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Biblioteca (s) : |
INIA Salto Grande. |
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Fecha : |
24/10/2014 |
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Actualizado : |
17/10/2019 |
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Tipo de producción científica : |
Artículos en Revistas Indexadas Internacionales |
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Autor : |
LADO, J.; RODRIGO, M.J.; CRONJE, P.; ZACARÍAS, L. |
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Afiliación : |
JOANNA LADO LINDNER, Instituto Nacional de Investigación Agropecuaria (INIA), Uruguay; M.J. RODRIGO, IATA (Instituto de Agroquímica y Tecnología de Alimentos), España; P. CRONJE, Citrus Research International (CRI), University of Stellenbosch, Sudáfrica; L. ZACARÍAS, IATA (Instituto de Agroquímica y Tecnología de Alimentos), España. |
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Título : |
Involvement of lycopene in the induction of tolerance to chilling injury in grapefruit. |
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Fecha de publicación : |
2015 |
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Fuente / Imprenta : |
Postharvest Biology & Technology, 2015, v.100, p. 176-186. |
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ISSN : |
0925-5214 |
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DOI : |
10.1016/j.postharvbio.2014.10.002 |
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Idioma : |
Inglés |
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Contenido : |
ABSTRACT.
Grapefruit are among the more sensitive Citrus varieties likely to develop chilling injury (CI) symptoms during postharvest storage at low temperatures. Comparative observations of the incidence of CI in fruit of white Marsh (MSH) and red Star Ruby (SR) grapefruit during postharvest storage at 2 C plus 7 days at 20 C to simulate shelf-life revealed that (1) the former was consistently more sensitive to CI, developing cold damage uniformly throughout the whole rind surface, and (2) more strikingly, CI symptoms in fruit of SR grapefruit were restricted to the yellow areas of the rind and the red-colored zones were almost absent of cold damage. This tolerance to CI in red flavedo was associated with high carotenoid (2) and lycopene (14) contents, as compared with yellow-colored flavedo. Absence of chilling damage in red areas of SR grapefruit rind was confirmed by cellular ultrastructure observations, in which these epidermal cells were intact, with a well-defined structure and compact vacuoles filled with content. Cells of yellow-colored tissue developing CI, were collapsed, with a contracted vacuole and shrinking organelles. To explore whether the tolerance to CI in red areas of grapefruit rind was due to an elevated lycopene concentration, chemical and environmental stimulation of this carotenoid was performed in
fruit of both grapefruit varieties. Application of the inhibitor of the lycopene cyclase activity, CPTA (2-(4- chlorophenylthio) triethylamine hydrochloride) induced red coloration, increased lycopene accumulation (32) and significantly delayed development of CI symptoms in the rind the CI-sensitive MSH.
Bagging of SR grapefruit enhanced a homogenous red coloration and substantially induced lycopene accumulation (75). CI symptoms in bagged fruit were notably delayed and reduced, as compared with non-bagged yellow fruit, upon subsequent storage at 2 C for up to 58 days and 7 days at 20 C. Analysis of the expression of ethylene biosynthetic genes (ACS1, ACS2 and ACO) revealed a significant induction in chilling-damaged tissue of both varieties that was almost absent in red chilling-tolerant tissue. Similarly, accumulation of transcripts of the ethylene receptors ETR1 and ETR3 were also associated with chilling damage, but a cold factor appears to also mediate the expression of these genes. Taken together, our results indicate that high lycopene concentration appears to be responsible for the induction of tolerance to chilling in the red-colored areas of the flavedo of grapefruit during postharvest storage at low temperatures.
ã 2014 Elsevier B.V. All rights reserved. MenosABSTRACT.
