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1.
Plant Physiol Biochem ; 195: 275-287, 2023 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-36652849

RESUMEN

The pericarp of fruit can be differentiated into endocarp, mesocarp, and exocarp. To explore the differences in gene expression and metabolites in different tissues of the pericarp, the fruits of sumac (Toxicodendron vernicifluum) were separated into endocarp and mesocarp-exocarp. The metabolites and transcriptome of exocarp-mesocarp and endocarp of Toxicodendron vernicifluum were analyzed by HPLC-QTOF-MS/MS and RNA sequencing, respectively. A total of 52 phenolic compounds were identified, including 3 phenylpropane derivatives, 10 urushiol compounds and 39 flavonoids. The exocarp-mesocarp contained more urushiol compounds and flavonoid glycosides while the endocarp contained more biflavonoids, such as rhusflavone and dihydromorelloflavone. The characteristic component of endocarp was rhusflavone and the characteristic component of exocarp-mesocarp was urushiol (triene). Most of the genes involved in flavonoid synthesis pathway were upregulated in endocarp compared with exocarp-mesocarp and positively correlated with the content of flavonoids. The candidate genes related to the synthesis of components of flavonoid glycosides and biflavonoids were screened. Metabolomic and transcriptomic analyses provide new insights into the synthesis and distribution of flavonoid glycosides and biflavonoids in the fruits of Toxicodendron vernicifluum.


Asunto(s)
Biflavonoides , Rhus , Toxicodendron , Flavonoides/genética , Flavonoides/metabolismo , Toxicodendron/genética , Toxicodendron/metabolismo , Rhus/genética , Rhus/metabolismo , Biflavonoides/genética , Biflavonoides/metabolismo , Glicosilación , Espectrometría de Masas en Tándem , Perfilación de la Expresión Génica , Fenoles/metabolismo , Transcriptoma/genética , Glicósidos/metabolismo , Frutas/genética , Frutas/metabolismo
2.
Molecules ; 24(9)2019 May 07.
Artículo en Inglés | MEDLINE | ID: mdl-31067628

RESUMEN

Ancient apple cultivars usually have higher nutraceutical value than commercial ones, but in most cases their variability in pomological traits does not allow us to discriminate among them. Fruit of two Tuscany ancient apple cultivars, 'Casciana' and 'Rotella', picked from eight different orchards (four for each cultivar) were analyzed for their pomological traits, organoleptic qualities, polyphenolic profile and antiradical activity. The effectiveness of a polyphenol-based cluster analysis was compared to molecular markers (internal transcribed spacers, ITS1 and ITS2) to unequivocally discern the two apples. 'Casciana' and 'Rotella' fruit had a higher nutraceutical value than some commercial cultivars, in terms of phenolic abundance, profile and total antiradical activity. Although pedo-climatic conditions of different orchards influenced the phenolic profile of both apples, the polyphenolic discriminant analysis clearly separated the two cultivars, principally due to higher amounts of procyanidin B2, procyanidin B3 and p-coumaroylquinic acid in 'Casciana' than in 'Rotella' fruit. These three polyphenols can be used proficiently as biochemical markers for distinguishing the two apples when pomological traits cannot. Conversely, ITS1 and ITS2 polymorphism did not allow us to distinguish 'Casciana' from 'Rotella' fruit. Overall, the use of polyphenolic fingerprint might represent a valid tool to ensure the traceability of products with a high economic value.


Asunto(s)
Biomarcadores , Frutas/genética , Malus/genética , Polifenoles/genética , Biflavonoides/química , Biflavonoides/genética , Catequina/química , Catequina/genética , Flavonoides/química , Flavonoides/genética , Frutas/química , Italia , Malus/química , Malus/clasificación , Extractos Vegetales/química , Polifenoles/química , Proantocianidinas/química , Proantocianidinas/genética
3.
Planta ; 245(5): 1021-1035, 2017 May.
Artículo en Inglés | MEDLINE | ID: mdl-28188424

RESUMEN

MAIN CONCLUSION: A coordinated regulation of different branches of the flavonoid pathway was highlighted that may contribute to elucidate the role of this important class of compounds during the early stages of apple fruit development. Apple (Malus × domestica Borkh.) is an economically important fruit appreciated for its organoleptic characteristics and its benefits for human health. The first stages after fruit set represent a very important and still poorly characterized developmental process. To enable the profiling of genes involved in apple early fruit development, we combined the suppression subtractive hybridization (SSH) protocol to next-generation sequencing. We identified and characterized genes induced and repressed during fruit development in the apple cultivar 'Golden Delicious'. Our results showed an opposite regulation of genes coding for enzymes belonging to flavonoid and monolignol pathways, with a strong induction of the former and a simultaneous repression of the latter. Two isoforms of phenylalanine ammonia-lyase and 4-coumarate:CoA ligase, key enzymes located at the branching point between flavonoid and monolignol pathways, showed opposite expression patterns during the period in analysis, suggesting a possible regulation mechanism. A targeted metabolomic analysis supported the SSH results and revealed an accumulation of the monomers catechin and epicatechin as well as several forms of procyanidin oligomers in apple fruitlets starting early after anthesis, together with a decreased production of other classes of flavonoids such as some flavonols and the dihydrochalcone phlorizin. Moreover, gene expression and metabolites accumulation of 'Golden Delicious' were compared to a wild apple genotype of Manchurian crabapple (Malus mandshurica (Maxim.) Kom.). Significant differences in both gene expression and metabolites accumulation were found between the two genotypes.


Asunto(s)
Biflavonoides/metabolismo , Catequina/metabolismo , Flavonoides/metabolismo , Malus/enzimología , Proantocianidinas/metabolismo , Biflavonoides/genética , Catequina/genética , Coenzima A Ligasas/genética , Coenzima A Ligasas/metabolismo , Flavonoides/genética , Secuenciación de Nucleótidos de Alto Rendimiento , Malus/genética , Malus/crecimiento & desarrollo , Fenilanina Amoníaco-Liasa/genética , Fenilanina Amoníaco-Liasa/metabolismo , Proantocianidinas/genética , Isoformas de Proteínas , Análisis de Secuencia de ADN , Técnicas de Hibridación Sustractiva
4.
Arch Biochem Biophys ; 518(2): 127-32, 2012 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-22203090

RESUMEN

Both CYP158A1 and CYP158A2 are able to catalyze an oxidative C-C coupling reaction producing biflaviolin or triflaviolin in Streptomyces coelicolor A3(2). The substrate-bound crystal structures of CYP158A2 and CYP158A1 reveal that the side chain of Ile87 in CYP158A2 points to the active site contacting the distal flaviolin molecule, however, the bulkier side chain of Lys90 in CYP158A1 (corresponding to Ile87 in CYP158A2) is toward the distal surface of the protein. These results suggest that these residues could be important in determining product regiospecificity. In order to explore the role of the two residues in catalysis, the reciprocal mutants, Ile87Lys and Lys90Ile, of CYP158A2 and CYP158A1, respectively, were generated and characterized. The mutant Ile87Lys enzyme forms two isomers of biflaviolin instead of three isomers of biflaviolin in wild-type CYP158A2. CYP158A1 containing the substitution of lysine with isoleucine has the same catalytic activity compared with the wild-type CYP158A1. The crystal structure of Ile87Lys showed that the BC loop in the mutant is in a very different orientation compared with the BC loop in both CYP158A1/A2 structures. These results shed light on the mechanism of the oxidative coupling reaction catalyzed by cytochrome P450.


Asunto(s)
Proteínas Bacterianas/química , Sistema Enzimático del Citocromo P-450/química , Isoleucina/química , Streptomyces coelicolor/enzimología , Sustitución de Aminoácidos , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Biflavonoides/química , Biflavonoides/genética , Biflavonoides/metabolismo , Catálisis , Dominio Catalítico , Cristalografía por Rayos X , Sistema Enzimático del Citocromo P-450/genética , Sistema Enzimático del Citocromo P-450/metabolismo , Isoleucina/genética , Isoleucina/metabolismo , Mutación Missense , Oxidación-Reducción , Streptomyces coelicolor/genética
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