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Table 3 13C-NMR chemical shifts of hydrolysis products of G-Rc by BG-1

From: Purification and characterization of a novel ginsenoside Rc-hydrolyzing β-glucosidase from Armillaria mellea mycelia

Carbon no

G-Rd

C-Mc1

G-F2

C-Mc

C-K

Aglycone moiety

 1

39.0

39.6

38.9

39.9

39.8

 2

26.6

27.2

26.5

26.6

26.6

 3

88.8

89.2

88.6

78.5

78.7

 4

39.5

40.1

39.5

39.8

39.9

 5

56.2

56.8

56.1

56.6

56.8

 6

18.3

18.2

18.2

18.3

19.2

 7

35.0

35.5

34.9

35.6

35.6

 8

39.9

40.4

39.8

40.0

40.0

 9

50.0

50.6

50.0

50.7

50.8

 10

36.7

37.3

36.7

37.8

37.8

 11

30.6

30.6

30.6

30.6

31.3

 12

70.1

70.6

70.1

70.6

70.6

 13

49.3

49.8

49.5

49.9

50.0

 14

51.4

52.0

51.2

51.8

52.0

 15

30.7

30.4

29.8

31.1

31.4

 16

26.5

27.0

26.4

26.2

26.3

 17

51.5

51.8

51.5

52.1

51.9

 18

16.1

16.7

16.1

16.7

16.5

 19

15.8

16.4

15.7

16.5

16.8

 20

83.2

82.8

83.1

83.8

83.8

 21

22.3

22.3

22.3

22.8

22.8

 22

35.9

36.5

35.8

36.6

36.7

 23

23.1

23.6

23.1

23.6

23.7

 24

125.8

126.4

125.7

125.3

126.5

 25

130.8

131.3

130.8

131.4

131.4

 26

25.7

26.2

25.6

26.2

26.2

 27

17.6

17.2

17.6

17.8

17.9

 28

27.9

28.5

27.9

27.2

28.8

 29

16.5

16.7

16.6

16.8

16.7

 30

17.2

17.8

17.1

17.8

17.6

3-Glucopyranosyl (inner)

 1′

105.0

105.4

106.7

  

 2′

83.2

76.2

75.6

  

 3′

78.1

79.3

77.8

  

 4′

71.5

72.3

71.7

  

 5′

78.1

79.1

78.2

  

 6′

62.6

63.0

62.8

  

3-Glucopyranosyl (outer)

 1″

105.9

    

 2″

77.0

    

 3″

79.1

    

 4″

71.5

    

 5″

78.1

    

 6″

62.7

    

20-Glucopyranosyl

 1′

98.1

98.5

98.1

98.5

98.7

 2′

75.0

75.2

75.0

75.4

75.6

 3′

77.8

78.6

79.0

79.7

77.8

 4′

71.4

72.1

71.3

72.6

72.1

 5′

78.0

76.9

78.5

77.0

78.5

 6′

62.5

68.8

62.5

68.9

63.4

20-Arabinofuranosyl

 1″

 

110.5

 

110.5

 

 2″

 

83.7

 

83.7

 

 3″

 

78.7

 

78.6

 

 4″

 

86.5

 

86.5

 

 5″

 

63.0

 

83.1