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  • Wiley  (5)
  • Shi, Ping  (5)
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  • Wiley  (5)
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  • 1
    In: FEBS Letters, Wiley, Vol. 596, No. 3 ( 2022-02), p. 369-380
    Abstract: Aspirin is a commonly used anti‐inflammatory, analgesic and antithrombotic drug. It has attracted attention due to its potential antifungal therapeutic effect; however, the molecular mechanism is poorly understood. Here, the effects of aspirin on the cell wall of Saccharomyces cerevisiae were explored. We observed by scanning electron microscopy that aspirin could damage the cell wall ultrastructure. Meanwhile, a cellular surface hydrophobicity (CSH) assay showed that aspirin increased the hydrophobicity of the yeast cell surface. A drug sensitivity assay indicated that the overexpression of dolichol phosphate mannose synthase 1 ( DPM1 ) reversed the cell wall damage and decreased the CSH induced by aspirin. Importantly, aspirin decreased the expression and enzyme activity of DPM1 in S. cerevisiae . Molecular docking results demonstrated that aspirin could directly bind to the Ser141 site of DPM1. Similarly, we found that aspirin damaged the cell wall and inhibited the expression of DPM1 in Candida albicans . These findings improve the current understanding of the action mode of aspirin and provide new strategies for antifungal drug design.
    Type of Medium: Online Resource
    ISSN: 0014-5793 , 1873-3468
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 1460391-3
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Wiley ; 2015
    In:  Journal of Food Safety Vol. 35, No. 1 ( 2015-02), p. 108-118
    In: Journal of Food Safety, Wiley, Vol. 35, No. 1 ( 2015-02), p. 108-118
    Abstract: This study aimed to identify and evaluate the probiotic properties of five E nterococcus strains isolated from the silage using in vitro screening assays. Their metabolites, antibiotic susceptibility, antimicrobial activity, as well as their survival in the gastrointestinal tract ( GIT ) and adhesive ability to human intestinal cells were investigated. Among eight selected antibiotics, all the isolates showed sensitive traits to six particular antibiotics including tetracycline and vancomycin. L 2– L 5 showed inhibition zones against E scherichia coli and S almonella except that L 6 only inhibited the growth of E . coli . The GIT proved that all the strains were able to survive in low pH and bile salt conditions and they all can adhere to LS ‐174 T intestinal cells. L 2 and L 5 were then chosen to examine their competition activity toward E . coli and inflammatory response. The results showed that both strains exhibited strong competition activities toward E . coli. The displacement ratios were 98.4 and 97.7%, respectively. Compared with E . coli , L 2 showed lower stimulation of interleukin ( IL )‐8 and IL ‐1 β , while L 5 induced higher levels of cytokines to provoke an inflammatory response. Finally, the in vivo effect of L 2 was investigated. The data showed that L 2 was harmless. The results obtained suggest that L 2 is potentially probiotic. Practical Application E nterococci are lactic acid bacteria that occur frequently in large numbers in various foods including vegetable, meat and dairy products. However, some of these bacteria are also recognized as nosocomial pathogens. Several properties may be evaluated to prove the potential of the bacteria before using them as probiotics. Results of this study indicated that five E nterococcus strains isolated from the mixed grass and corn stalk silage exhibited different capacties of antibiotic susceptibility, antimicrobial activity, tolerance to gastrointestinal conditions, adhesion to intestinal cells, and competitive exclusion of E . coli adhesion to epithelial cells and stimulation of immunity. Among these strains, L 2 shows above‐average results in all probiotic criteria observed in vitro . Additionally, L 2 was evaluated to be safe in mice feeding. The findings of our study suggest that L 2 isolated from the silage may be potentially used as probiotic in humans.
    Type of Medium: Online Resource
    ISSN: 0149-6085 , 1745-4565
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2015
    detail.hit.zdb_id: 2179788-2
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  • 3
    Online Resource
    Online Resource
    Wiley ; 2020
    In:  Journal of Basic Microbiology Vol. 60, No. 4 ( 2020-04), p. 372-379
    In: Journal of Basic Microbiology, Wiley, Vol. 60, No. 4 ( 2020-04), p. 372-379
    Abstract: Although highly accurate molecular processes and various messenger RNA (mRNA) quality control and ribosome proofreading mechanisms are used by organisms to transcribe their genes and maintain the fidelity of genetic information, errors are inherent in all biological systems. Low‐level translation errors caused by an imbalance of homologous and nonhomologous amino acids caused by stress conditions are particularly common. Paradoxically, advantageous phenotypic diversity can be generated by such errors in eukaryotes through unknown molecular processes. Here, we found that the significant cadmium‐resistant phenotype was correlated with an increased mistranslation rate of the mRNA in Saccharomyces cerevisiae . This phenotypic change was also related to endogenous sulfur amino acid starvation. Compared with the control, the mistranslation rate caused by cadmium was significantly increased ( p   〈  .01). With the increase of cysteine contents in medium, the mistranslation rate of WT(BY4742a) decreased significantly ( p   〈  .01). This demonstrates that cadmium treatment and sulfur amino acid starvation both can induce translation errors. Although cadmium uptake is independent of the Sul1 transporter, cadmium‐induced mRNA mistranslation is dependent on the sulfate uptake of the Sul1p transporter. Furthermore, cadmium‐induced translation errors depend on methionine biosynthesis. Taken together, cadmium causes endogenous sulfur starvation, leading to an increase in the mRNA mistranslation, which contributes to the resistance of yeast cells to cadmium. We provide a new pathway mediating the toxicity of cadmium, and we propose that altering mRNA mistranslation may portray a different form of environmental adaptation.
