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Chromium has been studied since the end of the 19th century, when carcinogenic effects of hexavalent Cr were discovered. Essentiality of trivalent Cr was demonstrated in 1959; Cr3+ has been studied in humans and laboratory animals since the 1970s and it is only since the 1990s that Cr has been studied as an essential element in livestock animals with the same intensity. Trivalent Cr is essential to normal carbohydrate, lipid and protein metabolism. It is biologically active as part of an oligopeptide - chromodulin - potentiating the effect of insulin by facilitating insulin binding to receptors at the cell surface. Cr absorption is low, ranging between 0.4 and 2.0% for inorganic compounds while the availability of organic Cr is more than 10 times higher. Absorbed Cr circulates in blood bound to the beta-globulin plasma fraction and is transported to tissues bound to transferrin. Absorbed Cr is excreted primarily in urine, by glomerular filtration; a small amount is excreted through perspiration, bile and in milk. This review describes Cr metabolism, the different biological functions of Cr and symptoms of Cr deficiency.

Introduction. Consumers and processors value tomatoes with high fruit sugar content; however, most breeding and cultural practices negatively impact this trait. Wild tomato species can accumulate two- to three-fold more fruit sugar than cultivars and are proving to be valuable both as a source of high-sugar loci to broaden the genetic base of currently produced cultivars, and as research material to understand this trait. Synthesis. While cutting-edge genomic approaches have taught us much about fruit phenotypes, it is still important to assess fruit enzyme activities and metabolic fluxes in lines with contrasting fruit sugar accumulation. These metabolic functions are closest to the ripe fruit sugar trait. In this review, we focus our attention on the biochemical pathways, especially starch biosynthesis, that may influence tomato fruit sugars. We try where possible to put this information into a physiological context because together they influence yield. We compare and contrast sugar metabolism in cultivars and wild tomato species and identify factors that may influence differences in their fruit size. Conclusion. Although difficult, we show that it is possible to develop fruit with high horticultural yield and use the breeding line ‘Solara’ as an example. In addition, we suggest avenues of further investigation to understand the regulation and control of fruit carbohydrate content. Introduction. Les consommateurs et les industriels apprécient les tomates avec un fort taux en sucres, mais la plupart des pratiques culturales et d’amélioration ont un impact négatif sur ce caractère. Les espèces de tomate sauvage peuvent accumuler 2 ou 3 fois plus de sucres dans le fruit que des cultivars et elles s’avèrent précieuses à la fois comme une source de loci à haute teneur en sucres pour élargir la base génétique des cultivars actuellement produits, et comme matériel de recherche pour comprendre ce caractère. Synthèse. Alors que les approches génomiques de pointe nous ont appris beaucoup sur le phénotype des fruits, il reste important d’évaluer l’activité des enzymes de fruits et les flux métaboliques dans des lignées présentant des situations contrastées d’accumulation de sucres dans les fruits. Ces fonctions métaboliques sont les plus proches du caractère de teneur en sucres dans le fruit mûr. Dans cette synthèse, nous nous sommes focalisés sur les voies biochimiques, en particulier sur la biosynthèse de l’amidon qui peut influencer les sucres dans le fruit des tomates. Nous essayons autant que possible de mettre cette information dans un contexte physiologique car, ensemble, ils influencent le rendement. Nous comparons et mettons en contraste le métabolisme des sucres dans les cultivars et les espèces sauvages de tomate et nous identifions les facteurs qui peuvent influencer des différences de taille des fruits. Conclusion. Bien que cela soit difficile, nous montrons qu’il est possible de produire des fruits présentant un rendement horticole élevé et nous utilisons la lignée sélectionnée “ Solara ” comme exemple. En outre, nous suggérons des pistes de recherches supplémentaires pour comprendre la régulation et le contrôle du contenu en glucides des fruits. Introducción. Los consumidores e industriales aprecian los tomates con un fuerte índice de azúcares, pero la mayoría de las prácticas relativas al cultivo y de mejora tienen un impacto negativo sobre este rasgo característico. Las especies de tomate salvaje pueden acumular 2 ó 3 veces más azúcares en el fruto que los cultivares, y resultan ser apreciadas como fuente de loci de alto contenido en azúcares para aumentar la base genética de los cultivares actualmente producidos y como material de investigación para comprender dicho rasgo característico. Síntesis. A pesar de que los acercamientos genómicos punteros nos hayan enseñado mucho sobre el fenotipo de los frutos, sigue siendo importante evaluar la actividad de las encimas de los frutos, así como los flujos metabólicos en líneas que presenten situaciones contrastadas de acumulación de azúcares en los frutos. Dichas funciones metabólicas son las que más se acercan al rasgo característico del contenido de azúcares en el fruto maduro. En esta síntesis, nos centramos en las vías bioquímicas, particularmente en la biosíntesis del almidón, que puede influenciar los azúcares en el fruto del tomate. Intentamos, en la medida de lo posible, situar esta información en un contexto fisiológico, ya que, conjuntamente, influencian el rendimiento. Comparamos y contrastamos el metabolismo de los azúcares en los cultivares y en las especies salvajes de tomate, e identificamos los factores que pueden influenciar las diferencias en el tamaño de los frutos. Conclusión. A pesar de la dificultad, ilustramos la posibilidad de producir frutos que presenten un elevado rendimiento y utilizamos la línea seleccionada “ Solara ” como ejemplo. Además, sugerimos vías de investigación suplementarias para comprender la regulación y el control del contenido de glúcidos de los frutos.

