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Purification and Characterization of an Extracellular Protease from Bacillus pumilus CN8
Mei-Hu Ma,Yong-Guo Jin,Hao-Li Li,Jun Wang,Ha-Na Kim,오덕환 한국식품위생안전성학회 2011 한국식품위생안전성학회지 Vol.26 No.1
The protease produced by a Bacillus pumilus CN8 strain was purified by DEAE-Cellulose-52 ion exchange. It has a molecular weight of approximately 96,920 Dalton. In the present study, this protease showed strong activity over a broad range of pH (6.5-9.5) and temperature from 40℃ to 60℃, and the protease performed the maximal activity at pH 7.3 at 42℃. The effect of metal ions on protease activity showed that K+ could slightly increase the protease activity, and other ions such as Zn²+, Fe²+, Na+, Ca²+, Mg²+ had no significant activation or inhibition to the protease (P > 0.05), and the more important is that Cu²+, Mn²+, Sn²+, Cd²+ had a strong inhibitory effect on the protease activity.
Chloride Diffusivity of High-Performance Concrete due to Early-Age Shrinkage Cracking
Li-Na Ma,Yanhua Zhao,Jinxin Gong 대한토목학회 2019 KSCE JOURNAL OF CIVIL ENGINEERING Vol.23 No.12
Due to the addition of mineral admixtures, early-age shrinkage cracking is a common feature in high-performance concrete (HPC). Chloride diffusivity of HPC due to early-age shrinkage cracking was investigated through rapid chloride migration (RCM) method. Restrained/unrestrained slabs made of HPC containing fly ash (FA) and ground granulated blast-furnace slag (GGBS) were left outdoors for early-age shrinkage cracking, and then cylindrical samples were drilled from slabs for RCM test to quantify the chloride diffusion coefficient, wherein a crack influence factor was introduced to account for the contribution of cracking in the chloride diffusivity progress. Test results from unrestrained HPC reveal that the addition of mineral admixtures could densify the pore structure of HPC thus improved the chloride diffusion coefficient, though FA had a delayed effect. The RCM tests from restrained HPC indicate that the crack indeed had an effect on the chloride ion transportation, but pore structure still dominated the chloride ingress. For a fixed cement replacement, the more the GGBS in the mix, the higher the contribution of cracking to chloride ion penetration.
Chen, Peng,Wang, Xiu-Li,Ma, Zhong-Sen,Xu, Zhong,Jia, Bo,Ren, Jin,Hu, Yu-Xin,Zhang, Qing-Hua,Ma, Tian-Gang,Yan, Bing-Di,Yan, Qing-Zhu,Li, Yan-Lei,Li, Zhen,Yu, Jin-Yan,Gao, Rong,Fan, Na,Li, Bo,Yang, Jun Asian Pacific Journal of Cancer Prevention 2012 Asian Pacific journal of cancer prevention Vol.13 No.7
HMGN5 is a typical member of the HMGN (high mobility group nucleosome-binding protein) family which may function as a nucleosomal binding and transcriptional activating protein. Overexpression of HMGN5 has been observed in several human tumors but its role in tumorigenesis has not been fully clarified. To investigate its significance for human lung cancer progression, we successfully constructed a shRNA expression lentiviral vector in which sense and antisense sequences targeting the human HMGN5 were linked with a 9-nucleotide loop. Inhibitory effects of siRNA on endogenous HMGN5 gene expression and protein synthesis were demonstrated via real-time RT-PCR and western blotting. We found HMGN5 silencing to significantly inhibit A549 and H1299 cell proliferation assessed by MTT, BrdU incorporation and colony formation assays. Furthermore, flow cytometry analysis showed that specific knockdown of HMGN5 slowed down the cell cycle at the G0/G1 phase and decreased the populations of A549 and H1299 cells at the S and G2/M phases. Taken together, these results suggest that HMGN5 is directly involved in regulation cell proliferation in A549 and H1299 cells by influencing signaling pathways involved in cell cycle progression. Thus, our finding suggests that targeting HMGN5 may be an effective strategy for human lung cancer treatment.
