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11.
Regulation of plant defense responses in Arabidopsis by EDR2, a PH and START domain-containing protein 总被引:1,自引:0,他引:1
Tang D Ade J Frye CA Innes RW 《The Plant journal : for cell and molecular biology》2005,44(2):245-257
We have identified an Arabidopsis mutant that displays enhanced disease resistance (edr2) to the biotrophic powdery mildew pathogen Erysiphe cichoracearum. Inhibition of fungal growth on edr2 mutant leaves occurred at a late stage of the infection process and coincided with formation of necrotic lesions approximately 5 days after inoculation. Double-mutant analysis revealed that edr2-mediated resistance is suppressed by mutations that inhibit salicylic acid (SA)-induced defense signaling, including npr1, pad4 and sid2, demonstrating that edr2-mediated disease resistance is dependent on SA. However, edr2 showed normal responses to the bacterial pathogen Pseudomonas syringae pv. tomato strain DC3000. EDR2 appears to be constitutively transcribed in all tissues and organs and encodes a novel protein, consisting of a putative pleckstrin homology (PH) domain and a steroidogenic acute regulatory protein-related lipid-transfer (START) domain, and contains an N-terminal mitochondrial targeting sequence. The PH and START domains are implicated in lipid binding, suggesting that EDR2 may provide a link between lipid signaling and activation of programmed cell death mediated by mitochondria. 相似文献
12.
Stearoyl-CoA desaturase 1 (SCD1) catalyzes the synthesis of monounsaturated fatty acids (MUFA) from saturated FA. Mice with whole-body or skin-specific deletion of SCD1 are resistant to obesity. Here, we show that mice lacking SCD1 in adipose and/or liver are not protected from either genetic- (agouti; A(y)/a) or diet-induced obesity (DIO) despite a robust reduction in SCD1 MUFA products in both subcutaneous and epididymal white adipose tissue. Adipose SCD1 deletion had no effect on glucose or insulin tolerance or on hepatic triglyceride (TG) accumulation. Interestingly, lack of SCD1 from liver lowered the MUFA levels of adipose tissue and vice versa, as reflected by the changes in FA composition. Simultaneous deletion of SCD1 from liver and adipose resulted in a synergistic lowering of tissue MUFA levels, especially in the A(y)/a model in which glucose tolerance was also improved. Lastly, we found that liver and plasma TG show nearly identical genotype-dependent differences in FA composition, indicating that FA composition of plasma TG is predictive for hepatic SCD1 activity and TG FA composition. The current study suggests that SCD1 deletion from adipose and/or liver is insufficient to elicit protection from obesity, but it supports the existence of extensive lipid cross-talk between liver and adipose tissue. 相似文献
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14.
M. Danova A. Riccardi S. Brugnatelli R. Fiocca M. Girino L. Villani P. Giordano P. Dionigi M. Giordano R. Buttini G. Ucci G. Mazzini 《The Histochemical journal》1988,20(3):125-130
Summary Bromodeoxyuridine (BUDR) is a non-radioactive thymidine analogue which is incorporated into the DNA of proliferating cells. This allows evaluation of the size of the S-phase as the BUDR labelling index (BUDR-LI) not onlyin vitro but alsoin vivo, since BUDR is not toxic at the doses needed to label cells. To ascertain whetherin vivo BUDR incorporation can be detected on routine histological material we tested several different procedures prior to immunoperoxidase staining, on formalin-fixed, paraffin-embedded sections from five patients with gastric cancer, who received BUDR (250 mg m–2, intravenous) 4 h before surgery. To determine the optimal conditions for detecting BUDR in formalin-fixed tissues, immunohistochemical testing for BUDR was performed simultaneously on duplicate sections fixed with 70% ethanol. It was found that hydrolysis with 3N HCl at 37° C for 30 min and digestion with 0.5% in at 37° C for 30 min were sufficient to detect BUDR immunoreactivity in formalin-fixed sections.The method presented extends the range of applications of thein vivo BUDR technique for cell kinetics studies in human neoplasms because it can be used on routinely fixed archival material, with the advantage of correlating the kinetic data with histopathological characters. 相似文献
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16.
