PHENOL BIODEGRADATION BY RALSTONIA PICKETTII EXTRACTED FROM PETROLEUM REFINERY OIL SLUDGE

Phenol-degrading bacterial strains have been extracted from oil-sludge samples collected from a local refinery. A selective medium was used to isolate the active strain capable of utilizing phenol as a sole carbon source, which was identified as Ralstonia pickettii. The growth kinetics of mixed and isolated R. pickettii suspensions were investigated using different initial concentrations of phenol in the range of 25 to 200 g m^?3 at 35°C and pH of 8.5. The results were compared to those of a commercially available mixed bacterial suspension, which was either acclimatized to 100 g m^?3 phenol concentration, extracted from PVA particles that were subjected to real petroleum refinery wastewater containing phenol, or an isolated active strain grown on a selective medium that was identified as Pseudomonas putida. The effect of substrate inhibition was observed using all bacterial suspensions, and the growth results were used to determine the parameters of a suitable kinetic model. It was found that the phenol biodegradation ability of the indigenous bacteria, R. pickettii, isolated from refinery sludge was comparable to that of the commercially available bacteria.     

Application of the accelerated shelf life testing method (ASLT) to study the survival rates of freeze‐dried Lactococcus starter cultures

The survival rates of two freeze‐dried strains, Lactococcus lactis var diacetylactis and Lactococcus lactis var lactis, were evaluated using the Accelerated Shelf Life Testing (ASLT) method. The strains were initially isolated from a brand of a Tunisian fermented milk product. Lactococcus cell survival observed at higher temperatures was used to extrapolate to shelf life at a lower storage temperature of 4 °C. The apparent kinetics of the survival rate loss were estimated and the effect of storage temperature was quantified by determining the inactivation energies for various samples. The work has shown an overall higher survival rate of the strain Lactococcus lactis var diacetylactis. An average half‐life of a strain maintained at 25 °C was equal to about 7 days as compared with about 43 days at 4 °C. The addition of lyoprotectants such glycerol, saccharose and calcium carbonate to the drying medium, improved the survival of such bacteria. © 2001 Society of Chemical Industry     

Microbial aspects of linear alkylbenzene sulfonate degradation in coastal water

Viable and total bacteria were determined during linear alkylbenzene sulfonate (LAS) degradation in coastal seawater. Viable bacteria were determined by plate counts on marine agar media, while total bacteria were determined by flow cytometry after SYTO-13 staining. LAS degradation was monitored by high-performance liquid chromatography analysis. Seawater samples with LAS at 5 mg/L, incubated in the laboratory (20°C, 100 rpm, 30 d), showed in most cases a similar evolution in bacterioplankton abundance over time, characterized by three phases: (i) a progressive increase in bacterial density; (ii) a later decrease; and (iii) a fluctuating stationary phase. Bacterioplankton degraded the LAS by growing to populations with a high percentage of viable bacteria. The bacteria were rapidly grazed by protozoa, preventing anomalous high bacterial growth and ensuring the later channeling of LAS carbon to upper trophic levels.     

Study of nanofiber scaffolds of PAA,PAA/CS,and PAA/ALG for its potential use in biotechnological applications

In recent times, electrospun nanofibers have been widely studied from several biotechnological approaches; in this work, poly(acrylic acid) (PAA) solutions mixed with chitosan and alginate were electrospun and characterized to determine the behavior of these fibers when used in combination with bacteria, different samples were incubated with the bacterial strains: Streptomyces spp., Micromonospora spp., and Escherichia coli and a OD600 test was performed. The formation of nanofibers via electrospinning and the physicochemical properties of the obtained fibers were evaluated. Results showed that the presence of chitosan enhanced the thermal stability of PAA, since PAA/alginate fibers lost 5% of their mass at 41°C, whereas PAA/chitosan lost this amount at around 125°C. The fibers demonstrated suitable characteristics to be used as a bacteria bioreactor.     

