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CO2 Adsorption on the B12N12 Nanocage Encapsulated with Alkali Metals: A Density Functional Study
Haiyan Zhu,Qiyan Zhang,Qinfu Zhao,He Zhao,Yifan Feng,Bingbing Suo,Huixian Han,Qi Song,Yawei Li,Wenli Zou,Haiyan Zhu 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2019 NANO Vol.14 No.3
Density functional theory (DFT) calculations have been carried out to study the capacity of the B12N12 nanocage encapsulated with alkali metals (Li, Na, K) for the CO2 adsorption and activation. It is found that after encapsulating alkali metals, the alkali metal atoms are closer to one side of clusters instead of exactly lying at the center, and a considerable charge transfers from the inner alkali metal atoms to the B12N12 cage. Besides, the HOMO–LUMO gap (HLG) values of Li@B12N12, Na@B12N12 and K@B12N12 are decreased to about 6 eV, being much smaller than that of the pristine B12N12. Although the geometry structure parameters and the energy differences of M06-2X are slightly different from the ones of ωB97X-D, some identical results of two kinds of functional can be obtained. CO2 can be adsorbed chemically and physically on majority bonds of all the clusters, except for some bonds with large change in bond length and bond indices. The encapsulation of alkali-metal atoms may enhance the physical and chemical adsorption of CO2 on the surface of the clusters, in which Na@B12N12 and K@B12N12 are the most powerful physical and chemical adsorbent for CO2, respectively.
( Feng Yun Gong ),( Ding Yu Zhang ),( Jiang Guo Zhang ),( Li Li Wang ),( Wei Li Zhan ),( Jun Ying Qi ),( Jian Xin Song ) 생화학분자생물학회(구 한국생화학분자생물학회) 2014 BMB Reports Vol.47 No.4
To gain insights into the effect of MexB gene under the short interfering RNA (siRNA), we synthesized 21 bp siRNA duplexes against the MexB gene. RT-PCR was performed to determine whether the siRNA inhibited the expression of MexB mRNA. Changes in antibiotic susceptibility in response to siRNA were measured by the E-test method. The efficacy of siRNAs was determined in a murine model of chronic P. aeruginosa lung infection. MexB-siRNAs inhibited both mRNA expression and the activity of P. aeruginosa in vitro. In vivo, siRNA was effective in reducing the bacterial load in the model of chronic lung infection and the P. aeruginosa-induced pathological changes. MexB-siRNA treatment enhanced the production of inflammatory cytokines in the early infection stage (P < 0.05). Our results suggest that targeting of MexB with siRNA appears to be a novel strategy for treating P. aeruginosa infections. [BMB Reports 2014; 47(4): 203-208]
Synthesis of rod-like titanium doped hydroxyapatite nanopowder
Li-li Wang,Xiu-feng Wang,Cheng-long Yu,Yan-qi Zhao 한양대학교 세라믹연구소 2013 Journal of Ceramic Processing Research Vol.14 No.6
Rod-like titanium doped hydroxyapatite (Ti-doped HA) nanopowder was synthesized using Ca(NO3)2 • 4H2O, (NH4)2HPO4 and tetraethylorthotitanate as precursor materials via a combination of chemical co-precipitation and microwave techniques route. The effect of the content of titanium in Ti-doped HA (0.2-2.4 wt.%) on sintering behavior, crystal size, shape and morphology was investigated. The results suggested that the addition of titanium to HA structure did restrain HA decomposition and thermal reaction between HA and titanium, which resulted in improved thermal stability of HA at high sintering temperature. The grain size of sintered Ti-doped HA, which was much smaller than that of pure HA. 0.8 wt.% addition of titanium to HA, was optimum for producing nanometer-sized rod-like Ti-doped HA crystal with improved thermal stability.
