Biodegradation of anthracene by Aspergillus fumigatus

An anthracene-degrading strain, identified as Aspergillus fumigatus, showed a favorable ability in degradation of anthracene. The degradation efficiency could be maintained at about 60% after 5d with initial pH of the medium kept between 5 and 7.5, and the optimal temperature of 30 °C. The activity of this strain was not affected significantly by high salinity. Exploration on co-metabolism showed that the highest degradation efficiency was reached at equal concentration of lactose and anthracene. Excessive carbon source would actually hamper the degradation efficiency. Meanwhile, the strain could utilize some aromatic hydrocarbons such as benzene, toluene, phenol etc. as sole source of carbon and energy, indicating its degradation diversity. Experiments on enzymatic degradation indicated that extracellular enzymes secreted by A. fumigatus could metabolize anthracene effectively, in which the lignin peroxidase may be the most important constituent. Analysis of ion chromatography showed that the release of anions of A. fumigatus was not affected by addition of anthracene. GC-MS analysis revealed that the molecular structure of anthracene changed with the action of the microbe, generating a series of intermediate compounds such as phthalic anhydride, anthrone and anthraquinone by ring-cleavage reactions.     

Biodegradation of 2,4,6-trinitrophenol by Rhodococcus sp. isolated from a picric acid-contaminated soil

A picric acid-degrading bacterium, strain NJUST16, was isolated from a soil contaminated by picric acid and identified as a member of Rhodococcus sp. based on 16S rRNA sequence. The degradation assays suggested that the strain NJUST16 could utilize picric acid as the sole source of carbon, nitrogen and energy. The isolate grew optimally at 30 degrees C and initial pH 7.0-7.5 in the mineral salts medium supplemented with picric acid. It was basically consistent with degradation of picric acid by the isolate. Addition of nitrogen sources such as yeast extract and peptone accelerated the degradation of picric acid. However, the stimulation was concentration dependent. The degradation was accompanied by release of stoichiometric amount of nitrite and acidification. The degradation of picric acid at relatively high concentrations (>3.93 mM) demonstrated that the degradation was both pH and nitrite dependent. Neutral and slightly basic pH was crucial to achieve high concentrations of picric acid degradation by the NJUST16 strain.     

Enantioselective degradation and unidirectional chiral inversion of 2-phenylbutyric acid, an intermediate from linear alkylbenzene, by Xanthobacter flavus PA1

Microbial degradation of the chiral 2-phenylbutyric acid (2-PBA), a metabolite of surfactant linear alkylbenzene sulfonates (LAS), was investigated using both racemic and enantiomer-pure compounds together with quantitative stereoselective analyses. A pure culture of bacteria, identified as Xanthobacter flavus strain PA1 isolated from the mangrove sediment of Hong Kong Mai Po Nature Reserve, was able to utilize the racemic 2-PBA as well as the single enantiomers as the sole source of carbon and energy. In the presence of the racemic compounds, X. flavus PA1 degraded both (R) and (S) forms of enantiomers to completion in a sequential manner in which the (S) enantiomer disappeared much faster than the (R) enantiomer. When the single pure enantiomer was supplied as the sole substrate, a unidirectional chiral inversion involving (S) enantiomer to (R) enantiomer was evident. No major difference was observed in the degradation intermediates with either of the individual enantiomers when used as the growth substrate. Two major degradation intermediates were detected and identified as 3-hydroxy-2-phenylbutanoic acid and 4-methyl-3-phenyloxetan-2-one, using a combination of liquid chromatography-mass spectrometry (LC-MS), and ¹H and ¹³C nuclear magnetic resonance (NMR) spectroscopy. The biochemical degradation pathway follows an initial oxidation of the alkyl side chain before aromatic ring cleavage. This study reveals new evidence for enantiomeric inversion catalyzed by pure culture of environmental bacteria and emphasizes the significant differences between the two enantiomers in their environmental fates.     

