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Table 1 Influence of BA and Kin on induction of multiple shoots in seedling-derived shoot tip explants of G. tenuifolia

From: In vitro propagation and analysis of secondary metabolites in Glossogyne tenuifolia (Hsiang-Ju) - a medicinal plant native to Taiwan

Cytokinin*

NAA

No. of explants cultured

Shoot length (mm)**

Explants induced multiple Shoots (%)**

Average No. of shoots / explant**

Explants induced callus (%)**

Fresh weight/shoot (mg)**

(mg/L)

(mg/L)

0

0

30

26.7 ± 2.1 cd

53.3 ± 9.1 bc

1.8 ± 0.3 c

0.0 ± 0.0 d

128.0 ± 16.7 d

0

0.1

30

40.8 ± 2.2 a

50.0 ± 9.1 bc

1.8 ± 0.2 c

56.7 ± 9.0 b

379.5 ± 33.4 c

BA 0.1

0.1

30

24.4 ± 1.3 d

93.3 ± 4.6 a

4.1 ± 0.4 b

33.3 ± 8.6 c

364.1 ± 43.6 c

BA 0.5

0.1

30

24.2 ± 1.4 d

100.0 ± 0.0 a

7.3 ± 0.6 a

13.3 ± 6.2 d

666.2 ± 68.4 b

BA 1.0

0.1

30

26.2 ± 1.7cd

100.0 ± 0.0 a

7.4 ± 0.6 a

95.0 ± 4.9 a

894.9 ± 78.4 a

Kin 0.1

0.1

30

40.1 ± 3.5 a

43.3 ± 9.0 c

1.8 ± 0.2 c

50.0 ± 9.1 bc

319.8 ± 44.2 c

Kin 0.5

0.1

30

32.8 ± 2.4 bc

70.0 ± 8.4 b

2.5 ± 0.3 c

80.0 ± 7.3 a

306.7 ± 32.6 c

Kin 1.0

0.1

30

34.6 ± 2.1 ab

56.7 ± 9.0 bc

2.3 ± 0.3 c

100.0 ± 0.0 a

253.0 ± 26.0cd

  1. *Basal medium: ½X MS basal medium supplemented with 3% sucrose and 0.9% Difco Bacto-agar. Observations were recorded after 35 days of culture.
  2. **Means followed by the same letter are not significantly different at 5% level by LSD (least significant difference) test.