Bavi Khadijeh, Khavari-Nejad Ramazan Ali, Najafi Farzaneh, Ghanati Faezeh
Department of Plant Sciences, Faculty of Biological Sciences, Kharazmi University, P.O.Box: 15719-14911, Tehran, Iran.
Department of Plant Biology, Faculty of Biological Sciences, Tarbiat Modares University, P.O.Box: 14115-111, Tehran, Iran.
3 Biotech. 2022 Aug;12(8):163. doi: 10.1007/s13205-022-03235-x. Epub 2022 Jul 9.
is an important medicinal plant with antioxidant and anticancer properties attributed to its phytochemicals. To develop a method for bulk production of valuable phytochemicals, cell suspension culture of were grown in liquid B5 medium and then treated in their log growth phase with chitosan (0, 10, 20, and 40 mg L) and yeast extract (0, 400, 800, and 1200 mg L) for 3 days. The levels of hydrogen peroxide (HO), nitric oxide (NO), malondialdehyde (MDA), and the main terpenoids and phenylpropanoids in the cell extracts were determined by HPLC and spectrophotometric techniques. The HO and MDA levels significantly increased in the cells treated with both yeast extract and chitosan, while the NO level increased in those exposed to yeast extract. At their highest concentrations, both elicitors significantly increased PAL and TAL activities, as well as phenolic acids and flavonoids contents. Chitosan only induced the production of caffeic acid (22 µg g DW), benzoic acid (2 µg g DW), 4-hydroxy benzoic acid (6 µg g DW), epicatechin (63 µg g DW), and apigenin (5 µg g DW) in the cells, while yeast extract increased the contents of phenylpropanoids gallic acid (50 µg g DW), vanillin (35 µg g DW), salicylic acid (24 µg g DW), catechin (130 µg g DW) and terpenoids carvacrol (7 µg g DW) and thymol (24 µg g DW). In conclusion, changes in the production of phenolics and terpenoids are a defensive mechanism in cells treated by yeast extract and chitosan.
The online version contains supplementary material available at 10.1007/s13205-022-03235-x.
是一种重要的药用植物,因其植物化学物质具有抗氧化和抗癌特性。为了开发一种大量生产有价值植物化学物质的方法,在液体B5培养基中培养细胞悬浮培养物,然后在对数生长期用壳聚糖(0、10、20和40毫克/升)和酵母提取物(0、400、800和1200毫克/升)处理3天。通过高效液相色谱法和分光光度技术测定细胞提取物中过氧化氢(HO)、一氧化氮(NO)、丙二醛(MDA)以及主要萜类化合物和苯丙素类化合物的含量。用酵母提取物和壳聚糖处理的细胞中HO和MDA水平显著增加,而暴露于酵母提取物的细胞中NO水平增加。在最高浓度下,两种诱导剂均显著提高苯丙氨酸解氨酶(PAL)和酪氨酸解氨酶(TAL)活性以及酚酸和黄酮类化合物含量。壳聚糖仅诱导细胞中咖啡酸(22微克/克干重)、苯甲酸(2微克/克干重)、4-羟基苯甲酸(6微克/克干重)、表儿茶素(63微克/克干重)和芹菜素(5微克/克干重)的产生,而酵母提取物增加了苯丙素类化合物没食子酸(50微克/克干重)、香草醛(35微克/克干重)、水杨酸(24微克/克干重)、儿茶素(130微克/克干重)以及萜类化合物香芹酚(7微克/克干重)和百里酚(二十四微克/克干重)的含量。总之,酚类和萜类化合物产量的变化是酵母提取物和壳聚糖处理的细胞中的一种防御机制。
在线版本包含可在10.1007/s13205-022-03235-x获取的补充材料。