The biodegradation pathway of triethylamine and its biodegradation by immobilized Arthrobacter protophormiae cells

A bacterial strain named R4 was isolated from a wastewater treatment pool containing triethylamine (TEA) as the sole source of carbon and nitrogen. Strain R4 was identified as Arthrobacter protophormiae based on 16S rRNA gene sequence analysis and morphological and physiological properties. The optimal pH, temperature and concentration of NaCl for TEA degradation by strain R4 were 7.0, 30°C and 0.5%, respectively. Strain R4 could completely degrade 100 mg l(-1) TEA to ammonia in 32 h, and could also effectively degrade diethylamine (DEA) and ethylamine (EA) to ammonia. The degradation of TEA was strongly inhibited by some metal ions (Cu(2+), Mn(2+), Zn(2+), Co(2+), Ni(2+) and Ag(+)) (1.0mM). Addition of either SO(4)(2-) or NH(4)(+) reduced the degradation efficiency of TEA by strain R4 to a certain extent. The inhibition became significant when the concentration of SO(4)(2-) and NH(4)(+) reached to 11 mM and 30 mM, respectively. Cell-free extracts prepared from cells grown in TEA exhibited TEA monooxygenase, DEA monooxygenase and EA monooxygenase activity. Here, we propose the metabolic pathway of TEA degradation in strain R4. The efficiency of TEA removal by immobilized cells of strain R4 was found to be equivalent to that of free cells. In addition, the immobilized cells could be reused without reduction in their ability to degrade TEA.     

Biodegradation of p-nitrophenol by Rhodococcus sp. CN6 with high cell surface hydrophobicity

Rhodococcus sp. CN6, isolated from a pesticide industry's effluent-sediment, was able to completely degrade and utilize 100mg/L p-nitrophenol (PNP) as the sole carbon, nitrogen and energy sources for growth in the minimal salt media (MSM) within 12h. To study the applicability of the strain for bioremediation of PNP, its degradation potential was examined in the presence of different supplemented carbon and nitrogen sources in MSM with 100mg/L PNP. Dextrin was experienced as the best supplemented carbon source used by the strain CN6 during degrading PNP. Addition of ammonium nitrate could also increase the PNP degradation rate. Preliminary studies on the surface characters of Rhodococcus sp. CN6 were undertaken for the sake of exploring its high efficiency on the degradation of PNP. Microbial adherence to hydrocarbons (MATH) assays illuminated that the strain CN6 was of higher hydrophobicity while grown on higher concentration of PNP. The results suggested that the strain CN6 could be used as a potential and efficient PNP degrader for the bioremediation of contaminated sites.     

Solar photocatalytic degradation of 2-sec-butyl-4,6-dinitrophenol (DNBP) using TiO2/SiO2 aerogel composite photocatalysts

Silica aerogels and TiO₂/silica aerogel composite photocatalysts were synthesized by sol–gel technique at ambient pressure using orthosilioate and tetra-n-butyl titanate as precursors, respectively. The prepared composite photocatalysts were characterized by XRD, TEM, BET surface area, FT-IR and UV–vis absorption spectra. The results showed that the TiO₂/silica aerogel composite photocatalysts possess high surface area. The addition of silica aerogels inhibited the grain growth and phase transformation of anatase to rutile during calcination. The TiO₂/silica aerogel composite sample calcined at 500 °C with an optimal silica aerogel content of 7 wt.% afforded the highest photocatalytic activity. The photocatalytic degradation of 2-sec-butyl-4,6-dinitrophenol (DNBP) was investigated by using this novel TiO₂/silica aerogel composite photocatalyst under solar light irradiation. The effects of irradiation time, pH, catalyst concentration, temperature and initial DNBP concentration were examined as operational parameters. The optimal operational parameters were found as follows: pH as solution pH 4.82, 8 g L⁻¹ catalyst concentration, 20 °C, and 240 min irradiation time. The kinetics of DNBP degradation by TiO₂/silica aerogel composite fit well a pseudo-first-order kinetic model. The repeatability of photocatalytic activity was also tested. This study showed the feasible and potential use of TiO₂/silica aerogel composite photocatalysts in degradation of toxic organic contaminants.     

Degradation of pyridine by one Rhodococcus strain in the presence of chromium (VI) or phenol

A Rhodococcus strain, Chr-9, which has the ability to degrade pyridine and phenol and reduce chromium (VI) (Cr (VI)) was isolated. The strain could grow with pyridine as the sole carbon and nitrogen source, and its pyridine-degradation capability was enhanced by 100 mg l(-1) phenol; however, the degradation of pyridine was inhibited when the phenol concentration was greater than 400 mg l(-1). The hydroxylation of pyridine suggested that the stimulation and inhibition of phenol to the pyridine degradation may be attributed to competition of phenol and pyridine for the hydroxylase gene. Strain Chr-9 was also able to reduce Cr (VI) when glucose and LB was used as the carbon source; however, the Cr (VI) reduction did not occur when pyridine was the sole carbon and energy source. In addition, strain Chr-9 could reduce Cr (VI) and simultaneously degrade pyridine in the presence of glucose. To the best of our knowledge, strain Chr-9 is the first Rhodococcus strain reported to degrade pyridine in the presence of Cr (VI), and the first strain with the pyridine degradation being stimulated by low concentrations of phenol.     

