Liu Liancheng, Dong Juan'e, Zhang Jingyi, Dang Xiaolin, Xing Bingyu, Yang Xiling
College of Life Sciences, Northwest Agriculture and Forestry University, Yangling 712100, Shaanxi, China.
Sheng Wu Gong Cheng Xue Bao. 2012 Nov;28(11):1359-69.
We studied the influence of the concentration of Ca2+ (0-50 mmol/L) in culture medium on the synthesis of rosmarinic acid (RA) and related enzymes in Salvia miltiorrhiza suspension cultures. Using verpamil (VP, a calcium channel antagonist) and ionophore A23187, we studied the mechanism of secondary metabolites of Salvia miltiorrhiza suspension cultures influenced by the concentration of Ca2+ in the culture medium. The synthesis of intracellular RA in 6-day incubation was significantly dependent on the medium Ca2+ concentration. At the optimal Ca2+ concentration of 10 mmol/L, a maximal RA content of 20.149 mg/g biomass dry weight was reached, which was about 37.3% and 20.4% higher than that at Ca2+ concentrations of 1 and 3 mmol/L, respectively. The variation of the activity of PAL and TAT, two key enzymes of the two branches of RA, could be affected by the concentration of Ca2+ in culture medium. The change of their activity occurred prior to the accumulation of RA, which suggested both of the key enzymes be involved in the synthesis of RA. Meanwhile, the enzymatic action of PAL was more distinct than TAT. The treatment of VP and A23187, respectively, indicated that the influence of RA affected by the concentration of Ca2+ in the culture medium was accomplished by the intracellular Ca2+, and the flow of Ca2+ from the extracellular to the intracellular environment could also participate in this process.
我们研究了培养基中Ca2+浓度(0 - 50 mmol/L)对丹参悬浮培养物中迷迭香酸(RA)合成及相关酶的影响。使用维拉帕米(VP,一种钙通道拮抗剂)和离子载体A23187,我们研究了培养基中Ca2+浓度对丹参悬浮培养物次生代谢产物的影响机制。6天培养期内细胞内RA的合成显著依赖于培养基中Ca2+浓度。在最佳Ca2+浓度10 mmol/L时,RA最大含量达到20.149 mg/g生物量干重,分别比Ca2+浓度为1 mmol/L和3 mmol/L时高约37.3%和20.4%。RA两个分支的两个关键酶PAL和TAT的活性变化会受到培养基中Ca2+浓度的影响。它们活性的变化发生在RA积累之前,这表明这两个关键酶都参与了RA的合成。同时,PAL的酶促作用比TAT更明显。分别用VP和A23187处理表明,培养基中Ca2+浓度对RA的影响是通过细胞内Ca2+实现的,Ca2+从细胞外环境向细胞内环境的流动也可能参与这一过程。