2015
DOI: 10.1002/jobm.201500477
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Molecular identification of indigenous manganese solubilising bacterial biodiversity from manganese mining deposits

Abstract: Manganese (Mn) ranks twelfth among the most exuberant metal present in the earth's crust and finds its imperative application in the manufacturing steel, chemical, tannery, glass, and battery industries. Solubilisation of Mn can be performed by several bacterial strains which are useful in developing environmental friendly solutions for mining activities. The present investigation aims to isolate and characterize Mn solubilising bacteria from low grade ores from Sanindipur Manganese mine of Sundargh district i… Show more

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Cited by 44 publications
(8 citation statements)
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“…In fact, Lysinibacillus spp. were isolated from a Mn mining soil (Liu et al, 2013) and a Brazilian Mn mine (Barboza et al, 2015), and were able to solubilize low grade ores from a Mn deposit (Ghosh et al, 2016). Chen et al (2019) isolated the Mn-oxidizing bacterium Massilia sp.…”
Section: Mineralogical and Microbiological Implicationsmentioning
confidence: 99%
“…In fact, Lysinibacillus spp. were isolated from a Mn mining soil (Liu et al, 2013) and a Brazilian Mn mine (Barboza et al, 2015), and were able to solubilize low grade ores from a Mn deposit (Ghosh et al, 2016). Chen et al (2019) isolated the Mn-oxidizing bacterium Massilia sp.…”
Section: Mineralogical and Microbiological Implicationsmentioning
confidence: 99%
“…K6 based on the sequence homology value in the 16S rDNA region with the closest species using the BLAST method from NCBI. 16S rDNA is a useful and powerful marker indicating the presence of bacteria in biological samples, and used as a new technique for bacteria identification at the species level (Srinivasan et al, 2015;Ghosh, 2016). 16S rDNA has areas with a conservative base order (conserved region) and regions with a variable base sequence (variable region) for diversity analysis.…”
Section: Molecular Identificationmentioning
confidence: 99%
“…The cell morphology was investigated using Phase contrast microscope-BX43 (Olympus, japan). Eventually, the strains were preserved on MRS agar slant in a refrigerated condition [17,18].…”
Section: Isolation and Medium Of Growthmentioning
confidence: 99%
“…The PCR products were electrophoresed. The amplified DNA pellet was dissolved in 10 mm TE buffer and 2 µl of the dissolved sample was analyzed using gel electrophoresis at 120 v for 60min to visualize the present DNA fragments (18). However, the purity was assessed by determining A260/280 ratio through spectrophotometric method (UH5000, Hitachi, Japan).…”
Section: Dna Extraction and Amplificationmentioning
confidence: 99%