alexa Enhancement of Crude Oil Biodegradation by Immobilizing of different Bacterial Strains on Porous PVA Hydrogels or Combining of them with their produced Biosurfactants | Open Access Journals
Journal of Petroleum & Environmental Biotechnology
Like us on:
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Enhancement of Crude Oil Biodegradation by Immobilizing of different Bacterial Strains on Porous PVA Hydrogels or Combining of them with their produced Biosurfactants

Abdeen Z1*, Huda K El-Sheshtawy2 and Moustafa YMM3
1Petrochemical Department, Egyptian Petroleum Research Institute, Nasr City, Cairo, Egypt
2Processes Development Department, Egyptian Petroleum Research Institute, Nasr City, Cairo, Egypt
3Evaluations and Analysis Department, Egyptian Petroleum Research Institute, Nasr City, Cairo, Egypt
Corresponding Author : Abdeen Z
Petrochemical Department
Egyptian Petroleum Research Institute
Nasr City, Cairo, Egypt
Tel: 20 1154459620
E-mail: [email protected]
Received August 30, 2014; Accepted October 01, 2014; Published October 17, 2014
Citation: Abdeen Z, El-Sheshtawy HK, Moustafa YMM (2014) Enhancement of Crude Oil Biodegradation by Immobilizing of different Bacterial Strains on Porous PVA Hydrogels or Combining of them with their produced Biosurfactants. J Pet Environ Biotechnol 5:192. doi:10.4172/2157-7463.1000192
Copyright: © 2014 Abdeen Z, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Journal of Petroleum & Environmental Biotechnology


The degradation of the crude oil in wastewater by each of freely microorganisms and by immobilized them on each of crosslinked poly (vinyl alcohol) hydrogel (CPVA) and its foam (CPVAF) was reported. Also, it was studied by using biosurfactants (Bios) with free cells. The macroporous CPVAF was prepared by adding CaCO3 as poreforming agent and epichlorohydrin as crosslinker. The prepared polymers are examining by FTIR, XRD, TGA, DSC and SEM analysis. The microorganisms of B.l., R.e. and P.x. isolated from contaminated effluents were investigated. The ability of these microorganisms to degrade the n-paraffin and PAHs was assessed by GC and HPLC analysis, respectively. Moreover, their stabilities and activities were tested in the growth count of bacteria study. The crosslinked CPVA carrier demonstrated better thermal stability and improvement in the microorganism efficiency with respect to hydrocarbons degradation than these of the CPVAF carrier. Scanning electron microscopy showed the presence of extracellular structures that could play an important role in the immobilization stability of cells on polymers. As well, GC analysis revealed that the percentage biodegradation ability of immobilized cells R.e. on CPVAF for the total n-paraffin was approximately, 100%. While, the HPLC analysis showed that the percentage biodegradation of cells for PAHs was enhancement by immobilized them on CPVA and also, at adding Bios to them. The results suggest that the potential of using each of CPVA, PVAF as cell carriers and Bios separately, to free cells to enhancing the biodegradation of petroleum hydrocarbons in an open marine environment.