Ying Yang,Dong Wang,Lei Cui,Hong-Hao Ma,Li Zhang,Hong-Yun Lian,Qing Zhang,Xiao-Xi Zhao,Li-Ping Zhang,Yun-Ze Zhao,Na Li,Tian-You Wang,Zhi-Gang Li,Rui Zhang 대한암학회 2021 Cancer Research and Treatment Vol.53 No.1
Purpose We sought to investigate the effectiveness and safety of dabrafenib in children with BRAFV600E-mutated Langerhans cell histiocytosis (LCH). Materials and Methods A retrospective analysis was performed on 20 children with BRAFV600E-mutated LCH who were treated with dabrafenib. Results The median age at which the patients started taking dabrafenib was 2.3 years old (range, 0.6 to 6.5 years). The ratio of boys to girls was 2.3:1. The median follow-up time was 30.8 months (range, 18.9 to 43.6 months). There were 14 patients (70%) in the risk organ (RO)+ group and six patients (30%) in the RO– group. All patients were initially treated with traditional chemotherapy and then shifted to targeted therapy due to poor control of LCH or intolerance to chemotherapy. The overall objective response rate and the overall disease control rate were 65% and 75%, respectively. During treatment, circulating levels of cell-free BRAFV600E (cfBRAFV600E) became negative in 60% of the patients within a median period of 3.0 months (range, 1.0 to 9.0 months). Grade 2 or 3 adverse effects occurred in five patients. Conclusion Some children with BRAFV600E-mutated LCH may benefit from monotherapy with dabrafenib, especially high-risk patients with concomitant hemophagocytic lymphohistiocytosis and intolerance to chemotherapy. The safety of dabrafenib is notable. A prospective study with a larger sample size is required to determine the optimal dosage and treatment duration.
Li, Na,Sun, Huaqin,Wu, Qiaqing,Tao, Dachang,Zhang, Sizhong,Ma, Yongxin Korean Society for Biochemistry and Molecular Biol 2007 Journal of biochemistry and molecular biology Vol.40 No.2
We have cloned a novel mouse zinc finger protein gene Znf313 by rapid amplification of cDNA ends (RACE) according to the homologue of human ZNF313 gene. The cDNA is 2,163 base pairs (bp) in length and encodes a 229 amino acids (aa) protein with a $C_3HC_4$ ring finger domain and three $C_2H_2$ domains. 89% and 93% nucleotide (nt) and aa sequence identity is observed with its human homologue. Revealed by Northern blot and RT-PCR, full mRNA consists of 2.16 kb and widely expresses in tissues as a single transcript, most abundantly in heart, liver, kidney and testis. The expression of Znf313 in testis is detected in all development stages. Western blot analysis also reveals that Znf313 is expressed in the tissues. Immunohistochemical staining and subcellular localization demonstrate that Znf313 is expressed both in the cytoplasm and nucleus whereas predominantly localized in the nucleus. Present data suggests that Znf313 gene might play a fundamental role in gene transcription and regulation in organism and relates to spermatogenesis.
Dapeng Li,Peng Zhang,Jiangtao Duan,Yaxin Wu,Na Ding,Zhenyu Wan,Longqi Chen,Jingli Xu,Suxiang Ge,Juntao Ma 한국공업화학회 2022 Journal of Industrial and Engineering Chemistry Vol.114 No.-
Utilization of fly ash (FA) wastes as the carriers of catalysts for the environmental application is an economicand practical strategy for their low cost, easy accessibility and thermal stability. However, mostcatalysts immobilized on fly ash were metal or metal oxides, some potential catalysts such as metalphthalocyanine complexes have not been reported upon their heterogeneous catalysis with FA as the carriers. In this paper, highly active iron octacarboxyphthalocyanine were immobilized onto the bird nestlikesurfaces of fly ash microspheres after NaOH activation. It is noted that the FeOCPc@FA compositeswith only 2 wt.% exhibited the high catalytic efficiency in the organic dye degradation. The high concentrationof 30 mg/L rhodamine B and methylene blue could be fast decolorized in the presence ofFeOCPc@FA–2 % and KHSO5. Moreover, the ultrafast decolorization of these dyes could be observed inthe catalytic system composed of FeOCPc@FA–2 %, KHSO5 and BuOOH (tert-butyl hydroperoxide). Simultaneous activation of KHSO5 and BuOOH could be realized in our designed catalytic system. Based on the structural characterizations of composites and active species generated during the catalyticprocesses, the probable generation pathway of metal–oxygen active species and various radicals wereanalyzed to explicate the catalytic mechanism. Our investigation provides a high efficiency, low costand environmentally friendly strategy for advanced oxidation treatment of organic pollutants.
