Publication:
Activation of lucidin‐3‐O‐primveroside mutagenicity by hesperidinase

dc.contributor.authorMalyn Chulasirien_US
dc.contributor.authorTaijiro Matsushimaen_US
dc.contributor.authorKunitoshi Yoshihiraen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherJapan Bioassay Research Centeren_US
dc.contributor.otherNational Institute of Health Sciences Tokyoen_US
dc.date.accessioned2018-07-04T07:03:00Z
dc.date.available2018-07-04T07:03:00Z
dc.date.issued1995-01-01en_US
dc.description.abstractAt the maximum dose tested, 100 μg/plate, lucidin‐3‐O‐primveroside (LUC‐Prv) exhibited mutagenic potential in Salmonella typhimurium TA100 without S9 mix but not with the addition of this preparation. When the pH of the tested system was reduced from 7.4 to 6.5, the same results were obtained. However, after hesperidinase treatment at pH 6.5, higher mutagenicity was demonstrated, and the mutagenicity of the hydrolysis product in TA100 decreased in the presence of S9 mix. When the preincubation time of the mixture was kept longer, i.e. 30, 60 and 120 min, the number of revertants in TA100 without S9 mix became higher. When the concentration of hesperidinase was varied from 5 × 10−5 to 2.5 × 10−2 unit, no change in the number of revertants was observed. In contrast, LUC‐Prv and its hydrolysis products demonstrated no mutagenicity in TA98 by the same tested system. Copyright © 1995 John Wiley & Sons, Ltd.en_US
dc.identifier.citationPhytotherapy Research. Vol.9, No.6 (1995), 421-424en_US
dc.identifier.doi10.1002/ptr.2650090607en_US
dc.identifier.issn10991573en_US
dc.identifier.issn0951418Xen_US
dc.identifier.other2-s2.0-0029033237en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/17506
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0029033237&origin=inwarden_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleActivation of lucidin‐3‐O‐primveroside mutagenicity by hesperidinaseen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0029033237&origin=inwarden_US

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