Immobilization; Crosslinked poly (vinyl alcohol) hydrogel; Foam; Biodegradation; Biosurfactants; Hydrocarbons.
Biodegradation of petroleum hydrocarbons is a complex process that depends on the nature and the amount of the hydrocarbons present, saturates, aromatics, asphaltenes and the polar compounds [1]. The polycyclic aromatic hydrocarbons (PAHs) [2] are a minor constituent of crude oils; however, they are widespread environmental pollutants. They are generated from petroleum and many pyrolysis processes. They form concern because of their potentially deleterious effects on human health and many can be recalcitrant in the environment [3]. Bioremediation can be described as the conversion of chemical compounds by living organisms, especially microorganisms, into energy, cell mass and biological waste products [4]. Bacteria can convert PAHs completely to biomass, CO2, and H2O. A wide range of different bacteria is able to completely assimilate a defined range of compound, or exhibit just partial metabolism [5]. Therefore, the use of pure cultures of microorganisms, specially adapted to metabolize the contaminant, is envisaged as an attractive alternative. Rhodococcus erythropolis is well known microorganism containing a large set of enzymes that allows carrying out an enormous number of bioconversion and degradation [6,7]. Biosurfactants are biological compounds that exhibit high surface-active properties [8] and are produced by a wide variety of microbes. Wide spectra of microbial compounds, including glycolipids, lipopeptides, fatty acids, and polymeric biosurfactants, have been found to have surface activity [9]. They have important advantages, such as biodegradability, low toxicity, and various possible structures, relative to chemically synthesized surfactants [10]. So, they were use in environmental applications, such as in bioremediation [11] and in enhanced oil recovery [12]. Microbial cells can be immobilized on various hydrophilic polymeric entrapment matrices such as hydrogels [13]. Among hydrophilic polymers, poly (vinyl alcohol) PVA, poly (hydroxyethylmetacrylate) PHEMA and others, are the most often used for hydrogel’s synthesis [14-17]. Poly (vinyl alcohol) (PVA) is a water-soluble material that has been widely used for immobilization of bioactive materials [18]. Because of, PVA is innocuous for bioactive matter and possesses many attractive properties [19], it is a potential bio-carrier material that can be applied in the fermentation industry [20], chemistry [21], and the environment [22]. The chemical stability and mechanical properties can be improved by physical or chemical crosslinking [19]. Nevertheless, research on the preparation and use of PVA foam for microbial immobilization is rarely reported. Therefore, there is a great scope for designing better PVA foam carriers for immobilizing microorganisms and developing new technologies for wastewater bio-treatment. In this work, hydrogel composites based on PVA and calcium carbonate were prepared and foamed by adding hydrochloric acid, to produce a macroporous carrier [23]. Epichlorohydrin was then used as a chemical crosslinking agent to form network structures as well as to improve the foam’s stability. Further investigation has revealed the desirable properties of crosslinked PVA foam (CPVAF) as a carrier of immobilized microorganisms. A crosslinked prepared PVA (CPVA) carrier was chosen for comparison and it was used for the preparation of the immobilization matrix. The main advantages in the use of immobilized cells in comparison with suspended ones include the retention in the reactor of higher concentration of microorganisms, easy removal of bacteria after use from the reaction mixture, providing the ability to control reaction time, reuse of cells for many reaction cycles, lowering the total production cost of cells-mediated reactions, provide pure products [24-26]. The efficiencies of each of free, immobilized cells (Bacillus licheniformis, Rhodococcuserythropolishas and Pseudomonas xanthomarina) on CPVAF and CPVA matrixes crosslinked by epichlorohydrin [17], and their biosurfactants in degradation of crude oil in water were evaluated. In addition, we evaluated the capability of each of CPVA and CPVAF in water, as immobilizers to the enhancement the degradation efficacy of each microorganism to degrade the pollutants.
Materials and Methods
Materials and microorganism
The PVA used in this study was analytical grade and was purchased from Merck, Germany. The average Mw of the PVA was 127,000 and the degree of hydrolysis was 89%. Epichlorohydrin (EP), calcium carbonate, sodium hydroxide, hydrochloric acid and other chemicals were all obtained from Beijing Chemical Reagent Factory (China) and used without further purification. The crude oil used in the present work, was Asphaltenic crude oil. The microorganisms used in this study were, Bacillus licheniformis ATCC10716 (B.l.) and Rhodococcus erythropolis ATCC13260 (R.e.) supplied by the microbial resources center (MIRCEN), Faculty of Agriculture, Ain Shams University, Cairo, Egypt. Also, Pseudomonas xanthomarina KMM 1447 (P.x.) bacterial was isolated from Gemsa Bay (Red Sea).
Molecular identification of the bacterial strain isolated from the Red Sea
An analysis of 16S rRNA was performed to taxonomically characterize the isolated strains (Sigma Scientific Services Co., Egypt). The cell of the bacterial strain was harvested through the enrichment medium up to 2×109 bacterial cells. DNA was extracted using protocol of Gene Jet genomic DNA purification Kit (Thermo) (Sigma Scientific Services Co., Egypt). To amplify the 16S rDNA gene, a polymerase chain reaction (PCR) was performed using two primers, the forward primer (5’-AGA GTT TGA TCC TGG CTCA-3’) and the reverse primer (5’-GGT TAC CTT GTT ACG ACT-3’). PCR was cleaned up to the PCR product using GeneJET™ PCR Purification Kit. A 45 ul of Binding Buffer was added to completed PCR mixture. The mixture was then thoroughly, transferred from step 1 to the GeneJET™ purification column. The mixture was centrifugated for 30-60 s at >12000 x g, then the flow were discarded. A 100 ul of wash buffer was added to the GeneJET™ purification column and centrifuged for 30-60 s. Then, discarded the flow-through and placed the purification column back into the collection tube. The mixture was centrifugated the empty GeneJET™ purification column for an additional one min. to completely remove any residual wash buffer. The purification column was transferred to a clean 1.5 ml micro centrifuge tube. A 25 ul of elution buffer was added to the center of the GeneJET™ purification column membrane and centrifuged for one min. The GeneJET™ purification column was discarded and the purified DNA was stored at -20°C. Following purification of the PCR products, the DNA sequence of the positive clone was subjected to a similarity search BLAST on the NCBI website (, and deposited into GenBank. Many relevant 16S rRNA gene sequences with validly published names were selected as references from the Gen- Bank.
