Interference with oxidative phosphorylation enhances anoxic expression of rice α-amylase genes through abolishing sugar regulation

Rice has the unique ability to express α-amylase under anoxic conditions, a feature that is critical for successful anaerobic germination and growth. Previously, anaerobic conditions were shown to up-regulate the expression of Amy3 subfamily genes (Amy3B/C, 3D, and 3E) in rice embryos. These genes are known to be feedback regulated by the hydrolytic products of starchy endosperm such as the simple sugar glucose. It was found that oxygen deficiency interferes with the repression of Amy3D gene expression imposed by low concentrations of glucose but not with that imposed by higher amounts. This differential anoxic de-repression depending on sugar concentration suggests the presence of two distinct pathways for sugar regulation of Amy3D gene expression. Anoxic de-repression can be mimicked by treating rice embryos with inhibitors of ATP synthesis during respiration. Other sugar-regulated rice α-amylase genes, Amy3B/C and 3E, behave similarly to Amy3D. Treatment with a respiratory inhibitor or anoxia also relieved the sugar repression of the rice CIPK15 gene, a main upstream positive regulator of SnRK1A that is critical for Amy3D expression in response to sugar starvation. SnRK1A accumulation was previously shown to be required for MYBS1 expression, which transactivates Amy3D by binding to a cis-acting element found in the proximal region of all Amy3 subfamily gene promoters (the TA box). Taken together, these results suggest that prevention of oxidative phosphorylation by oxygen deficiency interferes with the sugar repression of Amy3 subfamily gene expression, leading to their enhanced expression in rice embryos during anaerobic germination

Recent Trends and Perspectives on Defect-Oriented Testing

Electronics employed in modern safety-critical systems require severe qualification during the manufacturing process and in the field, to prevent fault effects from manifesting themselves as critical failures during mission operations. Traditional fault models are not sufficient anymore to guarantee the required quality levels for chips utilized in mission-critical applications. The research community and industry have been investigating new test approaches such as device-aware test, cell-aware test, path-delay test, and even test methodologies based on the analysis of manufacturing data to move the scope from OPPM to OPPB. This special session presents four contributions, from academic researchers and industry professionals, to enable better chip quality. We present results on various activities towards this objective, including device-aware test, software-based self-test, and memory test

Contribution of the Microbial Communities Detected on an Oil Painting on Canvas to Its Biodeterioration

In this study, we investigated the microbial community (bacteria and fungi) colonising an oil painting on canvas, which showed visible signs of biodeterioration. A combined strategy, comprising culture-dependent and -independent techniques, was selected. The results derived from the two techniques were disparate. Most of the isolated bacterial strains belonged to related species of the phylum Firmicutes, as Bacillus sp. and Paenisporosarcina sp., whereas the majority of the non-cultivable members of the bacterial community were shown to be related to species of the phylum Proteobacteria, as Stenotrophomonas sp. Fungal communities also showed discrepancies: the isolated fungal strains belonged to different genera of the order Eurotiales, as Penicillium and Eurotium, and the non-cultivable belonged to species of the order Pleosporales and Saccharomycetales. The cultivable microorganisms, which exhibited enzymatic activities related to the deterioration processes, were selected to evaluate their biodeteriorative potential on canvas paintings; namely Arthrobacter sp. as the representative bacterium and Penicillium sp. as the representative fungus. With this aim, a sample taken from the painting studied in this work was examined to determine the stratigraphic sequence of its cross-section. From this information, “mock paintings,” simulating the structure of the original painting, were prepared, inoculated with the selected bacterial and fungal strains, and subsequently examined by micro-Fourier Transform Infrared spectroscopy, in order to determine their potential susceptibility to microbial degradation. The FTIR-spectra revealed that neither Arthrobacter sp. nor Penicillium sp. alone, were able to induce chemical changes on the various materials used to prepare “mock paintings.” Only when inoculated together, could a synergistic effect on the FTIR-spectra be observed, in the form of a variation in band position on the spectrum.The FTIR analyses performed in this study were financed by the Junta de Andalucía (RNM-325 group). The molecular analyses performed in this study were financed by the Austrian Science Fund (FWF) project ‘Hertha-Firnberg T137’ and the Spanish Ministry of Science and Innovation (Project CTQ2008-06727-C03-03). G. Piñar also thanks the “Elise-Richter V194-B20” projects

