4.7 Article

Artificial Fluorescent Glucosinolates (F-GSLs) Are Transported by the Glucosinolate Transporters GTR1/2/3

Journal

Publisher

MDPI
DOI: 10.3390/ijms24020920

Keywords

glucosinolate transporters; GTR; fluorescent glucosinolates; fluorescent substrates

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Glucosinolate transporters (GTR1/2/3) from the NPF family are crucial for the transport, accumulation, and distribution of glucosinolates. By synthesizing fluorescent glucosinolates, the ability of GTR1/2/3 from Arabidopsis thaliana to import these compounds was investigated. Five out of seven fluorescent glucosinolates were successfully imported by at least one GTR. The uptake mechanism of fluorescent glucosinolates was found to be similar to that of natural glucosinolates.
The glucosinolate transporters 1/2/3 (GTR1/2/3) from the Nitrate and Peptide transporter Family (NPF) play an essential role in the transport, accumulation, and distribution of the specialized plant metabolite glucosinolates. Due to representing both antinutritional and health-promoting compounds, there is increasing interest in characterizing GTRs from various plant species. We generated seven artificial glucosinolates (either aliphatic or benzenic) bearing different fluorophores (Fluorescein, BODIPY, Rhodamine, Dansylamide, and NBD) and investigated the ability of GTR1/2/3 from Arabidopsis thaliana to import the fluorescent glucosinolates (F-GSLs) into oocytes from Xenopus laevis. Five out of the seven F-GSLs synthesized were imported by at least one of the GTRs. GTR1 and GTR2 were able to import three F-GSLs actively above external concentration, while GTR3 imported only one actively. Competition assays indicate that the F-GSLs are transported by the same mechanism as non-tagged natural glucosinolates. The GTR-mediated F-GSL uptake is detected via a rapid and sensitive assay only requiring simple fluorescence measurements on a standard plate reader. This is highly useful in investigations of glucosinolate transport function and provides a critical prerequisite for elucidating the relationship between structure and function through high-throughput screening of GTR mutant libraries. The F-GSL themselves may also be suitable for future studies on glucosinolate transport in vivo.

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