Culture conditions
Culture medium and production of different biosurfactants: The bacterial strains were streaked on a nutrient agar slants and incubated for 24 h at 30°C. Two loops of each culture were inoculated in 40 ml of nutrient broth in a 100 ml Erlenmeyer flask and incubated in a rotary shaker 150 rpm at 30°C for 8-12 h until cell numbers reached 108 CFU/ml. For biosurfactant synthesis, a mineral salt medium with the following composition was utilized: 2.0 g/l of Na2HPO4, 2.0 g/l of KH2PO4, 0.01 g/l of MgSO4.7H2O, 2.5 g/l of NaNO3, 0.8 g/l of NaCl, 0.2 g/l of CaCl2, 0.8 g/l of KCl, 0.001 g/l of FeSO4. 7H2O and 5 ml of a trace element solution. Trace element solution contained 0.116 g/l of FeSO4·7H2O, 0.232 g/l of H3BO3, 0.41 g/l of CoCl2·6H2O, 0.008 g/l of CuSO4·5H2O, 0.008 g/l of MnSO4·H2O, 0.022 g/l of [NH4]6Mo7O24 and 0.174 g/l of ZnSO4 [27]. The carbohydrate (glucose) was added to make a final concentration 2%, and the concentration of yeast extract was 3%. Cultivation studies have been done in 500 ml flasks containing 150 ml medium at 30°C for 72 h.
Preparation of PVA hydrogel crosslinked by epichlorohydrin (CPVA) [16]
CPVA was prepared by adding PVA to 100 ml of distilled water and blending by a mechanical stirrer in a boiling water bath for 1 h. After the mixture cooled to room temperature, stoichiometric amounts of each of epichlorohydrin (EP) as the crosslinker and potassium hydroxide solution were added separately to the mixture with stirring it gently, at 35°C for 2 h. The amount ratios of PVA/E/KOH were: 100/20/25, 100/60/65, 100/100/105 and 100/125/130, 100/140/150. Five CPVA hydrogel disc samples were prepared.
Preparation of crosslinked PVA hydrogel foam (CPVAF)
CPVAF was prepared as follows: calcium carbonate powder and PVA were added in ratio 1:2 to 100 ml distilled water and blended by a mechanical stirrer in a boiling water bath for 1 h. After the mixture cooled to room temperature, the certain amount of hydrochloric acid (5 M) was added and the mixture was stirred vigorously to dissolve the calcium carbonate and produce CO2 gas bubbles. Then the molded foam was submerged in 200 ml NaOH (1 M) containing 1 ml of EP and stirred gently at 35°C for 2 h. All prepared CPVA and CPVAF gels were cut into discs of about 0.5 cm thickness and 1.2 cm diameter and maintained in sterile conditions until their use for cell immobilization [24].
Biodegradation test of the crude oil using free cells in presence/ absence of different biosurfactants and by immobilizing of these cells on (CPVA and CPVAF) gels
To assess the efficiency of different bacterial strains to degrade the crude oil, 2 ml of inoculum (7.5 log count) was inoculated into the medium mineral salt medium MSM (100 ml) in a 250 ml erlenmeyer flask. The cultures were incubated in a temperature controlled shaker incubator at 150 rpm at 30°C for 15 days, using (1g) crude petroleum oil as a sole carbon source with/ without adding the discs of CPVA and CPVAF gels separately. The biosurfactant was produced by using the medium MSM with (1g) glucose as a sole carbon source for 72 h followed by addition of (1 g) crude oil until the end of incubation period. A sample without inoculum was taken as a control. Hence, the flasks were incubated at 30°C, 150 rpm, pH 7.5 for 15 days [28]. After incubation period, the bacterial count was determined and the crude oil samples were extracted from different microcosm and gravimetric analysis was also determined as follow:
Determination of the growth counts for different bacterial in presence/ absence biosurfactant and at immobilized these bacterial on CPVA and CPVAF gels: The bacterial counts were implemented by using the plate count technique where the different microcosms samples (1ml) was serially diluted in a sterile saline. Then inoculation in Luria broth (LB) plates medium containing (g/l of distilled water), 10.0 g/l of NaCl, 10.0 g/l of tryptone and 5.0 g/l of extracted yeast, the medium was adjusted to pH 7.0. The cultures were then incubated at 30°C for 48 h, then; the plate count in the range 30-300 Calonies was recorded. The bacterial count /ml (average colony forming unit (CFU)/ ml) was calculated from the following equation:
Bacterial count / ml = colony count / plate x dilution factor [29].
Gravimetric estimation for the extracted crude oil after its biodegradation: After incubating period (15 days), the polluted bacterial broth (100 ml) was thoroughly shaken with carbon tetrachloride (50 ml 3 times) in a separating funnel and the three fractions were collected in case of crude oil samples. The collected organic layer was dried over anhydrous sodium sulphate and the solvent was removed by a rotary evaporator till reached a constant weight. The oil sample was accurately weighed, the percentage of the biodegradation oil was calculated and the alteration in its chemical composition was studied by chromatographic analysis (GC and HPLC) [2,30].
Characterization of CPVA and CPVAF hydrogels
