The strain used in this study was isolated from soil sample near oil shop at Salem, Tamil Nadu, India. Serial dilution was performed and then plated on to tributrin agar base containing 1% tributrin and Tween 80 at pH 8.0. Lipase/esterase production was detected by observing clear zones around isolated colonies.6 Lipase activity was then detected by growth on Rhodamine B agar medium at 30 °C for 72 h.7 Colonies which showed orange fluorescence under

UV irradiation indicated true lipase activity and non-lipolytic bacteria formed pink colonies.8 Based on the morphological and biochemical features as well as by 16S rRNA sequencing identification was performed. The extracted genomic DNA was used as template and amplified by PCR with the aid of 16S rDNA Primers – 16S Forward Selleckchem Sotrastaurin Primer: 5′-AGAGTTTGATC(AC)TGGCTCAG-3′,16S Reverse Primer: 5′-AAGGAGGTG(AT)TCCA(AG)CC-3′. The resultant amplified product was sequenced and compared with other related sequences using

BLAST programme. Further, the nucleotide sequences of the isolate was aligned using CLUSTAL W mega version 5. One loopful culture from a nutrient agar slant was inoculated in 50 ml tryptone soy broth Selleck SB431542 medium and incubated at 50 °C overnight. Five milliliter was inoculated in to the medium containing 1% olive oil, 0.02% CaCl2·2H2O, 0.01% MgSO4·7H2O and 0.04% FeCl3·6H2O, then incubated for 72 h at 50 °C under shaking condition at 150 rpm. The initial pH of the medium was adjusted to pH 7.0.9 To measure the bacterial growth and lipase production with respect to the incubation time, culture samples were removed at 2 h interval and centrifuged at 5000 g for 10 min. Pellets were resuspended in 1 ml of 0.01 M phosphate buffer, pH 7 and the absorbance was measured at 600 nm.10 Culture supernatants were used to determine lipolytic activity. The effect of pH on lipase Carnitine palmitoyltransferase II production was studied by adjusting the pH of culture media to 6.0, 7.0, 8.0, 9.0, 10.0 and 11.0 respectively by the addition of 1.0 N HCl/NaOH prior to sterilization. One milliliter of 48 h old culture was inoculated and incubated at 37 °C for 10 min by shaking. Similarly, the effect of temperature

was studied by incubating at 30 °C–70 °C, at pH 7.0 for 10 min. Likewise, the effect of tryptone, CaCl2 and HgCl2, Triton X100 and Hexane was studied with concentrations ranging from 0.5% to 2.5% and 0.2% to 1.2%. Short chain, long chain oils such as butter fat and olive oil at a concentration of 0.5%–3% was used to determine lipase production in crude sample. The crude enzyme was obtained by centrifugation at 5,000 rpm at 4 °C for 10 min. Lipase activity was assayed according to the method of Sadasivam and Manickam 1996.11 Two milliliter of 0.1 M phosphate buffer, 1 ml of olive oil and 1 ml crude enzyme was incubated at 40 °C for 30 min.11 The reaction was stopped by adding 5 ml ethanol before titration against 0.1 N NaOH using phenolphthalein as indicator until the end point is reached.