Department of Medicinal Plant and Mushroom Biotechnology, Jagiellonian University, Medical College, 30-688 Kraków, Poland.
Molecules. 2024 Sep 29;29(19):4622. doi: 10.3390/molecules29194622.
A precursor feeding strategy was used for the first time in agitated microshoot cultures of . This strategy involved the addition of biogenetic precursors of simple phenolic acids (phenylalanine, cinnamic acid, and benzoic acid) and depsides (caffeic acid) into the culture media, with an assessment of its effect on the production of these bioactive compounds. The in vitro cultures were maintained in Murashige-Skoog medium (1 mg/L BAP and 1 mg/L NAA). Precursors at five concentrations (0.1, 0.5, 1.0, 5.0, and 10.0 mmol/L) were fed into the medium at the time of culture initiation (point "0") and independently on the 10th day of growth cycles. The contents of 23 compounds were determined in methanolic extracts of biomass collected after 20 days of growth cycles using an HPLC method. All extracts contained the same four depsides (chlorogenic, neochlorogenic, rosmarinic, and cryptochlorogenic acids) and the same four simple phenolic acids (protocatechuic, vanillic, caffeic, and syringic acids). Chlorogenic and neochlorogenic acids were the predominant compounds in all extracts (max. 388.39 and 263.54 mg/100 g d.w.). The maximal total contents of all compounds were confirmed after feeding with cinnamic acid (5 mmol/L, point "0") and caffeic acid (10 mmol/L, point "0"), which caused a 2.68-fold and 2.49-fold increase in the contents of the estimated compounds vs. control cultures (603.03 and 558.48 mg/100 g d.w., respectively). The obtained results documented the efficacy of the precursor feeding strategy in enhancing the production of bioactive compounds in agitated cultures of and suggest a potential practical application value.
首次在 的搅动微芽培养物中使用前体喂养策略。该策略涉及将生物合成的简单酚酸(苯丙氨酸、肉桂酸和苯甲酸)和缩酚酸(咖啡酸)前体添加到培养基中,并评估其对这些生物活性化合物生产的影响。体外培养在 Murashige-Skoog 培养基(1 mg/L BAP 和 1 mg/L NAA)中进行。前体以五种浓度(0.1、0.5、1.0、5.0 和 10.0 mmol/L)在培养起始时(“0”点)和生长周期的第 10 天分别添加到培养基中。使用 HPLC 方法在生长周期 20 天后收集的生物质甲醇提取物中测定了 23 种化合物的含量。所有提取物均含有相同的四种缩酚酸(绿原酸、新绿原酸、迷迭香酸和隐绿原酸)和相同的四种简单酚酸(原儿茶酸、香草酸、咖啡酸和丁香酸)。绿原酸和新绿原酸是所有提取物中的主要化合物(最高 388.39 和 263.54 mg/100 g d.w.)。在用肉桂酸(5 mmol/L,“0”点)和咖啡酸(10 mmol/L,“0”点)喂养后,确认了所有化合物的最大总含量,这导致估计化合物的含量与对照培养物相比增加了 2.68 倍和 2.49 倍(分别为 603.03 和 558.48 mg/100 g d.w.)。所得结果证明了前体喂养策略在增强 搅动培养物中生物活性化合物生产方面的有效性,并表明其具有潜在的实际应用价值。