Effect of ZnO on the structural,physio-mechanical properties and thermal shock resistance of Li2O–Al2O3–SiO2 glass-ceramics

The composition of lithium aluminosilicate (LAS) with different zinc oxide-magnesium oxide (ZnO–MgO) contents that ranged from 0 to 1.45 wt percent (wt%) was investigated to determine the thermal shock resistance properties of the glass-ceramics. The LAS glasses were melted in an alumina crucible at 1550 °C for 5 h, and the green compact samples were then heat-treated at 1100 °C for 3.5 h. The presence of zinc oxide (ZnO) in the compositions did not change the major crystal phase of β-spodumene. However, the addition of ZnO shifted the pronounced peak to a lower angle and increased the percentage of crystallinity from 55% to 59%. Additionally, the function of ZnO in LAS glass-ceramics as the network modifier was confirmed through Fourier Transform Infrared Spectroscopy (FTIR) analysis. The physio-mechanical properties were improved when 1.45 wt% ZnO was added to the LAS glass-ceramics. The results showed increased density (2.42 g/cm³), low porosity (0.85%), high flexural strength (125.23 MPa), and low coefficient of thermal expansion (25–800 °C) (CTE_{(25–800 °C)}) value of 1.73 × 10^?6 °C^?1. Meanwhile, the thermal shock resistance properties evaluation of the LAS glass-ceramics at different ZnO contents were conducted at different thermal shock temperatures of 200 °C, 500 °C, and 800 °C. The critical temperature of the LAS specimens with 1.45 wt% ZnO demonstrated the ability to withstand a thermal shock at 800 °C while preserving 87% of their initial strength of 108.40 MPa, exemplifying the best LAS glass-ceramics properties for rapid high-temperature change applications.     

Survival,oxidative stability,and surface characteristics of spray dried co-microcapsules containing omega-3 fatty acids and probiotic bacteria

The objective of the study was to determine optimum inlet and outlet air temperatures of spray process for producing co-microcapsules containing omega-3 rich tuna oil and probiotic bacteria L. casei. These co-microcapsules were produced using whey protein isolate and gum Arabic complex coacervates as shell materials. Improved bacterial viability and oxidative stability of omega-3 oil were used as two main criteria of this study. Three sets of inlet (130°C, 150°C, and 170°C) and outlet (55°C, 65°C, and 75°C) air temperatures were used in nine combinations to produce powdered co-microcapsule. The viability of L. casei, oxidative stability of omega-3 oil, surface oil, oil microencapsulation efficiency, moisture content, surface elemental composition and morphology of the powdered samples were measured. There is no statistical difference in oxidative stability at two lower inlet air temperatures (130°C and 150°C). However, there was a significant decrease in oxidative stability when higher inlet temperature (170°C) was used. The viability of L. casei decreased with the increase in the inlet and outlet air temperatures. There was no difference in the surface elemental compositions and surface morphology of powdered co-microcapsules produced under these nine inlet/outlet temperature combinations. Of the range of conditions tested the co-microcapsules produced at inlet-outlet temperature 130–65°C showed the highest bacterial viability and oxidative stability of omega-3 and having the moisture content of 4.93?±?0.05% (w/w). This research shows that powdered co-microcapsules of probiotic bacteria and omega-3 fatty acids with high survival of the former and high stability against oxidation can be produced through spray drying.     

Some properties of bacterial cellulose produced by new native strain Gluconacetobacter sp. A06O2 obtained from Turkish vinegar

The aim of the study was to isolate and identify an acetic acid bacterial strain having high cellulose yield and to investigate some physicochemical properties of bacterial cellulose (BC). Acetic acid bacteria were isolated by using 62 samples (vinegar, fruit, vegetable, and soil) from different region of Turkey. The cellulose production ability of 153 isolates was determined. A strain (A06O2) having high and stable cellulose yield was identified by biochemical tests and 16S rRNA gene sequencing and compared with type strain Gluconacetobacter xylinus NRRL B‐759. Based on the results, strain A06O2 was named at the genus level as Gluconacetobacter, however, species level identification could not be made. Celluloses from both strains were purified to investigate the physicochemical properties such as thermal properties, solubility in various solvents, elemental composition, tensile properties, and surface properties by FTIR and SEM. The results showed that the cellulose samples of two bacterial strains differed in the physicochemical properties. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Bacterial-barnacle interaction: Potential of using juncellins and antibiotics to alter structure of bacterial communities

