172 research outputs found

    The variation of morphological features and mineralogical components of biological soil crusts in the Gurbantunggut Desert of Northwestern China

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    Increasingly complex life forms were found in older biological soil crusts in the Gurbantaunggut Desert in Northwestern China. These crusts may play a critical role in mineral erosion and desert soil formation by modifying the weathering environment and ultimately affecting mineralogical variance. To test this hypothesis, variations in the morphological features and mineralogical components of successional biological soil crusts at 1 cm were studied by optical microscopy, SEM and grain size analysis. Concentrations of erosion-resistant minerals decreased with crust succession, while minerals susceptible to weathering increased with crust development. Neogenetic minerals were found in late stage crusts, but not in early stage crusts. Silt and clay concentrations were highest in early formation crusts and soil mean particle size decreased with crust succession. Cyanobacteria, lichen and moss were shown to erode and etch rocks, and secondary minerals produced by weathering were localized with the living organisms. Thus, more developed crusts appeared to contribute to greater mineral weathering and may be a major cause of mineralogical variance seen in the Gurbantunggut Desert. The greater activity and complexity of older crusts, as well as their improved moisture condition may function to accelerate mineral weathering. Therefore, protection and recovery of biological crusts is vital for desert soil formation

    Microalgal species variation at different successional stages in biological soil crusts of the Gurbantunggut Desert, Northwestern China

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    Biological soil crusts (BSC), most notably lichen crusts, develop and diversify in the Gurbantunggut Desert, the largest fixed and semi-fixed desert in China. Four different successional stages of BSC, including bare sand, microalgal crusts, lichen crusts, and moss crusts, were selected to determine successional changes in microalgal species composition and biomass and formation of BSC. A 10 x 10-m observation plot was established in an interdune region of the Gurbantunggut Desert and data were collected over an 8-year study period. The main results were: (1) different successional stages of BSC significantly affected the content of soil organic C and total and available N but not the total and available P and K content of soil; (2) composition of microalgal communities differed among the four successional stages; (3) significant differences in microalgal biomass were observed among the four successional stages; (4) bare sand was mainly uncompacted sand gains; (5) filamentous cyanobacteria, particularly Microcoleus vaginatus, were the dominant species in the early phase of crust succession. The presence of fungal mycelium and moss rhizoids prevented water and wind erosion

    Identification of Amino Acids Essential for Estrone-3-Sulfate Transport within Transmembrane Domain 2 of Organic Anion Transporting Polypeptide 1B1

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    As an important structure in membrane proteins, transmembrane domains have been found to be crucial for properly targeting the protein to cell membrane as well as carrying out transport functions in transporters. Computer analysis of OATP sequences revealed transmembrane domain 2 (TM2) is among those transmembrane domains that have high amino acid identities within different family members. In the present study, we identify four amino acids (Asp70, Phe73, Glu74, and Gly76) that are essential for the transport function of OATP1B1, an OATP member that is specifically expressed in the human liver. A substitution of these four amino acids with alanine resulted in significantly reduced transport activity. Further mutagenesis showed the charged property of Asp70 and Glu74 is critical for proper function of the transporter protein. Comparison of the kinetic parameters indicated that Asp70 is likely to interact with the substrate while Glu74 may be involved in stabilizing the binding site through formation of a salt-bridge. The aromatic ring structure of Phe73 seems to play an important role because substitution of Phe73 with tyrosine, another amino acid with a similar structure, led to partially restored transport function. On the other hand, replacement of Gly76 with either alanine or valine could not recover the function of the transporter. Considering the nature of a transmembrane helix, we proposed that Gly76 may be important for maintaining the proper structure of the protein. Interestingly, when subjected to transport function analysis of higher concentration of esteone-3-sulfate (50 µM) that corresponds to the low affinity binding site of OATP1B1, mutants of Phe73, Glu74, and Gly76 all showed a transport function that is comparable to that of the wild-type, suggesting these amino acids may have less impact on the low affinity component of esteone-3-sulfate within OATP1B1, while Asp 70 seems to be involved in the interaction of both sites

    Sesquiterpenes and lignans from the flower buds of Daphne genkwa and their nitric oxide inhibitory activities.

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    Chemical investigation of the Daphne genkwa has led to the isolation of four sesquiterpenes (1a/1b, 2 and 3), including one pair of sesquiterpene enantiomers (1a/1b), 1a is a new compound (+)-4-hydroxy-10-epirotundone, and twelve lignans (4-15). Their structures were elucidated by spectroscopic analysis, and the absolute configurations of 1a/1b were determined by CD analysis. All compounds were examined for their inhibitory effects on the nitric oxide (NO) production induced by lipopolysaccharide (LPS) in BV-2 microglial cells, and compounds 7-10 exhibited pronounced inhibition on NO production with IC50 values in the range of 5.8-10.2 μM, being more active than the positive control, quercetin (IC50 = 17.0 μM)

    Clara Cell 10-kDa Protein Gene Transfection Inhibits NF-κB Activity in Airway Epithelial Cells

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    Clara cell 10-kDa protein (CC10) is a multifunctional protein with anti-inflammatory and immunomodulatory effects. Induction of CC10 expression by gene transfection may possess potential therapeutic effect. Nuclear factor κB (NF-κB) plays a key role in the inflammatory processes of airway diseases.To investigate potential therapeutic effect of CC10 gene transfection in controlling airway inflammation and the underlying intracellular mechanisms, in this study, we constructed CC10 plasmid and transfected it into bronchial epithelial cell line BEAS-2B cells and CC10 knockout mice. In BEAS-2B cells, CC10's effect on interleukin (IL)-1β induced IL-8 expression was explored by means of RT-PCR and ELISA and its effect on NF-κB classical signaling pathway was studied by luciferase reporter, western blot, and immunoprecipitation assay. The effect of endogenous CC10 on IL-1β evoked IL-8 expression was studied by means of nasal explant culture. In mice, CC10's effect on IL-1β induced IL-8 and nuclear p65 expression was examined by immunohistochemistry. First, we found that the CC10 gene transfer could inhibit IL-1β induced IL-8 expression in BEAS-2B cells. Furthermore, we found that CC10 repressed IL-1β induced NF-κB activation by inhibiting the phosphorylation of IκB-α but not IκB kinase-α/β in BEAS-2B cells. Nevertheless, we did not observe a direct interaction between CC10 and p65 subunit in BEAS-2B cells. In nasal explant culture, we found that IL-1β induced IL-8 expression was inversely correlated with CC10 levels in human sinonasal mucosa. In vivo study revealed that CC10 gene transfer could attenuate the increase of IL-8 and nuclear p65 staining in nasal epithelial cells in CC10 knockout mice evoked by IL-1β administration.These results indicate that CC10 gene transfer may inhibit airway inflammation through suppressing the activation of NF-κB, which may provide us a new consideration in the therapy of airway inflammation

    Protective mechanisms of medicinal plants targeting hepatic stellate cell activation and extracellular matrix deposition in liver fibrosis

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