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Biodegradation of [14C]phenol in secondary sewage and landfill leachate measured by double-vial radiorespirometry.

Double-vial radiorespirometry was used to estimate the biodegradation rates of 14C-labeled phenol in a landfill leachate and a secondary treated domestic wastewater. Rates were found to be comparable for each material at each of the three concentrations tested. Sewage microorganisms immediately began biodegrading the [14C]phenol; landfill leachate microorganisms required a lag period before maximum biodegradation of the [14C]phenol. The apparent rate of [14C]phenol biodegradation was 2.4 times faster in the sewage than in the landfill leachate. Double-vial radiorespirometry was shown to be an effective method for screening biodegradation rates in aquifers.

Biodegradation, Environmental↗

Screening test for assessment of ultimate biodegradability: linear alkylbenzene sulfonates.

A relatively simple shake-flask system for determining CO2 evolution was developed to assess the ultimate biodegradability by soil and sewage micro-organisms of chemicals which enter the environment. Linear alkylbenzene sulfonates (LAS) were used as model compounds to evaluate the method and were found to undergo substantial biodegradation in this dilute system. At the 30 mg/liter test concentration, higher-molecular-weight LAS compounds were biodegraded at a slower rate and to a lesser extent than lower-molecular-weight LAS, an effect which was eliminated or greatly reduced upon incremental addition of the LAS to the test medium during the first week of incubation. LA35S was used to demonstrate rapid LAS desulfonation, and 14CO2 evolution studies with (14C) benzene ring-labeled LAS indicated concomitant biodegradation of the entire LAS molecule as well as the LAS aromatic component. The test can be employed to examine numerous compounds at the same time and is readily adapted to studies of the effect of variation in temperature and oxygen concentration on biodegradation.

Bacteria↗

Hydrocarbon biodegradation in oxygen-limited sequential batch reactors by consortium from weathered, oil-contaminated soil.

We studied the use of sequential batch reactors under oxygen limitation to improve and maintain consortium ability to biodegrade hydrocarbons. Air-agitated tubular reactors (2.5 L) were operated for 20 sequential 21-day cycles. Maya crude oil-paraffin mixture (13,000 mg/L) was used as the sole carbon source. The reactors were inoculated with a consortium from the rhizosphere of Cyperus laxus, a native plant that grows naturally in weathered, contaminated soil. Oxygen limitation was induced in the tubular reactor by maintaining low oxygen transfer coefficients (k(L)a < 20.6 h(-1)). The extent and biodegradation rates increased significantly up to the fourth cycle, maintaining values of about 66.33% and 460 mg x L(-1) x d(-1), respectively. Thereafter, sequential batch reactor operation exhibited a pattern with a constant general trend of biodegradation. The effect of oxygen limitation on consortium activity led to a low biomass yield and non-soluble metabolite (0.45 g SS/g hydrocarbons consumed). The average number of hydrocarbon-degrading microorganisms increased from 6.5 x 10(7) (cycles 1-3) to 2.2 x 10(8) (cycles 4-20). Five bacterial strains were identified: Achromobacter (Alcaligenes) xylosoxidans, Bacillus cereus, Bacillus subtilis, Brevibacterium luteum, and Pseudomonas pseudoalcaligenes. Asphaltene-free total petroleum hydrocarbons, extracted from a weathered, contaminated soil, were also biodegraded (97.1 mg x L(-1) x d(-1)) and mineralized (210.48 mg CO2 x L(-1) x d(-1)) by the enriched consortium without inhibition. Our results indicate that sequential batch reactors under oxygen limitation can be used to produce consortia with high and constant biodegradation ability for industrial applications of bioremediation.

Bacteria↗

Marked inflammatory sequelae to implantation of biodegradable and nonbiodegradable polymers in porcine coronary arteries.

