Figures (4)  Tables (2)
    • Figure 1. 

      Classification of metabolites for tea plant and its related species and varieties.

    • Figure 2. 

      Group number of tea plants determined based on Calinski criterion.

    • Figure 3. 

      Volcano plots of DAMs. (a) DAMs of natural population (red dots represent the content of DAMs that are higher in Group 2 compared to Group 1, green dots represent the content of DAMs that are higher in Group 1 compared to Group 2); (b) DAMs between Camellia sinensis and its relatives (red dots represent the content of DAMs that are higher in Camellia sinensis compared to relatives of Camellia sinensis, blue dots represent the content of DAMs that are higher in relatives of Camellia sinensis compared to Camellia sinensis).

    • Figure 4. 

      Top 30 DAMs of five tea plant species and varieties.

    • Representative group*MetaboliteClassRelative peak area
      CSACSPCSSCTFCTM
      CSSL-Pyroglutamic acidAmino acids and their derivatives5.E+077.E+078.E+074.E+074.E+07
      CSSL-SerineAmino acids and their derivatives1.E+061.E+062.E+061.E+061.E+06
      CSSSinapaldehyde glucosideCarbohydrates3.E+052.E+054.E+052.E+052.E+05
      CSS7-EthoxycoumarinCoumarins1.E+058.E+042.E+051.E+058.E+04
      CSSD-Quinic acidQuinates and their derivatives3.E+063.E+064.E+062.E+062.E+06
      CSAN-Acetyl-DL-tryptophanAmino acids and their derivatives1.E+064.E+053.E+053.E+051.E+06
      CSAAzelaic acidOrganic acids2.E+051.E+059.E+042.E+052.E+05
      CTF7-HydroxycoumarineCoumarins3.E+062.E+063.E+064.E+063.E+06
      CTFdiGC-GABenzoic acid derivatives2.E+072.E+071.E+073.E+072.E+07
      CTF2-Acetamido-2-deoxyglucoseCarbohydrates2.E+062.E+061.E+063.E+062.E+06
      CTFKaempferitrinFlavonol glycosides2.E+045.E+052.E+046.E+063.E+04
      CTFNictoflorinFlavonol glycosides2.E+057.E+052.E+057.E+062.E+05
      CTFTraumatic acidOrganic acids5.E+053.E+053.E+056.E+055.E+05
      CTFNeochlorogenic acidQuinates and their derivatives7.E+062.E+062.E+061.E+079.E+06
      CTM5'-Xanthylic acidQuinates and their derivatives5.E+053.E+053.E+055.E+056.E+05
      CTMChlorogenic acidQuinates and their derivatives1.E+071.E+074.E+069.E+062.E+07
      * CSS: C. sinensis var. sinensis (L.) O. Kuntze; CSA: C. sinensis var. assamica (Masters) Kitamura; CSP: C. sinensis var. pubilimba Chang; CTF: C. tachangensis F. C. Zhang; CTM: C. taliensis (W. W. Smith) Melchior.

      Table 1. 

      Signature metabolites of five tea plant species and varieties.

    • NameClassificationFormula
      GC-GCGAnthocyaninsC37 H30 O18
      Procyanidin B1AnthocyaninsC30 H26 O12
      Procyanidin B3AnthocyaninsC30 H26 O12
      Procyanidin B4AnthocyaninsC30 H26 O12
      Procyanidin C1AnthocyaninsC30 H26 O12
      Tricatechins1AnthocyaninsC45 H38 O18
      Tricatechins2AnthocyaninsC45 H38 O18
      Tricatechins3AnthocyaninsC45 H38 O18
      GC-diGABenzoic acid derivativesC29 H22 O15
      EriocitrinFlavanol glycosidesC27 H32 O15
      Eriodictyol C-hexosideFlavanone glycosidesC21 H22 O11
      NaringinFlavanone glycosidesC27 H32 O14
      Naringin dihydrochalconeFlavanone glycosidesC27 H34 O14
      PruninFlavanone glycosidesC21 H22 O10
      BaicalinFlavone glycosidesC21 H18 O11
      CynarosideFlavone glycosidesC21 H20 O11
      Luteolin 7-O-(6-O-malonyl-β-D-glucoside)Flavone glycosidesC24 H22 O14
      SchaftosideFlavone glycosidesC26 H28 O14
      AstilbinFlavonol glycosidesC21 H22 O11
      BaimasideFlavonol glycosidesC27 H30 O17
      IsoquercetinFlavonol glycosidesC21 H20 O12
      KaempferinFlavonol glycosidesC21 H20 O10
      KaempferitrinFlavonol glycosidesC27 H30 O14
      Myricetin 3-O-galactosideFlavonol glycosidesC21 H20 O13
      NictoflorinFlavonol glycosidesC27 H30 O15
      Quercetin 3-O-α-D-xylopyranosideFlavonol glycosidesC20 H18 O11
      QuercitrinFlavonol glycosidesC21 H20 O11
      RutinFlavonol glycosidesC27 H30 O16
      TilirosideFlavonol glycosidesC30 H26 O13
      VitexinFlavonol glycosidesC21 H20 O10
      Vitexin-2''-O-rhamnosideFlavonol glycosidesC27 H30 O14
      MalonylgenistinIsoflavone glycosidesC24 H22 O13

      Table 2. 

      Polymers of flavonoids.