The structures of carriers CPVA and CPVAF were characterized before and after foaming, by using the FT-IR spectra that, recorded using a Nicolet IS-10 FT-IR spectrophotometer. Also, the thermal stabilities of the CPVA and CPVAF carriers were studied using a Thermogravimetric analyzer (TGA) and Differential scanning calorimetry (DSC). All TGA spectra were recorded under a nitrogen atmosphere up to 600°C using a programmed rate of 10°C/min and the DSC spectra were obtained with a DSC-30 under N2 atmosphere at a heating rate of 20°C/min. X-ray diffraction patterns were recorded on X` Pert (Berlin, Germany) D500 diffract meter with a back mon°Chromatic and a Cu anticathode. The phase morphology was studied using a JSM-T20 (JEOL, Tokyo, Japan) scanning electron microscope (SEM). For scanning electron observations, the surface of the sample was mounted on a standard specimen stub. A thin coating (~ 10-6 m) of gold was deposited into the sample surface and attached to the stub prior to SEM examination in the microscope to avoid electrostatic charging during examination. The Swelling behavior of the prepared hydrogels was estimated by immersing a known weight of the sample disc in solutions of pH 7 at 30°C until the swelling equilibrium was reached. The disc was removed, dried with absorbent paper to get rid of excess water then weighed. The degrees of swelling (DS) for these samples were calculated at time intervals (5, 15, 30, 60, 120, 180 minutes) with respect to CPVA (A) and CPVAF (B) samples, with the following equation:
DS = (m- m’) / m’ (1),
Where m and m’ denote the weights of hydrogel and dried hydrogel sample, respectively [31].
Gas chromatographic analysis
Biodegradation of the crude oil was monitored using an Agilent 6890+ gas chromatography instrument according to the testing method IP 318 [32]. The detector was a flame ionization detector 325°C, separation was completed on HP-1 capillary column (100% methyl silicone siloxane, 30 m length, 0.35mm internal diameter and 0.25 mm thickness film), a dose of 0.5 μl was used using a splitter injector 300°C and the oven temperature 100-320°C reached applying a heating rate of 5°C/min. The carrier gas was nitrogen (2ml/min). Identification of the n-paraffins peaks was confirmed by chromatography a reference mixture of n-paraffins of a known composition under the same operating conditions.
High performance liquid chromatographic (HPLC) analysis [33]
The Identification and quantification of PAHs in the crude oil remained after biodegradation and the corresponding control sample were performed using HPLC. The apparatus used was model Waters HPLC 600 E, equipped with dual UV absorbance detector, model Waters 2487 and auto-sample Waters 717 plus attached to computerized system with millennium 3.2 soft ware. The condition of separation [34] is as follow: Column (Supelcosil.LC-PAH, 5 μm particles, 15 cm length and 4.6 mm internal diameter), Mobile phase (gradient acetonitrile: water 60 to 100% acetonitrile (v/v) over 45 minutes), Flow rate (0-2 min. 0.2 ml/min, 2-45 min. 1.0 ml/min) and Dector (Set at 254 nm).
Results and Discussions
Hydrogels characterization
PVA contributed to strength and durability of the carriers. To get high strength, the percentage of PVA in the experiment was 10% concentrations, the higher than 10% resulted viscous solutions [15]. The amounts and the ratio of the pore-forming agents are the important factors which decide the aperture uniformity and size distribution, and the elasticity of the foams. The infrared spectra of PVA crosslinked (CPVA) [16] and crosslinked PVA foam (CPVAF) are represented in Figure 1A and 1B, respectively. FTIR spectra shows broad peak at 3440 to 3100 cm–1 reveals stretching vibrations of the hydroxyl groups and the peak at 2940 to 2900 cm–1 is due to C-H stretching vibrations. The CPVA spectra shows abroad bonded hydroxyl peak around 3263 cm-1, but the hydroxyl peak of CPVAF was obviously less condensed broad, and was shifted to 3313 cm–1. The intramolecular and intermolecular hydrogen bonds of the OH groups of PVA and other molecule, shifted the band of –OH group to lower frequencies as shown in spectra of CPVA .The CaCO3 shows absorption bands at 1419, 871and 713 cm–1, which are attributed to the Ca-O Stretching vibration and bending vibration. This result shows that network structures were formed on the chains of the CPVA with a certain amount of hydroxyl. The stronger peak of CPVA and CPVAF carriers were at 1090 cm–1 (C–O–C), as a result of the formation of crosslinked network structures. FTIR spectra showed the bands at 1646, 1568 and 1654 cm–1 indicated presence of the residual vinyl acetate groups in the PVA chains (C=C) and the traces of water molecules (bending vibration). These peaks are very weak in spectra of CPVAF due to the more crosslinked hydrogels, than in the CPVA one. The peak around 1095 cm–1 denotes C-O stretching of the secondary alcoholic groups [16]. The swelling behaviors of the chemically crosslinked CPVA [20] and CPVAF carriers, pH (7) at 30oC were represented in Figures 2 and 3. The equilibrium swelling rates versus concentrations or the crosslinker ratios relationship is represented in Figure 2. The water uptake is found to decrease for CPVA matrix at increasing the ratio of crosslinker than certain ratio in PVA/E/ KOH (100/125/130). This behavior can be explained by the existence of an important crosslinking density which is in accordance with an increase in the crosslinker ratio to optimum swelling properties (9.1), after what , this property decrease (from 9.1 to 6.2) with an increasing in crosslinking density [20]. For CPVA and CPVAF, water uptake increases with increase of time, but the swelling property of CPVA is higher than in CPVAF and this was may suggested for occurring a high crosslinking density in CPVAF resulting in lowering the water uptake. Also, The PVAF hydrogel has the more porous with large size that may be decrease the retention water and, furthermore the presence the oxygen of CaCO3 may form physical bonding with hydroxyl group of PVA leading to a decrease in the penetration of water molecules into the hydrogel network. The thermal analysis of the carriers prepared was used to compare the differences in the polymeric arrangements of the carriers. The thermogravimetry (TG) curves are presented in Figure 4. The CPVA carrier had three main degradation steps: the first was at 189 and 260°C and 10% loss weight was ascribed to the release of volatile compounds, mainly water, which were present in the hydrophilic material. The second stage was between 260 and 400°C regarded as the elimination of acetic acid to form a polyene, whereas the third step was between 400 and 485°C corresponding to the breakage of the main chain. There was total 82% lost at last might be attributed to the decomposition of CPVA. TG curves for the CPVAF carrier also showed three consequent stages: The first was come between 160 and 