BACKGROUND: With the thrombogenic tendency and permanent implant nature of metallic stents, synthetic polymers have been proposed as candidate materials for stents and local drug delivery designs. We investigated the biocompatibility of several synthetic polymers after experimental placement in the coronary artery. METHODS AND RESULTS: Five different biodegradable polymers (polyglycolic acid/polylactic acid [PGLA], polycaprolactone [PCL], polyhydroxybutyrate valerate [PHBV], polyorthoester [POE], and polyethyleneoxide/polybutylene terephthalate [PEO/ PBTP]) and three nonbiodegradable polymers (polyurethane [PUR], silicone [SIL], and polyethylene terephthalate [PETP]) were tested as strips deployed longitudinally across 90 degrees of the circumferential surface of coil wire stents. Appropriately sized polymer-loaded stents were implanted in porcine coronary arteries of 2.5- to 3.0-mm diameter. Four weeks after implantation, stent patency was assessed by angiography followed by microscopic examination of the coronary arteries. The biodegradable PCL, PHBV, and POE and the nonbiodegradable PUR and SIL evoked extensive inflammatory responses and fibrocellular proliferation (thickness of tissue response: 0.79 +/- 0.22, 1.12 +/- 0.01, 2.36 +/- 0.60, 1.24 +/- 0.36, and 1.43 +/- 0.15 mm, respectively). Less but still severe responses were observed for the biodegradable PGLA and PEO/PBTP (0.46 +/- 0.18 and 0.61 +/- 0.23 mm, respectively) and for the nonbiodegradable PETP (0.46 +/- 0.11 mm). CONCLUSIONS: An array of both biodegradable and nonbiodegradable polymers has been demonstrated to induce a marked inflammatory reaction within the coronary artery with subsequent neointimal thickening, which was not expected on the basis of in vitro tests. The observed tissue response may be attributable to a combination of parent polymer compound, biodegradation products, and possibly implant geometry.

Animals↗

Effect of ethoxylate number and alkyl chain length on the pathway and kinetics of linear alcohol ethoxylate biodegradation in activated sludge.

Batch activated-sludge die-away studies were conducted with various pure homologs to determine the effect of ethoxylate number and alkyl chain length on the kinetics of primary and ultimate biodegradation of linear alcohol ethoxylates. The 14C-(ethoxylate) homologs C14E1, C14E3, C14E6, and C14E9 were used to investigate the effect of ethoxylate number, and 14C-(ethoxylate) homologs C12E6, C14E6, and C16E6 were used to examine the effect of chain length. Activated sludge was dosed with a trace concentration (0.2 microM) of each homolog, and the disappearance of parent, formation of metabolites, production of 14CO2, and uptake into solids were monitored with time. Ethoxylate number had little effect on the first-order decay rates for primary biodegradation, which ranged from 61 to 78 h(-1). However, alkyl chain length had a larger effect, with the C16 chain-length homolog exhibiting a slower rate of parent decay (18 h(-1)) compared to its corresponding C12 and C14 homologs (61-69 h(-1)). Ethoxylate number affected the mechanism of biodegradation, with fission of the central ether bond to yield the corresponding fatty alcohol and (poly)ethylene glycol group increasing in dominance with increasing ethoxylate number. Based upon the measured rates of primary biodegradation, removal of parent during activated-sludge treatment was predicted to range between 99.7 and 99.8% for all homologs except C16E6, which had a predicted removal of 98.9%. Based upon the measured rates of ultimate biodegradation, removal of ethoxylate-containing metabolites was predicted to exceed 83% for all homologs. These predictions corresponded closely with previously published removal measurements in laboratory continuous activated-sludge systems and actual treatment plants.

Alcohols↗

Prediction of polycyclic aromatic hydrocarbon biodegradation in contaminated soils using an aqueous hydroxypropyl-beta-cyclodextrin extraction technique.

