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1.
Chemosphere ; 235: 734-748, 2019 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-31280042

RESUMEN

Jasmonic acid (JA) is an important phytohormone associated in defense responses against stress. Crop plants experience heavy metal toxicity and needs to be explored to enhance the crop production. Lead (Pb) is one of the dangerous heavy metal that pollutes soil and water bodies and is released from various sources like discharge from batteries, automobile exhaust, and paints. The present study was designed to evaluate the role of JA (100 nM) on photosynthetic pigments, secondary metabolites, organic acids, and metal ligation compounds in tomato seedlings under different concentrations of Pb (0.25, 0.50, and 0.75 mM). It was observed that Pb treatment declined pigment content, relative water content, and heavy metal tolerance index. Expression of chlorophyllase was also enhanced in Pb-treated seedlings. Seeds primed with JA lowered the expression of chlorophyllase under Pb stress. JA application enhanced the contents of secondary metabolites (total phenols, polyphenols, flavonoids, and anthocyanin) which were confirmed with enhanced expression of chalcone synthase and phenylalanine ammonia lyase in Pb-exposed seedlings. Treatment of JA further elevated the levels of organic acids and metal chelating compounds under Pb toxicity. JA up-regulated the expression of succinate dehydrogenase and fumarate hydratase in Pb-exposed seedlings. Results revealed that seeds primed with JA reduced Pb toxicity by elevating, the levels of photosynthetic pigments, secondary metabolites, osmolytes, metal ligation compounds, organic acids, and polyamine accumulation in tomato seedlings.


Asunto(s)
Ciclopentanos/química , Plomo/química , Oxilipinas/química , Contaminantes del Suelo/química , Solanum lycopersicum/fisiología , Ciclopentanos/metabolismo , Expresión Génica , Inactivación Metabólica/genética , Plomo/metabolismo , Plomo/toxicidad , Solanum lycopersicum/genética , Solanum lycopersicum/metabolismo , Oxilipinas/metabolismo , Fenoles/metabolismo , Fotosíntesis , Reguladores del Crecimiento de las Plantas/metabolismo , Polifenoles/metabolismo , Plantones/metabolismo , Semillas/metabolismo , Contaminantes del Suelo/toxicidad
2.
Sci Rep ; 9(1): 3524, 2019 03 05.
Artículo en Inglés | MEDLINE | ID: mdl-30837530

RESUMEN

Lead (Pb) toxicity is a major environmental concern affirming the need of proper mitigation strategies. In the present work, potential of combined treatment of 24-Epibrassinolide (24-EBL) and Salicylic acid (SA) against Pb toxicity to Brassica juncea L. seedlings were evaluated. Seedlings pre-imbibed in EBL (0.1 mM) and SA (1 mM) individually and in combination, were sown in Pb supplemented petri-plates (0.25, 0.50 and 0.75 mM). Various microscopic observations and biochemical analysis were made on 10 days old seedlings of B. juncea. The toxic effects of Pb were evident with enhancement in in-situ accumulation of Pb, hydrogen peroxide (H2O2), malondialdehyde (MDA), nuclear damage, membrane damage, cell death and polyamine. Furthermore, free amino acid were lowered in response to Pb toxicity. The levels of osmoprotectants including total carbohydrate, reducing sugars, trehalose, proline and glycine betaine were elevated in response to Pb treatment. Soaking treatment with combination of 24-EBL and SA led to effective amelioration of toxic effects of Pb. Reduction in Pb accumulation, reactive oxygen content (ROS), cellular damage and GSH levels were noticed in response to treatment with 24-EBL and SA individual and combined levels. The contents of free amino acid, amino acid profiling as well as in-situ localization of polyamine (spermidine) was recorded to be enhanced by co-application of 24-EBLand SA. Binary treatment of 24-EBL and SA, further elevated the content of osmoprotectants. The study revealed that co-application of combined treatment of 24-EBL and SA led to dimination of toxic effects of Pb in B. juncea seedlings.