Evidence for the Presence of Long-Lived Plasma Cells in Nasal Polyps
Ya-Na Zhang,Jia Song,Guan-Ting Zhai,Hai Wang,Ren-Zhong Luo,Jing-Xian Li,Bo Liao,Jin Ma,Heng Wang,Xiang Lu,Da-Bo Liu,Zheng Liu 대한천식알레르기학회 2020 Allergy, Asthma & Immunology Research Vol.12 No.2
Purpose: Plasma cells and immunoglobulins (Igs) play a pivotal role in the induction and maintenance of chronic inflammation in nasal polyps. During secondary immune responses, plasma cell survival and Ig production are regulated by the local environment. The purpose of the present study was to investigate the presence of long-lived plasma cells (LLPCs) and specific survival niches for LLPCs in human nasal polyps. Methods: Nasal mucosal samples were cultured with an air-liquid interface system and the Ig levels in culture supernatants were analyzed by enzyme-linked immunosorbent assay. The characteristics of LLPCs in nasal polyps were determined by immunohistochemistry and immunofluorescence. The expression of neurotrophins as well as their receptors was detected by quantitative real-time polymerase chain reaction, immunohistochemistry, immunofluorescence, and Western blotting. Results: The numbers of CD138+ total plasma cells and BCL2+ plasma cells were increased in both eosinophilic and non-eosinophilic nasal polyps compared with those in normal tissues. The production of IgG, IgA, and IgE was detected in culture supernatants even after a 32-day culture of nasal polyps. Although the total numbers of plasma cells were decreased in nasal polyps after culture, the numbers of BCL2+ plasma cells remained stable. The expression of nerve growth factor (NGF) as well as tropomyosin receptor kinase (Trk) A, a high-affinity receptor for NGF, was upregulated in both eosinophilic and non-eosinophilic nasal polyps. In addition, BCL2+ plasma cell numbers were positively correlated with NGF and TrkA mRNA expression in nasal mucosal tissues. Polyp plasma cells had the expression of TrkA. Conclusions: Human nasal polyps harbor a population of LLPCs and NGF may be involved in their prolonged survival. LLPCs may be a novel therapeutic target for suppressing the local Ig production in nasal polyps.
Zhanjie Ren,Na Ji,Kebao Jia,Li Wang,Harvest F. Gu,Jun Ma 한국유전학회 2015 Genes & Genomics Vol.37 No.1
Intercellular adhesion molecule-1 (ICAM-1) isan inflammation cytokine. Previous studies have demonstratedthat genetic polymorphisms in the ICAM-1 gene areassociated with chronic inflammation and diabeticnephropathy. The present study aimed to investigate theassociation of ICAM-1 gene polymorphisms with type 2diabetes (T2D) and diabetic peripheral neuropathy (DPN)in a Chinese Han population. Four valid single nucleotidepolymorphisms (SNPs) in the ICAM-1 gene were genotypedin 672 control subjects, 787 T2D patients with andwithout DPN with TaqMan allelic discrimination. Singlemarker association analyses indicated that A allele of SNPrs5498 was associated with DPN (P = 0.037, OR 1.715,95 % CI 1.027–2.865). Further analyses of clinicalparameters according to the genotypes of this polymorphismdemonstrated that T2D patients with DPN carryingAA and AG genotypes had higher risk of coronary heartdisease compared with those carrying GG genotype(30.6 % vs. 11.5 %, P = 0.040). In SNP rs1799969, thedifference of minor allele frequencies between the patientswithout and with DPN was found (0.02 vs 0.01, P = 0.014,OR 3.695, 95 % CI 1.211–11.277). SNP rs281432 hadhigher frequency of G allele in all T2D patients comparedwith control subjects (0.35 vs. 0.31, P = 0.041, OR 1.200,95 % CI 1.008–1.428). The present study provides evidencethat rs5498 (A/G E469K) polymorphism is associatedwith DPN in T2D, and also implicates that theassociation of ICAM-1 with DPN may be related to othervascular complications.