[1]赵慧.福建茶产业发展现状与对策建议 [J]. 发展研究, 2018, 71-76.[2]梅宇, 林璇.2017中国白茶产销形势分析报告 [J]. 福建茶叶, 2017, 39: 3-5.[3]范方媛, 杨梦璇, 龚淑英, 等.基于近红外光谱技术的白茶3种典型感官滋味特征属性定量评价模型研究 [J]. 茶叶科学, 2018, 38: 296-304. DOI: 10.3969/j.issn.1000-369X.2018.03.010.[4]周琼琼, 孙威江, 叶艳, 等.不同年份白茶的主要生化成分分析 [J]. 食品工业科技, 2014, 35: 351-354+359. DOI: 10.13386/j.issn1002-0306.2014.09.068.[5]RUIZ C E, CABRERA L, LóPEZ-JIMéNEZ J á, et al.Effects of long-term ingestion of white tea on oxidation produced by aging and acute oxidative damage in rats [J]. Journal of Physiology & Biochemistry, 2017, 74: 1-7. DOI: 10.1007/s13105-017-0591-z.[6]LóPEZ V, CALVO M I.White Tea ( Camellia sinensis Kuntze) Exerts Neuroprotection against Hydrogen Peroxide-Induced Toxicity in PC12 Cells [J]. Plant Foods for Human Nutrition, 2011, 66: 22-6. DOI: 10.1007/s11130-010-0203-3.[7]HAJIAGHAALIPOUR F, KANTHIMATHI M S, SANUSI J, et al.White tea ( Camellia sinensis ) inhibits proliferation of the colon cancer cell line, HT-29, activates caspases and protects DNA of normal cells against oxidative damage [J]. Food Chemistry, 2015, 169: 401-410. DOI: 10.1016/j.foodchem.2014.07.005.[8]DAI W, XIE D, LU M, et al.Characterization of white tea metabolome: Comparison against green and black tea by a nontargeted metabolomics approach [J]. Food Research International, 2017, 96: 40-45. DOI: 10.1016/j.foodres.2017.03.028.[9]陈林, 陈键, 王丽丽, 等.不同茶类制法对茶多酚和游离氨基酸化学模式的影响 [J]. 福建农业学报, 2017, 32: 287-293. DOI: 10.19303/j.issn.1008-0384.2017.03.012.[10]CARLONI P, TIANO L, PADELLA L, et al.Antioxidant activity of white, green and black tea obtained from the same tea cultivar [J]. Food Research International, 2013, 53: 900-908. DOI: 10.1016/j.foodres.2012.07.057.[11]HORANNI R, ENGELHARDT U H.Determination of amino acids in white, green, black, oolong, pu-erh teas and tea products [J]. Journal of Food Composition and Analysis, 2013, 31: 94-100. DOI: 10.1016/j.jfca.2013.03.005.[12]《中国农业百科全书》委员会茶业卷委员会.中国农业百科全书, 茶业卷[M]. 北京: 农业出版社, 1988: 57-217.[13]CHEN S, LI M, ZHENG G, et al.Metabolite Profiling of 14 Wuyi Rock Tea Cultivars Using UPLC-QTOF MS and UPLC-QqQ MS Combined with Chemometrics [J]. Molecules, 2018, 23: 104. DOI: 10.3390/molecules23020104.[14]DOU J, LEE V S Y, TZEN J T, et al.Identification and comparison of phenolic compounds in the preparation of oolong tea manufactured by semifermentation and drying processes [J]. Journal of Agricultural & Food Chemistry, 2007, 55: 7462-7468. DOI: 10.1021/jf0718603.[15]HASHIMOTO F, NONAKA G I, NISHIOKA I.Tannins and related compounds. XC. 8-C-Ascorbyl (-)-epigallocatechin 3-O-gallate and novel dimeric flavan-3-ols, oolonghomobisflavans A and B, from oolong tea (3) [J]. Pharmaceutical Bulletin, 1989, 37: 3255-3263. DOI: 10.1248/cpb.37.3255.[16]DAI W, QI D, YANG T, et al.Nontargeted Analysis Using Ultraperformance Liquid Chromatography–Quadrupole Time-of-Flight Mass Spectrometry Uncovers the Effects of Harvest Season on the Metabolites and Taste Quality of Tea (Camellia sinensis L.) [J]. Journal of Agricultural and Food Chemistry, 2015, 63: 9869-9878. DOI: 10.1021/acs.jafc.5b03967.[17]JIANG X, LIU Y, WU Y, et al.Analysis of accumulation patterns and preliminary study on the condensation mechanism of proanthocyanidins in the tea plant [Camellia sinensis] [J]. Scientific Reports, 2015, 5: 8742-8742. DOI: 10.1038/srep08742.[18]TAUTENHAHN R, CHO K, URITBOONTHAI W, et al.An accelerated workflow for untargeted metabolomics using the METLIN database [J]. Nature Biotechnology, 2012, 30: 826-828. DOI: 10.1038/nbt.2348.[19]HANHINEVA K, ROGACHEV I, KOKKO H, et al.Non-targeted analysis of spatial metabolite composition in strawberry (Fragariaxananassa) flowers [J]. Phytochemistry, 2008, 69: 2463-2481. DOI: 10.1016/j.phytochem.2008.07.009.