Characterization of a Novel cry1-Type Gene from Bacillus thuringiensis subsp. alesti Strain LY-99
Qi, Xu Feng,Li, Ming Shun,Choi, Jae-Young,Roh, Jong-Yul,Song, Ji Zhen,Wang, Yong,Jin, Byung-Rae,Je, Yeon-Ho,Li, Jian Hong Korean Society of Sericultural Science 2009 International Journal of Industrial Entomology Vol.18 No.1
B. thuringiensis strain LY-99 belonging to subsp. alesti (H3a3c), was isolated from Chinese tobacco warehouse and showed significantly high toxicity to Plutella xylostella. For the identification of the cry1-type genes from B. thuringiensis LY-99, an extended multiplex PCRrestriction fragment length polymorphism (PCRRFLP) method was established by using two pairs of universal primers based on the conserved regions of the cry1-type genes to amplify around 2.4 kb cry1-type gene fragments. Then the DNA fragment was cloned into pGEM-T Easy vector and digested with EcoRI and EcoRV enzymes. Through this method, a known cry1-type gene was successfully identified from the reference strain, B. thuringiensis subsp. alesti. In addition, the RFLP patterns revealed that B. thuringiensis LY-99 included a novel cry1A-type gene in addition to cry1Aa, cry1Ac, cry1Be and cry1Ea genes. The novel cry1A-type gene was designated cry1Ah2 (Genbank accession No DQ269474). An inverse PCR method was used to amplify the flank regions of cry1Ah2 gene. Finally, 3143 bp HindIII fragment from B. thuringiensis LY-99 plasmid DNA including 5' region and partial ORF was amplified, and sequence analysis revealed that cry1Ah2 gene from LY-99 showed 89.31% of maximum sequence similarity with cry1Ac1 crystal protein gene. In addition, the deduced amino acid sequence of Cry1Ah2 protein shared 87.80% of maximum identity with that of Cry1Ac2. This protein therefore belongs to a new class of B. thuringiensis crystal proteins.
Molecular Characterization of A Novel Bacillus thuringiensis Strain from China
Qi Xu Feng,Li Ming Shun,Choi Jae Young,Kim Yang-Su,Wang Yong,Kang Joong Nam,Choi Heekyu,Je Yeon Ho,Song Ji Zhen,Li Jian Hong Korean Society of Sericultural Science 2005 International Journal of Industrial Entomology Vol.11 No.1
A strain of Bacillus thuringiensis that showed significantly high toxicity to Plutella xylostella was isolated from a dust sample collected from Chinese tobacco warehouse and characterized. The isolate named B. thuringiensis LY-99 was determined to belong to subsp. alesti (H3a3c) by an H antisera agglutination test and produced bipyramidal inclusions. Plasmid and crystal protein patterns of the LY-99 were different from those of the reference strain, subsp. alesti. PCR analysis with specific primers revealed that this isolate contained abundant cry genes including crylAa, crylAc, crylB, crylD, crylE, crylF and cry2 genes, which was absolutely different from cry gene profile of the subsp. alesti. In addition, insecticidal activity of the LY-99 against P. xylostella larvae was about 44 times higher than that of the subsp. alesti.
Qi Feng Li,Chen Guang Liu,김재창 한국화학공학회 2009 Korean Journal of Chemical Engineering Vol.26 No.1
The synthesis of thiophene from the reaction of n-Butanol and carbon disulfide was performed in a fixedbed reactor in the presence of promoted chromia on γ-alumina. A high selectivity to thiophene (87%) and a long lifetime of the catalyst (55 hour) was obtained at 450℃with a 1 : 6 n-Butanol to carbon disulfide molar ratio and LHSV 1 h−1 over γ-Al2O3 promoted by 7% K2CO3 with 15% Cr2O3 loaded. The catalytic behavior of these catalysts can be attributed to their dual-functional acidity and dehydrogenating and cyclized properties.