This study investigated the use of an aqueous hydroxypropyl-beta-cyclodextrin (HPCD) shake extraction to predict the degree of microbial degradation of polycyclic aromatic hydrocarbons (PAHs) in soils. Three different aged PAH-contaminated soils were studied: A soil from a former coke works (CW) and two artificially contaminated soils (AC1 and AC2). First, the catabolic activity of the indigenous soil microflora was assessed with 14C-respirometry, using a range of 14C-labeled aromatic compounds. Extensive mineralization of several compounds occurred in the CW and the AC2 soils, suggesting that both soils contained catabolically active microorganisms. No significant mineralization occurred in the AC1 soil, implying that either it did not contain an indigenous PAH-degrading microbial population or that degradation, but not mineralization, occurred. The soils then were subjected to three sets of analyses: dichloromethane (DCM) soxhlet extraction, six-week biodegradation assay followed by DCM extraction, and extraction with HPCD followed by DCM extraction. A general decrease in PAHs present in the soils occurred after the biodegradation assay. In the CW and the AC1 soils, strong correlations were observed between the amount of PAHs biodegraded and the fraction of PAHs removed from the soils using the HPCD extraction. However, the AC2 soil showed a more modest correlation between the biodegradable fraction and the HPCD extractable fraction, with the HPCD extraction slightly underestimating the extent of PAH biodegradation. The results of this study indicated that an aqueous HPCD extraction may be a useful tool in assessing the microbial availability of aged contaminant mixtures in soils, although further validation is required.

2-Hydroxypropyl-beta-cyclodextrin↗

Biodegradation of a variety of bisphenols under aerobic and anaerobic conditions.

There is a group of compounds structurally similar to bisphenol-A (BPA), namely bisphenols (BPs), and some of them are considered to be able to partially replace BPA. In order to assess their biodegradability in the aquatic environment, a variety of BPs; BPA, bis(4-hydroxyphenyl)methane (BPF), bis(4-hydroxyphenyl)ethane (BPE), 2,2-bis(4-hydroxy-phenyl)butane (BPB), 2,2-bis(4- hydroxy-3-methylphenyl)propane (BPP), bis(4-hydroxyphenyl)sulfone (BPS), thiodiphenol (TDP) and 4,4'-dihydroxybenzophenone (HBP); were subjected to biodegradation tests under both aerobic and anaerobic conditions. For the aerobic degradation test, a kind of river-die-away method using several river water samples was used, while pond sediments were used for the anaerobic degradation tests in sealed anoxic bottles. As a whole, the examined BPs could be ranked by their biodegradability under aerobic conditions; BPF, HBP > > BPA > BPP > BPE > BPB > TDP > > BPS. On the other hand, the tendency for the anaerobic biodegradability was; BPF > HBP > BPS, BPA, TDP > BPE > BPB. From the viewpoint of biodegradability, BPF seems to be more environmentally-friendly than BPA and, therefore, may be a candidate to replace BPA for reducing the environmental risks.

Bacteria, Aerobic↗

Anaerobic biodegradation of chlorinated aliphatic compounds using packed bed reactors.

The feasibility of anaerobic packed bed reactors with tezontle (volcanic stone widely available in Mexico) and mineral granular activated carbon (GAC) was explored for the degradation of the main chlorinated aliphatic compounds present in the effluent from chemical industry for ethylene and polyvinyl chloride production. The biofilm on the support materials was developed using as inoculums anaerobic sludge. The biodegradation of the halogenated aliphatic compounds (1,2-dichloroethane; 1, 1, 1 -trichloroethane; trichloroethylene and carbon tetrachloride) was possible without addition of external electron donors. High COD removal was obtained in the reactors with both materials. The use of GAC as a biomass support allows a complete biodegradation of the chlorinated aliphatic compounds at organic loads up to 1.24 kgCOD.m(-3).d(-1), with 94% of COD removal and with a biodegradation rate of 2.062 gCOD.kgGAC(-1).d(-1). The reactor with tezontle also had high biodegradation capacity, but the biodegradation of the 1, 1 -dichloroethene, which appeared as intermediate product, was not reached at the required level in the studied range of organic loads.

Anaerobiosis↗

Factors affecting biodegradation of 2-chlorophenol by Alcaligenes sp. in aerobic reactors.