In preparation for studies using natural products to probe interactions between bacterial consortia and settlement stage barnacles, we isolated 16 strains of bacteria associated with barnacles and examined: (1) effects of films of bacterial isolates on barnacle settlement, and (2) bacteriostatic effects of juncellins and standard antibiotics. Bacteria were isolated from the biofilm associated withBalanus amphitrite. On the basis of morphological and biochemical characteristics, bacteria were classified into five major groups:Aeromonas, Alcaligenes, Flavobacterium, Pseudomonas, andVibrio. Barnacle settlement was inhibited by allVibrio films and 64% of the other isolates. No film stimulated barnacle settlement. Juncellins were approximately as potent as standard antibiotics for all bacterial species tested.Vibrio spp. were most resistant to juncellins.     

Activation of soil respiration and shift of the microbial population balance in soil as a response to Lavandula stoechas essential oil

Lavandula stoechas, a native plant of Greece, is rich in essential oil and fenchone is its major constituent. We examined the effect of the essential oil and its main constituents on soil metabolism and microbial growth. Addition of the essential oil or fenchone to soil samples induced a remarkable increase in soil respiration. This was accompanied by an increase in the soil bacterial population of three orders of magnitude. This sizable population was not qualitatively similar to that of the control soil samples. One bacterial strain dominated soil samples treated with L. stoechas essential oil or fenchone. By use of the disk diffusion assay, we evaluated the capacity of three bacterial strains that we isolated from the soil samples, as well as Escherichia coli and Bacillus subtilis (reference strains), to grow in the presence of the essential oil and three of its main constituents (fenchone, cineol, -pinene). The substances tested did not inhibit the growth of the strain found to dominate the bacterial populations of treated soil samples; they severely inhibited B. subtilis. The other two isolated strains could also grow in liquid cultures in the presence of different quantities of essential oil or fenchone. Addition of fenchone at the end of the exponential phase increased the cell numbers of the strain that dominated the bacterial populations of treated soil samples, indicating use of the substrate added. On the basis of these results, we propose a scheme of successional stages during the decomposition process of the rich-in-essential-oil litter of aromatic plants that abound in the Mediterranean environment.     

Reduction of hexavalent chromium by Bacillus sp. isolated from chromite mine soils and characterization of reduced product

BACKGROUND: The reduction of highly mobile and toxic hexavalent chromium by bacterial strains is considered to be a viable alternative to reduce Cr(VI) contamination, in soils and water bodies, emanating from the overburden dumps of chromite ores and mine drainage. The present study reports the isolation of Cr(VI) resistant bacterial strains from an Indian chromite mine soil and their potential use in reduction of hexavalent chromium. RESULTS: Among the isolates, a bacterial strain (CSB‐4) was identified as Bacillus sp. based on standard biochemical tests and partial 16SrRNA gene sequencing, which was tolerant to as high as 2000 mg L^?1 Cr(VI) concentration. The strain was capable of reducing Cr(VI) to Cr(III) in different growth media. Under the optimized conditions pH ～7.0, 100 mg L^?1 Cr(VI), 35 °C temperature and stirring speed 100 rpm, CSB‐4 reduced more than 90% of Cr(VI) in 144 h. The time course reduction data fitted well an exponential rate equation yielding rate constants in the range 3.22 × 10^?2 to 6.5 × 10^?3 h^?1 for Cr(VI) concentration of 10–500 mg L^?1. The activation energy derived from temperature dependence rate constants between 25 and 35 °C was found to be 99 kJ mol^?1. The characterization of reduced product associated with bacterial cells by SEM‐EDS, FT‐IR and XRD was also reported. CONCLUSION: Reasonably high tolerance and reduction ability of indigenous Bacillus sp. (CSB‐4) for Cr(VI) under a wide range of experimental conditions show promise for its possible use in reclamation of chromite ore mine areas including soils and water bodies. Copyright © 2010 Society of Chemical Industry     

Deoxycholic acid formation in gnotobiotic mice associated with human intestinal bacteria

