Please use this identifier to cite or link to this item: https://doi.org/10.1073/pnas.2017890118
Title: Retrograde sulfur flow from glucosinolates to cysteine in Arabidopsis thaliana
Authors: Sugiyama, Ryosuke 
Li, Rui
Kuwahara, Ayuko
Nakabayashi, Ryo
Sotta, Naoyuki
Mori, Tetsuya
Ito, Takehiro
Ohkama-Ohtsu, Naoko
Fujiwara, Toru
Saito, Kazuki
Nakano, Ryohei Thomas
Bednarek, Pawel
Hirai, Masami Yokota
Keywords: Glucosinolate
Specialized metabolism
Stress response
Sulfur
Issue Date: 25-May-2021
Publisher: National Academy of Sciences
Citation: Sugiyama, Ryosuke, Li, Rui, Kuwahara, Ayuko, Nakabayashi, Ryo, Sotta, Naoyuki, Mori, Tetsuya, Ito, Takehiro, Ohkama-Ohtsu, Naoko, Fujiwara, Toru, Saito, Kazuki, Nakano, Ryohei Thomas, Bednarek, Pawel, Hirai, Masami Yokota (2021-05-25). Retrograde sulfur flow from glucosinolates to cysteine in Arabidopsis thaliana. Proceedings of the National Academy of Sciences of the United States of America 118 (22) : e2017890118. ScholarBank@NUS Repository. https://doi.org/10.1073/pnas.2017890118
Rights: Attribution 4.0 International
Abstract: Specialized (secondary) metabolic pathways in plants have long been considered one-way routes of leading primary metabolite precursors to bioactive end products. Conversely, endogenous degradation of such “end” products in plant tissues has been observed following environmental stimuli, including nutrition stress. Therefore, it is of general interest whether specialized metabolites can be reintegrated into primary metabolism to recover the invested resources, especially in the case of nitrogen- or sulfur-rich compounds. Here, we demonstrate that endogenous glucosinolates (GLs), a class of sulfur-rich plant metabolites, are exploited as a sulfur source by the reallocation of sulfur atoms to primary metabolites such as cysteine in Arabidopsis thaliana. Tracer experiments using 34S- or deuterium-labeled GLs depicted the catabolic processing of GL breakdown products in which sulfur is mobilized from the thioglucoside group in GL molecules, potentially accompanied by the release of the sulfate group. Moreover, we reveal that beta-glucosidases BGLU28 and BGLU30 are the major myrosinases that initiate sulfur reallocation by hydrolyzing particular GL species, conferring sulfur deficiency tolerance in A. thaliana, especially during early development. The results delineate the physiological function of GL as a sulfur reservoir, in addition to their well-known functions as defense chemicals. Overall, our findings demonstrate the bidirectional interaction between primary and specialized metabolism, which enhances our understanding of the underlying metabolic mechanisms via which plants adapt to their environments. © 2021 National Academy of Sciences. All rights reserved.
Source Title: Proceedings of the National Academy of Sciences of the United States of America
URI: https://scholarbank.nus.edu.sg/handle/10635/233851
ISSN: 0027-8424
DOI: 10.1073/pnas.2017890118
Rights: Attribution 4.0 International
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