Penicillum janthinellum SDX7 was isolated from aged petroleum hydrocarbon-affected soil at the site of Anand, Gujarat, India, and was tested for different pH, temperature, agitation and concentrations for optimal growth of the isolate that was capable of degrading upto 95%, 63% and 58% of 1%, 3% and 5% kerosene, respectively, after a period of 16 days, at optimal growth conditions of pH 6.0, 30 °C and 180 rpm agitation. The GC/MS chromatograms revealed that then-alkane fractions are easily degraded; however, the rate might be lower for branched alkanes, n-alkylaromatics, cyclic alkanes and polynuclear aromatics. The test doses caused a concentration-dependent depletion of carbohydrates of P. janthinellum SDX7 by 3% to 80%, proteins by 4% to 81% and amino acids by 8% to 95% upto 16 days of treatment. The optimal concentration of 3% kerosene resulted in the least reduction of the metabolites of P. janthinellum such as carbohydrates, proteins and amino acids with optimal growth compared to 5% and 1% (v/v) kerosene doses on the 12th and 16th day of exposure. Phenols were found to be mounted by 43% to 66% at lower and higher concentrations during the experimental period. Fungal isolate P. janthinellum SDX7 was also tested for growth on various xenobiotic compounds.

The current study suggests that the fungal isolates P. decumbens PDX7, P. janthinellum SDX7, and A. terreus PKX4 degraded kerosene by 95%, 96%, and 75% and diesel by 79%, 75%, and 70% after 16 days based on the ability of utilizing these compounds as sole carbon sources. GC-MS chromatograms revealed that n-alkane fractions are easily degraded; however, the rate is lower for branched alkanes, n-alkyl aromatics, cyclic alkanes, and polynuclear aromatics displaying delayed and lower degradation. The ratio of aromatic/aliphatic hydrocarbons >0.8 indicates the efficiency of these fungi in removing the aromatic hydrocarbons of the petroleum products. All of the treated fungal strains exhibited higher MnP, laccase, and dehydrogenase activities on the twelfth and sixteenth days as compared to the initial fourth and eighth days. In addition, P. decumbens PDX7 and P. janthinellum SDX7 displayed higher enzymatic activities as compared to A. terreus PKX4. Fungal isolates were also tested for their growth on various xenobiotic compounds as sole carbon sources.

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The study was aimed to determine the chronic toxicity of Polynuclear aromatic hydrocarbon – Anthracene in response to pigments and metabolic study on three different cyanobacterial species such as Synechocystis sp., Anabaena fertilissima, and Nostoc muscorum. Test organisms were treated at different doses and encountered LC50/Mean Lethal Concentration (at which 50% lethality/ growth reduction occur) separately at 7.0 ppm for Synechocystis sp, 5.0 ppm for Anabaena fertilissima and 1.5 ppm for Nostoc muscorum. The influence of anthracene on pigments, metabolites and enzymes was carried out. The test doses caused concentration dependent and decreased pigments like carotenoids and phycobilliproteins. Depletion of carbohydrate by 65 to 80% and proteins by 58 to 78% was encountered with rise in Anthracene concentrations after 16th day exposure in case of Synechocystis sp however, phenols were found to raise by 26 to 37% with increased anthracene concentrations. Similar trend also observed in other two tested blue green algae. Thus the Synechocystis sp.is more tolerant to anthracene treatments as compare to Anabaena fertillissima but Nostoc muscorum showed highest sensitivity to anthracene.Int J Appl Sci Biotechnol, Vol 3(3): 381-386