270°C, and the weight loss was increased to 14% at 160°C, indicated an increase in carrier hydrophilicity than in CPVA [3]. The second stage was from 270 to 578.0°C and finally, the last stage was from 578.0 and 790.8°C. There was total 64% lost at last temperature. Also, the degradation events showed an increase in the thermal stability of the carrier as a result of adding foaming reagent to crosslinking PVA. The DSC curves of the carriers are presented in Figure 5. The sample carriers were included to establish a detailed behavior of the organization of polymeric chains. CPVAF exhibited an endothermic peak at about 223°C, corresponding to the melting temperature of PVA. The melting temperature was much increased for CPVA. This implied that foaming limited the mobility of the PVA chains. The addition of CaCO3 to the polymeric carrier increased the distance between the chains, regardless of whether the polymer became more crosslinked or branched, which made the organization of PVA in crystalline lattices difficult and formed network structures. The XRD patterns for CPVA (A) and CPVAF (B) carriers were given in Figure 6. The diffraction peak at around 18.4°C was a characteristic peak of the crystalline structure of PVA and it was shifted to less 2θ due to the some deformation in PVA crystallinty as a result of crosslinking. However, its intensity weakened significantly, indicating that the crystalline structure of PVA was changed after the introduction of CaCO3. It may be due to the intermolecular and intramolecular hydrogen bonding between the carbonyl groups in CaCO3and hydroxyl groups in PVA, which inhibited the formation of crystal structure. This promotes the formation of physically crosslinked PVA hydrogel in CPVAF so it becomes more crosslinked structure. Figure 7 shows the surface morphologies of CPVA (A) and CPVAF (B) by scanning electron microscope. It can be seen from Figure 7B that CPVAF were perfectly porous in shape with a rough surface. But, Figure 7A of CPVA shows the less pour in size than in 7B of CPVAF, also, it can be seen that the obtained surfaces of each CPVA (A) and CPVAF(B) were porous and the pore sizes were heterogeneous because reaction between CaCO3 and HCl was not uniform throughout the samples. So, CPVA has the more narrow pours, as a result it has the properties are favorable for producing good adsorption capacity. Therefore, an ideal hydrogel carrier should possess a highly porous structure to facilitate the non hindered diffusion of solutes and dissolved gases.
The chemical structure of the biosurfactants produced by different bacterial strains
Biosurfactants [9,10] are surfactants that are produced extracellularly or as part of the cell membrane by bacteria, yeasts and fungi. They can be potentially as effective with some distinct advantages over the highly used synthetic surfactants including high specificity, biodegradability and biocompatibility. In this work the scope was on certain types of the biosurfactants were produced by different bacterial strains that obtained from contaminated area in our country. The function of these biosurfactant was the increased the solubility of some hydrocarbon compounds so, it enhance the efficiency of microorganisms to degrade a crude oil. It was found that, the biosurfactants are grouped as glycolipids, lipopeptides, phospholipids, fatty acids, neutral lipids, polymeric and particulate compounds [35]. Most of these compounds are either anionic or neutral. Only a few are cationic such as those containing amine groups. The hydrophobic part of the molecule is based on long-chain fatty acids, hydroxy fatty acids or α-alkyl-β-hydroxy fatty acids. The hydrophilic portion can be a carbohydrate, amino acid, cyclic peptide, phosphate, carboxylic acid or alcohol. In this study, the microorganisms (Bacillus licheniformis, Rhodococcus erythropolis and Pseudomonas xanthomarina ) produced three types of the biosurfactants with different structures, cyclic lipopeptide surfactin, phosphatidyl ethanolamine and rhamnolipids respectivly. The structure of the producing biosurfactant was affected by some factors such as type of microorganism, pH, nutrient composition, substrate and temperature used. Where, in our work we choose the conditions that are suitable for the medium of microorganism in our country.
1. The bacterium Bacillus licheniformis has been produced surfactin biosurfactant with a cyclic structure that has affect on enhanced the ability of microorganism to degrade some of hydrocarbon compounds. Where, it increases the solubility of these compounds to increase the capability of microorganism to degrade them.
The Chemical structure of the biosurfactant that produced by Bacillus licheniformis.
2. The bacterium Rhodococcus erythropolis has been produced Phosphatidyl ethanolamine biosurfactant, with cationic structure contained the amino group with positive charges facility the solubility of some of hydrocarbon compounds and their degraded by cells.
3. The isolated bacterial strain Pseudomonas xanthomarina has been produced rhamnolipids. From the literature review the Pseudomonas sp. produced rhamnolipids biosurfactant rhamnolipids. This strain was first identified using molecular identification and performed by amplifying and sequencing the 16S rRNA gene sequences. The results of the identification procedure showed that the isolated bacteria belong to the Pseudomonas xanthomarina KMM 1447. It was found this type of surfactin has hydrophilic groups (COOH- and OH-) was lower the surface tension and so, the interfacial tensions at pH7, for some hydrocarbon compounds to be degraded by microorganism. Also, it contains a hydrophilic and a hydrophobic domain, may be facilitate the uptake of hydrocarbons into the producing cells
Application to hydrocarbon biodegradation
