Synthetic studies of bi-fluorescence-labeled maltooligosaccharides as substrates for α-amylase on the basis of fluorescence resonance energy transfer (FRET)

Bioorganic and Medicinal Chemistry

Volumn 20, Issue 1, 2012, Pages 435-445

  Oka, Hiroyuki ^a,b   Koyama, Tetsuo ^a   Hatano, Ken ^a   Matsuoka, Koji ^a  

^a SAITAMA UNIVERSITY   (Japan)

^b Scientific Investigation Laboratory   (Japan)

Author keywords

Amylase; Fluorescence resonance energy transfer; Maltooligosaccharides; Synthetic substrates

Indexed keywords

4 O (2,3,4,6 TETRA O ACETYL BETA DEXTRO GLUCOPYRANOSYL) 2,3,6 TRI O ACETYL BETA DEXTRO GLUCOPYRANOSE THIOACETATE; AMINO ETHYL THIOPENTYL 4 O (6 O NAPHTHYLMETHYL BETA DEXTRO GLUCOPYRANOSYL) 1 THIO BETA DEXTRO GLUCOPYRANOSIDE; AMYLASE; DANSYL AMIDO ETHYL THIOPENTYL 4 O (6 O NAPHTHYLMETHYL BETA DEXTRO GLUCOPYRANOSYL) 1 THIO BETA DEXTRO GLUCOPYRANOSIDE; MALTOOLIGOSACCHARIDE DERIVATIVE; MALTOTETRAOSE DERIVATIVE; MALTOTETRAPYRANOSIDE DERIVATIVE; MALTOTRIAOSIDE DERIVATIVE; N PENTENYL 1 THIO BETA DEXTRO MALTOHEPTAOSIDE; N PENTENYL 1 THIO BETA DEXTRO MALTOHEXAOSIDE; N PENTENYL 1 THIO BETA DEXTRO MALTOPENTAOSIDE; N PENTENYL 1 THIO BETA DEXTRO MALTOTETRAOSIDE; N PENTENYL 1 THIO BETA DEXTRO MALTOTRIAOSIDE; N PENTENYL 4 O (2,3 DI O ACETYL 4,6 O NAPHTHYLMETHYLIDENE BETA DEXTRO GLUCOPYRANOSYL) 2,3,6 TRI O ACETYL 1 THIO BETA DEXTRO GLUCOPYRANOSIDE; N PENTENYL 4 O (2,3 DI O ACETYL 6 O NAPHTHYLMETHYL BETA DEXTRO GLUCOPYRANOSYL) 2,3,6 TRI O ACETYL 1 THIO BETA DEXTRO GLUCOPYRANOSIDE; N PENTENYL 4 O (2,3,4,6 TETRA O ACETYL BETA DEXTRO GLUCOPYRANOSYL) 2,3,6 TRI O ACETYL 1 THIO BETA DEXTRO GLUCOPYRANOSIDE; N PENTENYL 4 O (6 O NAPHTHYLMETHYL BETA DEXTRO GLUCOPYRANOSYL) 1 THIO BETA DEXTRO GLUCOPYRANOSIDE; N PENTENYL 4 O (BETA DEXTRO GLUCOPYRANOSY) 1 THIO BETA DEXTRO GLUCOPYRANOSIDE; OLIGOSACCHARIDE; PYRANOSIDE DERIVATIVE; THIOACETATE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBOHYDRATE ANALYSIS; CARBOHYDRATE METABOLISM; CARBOHYDRATE SYNTHESIS; CHEMICAL LABELING; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONTROLLED STUDY; ENZYME ANALYSIS; ENZYME METABOLISM; ENZYME SUBSTRATE; EXCITATION; FLUORESCENCE RESONANCE ENERGY TRANSFER; HUMAN; SALIVA;

ALPHA-AMYLASES; FLUORESCENCE RESONANCE ENERGY TRANSFER; FLUORESCENT DYES; HUMANS; HYDROLYSIS; OLIGOSACCHARIDES; SALIVA; SUBSTRATE SPECIFICITY;

TETRA;

EID: 84855192722     PISSN: 09680896     EISSN: 14643391     Source Type: Journal    
DOI: 10.1016/j.bmc.2011.10.065     Document Type: Article

References (15)

1. P. Wu, and L. Bland Anal. Biochem. 218 1994 1
2. S. Cottaz, B. Brasme, and H. Driguez Eur. J. Biochem. 2000 5593
3. K. Matsuoka, S. Nishimura, and Y.C. Lee Tetrahedron: Asymmetry 5 1994 2335
4. K.B. Lee, K. Matsuoka, S. Nishimura, and Y.C. Lee Anal. Biochem. 230 1995 31
5. K. Matsuoka, S. Nishimura, and Y.C. Lee Carbohydr. Res. 276 1995 31
6. V. Ferro, M. Medldal, and K. Bock J. Chem. Soc., Perkin Trans. 1 1994 2169
7. N. Payre, S. Cottaz, and H. Drigues Angew. Chem., Int. Ed. Engl. 34 1995 1239
8. S.-I. Nishimura, N. Kimura, K. Matsuoka, and Y.C. Lee Carbohydr. Lett. 4 2001 77
9. T. Murayama, T. Tanabe, H. Ikeda, and A. Ueno Bioorg. Med. Chem. 14 2006 3691
10. M. Shigemura, T. Moriyama, T. Endo, H. Shibuya, H. Suzuki, M. Nishimura, H. Chiba, and K. Matsuno Clin. Chem. Lab. Med. 42 2004 677
11. M.A. Abou-Seif, and A.A. Youssefb Clin. Chem. Acta 346 2004 161
12. H. Oka, T. Koyama, K. Hatano, D. Terunuma, and K. Matsuoka Bioorg. Med. Chem. Lett. 20 2010 1969
13. N. Sakairi, L.X. Wang, and H. Kuzuhara J. Chem. Soc., Chem. Commun. 1991 289
14. K.G. Rice Anal. Biochem. 297 2001 117
15. T. Suganuma, R. Matsuno, M. Ohnishi, and K. Kiromi J. Biochem. 84 1978 293