Fertile Plant Regeneration from Protoplasts of the Korean Lettuce Cultivar “Cheongchima” (Lactuca sativa L.)

Protoplasts were isolated from the primary leaves of lettuce (Lactuca sativa L.) seedlings 10 days after in vitro germination. The leaves were stripped and incubated in an enzyme mixture consisting of 1.2% Cellulase R-10 and 0.3% Macerozyme R-10 in cell and protoplast washing solution (CPW) overnigh...

Full description

Saved in:
Bibliographic Details
Published inJournal of Agriculture & Life Science Vol. 56; no. 5; pp. 45 - 50
Main Authors Son, Bo-Hwa, Park, Chul-Gyoo, Khakurel, Dhruba, Hwang, Hae-Jun, Kim, Tea-Won, Jeon, Byeong-Gyun, Lee, Sung-Ho
Format Journal Article
LanguageEnglish
Published 경상국립대학교 농업생명과학연구원 31.10.2022
Subjects
Online AccessGet full text
ISSN1598-5504
2383-8272
DOI10.14397/jals.2022.56.5.45

Cover

More Information
Summary:Protoplasts were isolated from the primary leaves of lettuce (Lactuca sativa L.) seedlings 10 days after in vitro germination. The leaves were stripped and incubated in an enzyme mixture consisting of 1.2% Cellulase R-10 and 0.3% Macerozyme R-10 in cell and protoplast washing solution (CPW) overnight. The average protoplast yield was 8.25 x 106 protoplasts per g of fresh leaf tissue. When protoplasts were cultured at a density of 3.0 × 105 protoplasts/mL in agarose solid KM8P/KM8 medium, first and second divisions were observed in the protoplasts within a week. Protoplast-derived microcolonies formed after 4 weeks of culture, and visible colonies were present after 3 months of culture. Protoplast-derived microcalli were transferred to Murashige and Skoog medium supplemented with 2.0 mg/L kinetin and 0.1 mg/L NAA and incubated in the light for 3 weeks. They grew into callus, which then regenerated into plants after 7 weeks of culture. The regenerated plants grew as apparently normal flowering fertile plants.
ISSN:1598-5504
2383-8272
DOI:10.14397/jals.2022.56.5.45