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Antigenotoxic potential of glucomannan on four model test systems
V Vlcková1, V Dúhová, S Svidová
1Department of Genetics, Faculty of Natural Sciences, Comenius University, Bratislava, Slovak Republic. vlckova@fns.uniba.sk
Abstract:
Antimutagenic, anticlastogenic, and bioprotective effect of polysaccharide glucomannan (GM) isolated from Candida utilis was evaluated in four model test systems. The antimutagenic effect of GM against 9-aminoacridine (9-AA)- and sodium azide (NaN3)-induced mutagenicity was revealed in the Salmonella typhimurium strains TA97 and TA100, respectively. GM showed anticlastogenic effect against N-nitroso-N'-methylurea (NMU) induced chromosome aberrations in the Vicia sativa assay. The bioprotective effect of GM co-treated with methyl-methane-sulphonate (MMS) was also established in Chlamydomonas reinhardtii repair deficient strains uvs10 and uvs14. The statistically significant antimutagenic potential of GM was not proved against 4-nitro-quinoline-1-oxide (4-NQO)-induced mutagenicity in Saccharomyces cerevisiae D7 assay. It may be due to bioprotectivity of alpha-mannan and beta-glucan, which are integral part of S. cerevisiae cell walls. Due to the good water solubility, low molecular weight (30 kDa), antimutagenic/anticlastogenic, and bioprotective activity against chemical compounds differing in mode of action, GM appears to be a promising natural protective (antimutagenic) agent.
Insights
Glucomannan (GM) from Candida utilis demonstrates significant antimutagenic and anticlastogenic effects in various test systems. This natural polysaccharide shows promise as a protective agent against chemical mutagens.
Area of Science:
- Biochemistry
- Molecular Biology
- Genetics
Background:
- Polysaccharides are known for their diverse biological activities.
- Glucomannan (GM) is a polysaccharide with potential health benefits.
- Evaluating the protective effects of natural compounds is crucial for developing new therapeutic agents.
Purpose of the Study:
- To evaluate the antimutagenic, anticlastogenic, and bioprotective effects of glucomannan (GM) isolated from Candida utilis.
- To assess GM's efficacy across four different model test systems.
- To determine GM's potential as a natural protective agent against chemical mutagens.
Main Methods:
- Assessing antimutagenic activity using Salmonella typhimurium strains TA97 and TA100 against 9-aminoacridine (9-AA) and sodium azide (NaN3).
- Evaluating anticlastogenic effect against N-nitroso-N'-methylurea (NMU) induced chromosome aberrations in Vicia sativa.
- Testing bioprotective effect in Chlamydomonas reinhardtii repair deficient strains (uvs10, uvs14) with methyl-methane-sulphonate (MMS).
- Investigating antimutagenic potential against 4-nitro-quinoline-1-oxide (4-NQO) in Saccharomyces cerevisiae D7.
Main Results:
- GM exhibited significant antimutagenic effects against 9-AA and NaN3 induced mutagenicity.
- GM demonstrated anticlastogenic activity against NMU-induced chromosome aberrations.
- GM showed bioprotective effects when co-treated with MMS in Chlamydomonas reinhardtii.
- No statistically significant antimutagenic potential was observed against 4-NQO in Saccharomyces cerevisiae.
Conclusions:
- Glucomannan (GM) from Candida utilis possesses notable antimutagenic, anticlastogenic, and bioprotective properties.
- GM's efficacy varies depending on the mutagen and test system, potentially due to interactions with cell wall components like in Saccharomyces cerevisiae.
- With its favorable properties (water solubility, low molecular weight), GM is a promising natural protective agent against chemical mutagens.
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