In humans and animals, intestinal flora is indispensable for bile acid transformation. The goal of our study was to establish gnotobiotic mice with intestinal bacteria of human origin in order to examine the role of intestinal bacteria in the transformation of bile acids in vivo using the technique of gnotobiology. Eight strains of bile acid-deconjugating bacteria were isolated from ex-germ-free mice inoculated with a human fecal dilution of 10⁻⁶, and five strains of 7α-dehydroxylating bacteria were isolated from the intestine of limited human flora mice inoculated only with clostridia. The results of biochemical tests and 16S rDNA sequence analysis showed that seven out of eight bile acid-deconjugating strains belong to a bacteroides cluster (Bacteroides vulgatus, B. distasonis, and B. uniformis), and one strain had high similarity with Bilophila wadsworthia. All five strains that converted cholic acid to deoxycholic acid had greatest similarity with Clostridium hylemonae. A combination of 10 isolated strains converted taurocholic acid into deoxycholic acid both in vitro and in the mouse intestine. These results indicate that the predominant bacteria, mainly Bacteroides, in human feces comprise one of the main bacterial groups for the deconjugation of bile acids, and clostridia may play an important role in 7α-dehydroxylation of free-form primary bile acids in the intestine although these strains are not predominant. The gnotobiotic mouse with bacteria of human origin could be a useful model in studies of bile acid metabolism by human intestinal bacteria in vivo.     

Production of ellagic acid from degradation of valonea tannins by Aspergillus niger and Candida utilis

Two fungal strains, effective in converting valonea (Quercus aegilops) tannins into ellagic acid (EA), were isolated from soil contaminated by valonea tannins, and were tentatively identified as Aspergillus niger and Candida utilis. Properties of EA accumulation by the two isolates from valonea tannins' fermentation were studied. Both the strains preferred sucrose to glucose as the additional carbon and energy source. The most suitable concentrations of valonea tannins in fermentation media for EA accumulation by A niger and C utilis were 5.0 and 9.0 g dm^?3 with EA yields of 12.1 and 8.9% (w/w), respectively. The optimal temperature for the two strains was 28 °C, while the preferred pH values of the fermentation media were 4.5–5.0 for A niger and 4.8–5.2 for C utilis. The tannin tolerances of A niger and C utilis were adapted to 20 and 25 g dm^?3 by gradually increasing the concentrations of valonea tannins in the culture media. The adapted strain of A niger was able to completely degrade 20 g dm^?3 valonea tannins with an EA yield of 14.3% in 9 days. Meanwhile, the adapted strain of C utilis decreased the valonea tannins' level from 25 to 9.1 g dm^?3 with an EA yield of 11.48%. The degradation ability of A niger came from tannase whose activity in the medium was 63 U cm^?3 at the ninth day of fermentation, and that of C utilis was due to both tannase and polyphenol oxidase (PPO) whose activities were 32 U cm^?3 and 29 U cm^?3 at the ninth day. The coculture of both the adapted strains could completely degrade 25 g dm^?3 valonea tannins in only 7 days with a remarkably increased EA yield (21%). The activities of tannase and PPO of the coculture at the seventh day were 66 U cm^?3 and 47 U cm^?3 respectively, which proved the synergistic effect of the two enzymes on valonea tannins' degradation and EA accumulation. Copyright © 2005 Society of Chemical Industry     

Correlation between crystallinity and thermal expansion in LiAlSiO4 ceramics prepared by spark plasma sintering

LiAlSiO₄ (LAS) ceramics are prepared by using the sol-gel method followed by spark plasma sintering. XRD patterns and SEM images verify that the ceramics contain amorphous and LAS phases and that microcracks appear in the sample prepared at 900 °C due to its larger grain size. Compared with applied pressure and soaking time, sintering temperature has a greater impact on the crystallinity and density of the ceramics during sintering. High-temperature XRD results reveal that the LAS phase exhibits its intrinsic negative thermal expansion independently in all samples regardless of crystallinity. The coefficients of thermal expansion (CTE) measured by the dilatometric method change from positive values in samples prepared at 600 and 650 °C to near zero in samples prepared at 700 and 800 °C and then to a negative value in the sample prepared at 900 °C. The combined effects of an amorphous phase with a positive CTE and the LAS phase with a negative CTE are responsible for the observed transformation of thermal expansion in the samples. The calculated total CTEs of the glass-ceramic bulks are in agreement with the results measured through the dilatometric method in samples prepared at 650–800 °C. Microcracks in the sample prepared at 900 °C cause a more negative bulk CTE than the calculated CTE.     

