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. 2022 Oct 28;4(2):100468. doi: 10.1016/j.xplc.2022.100468

Figure 3.

Figure 3

AtABCG14 displayed different efflux transport activities toward multiple CK species in YPH499 yeast cells.

(A) Immunoblotting of the heterologous expression of GFP-AtABCG14 in YPH499 yeast cells harboring GFP-AtABCG14 using GFP antibody. YPH499 yeast cells transformed with an empty vector were used as a control.

(B and C) Quantification of the isotope-labeled CKs 2H5-tZ, 2H5-tZR, 2H6-iP, 2H6-iPR, 15N4-cZ, or 2H3-DHZ in YPH499 yeast cells harboring GFP-AtABCG14 or an empty vector after feeding with the respective isotope-labeled CKs (B) or the respective isotope-labeled CKs and vanadate (C) for 20 min. Data are means ± SD (n = 4).

(D) Exported 2H5-tZ content from YPH499 yeast cells harboring GFP-AtABCG14 or an empty vector after feeding with 2H5-tZ.

Data are means ± SE (n = 4). ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001, Student’s t-test.