An effective method for Agrobacterium tumefaciens-mediated transformation of Jatropha curcas L. using cotyledon explants. Issue 1 (1st January 2020)

• Record Type: Journal Article
• Authors: Liu, Ying; Yang, Xiaoyan; Zhao, Yahuan; Yang, Yuesheng; Liu, Zhenlan
• Is Part Of: Bioengineered. Volume 11:Issue 1(2020)
• Page Start: 1146
• Page End: 1158
• Publication Date: 2020-01-01
• Subjects: Cotyledon explants -- Jatropha curcas L. -- bud regeneration -- Thidiazuron -- transformation; Biomedical engineering -- Periodicals; Biotechnology -- Periodicals; Microbiology -- Periodicals; 660.6
• DOI: 10.1080/21655979.2020.1831363
• Languages: English
• ISSNs: 2165-5987

Abstract

ABSTRACT: Jatropha curcas is one of oilseed crops and has been considered as an energy crop. In the present study, efficient plant regeneration protocol and transformation method were developed for J. curcas . Because the regeneration efficiency of adventitious bud from cotyledon explants of J. curcas induced by traditional methods is low, and it takes a long time to get complete plants. It is necessary to establish a new regeneration system to improve regeneration efficiency. Cotyledon explants were dipped into TDZ solution at different concentrations respectively for various times to obtain higher efficiency of adventitious bud regeneration. This new regeneration method was then applied to genetic transformation of J. curcas . Cotyledon explants were precultured for 1 day after treated with high concentration of Thidiazuron (TDZ) solution (20 mg/L for 40 min), followed by Agrobacterium tumefaciens infection. After co-cultured for 2 days, the explants were placed on the induction hormone-free media for bud regeneration and resistant screening. After 30 days, selected shoot buds were transferred onto elongation medium for 15 days. Young leaf sections of the regenerated shoots were used for PCR (Polymerase chain reaction) detection of the transgenic shoots. The PCR positive shoots were isolated and used for in vitro grafting. The intact plants were obtained within 20 days. GUS (β-Glucosidase) staining and Southern analysis confirmed the transformation events. Briefly, a transformation efficiency of 34.32% was achieved and an intact transgenic plant could be obtained within 65 days. GRAPHICAL ABSTRACT: