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1.
J Agric Food Chem ; 58(8): 5114-21, 2010 Apr 28.
Article in English | MEDLINE | ID: mdl-20369803

ABSTRACT

Mountain papaya ( Vasconcellea pubescens ) is a climacteric fruit that develops a strong and characteristic aroma during ripening. Esters are the main volatile compounds produced by the fruit, and most of them are dependent on ethylene. As esters are synthesized through alcohol acyltransferases (AAT), a full-length cDNA (VpAAT1) was isolated that displayed the characteristic motifs of most plant acyltransferases. The full-length cDNA sequence was cloned and expressed in yeasts, obtaining a functional enzyme with high AAT activity toward the formation of benzyl acetate. The transcript accumulation pattern provided by qPCR analysis showed that the VpAAT1 gene is expressed exclusively in fruit tissues and that a high level of transcripts is accumulated during ripening. The increase in VpAAT1 transcripts in fruit is coincident with the increase in AAT activity; transcript accumulation is induced by ethylene, and it is avoided by 1-methylcyclopropene (1-MCP) treatment. The data indicate that VpAAT1 is involved in aroma formation and that ethylene plays a major role in regulating its expression.


Subject(s)
Carica/metabolism , Proteins/genetics , Amino Acid Sequence , Carica/physiology , Esters , Molecular Sequence Data , Proteins/chemistry , Proteins/metabolism , Sequence Homology, Amino Acid , Temperature
2.
J Agric Food Chem ; 55(13): 5213-20, 2007 Jun 27.
Article in English | MEDLINE | ID: mdl-17542607

ABSTRACT

Alcohol acyltransferases (AAT) play a key role in the biosynthesis of ester aroma volatiles in fruit. Three ripening-specific recombinant AATs of cantaloupe Charentais melon fruit (Cm-AAT1, Cm-AAT3, and Cm-AAT4) are capable of synthesizing thioether esters with Cm-AAT1 being by far the most active. All proteins, as well as AAT(s) extracted from melon fruit, are active as tetramers of around 200 kDa. Kinetic analysis demonstrated that CoA-SH, a product of the reaction, is an activator at low concentrations and an inhibitor at higher concentrations. This was confirmed by the addition of phosphotransacetylase at various concentrations, capable of modulating the level of CoA-SH in the reaction medium. Site-directed mutagenesis of some amino acids that were specific to the Cm-AAT sequences into amino acids that were consensus to other characterized AATs greatly affected the selectivity of the original protein and the number of esters produced.


Subject(s)
Acyltransferases/chemistry , Acyltransferases/metabolism , Alcohols/metabolism , Coenzyme A/physiology , Cucurbitaceae/enzymology , Fruit/enzymology , Acyltransferases/genetics , Amino Acid Sequence , Molecular Sequence Data , Mutagenesis, Site-Directed , Recombinant Proteins/metabolism , Structure-Activity Relationship , Substrate Specificity
3.
Plant Mol Biol ; 61(4-5): 675-85, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16897483

ABSTRACT

Alcohol dehydrogenases (ADH) participate in the biosynthetic pathway of aroma volatiles in fruit by interconverting aldehydes to alcohols and providing substrates for the formation of esters. Two highly divergent ADH genes (15% identity at the amino acid level) of Cantaloupe Charentais melon (Cucumis melo var. Cantalupensis) have been isolated. Cm-ADH1 belongs to the medium-chain zinc-binding type of ADHs and is highly similar to all ADH genes expressed in fruit isolated so far. Cm-ADH2 belongs to the short-chain type of ADHs. The two encoded proteins are enzymatically active upon expression in yeast. Cm-ADH1 has strong preference for NAPDH as a co-factor, whereas Cm-ADH2 preferentially uses NADH. Both Cm-ADH proteins are much more active as reductases with K (m)s 10-20 times lower for the conversion of aldehydes to alcohols than for the dehydrogenation of alcohols to aldehydes. They both show strong preference for aliphatic aldehydes but Cm-ADH1 is capable of reducing branched aldehydes such as 3-methylbutyraldehyde, whereas Cm-ADH2 cannot. Both Cm-ADH genes are expressed specifically in fruit and up-regulated during ripening. Gene expression as well as total ADH activity are strongly inhibited in antisense ACC oxidase melons and in melon fruit treated with the ethylene antagonist 1-methylcyclopropene (1-MCP), indicating a positive regulation by ethylene. These data suggest that each of the Cm-ADH protein plays a specific role in the regulation of aroma biosynthesis in melon fruit.