Cold-active enzymes from cold-adapted bacteria

The properties of amylase, lipase and protease, excreted by newly isolated bacteria from snow-covered soil, salmon intestine and crab intestine, have been investigated. One amylase, one lipase, and three proteases have been characterized by shifts in their apparent optimal activities toward low temperatures and by reductions in their activation energy values. The discovered enzymes were rapidly inactivated at temperatures above the optimum (30 to 40°C). These results suggest that the enzymes are cold-active. The best cold-active protease producer, isolated from salmon intestine, has been identified as Flavobacterium balustinum by the analysis of 16S rRNA. The optimal growth temperature of this bacterium was 20°C, but a higher amount of protease activity was present at 10°C.     

Mixed Micellization of Sodium Dodecylbenzene Sulfonate with Polyoxyethylene Lauryl Ether Surfactants (POLE4 and POLE23) in n-Butanol Aqueous Solution

The values of critical micelle concentration and counterion binding constant for the mixed micellizations of sodium dodecylbenzenesulfonate (DBS) with polyoxyethylene(4) lauryl ether (POLE4) and polyoxyethylene(23) lauryl ether (POLE23) in aqueous solution of n-butanol at 25 °C were determined as a function of the overall mole fraction of DBS by using the electric conductivity and the surface tension methods. Various thermodynamic parameters were calculated and analyzed for the mixed micellization of DBS/POLE4 and DBS/POLE23 systems by means of the equations derived from the nonideal mixed micellar model. The results show that DBS/POLE23 mixed system has a greater deviation from the ideal model than DBS/POLE4 mixed system. These deviations of thermodynamic parameters for both mixed systems become greater with the addition and concentration increase of n-butanol.     

Isolation,Screening, and Characterization of Naphthalene-Degrading Bacteria from Zarand Mine,Iran

ABSTRACT

PAHs are aromatic hydrocarbons with two or more fused benzene rings. They are formed during the thermal breakdown of organic molecules and their succeeding recombination. Naphthalene is the simplest (PAHs) that is carcinogenic. Bioremediation method is considered as an economical and safe approach for the elimination of aromatic compounds from environment. The bacteria were capable to grow on various hydrocarbons like naphthalene. The aim of this research is to isolate and identify naphthalene-degrading bacteria from the coal mine of Zarand. Four samples of water and sludge from various sites of the mine were collected. These sites include the following: Main coal vacate site (MC), Inoculum Sump site (IB), Sludge aggregate site (SA), and Near sludge aggregate site (NF). In this study, 12 bacterial strains that utilize naphthalene at initial concentration 200 mg/L (ppm) as carbon and energy sources for growth were isolated from the Zarand mine in Iran. In addition, bacterial cell density was assayed by measuring the OD₆₀₀. In addition, total naphthalene-degrading bacteria were quantified with the most probable number (MPN) procedure using microtiter plates and the colony-forming unit (CFU) method. The results had shown that most of the naphthalene degrader bacteria aggregated in (SA) site. Six bacteria, isolated from wastewater and oil-contaminated soil showed great potential as naphthalene degraders up to 400 (ppm) and selected for biochemical characteristics. Naphthalene tolerance of the strains in various concentrations of naphthalene indicates that the strain 38 N can grow best at 600 (ppm) naphthalene. This strain was identified based on 16S rRNA gene analysis that showed belonging to Sphingobacterium multivorum AHB38N.     

