Fazal Hina, Abbasi Bilal Haider, Ahmad Nisar, Ali Mohammad
1Department of Plant Sciences, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, 45320 Pakistan.
Pakistan Council of Scientific and Industrial Research (PCSIR) Laboratories Complex, Peshawar, 25120 Pakistan.
Physiol Mol Biol Plants. 2018 Nov;24(6):1307-1315. doi: 10.1007/s12298-018-0567-7. Epub 2018 Jun 18.
The objective of the current study was to monitor the variations caused by the application of exogenous melatonin on growth kinetics and production of stress enzymes in . Leaf and petiole explants were used for callogenesis. These explants were inoculated on Murashige and Skoog media containing various concentrations of melatonin alone or in combination with 2.0 mg/l naphthalene acetic acid. Herein, a maximum of 3.18-g/100 ml fresh biomass accumulation was observed on day 35 during log phase of growth kinetics at 1.0 mg/l melatonin concentration from leaf explants. While 0.5 and 1.0 mg/l melatonin enhanced the biomass accumulation from petiole explants. Moreover, the synergistic combination of melatonin and naphthalene acetic acid also promoted growth from leaf and petiole explants. Leaf derived callus cultures treated with 1.0 mg/l melatonin induced the production of total protein content (90.47 μg BSAE/mg FW) and protease activity (4.77 U/g FW). While the calli obtained from petiole explants have shown highest content of total protein (160.8 μg BSAE/mg FW) and protease activity (5.35 U/g FW) on media containing 0.5 mg/l melatonin. Similarly, 0.5 mg/l melatonin enhanced superoxide dismutase (3.011 nM/min/mg FW) and peroxidase (1.73 nM/min/mg FW) enzymes from leaf derived callus cultures. The combination of 1.0 and 1.5 mg/l naphthalene acetic acid enhanced content of total protein and protease activity in leaf and petiole derived cultures. These results suggested that the application of melatonin play a positive role in biomass accumulation and production of stress enzymes in .
本研究的目的是监测外源褪黑素的应用对[具体植物名称未给出]生长动力学和应激酶产生的影响。叶片和叶柄外植体用于愈伤组织诱导。将这些外植体接种在含有不同浓度褪黑素单独或与2.0毫克/升萘乙酸组合的Murashige和Skoog培养基上。在此,在生长动力学的对数期第35天,从叶片外植体在1.0毫克/升褪黑素浓度下观察到最大鲜生物量积累为3.18克/100毫升。而0.5和1.0毫克/升褪黑素增强了叶柄外植体的生物量积累。此外,褪黑素和萘乙酸的协同组合也促进了叶片和叶柄外植体的生长。用1.0毫克/升褪黑素处理的叶片来源的愈伤组织培养物诱导了总蛋白含量(90.47微克牛血清白蛋白当量/毫克鲜重)和蛋白酶活性(4.77单位/克鲜重)的产生。而从叶柄外植体获得的愈伤组织在含有0.5毫克/升褪黑素的培养基上显示出最高的总蛋白含量(160.8微克牛血清白蛋白当量/毫克鲜重)和蛋白酶活性(5.35单位/克鲜重)。同样,0.5毫克/升褪黑素增强了叶片来源的愈伤组织培养物中的超氧化物歧化酶(3.011纳摩尔/分钟/毫克鲜重)和过氧化物酶(1.73纳摩尔/分钟/毫克鲜重)活性。1.0和1.5毫克/升萘乙酸的组合提高了叶片和叶柄来源的培养物中的总蛋白含量和蛋白酶活性。这些结果表明,褪黑素的应用对[具体植物名称未给出]的生物量积累和应激酶的产生起到了积极作用。