Establishment of Highly Efficient Plant Regeneration, Callus Transformation and Analysis of Botrytis cinerea-Responsive PR Promoters in Lilium brownii var. viridulum

作者：Fu, Yongyao; Shu, Liling; Li, Hanyi; Zhang, Xingming; Liu, Xuan; Ou, Zhengying; Liang, Xiaomeng; Qi, Xiangying^*; Yang, Liping^*

来源：Plants-Basel, 2023, 12(10): 1992.

DOI：10.3390/plants12101992

• Lilium brownii var
• viridulum
• plant regeneration
• callus
• genetic transformation
• Botrytis cinerea

Lilium brownii var. viridulum, commonly called Longya lily, is a well-known flower and vegetable plant in China that has poor tolerance to Botrytis fungal disease. The molecularimprovement has mainly been restricted to an efficient regeneration and transformation system. In this study, the highly efficient regeneration of Longya lily was established through the optimization of embryogenic callus, adventitious shoot and rooting induction. The major factors influencing transformation (antibiotics, Agrobacterium concentration, infection time, suspension solution and coculture medium) were examined. The expression responses of PR promoters (ZmPR4 and BjCHI1) to B. cinerea were assessed in transgenic calli. The results showed that Murashige and Skoog (MS) medium with 1.0 mg center dot L-1 picloram (PIC) and 0.2 mg center dot L-1 1-naphthaleneacetic acid (NAA) under light conditions and MS with 0.5 mg center dot L-1 6-benzylaminopurine (6-BA) and 1.0 mg center dot L-1 NAA under darkness were optimal for embryogenic callus induction (64.67% rate) and proliferation (3.96 coefficient). Callus inoculation into MS containing 2.0 mg center dot L-1 thidiazuron (TDZ), 0.4 mg center dot L-1 NAA, 1.0 mg center dot L-1 TDZ and 0.5 mg center dot L-1 NAA led to shooting induction (92.22 of rate) and proliferation (3.28 of coefficient) promotion, respectively. The rooting rate reached 99.00% on MS with 0.3 mg center dot L-1 NAA. Moreover, a transformation rate of 65.56% was achieved by soaking the callus in Agrobacterium at an OD600 of 0.4 for 10 min in modified MS without NH4NO3 as the suspension solution and coculture medium before selecting 75 mg center dot L-1 hygromycin and 300 mg center dot L-1 cefotaxime. Only the BjCHI1 promoter was obviously expressed in transgenic calli. These results could facilitate the generation of Longya lily transgenic plants with improved B. cinerea resistance.