2015
DOI: 10.1016/j.cej.2014.08.111
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Engineering and microbiological aspects of BTEX removal in bioreactors under sulfate-reducing conditions

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Cited by 30 publications
(27 citation statements)
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“…In the marine sediments, the degradation of crude oil was limited by the availability of N and P. But addition of simple empirical estimates of the nutrient proportions may not be sufficient for successful remediation (Singh et al 2015). Labile organic enhancer substrates used like acetate (Stasik et al 2015) and ethanol (Firmino et al 2015) exhibited negative results possibly due to product inhibition in the degradative pathway. (Mukherjee and Bordoloi 2012) had reported the essential presence of minimum amount of phosphate and nitrate sources and the fact that S. silvestris AM1 could produce bioemulsifier only in ZM medium,1/10th ZM medium was chosen.…”
Section: Microcosm Studiesmentioning
confidence: 95%
“…In the marine sediments, the degradation of crude oil was limited by the availability of N and P. But addition of simple empirical estimates of the nutrient proportions may not be sufficient for successful remediation (Singh et al 2015). Labile organic enhancer substrates used like acetate (Stasik et al 2015) and ethanol (Firmino et al 2015) exhibited negative results possibly due to product inhibition in the degradative pathway. (Mukherjee and Bordoloi 2012) had reported the essential presence of minimum amount of phosphate and nitrate sources and the fact that S. silvestris AM1 could produce bioemulsifier only in ZM medium,1/10th ZM medium was chosen.…”
Section: Microcosm Studiesmentioning
confidence: 95%
“…The PCR mixture (50 lL) contained 10 lL of reaction buffer (5X), 5 lL of MgCl 2 (25 mM), 0.25 lL of Taq polymerase (5 u Á lL À1 ) (Promega, USA), 1.0 or 1.5 lL of deoxynucleotide triphosphates (10 mM), l lL of the extracted DNA, 1.0 or 1.5 lL of PCR primers (10 lM) and Milli-Q water up to a final volume of 50 lL. The PCR thermocycling program used was previously described by Firmino et al [21].…”
Section: Microbial Community Analysesmentioning
confidence: 99%
“…DGGE was performed in a D-Code Universal Mutation Detection System (Bio Rad Laboratories, USA) using polyacrylamide gels with a urea/formamide denaturing gradient of 42-67% and 30-60% for bacterial and archaeal communities, respectively and superimposed with a porous gradient of acrylamide/bisacrylamide (6-10%). The electrophoresis conditions and gel staining were previously described by Firmino et al [21].…”
Section: Microbial Community Analysesmentioning
confidence: 99%
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