Effect of lead treatment on medicarpin accumulation and on the gene expression of key enzymes involved in medicarpin biosynthesis in Medicago sativa L

被引:14
|
作者
Ghelich, Sima [1 ]
Zarinkamar, Fatemeh [1 ]
Soltani, Bahram Mohammad [1 ]
Niknam, Vahid [2 ,3 ]
机构
[1] Tarbiat Modares Univ, Fac Biol Sci, Tehran, Iran
[2] Univ Tehran, Sch Biol, Coll Sci, Tehran, Iran
[3] Univ Tehran, Ctr Excellence Phylogeny Living Organisms, Coll Sci, Tehran, Iran
关键词
Lead; Medicarpin; PAL; CHS; VR; Isoflavonoids; Medicago sativa L; PHENYLALANINE AMMONIA-LYASE; PHENYLPROPANOID PATHWAY; ISOFLAVONE REDUCTASE; VESTITONE REDUCTASE; PLANT DEFENSE; TOXICITY; RESPONSES; ROOTS; MAIZE; PB;
D O I
10.1007/s11356-014-3335-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Lead (Pb) is the most common heavy metal contaminant in the environment. The present study was undertaken to determine the effect of Pb treatment on medicarpin production and accumulation in Medicago sativa L. To this aim, 7- and 30-day-old plants were treated with 0, 120, 240, 500, and 1,000 mu M Pb during 10 days. The content of medicarpin was determined by HPLC, and the extent of medicarpin production was deduced from the result of semiquantitative RT-PCR performed on PAL, CHS, and VR genes. HPLC results indicated that medicarpin concentration has been reduced in the roots, while its exudation to the culture medium has been increased. RT-PCR results indicated that the transcript levels of PAL, CHS, and VR genes have not been affected following Pb stress in seedlings. At the vegetative stage, transcript levels of PAL and CHS genes have been reduced in the roots. However, the transcript level of VR gene increased at 120 and 240 mu M Pb, while it decreased at higher concentrations. In the shoot, the transcript levels of PAL, CHS, and VR genes were increased following increased concentration of lead in the medium. Overall, q-PCR results suggest that medicarpin biosynthesis has been induced in the shoots and reduced in the roots of the plants treated with a toxic concentration of Pb.
引用
收藏
页码:14091 / 14098
页数:8
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