TY - JOUR
T1 - OsTH1 is a key player in thiamin biosynthesis in rice
AU - Faustino, Maria
AU - Lourenço, Tiago
AU - Strobbe, Simon
AU - Cao, Da
AU - Fonseca, André
AU - Rocha, Isabel
AU - Van Der Straeten, Dominique
AU - Oliveira, M. Margarida
N1 - Funding Information:
MMO gratefully acknowledges FCT (Funda\u00E7\u00E3o para a Ci\u00EAncia e a Tecnologia) financial support through the project Rice2B (2022.02916.PTDC, https://doi.org/10.54499/2022.02916.PTDC ) \u201CModelling vitamins B1 and B2 biosynthesis and biofortification in rice\u201D, the Plants for Life PhD fellowship of MF (PD/BD/148694/2019), the contract of TL (CEECIND/03641/2017), and the Research Unit \u201CGREEN-IT\u2014Bioresources for Sustainability\u201D (UIDB/04551/2020, https://doi.org/10.54499/UIDB/04551/2020 and UIDP/04551/2020, https://doi.org/10.54499/UIDP/04551/2020 ). DVDS gratefully acknowledges funding from the Research Foundation Flanders (FWO; G064119N), Ghent University (Bijzonder Onderzoeksfonds (BOF) GOA 01G00409 and BOF-BAS) and Horizon2020-ERA-NET (BIOFAIR project).
Publisher Copyright:
© The Author(s) 2024.
PY - 2024/6/12
Y1 - 2024/6/12
N2 - Thiamin is a vital nutrient that acts as a cofactor for several enzymes primarily localized in the mitochondria. These thiamin-dependent enzymes are involved in energy metabolism, nucleic acid biosynthesis, and antioxidant machinery. The enzyme HMP-P kinase/thiamin monophosphate synthase (TH1) holds a key position in thiamin biosynthesis, being responsible for the phosphorylation of HMP-P into HMP-PP and for the condensation of HMP-PP and HET-P to form TMP. Through mathematical kinetic model, we have identified TH1 as a critical player for thiamin biofortification in rice. We further focused on the functional characterization of OsTH1. Sequence and gene expression analysis, along with phylogenetic studies, provided insights into OsTH1 bifunctional features and evolution. The indispensable role of OsTH1 in thiamin biosynthesis was validated by heterologous expression of OsTH1 and successful complementation of yeast knock-out mutants impaired in thiamin production. We also proved that the sole OsTH1 overexpression in rice callus significantly improves B1 concentration, resulting in 50% increase in thiamin accumulation. Our study underscores the critical role of OsTH1 in thiamin biosynthesis, shedding light on its bifunctional nature and evolutionary significance. The significant enhancement of thiamin accumulation in rice callus upon OsTH1 overexpression constitutes evidence of its potential application in biofortification strategies.
AB - Thiamin is a vital nutrient that acts as a cofactor for several enzymes primarily localized in the mitochondria. These thiamin-dependent enzymes are involved in energy metabolism, nucleic acid biosynthesis, and antioxidant machinery. The enzyme HMP-P kinase/thiamin monophosphate synthase (TH1) holds a key position in thiamin biosynthesis, being responsible for the phosphorylation of HMP-P into HMP-PP and for the condensation of HMP-PP and HET-P to form TMP. Through mathematical kinetic model, we have identified TH1 as a critical player for thiamin biofortification in rice. We further focused on the functional characterization of OsTH1. Sequence and gene expression analysis, along with phylogenetic studies, provided insights into OsTH1 bifunctional features and evolution. The indispensable role of OsTH1 in thiamin biosynthesis was validated by heterologous expression of OsTH1 and successful complementation of yeast knock-out mutants impaired in thiamin production. We also proved that the sole OsTH1 overexpression in rice callus significantly improves B1 concentration, resulting in 50% increase in thiamin accumulation. Our study underscores the critical role of OsTH1 in thiamin biosynthesis, shedding light on its bifunctional nature and evolutionary significance. The significant enhancement of thiamin accumulation in rice callus upon OsTH1 overexpression constitutes evidence of its potential application in biofortification strategies.
UR - http://www.scopus.com/inward/record.url?scp=85195897223&partnerID=8YFLogxK
U2 - 10.1038/s41598-024-62326-2
DO - 10.1038/s41598-024-62326-2
M3 - Article
C2 - 38866808
AN - SCOPUS:85195897223
SN - 2045-2322
VL - 14
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 13591
ER -