Regeneration System and Influencing Factors of Maize in Ningxia
Lei Shi
Abstract
Lei Shi
Abstract
Using immature embryo of four maize varieties in Ningxia as explants and utilizing the plant tissue culture method,the effect of medium type,genotype,exogenous hormone and cephamycin(Cef) on in vitro culture and regeneration was studied.The results showed that different medium type and genotype showed different ability of embryogenic callus inducing.Ⅰand Ⅱ had more high rate of induction,Ningyu 12 and Ning 0816 had high rate as 85.3% and 82.1% respectively;6-BA were the most important factor for the induction of differentiation of embryogenic callus,6-BA could promote the differentiation of embryogenic callus.Respectively,when 500 mg/L of Cef was added,the differentiation of callus was significant inhibited.The best inducing medium was N6 +Casein hydrolysate 200 mg/L+Pro 690 mg/L+2,4-D 2.0 mg/L + Sugar 30 g/L+Inositol 100 mg/L+AgNO310 mg/L,The best differentiation medium was: N6+6-BA1.0 mg/L+Sugar 50 g/L.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Using immature embryo of four maize varieties in Ningxia as explants and utilizing the plant tissue culture method,the effect of medium type,genotype,exogenous hormone and cephamycin(Cef) on in vitro culture and regeneration was studied.The results showed that different medium type and genotype showed different ability of embryogenic callus inducing.Ⅰand Ⅱ had more high rate of induction,Ningyu 12 and Ning 0816 had high rate as 85.3% and 82.1% respectively;6-BA were the most important factor for the induction of differentiation of embryogenic callus,6-BA could promote the differentiation of embryogenic callus.Respectively,when 500 mg/L of Cef was added,the differentiation of callus was significant inhibited.The best inducing medium was N6 +Casein hydrolysate 200 mg/L+Pro 690 mg/L+2,4-D 2.0 mg/L + Sugar 30 g/L+Inositol 100 mg/L+AgNO310 mg/L,The best differentiation medium was: N6+6-BA1.0 mg/L+Sugar 50 g/L.
Key concepts: Callus, Explant culture, Sucrose, Tissue culture, Regeneration (biology), Sugar, Botany, Biology