Nia30(145) transformants with very low nitrate reductase activity provide an in vivo screen to identify processes that are regulated by nitrate. Nia30(145) resembles nitrate-limited wild-type plants with respect to growth rate and protein and amino acid content but accumulates large amounts of nitrate when it is grown on high nitrate. The transcripts for nitrate reductase (NR), nitrite reductase, cytosolic glutamine synthetase, and glutamate synthase increased; NR and nitrite reductase activity increased in leaves and roots; and glutamine synthetase activity increased in roots. The transcripts for phosphoenolpyruvate carboxylase, cytosolic pyruvate kinase, citrate synthase, and NADP-isocitrate dehydrogenase increased; phosphoenolpyruvate carboxylase activity increased; and malate, citrate, isocitrate, and alpha-oxoglutarate accumulated in leaves and roots. There was a decrease of the ADP-glucose pyrophosphorylase transcript and activity, and starch decreased in the leaves and roots. After adding 12 mM nitrate to nitrate-limited Nia30(145), the transcripts for NR and phosphoenolpyruvate carboxylase increased, and the transcripts for ADP-glucose pyrophosphorylase decreased within 2 and 4 hr, respectively. Starch was remobilized at almost the same rate as in wildtype plants, even though growth was not stimulated in Nia30(145). It is proposed that nitrate acts as a signal to initiate coordinated changes in carbon and nitrogen metabolism.

During oil deposition in developing seeds of Arabidopsis, photosynthate is imported in the form of carbohydrates into the embryo and converted to triacylglycerols. To identify genes essential for this process and to investigate the molecular basis for the developmental regulation of oil accumulation, mutants producing wrinkled, incompletely filled seeds were isolated. A novel mutant locus, wrinkled1 (wri1), which maps to the bottom of chromosome 3 and causes an 80% reduction in seed oil content, was identified. Wild-type and homozygous wri1 mutant plantlets or mature plants were indistinguishable. However, developing homozygous wri1 seeds were impaired in the incorporation of sucrose and glucose into triacylglycerols, but incorporated pyruvate and acetate at an increased rate. Because the activities of several glycolytic enzymes, in particular hexokinase and pyrophosphate-dependent phosphofructokinase, are reduced in developing homozygous wri1 seeds, it is suggested that WRI1 is involved in the developmental regulation of carbohydrate metabolism during seed filling

The mechanisms by which higher plants recognize and respond to sugars are largely unknown. Here, we present evidence that the first enzyme in the hexose assimilation pathway, hexokinase (HXK), acts as a sensor for plant sugar responses. Transgenic Arabidopsis plants expressing antisense hexokinase (AtHXK) genes are sugar hyposensitive, whereas plants overexpressing AtHXK are sugar hypersensitive. The transgenic plants exhibited a wide spectrum of altered sugar responses in seedling development and in gene activation and repression. Furthermore, overexpressing the yeast sugar sensor YHXK2 caused a dominant negative effect by elevating HXK catalytic activity but reducing sugar sensitivity in transgenic plants. The result suggests that HXK is a dual-function enzyme with a distinct regulatory function not interchangeable between plants and yeast

Maize (Zea mays L.) plants were grown to the nine-leaf stage. Despite a saturating N supply, the youngest mature leaves (seventh position on the stem) contained little NO3- reserve. Droughted plants (deprived of nutrient solution) showed changes in foliar enzyme activities, mRNA accumulation, photosynthesis, and carbohydrate and amino acid contents. Total leaf water potential and CO2 assimilation rates, measured 3 h into the photoperiod, decreased 3 d after the onset of drought. Starch, glucose, fructose, and amino acids, but not sucrose (Suc), accumulated in the leaves of droughted plants. Maximal extractable phosphoenolpyruvate carboxylase activities increased slightly during water deficit, whereas the sensitivity of this enzyme to the inhibitor malate decreased. Maximal extractable Suc phosphate synthase activities decreased as a result of water stress, and there was an increase in the sensitivity to the inhibitor orthophosphate. A correlation between maximal extractable foliar nitrate reductase (NR) activity and the rate of CO2 assimilation was observed. The NR activation state and maximal extractable NR activity declined rapidly in response to drought. Photosynthesis and NR activity recovered rapidly when nutrient solution was restored at this point. The decrease in maximal extractable NR activity was accompanied by a decrease in NR transcripts, whereas Suc phosphate synthase and phosphoenolpyruvate carboxylase mRNAs were much less affected. The coordination of N and C metabolism is retained during drought conditions via modulation of the activities of Suc phosphate synthase and NR commensurate with the prevailing rate of photosynthesis

