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논문 기본 정보

자료유형
학술저널
저자정보
Sung-Hee Kim (Seoul National University) Myoung-Hee Lee (Seoul National University) Sung-Jae Yang (Seoul National University) Jung-Woo Kim (Seoul National University) Hyunju Cha (Seoul National University) Jae-Ho Cha (Pusan National University) Van Dao Nguyen (Hanoi Open University) Kwan-Hwa Park (Seoul National University)
저널정보
한국식품과학회 Food Science and Biotechnology Food Science and Biotechnology vol 17. no 2
발행연도
2008.4
수록면
302 - 307 (6page)

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초록· 키워드

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Novel amylase inhibitors were synthesized via transglycosylation by Thermotoga maritima glucosidase (TMG). TMG hydrolyzes acarbose, acarviosine-glucose, and maltooligosaccharide by releasing <sup>14</sup>C-labeled glucose from the reducing end of each molecule. When TMG was incubated with acarviosine-glucose (the donor) and glucose (the acceptor), two major transfer products, compounds 1 and 2, were formed via transglycosylation. The structures of the transfer products were determined using thin-layer chromatography (TLC), high-performance ion chromatography (HPIC), and <sup>13</sup>C nuclear magnetic resonance (NMR) spectroscopy. The results indicate that acarviosine was transferred to glucose at either C-6, to give a α-(1→6) glycosidic linkage, or at C-3, to produce an α-(1→3) glycosidic linkage. The transfer products showed a mixed-type inhibition against porcine pancreatic α-amylase; therefore, they may be useful not only as inhibitors but also as acarbose transition-state analogs to study the mechanism of amylase inhibition.

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Abstract
Introduction
Materials and Methods
Results and Discussion
Acknowledgments
References

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