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dc.contributor.authorBaktir, Afaf
dc.contributor.authorZaini, Noor Cholies
dc.contributor.authorMurdiyatmo, Untung
dc.contributor.authorKuntaman
dc.date.accessioned2011-03-28T07:11:08Z
dc.date.available2011-03-28T07:11:08Z
dc.date.issued2005
dc.identifier.issn0854-8587
dc.identifier.urihttp://repository.ipb.ac.id/handle/123456789/43387
dc.description.abstractDextranase of Arthrobacter sp. strain B7 (B7DEX enzyme) was characterized in this study. This enzyme hydrolyzed sucrose and dextran, but not other glucans (starch, nigeran, cellulose, β-soluble glucan). It also hydrolyzed glucan from dental plaque with the activity of 7.38 + 0.66 U/ml, where the activity toward dextran was 31.88 + 1.24 U/ml. The enzyme exhibited the pH optimum of 7 and the temperature optimum of 50 oC. Its optimum stability was at pH 7 and 50 oC. The enzyme was inhibited by Fe3+, Cu2+, Zn2+, and Ag+, but not by the anionic detergent (SDS) and the nonionic detergent (Triton-X). The enzyme was activated by Ca2+, Na+, Mg2+, and saliva.en
dc.publisherIPB (Bogor Agricultural University)
dc.relation.ispartofseriesVol 12;No 4
dc.titleThe Potency of Dextranase from Arthrobacter sp. Strain B7 as Dental Plaque Removalen
dc.title.alternativeHAYATI Journal of Biosciences Vol. 12 No.4 Tahun 2005en


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