Skip to main content

Table 2 Effect of different media types and combinations and concentrations of PGRs on direct regeneration from anther culture in Bomby

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

% Acclimatization

M1

MS + 4 mg/L NAA + 1 mg/L BAP

1.46 ± 0.02a

14.34 ± 0.24e2

2.35 ± 0.003a

1.87 ± 0.003a

M2

MS + 4 mg/L NAA + 0.1 mg/L BAP

0.83 ± 0.02b

14.37 ± 0.28e2

1.87 ± 0.018b

1.22 ± 0.003b

M3

MS + 4 mg/L NAA + 0.5 mg/L BAP

0.64 ± 0.02c

17.94 ± 0.11c2

1.58 ± 0.006c

1.22 ± 0.003b

M4

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

0.58 ± 0.02 cd

23.55 ± 0.16a2

1.22 ± 0.009d

0.71 ± 0.00c

M5

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

0.41 ± 0.02ef

22.64 ± 0.48b2

0.71 ± 0.00e

0.71 ± 0.00c

M6

B5 + 4 mg/L NAA + 1 mg/L BAP

0.73 ± 0.02bc

15.85 ± 0.07d2

1.22 ± 0.007d

0.71 ± 0.00c

M7

B5 + 4 mg/L NAA + 0.1 mg/L BAP

0.70 ± 0.02bc

14.23 ± 0.17e2

1.87 ± 0.015b

1.22 ± 0.009b

M8

B5 + 4 mg/L NAA + 0.5 mg/L BAP

0.60 ± 0.02 cd

13.00 ± 0.14f2

0.71 ± 0.00e

0.71 ± 0.00c

M9

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

0.49 ± 0.02de

16.55 ± 0.29d2

0.71 ± 0.00e

0.71 ± 0.00c

M10

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

0.41 ± 0.02ef

14.24 ± 0.33e2

0.71 ± 0.00e

0.71 ± 0.00c

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

0.31 ± 0.02 fg

11.29 ± 0.26g2

0.71 ± 0.00e

0.71 ± 0.00c

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

0.26 ± 0.02 g

10.67 ± 0.25g2

0.71 ± 0.00e

0.71 ± 0.00c

 

CV

3.56

2.82

1.11

0.56

  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 differ significantly (α ≤ 0.05)