth rate from VFAs. VFAs generated from thermophilic alkaline sludge fermentation were a suitable carbon source for PHA production by mixed cultures.