The influence of variations in carbon source concentration, cell inocula, pH, presence of other substrates, and other organisms on the biodegradation of 2-chlorophenol (2-CP) was studied for Alcaligenes sp. isolated from natural sources. Assays of biodegradation were performed in batch and continuous-flow fluidized-bed aerobic reactors. Evaluation of biodegradation was performed by determining total phenols, chemical oxygen demand (COD), and 2-CP by ultraviolet (UV) spectrophotometry. Measurement of microbial growth was carried out by the plate count method. Bioassays of acute toxicity were performed to evaluate detoxification by using Daphnia magna. Results obtained show that under batch conditions with initial inocula of 10(6) cells/mL the strain grew exponentially with 100, 200, and 300 mg/L of 2-CP within 48 hr. A lag period was observed with low cell density inocula (10(5) cells/mL). The strain showed marked delay in the biodegradation of 2-CP at pH 5. Removal of target substrate from mixtures containing other carbon sources demonstrated the possibility of concurrent growth. Mineralization of 2-CP was assessed by gas chromatography carried out at the end of the batch assays and at the exit of the continuous-flow reactor. The presence of other organisms (bacteria, rotifers, ciliate, and algae) that developed in the fluidized-bed reactor did not affect the efficacy of the biodegradation of 2-CP. The removal of 2-CP in the two assayed systems was over 97% in all cases. Toxicity was not detected at the exit of the continuous reactor.

Alcaligenes↗

A two-stage anaerobic system for biodegrading wastewater containing terephthalic acid and high strength easily degradable pollutants.

The high strength easily biodegradable pollutants (represented by CODE) are strong inhibitors of terephthalic acid (TA) anaerobic biodegradation. At the same time, TA can inhibit easily biodegradable pollutants removal under anaerobic conditions to a limited extent. This mutual inhibition could happen and cause a low removal efficiency of both TA and CODE, when the effluent from TA workshops containing TA and easily biodegradable pollutants are treated by a single anaerobic reactor system. Based upon the treatment kinetics analysis of both TA degradation and CODE removal, a two-stage up-flow anaerobic sludge blanket and up-flow fixed film reactor(UASB-UAFF) system for dealing with this kind of wastewater was developed and run successfully at laboratory scale. An UASB reactor with the methanogenic consortium as the first stage removes the easily biodegradable pollutants(CODE). An UAFF reactor as the second stage is mainly in charge of TA degradation. At a CODE loading of 15.3 g/(L.d) and a TA loading of 1.4 g/(L.d), HRT 18.5 h, the CODE and TA removal rate of the system reached 89.2% and 71.6%, respectively.

Acetates↗

Biodegradation during contaminant transport in porous media: 6. Impact of sorption on coupled degradation-transport behavior.

Bioavailability is one of the critical factors influencing the biodegradation and bioremediation of organic compounds. The bioavailability of many organic contaminants is controlled in part by the nature, magnitude, and rate of sorption/desorption processes. This study investigates the impact of sorption and associated retardation on the bioavailability and biodegradation of aromatic hydrocarbons during transport in porous media. Miscible-displacement experiments were conducted using naphthalene and 2-naphthol as the model sorbing compounds and salicylate, a degradation product of naphthalene, as a nonsorbing reference compound. Two porous media were used, one (Eustis soil, FL, USA) with moderate sorption capacity and one (quartz sand) with no measurable sorption of the compounds. The porous media were sterilized and inoculated with Pseudomonas putida RB1353, an organism that degrades naphthalene and its derivatives. The biodegradation and transport of all three substrates in quartz sand were significantly influenced by microbial lag, the effects of which were observed within two to three pore volumes (3-4.5 h). This was also true for salicylate transport in the Eustis soil system. Conversely, biodegradation lag effects were not observed for naphthalene or 2-naphthol in the Eustis soil system. In addition, the masses of naphthalene and 2-naphthol degraded were significantly greater for the Eustis soil system compared to the quartz sand system. As noted previously, naphthalene and 2-naphthol were sorbed by the Eustis soil but not the quartz sand, while salicylate was not sorbed by either media. These results indicate that the increased residence time associated with sorption of naphthalene and 2-naphthol by Eustis soil enhanced overall biodegradation and obviated the impact of lag on observed transport behavior.

Adsorption↗

Predicting ready biodegradability of premanufacture notice chemicals.

