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Enzymatic Modification of Cellulose Using Leuconostoc mesenteroides B-742CBM Dextransucrase
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  • Enzymatic Modification of Cellulose Using Leuconostoc mesenteroides B-742CBM Dextransucrase
  • Enzymatic Modification of Cellulose Using Leuconostoc mesenteroides B-742CBM Dextransucrase
저자명
Kim. Do-Man,Kim. Young-Min,Park. Mi-Ran,Ryu. Hwa-Ja,Park. Don-Hee,Robyt. John F.
간행물명
Journal of microbiology and biotechnology
권/호정보
1999년|9권 5호|pp.529-533 (5 pages)
발행정보
한국미생물생명공학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

In addition to catalyzing the synthesis of dextran from sucrose as a primary reaction, dextransucrase also catalyzes the transfer of glucose from sucrose to other carbohydrates that are present or are added to the reaction digest. We have synthesized new glucans having new structures and new characteristics, by transferring D-glucose of sucrose to $alpha$-cellulose and by using the constitutive dextransucrase obtained from Leuconostoc mesenteroides B-742CBM. The final reaction products were composed of soluble- and insoluble-glucans. The yields of soluble- and insoluble-glucans were theoretically 21% $pm$ 2.2 and 68% $pm$ 5.1, respectively. The remainder of the reaction products was recovered as a mixture of olgiosaccharides that could not be precipitated by 67%(v/v) ethanol. Treating the modified glucans with endo-dextranase and/or cellulase, oligosaccharides were produced that were not formed from the hydrolysis of native cellulose or B-742CBM dextran. The modification of the cellulose was confirmed by methylation and acid hydrolysis of the soluble-and insoluble-glucan. Both (1->4) and(1->6) glycosidic linkages were found in both of the glucans.