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MOESM3 of Effective Agrobacterium-mediated transformation protocols for callus and roots of halophyte ice plant (Mesembryanthemum crystallinum)

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posted on 2019-01-07, 05:00 authored by Hau-Hsuan Hwang, Chih-Hao Wang, Hsiao-Huei Chen, Jia-Fang Ho, Shin-Fei Chi, Fan-Chen Huang, Hungchen Yen
Additional file 3: Figure S1. The establishment of transgenic ice plant callus expressing the yellow fluorescent protein (YFP). (A) Representative untransformed ice plant callus grown on CIM with (1) 0 mg L−1 and (2) 25 mg L−1 glufosinate ammonium. Bar = 1 cm. (A-3) Fresh weight of untransformed ice plant callus grown on CIM with 0, 25, 50, 75, and 100 mg L−1 glufosinate ammonium (GLA). ΔFW: increased fresh weight mass. Average values of the increased fresh weight from at least three independent experiments. *P < 0.05 comparing with and without GLA by pairwise Student t-test. (B) Fluorescent observation of YFP-transformed callus-derived cells. (B1-3) Untransformed callus-derived cells; (B4-6) YFP-transformed callus-derived cells; (B1, B4) Bright field images; (B2, B5) Confocal microscopy images with the YFP filter; (B3, B6) merged images. Bar = 20 μm. (C) Genomic DNA PCR results of YFP (upper panel) and phosphoenolpyruvate carboxylase (PPC1) (lower panel) in plant callus. 1, 2: independent transformed plant callus lines; NC: untransformed callus as a negative control; arrow: predicted length of PCR product.

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Ministry of Science and Technology, Taiwan

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