Regulation of gene expression by nutrients is an important mechanism in the adaptation of mammals to their nutritional environment. This is especially true for enzymes involved in the storage of energy, such as the lipogenic and glycolytic enzymes in liver and adipose tissue. Transcription of the genes for lipogenic and glycolytic enzymes is stimulated by glucose in adipose tissue, liver, and pancreatic beta-cells. Several lines of evidence suggest that glucose must be metabolized to glucose-6-phosphate to stimulate gene transcription. In adipose tissue, insulin increases the expression of lipogenic enzymes indirectly by stimulating glucose uptake. In the liver, insulin also acts indirectly by stimulating the expression of glucokinase and, hence, by increasing glucose metabolism. Glucose response elements have been characterized for the L-pyruvate kinase and S 14 genes. They have in common the presence of a sequence 5'-CACGTG-3', which binds a transcription factor called USF (upstream stimulatory factor). Another glucose response element, which uses a transcription factor named Sp1, has been characterized in the gene for the acetyl-coenzyme A carboxylase. The mechanisms linking glucose-6-phosphate to the glucose-responsive transcription complex are largely unknown

Sucrose synthase (SuSy; EC 2.4.1.13; sucrose + UDP reversibly UDPglucose + fructose) has always been studied as a cytoplasmic enzyme in plant cells where it serves to degrade sucrose and provide carbon for respiration and synthesis of cell wall polysaccharides and starch. We report here that at least half of the total SuSy of developing cotton fibers (Gossypium hirsutum) is tightly associated with the plasma membrane. Therefore, this form of SuSy might serve to channel carbon directly from sucrose to cellulose and/or callose synthases in the plasma membrane. By using detached and permeabilized cotton fibers, we show that carbon from sucrose can be converted at high rates to both cellulose and callose. Synthesis of cellulose or callose is favored by addition of EGTA or calcium and cellobiose, respectively. These findings contrast with the traditional observation that when UDPglucose is used as substrate in vitro, callose is the major product synthesized. Immunolocalization studies show that SuSy can be localized at the fiber surface in patterns consistent with the deposition of cellulose or callose. Thus, these results support a model in which SuSy exists in a complex with the beta-glucan synthases and serves to channel carbon from sucrose to glucan.

Classical quorum-sensing (autoinduction) regulation, as exemplified by the lux system of Vibrio fischeri, requires N-acyl homoserine lactone (AHL) signals to stimulate cognate transcriptional activators for the cell density-dependent expression of specific target gene systems. For Pantoea stewartii subsp. stewartii, a bacterial pathogen of sweet corn and maize, the extracellular polysaccharide (EPS) stewartan is a major virulence factor, and its production is controlled by quorum sensing in a population density-dependent manner. Two genes, esaI and esaR, encode essential regulatory proteins for quorum sensing. EsaI is the AHL signal synthase, and EsaR is the cognate gene regulator, esaI, delta esaR, and delta esaI-esaR mutations were constructed to establish the regulatory role of EsaR. We report here that strains containing an esaR mutation produce high levels of EPS independently of cell density and in the absence of the AHL signal. Our data indicate that quorum-sensing regulation in P. s. subsp. stewartii, in contrast to most other described systems, uses EsaR to repress EPS synthesis at low cell density, and that derepression requires micromolar amounts of AHL. In addition, derepressed esaR strains, which synthesize EPS constitutively at low cell densities, were significantly less virulent than the wild-type parent. This finding suggests that quorum sensing in P. s. subsp. stewartii may be a mechanism to delay the expression of EPS during the early stages of infection so that it does not interfere with other mechanisms of pathogenesis

Reactive oxygen species (ROS) are both signal molecules and direct participants in plant defense against pathogens. Many fungi synthesize mannitol, a potent quencher of ROS, and there is growing evidence that at least some phytopathogenic fungi use mannitol to suppress ROS-mediated plant defenses. Here we show induction of mannitol production and secretion in the phytopathogenic fungus Alternaria alternata in the presence of host-plant extracts. Conversely, we show that the catabolic enzyme mannitol dehydrogenase is induced in a non-mannitol-producing plant in response to both fungal infection and specific inducers of plant defense responses. This provides a mechanism whereby the plant can counteract fungal suppression of ROS-mediated defenses by catabolizing mannitol of fungal origin.