Characterization of phenol degradation by Rhizobium sp. CCNWTB 701 isolated from Astragalus chrysopteru in mining tailing region

To screen high strength phenol degrading bacteria, we selected 108 rhizobial strains isolated from nodules of eight wild legumes species in the mining tailing region of Shaanxi province, northwest of China, and cultivated them in a basal salt (BS) medium supplemented with different phenol concentrations as a sole carbon source. The results showed that some of the strains could use phenol as sole carbon source. In order to study the characteristics of phenol degradation, the strain CCNWTB701 isolated from Astragalus chrysopteru was used as well, due to the fact that it was very efficient in phenol degradation. The phenol degradation was around 99.5 and 78.3%, with an initial concentration of 900 and 1000 mg/l phenol in 62 and 66 h, respectively. Kinetic studies indicated that the strain had a high KS (743.1 microM) and an extremely high KSI (10,469 microM) in Haldane's model. The phylogenetic analysis based on 16S rRNA gene sequences showed that CCNWTB701 belonged to the Rhizobium genus, and it was closely related to Rhizobium mongolense and Rhizobium gallicum.     

Effects of some organic pollutants on the exopolysaccharides (EPSs) produced by some Pseudomonas spp. strains

In this study, isolation and characterization of exopolysaccharides produced by Pseudomonas aeruginosa B1, P. fluorescens B5, P. stutzeri B11 and P. putida B15 which had been seen to produce exopolymers of potential interest in biotechnological applications were examined. To initiate the observation of the organic pollutants–polymer interactions, the yield and properties of their extracellular polysaccharide were researched. The exopolysaccharide production by these strains during growth in nutrient broth medium (control) was 41–75 mg L⁻¹. Also, P. aeruginosa B1, P. fluorescens B5, P. stutzeri B11 and P. putida B15 had exhibited high production of EPSs in presence of various organic pollutants (2,4-D, benzene, BTX and gasoline, respectively) in mineral salt medium (MSM) as a sole carbon source. EPS production by the 4 strains ranged from 40 mg L⁻¹ to 8 mg L⁻¹. Monosaccharide composition of EPS produced by these cultures were analyzed by HPLC. Results indicated that EPSs of strains contained neutral sugars and acetylated amino sugars. The neutral sugars in the EPS were mainly composed of glucose, arabinose, glycerol, ribose. The presence of galactronic acid, N-acetyl-d-galactosamin and N-acetyl-d-glucosamine indicated the acidic nature of the polysaccharide. Glycerol was the basic structural unit of EPS produced by the strains except P. stutzeri B11 (MSM with 1% BTX). Strain B1 (in NB medium) was found to be composed of neutral sugars (100%) while strain B1 [in MSM medium with 0.2% (v/v) 2.4-D] contained neutral sugars (70.0%), acetylated amino sugars (30.0%). Also, EPS content of strain B5 (in the NB medium) was neutral sugars (99.8%), acetylated amino sugars (0.2%) while the strain B5 [in MSM medium containing the 1% (v/v) benzene] was found to contain neutral sugars (99.9%), acetylated amino sugars (0.1%). However, EPS monomer composition by strain B11 was detected as neutral sugars (99.77%), acetylated amino sugars (0.23%) in NB medium while the strain B11 [in MSM medium with 1% (v/v) BTX] contained neutral sugars (98.2%) and acetylated amino sugars (1.8%). Lastly, in NB medium by strain B15 was found to contain neutral sugars (99.9%) and acetylated amino sugars (0.1%) while in MSM medium in the presence of 1% (v/v) gasoline it was found to contain neutral sugars (83.6%), acetylated amino sugars (16.4%). Monomer composition of control EPSs changed to different structures in the presence of various organic pollutants. Diversities of organic compounds as carbon source affected the monomer composition of EPS produced by some Pseudomonas spp. cultures.     