The high cell-retention capacity making CPVA and CPVAF polymers have an effective matrix, where they have the same condition, such as the polymer weight, time of incubation, pH, temperatures and the type of the cell. So, the high cell-retention capacities were expressed about the growth count of cell strains and not the potential of cell to degrade the oil. Where, this was attributed to adapting the cell to utilize some types of components present in oil. As shown at Table 1, the percentage of biodegradation of petroleum hydrocarbon samples, were arranged in this order, R.e. >B.l. > P.x. and Bio2> Bio 3 >Bio1, with respect to free cells and their produced biosurfactants respectively. The capabilities of B.l. and P.x. to oil degradation were enhanced at immobilized them on CPVA and restricted with CPVAF. No further degradation of petroleum hydrocarbon was observed at immobilized R.e. cell on CPVA and its degradation ability was restricted with CPVAF. The data obtained from the degradation of petroleum hydrocarbon by immobilized cells in all the matrices suggest that the rate of degradation was much higher than that with freely suspended cells. This may be due to a kind of membrane stabilization, which is assumed to be responsible for the cell protection and better degradation rates in the adsorbed cells. However, the fact that the rate of degradation was less in the CPVAF foamed than in CPVA matrices, may be attributed to the slow diffusion of the compounds (oil)into the gel discs. And also, may be as a result of releasing of some cells from gel disc into the medium, because of the large size porosity of the gel matrices.
Growth count of microorganisms
Three different types of the bacterial strains were used to evaluate their potential for degradation of petroleum hydrocarbons. Their degradation efficiency was improved by each of, adding their producing biosurfactants, and also, by immobilized each of them on two different types of polymers, CPVA and CPVAF. The growth of the different bacterial strains inoculated into the mineral salt medium MSM on the crude oil as a sole carbon and energy sources in presence /absence each of the CPVA and CPVAF gels discs separately and also biosurfactants, were indicated in Table 2. The count was determined after incubated them at 30°C, 150 rpm, pH 7.5 for 15 days [28]. As shown in Table 2, the bacterial count on crude oil, was increased in these order where, R.e. >P.x.>B.l., but, when adding the biosurfactant (Bio), the order will be change to, P.x.> R.e.>B.l. Where the growth count of bacterial P.X. enhanced with adding its producing biosurfactant 3(Bio3), and also, when immobilizing it on each of CPVA and CPVAF. On other hand the growth count of bacterium B.l. and R.e. were inhibited or restricted by immobilizing the on the polymer CPVAF, but enhanced with CPVA in case bacteria B.l. and somewhat restricted with R.e.
The degradation of paraffins compounds
The residual of the n-paraffin after biodegradation was identified using GC as shown in Table 3. The UCM% was high (84.68) in control sample than of the most residual samples, suggesting that the control sample we obtained was exposed to the most chronic oil pollution. Also, was noticed that the most remaining percentages of the n-paraffin after biodegradation are higher than its of the crude oil control, suggesting that occurring more biodegradation for UCM than that for paraffin compounds. The results revealed that the bacterium, Bacillus lichneformis ATCC 10716 (B.l.), Rhodococcus erythropolis ATCC 13260 (R.e.) and Pseudomonas xanthomarina KMM 1447 strains, that, were isolated from a biological waste-water, have the capability to utilizing paraffins as the sole source of carbon and energy and this capability was increased in this order, R.e.> P.x.>B.l. This is attributed to their efficiencies to degrade the non polar compounds (paraffin), but, the bacterial (B.l.) has the best degradation for unresolved complex mixture (UCM) with comparison with others bacterium. This ability increase when it was immobilized on each of CPVAF and CPVA polymers. On the other hand the paraffins biodegradations percentage, by R.e. and P.x. microorganisms were enhanced at adding to them their produced biosurfactants (Bio2 and Bio3) (19.05%, 19.77%, respectively). These percentages degradation increase at immobilized these cells on CPVA, but when R.e. was immobilized on CPVAF, the complete degradation for the paraffins and UCM, was determined to indicating that this polymer foaming type enhanced the biodegradation efficiency of R.e. to degrade completely the paraffin from C9 to C39 and UCM. As we can see, the macro porous CPVAF carrier could provide sufficient space for microbial growth. Also, the polarity of the produced biosurfactants by B.l., R.e. and P.x. was increased in this direction, (Bio 1< Bio 2 <Bio 3).
The degradation of PAHs
The brief identification and quantification of PAHs in the investigated of the crude oil remained after biodegradation and the corresponding control sample using HPLC, were shown in Table 4. The HPLC results showed that, the presence of 2,3 and 4,5,6- member rings of PAHs. In the control sample the percentage concentration of 4 -member rings is higher than that of the 5-member rings of PAHs. The results showed that the freely suspended Rhodococcus erythropolis (R.e.) can utilize 5-member rings of PAHs completely and degraded them to 3 and 4 -member rings of PAHs, Table 4. So, there no remaining of 5-member rings of PAHs was detected. On the other hand, the efficiency of Pseudomonas xanthomarina to degrade the 5-member rings of PAHs is less than that of the R.e. but, higher than that of B.l., where, the percentage concentration of the 5-member rings of PAHs is increase in presence B.l. than that in control sample. This result may be attributed to ability of this microorganism (B.l.) to degrade the 4 -member rings of PAHs that has certain polarity to lower 2-member rings of PAHs, that may be combined with each others to form the 5-member rings of PAHs. So, the degradation arrangement of polar compound by microorganism increase in this direction, R.e. > P.x.