[20]FERRERES F, SILVA B M, ANDRADE P B, et al.Approach to the study of C-glycosyl flavones by ion trap HPLC-PAD-ESI/MS/MS: application to seeds of quince (Cydonia oblonga) [J]. Phytochem Anal, 2010, 14: 352-359. DOI: 10.1002/pca.727.[21]MENET M C, SANG S, YANG C S, et al.Analysis of theaflavins and thearubigins from black tea extract by MALDI-TOF mass spectrometry [J]. Journal of Agricultural & Food Chemistry, 2004, 52: 2455-2461. DOI: 10.1021/jf035427e.[22]ZHENG X-Q, NIE Y, GAO Y, et al.Screening the cultivar and processing factors based on the flavonoid profiles of dry teas using principal component analysis [J]. Journal of Food Composition and Analysis, 2018, 67: 29-37. DOI: 10.1016/j.jfca.2017.12.016.[23]李朋亮.基于修饰代谢组学的绿茶中糖苷类品质成分研究 [D]. 武汉: 华中农业大学, 2018.[24]FRASER K, LANE G A, OTTER D E, et al.Non-targeted analysis by LC-MS of major metabolite changes during the oolong tea manufacturing in New Zealand [J]. Food Chemistry, 2014, 151: 394-403. DOI: 10.1016/j.foodchem.2013.11.054.[25]TAN J, DAI W, LU M, et al.Study of the dynamic changes in the non-volatile chemical constituents of black tea during fermentation processing by a non-targeted metabolomics approach [J]. Food Research International, 2016, 79: 106-113. DOI: 10.1016/j.foodres.2015.11.018.[26]尹军峰, 闵航, 许勇泉, 等.摊放环境对名优绿茶鲜叶茶多酚及儿茶素组成的影响 [J]. 茶叶科学, 2008, 22-27.[27]尹军峰, 许勇泉, 袁海波, 等.名优绿茶鲜叶摊放过程中主要生化成分的动态变化 [J]. 茶叶科学, 2009, 29: 102-110.[28]陶湘辉, 陈常颂, 林郑和, 等.茶叶EGCG在不同茶类加工过程的变化初探 [J]. 茶叶科学技术, 2010, 27-30. DOI: 10.3969/j.issn.1007-4872.2010.03.008.[29]王丽, 叶乃兴, 郑德勇, 等.加工工艺对白茶、乌龙茶、红茶生化成分及抗氧化活性的影响 [J]. 福建茶叶, 2016, 38: 4-7. DOI: 10.3969/j.issn.1005-2291.2016.04.003.[30]SUZUKI T, YAMAZAKI N, SADA Y I, et al.Tissue distribution and intracellular localization of catechins in tea leaves [J]. Bioscience Biotechnology & Biochemistry, 2003, 67: 2683-2686. DOI: 10.1271/bbb.67.2683.[31]GUI J, FU X, ZHOU Y, et al.Does Enzymatic Hydrolysis of Glycosidically Bound Volatile Compounds Really Contribute to the Formation of Volatile Compounds During the Oolong Tea Manufacturing Process? [J]. Journal of Agricultural & Food Chemistry, 2015, 63: 6905-6914. DOI: 10.1021/acs.jafc.5b02741.[32]KIM Y, GOODNER K L, PARK J D, et al.Changes in antioxidant phytochemicals and volatile composition of Camellia sinensis by oxidation during tea fermentation [J]. Food Chemistry, 2011, 129: 1331-1342. DOI: 10.1016/j.foodchem.2011.05.012.[33]SHITANDI A, NGURE F M, MAHUNGU S M.Tea Processing and its Impact on Catechins, Theaflavin and Thearubigin Formation [J]. Tea in Health and Disease Prevention, 2013, 193-205. DOI: 10.1016/B978-0-12-384937-3.00016-1.[34]DAI W, TAN J, LU M, et al.Metabolomics Investigation Reveals That 8-C N-Ethyl-2-pyrrolidinone-Substituted Flavan-3-ols Are Potential Marker Compounds of Stored White Teas [J]. J Agric Food Chem, 2018, 66: 7209-7218. DOI: 10.1021/acs.jafc.8b02038.[35]LI X, LIU G J, ZHANG W, et al.Novel Flavoalkaloids from White Tea with Inhibitory Activity against the Formation of Advanced Glycation End Products [J]. J Agric Food Chem, 2018, 66: 4621-4629. 10.1021/acs.jafc.8b00650.[36]解东超.紫娟茶中花青素及其在加工过程中变化规律研究 [D]. 北京: 中国农业科学院, 2017. DOI: 10.3969/j.issn.1000-369X.2018.03.010.[37]SANG S, LAMBERT J D, HO C, et al.The chemistry and biotransformation of tea constituents [J]. Pharmacological Research, 2011, 64: 87-99. DOI: 10.1016/j.phrs.2011.02.007.[38]HUNG W L, WANG S, SANG S, et al.Quantification of ascorbyl adducts of epigallocatechin gallate and gallocatechin gallate in bottled tea beverages [J]. Food Chemistry, 2018, 261: 246-252. DOI: 10.1016/j.foodchem.2018.04.050.[39]HASHIMOTO F, KASHIWADA Y, NONAKA G I, et al.Evaluation of tea polyphenols as anti-HIV agents [J]. Bioorganic & Medicinal Chemistry Letters, 1996, 6: 695-700. DOI: 10.1016/0960-894X(96)00095-9. |