2020
DOI: 10.1038/s41438-020-0248-x
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UGT74AF3 enzymes specifically catalyze the glucosylation of 4-hydroxy-2,5-dimethylfuran-3(2H)-one, an important volatile compound in Camellia sinensis

Abstract: 4-Hydroxy-2,5-dimethylfuran-3(2H)-one (HDMF) is an important odorant in some fruits, and is proposed to play a crucial role in the caramel-like notes of some teas. However, its biosynthesis and metabolism in tea plants are still unknown. Here, HDMF glucoside was unambiguously identified as a native metabolite in tea plants. A novel glucosyltransferase UGT74AF3a and its allelic protein UGT74AF3b specifically catalyzed the glucosylation of HDMF and the commercially important structural homologues 2 (or 5)-ethyl-… Show more

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Cited by 21 publications
(14 citation statements)
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“…Real‐time PCR was performed according to published protocols (Chen et al, 2020). The gene‐specific primer sequences are provided in Table S2.…”
Section: Methodsmentioning
confidence: 99%
“…Real‐time PCR was performed according to published protocols (Chen et al, 2020). The gene‐specific primer sequences are provided in Table S2.…”
Section: Methodsmentioning
confidence: 99%
“…The tea plant is one of the most economically important crop species in China, Japan, India, and Kenya. Tea plants synthesize, accumulate, and emit many volatile compounds, which play important roles in tea quality and plant performance 13 , 14 . Cold and drought are major environmental factors that affect the natural geographic distribution of plants 15 .…”
Section: Introductionmentioning
confidence: 99%
“…Heterologous protein expression and purification were carried out following the methods of a previous study (Chen et al, 2020c) with slight modifications. The full-length sequence of CsGES was digested with Bam H1 and Sma l1, and the resulting gene fragments were cloned into the expression vector pGEX-4T-1 (Amersham Biosciences, Freiburg, Germany).…”
Section: Heterologous Protein Expression and Purificationmentioning
confidence: 99%
“…Fluorescent quantitative cDNA templates were synthesized by reverse transcription using Hifair® III First-Strand cDNA Synthesis SuperMix for qPCR (gDNA digester plus) kit. Real-time PCR was performed according to previously published protocols (Chen et al, 2020c) using the gene-specific primer sequences (Table S1). The glyceraldehyde-3-phosphate dehydrogenase (GAPDH ) gene was used as an internal reference gene, and relative expression levels were calculated using the 2 -Δ῝Τ method (Jing et al, 2020).…”
Section: Quantitative Real-time Pcr Analysismentioning
confidence: 99%