Wang Wei, Zhao Zhen-Jiang, Xu Yufang, Qian Xuhong, Zhong Jian-Jiang
State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, China.
Appl Microbiol Biotechnol. 2006 Apr;70(3):298-307. doi: 10.1007/s00253-005-0089-4. Epub 2005 Jul 23.
Chemically synthesized 2-hydroxyethyl jasmonate (HEJA) was for the first time employed to induce the ginsenoside biosynthesis and to manipulate the product heterogeneity in plant cell cultures. The dose response and timing of HEJA elicitation were investigated in cell suspension cultures of Panax notoginseng. The optimal concentration and timing of HEJA addition for both cell growth and ginsenoside accumulation was identified to be 200 microM added on day 4. It was interestingly found that HEJA could stimulate ginsenosides biosynthesis and change their heterogeneity more efficiently than methyl jasmonate (MJA), i.e., the total ginsenoside content and the Rb/Rg ratio increased about 60 and 30% with HEJA elicitation than that by MJA, respectively. The activity of Rb1 biosynthetic enzyme, i.e., UDPG-ginsenoside Rd glucosyltransferase (UGRdGT), was also higher in the former case. A maximal production titer of ginsenoside Rg1, Re, Rb1, and Rd was 47.4+/-4.8, 52.3+/-4.4, 190+/-18, and 12.1+/-2.5 mg/l with HEJA elicitation, which was about 1.3-, 1.3-, 1.7-, and 2.1-fold than that using MJA, respectively. Early signal events in plant defense response, including oxidative burst and jasmonic acid (JA) biosynthesis, were also examined. Levels of H2O2 and NO in medium and L-phenylalanine ammonia lyase activity in cells were not affected by addition of MJA and HEJA. On the other hand, the JA content in cells was increased with external jasmonates elicitation, and it was inhibited with the addition of JA biosynthesis inhibitors. The results suggest that oxidative burst might not be involved in the jasmonates-elicited signal transduction pathway, and MJA and HEJA may induce the ginsenoside biosynthesis via induction of endogenous JA biosynthesis and key enzymes (such as UGRdGT) in the ginsenoside biosynthetic pathway of P. notoginseng cells. The information is useful for hyperproduction of plant-specific heterogeneous products.
首次使用化学合成的茉莉酸 2-羟乙酯(HEJA)来诱导人参皂苷生物合成并调控植物细胞培养物中的产物异质性。在三七细胞悬浮培养物中研究了 HEJA 诱导的剂量反应和时间。确定添加 HEJA 促进细胞生长和人参皂苷积累的最佳浓度和时间为第 4 天添加 200 μM。有趣的是,发现 HEJA 比茉莉酸甲酯(MJA)更有效地刺激人参皂苷生物合成并改变其异质性,即 HEJA 诱导时总人参皂苷含量和 Rb/Rg 比值分别比 MJA 诱导时增加约 60%和 30%。在前一种情况下,Rb1 生物合成酶即 UDPG-人参皂苷 Rd 糖基转移酶(UGRdGT)的活性也更高。HEJA 诱导时人参皂苷 Rg1、Re、Rb1 和 Rd 的最大产量滴度分别为 47.4±4.8、52.3±4.4、190±18 和 12.1±2.5 mg/l,分别约为使用 MJA 时的 1.3 倍、1.3 倍、1.7 倍和 2.1 倍。还研究了植物防御反应中的早期信号事件,包括氧化爆发和茉莉酸(JA)生物合成。培养基中 H2O2 和 NO 的水平以及细胞中 L-苯丙氨酸解氨酶的活性不受 MJA 和 HEJA 添加的影响。另一方面,细胞中的 JA 含量随外源茉莉酸酯诱导而增加,并因添加 JA 生物合成抑制剂而受到抑制。结果表明氧化爆发可能不参与茉莉酸酯诱导的信号转导途径,MJA 和 HEJA 可能通过诱导三七细胞人参皂苷生物合成途径中的内源性 JA 生物合成和关键酶(如 UGRdGT)来诱导人参皂苷生物合成。该信息对于植物特异性异质产物的过量生产很有用。