> B.l. The efficient of these microorganisms were enhanced by immobilized them on different types of polymers (CPVA and CPVAF) or by adding their produced biosurfactants to them. Biosurfactants accumulated at interfaces, forming micelles that lowered the surface tension and thereby enhanced the solubility of poorly soluble compounds in water [36]. So, it was shown (Table 4), that the degradation efficiency of the B.l. to degrade the low polar compound (4-member rings PAHs), was enhanced by adding its produced biosurfactant (Bio1) to it. But its potential to degrade the 5-member rings of PAHs, is not recorded only; furthermore the percentage concentration of these compounds increased (77.33%) than with the B.l. alone. Also, this behavior of biodegradation was noticed with adding the produced biosurfactant (Bio2) to R.e. strain, resulting in restricted the utilizing of this bacteria for the 5 -member rings of PAHs. It was found that, the combination of P.x. with its biosurfactant 3 (Bio3), enhanced its capability to degrade the 5-member rings of PAHs to 2 -member rings of PAHs. Moreover, this combination made them to utilize on the 4-member rings of PAHs, where, they were superior in removing these compounds to residue of 1.09%. The enhancement or restricting of these biosurfactants towards the degradation capabilities of these strains to degrade the crude oil may be attributed to their structures. So, due to the structure of Bio3 contains many hydrophilic groups act as adsorbance sites for crude oil and also, can react with polar compounds than others (paraffin) resulting in degradation these compounds. At immobilizing the strain B.l. on each of, CPVA and CPVAF polymers, it was found that, with CPVAF no significant degrading of 4 and 5-member rings of PAHs, was observed. Although, the efficient of this strain enhanced when it was immobilized on CPVA to remove these PAHs and the remains was 0.76 and 10.04% of each 4 and 5-member rings of PAHs respectively. This immobilizing method was enhanced the potential of this strain to degrade the 4 and 5-member rings of PAHs to 2-member rings of PAHs. But, this enhancement biodegradation proper decrease at immobilizing the R.e. strain on CPVA to degrade the 4 and 5-member rings of PAHs to 2 and 3-member rings of PAHs with the concentration of 43.32 and 32.62% respectively. However, this potential of this strain to degrade the 4 -member rings to the 3 -member rings was increased with CPVAF polymer. It was noticed that, the residual of the 5 -member rings increase more than that in the control sample, where, it may be as a result of the combination of low polar compounds. Also, this biodegradation behavior was occurred at immobilizing the P.x. strain on these polymers.
This study revealed that the more efficient degradation of fluoranthen (Flu) (4 -member rings) was completely by using P.x. cell combined with its biosurfactant or immobilized it on CPVA polymer. The high removal was occurred by freely P.x. and immobilized each of B.l. and R.e. cells on CPVA polymer or combined each of them with their produced biosurfactants. Also, chrysene (Chr) was removed completely by freely R.e. cell or by immobilized each of B.l., R.e. and P.x. cells on CPVAF and also, B.l. on CPVA. The superior removal was recorded by freely P.x. The complete degradation of Benzo [a] Pyrene (BaP) (5-member rings) was observed by immobilized each of B.l., R.e. and P.x. cells on CPVAF polymer and by freely R.e. cell. But, the superior degradation, was occurred by combination of P.x with its produced biosurfactant (Bio3), where, it being amphipathic molecules of the biosurfactant (Bio3) with a hydrophilic and a hydrophobic domain, may be facilitate the uptake of hydrocarbons into cells. It was observed that, the complete removal of Benzo [K] fluranthene (5-member rings) was only, by freely R.e cell and the good degradation was occurred by immobilized each of B.l., R.e. and P.x. cells on CPVA polymer and also, by immobilized R.e. cell on CPVAF polymer. As well, it was revealed the good degradation of Benzo [K] fluranthene by combined each of R.e.and P.x. cells with their produced biosurfactants and by freely P.x cell. Surfactants can increase the surface area of hydrophobic materials, in water environment, thereby increasing their water solubility. Hence, the presence of surfactants may increase the efficiency of microbial to degrade the pollutants. It was revealed that the physicochemical stability of the PVA carrier was increased and the hydroxyl groups created a hydrophilic micro-environment for the metabolism of the immobilized microorganisms. Thus there is a potential for the development of microbial technology for the treatment of waste water containing aromatic hydrocarbons.
The immobilization methods make the cells stay alive for a long time in the immobilized stage when the conditions are optimal. Bioremediation using immobilized cells has been widely investigated for numerous toxic chemicals such as paraffins and aromatic hydrocarbons. In the present study, the CPVA and CPVAF macroporous carriers were prepared based on PVA with a pore-forming agent (calcium carbonate) with respect for CPVAF and each of was crosslinked with epichlorohydrin. Calcium carbonates as foaming agent has lower toxicity to yeast cells. The CPVA and CPVAF hydrogel discs were showed; the higher stability in water but CPVA has greater biological activity than CPVAF hydrogels that has more crosslinked structure. The CPVA and CPVAF carriers can serve as a suitable material for immobilized microorganisms, as they have the better chemical and thermal stability. For immobilization of bacteria, the CPVA carrier supports the higher biomass density and microbial activity yield than the CPVAF carrier. The maximum growth count was for P.x. strain immobilized on CPVA (8×107 CFU/ml) and also at, presence of the Bio 3 with P.x (9×107 CFU/ml). The higher growth count may attribute to the greater mass transfer of the substrate (and oxygen) between the bulk solution and the immobilized on CPVA carrier or combined with Bio 3 microorganisms. The rate of degradation of oil by immobilized cells in various matrices is compared with that by freely suspended cells, and combined with their produced biosurfactants with regards to oil degrading capacity at various initial oil concentrations. The longevity of the hydrocarbons degrading activity was by immobilized cells and by presence of biosurfactant with cells. These preparation methods of CPVA, CPVAF and biosurfactants were inexpensive, low in toxicity, and easily performed; they can serve as a promising and economical technique for immobilizing microorganisms. In addition, may be after being modified, the CPVA and CPVAF could serve as valuable carriers or supports in the biotechnology and biochemistry fields.
We are grateful for the grant obtained from the members in Central Analytical Lab, Department of Processes Development and Petrochemicals Department, Egyptian Petroleum Research Institute (EPRI).

