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首页> 外文期刊>Revista Caatinga >CRESCIMENTO, ATIVIDADE ENZIMáTICA E ANTIOXIDANTE DE MANJERIC?O CULTIVADO IN VITRO
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CRESCIMENTO, ATIVIDADE ENZIMáTICA E ANTIOXIDANTE DE MANJERIC?O CULTIVADO IN VITRO

机译:曼杰的生长,酶活性和抗氧化剂?体外栽培

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Sweet basil is a perennial herb. Studies on in vitro cultivation of these plant species are scarce and inconclusive. This study was carried out to investigate the effect of culture medium concentration in combination with antioxidants and plant growth regulators on the in vitro growth and biochemical activity of sweet basil seedlings. Seeds of the ‘Genovese’ cultivar were inoculated into Murashige and Skoog culture medium supplemented with activated carbon and plant growth regulators 6 -benzylaminopurine and a-naphthaleneacetic acid. The seedlings were grown under controlled conditions for 80 days and their biometric and biochemical characteristics evaluated. More abnormal seedlings were observed in the 100% medium with 30 g L-1 sucrose, 0.4 g L-1 6-benzylaminopurine, and 0.2 g L-1 a-naphthaleneacetic acid (T4) and the medium without regulators (T1). However, the T4 culture medium resulted in a higher leaf number and shoot dry mass. Antioxidant activity was higher in the seedlings grown in the culture medium composed of 100% medium 3.0 g L-1 activated carbon 0.4 mg L-1 6-benzylaminopurine 0.2 mg L-1 a-naphthaleneacetic acid (T5) and that composed of 70% medium 3.0 g L-1 activated carbon 0.1 mg L-1 6-benzylaminopurine (T3). The enzyme superoxide dismutase showed higher activity in all culture media than catalase or ascorbate peroxidase. Sweet basil seedlings growing in T4 and T1 medium showed the highest growth rate of shoots and the lowest antioxidant activity, whereas seedlings grown in T3 medium had the highest catalase and ascorbate peroxidase activity.
机译:甜蜜的罗勒是一个多年生草本植物。这些植物物种的体外培养的研究稀缺和不确定。进行该研究以研究培养基培养基浓度与抗氧化剂和植物生长调节剂组合的影响甜罗勒幼苗的体外生长和生化活性。将“Genovese”品种的种子接种到补充有活性炭和植物生长调节剂6-苄氨基嘌呤和萘酸甲酸的Murashige和Skoog培养基。幼苗在受控条件下生长80天,并评估其生物化学和生物化学特性。在100%培养基中观察到更多异常的幼苗,其中30g L-1蔗糖,0.4g L-1 6-苄基氨基嘌呤,0.2g L-1 a-萘酸酸(T4)和没有调节剂的培养基(T1)。然而,T4培养基导致更高的叶子数和芽干肿块。在由100%培养基3.0g L-1活性炭0.4mg L-1 6-苄基氨基嘧啶0.2mg L-1a-萘酰基乙酸(T5)组成的培养基中生长的抗氧化活性较高,由70%组成培养基3.0g L-1活性炭0.1mg L-1 6-苄氨基嘌呤(T3)。酶超氧化物歧化酶在所有培养基中显示出高于过氧化氢酶或抗坏血酸过氧化物酶。生长在T4和T1培养基中的甜罗勒幼苗显示出芽的最高生长率和最低的抗氧化剂活性,而在T3培养基中生长的幼苗具有最高的过氧化氢酶和抗坏血酸过氧化物酶活性。

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