Grapefruit are among the more sensitive Citrus varieties likely to develop chilling injury (CI) symptoms during postharvest storage at low temperatures. Comparative observations of the incidence of CI in fruit of white Marsh (MSH) and red Star Ruby (SR) grapefruit during postharvest storage at 2 C plus 7 days at 20 C to simulate shelf-life revealed that (1) the former was consistently more sensitive to CI, developing cold damage uniformly throughout the whole rind surface, and (2) more strikingly, CI symptoms in fruit of SR grapefruit were restricted to the yellow areas of the rind and the red-colored zones were almost absent of cold damage. This tolerance to CI in red flavedo was associated with high carotenoid (2) and lycopene (14) contents, as compared with yellow-colored flavedo. Absence of chilling damage in red areas of SR grapefruit rind was confirmed by cellular ultrastructure observations, in which these epidermal cells were intact, with a well-defined structure and compact vacuoles filled with content. Cells of yellow-colored tissue developing CI, were collapsed, with a contracted vacuole and shrinking organelles. To explore whether the tolerance to CI in red areas of grapefruit rind was due to an elevated lycopene concentration, chemical and environmental stimulation of this carotenoid was performed in
fruit of both grapefruit varieties. Application of the inhibitor of the lycopene cyclase activity, CPTA (2-(4- chlorophenylthio) triethylamine hydrochlo... Presentar Todo |
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Thesagro : |
ALMACENAMIENTO EN FRIO; CITRUS; ESTRES TERMICO; FRIO; TECNOLOGIA POSCOSECHA; TOLERANCIA AL FRIO. |
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Asunto categoría : |
F01 Cultivo |
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Marc : |
LEADER 03375naa a2200253 a 4500
001 1051284
005 2019-10-17
008 2015 bl uuuu u00u1 u #d
022 $a0925-5214
024 7 $a10.1016/j.postharvbio.2014.10.002$2DOI
100 1 $aLADO, J.
245 $aInvolvement of lycopene in the induction of tolerance to chilling injury in grapefruit.$h[electronic resource]
260 $c2015
520 $aABSTRACT. Grapefruit are among the more sensitive Citrus varieties likely to develop chilling injury (CI) symptoms during postharvest storage at low temperatures. Comparative observations of the incidence of CI in fruit of white Marsh (MSH) and red Star Ruby (SR) grapefruit during postharvest storage at 2 C plus 7 days at 20 C to simulate shelf-life revealed that (1) the former was consistently more sensitive to CI, developing cold damage uniformly throughout the whole rind surface, and (2) more strikingly, CI symptoms in fruit of SR grapefruit were restricted to the yellow areas of the rind and the red-colored zones were almost absent of cold damage. This tolerance to CI in red flavedo was associated with high carotenoid (2) and lycopene (14) contents, as compared with yellow-colored flavedo. Absence of chilling damage in red areas of SR grapefruit rind was confirmed by cellular ultrastructure observations, in which these epidermal cells were intact, with a well-defined structure and compact vacuoles filled with content. Cells of yellow-colored tissue developing CI, were collapsed, with a contracted vacuole and shrinking organelles. To explore whether the tolerance to CI in red areas of grapefruit rind was due to an elevated lycopene concentration, chemical and environmental stimulation of this carotenoid was performed in fruit of both grapefruit varieties. Application of the inhibitor of the lycopene cyclase activity, CPTA (2-(4- chlorophenylthio) triethylamine hydrochloride) induced red coloration, increased lycopene accumulation (32) and significantly delayed development of CI symptoms in the rind the CI-sensitive MSH. Bagging of SR grapefruit enhanced a homogenous red coloration and substantially induced lycopene accumulation (75). CI symptoms in bagged fruit were notably delayed and reduced, as compared with non-bagged yellow fruit, upon subsequent storage at 2 C for up to 58 days and 7 days at 20 C. Analysis of the expression of ethylene biosynthetic genes (ACS1, ACS2 and ACO) revealed a significant induction in chilling-damaged tissue of both varieties that was almost absent in red chilling-tolerant tissue. Similarly, accumulation of transcripts of the ethylene receptors ETR1 and ETR3 were also associated with chilling damage, but a cold factor appears to also mediate the expression of these genes. Taken together, our results indicate that high lycopene concentration appears to be responsible for the induction of tolerance to chilling in the red-colored areas of the flavedo of grapefruit during postharvest storage at low temperatures. ã 2014 Elsevier B.V. All rights reserved.
650 $aALMACENAMIENTO EN FRIO
650 $aCITRUS
650 $aESTRES TERMICO
650 $aFRIO
650 $aTECNOLOGIA POSCOSECHA
650 $aTOLERANCIA AL FRIO
700 1 $aRODRIGO, M.J.
700 1 $aCRONJE, P.
700 1 $aZACARÍAS, L.
773 $tPostharvest Biology & Technology, 2015$gv.100, p. 176-186.
