Journal of Food Bioactives, ISSN 2637-8752 print, 2637-8779 online
Journal website www.isnff-jfb.com

Original Research

Volume 22, June 2023, pages 27-35


Study on antioxidant activity of Jujube seed oil

Figures

Figure 1.
Figure 1. Location of enzymes associated with oxidative stress in the cell.
Figure 2.
Figure 2. Technical route of this study.
Figure 3.
Figure 3. Structures of d-limonene, methyl N-methylanthranilate,α-farnesene, and γ-terpinene.
Figure 4.
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.
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.
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.
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.
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.
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.
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.ComponentsRTRelative contentMolecular Formula
1a-Pinene6.530.28C10H16
2y-Limonene6.580.33C10H16
3Didehydro pinane7.310.37C10H16
4D-Limonene8.517.87C10H16
5y -Terpinene9.374.23C10H16
6Terpinolene9.473.04C10H16
71,3,8-p-Menthatriene9.650.13C10H14
8trans-Alloocimene9.751.07C10H16
9cis-p-Mentha-2,8-dien-1-ol9.920.8C10H16O
10d-Citronellal10.041.65C10H18O
11Cyclohexene, 3-(3-methyl-1-butenyl)-, (E)-10.280.17C10H18
12Sabinene hydrate10.330.16C10H18O
13Terpinen-4-ol10.512.93C10H18O
14a-terpineol10.734.68C10H18O
15Isopiperitenol10.840.11C10H16O
16Citronellol11.082.18C10H20O
17methyl thymol ether11.170.65C11H16O
18Carvone11.390.6C10H14O
19piperitone11.530.18C10H16O
20perillyl aldehyde11.841.88C10H14O
21Thymol11.963.79C10H14O
22Carvacrol12.242.16C10H14O
23y -Elemene12.640.15C15H24
24cis-carane12.770.55C10H18
25Geranyl acetate12.930.38C12H20O2
26a-Copaene13.251.73C15H24
27β-Copaene13.461.24C15H24
28Methyl N-methylanthranilate13.9115.3C8H9NO2
29β-Caryophyllene14.053.05C15H24
30a-Caryophyllene14.530.78C15H24
31Germacrene D14.870.49C15H24
32a-Farnesene15.119.5C15H24
33Cadina-1(10),4-diene15.462.16C15H24
34a-Elemol15.940.44C15H26O
35Dodecanoic acid16.160.5C12H24O2
36a-Patchoulene16.450.37C15H24
37Caryophyllene oxide16.510.38C15H24O
38Tetradecanal16.640.2C14H28O
39aromadendrene oxide17.170.11C15H24O
40T-muurolol17.260.2C15H26O
41β-eudesmol17.440.45C15H26O
42β-santalol17.630.31C15H24O
43a-sinensal18.466.34C15H22O
442-Amylnonen-2-al19.720.18C14H26O
45Hexadecanoic acid20.361.85C16H32O2
46p-Camphorene21.090.15C20H32
47Methyl Linoleate22.090.23C19H34O2
48Methyl Linolenate22.160.14C19H32O2
49Linoleic acid22.550.69C18H32O2
50Dodecenylsuccinic anhydride22.720.15C16H26O3