Chemical substances other than pesticides, drugs, and food additives are regulated by the U.S. Environmental Protection Agency (U.S. EPA) under the Toxic Substances Control Act (TSCA), but the United States does not require that new substances be tested automatically for such critical properties as biodegradability. The resulting lack of submitted data has fostered the development of estimation methods, and the BioWIN models for predicting biodegradability from chemical structure have played a prominent role in premanufacture notice (PMN) review. Until now, validation efforts have used only the Japanese Ministry of International Trade and Industry (MITI) test data and have not included all models. To assess BioWIN performance with PMN substances, we assembled a database of PMNs for which ready biodegradation data had been submitted over the period 1995 through 2001. The 305 PMN structures are highly varied and pose major challenges to chemical property estimation. Despite the variability of ready biodegradation tests, the use of at least six different test methods, and widely varying quality of submitted data, accuracy of four of six BioWIN models (MITI linear, MITI nonlinear, survey ultimate, survey primary) was in the 80+% range for predicting ready biodegradability. Greater accuracy (>90%) can be achieved by using model estimates only when the four models agree (true for 3/4 of the PMNs). The BioWIN linear and nonlinear probability models did not perform as well even when classification criteria were optimized. The results suggest that the MITI and survey BioWIN models are suitable for use in screening-level applications.

Biodegradation, Environmental↗

Kinetics of biodegradation during remediation of consecutive accidental spills of chlorophenols in a sandy aquifer.

Kinetics of biodegradation of chlorophenols were studied in six sandy aquifer columns (0.06 m I.D.; 1.00 m L). Remediation of chlorophenols was enhanced by using a "closed-loop" configuration system, where local groundwater was recirculated through the polluted site in a controlled manner. Consecutive accidental spills of phenol, 2-monochlorophenol (2-MCP) and 2,4,6-trichlorophenol (2,4,6-TCP) as single pollutants were removed following first order kinetics. The removal of chlorophenols increased by one order of magnitude following consecutive accidental spills demonstrating adaptation of the resident micro flora. The biodegradation rate constants in this study were in the same range and agreed with those reported in the literature for biodegradation in aerobic aquifers. Following the fate of the resident micro flora (enhanced by adding NH4Cl and KH2PO4 at a ratio C/N/P equal to 120:10:1), biomass growth was observed in the sandy aquifer columns and particle size analyses of the aqueous phase recirculated through the polluted site experimentally proved aggregation of cells. Aggregation of cells has been hypothesized as one of the causes for low biodegradation rates found in the field compared to those calculated using biodegradation rate constants determined in batch culture.

Accidents↗

Biodegradable fixation of distal humeral physeal fractures.

Polyglycolic acid (PGA) has been used worldwide as a biodegradable suture material since 1970. Biodegradable polyglycolide implants were introduced in osteofixation of cancellous bone fractures in 1985. From September 1987 to September 1989, 19 consecutive children with physeal fractures of the distal humerus necessitating open reduction and internal fixation were treated by transphyseal biodegradable fixation using 1.5 x 60-mm2 self-reinforced polyglycolide (SR-PGA) pins. Included were nine displaced fractures of the lateral humeral condyle, five severe avulsions of the medial epicondyle of the humerus, four displaced fractures of the humeral capitellum, and one intraarticular fracture of the medial condyle of the humerus. After accurate reduction, two smooth Kirschner pins 1.5 mm in diameter were introduced across the growth plate for temporary fixation. The metallic pins then were removed one by one and subsequently replaced with the cylindrical SR-PGA pins 1.5 mm in diameter. After operation, a padded plaster splint was worn for four weeks. Neither secondary displacement nor signs of growth disturbance were seen during the 26-month follow-up time (mean, 17.2 months). Not only the reduction of the costs but also the psychological aspects should be considered when dealing with biodegradable fixation of physeal fractures in children. Transphyseal biodegradable fixation has established itself as a procedure of choice for handling simple physeal fractures.

Adolescent↗

Low temperature biodegradation of airport de-icing fluids.

