Figures
Figure 1. Location of enzymes associated with oxidative stress in the cell.
Figure 2. Technical route of this study.
Figure 3. Structures of d-limonene, methyl N-methylanthranilate,α-farnesene, and γ-terpinene.
Figure 4. Reducing power of jujube seed oil. The concentration of SJO used was 0.2 mg/mL,0.4 mg/mL,0.6 mg/mL,1 mg/mL,1.5 mg/mL, and 2 mg/mL, repectively. The positive control group received 0.2 mg/mL, 0.4 mg/mL, 0.6 mg/mL, 0.8 mg/mL,1 mg/mL, and 2 mg/mL of VC, respectfully. Data represent the mean ± SD of three independent trials.
Figure 5. DPPH radical scavenging activity of SJO. The concentration of SJO used was 1 mg/mL,4 mg/mL,5 mg/mL, 10 mg/mL, 15 mg/mL, and 20 mg/mL, respectively. The positive control group received 1 mg/mL VC and 1 mg/mL BHT. Data represent the mean ± SD of three independent trials.
Figure 6. Hydroxyl radical scavenging activity of SJO. The concentration of SJO used was 1 mg/mL, 2 mg/mL, 4 mg/mL, and 6 mg/mL. The positive control group received 1 mg/mL VC and 1 mg/mL BHT. Data represent the mean ± SD of three independent trials.
Figure 7. The survival rate of S. cerevisiae cells is directly exposed to increasing SJO concentrations. The concentration of SJO used was 25 μg/mL and 50 μg/mL. Data represent the mean ± SD of three independent trials.
Figure 8. Effect of 2 mM H2O2, 10 mM CCL4 on lipid peroxidation level of S. cerevisiae cells (WT, ctt1Δ, sod1Δ, gtt1Δ, gtt2Δ, and gsh1Δ) and the membrane protective effect of SJO. The concentration of SJO used was 5 μg/mL. Lipid peroxidation levels of non-stressed cells without SJO treatment were used as a control. Data represent the mean ± SD of three independent trials. In each oxidative stress group, the statistically different results were denoted by different letters, p < 0.05.
Figure 9. Effect of 2 mM H2O2, 10 mM CCl4 on survival of S. cerevisiae cells (WT, ctt1Δ, sod1Δ, gtt1Δ, gtt2Δ, and gsh1Δ) and the antioxidant effect of SJO. The concentration of SJO used was 25 μg/mL and 50 μg/mL. Data represent the mean ± SD of three independent trials. In each oxidative stress group, the statistically different results were denoted by different letters, p < 0.05.
Figure 10. Effect of 2 mM H2O2, 10 mM CCL4 on ROS level of S. cerevisiae (WT, ctt1Δ, sod1Δ, gtt1Δ, gtt2Δ, and gsh1Δ) and the ROS effect of SJO. The concentration of SJO used was 5 μg/mL. ROS levels of non-stressed cells without SJO treatment were used as a control. Data represent the mean ± SD of three independent trials. In each oxidative stress group, the statistically different results were denoted by different letters, p < 0.05.
Table
Table 1. Chemical composition of the jujube seed oil
No. | Components | RT | Relative content | Molecular Formula |
---|
1 | a-Pinene | 6.53 | 0.28 | C10H16 |
2 | y-Limonene | 6.58 | 0.33 | C10H16 |
3 | Didehydro pinane | 7.31 | 0.37 | C10H16 |
4 | D-Limonene | 8.5 | 17.87 | C10H16 |
5 | y -Terpinene | 9.37 | 4.23 | C10H16 |
6 | Terpinolene | 9.47 | 3.04 | C10H16 |
7 | 1,3,8-p-Menthatriene | 9.65 | 0.13 | C10H14 |
8 | trans-Alloocimene | 9.75 | 1.07 | C10H16 |
9 | cis-p-Mentha-2,8-dien-1-ol | 9.92 | 0.8 | C10H16O |
10 | d-Citronellal | 10.04 | 1.65 | C10H18O |
11 | Cyclohexene, 3-(3-methyl-1-butenyl)-, (E)- | 10.28 | 0.17 | C10H18 |
12 | Sabinene hydrate | 10.33 | 0.16 | C10H18O |
13 | Terpinen-4-ol | 10.51 | 2.93 | C10H18O |
14 | a-terpineol | 10.73 | 4.68 | C10H18O |
15 | Isopiperitenol | 10.84 | 0.11 | C10H16O |
16 | Citronellol | 11.08 | 2.18 | C10H20O |
17 | methyl thymol ether | 11.17 | 0.65 | C11H16O |
18 | Carvone | 11.39 | 0.6 | C10H14O |
19 | piperitone | 11.53 | 0.18 | C10H16O |
20 | perillyl aldehyde | 11.84 | 1.88 | C10H14O |
21 | Thymol | 11.96 | 3.79 | C10H14O |
22 | Carvacrol | 12.24 | 2.16 | C10H14O |
23 | y -Elemene | 12.64 | 0.15 | C15H24 |
24 | cis-carane | 12.77 | 0.55 | C10H18 |
25 | Geranyl acetate | 12.93 | 0.38 | C12H20O2 |
26 | a-Copaene | 13.25 | 1.73 | C15H24 |
27 | β-Copaene | 13.46 | 1.24 | C15H24 |
28 | Methyl N-methylanthranilate | 13.91 | 15.3 | C8H9NO2 |
29 | β-Caryophyllene | 14.05 | 3.05 | C15H24 |
30 | a-Caryophyllene | 14.53 | 0.78 | C15H24 |
31 | Germacrene D | 14.87 | 0.49 | C15H24 |
32 | a-Farnesene | 15.11 | 9.5 | C15H24 |
33 | Cadina-1(10),4-diene | 15.46 | 2.16 | C15H24 |
34 | a-Elemol | 15.94 | 0.44 | C15H26O |
35 | Dodecanoic acid | 16.16 | 0.5 | C12H24O2 |
36 | a-Patchoulene | 16.45 | 0.37 | C15H24 |
37 | Caryophyllene oxide | 16.51 | 0.38 | C15H24O |
38 | Tetradecanal | 16.64 | 0.2 | C14H28O |
39 | aromadendrene oxide | 17.17 | 0.11 | C15H24O |
40 | T-muurolol | 17.26 | 0.2 | C15H26O |
41 | β-eudesmol | 17.44 | 0.45 | C15H26O |
42 | β-santalol | 17.63 | 0.31 | C15H24O |
43 | a-sinensal | 18.46 | 6.34 | C15H22O |
44 | 2-Amylnonen-2-al | 19.72 | 0.18 | C14H26O |
45 | Hexadecanoic acid | 20.36 | 1.85 | C16H32O2 |
46 | p-Camphorene | 21.09 | 0.15 | C20H32 |
47 | Methyl Linoleate | 22.09 | 0.23 | C19H34O2 |
48 | Methyl Linolenate | 22.16 | 0.14 | C19H32O2 |
49 | Linoleic acid | 22.55 | 0.69 | C18H32O2 |
50 | Dodecenylsuccinic anhydride | 22.72 | 0.15 | C16H26O3 |