Bulchandani Neha, Shekhawat Gyan S
Department of Botany, Jai Narain Vyas University, Jodhpur, Rajasthan 342005 India.
3 Biotech. 2020 Nov;10(11):482. doi: 10.1007/s13205-020-02470-4. Epub 2020 Oct 21.
The study illustrates the system for enhanced production of a medicinally important unexplored compound, carvone occurring naturally in . The effect of salicylic acid (SA) on biomass yield, carvone biosynthesis, growth and major enzymatic antioxidant parameters in was evaluated. The effects of different combinations of benzyl adenine (BA) and 1-Naphthalene acetic acid (NAA) were tested. Murashige and Skoog (MS) medium comprising 1.76 µM BA + 3.24 µM NAA was the best for friable callus induction. The friable callus was used for the initiation of cell suspension culture. MS salts in combination with 4.4 µM BA and 2.6 µM NAA, 3% sucrose was appropriate for cell growth and bioactive compound accumulation. The cell suspension cultures were then treated with SA (0.1, 0.75 and 1.5 mM) as an elicitor for four weeks. An up regulation of enzymatic antioxidants, ascorbate peroxidase (APX); superoxide dismutase (SOD) and catalase (CAT) activity with increasing concentrations of SA whereas a reduction in guaiacol peroxidase (GPX) activity was recorded at the end of the growth phase. The results also showed that higher concentrations of SA significantly increased malondialdehyde (MDA) and Proline content. Cell suspension culture was then subjected to extraction and isolation. The quantification of carvone through HPLC analysis revealed highest amount of carvone (0.063%) in cell suspension culture treated with 0.1 mM concentration of SA whereas higher concentration 0.75 mM SA showed reduction in amount (0.035%) of carvone. SA elicited cell suspension culture offered an effective and favorable method to improve the production of carvone for its potential use in pharmaceuticals.
该研究阐述了用于提高一种具有重要药用价值但尚未被充分探索的化合物香芹酮产量的系统,香芹酮天然存在于……中。评估了水杨酸(SA)对……中生物量产量、香芹酮生物合成、生长以及主要酶促抗氧化参数的影响。测试了苄基腺嘌呤(BA)和1-萘乙酸(NAA)不同组合的效果。含有1.76 μM BA + 3.24 μM NAA的Murashige和Skoog(MS)培养基最适合诱导易碎愈伤组织。易碎愈伤组织用于启动细胞悬浮培养。MS盐与4.4 μM BA和2.6 μM NAA、3%蔗糖组合适合细胞生长和生物活性化合物积累。然后将细胞悬浮培养物用SA(0.1、0.75和1.5 mM)作为诱导剂处理四周。随着SA浓度增加,酶促抗氧化剂抗坏血酸过氧化物酶(APX)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性上调,而在生长阶段结束时记录到愈创木酚过氧化物酶(GPX)活性降低。结果还表明,较高浓度的SA显著增加了丙二醛(MDA)和脯氨酸含量。然后对细胞悬浮培养物进行提取和分离。通过高效液相色谱(HPLC)分析对香芹酮进行定量,结果显示在0.1 mM浓度SA处理的细胞悬浮培养物中香芹酮含量最高(0.063%),而较高浓度0.75 mM SA处理的香芹酮含量降低(0.035%)。SA诱导的细胞悬浮培养提供了一种有效且有利的方法来提高香芹酮产量,以便其在制药领域具有潜在用途。