Subject(s)
Alcohol Dehydrogenase/genetics , Alcohol Dehydrogenase/metabolism , Cucurbitaceae/enzymology , Fruit/enzymology , Fruit/growth & development , Gene Expression Regulation, Plant , Alcohol Dehydrogenase/chemistry , Aldehydes/metabolism , Amino Acid Sequence , Cucurbitaceae/genetics , Fruit/genetics , Gene Expression Regulation, Enzymologic , Kinetics , Molecular Sequence Data , NAD/metabolism , NADP/metabolism , Phylogeny , Substrate Specificity
4.
Plant Mol Biol ; 59(2): 345-62, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16247561

ABSTRACT

Volatile esters, a major class of compounds contributing to the aroma of many fruit, are synthesized by alcohol acyl-transferases (AAT). We demonstrate here that, in Charentais melon (Cucumis melo var. cantalupensis), AAT are encoded by a gene family of at least four members with amino acid identity ranging from 84% (Cm-AAT1/Cm-AAT2) and 58% (Cm-AAT1/Cm-AAT3) to only 22% (Cm-AAT1/Cm-AAT4). All encoded proteins, except Cm-AAT2, were enzymatically active upon expression in yeast and show differential substrate preferences. Cm-AAT1 protein produces a wide range of short and long-chain acyl esters but has strong preference for the formation of E-2-hexenyl acetate and hexyl hexanoate. Cm-AAT3 also accepts a wide range of substrates but with very strong preference for producing benzyl acetate. Cm-AAT4 is almost exclusively devoted to the formation of acetates, with strong preference for cinnamoyl acetate. Site directed mutagenesis demonstrated that the failure of Cm-AAT2 to produce volatile esters is related to the presence of a 268-alanine residue instead of threonine as in all active AAT proteins. Mutating 268-A into 268-T of Cm-AAT2 restored enzyme activity, while mutating 268-T into 268-A abolished activity of Cm-AAT1. Activities of all three proteins measured with the prefered substrates sharply increase during fruit ripening. The expression of all Cm-AAT genes is up-regulated during ripening and inhibited in antisense ACC oxidase melons and in fruit treated with the ethylene antagonist 1-methylcyclopropene (1-MCP), indicating a positive regulation by ethylene. The data presented in this work suggest that the multiplicity of AAT genes accounts for the great diversity of esters formed in melon.


Subject(s)
Acyltransferases/genetics , Acyltransferases/metabolism , Cucurbitaceae/enzymology , Cucurbitaceae/genetics , Esters/metabolism , Threonine/metabolism , Acyltransferases/chemistry , Amino Acid Sequence , Amino Acid Substitution , Esters/chemistry , Fruit/enzymology , Gene Expression Regulation, Enzymologic , Gene Expression Regulation, Plant , Molecular Sequence Data , Multigene Family , Mutagenesis, Site-Directed , Mutation , Phylogeny , Sequence Alignment , Sequence Homology, Amino Acid , Substrate Specificity , Threonine/genetics , Volatilization
5.
Cir. gen ; 15(2): 67-70, abr.-jun. 1993. ilus
Article in Spanish | LILACS | ID: lil-196043

ABSTRACT

Objetivo. Informar la experiencia de los autores en el tratamiento quirúrgico de 100 pacientes con tumor de cuello. Diseño. Análisis descriptivo, retrospectivo, de 100 pacientes con tumores de cuello operados en un lapso de tres años de un total de 1500 operaciones. Sede. Hospital General de México de la Secretaría de Salud servicios de cirugía gneral 104 y 306, pabellones 3 y 18. Resultados. Se trató de 90 mujeres y 10 hombres, con edades entre 15 y 80 años, con mayor frecuencia ubicados entre la cuarta y sexta década de la vida. la principal manifestación clínica fue tumor a nivel cervical que se localizó en 45 pacientes en la cara lateral derecha de cuello, en 25 en la izquierda y en 30 abarcó ambos lados. En el 88 por ciento la patología correspondió a enfermedad de tiroides y de éstos un 60 por ciento correspondieron a bocio en sus diversas variedades. La tiroidectomía sub total se utilizó en 58 por ciento, seguida de la hemitiroidectomía derecha en un 10 por ciento de los pacientes. La mortalidad fue del 1 por ciento.


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Biopsy , General Surgery , Antibody Formation/immunology , Head and Neck Neoplasms/therapy , Radiography
8.
s.l; s.n; 1975. 6 p. ilus.
Non-conventional in Spanish | Sec. Est. Saúde SP, HANSEN, Hanseníase Leprosy, SESSP-ILSLACERVO, Sec. Est. Saúde SP | ID: biblio-1237552
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