Catálogo de publicaciones - libros
Advances in Plant Ethylene Research: Proceedings of the 7th International Symposium on the Plant Hormone Ethylene
Angelo Ramina ; Caren Chang ; Jim Giovannoni ; Harry Klee ; Pierdomenico Perata ; Ernst Woltering (eds.)
Resumen/Descripción – provisto por la editorial
No disponible.
Palabras clave – provistas por la editorial
Plant Sciences; Plant Physiology; Plant Genetics & Genomics; Agriculture; Biotechnology; Developmental Biology
Disponibilidad
Institución detectada | Año de publicación | Navegá | Descargá | Solicitá |
---|---|---|---|---|
No detectada | 2007 | SpringerLink |
Información
Tipo de recurso:
libros
ISBN impreso
978-1-4020-6013-7
ISBN electrónico
978-1-4020-6014-4
Editor responsable
Springer Nature
País de edición
Reino Unido
Fecha de publicación
2007
Información sobre derechos de publicación
© Springer Science+Business Media B.V. 2007
Cobertura temática
Tabla de contenidos
Role of ethylene in triggering ROS production in the tomato mutant Nr subjected to acute ozone treatment
A. Castagna; L. Ederli; S. Pasqualini; A. Mensuali-Sodi; B. Baldan; A. Pardossi; A. Ranieri
Tropospheric ozone (O3) is believed to be the most important phytotoxic air pollutant in industrialised countries and one of the major anthropogenic stresses that threaten native and cultivated ecosystems. Although reactive oxygen species (ROS) generated following O3 exposure are believed to act as key molecules that elicit plant response to O3, the current information underlines the importance of the complex interactions between ROS and several phytohormones, among which ethylene (ET) (Kangasjärvi . 2005, Diara 2005).
6 - Ethylene Involvement In Biotic And Abiotic Stresses | Pp. 387-388
Ozone as a tool for studying stress responses in tomato (Solanum lycopersicum L.). III. Ethylene, cyanide and the development of foliar symptoms in the autonecrotic mutant V20368
M. G. Antonelli; R. Marabottini; E. Santangelo; A. Francini; E. Pellegrini; D. Di Baccio; L. Ederli; C. Nali; S. Pasqualini; G. P. Soressi; M. Ciaffi; G. Lorenzini; L. Sebastiani; M. Badiani
Plants’ exposure to ozone (O3) activates a multitude of defense reactions – among which the launch of a cell death program (PCD) leading to the development of visible foliar symptoms – which are also deployed in response to other abiotic or biotic stressors. Ethylene (ET) plays a key role in these events.
6 - Ethylene Involvement In Biotic And Abiotic Stresses | Pp. 389-390
The autonecrosis triggered by Cf-2/Rcr3esc interaction in tomato (Solanum lycopersicum L.) involves an ethylene burst and the enzymatic machinery protecting the respiratory apparatus of mitochondria
E. Santangelo; R. Marabottini; M. G. Antonelli; M. Badiani; S. Pasqualini; G. P. Soressi
High ethylene (ET) synthesis observed under stress conditions produces stoichiometric amounts of CNand CO2. Normally, plant tissues have ample capacity to detoxify the cytosolic CN??to β-cyanoalanine by the action of β-cyanoalanine synthase (β-CAS), mainly present in the mitochondrial fraction.
6 - Ethylene Involvement In Biotic And Abiotic Stresses | Pp. 391-392
Ethylene response of tomato fruits to the minimum dropping
H. Usuda; M. Kitagawa; Y. Ito; H. Umehara; N. Nakamura; P. Roy; H. Okadome; Y. Ishikawa; T. Satake; T. Shiina
Physical stresses such as shock and vibration deteriorate the quality of fresh fruits and vegetables not only by direct physical damage but also through the endogenous biological activities of the produce. Ethylene seems to be the most important factor of the stress response in the produce. In this paper we study the effects of slight dropping (1, 3, 10 times) on the ethylene and CO2 production of the whole tomato fruits and accumulation of the ACC synthase (ACS) mRNA in the tissue. The mature green tomato () fruits which were screened by ethylene production rate (less than 0.2 μlkg??h??) were used to avoid a contamination of climacteric phase fruit.
