2015
DOI: 10.1016/j.bios.2014.08.030
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Fast and sensitive optical toxicity bioassay based on dual wavelength analysis of bacterial ferricyanide reduction kinetics

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Cited by 19 publications
(6 citation statements)
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“…5d). Even the EC 50 , around 3.9 mg L -1 , coincided with that obtained with the reflectomery assay, and was in agreement with those previously reported for optical kinetic analysis of ferricyanide reduction [20] and with the standard method Microtox® [22]. According to this, chromatic analysis of BPDs represents a suitable method for quantitative determination of water toxicity, independently on the transduction method.…”
Section: Bacterial Entrapment Efficiency and Stability On Pdssupporting
confidence: 90%
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“…5d). Even the EC 50 , around 3.9 mg L -1 , coincided with that obtained with the reflectomery assay, and was in agreement with those previously reported for optical kinetic analysis of ferricyanide reduction [20] and with the standard method Microtox® [22]. According to this, chromatic analysis of BPDs represents a suitable method for quantitative determination of water toxicity, independently on the transduction method.…”
Section: Bacterial Entrapment Efficiency and Stability On Pdssupporting
confidence: 90%
“…This intriguing fact may be derived from inherent nature of kinetic and single measurement analysis. That is, kinetic analysis relies on a reversible and non-accumulative magnitude, and conversely single point analysis relies on an irreversible and accumulative magnitude [20]. Thus, the present cellulose-based bioassay represents a low-cost, simple, robust and reliable strategy for quick in-situ determination of toxicity with minimal instrumentation and without problems of portability.…”
Section: Bacterial Entrapment Efficiency and Stability On Pdsmentioning
confidence: 99%
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“…Being a model organism for laboratories, almost every aspect of E.coli, from its genome to its proteinmaking capability, has been exploited (Lee, 2009). In bacterial metabolism, oxygen acts as the hydrogen acceptor in the TCA cycle under the aerobic condition for growth and respiration (Hadjipetrou, 1966).…”
Section: Introductionmentioning
confidence: 99%
“…The starting iron donors for PB formation are a specific concentration mixture of potassium ferricyanide and ferric ammonium citrate. Bacteria readily reduce ferricyanide to ferrocyanide. However, this reduced form cannot spontaneously react with ferric ammonium citrate at the provided dilution. The bond between iron and citrate cannot be spontaneously broken by the presence of ferrocyanide or bacteria but requires light activation.…”
mentioning
confidence: 99%