Asunto(s)
Brasinoesteroides/farmacología , Plomo/metabolismo , Planta de la Mostaza/metabolismo , Ácido Salicílico/farmacología , Esteroides Heterocíclicos/farmacología , Aminoácidos/metabolismo , Daño del ADN/efectos de los fármacos , Glutatión/metabolismo , Peróxido de Hidrógeno/metabolismo , Plomo/toxicidad , Malondialdehído/metabolismo , Microscopía Confocal , Planta de la Mostaza/efectos de los fármacos , Planta de la Mostaza/crecimiento & desarrollo , Poliaminas/metabolismo , Especies Reactivas de Oxígeno/metabolismo , Plantones/efectos de los fármacos , Plantones/metabolismo , Trehalosa/metabolismo
3.
Dalton Trans ; 42(13): 4456-63, 2013 Apr 07.
Artículo en Inglés | MEDLINE | ID: mdl-23385981

RESUMEN

Hexaphenylbenzene (HPB) derivatives 5 and 7 having rhodamine B moieties have been designed and synthesized, and have been shown to display solvent dependent. Fluorescence resonance energy transfer (FRET) and through bond energy transfer (TBET) in the presence of Hg(2+) ions among the various cations (Cu(2+), Pb(2+), Zn(2+), Ni(2+), Cd(2+), Ag(+), Ba(2+), Mg(2+), K(+), Na(+), and Li(+)) have been tested. Derivative 5 displays quite high through bond energy transfer efficiency in the presence of Hg(2+) ions in methanol whereas derivative 7 exhibits better FRET efficiency in the presence of Hg(2+) ions in THF and CH(3)CN than derivative 5.

4.
Dalton Trans ; 41(34): 10182-8, 2012 Sep 14.
Artículo en Inglés | MEDLINE | ID: mdl-22842337

RESUMEN

A new terphenyl-based macrocycle 5 incorporating phenanthroline as a fluorophore has been designed, synthesized and examined for its recognition ability toward various cations (Pb(2+), Hg(2+), Ba(2+), Cd(2+), Ag(+), Zn(2+), Cu(2+), Ni(2+), Co(2+), K(+), Mg(2+), Na(+) and Li(+)) by UV-vis, fluorescence and NMR spectroscopy. The receptor 5 showed highly selective 'Off-On' fluorescence signaling behavior for Zn(2+) ions in THF. Interestingly, the addition of H(2)PO(4)(-) ions to the [5-Zn] complex regulates the binding site for additional Zn(2+) ions and hence leads to a blue-shifted emission band.


Asunto(s)
Fenantrolinas/química , Ácidos Fosfóricos/química , Espectrofotometría Ultravioleta , Compuestos de Terfenilo/química , Zinc/análisis , Iones/química , Metales/química
5.
Dalton Trans ; 41(2): 403-7, 2012 Jan 14.
Artículo en Inglés | MEDLINE | ID: mdl-21931914

RESUMEN

A new terphenyl based chemosensor 3 has been designed and synthesized. The binding behavior of 3 and its chemosensing ensemble 3-Hg toward various anions (F(-), Cl(-), Br(-), I(-), HSO(4)(-), H(2)PO(4)(-), CH(3)COO(-), NO(3)(-), N(3)(-), SO(4)(2-), SO(3)(2-), and Cr(2)O(7)(2-)) has been investigated by UV-Vis, fluorescence and NMR spectroscopy. Compound 3 shows a sensitivity for both F(-) and CH(3)COO(-) ions among various anions tested, whereas the ensemble 3-Hg shows a better selectivity for CH(3)COO(-) ions. The ensemble is utilized for CH(3)COO(-) recognition in a blood plasma like system.


Asunto(s)
Acetatos/sangre , Colorantes Fluorescentes/síntesis química , Compuestos Organomercuriales/síntesis química , Compuestos de Terfenilo/síntesis química , Acetatos/química , Colorantes Fluorescentes/química , Estructura Molecular , Compuestos Organomercuriales/química , Espectrometría de Fluorescencia , Espectrofotometría Ultravioleta , Compuestos de Terfenilo/química
6.
Inorg Chem ; 48(24): 11677-84, 2009 Dec 21.
Artículo en Inglés | MEDLINE | ID: mdl-19877709

RESUMEN

New terphenyl-based reversible receptors 1-4 with pyrene and quinoline as the fluorophores have been designed, synthesized, and examined for their cation recognition abilities toward various cations (Sm(3+), Nd(3+), Pb(2+), Hg(2+), Ba(2+), Cd(2+), Ag(+), Zn(2+), Cu(2+), Ni(2+), Co(2+), Fe(2+), Fe(3+), K(+), Mg(2+), Na(+), and Li(+)) by UV-vis, fluorescence, and NMR spectroscopy. The prepared receptors showed the highly selective and sensitive "Off-On" fluorescence signaling behavior for Hg(2+) ions in THF and mixed aqueous media (THF:H(2)O, 9.5:0.5).


Asunto(s)
Colorantes Fluorescentes/química , Mercurio/análisis , Compuestos de Terfenilo/química , Colorantes Fluorescentes/síntesis química , Estructura Molecular , Pirenos/química , Quinolinas/química , Compuestos de Terfenilo/síntesis química
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