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没食子酸丙酯处理通过增强抗坏血酸库和抗氧化酶活性诱导绿色微藻巴达维亚盐藻的耐盐胁迫能力。

The induction of salt stress tolerance by propyl gallate treatment in green microalga Dunaliella bardawil, through enhancing ascorbate pool and antioxidant enzymes activity.

作者信息

Einali Alireza

机构信息

Department of Biology, Faculty of Science, University of Sistan and Baluchestan, Zahedan, Iran.

出版信息

Protoplasma. 2018 Mar;255(2):601-611. doi: 10.1007/s00709-017-1173-1. Epub 2017 Oct 8.

Abstract

The effect of propyl gallate (PG), a synthetic antioxidant, on antioxidant responses and salinity tolerance was investigated in the cells of the green microalga, Dunaliella bardawil. Algal suspensions grown at three salinity levels of 1, 2, and 3 M NaCl were incubated with 1 mM of PG. The number of cells was significantly lower in all PG-treated cells compared to untreated controls. Despite PG-induced cell death, the fresh weight of all PG-treated cells was considerably higher than controls. PG-treated cells had enhanced antioxidant capacity because of increased levels of Chlorophyll a, β-carotene, reduced ascorbate, protein, and enzymatic activities, but accumulated lower levels of malonyldialdehyde and hydrogen peroxide compared to untreated cells. The results suggest that PG acts as a signal molecule both directly by reducing of free radical oxidants and indirectly by augmenting ascorbate pool levels, β-carotene production, and antioxidant enzymes activity to boost the capacity of antioxidant systems and radical oxygen species scavenging. Therefore, induction of salt stress tolerance by PG in D. bardawil is associated with metabolic adjustments through activation or synthesis of both enzymatic and non-enzymatic molecules involved in antioxidant systems.

摘要

研究了合成抗氧化剂没食子酸丙酯(PG)对绿色微藻巴氏杜氏藻细胞抗氧化反应和耐盐性的影响。将在1、2和3M NaCl三个盐度水平下生长的藻类悬浮液与1mM的PG一起孵育。与未处理的对照相比,所有经PG处理的细胞中的细胞数量显著降低。尽管PG诱导细胞死亡,但所有经PG处理的细胞的鲜重均明显高于对照。由于叶绿素a、β-胡萝卜素、还原型抗坏血酸、蛋白质水平和酶活性的增加,经PG处理的细胞具有增强的抗氧化能力,但与未处理的细胞相比,丙二醛和过氧化氢的积累水平较低。结果表明,PG既通过减少自由基氧化剂直接作为信号分子,又通过增加抗坏血酸池水平、β-胡萝卜素产量和抗氧化酶活性间接作为信号分子,以增强抗氧化系统的能力和清除活性氧。因此,PG诱导巴氏杜氏藻的耐盐胁迫与通过激活或合成参与抗氧化系统的酶和非酶分子进行的代谢调节有关。

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