7 and 8 Bioremediation or biotransformation finds a suitable way to remove those toxic chemicals either by complete degradation or by transforming them to nontoxic ones.9, 10 and 11 A new bacterial strain was isolated from the site of Haldia Oil Refinery, West Bengal, India that was capable of mineralizing different PAHs.12 Biochemical characterization of the strain showed that it has high Modulators gelatinase activity. Soil was collected from 1 ft depth of the

selected site and its pH was measured following the standard method.13 A mineral salt medium (MSM) was prepared with a composition of NH4Cl 2.0 g, KH2PO4 5.0 g, Na2HPO4 4.0 g, MnSO4 0.2 g, MgSO4 0.2 g, FeCl3 0.05 g, CaCl2 0.001 g and other trace elements14 and pH 7.2. One gram soil 3-deazaneplanocin A was dissolved in 10 ml autoclaved mineral medium, mixed thoroughly, centrifuged at 1000 rpm, supernatant collected selleck products and centrifuged at 10,000 rpm for 10 min. Pellet was washed and centrifuged with MSM twice, then suspended in 5 ml mineral medium. The suspension was inoculated to a flask containing 100 ml MSM where 10 mg of benzo(a)pyrene (Sigma) was added as sole source of carbon. Another set was done that contained

no carbon source (placebo), both incubated at 30 °C, 120 rpm. After 10 days of incubation 1 ml of soup was collected from each flask and inoculated to PAH supplement MSM medium and placebo respectively and incubated for MTMR9 10 days. Then soup from respective flask inoculated on two different nutrient agar plates. A set of four test tubes were taken each containing 25 ml mineral medium with 20 mg filter sterilized anthracene dissolved in acetone, acetone was removed by evaporation. The randomly selected four isolates were inoculated (106 cells) and incubated at 30 °C, 100 rpm for 10 days. Then absorbance was taken at 600 nm. Better degrading (anthracene) isolates were further checked if they degrade a relatively complex PAH molecule, fluoranthene. The isolates were inoculated separately on MSM-agar

plate, then acetone solution of fluoranthene was sprayed over the plates,15 solvent was evaporated and then incubated at 30 °C for 4 days. To study the bacterial growth two flasks were used separately, one containing mineral medium and solid crystals of fluoranthene and another that with pyrene as sole source of carbon. Bacterial suspension was added to the flask with an initial value of O.D600 0.1, and then incubated at 30 °C and 100 rpm. Bacterial growth was measured by taking optical density at 600 nm. To study the degradation rate two sets of 50 ml Erlenmeyer flaks were taken, each containing 10 ml mineral medium amended with 50 ppm fluoranthene or pyrene, dissolved in ethyl acetate. Ethyl acetate was evaporated before adding bacteria and incubated at 100 rpm for 12 days in the dark at 30 °C.16 Also a negative control was used where no bacteria added.