Plant Responses to Arsenic: the Role of Nitric Oxide

被引:26
作者
Farnese, Fernanda S. [1 ]
de Oliveira, Juraci A. [2 ]
Gusman, Grasielle S. [3 ]
Leao, Gabriela A. [1 ]
Ribeiro, Cleberson [2 ]
Siman, Luhan I. [2 ]
Cambraia, Jose [2 ]
机构
[1] Univ Fed Vicosa, Dept Plant Biol, BR-36570000 Vicosa, MG, Brazil
[2] Univ Fed Vicosa, Dept Gen Biol, BR-36570000 Vicosa, MG, Brazil
[3] Univ Fed Minas Gerais, Coll Pharm, BR-31270901 Belo Horizonte, MG, Brazil
关键词
Antioxidants; Toxicity; Phytochelatins; Cellular Signaling; Sulfate Uptake; HYDROGEN-PEROXIDE; METABOLISM; STRESS; HYPERACCUMULATION; PHYTOCHELATINS; ACCUMULATION; TOLERANCE;
D O I
10.1007/s11270-013-1660-8
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Arsenic (As) toxicity and the effects of nitric oxide (NO), supplied as sodium nitroprusside (SNP), were analyzed in Pistia stratiotes. The plants, which were grown in nutrient solution at pH 6.5, were exposed to four treatments for 24 h: control; SNP (0.1 mg L-1); As (1.5 mg L-1); and As + SNP (1.5 and 0.1 mg L-1). As accumulated primarily in the roots, indicating the low translocation factor of P. stratiotes. The As accumulation triggered a series of changes with increasing production of reactive oxygen intermediates and damage to cell membranes. The application of SNP was able to mitigate the harmful effects of As. This attenuation was probably due to the action of the SNP as an antioxidant, reducing the superoxide anion concentration, and as a signaling agent. Acting as a signal transducer, SNP increased the activity of enzymatic antioxidants (POX, CAT, and APX) in the leaves and stimulated the entire phytochelatins biosynthetic pathway in the roots (increased sulfate uptake and synthesis of amino acids, non-proteinthiols, and phytochelatins). The As also stimulated the phytochelatins biosynthesis, but this effect was limited, probably because plants exposed only to pollutant showed small increments in the sulfate uptake. Thus, NO also may be involved in gene regulation of sulfate carriers.
引用
收藏
页数:11
相关论文
共 33 条
[1]   Nitric oxide as a bioactive signalling molecule in plant stress responses [J].
Arasimowicz, Magdalena ;
Floryszak-Wieczorek, Jolanta .
PLANT SCIENCE, 2007, 172 (05) :876-887
[2]  
Beauchamp C., 1971, ANAL BIOCHEM, V44, P267
[3]   Measurement of superoxide radical and hydrogen peroxide production in isolated cells and subcellular organelles [J].
Boveris, A ;
Alvarez, S ;
Bustamante, J ;
Valdez, L .
SUPEROXIDE DISMUTASE, 2002, 349 :280-287
[4]   METHOD FOR CHARACTERIZING RELATION BETWEEN NUTRIENT CONCENTRATION AND FLUX INTO ROOTS OF INTACT PLANTS [J].
CLAASSEN, N ;
BARBER, SA .
PLANT PHYSIOLOGY, 1974, 54 (04) :564-568
[5]   CHARACTERIZATION OF PHOSPHATASE OF INTACT MAIZE ROOTS [J].
CLARK, RB .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1975, 23 (03) :458-460
[6]   A critical evaluation of the effect of sorbitol on the ferric-xylenol orange hydroperoxide assay [J].
Gay, C ;
Gebicki, JM .
ANALYTICAL BIOCHEMISTRY, 2000, 284 (02) :217-220
[7]   SUPEROXIDE DISMUTASES .1. OCCURRENCE IN HIGHER-PLANTS [J].
GIANNOPOLITIS, CN ;
RIES, SK .
PLANT PHYSIOLOGY, 1977, 59 (02) :309-314
[8]   Cross Talk among Calcium, Hydrogen Peroxide, and Nitric Oxide and Activation of Gene Expression Involving Calmodulins and Calcium-Dependent Protein Kinases in Ulva compressa Exposed to Copper Excess [J].
Gonzalez, Alberto ;
de los Angeles Cabrera, M. ;
Josefa Henriquez, M. ;
Contreras, Rodrigo A. ;
Morales, Bernardo ;
Moenne, Alejandra .
PLANT PHYSIOLOGY, 2012, 158 (03) :1451-1462
[10]   Arsenate and arsenite: the toxic effects on photosynthesis and growth of lettuce plants [J].
Gusman, Grasielle S. ;
Oliveira, Juraci A. ;
Farnese, Fernanda S. ;
Cambraia, Jose .
ACTA PHYSIOLOGIAE PLANTARUM, 2013, 35 (04) :1201-1209