    Type of Medium: Online Resource
    ISSN: 0233-111X , 1521-4028
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 1480967-9
    detail.hit.zdb_id: 632513-0
    detail.hit.zdb_id: 203025-1
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    Wiley ; 2021
    In:  Journal of Biochemical and Molecular Toxicology Vol. 35, No. 5 ( 2021-05)
    In: Journal of Biochemical and Molecular Toxicology, Wiley, Vol. 35, No. 5 ( 2021-05)
    Abstract: Clioquinol has been reported to act as a potential therapy for neurodegenerative diseases and cancer. However, the underlying mechanism is unclear. We have previously reported that clioquinol induces S‐phase cell cycle arrest through the elevation of calcium levels in human neurotypic SH‐SY5Y cells. In this study, different types of cells were observed to detect if the effect of clioquinol on intracellular calcium levels is cell type‐specific. The Cell Counting Kit‐8 assay showed that clioquinol exhibited varying degrees of concentration‐dependent cytotoxicity in different cell lines, and that the growth inhibition caused by it was not related to cell source or carcinogenesis. In addition, the inhibition of cell growth by clioquinol was positively associated with its effect on intracellular calcium content ([Ca 2+ ] i ). Furthermore, the elevation of [Ca 2+ ] i induced by clioquinol led to S‐phase cell cycle arrest. Similar to our previous studies, the increase in [Ca 2+ ] i was attributed to changes in the expression levels of the calcium pump SERCA2. Comparison of expression levels of SERCA2 between cell lines showed that cells with high levels of SERCA2 were more sensitive to clioquinol. In addition, analysis using UALCAN and the Human Protein Atlas also showed that the expression of SERCA2 in the corresponding human tissues was similar to that of the cells tested in this study, suggesting potential in the application of clioquinol in the future. In summary, our results expand the understanding of the molecular mechanism of clioquinol and provide an important strategy for the rational use of clioquinol.
    Type of Medium: Online Resource
    ISSN: 1095-6670 , 1099-0461
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 1481995-8
    SSG: 12
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  • 5
    Online Resource
    Online Resource
    Wiley ; 2018
    In:  IUBMB Life Vol. 70, No. 8 ( 2018-08), p. 753-762
    In: IUBMB Life, Wiley, Vol. 70, No. 8 ( 2018-08), p. 753-762
    Abstract: As a lipin family founding member, lipin1 exerts dual functions as a phosphatidate phosphatase enzyme and/or a co‐transcriptional regulator in lipid metabolism. In fact, it is also involved in many other cell processes. In this study, we utilized pull down assay coupled with mass spectrometry (MS) to unravel protein–protein interaction networks of lipin1 in 293T human embryonic kidney cells. Pull‐down assay on the Ni 2+ ‐chelating column was used to isolate lipin1 complexes from 293T cells transfected with 6‐His tagged lipin1. The lipin1 complexes were analyzed on Q Exactive mass spectrometer. A total of 30 proteins were identified from label free quantitation of the MS data by Proteome Discoverer platform. The physical interaction between lipin1 and eEF1A1 was further affirmed in 293T cells transfected with 6‐His tagged lipin1 and hepatocyte SMMC7721 cells by protein immunoprecipitation and immunofluorescence microscopy. Lipin1 also interacted with HIST1H2BK, which was confirmed in SMMC7721 cells by protein immunoprecipitation. Our proteomic analysis implicated lipin1 in novel roles in various cellular processes. © 2018 IUBMB Life, 70(8):753–762, 2018
    Type of Medium: Online Resource
    ISSN: 1521-6543 , 1521-6551
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2018
    detail.hit.zdb_id: 2009952-6
    detail.hit.zdb_id: 2485214-4
    SSG: 12
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