Please use this identifier to cite or link to this item: https://doi.org/10.1073/pnas.2017890118
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dc.titleRetrograde sulfur flow from glucosinolates to cysteine in Arabidopsis thaliana
dc.contributor.authorSugiyama, Ryosuke
dc.contributor.authorLi, Rui
dc.contributor.authorKuwahara, Ayuko
dc.contributor.authorNakabayashi, Ryo
dc.contributor.authorSotta, Naoyuki
dc.contributor.authorMori, Tetsuya
dc.contributor.authorIto, Takehiro
dc.contributor.authorOhkama-Ohtsu, Naoko
dc.contributor.authorFujiwara, Toru
dc.contributor.authorSaito, Kazuki
dc.contributor.authorNakano, Ryohei Thomas
dc.contributor.authorBednarek, Pawel
dc.contributor.authorHirai, Masami Yokota
dc.date.accessioned2022-10-26T09:20:20Z
dc.date.available2022-10-26T09:20:20Z
dc.date.issued2021-05-25
dc.identifier.citationSugiyama, 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
dc.identifier.issn0027-8424
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/233851
dc.description.abstractSpecialized (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.
dc.publisherNational Academy of Sciences
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.subjectGlucosinolate
dc.subjectSpecialized metabolism
dc.subjectStress response
dc.subjectSulfur
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.doi10.1073/pnas.2017890118
dc.description.sourcetitleProceedings of the National Academy of Sciences of the United States of America
dc.description.volume118
dc.description.issue22
dc.description.pagee2017890118
dc.published.statePublished
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