Department of Biology and Pharmaceutical Botany, Medical University of Lodz, 90-151 Lodz, Poland.
Department of Pharmaceutical Biology, Medical University of Warsaw, 02-097 Warsaw, Poland.
Molecules. 2024 Jun 3;29(11):2626. doi: 10.3390/molecules29112626.
Callus cultures of the Iranian medicinal plant were initiated from three-week-old seedlings on Murashige and Skoog (MS) medium supplemented with α-naphthaleneacetic acid (NAA) and various cytokinins. Although all tested hormonal variants of the medium and explant enabled callus induction, the most promising growth was noted for -(2-chloro-4-pyridyl)-'-phenylurea (CPPU)-induced calli. Three lines obtained on this medium (cotyledon line-CL, hypocotyl line-HL, and root line-RL) were preselected for further studies. Phenolic compounds in the callus tissues were identified using UPLC-MS (ultra-performance liquid chromatography-mass spectrometry) and quantified with HPLC (high-performance liquid chromatography). All lines exhibited intensive growth and contained twelve phenolic acid derivatives, with rosmarinic acid predominating. The cotyledon-derived callus line displayed the highest growth index values and polyphenol content; this was exposed to different light-emitting diodes (LED) for improving biomass accumulation and secondary metabolite yield. Under LED treatments, all callus lines exhibited enhanced RA and total phenolic content compared to fluorescent light, with the highest levels observed for white (48.5-50.2 mg/g dry weight) and blue (51.4-53.9 mg/g dry weight) LEDs. The selected callus demonstrated strong antioxidant potential in vitro based on the 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS), 2,2-diphenyl-1-picrylhydrazyl (DPPH), and ferric reducing antioxidant power (FRAP) tests. Our findings confirm that the callus system is suitable for enhanced rosmarinic acid production; the selected optimized culture provide high-quality plant-derived products.
伊朗药用植物的愈伤组织培养是从三周龄的幼苗在添加α-萘乙酸(NAA)和各种细胞分裂素的Murashige 和 Skoog(MS)培养基上开始的。虽然测试的培养基和外植体的所有激素变体都能诱导愈伤组织,但最有希望的生长是在 -(2-氯-4-吡啶基)-'-苯基脲(CPPU)诱导的愈伤组织中观察到的。在该培养基上获得的三条线(子叶线-CL、下胚轴线-HL 和根线-RL)被预先选择进行进一步研究。使用 UPLC-MS(超高效液相色谱-质谱)鉴定愈伤组织中的酚类化合物,并使用 HPLC(高效液相色谱)进行定量。所有的系都表现出强烈的生长,并含有十二种酚酸衍生物,以迷迭香酸为主。子叶衍生的愈伤组织系显示出最高的生长指数值和多酚含量;该系暴露于不同的发光二极管(LED)下,以提高生物量积累和次生代谢产物产量。在 LED 处理下,与荧光灯相比,所有愈伤组织系的 RA 和总酚含量均有所提高,其中白光(48.5-50.2mg/g 干重)和蓝光(51.4-53.9mg/g 干重)LED 的含量最高。根据 2,2'-联氮双(3-乙基苯并噻唑啉-6-磺酸)(ABTS)、2,2-二苯基-1-苦基肼(DPPH)和铁还原抗氧化能力(FRAP)试验,选择的愈伤组织在体外表现出很强的抗氧化潜力。我们的研究结果证实,愈伤组织系统适合于增强迷迭香酸的产生;所选的优化培养物提供高质量的植物衍生产品。
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