The biodegradabilities of glycol- and acetate-based aircraft de-icing fluids on airport surfaces have been investigated at three temperatures between 0 degrees C and 10 degrees C. The aqueous solubilities of these substances can result in high BOD loadings in runoff and pose serious toxicity problems in receiving waters. The measured surface biodegradation rates for de-icing products based on ethylene/diethylene glycol (Konsin), propylene glycol (Kilfrost) and potassium acetate (Clearway) at 4 degrees C were 0.082, 0.073 and 0.033 day(-1). The resulting reductions in the potential BOD loadings, of a single application of a typical mixture of these products, over a 5 day biodegradation period are predicted to be 32.9%, 30.2% and 21.4%, respectively at 8 degrees C, 4 degrees C and 1 degrees C. For consecutive daily applications, the comparable cumulative reductions over 5 days are 20.8%, 18.9% and 13.3%. The subsequent savings in the amount of treatment required for airport runoff prior to safe discharge to receiving waters are discussed and hence the relevance of surface biodegradation processes to the design of stormwater treatment systems involving the wash-off of biodegradable pollutants following retention on urban surfaces.

Aircraft↗

Comparison of yeast (Candida maltosa) and bacterial (Rhodococcus erythropolis) phenol hydroxylase activity and its properties in the phenolic compounds biodegradation.

Aromatic contaminants of the environment, to which belongs phenol and its derivatives, are toxic and in most of the cases hard to degrade. Removal of these pollutants by biological, gentle and effective way, depends on specific environmental conditions in the locality and on the biodegradation potential of the used microbial population. Closer characterization of the biodegradation and enzyme mechanisms is therefore an essential assumption of the successful implementation of microbes. This paper is focused on comparison of the biodegradation activity between the soil yeast Candida maltosa and bacteria Rhodococcus erythropolis towards various aromatics connected with determination of the first enzyme of the phenol biodegradation pathway: phenol hydroxylase (PH). The effect of substrate type, substrate concentration, growth phase of the microorganisms and presence of humic acids in the cultivation medium, on phenol biodegradation and PH activity are discussed.

Air Pollutants↗

Methanotrophic biodegradation of cis-1,2-dichloroethylene in a continuously fed fixed-film bioreactor.

Co-metabolic biodegradation of cis-dichloroethylene (cis-DCE) was investigated in a bench-scale fixed-film bioreactor inoculated with a mixed culture of methane oxidising bacteria. The aim of this work was to identify factors that affect the cis-DCE biodegradation. It was observed that the presence of methane was necessary to enhance the biodegradation of cis-DCE, but an excess of methane inhibited the cis-DCE removal. cis-DCE did not inhibit the methane biodegradation at concentrations up to 300 microg/L. Maximum cis-DCE removal was observed with a methane bulk concentration ranging from 0.2 to 0.7 mg/L. It was found that the activity of the biofilm was located in the upper 100 microm of the biofilm. On the basis of this study it is concluded that careful control of the oxygen and methane concentrations as well as of the biofilm thickness is necessary in order to optimise the biodegradation of cis-DCE in fixed film bioreactors.

Biodegradation, Environmental↗

BTE-OX biodegradation kinetics with MTBE through bioaugmentation.

The biodegradation kinetics of BTE-oX and MTBE, mixed all together, in the presence of bioaugmented bacterial populations as high as 880 mg/L VSS was evaluated. The effect of soil in aqueous samples and the effect of Tergitol NP-10 on substrate biodegradation rates were also evaluated. Biodegradation kinetics was evaluated for 36 hours, every 6 hours. Benzene and o-xylene biodegradation followed a first-order one-phase kinetic model, whereas toluene and ethylbenzene biodegradation was well described by a first-order two-phase kinetic model in all samples. MTBE followed a zero-order removal kinetic model in all samples. The presence of soil in aqueous samples retarded BTE-oX removal rates, with the highest negative effect on o-xylene. The presence of soil enhanced MTBE removal rate. The addition of Tergitol NP-10 to aqueous samples containing soil had a positive effect on substrate removal rate in all samples. Substrate percent removals ranged from 95.4-99.7% for benzene, toluene and ethylbenzene. O-xylene and MTBE percent removals ranged from 55.9-90.1% and 15.6-30.1%, respectively.

Benzene↗