首页> 美国卫生研究院文献>Molecules >Interactive Effect of Melatonin and UV-C on Phenylpropanoid Metabolite Production and Antioxidant Potential in Callus Cultures of Purple Basil (Ocimum basilicum L. var purpurascens)
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Interactive Effect of Melatonin and UV-C on Phenylpropanoid Metabolite Production and Antioxidant Potential in Callus Cultures of Purple Basil (Ocimum basilicum L. var purpurascens)

机译:褪黑素和UV-C交互作用对紫色罗勒愈伤组织培养物中苯丙氨酸代谢产物的产生和抗氧化能力的影响。紫罗兰(Ocimum basilicum L. var purpurascens)

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摘要

The present study evaluated the interactive effect of melatonin and UV-C on phenylpropanoid metabolites profile and antioxidant potential of L. Callus was treated with varying concentrations of melatonin and UV-C radiations for different time durations, either alone and/or in combination. Individual treatments of both UV-C and melatonin proved to be more effective than combine treatments. Results indicated that UV-C (10 min) exposure increased rosmarinic acid (134.5 mg/g dry weight (DW)), which was 2.3-fold greater than control. Chichoric acid (51.52 mg/g DW) and anthocyanin (cyanide 0.50 mg/g DW) were almost 4.1-fold, while peonidin was found 2.7-fold higher in UV-C (50 min) exposure. In the case of melatonin, 1.0 mg/L concentrations showed maximum rosmarinic acid (79.4 mg/g DW) accumulation; i.e., 1.4-fold more, as compared to the control. However, 2 mg/L melatonin accumulate chichoric acid (39.99 mg/g DW) and anthocyanin (cyanide: 0.45 mg/g DW and peonidin: 0.22 mg/g DW); i.e., 3.2, 3.7 and 2.0-fold increase, as compared to the control, respectively. On the other hand, melatonin-combined treatment (melatonin (Mel) (4 mg/L) + UV-C (20 min)) was proved to be effective in caffeic acid elicitation, which was 1.9-fold greater than the control. Furthermore, antioxidant potential was evaluated by both in vitro (DPPH, ABTS and FRAP assays) and methods. Maximum in vitro antioxidant activity (DPPH: 90.6% and ABTS: 1909.5 µM) was observed for UV-C (50 min)-treated cultures. The highest in vitro antioxidant activity measured with the ABTS assay as compared to the FRAP assay, suggesting the main contribution of antioxidants from basil callus extracts acting through a hydrogen atom transfer (HAT) over an electron transfer (ET)-based mechanism. Cellular antioxidant assay was evaluated by production of ROS/RNS species using yeast cell cultures and further confirmed the protective action of the corresponding callus extracts against oxidative stress. Overall, both melatonin and UV-C are here proved to be effective elicitors since a positive correlation between the induced production of phenolic compounds, and antioxidant action of basil callus extracts were observed.
机译:本研究评估了褪黑素和UV-C相互作用对苯丙氨酸代谢产物和L的抗氧化能力的影响。愈伤组织用不同浓度的褪黑素和UV-C辐射处理,持续时间不同,可以单独使用和/或组合使用。紫外线-C和褪黑激素的单独治疗被证明比联合治疗更有效。结果表明,UV-C(10分钟)暴露增加了迷迭香酸(134.5 mg / g干重(DW)),比对照大2.3倍。甲壳酸(51.52 mg / g DW)和花色苷(氰化物0.50 mg / g DW)几乎是4.1倍,而peonidin在UV-C(50分钟)暴露下则高2.7倍。就褪黑激素而言,1.0 mg / L的浓度显示最大的迷迭香酸(79.4 mg / g DW)积累;即,与对照相比,增加了1.4倍。然而,2 mg / L褪黑素会积聚Chichoric酸(39.99 mg / g DW)和花色苷(氰化物:0.45 mg / g DW和peonidin:0.22 mg / g DW);即,与对照相比分别增加了3.2倍,3.7倍和2.0倍。另一方面,褪黑素联合治疗(褪黑素(Mel)(4 mg / L)+ UV-C(20分钟))被证明对咖啡酸的诱导有效,比对照高1.9倍。此外,通过体外(DPPH,ABTS和FRAP分析)和方法评估了抗氧化剂的潜力。对于经UV-C(50分钟)处理的培养物,观察到最大的体外抗氧化剂活性(DPPH:90.6%和ABTS:1909.5 µM)。与FRAP分析相比,使用ABTS分析测得的体外抗氧化活性最高,表明罗勒愈伤组织提取物中的抗氧化剂的主要作用是通过基于氢原子转移(HAT)的电子转移(ET)机制。通过使用酵母细胞培养物生产ROS / RNS物种评估了细胞抗氧化剂的含量,并进一步证实了相应愈伤组织提取物对氧化应激的保护作用。总体而言,褪黑激素和UV-C在这里被证明是有效的引发剂,因为在酚类化合物的诱导生产与罗勒愈伤组织提取物的抗氧化作用之间存在正相关。

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