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外源诱导物对百里香植株再生过程中脂氧合酶活性的影响
引用本文:李翠霞,李志忠,张继.外源诱导物对百里香植株再生过程中脂氧合酶活性的影响[J].草业科学,2012,29(9):1390-1395.
作者姓名:李翠霞  李志忠  张继
作者单位:1. 兰州理工大学生命科学与工程学院,甘肃兰州730050 西北师范大学生命科学院,甘肃兰州730030
2. 兰州理工大学生命科学与工程学院,甘肃兰州,730050
3. 西北师范大学生命科学院,甘肃兰州,730030
基金项目:基金项目:国家自然科学基金,甘肃省科技厅自然科学基金
摘    要:以1/2 MS为基本培养基,分别用不同浓度梯度的蔗糖、NO3-/NH4+、丙氨酸、谷氨酸和丙酮酸处理百里香(Thymus vulgaris)再生植株30 d后,测定其对脂氧合酶(LOX)活性的影响。另外,培养百里香20、30和 40 d 后分别用茉莉酸甲酯、水杨酸和壳聚糖等外源因子对百里香进行处理,在不同的处理时间下测定LOX活性,探讨外源因素对增殖百里香中LOX活性的影响。结果表明,碳氮源调控30 d百里香,蔗糖浓度为4%、NO3-/NH4+比例为2∶1时最高;前体调控添加0.6 mmol·L-1苯丙氨酸和0.4 mmol·L-1谷氨酸诱导LOX活性达到最大值,丙酮酸对LOX酶活几乎无影响;20 d百里香经1.0 mmol·L-1 MeJA喷施诱导48 h后LOX活性为对照的655.4%,经150 mg·L-1 SA诱导12 h后LOX活性为对照的503.8%,经200 mg·L-1壳聚糖诱导24 h后LOX的活性为对照的429.1%。30 d百里香经0.5 mmol·L-1 MeJA诱导48 h后LOX的活性为对照的688.1%,经150 mg·L-1 SA诱导12 h后LOX的活性为对照的383.8%,经200 mg·L-1壳聚糖诱导24 h后LOX的活性为对照的360.8%。40 d百里香在外源处理因素作用下对LOX活性作用不明显。可见,在不同时期用不同处理因素对百里香再生植株进行处理能显著调节LOX的活性。

关 键 词:百里香  脂氧合酶  诱导因素  酶活性

Effects of different factors on fatty acid oxidation activity of thyme
LI Cui-xia,LI Zhi-zhong,ZHANG Ji.Effects of different factors on fatty acid oxidation activity of thyme[J].Pratacultural Science,2012,29(9):1390-1395.
Authors:LI Cui-xia  LI Zhi-zhong  ZHANG Ji
Institution:1.College of Life Science and Engineering,Lanzhou University of Technology,Lanzhou 730050,China; 2.College of Life Science Northwest Normal University,Lanzhou 730030,China)
Abstract:Plantlets of thyme were cultured on the 1/2 MS medium that containing surcose with different concentrations, NO3-/NH4+, phenylalanine, glutamic acid and pyruvic acid. The LOX activity of thyme was tested after 30 d. Furthermore, the plantlets were induced for 0~120 h by MeJA, SA and chitosan at different culture for 20 d, 30 d and 40 d, and LOX activity was tested. The results showed that the highest LOX activity was obtained when the plantlets of thyme were cultured on the 1/2 MS medium with 4% sugar and 2∶1 NO3-/NH4+ ratio for 30 d. The LOX activities were increased respectively when adding 0.6 mmol·L-1 precursor regulation L phenylalanine, 0.4 mmol·L-1 glutamic acid. The LOX activities of plantlets cultured for 20 d were 655.4%, 503.8% and 429.1% more than control by adding 1.0 mmol·L-1 MeJA,150 mg·L-1 SA, and 200 mg·L-1 chitosan. The LOX activities of plantlets cultured for 30 d were increased to 688.1%, 383.8% and 383.3% when adding 0.5 mmol·L-1 MeJA, 150 mg·L-1 SA, and 200 mg·L-1 chitosan, respectively. The LOX activities of plantlets cultured for 40 d did not change. Therefore, the LOX activity was affected by adding different inducer at different time.
Keywords:thyme  Lipoxygenase  inducing factors  enzyme activity
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