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1. (Article ID: 6563)
Nakao Y, Kozutsumi Y, Funakoshi I, Kawasaki T, Yamashina I, Mutsaers JH, van Halbeek H, Vliegenthart JFG
Structures of oligosaccharides on b-galactosidase from Aspergillus oryzae
Journal of Biochemistry 102 (1987)
171-179
The carbohydrate portions of β-galactosidase from Aspergillus oryzae were found to be composed of two types of sugar chains. They were released equally well with endo-β-N-acetylglucosaminidase H, but were distinct in their chain length. The long sugar chains (fraction I), corresponding to 4% of the total carbohydrate chains, were composed of galactomannan-type oligosaccharides, which consisted of mannose, galactose, glucose, and glucosamine in the molar ratios of 30.0, 16.4, 1.4, and 2.1 per mol of aspartic acid, respectively. The short sugar chains (fraction II), corresponding to 96% of the total carbohydrate chains, consisted of mannose, galactose, glucose, and glucosamine in the molar ratios of 9.4, 0.6, 0.3, and 1.7 per mol of aspartic acid, respectively. Both types of sugar chains were fractionated into neutral and acidic subfractions. The neutral subfraction of fraction I (I-N), corresponding to 1% of the total carbohydrate chains, was very heterogeneous in length and was resistant to digestion with α-mannosidase and β-galactosidase. The neutral subfraction of fraction II (II-N), corresponding to 91% of the total carbohydrate, was composed of a mixture of oligosaccharides with oligomanneoside chains (Mann GlcNAcol). The major components were similar to high mannose-type oligosaccharides of mammalian origin in their composition and size (n = 5-9). However, digestion of II-N with α-1,2-mannosidase produced considerable amounts of Man6GlcNAcol, an unusual product in the case of high mannose-type oligosaccharides of mammalian origin, in addition to the common one, Man5GlcNAcol.
NCBI PubMed ID: 3117779Journal NLM ID: 0376600Publisher: Japanese Biochemical Society
Institutions: Department of Biological Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University
Methods: 1H NMR, gel filtration, paper chromatography, enzymatic digestion, method of Hewitt, resorcinol method of Jourdian
The publication contains the following compound(s):
- Compound ID: 16862
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a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-3)-+
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a-D-Manp-(1-2)-a-D-Manp-(1-6)-+ |
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a-D-Manp-(1-2)-a-D-Manp-(1-3)-a-D-Manp-(1-6)-b-D-Manp-(1-4)-D-GlcNAc-ol |
Show graphically |
Structure type: oligomer
Compound class: N-glycan
Reference(s) to other database(s): GTC:G29042WW, CCSD:
16060, CBank-STR:19045
- Compound ID: 16863
|
a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Manp-(1-3)-+
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a-D-Manp-(1-3)-+ |
| |
a-D-Manp-(1-2)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-b-D-Manp-(1-4)-D-GlcNAc-ol |
Show graphically |
Structure type: oligomer
Compound class: N-glycan
Reference(s) to other database(s): GTC:G23232XI, CCSD:
16061, CBank-STR:18325
- Compound ID: 16864
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a-D-Manp-(1-3)-+
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a-D-Manp-(1-6)-+ |
| |
a-D-Manp-(1-3)-a-D-Manp-(1-6)-b-D-Manp-(1-4)-D-GlcNAc-ol |
Show graphically |
Structure type: oligomer
Compound class: N-glycan
Reference(s) to other database(s): GTC:G84020NP, CCSD:
2738, CBank-STR:14218
- Compound ID: 16865
|
a-D-Manp-(1-3)-+
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a-D-Manp-(1-3)-+ |
| |
a-D-Manp-(1-6)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-b-D-Manp-(1-4)-D-GlcNAc-ol |
Show graphically |
Structure type: oligomer
Compound class: N-glycan
Reference(s) to other database(s): GTC:G66679EK, CCSD:
2769, CBank-STR:15772
- Compound ID: 16866
|
a-D-Manp-(1-2)-a-D-Manp-(1-3)-+
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a-D-Manp-(1-6)-+ |
| |
a-D-Manp-(1-3)-a-D-Manp-(1-6)-b-D-Manp-(1-4)-D-GlcNAc-ol |
Show graphically |
Structure type: oligomer
Compound class: N-glycan
Reference(s) to other database(s): GTC:G86459PH, CCSD:
2776, CBank-STR:16047
- Compound ID: 16867
|
a-D-Manp-(1-2)-a-D-Manp-(1-3)-+
|
a-D-Manp-(1-3)-+ |
| |
a-D-Manp-(1-6)-a-D-Manp-(1-6)-a-D-Manp-(1-6)-b-D-Manp-(1-4)-D-GlcNAc-ol |
Show graphically |
Structure type: oligomer
Compound class: N-glycan
Reference(s) to other database(s): GTC:G27870HB, CCSD:
2820, CBank-STR:17153
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