Metal biosorption by magnetotactic bacteria isolated from fresh water sediments and characterization of extracted magnetosomes.

The focus of the present study is to isolate and identify magnetotactic bacteria from fresh water sediments in Salem region, Tamil Nadu. Fresh water sediments were collected and characterized by X-ray diffraction to detect the crystalline nature of particles. Totally 12 isolates were screened for the metal biosorption efficiency in modified nutrient agar plates with 10 mg (lower concentration) of four different metals viz., manganese chloride, zinc sulphate, copper sulphate and potassium dichromate. Followed by testing their ability to tolerate higher concentration of metals viz., 20 mg, 30 mg, 50 mg, 70 mg, 90 mg and 150 mg/50 ml was analyzed. Only four bacteria survived the highest concentration of manganese and zinc (3000 µg/ml), CuSO4 and K2Cr2O7 at a concentration of 1400 µg/ml and 1800 µg/ml, respectively. The four bacterial strains Stenotrophomonas maltophilia, two Pseudomonas aeruginosa strains and Achromobacter xylosoxidans were grown in modified nutrient broth (NB) and Luria Bertani (LB) incorporated with metals such as manganese, zinc, copper and chromium and tested for their efficacy to sustain metal stress. Since the two bacterial strains (SBY and KY1) were able to grow in both medium with a potential to with stand higher metal concentration these strains were further studied. A metal tolerant magnetotactic bacterial strain Pseudomonas aeruginosa SBY was confirmed by TEM analysis to detect the accumulated metal within the cell. As bacterial strains were capable of tolerating higher concentration of metal, they may have a vital role in environmental bioremediation.

Molecular characterization and antioxidant assay of pigment producing bacteria, Sphingomonas paucimobilis and Microbacterium arborescens isolated from fresh water sediments.

This study focuses on isolation of pigment producing bacteria from fresh water sediment. The isolated bacteria were grown in nutrient broth and the maximum absorbance of 2.512 was obtained for the extracted pigment at 500 nm. The effective strains were optimized, pH 11 and temperature 30 °C was found to be more favorable for its maximum growth. The isolates were identified based on their molecular characterestics as Microbacterium arborescens and Sphingomonas paucimobilis, molecular size of the amplified 16S rRNA gene sequence was found to be approximately 1270 and 765 bp respectively. The antioxidant property of the pigment was analyzed using DPPH and ABTS assay. The IC50 value of Microbacterium arborescens was higher in all the three assays in comparison with Sphingomonas paucimobilis. The extracted pigment was characterized for the presence of compounds using GC-MS and FTIR analysis to determine the functional groups. As the pigment obtained from M. arborescens had shown better antioxidant activity it may be used as colorant in food industrial applications.