Degradation of phenanthrene by bacterial strain isolated from soil in oil refinery fields in Shanghai China

A bacterial strain Pseudomonas stutzeri ZP2 was identified with phenanthrene-degrading ability based on Gram staining, oxydase reaction, biochemical tests, FAME analysis, G+C content and 16S rDNA gene sequence analysis. It is the first time that P. stutzeri is reported to process the capability for phenanthrene degradation. The strain was isolated from soil samples contaminated with polycyclic aromatic hydrocarbon (PAH)-containing waste from an oil refinery field in Shanghai, China. Strain P sp. ZP2 can utilize naphthalene, phenanthrene and Tween 80 as its sole carbon source and can degrade phenanthrene very fast, 6 days for 96% phenanthrene at 250 ppm concentration. The optimal growth conditions of strain ZP2 was determined to be at pH 8.0, 37 degrees C, respectively. The results also indicate that strain ZP2 can remove more than 90% of phenanthrene at any concentrations ranged from 250 to 1000 ppm in 6 days. It suggests that strain ZP2 can endure high concentrations of phenanthrene. Besides, the effects of non-ionic surfactants such as Brij 30, Triton X100 and Tween 80, on the phenanthrene degradation were examined. Therefore, this strain may find great application in bioremediation practices.     

Chlorination of organophosphorus pesticides in natural waters

Unknown second-order rate constants for the reactions of three organophosphorus pesticides (chlorpyrifos, chlorfenvinfos and diazinon) with chlorine were determined in the present study, and the influence of pH and temperature was established. It was found that an increase in the pH provides a negative effect on the pesticides degradation rates. Apparent second-order rate constants at 20 degrees C and pH 7 were determined to be 110.9, 0.004 and 191.6 M(-1) s(-1) for chlorpyrifos, chlorfenvinfos and diazinon, respectively. A higher reactivity of chlorine with the phosphorothioate group (chlorpyrifos and diazinon) than with the phosphate moiety (chlorfenvinfos) could explain these results. Intrinsic rate constant for the elementary reactions of chlorine species with chlorpyrifos and diazinon were also calculated, leading to the conclusion that the reaction between hypochlorous acid and the pesticide is predominant at neutral pH. The elimination of these pesticides in surface waters was also investigated. A chlorine dose of 2.5 mg L(-1) was enough to oxidize chlorpyrifos and diazinon almost completely, with a formation of trihalomethanes below the EU standard for drinking water. However, the removal of chlorfenvinfos was not appreciable. Therefore, chlorination is a feasible option for the removal of organophosphorus pesticides with phosphorothioate group during oxidation and disinfection processes, but not for the elimination of pesticides with phosphate moiety.     

Degradation of quinoline by Rhodococcus sp. QL2 isolated from activated sludge

A novel aerobic gram-positive bacterial strain capable of utilizing quinoline as sole source of carbon, nitrogen and energy was isolated from activated sludge of a coke plant wastewater treatment process. The isolate was identified as Rhodococcus sp. QL2 based on its morphology, physiochemical properties in addition to the results from 16S rDNA sequence analysis. The optimum temperature and the pH for its growth were 35–40 °C and 8.0, respectively. Extra nitrogen sources stimulated the bacterial growth on quinoline. Strain QL2 had strong quinoline degradability, and its degradation kinetics could be described with Haldane's model. Strain QL2 also had a broad range of substrate utilization. Identification of intermediates by GC/MS showed Rhodococcus sp. QL2 degraded quinoline via two pathways simultaneously.     

Isolation and characterization of a nitrobenzene degrading yeast strain from activated sludge

Strain Z1 was isolated from nitrobenzene-contaminated sludge. Strain Z1 was able to utilize nitrobenzene as a sole source of carbon, nitrogen, and energy under aerobic condition. Based on the morphology, physiological biochemical characteristics, and 26S rDNA D1/D2 domain sequence, strain Z1 was identified as Rhodotorula mucilaginosa. Strain Z1 mineralized up to 450mg L(-1) nitrobenzene. Kinetics of nitrobenzene degradation was described using the Andrews equation. The kinetic parameters were as follows: q(max)=1.50h(-1), K(s)=31.31mg L(-1), and K(i)=101.34mg L(-1). Strain Z1 had a high-salinity tolerance. It degraded nitrobenzene effectively in 5% NaCl (quality concentration). Even in the presence of aniline or phenol, strain Z1 degraded nitrobenzene efficiently. Strain Z1 therefore could be an excellent candidate for the bio-treatment of nitrobenzene industrial wastewaters.     