Strain isolation and optimization of process parameters for bioconversion of glycerol to lactic acid

BACKGROUND: The crude glycerol from biodiesel production represents an abundant and inexpensive source which can be used as raw material for lactic acid production. The first aim of this investigation was to select a strain suitable for producing lactic acid from glycerol with a high concentration and productivity. The second aim was to obtain the optimum fermentation conditions, as a basis for large‐scale lactate production in the future. RESULTS: Eight bacterial strains, which could aerobically convert glycerol to lactic acid, were screened from soil samples. One of the strains, AC‐521, which synthesized lactic acid with a higher concentration, was identified based on its 16S rDNA sequences and physiological characteristics. These results indicated that this strain was a member of Escherichia coli. The optimal fermentation conditions for Escherichia coli AC‐521 were 42 °C, pH 6.5, 0.85 min^?1 (K_La). CONCLUSION: Escherichia coli AC‐521 suitable for producing lactic acid from glycerol with high concentration and productivity was identified. After 88 h of fed‐batch fermentation, both the lactic acid concentration and glycerol consumption reached maximum, giving 85.8 g L^?1 of lactic acid with a productivity of 0.97 g L^?1 h^?1 and a yield of 0.9 mol mol^?1 glycerol. Copyright © 2009 Society of Chemical Industry     

Effects of water sorption at different temperatures on permanent changes in an epoxy

Crosslinked epoxy resins, tetraglycidyl 4,4′-diamino diphenyl methane cured with 4,4′-diamino diphenyl sulfone, were soaked in water at either 25°C or 70°C for varying lengths of time. The infrared spectra and DSC thermograms were obtained for samples that were soaked, or soaked and dried. There was a monotonic decrease in exothermic reaction energy with water content. The glass transition was also lowered, although samples soaked at 70°C showed a leveling in the T_g around 115°C. When the soaked samples were dried, the exothermic reaction energy showed near reversibility for samples soaked at 25°C while the 70°C samples were highly irreversible. IR of the latter samples showed that the 70°C water soaking resulted in reaction of some of the unreacted epoxide groups that remained after the initial cure.     

Cell growth kinetics and ice nucleation activity of pseudomonas syringae

The bacterium Pseudomonas syringae causes freezing of supercooled water at temperatures close to 0°C. In this study, the growth kinetics and ice nucleation activity (INA) of the bacterium P. syringae pv. syringae cit 7 were investigated in a batch and continuously operated laboratory scale bioreactor system. Under continuous culture conditions, the bacterial INA decreased with an increase in dilution rate. The maximum biomass and INA productivities were obtained at a dilution rate of 0.054 hr^?1 at 25°C and pH 7.0. The results of this investigation can be applied towards the large scale production of P. syringae bacteria for snow making and other commercial applications of ice nucleation.     

Studies on Biosurfactants Produced using Bacillus cereus Isolated from Seawater with Biotechnological Potential for Marine Oil-Spill Bioremediation

With the aim of producing a biotensioactive material for use in the remediation of marine environments, screening for biosurfactant-producing bacteria was conducted with strains isolated from seawater contaminated with petroleum derivatives. Gene sequencing revealed that all four promising biosurfactant-producing isolates belonged to the same genus and species, namely Bacillus cereus. The biosurfactant-producing bacteria were cultivated with different carbon (glucose, soybean oil, and waste frying soybean oil) and nitrogen (ammonium chloride, sodium nitrate, urea, and peptone) sources. B. cereus strain BCS0 was chosen as the best biosurfactant producer in a mineral medium with 2% frying oil and 0.12% peptone. Following the optimization of agitation and cultivation time, an agitation rate of 250 rpm and 48 h of cultivation were selected. Under these conditions, the surface tension was reduced to 27 mN m⁻¹ and the biosurfactant concentration was 3.5 g L⁻¹. The critical micelle concentration (CMC) of the biosurfactant was defined as 500 mg L⁻¹. The biosurfactant remained stable within large ranges of pH (2–10), salinity (2–10%), and temperature (5–120 °C). Under these conditions, motor oil emulsification rates were greater than 90%. Moreover, the biosurfactant properties remained unaltered after heating at 90 °C for 120 min. The biosurfactant enhanced the degradation of motor oil up to 96% in 27 days and exhibited considerable motor oil displacement capacity. Thus, the biosurfactant has potential in the application of remediation processes in marine environments.