6 - Ethylene Involvement In Biotic And Abiotic Stresses | Pp. 393-394
Ethylene production of Botrytis cinerea in vitro and during in planta infection of tomato fruits
S. M. Cristescu; F. J. M. Harren; Ernst Woltering
We present a new approach to study the pathogen-host interaction by online monitoring of ethylene release using a laser-based photoacoustic detector. The instrument allows detection of ethylene emission in a continuous flow system down to 10 pptv (pptv = parts-per-trillion volume, 1:1012) (Bijnen ., 1996) and has relatively high time resolution for measuring the dynamics of ethylene production by and by infected tomatoes. Moreover, it has been proved to be a powerful tool to study the relationship between ethylene released by the fungus and the enhanced ethylene production in infected tomato with respect to disease development.
6 - Ethylene Involvement In Biotic And Abiotic Stresses | Pp. 395-397
Ethylene production of two durum wheat cultivars exposed to cadmium
A. Mensuali-Sodi; L. Ercoli
Cadmium is a highly toxic heavy metal for all living organisms and causes a reduction of several physiological processes in plants. Cadmium tends to accumulate in several crops grown in soils containing Cd (Grant ., 1998). Grain and cereal products are primary sources of Cd, being able to accumulate Cd in grain (Greger and Löfstedt, 2004). Ethylene production has been often associated with response to Cd exposure in several species (Rodecap and Tingery, 1981; Bhattacharjee, 1997).
6 - Ethylene Involvement In Biotic And Abiotic Stresses | Pp. 399-400
Ferric reductase and iron transporter gene expression in different Arabidopsis ethylene mutants
M. J. García; F. J. Romera; R. Pérez-Vicente; C. Lucena; E. Alcántara
Dicotyledonous plants need to reduce Fe(III) to Fe(II), mediated by a ferric reductase (encoded by the gene in ), prior to its uptake through an Fe(II) transporter (encoded by the gene in ). The expression of both genes is up-regulated under Fe deficiency. In the last years evidence has been presented to support a role for ethylene as activator of the ferric reductase activity but it is not known whether ethylene affects transcription or other aspects of this activity (Romera and Alcántara, 2004).
6 - Ethylene Involvement In Biotic And Abiotic Stresses | Pp. 401-403
Modulating effects of ethylene and ethylene inhibitors in the control of fruit ripening
P. Tonutti; C. Bonghi; Angelo Ramina
The control of the ripening process in climacteric fruit mainly relies on the possibility of affecting ethylene biosynthesis and action. This can be achieved through genetic manipulation, by modulating environmental parameters (temperature, atmosphere composition) during storage, or using specific inhibitors of ethylene biosynthesis/perception. The effects of treatments with ethylene inhibitors on climacteric fruit, however, differ according to several factors including genotype.
7 - Biotechnology And Applied Aspects | Pp. 407-415
Issues with commercialization of 1-methylcyclopropene (1-MCP) for apples
C. B. Watkins; S. K. Jung; F. Razafimbelo; J. F. Nock
1-Methylcyclopropene (1-MCP) is an inhibitor of ethylene binding that can prevent ethylene-dependent responses in many fruits and vegetables (Blankenship and Dole, 2003; Watkins, 2006). 1-MCP has been commercialized as SmartFresh and food use registration has been obtained for a wide range of crops in several countries (Watkins, 2006).
7 - Biotechnology And Applied Aspects | Pp. 417-422
Comprehensive analysis of candidate genes involved in ethylene production and perception during apple ripening: phenotypic dissection and functional profiling
F. Costa; S. Stella; V. Soglio; L. Gianfranceschi; H. Schouten; W. E. Van de Weg; W. Guerra; S. Serra; S. Musacchi; S. Sansavini
The ripening of fleshy fruit is generally distinguished into two categories, climacteric and non-climacteric, based on the fruit’s ability to produce or ethylene in high concentrations during maturation. A gaseous hormone produced by higher plants, ethylene regulates a number of physiological processes ranging from fruit development to maturation and senescence (Yang and Hoffmann 1984; Giovannoni 2004).
7 - Biotechnology And Applied Aspects | Pp. 423-429