Hydrogen substitutes for the in situ generation of H2O2: an application in the Fenton reaction

This study investigates the ability of formic acid, hydrazine and hydroxylamine to act as H₂ substitutes in conducting phenol degradation by Fenton reaction using in situ generated hydrogen peroxide. The processes were performed with semi-heterogeneous (Pd/Al₂O₃ + soluble Fe²⁺) and fully heterogeneous (FePd/Al₂O₃) catalytic systems under ambient conditions. In contrast to bulk H₂O₂ production conditions, hydrazine is able to produce H₂O₂in situ followed by phenol degradation using Pd/Al₂O₃ + Fe²⁺ at pH 3 without the need for halide ions. However, a degree of mineralization exceeding 37% could not be achieved. The significant production of in situ H₂O₂ at the inherent acidic pH of hydroxylammonium sulfate in the presence of Pd/Al₂O₃ + Fe²⁺ was also found to differ from the bulk production of H₂O₂, in which no H₂O₂ was detected. A remarkable degree of mineralization (ca. 65%) as well as fast phenol degradation during the reaction started at pH 7 over FePd/Al₂O₃ may be an advantage of using hydroxylamine. On the other hand, using formic acid, H₂O₂ was produced at a moderate rate, thereby achieving higher efficiency in the mineralization of phenol. Most importantly, the catalysts were more stable in the presence of formic acid than hydrazine or hydroxylamine.     

Thermophilic biofiltration of H2S and isolation of a thermophilic and heterotrophic H2S-degrading bacterium, Bacillus sp. TSO3

Thermophilic biofiltration of H₂S-containing gas was studied at 60 °C using polyurethane (PU) cubes and as a packing material and compost as a source of thermophilic microorganisms. The performance of biofilter was enhanced by pH control and addition of yeast extract (YE). With YE supplement and pH control, H₂S removal efficiency remained above 95% up to an inlet concentration of 950 ppmv at a space velocity (SV) of 50 h⁻¹ (residence time = 1.2 min). H₂S removal efficiency strongly correlated with the inverse of H₂S inlet concentrations and gas flow rates. Thermophilic, sulfur-oxidizing bacteria, TSO3, were isolated from the biofilter and identified as Bacillus sp., which had high similarity value (99%) with Bacillus thermoleovorans. The isolate TSO3 was able to degrade H₂S without a lag period at 60 °C in liquid cultures as well as in the biofilter. High H₂S removal efficiencies were sustained with a periodic addition of YE. This study demonstrated that an application of thermophilic microorganism for a treatment of hot gases may be an economically attractive option since expensive pre-cooling of gases to accommodate mesophilic processes is not required.     

Biodegradation of phenol at high initial concentration by Alcaligenes faecalis

Strain Alcaligenes faecalis was isolated and identified as a member of the genus Alcaligenes by using BIOLOG and 16S rDNA sequence analysis. The phenol biodegradation tests showed that the phenol-degrading potential of A. faecalis related greatly to the different physiological phases of inoculum. The maximum phenol degradation occurred at the late phase of the exponential growth stages, where 1600 mg L(-1) phenol was completely degraded within 76 h. A. faecalis secreted and accumulated a vast quantity of phenol hydroxylase in this physiological phase, which ensured that the cells could quickly utilize phenol as a sole carbon and energy source. In addition, the kinetic behavior of A. faecalis in batch cultures was also investigated over a wide range of initial phenol concentrations (0-1600 mg L(-1)) by using Haldane model. It was clear that the Haldane kinetic model adequately described the dynamic behavior of the phenol biodegradation by the strain of A. faecalis.     

Synergistic degradation of 2-naphthol by Fusarium proliferatum and Bacillus subtilis in wastewater

