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서지반출
Chemical Modification of Botryosphaeran: Structural Characterization and Anticoagulant Activity of a Water-Soluble Sulfonated ($1{ ightarrow}3$)($1{ ightarrow}6$)-${eta}$-D-Glucan
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  • Chemical Modification of Botryosphaeran: Structural Characterization and Anticoagulant Activity of a Water-Soluble Sulfonated ($1{ ightarrow}3$)($1{ ightarrow}6$)-${eta}$-D-Glucan
  • Chemical Modification of Botryosphaeran: Structural Characterization and Anticoagulant Activity of a Water-Soluble Sulfonated ($1{ ightarrow}3$)($1{ ightarrow}6$)-${eta}$-D-Glucan
저자명
Brandi. Jamile,Oliveira. Eder C.,Monteiro. Nilson K.,Vasconcelos. Ana Flora D.,Dekker. Robert F.H.,Barbosa. Aneli M.,Silveira. J
간행물명
Journal of microbiology and biotechnology
권/호정보
2011년|21권 10호|pp.1036-1042 (7 pages)
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한국미생물생명공학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

The exopolysaccharide botryosphaeran ($EPS_{GLC}$; a ($1{ ightarrow}3$)($1{ ightarrow}6$)-${eta}$-D-glucan from Botryosphaeria rhodina MAMB-05) was sulfonated to produce a water-soluble fraction ($EPS_{GLC}$-S) using pyridine and chlorosulfonic acid in formamid. This procedure was then repeated twice to produce another fraction ($EPS_{GLC}$-RS) with a higher degree of substitution (DS, 1.64). The purity of each botryosphaeran sample (unsulfonated and sulfonated) was assessed by gel filtration chromatography (Sepharose CL-4B), where each polysaccharide was eluted as a single symmetrical peak. The structures of the sulfonated and re-sulfonated botryosphaerans were investigated using ultraviolet-visible (UV-Vis), Fourier-transform infrared (FT-IR), and $^{13}C$ nuclear magnetic resonance ($^{13}C$ NMR) spectroscopies. $EPS_{GLC}$ and $EPS_{GLC}$-RS were also assayed for anticoagulation activity, and $EPS_{GLC}$-RS was identified as an anticoagulant.