• Title/Summary/Keyword: levan acetate

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Levan acetate를 이용한 hydrocortisone의 방출 제어

  • Im, Seung;Lee, Gi-Yeong;Kim, Dong-Un;Choe, Chun-Sun
    • 한국생물공학회:학술대회논문집
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    • 2001.11a
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    • pp.849-852
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    • 2001
  • The preparation, characterization and drug release behaviour of hydrocortisone(HC) loaded levan acetate microparticles were investigated. Hydrophobic levan acetate was prepared by chemical modification of hydrophilic levan and micro particles were made by dialysis method or solvent evaporation method. The morphology of levan acetate was observed by SEM and drug release profiles were investigated at pH 7.4 and pH 1.2. Newly synthesised levan acetate can be used for carrier of drugs.

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Controlled Rrelease of Indomethacin using Biodegradable Polymer Microspheres (생분해성 고분자 미세구를 이용한 indomethacin의 방출제어)

  • Lim, Seung;Lee, Ki-Young;Lee, Moo-Sung;Choi, Chang-Nam;Kim, Young-Dae
    • KSBB Journal
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    • v.16 no.5
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    • pp.505-510
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    • 2001
  • The preparation, characterization and drug release behaviour of drug(indomethacin) loaded Poly(L-lactic acid)(PLA), tarmarind acetate and levan acetate mircospheres were investigated. Hydrophobic tarmarind acetate and levan acetate were prepared by chemical modification of hydrophilic tarmaried gum and levan and microspheres were made by a solvent evaporation method. In the case of poly(L-lactic acid) microspheres, drug release rate was effected by polymer-drug ratios and drum release was sustained by increasing of polymer content. The yield of microspheres were effected by many factors and the mean size was below 1 $\mu$m, The IND release profiles from tarmarind acetate and levan acetate micropheres were more slightly less than ploy(L-lactic acid) microspheres.

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Prebiotic Properties of Levan in Rats

  • Jang, Ki-Hyo;Kang, Soon-Ah;Cho, Yun-Hi;Kim, Yun-Young;Lee, Yun-Jung;Hong, Kyung-Hee;Seong, Kyung-Hwa;Kim, So-Hye;Kim, Chul-Ho;Rhee, Sang-Ki;Ha, Sang-Do;Choue, Ryo-Won
    • Journal of Microbiology and Biotechnology
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    • v.13 no.3
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    • pp.348-353
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    • 2003
  • Generally, two different types of fructose polymer are found in nature. One is inulin, whose fructosyl residues are linked mainly by a ${\beta}-(2,1)-linkage$, while the other is high-molecular-weight levan, whose fructosyl residues are linked mainly by a ${\beta}-(2,6)-linkage$. In contrast to the extensive studies on the prebiotic properties of inulin, there has been no report on the effect of levan on the large bowel microflora in viva. Therefore, to examine whether dietary levan can be used as a prebiotic, Sprague-Dawley male rats were fed one of two diets for 3 weeks: 1) basal diet plus sucrose; 2) basal diet plus 10% (wt/wt) levan. The cecal bowel mass, cecal and colon short-chain fatty acids (SCFAs), pH, and microflora were then compared. The intake of the levan-containing diet significantly increased the total cecal weight and wall weight. The analyses of the SCFAs in the cecal and colonic contents revealed that levan was converted into acetate, butyrate, and lactate, which resulted in acidic conditions. The intake of levan also significantly increased the total number of microorganisms by 5-fold and lactic acid-producing bacteria (LAB) 30-fold in the feces. Accordingly, the current work shows that levan can be used as a prebiotic for stimulating the growth of LAB in an animal model.

Purification and Characterization Sucrose phosohorylase in Leuconostoc mesenteroides NRRL B-1149 (Leuconostoc mesenteroides NRRL B-1149의 Sucrose phosohorylase의 분리와 특성 연구)

  • Lee Jin Ha;Park Jun Seong;Park Hyen Joung;Cho Jae Young;Choi Jeong Sik;Kim Do Man
    • KSBB Journal
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    • v.19 no.5
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    • pp.363-367
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    • 2004
  • Leuconostoc mesenteroides NRRL B-1149 produces various glucoseyltransferases for the synthesis of dextran, levan and glucose-1-phosphate using sucrose as a substrate. A sucrose phosphorylase (1149SPase) was purified from L. mesenteroides NRRL B-1149 culture by using hollow fiber filtration (30 kDa cut off), Toyopearl DEAE 650 M column chromatography and following two times of DEAE-Sepharose column chromatographies. The specific activity of the purified 1149SPase was 25.7 (U/mg) with $16\%$ yield. The 1149SPase showed a molecular size of 56 kDa on denatured $10\%$ SDS-PAGE. The N-terminal amino acid sequence of the enzyme was MEIQNKAM. The optimum pH and temperature of this enzyme were 6.2~6.5 and 37^{circ}C, respectively. It had an apparent K_{m} of 6.0 mM and K_{cat} of 1.62/s for sucrose. 1149SPase crystal was formed by hanging drop diffusion technique using 20 mM calcium chloride dihydrate, 100 mM sodium acetate trihydrate pH 4.6 and $30\%$ 2-methyl-2,4-pentanediol as vaporizing and reservation solution. The 1149SPase catalyzes transferring of glucose from isomaltose or sucrose to salicin and salicyl alcohol by disproportionation reaction or acceptor reaction and synthesized two acceptor products, respectively.