Current stocks and potential of carbon sequestration of the forest tree layer in Qinghai Province,China北大核心CSCD
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Aims Our objective was to estimate the carbon storage in the forest tree layer in Qinghai Province, China. Methods Based on forest resource inventory data and field investigation data, we estimated the carbon storage, sequestration rate and potentials in the forest tree layer in the Qinghai Province. Important findings The carbon density and total carbon storage of forest tree layer in Qinghai Province was 76.54 Mg·hm-2 and 27.38 Tg, respectively, of which four forest types (Picea spp. forest, Cupressus funebris forest, Betula spp. forest and Populus spp. forest) accounted for 86.67% while their areas were 96.23% of total forest areas in Qinghai. The carbon density and carbon storage of Picea spp. forest was 106.93 Mg·hm-2 and 14.78 Tg, respectively, which was the largest among all forest types. The carbon storage of the forest tree layer at different stand ages followed the sequence of over-mature forest > middle-aged forest > mature forest > near-mature forest > young forest. In addition, the carbon storage of forest tree layer in the province increased from 23.30 Tg in 2003 to 27.38 Tg in 2011. The average annual growth of carbon and carbon sequestration rate were 0.51 Tg and 1.06 Mg·hm-2·a-1, respectively. The maximum and minimum of carbon sequestration rate were respectively found in Cupressus funebris forest (0.44 Mg·hm-2·a-1) and Betula spp. forest (-1.06 Mg·hm-2·a-1). The mean carbon sequestration potential reached 8.50 Tg in 2011, with the highest value found in Picea spp. forest (3.40 Tg). These findings suggested high carbon sequestration potential of forest tree layer in Qinghai Province. Therefore, the carbon storage in Qinghai Province could be increased through better forest management and utilization. © 2018 Editorial Office of Chinese Journal of Plant Ecology. All rights reserved. 相似文献
17.
Effect of Alkylsilyl Side‐Chain Structure on Photovoltaic Properties of Conjugated Polymer Donors
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Haijun Bin Yankang Yang Zhengxing Peng Long Ye Jia Yao Lian Zhong Chenkai Sun Liang Gao He Huang Xiaojun Li Beibei Qiu Lingwei Xue Zhi‐Guo Zhang Harald Ade Yongfang Li 《Liver Transplantation》2018,8(8)
Side‐chain engineering is an important strategy for optimizing photovoltaic properties of organic photovoltaic materials. In this work, the effect of alkylsilyl side‐chain structure on the photovoltaic properties of medium bandgap conjugated polymer donors is studied by synthesizing four new polymers J70 , J72 , J73 , and J74 on the basis of highly efficient polymer donor J71 by changing alkyl substituents of the alkylsilyl side chains of the polymers. And the photovoltaic properties of the five polymers are studied by fabricating polymer solar cells (PSCs) with the polymers as donor and an n‐type organic semiconductor (n‐OS) m‐ITIC as acceptor. It is found that the shorter and linear alkylsilyl side chain could afford ordered molecular packing, stronger absorption coefficient, higher charge carrier mobility, thus results in higher Jsc and fill factor values in the corresponding PSCs. While the polymers with longer or branched alkyl substituents in the trialkylsilyl group show lower‐lying highest occupied molecular orbital energy levels which leads to higher Voc of the PSCs. The PSCs based on J70 :m‐ITIC and J71 :m‐ITIC achieve power conversion efficiency (PCE) of 11.62 and 12.05%, respectively, which are among the top values of the PSCs reported in the literatures so far. 相似文献
18.