2-Naphthol, which originates widely from various industrial activities, is toxic and thus harmful to human liver and kidney. A new compound biodegradation system was adopted to degrade 2-naphthol-contaminated wastewater. Enzymatic response to 2-naphthol biodegradation in the aqueous phase was also studied. As a co-metabolic substrate, salicylic acid could induce the two microorganisms to produce a large amount of degradation enzymes for 2-naphthol. The key enzymes were confirmed as polyphenol oxidase (PPO) and catechol 2,3-dioxygenase (C23O). The degradation extent of 2-naphthol, determined by high performance liquid chromatography (HPLC), was enhanced by nearly 15% on the 6th day after the addition of the co-metabolic substrate. The results obtained thus clearly indicated that the co-metabolic process was the most important factor affecting the degradation of the target contaminant. The optimal concentration of 2-naphthol was 150 mg L⁻¹, and the optimal pH value was 7.0. The degradation extent of 2-naphthol was further enhanced by nearly 10% after the addition of Tween 80, which increased the bioavailability of 2-naphthol. In a practical treatment of industrial wastewater from medical manufacture, the synergistic degradation system resulted in a high degradation efficiency of 2-naphthol although its lag time was a little long in the initial stage.     

Co-metabolic degradation of bensulfuron-methyl in laboratory conditions

The present study deals with the degradation of bensulfuron-methyl by microorganisms cultured with different sources of carbon, nitrogen and phosphorus. Addition of carbon source accelerated the degradation of bensulfuron-methyl under co-metabolism process. Sodium lactate was the best carbon source for the degradation of bensulfuron-methyl, compared to other carbon sources studied, and the degradation ratio of bensulfuron-methyl reached 79.5%, whereas only 34.6 and 29.7% were removed in the presence of glucose and sucrose, respectively. Supplement of nitrogen source also enhanced degradation of bensulfuron-methyl. However, no significant differences were observed in the loss of bensulfuron-methyl between organic nitrogen and inorganic source. Phosphate buffer was supplemented into the media to maintain neutral conditions for the advantage of the strain growth since increase in pH value was observed. An orthogonal array design was applied to arrange main factors singled out for investigating the influence of factor and interaction between them on the degradation of bensulfuron-methyl. Statistical analysis showed that the concentration of sodium lactate, bensulfuron-methyl and inoculum size were the main effects, and the interaction of sodium lactate and bensulfuron-methyl was of statistical significance.     

Biodegradation of beta-cypermethrin and 3-phenoxybenzoic acid by a novel Ochrobactrum lupini DG-S-01

A newly isolated bacterium DG-S-01 from activated sludge utilized beta-cypermethrin (beta-CP) and its major metabolite 3-phenoxybenzoic acid (3-PBA) as sole carbon and energy source for growth in mineral salt medium (MSM). Based on the morphology, physio-biochemical characteristics, and 16S rDNA sequence analysis, DG-S-01 was identified as Ochrobactrum lupini. DG-S-01 effectively degraded beta-CP with total inocula biomass A(590 nm) = 0.1-0.8, at 20-40 °C, pH 5-9, initial beta-CP 50-400 mg L(-1) and metabolized to yield 3-PBA leading to complete degradation. Andrews equation was used to describe the special degradation rate at different initial concentrations. Degradation rate parameters q(max), K(s) and K(i) were determined to be 1.14 d(-1), 52.06 mg L(-1) and 142.80 mg L(-1), respectively. Maximum degradation was observed at 30 °C and pH 7.0. Degradation of beta-CP was accelerated when MSM was supplemented with glucose, beef extract and yeast extract. Studies on biodegradation in liquid medium showed that over 90% of the initial dose of beta-CP (50 mg L(-1)) was degraded under the optimal conditions within 5d. Moreover, the strain also degraded beta-cyfluthrin, fenpropathrin, cyhalothrin and deltamethrin. These results reveal that DG-S-01 may possess potential to be used in bioremediation of pyrethroid-contaminated environment.     

Comparative photocatalytic study of two selected pesticide derivatives, indole-3-acetic acid and indole-3-butyric acid in aqueous suspensions of titanium dioxide

Heterogeneous photocatalysed degradation of two selected pesticide derivatives such as indole-3-acetic acid (IAA) and indole-3-butyric acid (IBA) has been investigated in aqueous suspensions of titanium dioxide by monitoring the change in substrate concentration employing UV spectroscopic analysis technique and depletion in total organic carbon (TOC) content as a function of irradiation time. The degradation kinetics was studied under different conditions such as pH, types of TiO_2, substrate and catalyst concentration, and in the presence of electron acceptor such as hydrogen peroxide (H₂O₂) besides molecular oxygen. The degradation rates were found to be strongly influenced by all the above parameters. The photocatalyst Degussa P25 showed comparatively highest photocatalytics. The pesticide derivative, indole-3-acetic acid was found to degrade slightly faster than indole-3-butyric acid.