L'umano nell'uomo: Vasilij Grossman tra ideologie e domande eterne

Vasilij Grossman (1905-1964) s'impone solo ora, con il recente successo delle ripubblicazioni in diverse lingue del suo capolavoro postumo Vita e destino, come una delle figure artistiche e filosofiche pi\uf9 interessanti del XX secolo. La dimensione letteraria di Grossman che affonda le radici nella pi\uf9 alta tradizione russa - \ue8 votata ad un realismo classico, aperto all'universale, costantemente teso all'espressione di domande ultime ed eterne che affermano l'uomo e la sua libert\ue0 contro il potere dell'ideologia. L'umano nell'uomo \ue8 questo nucleo originale presente in ogni uomo che impedisce al potere di schiacciare il singolo nella morsa dell'omologazione. Tra i meandri oscuri della storia del Novecento, la risposta di Grossman non \ue8 da intendersi solo in senso intellettuale: \ue8 una strada reale che la letteratura, nella sua bellezza "incarnata", manifesta come possibilit\ue0 aperta all'esperienza di ciascuno. I saggi che compongono questo volume il secondo di studi collettanei su Grossman - rappresentano un passo decisivo verso una conoscenza completa della vita e dell'opera del grande autore russo e ne documentano l'appartenenza ai classici della letteratura di ogni tempo

Session 17 Ecophysiology

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Hormonal regulation in different varieties of chenopodium quinoa willd. Exposed to short acute uv-b irradiation

Increased ultraviolet-B (UV-B) due to global change can affect plant development and metabolism. Quinoa tolerates extreme conditions including high UV levels. However, the physiological mechanisms behind its abiotic stress tolerance are unclear, especially those related to UV-B. We previously demonstrated that 9.12 kJ m−2 d−1 may induce UV-B-specific signaling while 18.24 kJ m−2 d−1 promotes a UV-B-independent response. Here, we explored the effects of these UV-B doses on hormonal regulation linked to plant morphology and defense among diverse varieties. Changes in fluorescence parameters of photosystem II, flavonoids and hormones (indoleacetic acid (IAA), jasmonic acid (JA), abscisic acid (ABA) and salicylic acid (SA)) were surveyed under controlled conditions. Here, we showed that the sensitivity to short acute UV-B doses in varieties from different habitats is influenced by their parental lines and breeding time. UV-B sensitivity does not necessarily correlate with quinoa’s geographical distribution. The role of flavonoids in the UV-B response seems to be different depending on varieties. Moreover, we found that the extent of changes in JA and SA correlate with UV-B tolerance, while the increase of ABA was mainly related to UV-B stress

The effect of soil moisture depletion on Stevia (Stevia rebaudiana Bertoni) grown in greenhouse conditions: Growth, steviol glycosides content, soluble sugars and total antioxidant capacity.

The purpose of the present study was to determine threshold values of soil moisture content for Ste-via (Stevia rebaudiana Bertoni) and to evaluate the effects of drought stress on the main metabolites ofthis species. For these purposes, a greenhouse experiment was carried out with four soil moisture lev-els and plant growth, steviol glycoside (SVglys) contents, soluble sugars and antioxidant capacity wereinvestigated at variable soil moisture content. Irrigation was scheduled at 3, 6, 9 and 12-day irrigationintervals, based on soil moisture content at 90, 75, 60 and 45% of field capacity (FC) respectively. Theresults showed that soil water depletion up to 60% FC (9-day irrigation interval) had no negative effecton plant growth and leaf dry weight, whereas a significant growth reduction occurred at 45% FC (12-dayirrigation interval). Similarly, the total SVglys content increased when soil moisture was depleted to 60%FC (9-day irrigation interval), but these metabolites contents decreased by 45% FC treatment. AlthoughStevia growth and SVglys content significantly decreased under severe drought stress (45% FC), the totalantioxidant capacity and soluble sugars increased in the identical condition. The obtained results suggestthat Stevia plants can grow well with a soil water content near to 60% FC, showing a good SVglys content.The Stevia tolerance to mild water stress is noteworthy, especially in water limited regions. In addition,it was found that soil water depleted to 45% FC was detrimental to Stevia in greenhouse conditions. Theimprovement of antioxidant capacity and soluble sugar content by soil water stress conditions could beconsidered as physiological and biochemical responses to a progressive drought stress in Stevia and maybe an acclimation response to drought stress

