• 제목/요약/키워드: methyl-${\beta}$-D-xylopyranoside

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Three Antioxidant Compounds of the Red Alga Liagora farinosa

  • Hannoda, Hala M.;Badr, Jihan M.;Yousef, Diaa T.A.
    • Natural Product Sciences
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    • 제13권2호
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    • pp.140-143
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    • 2007
  • Investigation of the chloroform soluble fraction of the red alga Liagora farinosa, collected from Hurghada at the Red Sea resulted in the isolation of three compounds; a nucleoside (thymidine) and two glycosides (methyl-${\beta}$-D-xylopyranoside and glycerol-2-${\alpha}$-D-glucopyranoside). The structures of the isolated compounds were established on the basis of different spectroscopic techniques as well as comparison with the previously published data. This is the first report for the isolation of the three compounds fron red algae; moreover, the compounds were examined for their antioxidant activity and showed variable activity.

Paenibacillus sp. DG-22에서의 β-xylosidase 생합성 조절 (Regulation of β-xylosidase biosynthesis in Paenibacillus sp. DG-22)

  • 이태형;임평옥;이용억
    • 생명과학회지
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    • 제17권3호통권83호
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    • pp.407-411
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    • 2007
  • 효소생산을 최적화하기 위해서 Paenibacillus sp. DG-22에서의 ${\beta}-xylosidase$ 생합성 조절을 연구하였다. Paenibacillus sp. DG-22의 ${\beta}-xylosidase$는 배양액에 존재하는 탄소원에 의해 조절되는 것으로 관찰되었다. ${\beta}-Xylosidase$의 합성은 xylan과 methyl ${\beta}-D-xylopyranoside$ (${\beta}MeXyl$)에 의해 유도되었으나 쉽게 대사되는 단당류에 의해서는 약간 억제되었다. ${\beta}MeXyl$${\beta}-xylosidase$의 유도를 위한 최적의 기질임을 확인하였고 가장 효과적인 유도는 10 mg/ml의 농도에서 얻어졌다. ${\beta}-Xylosidase$의 생산은 세포의 생장과 연관된 양상을 나타내었으며, 대수기 말에 최대양이 형성되었다. Glucose와 xylose가 존재하면 ${\beta}-xylosidase$의 활성 수준이 감소하는 것으로 보아 이 효소의 생합성은 catabolite repression을 받는것으로 보인다. SDS-PAGE와 활성염색 기술을 이용하여 ${\beta}Mexyl$가 이 효소의 생합성을 유도하며 약 80 kDa 크기의 하나의 ${\beta}-xylosidase$가 존재함을 알 수 있었다.

Phenolic Compounds from Desmodium caudatum

  • Li, Wei;Sun, Ya Nan;Yan, Xi Tao;Yang, Seo Young;Choi, Chun Whan;Kim, Young Ho
    • Natural Product Sciences
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    • 제19권3호
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    • pp.215-220
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    • 2013
  • Three C-glucosyl flavones (1 - 3), one xanthone (4), and four flavanonols (5 - 8) were isolated by various chromatographic methods from the leaves and stems of Desmodium caudatum (Thunb.) DC. Chemical structures of these compounds were elucidated by 1D and 2D NMR and mass spectroscopy. The compounds were identified as swertisin (1), spinosin (2), 7-methyl-apigenin-6-C-${\beta}$-glucopyranosyl-2"-O-${\beta}$-D-xylopyranoside (3), 1,3,5,6-tetrahydroxyxanthone (4), yokovanol (5), aromadendrin (6), 2'-hydroxy yokovanol (7), and 2'-hydroxy neophellamuretin (8). Compounds 2 - 4 were first isolated from D. caudatum, as well as the spectroscopic data for compound 3.

Isolation of Compounds from Cimicifugae Rhizoma and their Cytotoxic Activity

  • Cuong, To Dao;Lim, Chae-Jin;Kim, Sang-Won;Park, Ji-Eun;Hung, Tran Manh;Min, Byung-Sun
    • Natural Product Sciences
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    • 제17권2호
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    • pp.80-84
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    • 2011
  • Five known compounds, cimigenol (1), 25-O-acetylcimigenol (2), cimigenol 3-O-${\beta}$-D-xylopyranoside (3), ferulic acid methyl ester (4), and visnagin (5), were isolated from Cimicifugae Rhizoma (Ranunculaceae). The chemical structures of these compounds were determined on the basis of spectroscopic analyses including 2D NMR. Compounds 1 - 5 were evaluated for their cytotoxic activity against the HL-60, MCF-7, and A549 cancer cell lines in in vitro. Among them, compounds 4 and 5 showed moderate inhibitory activity against HL-60 cancer cell lines with $IC_{50}$ values of 24.8 and 18.1 ${\mu}M$, respectively.