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1.
Physiol Plant ; 115(2): 213-220, 2002 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-12060238

RESUMEN

The non-enzymatic modification of proteins through the Maillard reaction plays an important role in the loss of seed viability during seed storage. In the present study we examined whether the Maillard reaction reduces the activities of scavenging enzymes in Vigna radiata (mung bean) seeds during storage. Seeds were stored under various conditions for different duration. Maillard products were monitored by measuring protein fluorescence, and the activities of glutathione reductase (GR), superoxide dismutase (SOD), ascorbate peroxidase (APX), catalase (CAT) and peroxidase (POX) were determined. The accumulation of Maillard products in seed axes increased during storage with increasing moisture content and temperature, and was correlated with the decline in seed vigour. The activities of GR, CAT and APX decreased in proportion to the increase in Maillard products at all the moisture contents and temperatures tested. These enzymatic changes were also correlated with seed vigour. However, the activities of SOD and POX remained unchanged and appeared to be less sensitive to the Maillard reaction.

2.
FEBS Lett ; 586(24): 4282-8, 2012 Dec 14.
Artículo en Inglés | MEDLINE | ID: mdl-22801216

RESUMEN

Genome inspection revealed nine putative heme-binding, FixL-homologous proteins in Chlamydomonas reinhardtii. The heme-binding domains from two of these proteins, FXL1 and FXL5 were cloned, expressed in Escherichia coli, purified and characterized. The recombinant FXL1 and FXL5 domains stained positively for heme, while mutations in the putative ligand-binding histidine FXL1-H200S and FXL5-H200S resulted in loss of heme binding. The FXL1 and FXL5 [Fe(II), bound O(2)] had Soret absorption maxima around 415 nm, and weaker absorptions at longer wavelengths, in concurrence with the literature. Ligand-binding measurements showed that FXL1 and FXL5 bind O(2) with moderate affinity, 135 and 222 µM, respectively. This suggests that Chlamydomonas may use the FXL proteins in O(2)-sensing mechanisms analogous to that reported in nitrogen-fixing bacteria to regulate gene expression.


Asunto(s)
Proteínas Bacterianas/metabolismo , Chlamydomonas reinhardtii/metabolismo , Hemo/metabolismo , Hemoproteínas/metabolismo , Oxígeno/metabolismo , Secuencia de Aminoácidos , Proteínas Bacterianas/química , Proteínas Bacterianas/genética , Sitios de Unión , Chlamydomonas reinhardtii/genética , Escherichia coli/metabolismo , Genoma Bacteriano , Hemoproteínas/química , Hemoproteínas/genética , Histidina/química , Histidina Quinasa , Datos de Secuencia Molecular , Mutación , Fosforilación , Espectrofotometría
3.
Ann Bot ; 96(5): 737-43, 2005 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16033778

RESUMEN

AIMS: The molecular mechanisms that correlate with gravity perception and signal transduction in the tip of angiosperm primary roots are discussed. SCOPE: Gravity provides a cue for downward orientation of plant roots, allowing anchorage of the plant and uptake of the water and nutrients needed for growth and development. Root gravitropism involves a succession of physiological steps: gravity perception and signal transduction (mainly mediated by the columella cells of the root cap); signal transmission to the elongation zone; and curvature response. Interesting new insights into gravity perception and signal transduction within the root tip have accumulated recently by use of a wide range of experimental approaches in physiology, biochemistry, genetics, genomics, proteomics and cell biology. The data suggest a network of signal transduction pathways leading to a lateral redistribution of auxin across the root cap and a possible involvement of cytokinin in initial phases of gravicurvature. CONCLUSION: These new discoveries illustrate the complexity of a highly redundant gravity-signalling process in roots, and help to elucidate the global mechanisms that govern auxin transport and morphogenetic regulation in roots.


Asunto(s)
Gravitropismo/fisiología , Raíces de Plantas/crecimiento & desarrollo , Raíces de Plantas/fisiología , Transducción de Señal/fisiología , Canales Iónicos/fisiología , Reguladores del Crecimiento de las Plantas/fisiología , Proteínas de Plantas/metabolismo , Raíces de Plantas/genética
4.
J Exp Bot ; 54(384): 1057-67, 2003 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-12598575

RESUMEN

Two primary biochemical reactions in seed ageing (lipid peroxidation and non-enzymatic protein glycosylation with reducing sugars) have been studied under different seed water contents and storage temperatures, and the role of the glassy state in retarding biochemical deterioration examined. The viability loss of Vigna radiata seeds during storage is associated with Maillard reactions; however, the contribution of primary biochemical reactions varies under different storage conditions. Biochemical deterioration and viability loss are greatly retarded in seeds stored below a high critical temperature (approximately 40 degrees C above glass transition temperature). This high critical temperature corresponds to the cross-over temperature (T(c)) of glass transition where molecular dynamics changes from a solid-like system to a normal liquid system. The data show that seed ageing slows down significantly, even before seed tissue enters into the glassy state.


Asunto(s)
Fabaceae/metabolismo , Semillas/metabolismo , Metabolismo de los Hidratos de Carbono , Fabaceae/química , Fabaceae/crecimiento & desarrollo , Germinación/fisiología , Glucosa/metabolismo , Peroxidación de Lípido/fisiología , Reacción de Maillard , Semillas/química , Semillas/crecimiento & desarrollo , Temperatura , Factores de Tiempo , Agua/metabolismo
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