Browsing by Subject "Xerophyta"

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    Anomalous pressure volume curves of resurrection plants do not suggest negative turgor.
    (Oxford University Press, 2001) Willigen, Clare Vander; Farrant, Jill; Pammenter, N W
    Pressure-volume (PV) curves of the desiccation-tolerant angiosperms, Eragrostis nindensis, Craterostigma wilmsii and Xerophyta humilis, and the desiccation-sensitive species, E. curvula, were compared. The shape of curves for E. nindensis and C. wilmsii differed from the usual curvilinear form. Over the relative water content (RWC) range of approx. 70 to 25%, PV curves indicated water potentials higher than directly measured water activity on frozen-thawed tissue. Anatomical studies showed considerable cell wall folding and a consequent reduction in cell volume in these two species; this was not seen in X. humilis or E. curvula which showed normal PV curves. It is suggested that this wall folding may have prevented the development of negative turgor and physical stress in the cells, and contributed to desiccation tolerance. Copyright 2001 Annals of Botany Company.
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    A novel stress-inducible antioxidant enzyme identified from the resurrection plant Xerophyta viscosa Baker.
    (Springer, 2002) Mowla, Shaheen B; Thomson, Jennifer A; Farrant, Jill; Mundree, Sagadevan G
    A cDNA corresponding to 1-Cys peroxiredoxin, an evolutionarily conserved thiol-specific antioxidant enzyme, was isolated from Xerophyta viscosa Baker, a resurrection plant indigenous to Southern Africa and belonging to the family Velloziaceae. The cDNA, designated XvPer1, contains an open reading frame that encodes a polypeptide of 219 residues with a predicted molecular weight of 24.2 kDa. The XvPer1 polypeptide shows significant sequence identity (approx. 70%) to other recently identified plant 1-Cys peroxiredoxins and relatively high levels of sequence similarity (approx. 40%) to non-plant 1-Cys peroxiredoxins. The XvPer1 cDNA contains a putative polyadenylation site. As for all 1-Cys peroxiredoxins identified to date, the amino acid sequence proposed to constitute the active site of the enzyme, PVCTTE, is highly conserved in XvPer1. It also contains a putative bipartite nuclear localization signal. Southern blot analysis revealed that there is a single copy of XvPer1 in the X. viscosa genome. All angiosperm 1-Cys peroxiredoxins described to date are seed-specific and absent in vegetative tissues even under stress conditions; therefore, XvPer1 is unique in that it is expressed in the vegetative tissues of X. viscosa. The XvPer1 transcript was absent in fully hydrated X. viscosa tissue but levels increased in tissues subjected to abiotic stresses such as dehydration, heat (42 °C), high light intensity (1,500 µmol photons m–2 s–1) and when treated with abscisic acid (100 µM ABA) and sodium chloride (100 mM NaCl). Western blot analyses correlated with the patterns of expression of XvPer1 transcripts under different stress conditions. Immunofluorescence analyses revealed that XvPer1 is localized in the nucleus of dehydrated X. viscosa leaf cells. These results suggest that XvPer1 is a stress-inducible gene, which may function to protect nucleic acids within the nucleus against oxidative injury.
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    An overview of mechanisms of desiccation tolerance in selected angiosperm resurrection plants
    (Global Science Books, 2007) Farrant, Jill M; Brandt, Wolf B; Lindsey, George G
    The vegetative tissues of resurrection plants, like seeds, can tolerate desiccation to 5% relative water content (RWC) for extended periods and yet resume full metabolic activity on re-watering. In this review we will illustrate how this is achieved in a variety of angiosperm resurrection plants, our studies ranging from the ecophysiological to the biochemical level. At the whole plant level, leaf folding and other anatomical changes serve to minimise light and mechanical stress associated with drying and rehydration. The mechanisms of cell wall folding are described for Craterostigma wilmsii and Myrothanmus flabellifolia. Free radicals, radical oxygen species (ROS) usually generated under water-deficit stress by photosynthesis, are minimised by either homoiochlorophylly (e.g. C. wilmsii and M. flabellifolia) or poikilochlorophylly (e.g. Xerophyta sp.). The antioxidant systems of these plants effectively deal with ROS generated by other metabolic processes. In addition to antioxidants common to most plants, resurrection plants also accumulate polyphenols such as 3, 4, 5 tri-O-galloylquinic acid in M. flabellifolia, and seed-associated antioxidants (e.g. 1-cys-peroxiredoxin and metallothionines) as effective ROS scavengers. Sucrose accumulates at low RWC, presumably protecting the sub-cellular milieu against desiccation-induced macromolecular denaturation.