2007Journal of Northwest A&F UniversityRequires access

Optimizing for callus tissue culture system for the stem of Solanum tuberosum

Yingmei Li

Open publisher page 0 citations

Abstract

Four potato cultivars,Kexin No.12,Kexin No.13,Dongnong303 and Zaodabai were cultivated in vitro from stem explants.The results showed that the optimal medium of callus for Kexin No.12 and Kexin No.13 was MS+30 g/L sucrose+8g/L agar +2 mg/L6-BA+1 mg/L 2,4-D;Dongnong 303 was MS+2 mg/L 6-BA +0.5 mg/L 2,4-D;the optimal medium of Zaodabai was MS+30 g/L sucrose+8 g/L agar+2 mg/L 6-BA+0.5 mg/L 2,4-D;the adventitious callus induction rate were 100%,100%,100% and 90%,respectively by using these optimal induced medium.The best medium for adventitious bud differentiation from stem callus was MS+30 g/L sucrose+8 g/L agar+4.0 mg/L 6-BA+0.1 mg/L NAA+1.0 mg/L GA3 for Kexin13;MS+30 g/L sucrose+8 g/L agar+2.0 mg/L 6-BA+0.5 mg/L NAA+1.0 mg/L GA3 for Kexin12;MS+30 g/L sucrose+8 g/L agar+2.0 mg/L 6-BA+0.1 mg/L NAA+1.5 mg/L GA3 for Dongnong 303;MS+30 g/L sucrose+8 g/L agar+2.0 mg/L 6-BA+0.5 mg/L NAA+1.0 mg/L GA3 for Zaodabai.Under these optimal induced medium,the rates of adventitious bud differentiation were 80%,90%,100%,and 76.7%,respectively.

About this research paper

What this paper is about

Four potato cultivars,Kexin No.12,Kexin No.13,Dongnong303 and Zaodabai were cultivated in vitro from stem explants.The results showed that the optimal medium of callus for Kexin No.12 and Kexin No.13 was MS+30 g/L sucrose+8g/L agar +2 mg/L6-BA+1 mg/L 2,4-D;Dongnong 303 was MS+2 mg/L 6-BA +0.5 mg/L 2,4-D;the optimal medium of Zaodabai was MS+30 g/L sucrose+8 g/L agar+2 mg/L 6-BA+0.5 mg/L 2,4-D;the adventitious callus induction rate were 100%,100%,100% and 90%,respectively by using these optimal induced medium.The best medium for adventitious bud differentiation from stem callus was MS+30 g/L sucrose+8 g/L agar+4.0 mg/L 6-BA+0.1 mg/L NAA+1.0 mg/L GA3 for Kexin13;MS+30 g/L sucrose+8 g/L agar+2.0 mg/L 6-BA+0.5 mg/L NAA+1.0 mg/L GA3 for Kexin12;MS+30 g/L sucrose+8 g/L agar+2.0 mg/L 6-BA+0.1 mg/L NAA+1.5 mg/L GA3 for Dongnong 303;MS+30 g/L sucrose+8 g/L agar+2.0 mg/L 6-BA+0.5 mg/L NAA+1.0 mg/L GA3 for Zaodabai.Under these optimal induced medium,the rates of adventitious bud differentiation were 80%,90%,100%,and 76.7%,respectively.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Four potato cultivars,Kexin No.12,Kexin No.13,Dongnong303 and Zaodabai were cultivated in vitro from stem explants.The results showed that the optimal medium of callus for Kexin No.12 and Kexin No.13 was MS+30 g/L sucrose+8g/L agar +2 mg/L6-BA+1 mg/L 2,4-D;Dongnong 303 was MS+2 mg/L 6-BA +0.5 mg/L 2,4-D;the optimal medium of Zaodabai was MS+30 g/L sucrose+8 g/L agar+2 mg/L 6-BA+0.5 mg/L 2,4-D;the adventitious callus induction rate were 100%,100%,100% and 90%,respectively by using these optimal induced medium.The best medium for adventitious bud differentiation from stem callus was MS+30 g/L sucrose+8 g/L agar+4.0 mg/L 6-BA+0.1 mg/L NAA+1.0 mg/L GA3 for Kexin13;MS+30 g/L sucrose+8 g/L agar+2.0 mg/L 6-BA+0.5 mg/L NAA+1.0 mg/L GA3 for Kexin12;MS+30 g/L sucrose+8 g/L agar+2.0 mg/L 6-BA+0.1 mg/L NAA+1.5 mg/L GA3 for Dongnong 303;MS+30 g/L sucrose+8 g/L agar+2.0 mg/L 6-BA+0.5 mg/L NAA+1.0 mg/L GA3 for Zaodabai.Under these optimal induced medium,the rates of adventitious bud differentiation were 80%,90%,100%,and 76.7%,respectively.

Key concepts: Sucrose, Agar, Callus, Explant culture, Solanum tuberosum, Botany, Food science, Biology

Related papers

Back to paper searchBrowse research topicsOriginal source
Optimizing for callus tissue culture system for the stem of Solanum tuberosum — Research Paper | ScholarLens