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Table 1 Effect of different media types and combinations and concentrations of PGRs on direct regeneration from anther culture in Orobelle

From: Anther-derived microspore embryogenesis in pepper hybrids orobelle and Bomby

Media code

Treatments

% Embryo formation (Mean ± S.E.)

% callus formation

(Mean ± S.E.)

% Plant regenerated from embryo formed (Mean ± S.E.)

% Acclimatization (Mean ± S.E.)

M1

MS + 4 mg/L NAA + 1 mg/L BAP

1.85 ± 0.02a

13.80 ± 0.16e2

2.92 ± 0.03a

2.55 ± 0.06a

M2

MS + 4 mg/L NAA + 0.1 mg/L BAP

0.94 ± 0.02b

15.40 ± 0.15d2

2.12 ± 0.003b

1.58 ± 0.01b

M3

MS + 4 mg/L NAA + 0.5 mg/L BAP

0.84 ± 0.02b

17.84 ± 0.33c2

1.87 ± 0.02c

1.22 ± 0.003c

M4

MS + 5 mg/L NAA + 0.1 mg/L BAP + 0.05 mg/L biotin

0.59 ± 0.02cd

22.74 ± 0.58a2

0.71 ± 0.00f

0.71 ± 0.00d

M5

MS + 5 mg/L NAA + 1 mg/L BAP + 0.05 mg/L folic acid

0.49 ± 0.02cd

21.34 ± 0.16b2

0.71 ± 0.00f

0.71 ± 0.00d

M6

B5 + 4 mg/L NAA + 1 mg/L BAP

0.84 ± 0.02b

14.90 ± 0.01d2

1.58 ± 0.006d

1.22 ± 0.003c

M7

B5 + 4 mg/L NAA + 0.1 mg/L BAP

0.78 ± 0.02b

13.98 ± 0.04e2

1.58 ± 0.006d

1.22 ± 0.003c

M8

B5 + 4 mg/L NAA + 0.5 mg/L BAP

0.62 ± 0.02c

12.56 ± 0.22f2

1.22 ± 0.007e

0.71 ± 0.00d

M9

B5 + 4 mg/L NAA + 0.1 mg/L BAP + 1 g/L glutamine

0.51 ± 0.02 cd

15.36 ± 0.26d2

0.71 ± 0.00f

0.71 ± 0.00d

M10

B5 + 4 mg/L NAA + 1 mg/L BAP + 1 g/L glutamine

0.46 ± 0.02de

14.97 ± 0.03d2

1.23 ± 0.00e

0.71 ± 0.00d

M11

Double layer media—MS + 2%sucrose, 0.5% activated charcoal, gelrite- 2.6 g/L, Liquid upper layer contained half strength MS + 2% sucrose

0.37 ± 0.02ef

10.56 ± 0.03g2

0.71 ± 0.00f

0.71 ± 0.00d

M12

Double layer media—Nistch medium, Maltose- 2%, Activated Charcoal – 0.5%, gelrite- 2.6 g/L, Liquid top layer consists of Nistch medium and 2% maltose

0.32 ± 0.02f

9.50 ± 0.03h2

0.71 ± 0.00f

0.71 ± 0.00d

 

CV

3.24

1.18

1.41

0.68

  1. Media 1 to 10 – contain 0.25% activated charcoal, 15 mg/L AgNO3, 30 g/L sucrose and gelrite- 2.6 g/L in addition to the PGRs mentioned in the table
  2. % Plant regeneration and % plant acclimatization is calculated based on the total number of embryo formed from each respective treatments
  3. The mean data mentioned in the table are square root (% embryo formation, % callus formation % plant regenerated from embryo formed and % acclimatization) transformed values respectively
  4. Values are mean ± standard error and treatment values followed by different letters are significant (α ≤ 0.05)