Geraniol is a potent tea odorant and exists mainly as geranyl glycoside in . Understanding the mechanisms of geraniol biosynthesis at molecular levels in tea plants is of great importance for practical improvement of tea aroma. In this study, geraniol and its glycosides from tea plants were examined using liquid chromatography coupled with mass spectrometry. Two candidate geraniol synthase () genes () and two Nudix hydrolase genes ( and ) from the tea genome were functionally investigated through gene transcription manipulation and gene chemical product analyses. Our data showed that in tea leaves, levels of geranyl -primeveroside were dramatically higher than those of geranyl -glucoside, while free geraniol was undetectable in this study. A tempo-spatial variation of geranyl -primeveroside abundance in tea plants existed, with high levels in young and green tissues and low levels in mature or non-green tissues. Cytosolic CsNUDX1-cyto showed higher hydrolysis activity of geranyl-pyrophosphate to geranyl-monophosphate (GP) than did chloroplastidial CsNUDX1-chlo. A transgenic study revealed that expression of resulted in significantly more geranyl -primeveroside in transgenic compared with non-transgenic wild-type, whereas expression of had no effect. An antisense oligo-deoxynucleotide study confirmed that suppression of transcription in tea shoots led to a significant decrease in geranyl -primeveroside abundance. Additionally, transcript levels and geranyl -primeveroside abundances shared the same tempo-spatial patterns in different organs in the tea cultivar "Shucha Zao," indicating that is important for geranyl -primeveroside formation in tea plants. Results also suggested that neither of the two candidate GES genes in tea plants did not function as GES in transgenic . All our data indicated that is involved in geranyl -primeveroside production in tea plants. Our speculation about possible conversion from the chemical product of CsNUDX1-cyto to geranyl -primeveroside in plants was also discussed.
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http://dx.doi.org/10.3389/fpls.2022.833682 | DOI Listing |
J Agric Food Chem
March 2023
College of Horticulture, Northwest A&F University, Yangling, Shaanxi 712100, China.
Tea aroma components are often stored as glycosidically bound forms in the tea plant (). However, the determination of these glycosides in tea samples is far from optimal. In the present study, we developed a high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method for simultaneous quantification of eight primary aroma glycosides within 10 min.
View Article and Find Full Text PDFFront Plant Sci
May 2022
State Key Laboratory of Tea Plant Biology and Utilization, Anhui Agricultural University, Hefei, China.
Geraniol is a potent tea odorant and exists mainly as geranyl glycoside in . Understanding the mechanisms of geraniol biosynthesis at molecular levels in tea plants is of great importance for practical improvement of tea aroma. In this study, geraniol and its glycosides from tea plants were examined using liquid chromatography coupled with mass spectrometry.
View Article and Find Full Text PDFFood Chem
May 2019
Key Laboratory of Tea Biology and Resources Utilization, Ministry of Agriculture, Tea Research Institute, Chinese Academy of Agricultural Sciences, 9 Meiling South Road, Hangzhou, Zhejiang 310008, People's Republic of China. Electronic address:
The glycosides are presumed to influence the quality of green tea but the molecular mechanism behind remains unclear. To elucidate the contribution of glycosides to the flavor formation of green tea, changes of both glycosidically bound non-volatiles (GBNVs) and glycosidically bound volatiles (GBVs) during the manufacturing of green tea were investigated using a modification-specific metabolomics method. A total of 64 glycosides (47 GBNVs and 17 GBVs) were identified and their contents mainly changed during the pan firing and drying stages of green tea manufacturing.
View Article and Find Full Text PDFPlant Physiol
June 2015
Graduate School of Agriculture (S.O., K.T., Y.O., T.A., T.O.) and Research Institute of Green Science and Technology (H.D., T.O.), Shizuoka University, Shizuoka 422-8529, Japan;Research Institute, Suntory Global Innovation Center, Shimamoto, Mishima, Osaka 618-8503, Japan (E.O., H.T.);Bioorganic Research Institute, Suntory Foundation for Life Sciences, Shimamoto, Mishima, Osaka 618-8503, Japan (M.H., J.M.);Graduate School of Medicine, Yamaguchi University, Yamaguchi 753-8515, Japan (K.M.);Graduate School of Agricultural Science, Kobe University, Kobe 657-8501, Japan (M.M.); andGraduate School of Engineering, Shizuoka University, Hamamatsu 432-8561, Japan (N.W.)
Tea plants (Camellia sinensis) store volatile organic compounds (VOCs; monoterpene, aromatic, and aliphatic alcohols) in the leaves in the form of water-soluble diglycosides, primarily as β-primeverosides (6-O-β-D-xylopyranosyl-β-D-glucopyranosides). These VOCs play a critical role in plant defenses and tea aroma quality, yet little is known about their biosynthesis and physiological roles in planta. Here, we identified two UDP-glycosyltransferases (UGTs) from C.
View Article and Find Full Text PDFJ Agric Food Chem
November 2000
Laboratory of Food Chemistry, Department of Nutrition and Food Science, Ochanomizu University, 2-1-1 Ohtsuka, Bunkyo-ku, Tokyo 112, Japan.
Twenty-six synthetic glycosides constituting aglycons of the main tea aroma compounds ((Z)-3-hexenol, benzyl alcohol, 2-phenylethanol, methyl salicylate, geraniol, linalool, and four isomers of linalool oxides) were synthesized in our laboratory as authentic compounds. Those compounds were used to carry out a direct qualitative and quantitative determination of the glycosides as aroma precursors in different tea cultivars by capillary gas chromatographic-mass spectrometric (GC-MS) analyses after trifluoroacetyl conversion of the tea glycosidic fractions. Eleven beta-D-glucopyranosides, 10 beta-primeverosides (6-O-beta-D-xylopyranosyl-beta-D-glucopyranoside) with aglycons as the above alcohols, and geranyl beta-vicianoside (6-O-alpha-L-arabinopyranosyl-beta-D-glucopyranoside) were identified (tentatively identified in the case of methyl salicylate beta-primeveroside) in fresh tea leaves and quantified on the basis of calibration curves that had been established by using the synthetic compounds.
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