2006
DOI: 10.1016/j.bios.2005.10.009
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SOS-red fluorescent protein (RFP) bioassay system for monitoring of antigenotoxic activity in plant extracts

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Cited by 20 publications
(15 citation statements)
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“…However, other chemical investigations are needed to identify the compounds which could not be detected by GC-MS. Grover & Bala (1993) reported that, a pretreatment with an aqueous guava leaf extract was found to be effective in activating the mutagenicity of direct acting mutagens. Moreover, it has been reported that the aqueous whole plant extract afforded protection against mitomycin C, nalidixic acid and hydrogen peroxide induced mutagenicity (Bartolome et al, 2006).…”
Section: Discussionmentioning
confidence: 99%
“…However, other chemical investigations are needed to identify the compounds which could not be detected by GC-MS. Grover & Bala (1993) reported that, a pretreatment with an aqueous guava leaf extract was found to be effective in activating the mutagenicity of direct acting mutagens. Moreover, it has been reported that the aqueous whole plant extract afforded protection against mitomycin C, nalidixic acid and hydrogen peroxide induced mutagenicity (Bartolome et al, 2006).…”
Section: Discussionmentioning
confidence: 99%
“…A considerable battery of assays exists for the detection of different genotoxic effects of compounds in experimental systems, or for investigations of exposure to genotoxic agents in environmental or occupational settings. Treatment with the aqueous whole plant extracts of Psidium guajava afforded protection (anti-genotoxic activity) against mitomycin C, nalidixic acid and hydrogen peroxide (three genotoxins) (Bartolome et al, 2006). In another study, a pre-treatment with an aqueous guava leaf extract was found to be effective in inactivating the mutagenicity of direct-acting mutagens 4-nitro-o-phenylenediamine and 2-aminofluorene in the tester strains of Salmonella typhimurium.…”
Section: Antigenotoxic and Antimutagenic Effectsmentioning
confidence: 97%
“…Performance was usually poorer compared with bioluminescent recA ‐based reporters: lag times were longer and detection thresholds were higher, unless incubation times were very long. The recA ′:: DsRed plasmid, hosted in E. coli UTL2, was used in order to monitor antigenotoxic activity of plant extracts that exhibited some protection against MMC, NA and hydrogen peroxide (Bartolome et al. , 2006).…”
Section: Reporter Systemsmentioning
confidence: 99%