Tables and Figures at a glance


Table icon Table icon Table icon Table icon
Table 1 Table 2 Table 3 Table 4


Figures at a glance


Figure Figure Figure Figure
Figure 1 Figure 2 Figure 3 Figure 4


Figure Figure Figure
Figure 5 Figure 6 Figure 7
Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Relevant Topics

Recommended Conferences

Article Usage

  • Total views: 11832
  • [From(publication date):
    December-2014 - Sep 20, 2017]
  • Breakdown by view type
  • HTML page views : 8010
  • PDF downloads :3822

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

Agri, Food, Aqua and Veterinary Science Journals

Dr. Krish

[email protected]

1-702-714-7001 Extn: 9040

Clinical and Biochemistry Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Business & Management Journals


[email protected]

1-702-714-7001Extn: 9042

Chemical Engineering and Chemistry Journals

Gabriel Shaw

[email protected]

1-702-714-7001 Extn: 9040

Earth & Environmental Sciences

Katie Wilson

[email protected]

1-702-714-7001Extn: 9042

Engineering Journals

James Franklin

[email protected]

1-702-714-7001Extn: 9042

General Science and Health care Journals

Andrea Jason

[email protected]

1-702-714-7001Extn: 9043

Genetics and Molecular Biology Journals

Anna Melissa

[email protected]

1-702-714-7001 Extn: 9006

Immunology & Microbiology Journals

David Gorantl

[email protected]

1-702-714-7001Extn: 9014

Informatics Journals

Stephanie Skinner

[email protected]

1-702-714-7001Extn: 9039

Material Sciences Journals

Rachle Green

[email protected]

1-702-714-7001Extn: 9039

Mathematics and Physics Journals

Jim Willison

[email protected]

1-702-714-7001 Extn: 9042

Medical Journals

Nimmi Anna

[email protected]

1-702-714-7001 Extn: 9038

Neuroscience & Psychology Journals

Nathan T

[email protected]

1-702-714-7001Extn: 9041

Pharmaceutical Sciences Journals

John Behannon

[email protected]

1-702-714-7001Extn: 9007

Social & Political Science Journals

Steve Harry

[email protected]

1-702-714-7001 Extn: 9042

© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version