Plant growth retardants (PGRs) affect growth and secondary metabolite biosynthesis in Stevia rebaudiana Bertoni under drought stress

Beyond the inhibitory action against the gibberellin biosynthesis, some plant growth retardants (PGRs) can play an important role in regulating plant responses to abiotic stress through the induction of different tolerance mechanisms. The aim of the present study was the exploitation of the potential of PGRs in enhancing the resistance to drought stress in Stevia rebaudiana Bert. Therefore, the effects of three PGRs on stevia plants grown under drought stress condition were investigated. Stevia plants were first subjected to water stress and, second, treated with PGRs to detect PGRs effect on biometric, productive and phytochemical characteristics of drought stressed-plants. The control plants were uniformly irrigated at 3-day intervals, while water-stress conditions were imposed by watering the plants at 12-day intervals. Subsequently, the Chlorocholine chloride (CCC, as Copalyl diphosphate synthase inhibitor and Kaurene synthase inhibitor), Paclobutrazol (PBZ, as Kaurene oxidase inhibitor) and Daminozide (DAM, as anti-gibberellins) were applied in drought stressed-plants. The CCC and DAM were sprayed on stevia shoots, while PBZ was drenched. The obtained results showed that leaf dry weight of stevia plantswas significantly reduced by drought stress, but this parameter increased as a consequence of CCC and PBZ treatments. Drought stress also caused a significant reduction in total steviol glycoside (SVglys) content. This reduction was more pronounced in drought stressed-plants treated with CCC, while PBZ was able to counteract the SVglys reduction,with SVgly content similar to that observed in the control. Similarly, PBZ was able to increase the soluble sugar production and total antioxidant capacity in the leaves of stressed-stevia plants. These findings suggested that CCC and, in particular, PBZ had a protective effect on stevia growth under drought stress by induction of antioxidant defenses and soluble sugar production. CCC seems to inhibit gibberellin biosynthesis, preventing the SVglys production, while DAM and PBZ, as gibberellin inhibitors, didn't have a negative effect on SVglys production in drought stressed-plants. This observation seems to emphasize their role in limiting the rate of target enzymes of CCC in SVglys biosynthetic pathway.Moreover, the induction of glucose production, as a substrate for SVglys biosynthesis, could be a convincing evidence for SVglys promotion in PBZ treated-plants

Lung injury and degradation of extracellular matrix components by Asperigillus fumigatus serine proteinase.

Aspergillus fumigatus produces a variety of extracellular proteinases that are believed to be virulence factors towards Aspergillus-related lung disease. Among Aspergillus proteinases, the serine proteinase is thought to play a major virulent role because of its widespread production. Nevertheless, evidence of direct pulmonary injury caused by the A. fumigatus serine proteinase is still lacking. The purpose of our work was: (1) to provide evidence for a pivotal role of A. fumigatus serine proteinase in producing lung injury in an animal model, and (2) to investigate the broadness of the substrate specificity of the proteinase towards extracellular matrix components. To achieve this aim, the proteinase from an A. fumigatus strain isolated from human airways was purified by a four-step procedure, including cation exchange and hydrophobic interaction. High-performance capillary electrophoresis, SDS-PAGE, determination of K(m) towards synthetic substrates, and inhibitory studies were used to further characterize the A. fumigatus serine proteinase. With reference to extracellular matrix components, the A. fumigatus serine proteinase was shown to degrade human lung elastin at a higher rate than an equimolar amount of human neutrophil elastase. Human lung collagen, type I and type III collagens, as well as fibronectin, were quickly digested by the A. fumigatus serine proteinase. Finally, mice intratracheally injected with the proteinase showed a significant degree of lower respiratory tract destruction. We conclude that the A. fumigatus serine proteinase is capable per se of hydrolyzing the major structural barriers of the lung