Kui Jiang Guangye Zhang Guofang Yang Jianquan Zhang Zhengke Li Tingxuan Ma Huawei Hu Wei Ma Harald Ade He Yan 《Liver Transplantation》2018,8(9)
Ternary organic solar cells (OSCs) have attracted much research attention, as they can maintain the simplicity of the single‐junction device architecture while broadening the absorption range of OSCs. However, one main challenge that limits the development of ternary OSCs is the difficulty in controlling the morphology of ternary OSCs. In this paper, an effective approach to control the morphology is presented that leads to multiple cases of efficient nonfullerene ternary OSCs with efficiencies of up to 11.2%. This approach is based on a donor polymer with strong temperature dependent aggregation properties processed from hot solutions without any solvent additives and a pair of small molecular acceptors (SMAs) that have similar surface tensions and thus low propensity to form discrete phases. Such a ternary blend exhibits a simplified bulk‐heterojunction morphology that is similar to the morphology of previously reported binary blends. As a result, an almost linear relationship between VOC and film composition is observed for all nonfullerene ternary devices. Meanwhile, by carefully designing a control system with a large interfacial tension, a different phase separation and VOC dependence is demonstrated. This morphology control approach can be applicable to more material systems and accelerates the development of the ternary OSC field. 相似文献
19.
Effect of Ring‐Fusion on Miscibility and Domain Purity: Key Factors Determining the Performance of PDI‐Based Nonfullerene Organic Solar Cells
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Huawei Hu Yunke Li Jianquan Zhang Zhengxing Peng Lik‐kuen Ma Jingming Xin Jiachen Huang Tingxuan Ma Kui Jiang Guangye Zhang Wei Ma Harald Ade He Yan 《Liver Transplantation》2018,8(26)
Compared to the rapid development of nonfullerene organic solar cells (OSCs) based on the state‐of‐the‐art indacenodithiophene (IDT)‐based small molecule acceptors (SMAs), the progress for perylene diimide (PDI)‐based electron acceptors has lagged behind owing to the lack of understanding on the structure–morphology–performance relationship of PDI SMAs. Given the ease of synthesis for PDIs and their high intrinsic electron mobility, it is crucial to identify key material parameters that influence the polymer:PDI blend morphology and to develop rational approaches for molecular design toward high‐performance PDI‐based SMAs. In this study, three pairs of PDI‐based SMAs with and without ring‐fusion are investigated and it is found that ring‐fusion and domain purity are the key structural and morphological factors determining the fill factors (FFs) and efficiencies of PDI‐based nonfullerene OSCs. This data shows that nonfullerene OSCs based on the ring‐fused PDI‐based SMAs exhibit much higher average domain purity and thus increased charge mobilities, which lead to enhanced FFs compared to those solar cells based on nonfused PDIs. This is explained by higher Florry Huggins interaction parameters as observed by melting point depression measurements. This study suggests that increasing repulsive molecular interactions to lower the miscibility between the polymer donor and PDI acceptor is the key to improve the FF and performance of PDI‐based devices. 相似文献
20.
Influence of Donor Polymer on the Molecular Ordering of Small Molecular Acceptors in Nonfullerene Polymer Solar Cells
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Huawei Hu Kui Jiang Philip C. Y. Chow Long Ye Guangye Zhang Zhengke Li Joshua H. Carpenter Harald Ade He Yan 《Liver Transplantation》2018,8(5)
Nonfullerene polymer solar cells (PSCs) based on polymer donors and nonfullerene small molecular acceptors (SMAs) have recently attracted considerable attention. Although much of the progress is driven by the development of novel SMAs, the donor polymer also plays an important role in achieving efficient nonfullerene PSCs. However, it is far from clear how the polymer donor choice influences the morphology and performance of the SMAs and the nonfullerene blends. In addition, it is challenging to carry out quantitative analysis of the morphology of polymer:SMA blends, due to the low material contrast and overlapping scattering features of the π–π stacking between the two organic components. Here, a series of nonfullerene blends is studied based on ITIC‐Th blended with five different donor polymers. Through quantitative morphology analysis, the (010) coherence length of the SMA is characterized and a positive correlation between the coherence length of the SMA and the device fill factor (FF) is established. The study reveals that the donor polymer can significantly change the molecular ordering of the SMA and thus improve the electron mobility and domain purity of the blend, which has an overall positive effect that leads to the enhanced device FF for nonfullerene PSCs. 相似文献