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Registro original : |
INIA Salto Grande (SG) |
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Registro completo
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Biblioteca (s) : |
INIA La Estanzuela. |
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Fecha actual : |
21/02/2014 |
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Actualizado : |
19/04/2022 |
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Tipo de producción científica : |
Trabajos en Congresos/Conferencias |
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Autor : |
BANCHERO, G.; FERNANDEZ, M.; GANZÁBAL, A.; VÁZQUEZ, A.; QUINTANS, G. |
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Afiliación : |
GEORGGET ELIZABETH BANCHERO HUNZIKER, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; MARIA EUGENIA FERNANDEZ DIEZ, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; ANDRES RICARDO GANZÁBAL PLANINICH, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; JORGE ANDRÉS VÁZQUEZ TEXEIRA, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; GRACIELA QUINTANS ILARIA, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay. |
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Título : |
Manejo genético y nutricional para aumentar la tasa mellicera de nuestras majadas. |
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Fecha de publicación : |
2006 |
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Fuente / Imprenta : |
In: JORNADAS URUGUAYAS DE BUIATRÍA, 34., 2006, Paysandú, Uruguay. Paysandú, UY: Centro Médico Veterinario de Paysandú, SUB, SMVU. 2006. |
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Páginas : |
p. 71-76. |
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Idioma : |
Español |
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Contenido : |
Resumen: La tasa mellicera de nuestras majadas está en el orden de 6 a 15%. Sin embargo, algunos productores logran tasas melliceras de 50% o más. ¿Cómo lo hacen?. Utilizando biotipos prolíficos puros o sus cruzas con nuestras razas o dentro de nuestras razas realizando un manejo muy preciso de la nutrición previo al apareamiento. Por ejemplo, bajo las mismas condiciones de alimentación, la F1 entre el biotipo Ideal y Frisona Milchschaf permite incrementos en la tasa mellicera de 25 a 35 puntos porcentuales por encima del biotipo puro (10-15 vs 35-50%). Pero además, si sometemos a esa F1 a un "f1ushing" corto previo a la encarnerada, ésta puede alcanzar tasas melliceras de 80 a 85% mientras que las ovejas Ideal pueden llegar a
60%. En este artículo discutiremos los dos caminos y cuales son sus implicancias prácticas. |
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Thesagro : |
CRUZAMIENTO; OVEJA; OVINOS; OVULACION. |
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Asunto categoría : |
-- |
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URL : |
http://www.ainfo.inia.uy/digital/bitstream/item/16386/1/JB2006-71-76.pdf-Banchero.pdf
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Marc : |
LEADER 01536nam a2200217 a 4500
001 1036442
005 2022-04-19
008 2006 bl uuuu u01u1 u #d
100 1 $aBANCHERO, G.
245 $aManejo genético y nutricional para aumentar la tasa mellicera de nuestras majadas.$h[electronic resource]
260 $aIn: JORNADAS URUGUAYAS DE BUIATRÍA, 34., 2006, Paysandú, Uruguay. Paysandú, UY: Centro Médico Veterinario de Paysandú, SUB, SMVU. 2006.$c2006
300 $ap. 71-76.
520 $aResumen: La tasa mellicera de nuestras majadas está en el orden de 6 a 15%. Sin embargo, algunos productores logran tasas melliceras de 50% o más. ¿Cómo lo hacen?. Utilizando biotipos prolíficos puros o sus cruzas con nuestras razas o dentro de nuestras razas realizando un manejo muy preciso de la nutrición previo al apareamiento. Por ejemplo, bajo las mismas condiciones de alimentación, la F1 entre el biotipo Ideal y Frisona Milchschaf permite incrementos en la tasa mellicera de 25 a 35 puntos porcentuales por encima del biotipo puro (10-15 vs 35-50%). Pero además, si sometemos a esa F1 a un "f1ushing" corto previo a la encarnerada, ésta puede alcanzar tasas melliceras de 80 a 85% mientras que las ovejas Ideal pueden llegar a 60%. En este artículo discutiremos los dos caminos y cuales son sus implicancias prácticas.
650 $aCRUZAMIENTO
650 $aOVEJA
650 $aOVINOS
650 $aOVULACION
700 1 $aFERNANDEZ, M.
700 1 $aGANZÁBAL, A.
700 1 $aVÁZQUEZ, A.
700 1 $aQUINTANS, G.
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INIA La Estanzuela (LE) |
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