Browsing by Author "Rodrigues, Maria Luisa"
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- Crystal structures of the free and sterol-bound forms of beta-cinnamominPublication . Rodrigues, Maria Luisa; Archer, Margarida; Martel, Paulo; Miranda, Sandra; Thomaz, Mónica; Enguita, Francisco J.; Baptista, Ricardo P.; Melo, Eduardo P.; Sousa, Nelson; Cravador, A.; Carrondo, Maria A.The crystal structure of the elicitin h-cinnamomin (h-CIN) was determined in complex with ergosterol at 1.1 A° resolution. h-CIN/ergosterol complex crystallized in the monoclinic space group P21, with unit cell parameters of a =31.0, b =62.8, c =50.0 A° and b =93.4- and two molecules in the asymmetric unit. Ligand extraction with chloroform followed by crystallographic analysis yielded a 1.35 A° structure of h-CIN (P43212 space group) where the characteristic elicitin fold was kept. After incubation with cholesterol, a new complex structure was obtained, showing that the protein retains, after the extraction procedure, its ability to complex sterols. The necrotic effect of h-CIN on tobacco was also shown to remain unchanged. Theoretical docking studies of the triterpene lupeol to h-CIN provided an explanation for the apparent inability of h-CIN to bind this ligand, as observed experimentally. D 2005 Elsevier B.V. All rights reserved.
- Crystallisation and preliminary X-ray diffraction analysis of alpha-cinnamomin, an elicitin secreted by the phytopathogenic fungus Phytophthora cinnamomiPublication . Archer, Margarida; Rodrigues, Maria Luisa; Aurélio, M.; Biemans, R.; Cravador, A.; Carrondo, Maria A.Cinnamomin (CIN) belongs to a family of 10 kDa proteins designated as elicitins. Some of these proteins induce a hypersensitive response in diverse plant species, leading to resistance against fungal and bacterial plant pathogens. CIN was crystallized by the vapourdiffusion method using either ammonium sulfate or polyethyleneglycol (PEG) as precipitants in solutions buffered at around pH 7. These crystals are isomorphous and belong to the triclinic space group, with unit-cell parameters a = 31.69, b = 36.99, c = 44.09 A Ê , = 76.86, = 84.41, = 80.26 . A frozen crystal diffracted X-rays beyond 1.45 A Ê resolution on a synchrotron-radiation source.
- How plants cope with water stress in the field : photosynthesis and growthPublication . Chaves, Maria Manuela; Pereira, J. S.; Maroco, J.; Rodrigues, Maria Luisa; Ricardo, C. P.; Osório, Maria Leonor; Carvalho, Isabel Saraiva de; Faria, T.; Pinheiro, C.Plants are often subjected to periods of soil and atmospheric water deficit during their life cycle. The frequency of such phenomena is likely to increase in the future even outside today's arid/semi-arid regions. Plant responses to water scarcity are complex, involving deleterious and/or adaptive changes, and under field conditions these responses can be synergistically or antagonistically modified by the superimposition of other stresses. This complexity is illustrated using examples of woody and herbaceous species mostly from Mediterranean-type ecosystems, with strategies ranging from drought-avoidance, as in winter/spring annuals or in deep-rooted perennials, to the stress resistance of sclerophylls. Differences among species that can be traced to different capacities for water acquisition, rather than to differences in metabolism at a given water status, are described. Changes in the root : shoot ratio or the temporary accumulation of reserves in the stem are accompanied by alterations in nitrogen and carbon metabolism, the fine regulation of which is still largely unknown. At the leaf level, the dissipation of excitation energy through processes other than photosynthetic C-metabolism is an important defence mechanism under conditions of water stress and is accompanied by down-regulation of photochemistry and, in the longer term, of carbon metabolism.