Qi Fei-Yan,Zhu Zhou-Hai,Li Meng,Guan Ying,Peng Qi-Yuan,Lu She-Ming,Liu Zhi-Hua,Wang Ming-Feng,Miao Ming-Ming,Chen Zhang-Yu,Li Xue-Mei,Bai Jie,Yao Jian-Hua 한국유전학회 2022 Genes & Genomics Vol.44 No.11
Background: Smoking behavior is influenced by multiple genes, including the bitter taste gene TAS2R38. It has been reported that the correlation between TAS2R38 and smoking behavior has ethnicity-based differences. However, the TAS2R38 status in Chinese smokers is still unclear. Objective: This study aims to investigate the possible relationship between genetic variations in TAS2R38 (A49P, V262A and I296V) and smoking behaviors in the Han Chinese population. Methods: The haplotype analyses were performed and smoking behavior questionnaire was completed by 1271 individuals. Genetic association analyses for smoking behavior were analyzed using chi-square test. Further, for investigating the molecular mechanism of TAS2R38 variants effect on smoking behavior, we conducted TAS2R38-PAV and TAS2R38-AVI expression plasmids and tested the cellular calcium assay by cigarette smoke compounds stimulus in HEK293. Results: Significant associations of genetic variants within TAS2R38 were identified with smoking behavior. We found a higher PAV/PAV frequency than AVI/AVI in moderate and high nicotine dependence (FTND ≥ 4; X2 = 4.611, 1 df, p = 0.032) and strong cigarette smoke flavor intensity preference (X2 = 4.5383, 1 df, p = 0.033) in participants. Furthermore, in the in vitro cellular calcium assay, total particle matter (TPM), N-formylnornicotine and cotinine, existing in cigarette smoke, activated TAS2R38-PAV but not TAS2R38-AVI-transfected cells. Conclusion: Our data highlights that genetic variations in TAS2R38 are related to smoking behavior, especially nicotine dependence and cigarette smoke flavor intensity preference. Our findings may encourage further consideration of the taste process to identify individuals susceptible to nicotine dependence, particularly Han Chinese smokers.
Molecular Characterization of A Novel Bacillus thuringiensis Strain from China
( Xu Feng Qi ),( Ming Shun Li ),( Jae Young Choi ),( Yang Su Kim ),( Yong Wang ),( Joong Nam Kang ),( Hee Kyu Choi ),( Yeon Ho Je ),( Ji Zhen Song ),( Jian Hong Li ) 한국잠사학회 2005 International Journal of Industrial Entomology Vol.11 No.1
A strain of Bacillus thuringiensis that showed significantly high toxicity to Plutella xylostella was isolated from a dust sample collected from Chinese tobacco warehouse and characterized. The isolate named B. thuringiensis LY-99 was determined to belong to subsp. alesti (H3a3c) by an H antisera agglutination test and produced bipyramidal inclusions. Plasmid and crystal protein patterns of the LY-99 were different from those of the reference strain, subsp. alesti. PCR analysis with specific primers revealed that this isolate contained abundant cry genes including cry1Aa, cry1Ac, cry1B, cry1D, cry1E, cry1F and cry2 genes, which was absolutely different from cry gene profile of the subsp. alesti. In addition, insecticidal activity of the LY-99 against P. xylostella larvae was about 44 times higher than that of the subsp. alesti.
Characterization of a Novel cry1-Type Gene from Bacillus thuringiensis subsp. alesti Strain LY-99
Xu Feng Qi,Ming Shun Li,Jae Young Choi,Jong Yul Roh,Ji Zhen Song,Yong Wang,Byung Rae Jin,Yeon Ho Je,Jian Hong Li 한국잠사학회 2009 International Journal of Industrial Entomology Vol.18 No.1
B. thuringiensis strain LY-99 belonging to subsp. Alesti (H3a3c), was isolated from Chinese tobacco warehouse and showed significantly high toxicity to Plutella xylostella. For the identification of the cry1-type genes from B. thuringiensis LY-99, an extended multiplex PCR-restriction fragment length polymorphism (PCR-RFLP) method was established by using two pairs of universal primers based on the conserved regions of the cry1-type genes to amplify around 2.4 kb cry1-type gene fragments. Then the DNA fragment was cloned into pGEM-T Easy vector and digested with EcoRI and EcoRV enzymes. Through this method, a known cry1-type gene was successfully identified from the reference strain, B. thuringiensis subsp. alesti. In addition, the RFLP patterns revealed that B. thuringiensis LY-99 included a novel cry1A-type gene in addition to cry1Aa, cry1Ac, cry1Be and cry1Ea genes. The novel cry1A-type gene was designated cry1Ah2 (Genbank accession No DQ269474). An inverse PCR method was used to amplify the flank regions of cry1Ah2 gene. Finally, 3143 bp HindIII fragment from B. thuringiensis LY-99 plasmid DNA including 5` region and partial ORF was amplified, and sequence analysis revealed that cry1Ah2 gene from LY-99 showed 89.31% of maximum sequence similarity with cry1Ac1 crystal protein gene. In addition, the deduced amino acid sequence of Cry1Ah2 protein shared 87.80% of maximum identity with that of Cry1Ac2. This protein therefore belongs to a new class of B. thuringiensis crystal proteins.