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- 저자 : Yaozhou, Zhang (검색결과 5 건)
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Basic Properties and Engineering Application of Bentonite-Cement-Water Glass Grouting
Yao Zhou,Gui He Wang,Yu Fei Yuan 대한토목학회 2020 KSCE JOURNAL OF CIVIL ENGINEERING Vol.24 No.9
The cement manufacturing process causes environmental problems such as carbon dioxide emissions. Bentonite-cement-water glass grouting (BCG) is a grout with low environmental impact, designed to reduce the use of cement. The significance of this study is to explore the fundamental properties of BCGs with the bentonite contents of up to 50%, and the antiwash-out and permeability characteristics of BCG in comparison with cement-water glass grout (CG). The effects of water-to-solid ratios (W/S), bentonite content, water glass content and the volume ratio of bentonite-cement slurry to water glass slurry (Va: Vb) on the fundamental properties of BCGs were tested in the laboratory. The results show that the BCGs have excellent characteristics of high viscosity, low bleeding, short and controllable setting time, and high early strength. The BCGs have been applied to the pre-grouting of the water-rich sandy pebble stratum in the Wangfujing North Station section of Beijing Metro Line 8 and achieved better water sealing and reinforcement effects than CG.
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( Yao Zhou ),( Shengmin Zhou ),( Haijun Yu ),( Jingyi Li ),( Yang Xia ),( Baoyi Li ),( Xiaoli Wang ),( Ping Wang ) 한국미생물 · 생명공학회 2016 Journal of microbiology and biotechnology Vol.26 No.5
S-Nitrosoglutathione reductase (GSNOR) metabolizes S-nitrosoglutathione (GSNO) and has been shown to play important roles in regulating cellular signaling and formulating host defense by modulating intracellular nitric oxide levels. The enzyme has been found in bacterial, yeast, mushroom, plant, and mammalian cells. However, to date, there is still no evidence of its occurrence in filamentous fungi. In this study, we cloned and investigated a GSNOR-like enzyme from the filamentous fungus Aspergillus nidulans. The enzyme occurred in native form as a homodimer and exhibited low thermal stability. GSNO was an ideal substrate for the enzyme. The apparent Km and kcat values were 0.55 mM and 34,100 min-1, respectively. Substrate binding sites and catalytic center amino acid residues based on those from known GSNORs were conserved in this enzyme, and the corresponding roles were verified using site-directed mutagenesis. Therefore, we demonstrated the presence of GSNOR in a filamentous fungus for the first time.
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Xueyun Wu,Zhengbin Lv,Yaozhou Zhang,Dong Yang,Xiangcheng Zhu,Zhinan Xu,Zhiyang Feng,Ben Shen 한국생물공학회 2010 Biotechnology and Bioprocess Engineering Vol.15 No.4
The heterologous production of iso-migrastatin (iso-MGS) was successfully demonstrated in an engineered S. lividans SB11002 strain, which was derived from S. lividans K4-114, following introduction of pBS11001,which harbored the entire mgs biosynthetic gene cluster. However, under similar fermentation conditions, the iso-MGS titer in the engineered strain was significantly lower than that in the native producer - Streptomyces platensis NRRL 18993. To circumvent the problem of low iso-MGS titers and to expand the utility of this heterologous system for iso-MGS biosynthesis and engineering, systematic optimization of the fermentation medium was carried out. The effects of major components in the cultivation medium,including carbon, organic and inorganic nitrogen sources,were investigated using a single factor optimization method. As a result, sucrose and yeast extract were determined to be the best carbon and organic nitrogen sources, resulting in optimized iso-MGS production. Conversely, all other inorganic nitrogen sources evaluated produced various levels of inhibition of iso-MGS production. The final optimized R2YE production medium produced iso-MGS with a titer of 86.5 mg/L, about 3.6-fold higher than that in the original R2YE medium, and 1.5 fold higher than that found within the native S. platensis NRRL 18993 producer.
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Expression of Human Stem Cell Factor with Recombinant Baculovirus in BmN Cell Line and Silkworm
Xijie, Guo,Yongfeng, Jin,Mingguan, Yang,Yaozhou, Zhang Korean Society of Sericultural Science 2002 International Journal of Industrial Entomology Vol.4 No.1
A recombinant transfer vector pBacSCF was constructed by inserting huamn stem cell factor (hSCF) cDNA into plasmid pBacPAK8. BmN cells were co-transfected with modified Bombyx mori, nuclear polyhedrosis virus (BmBacPAK) DNA and the recmbinant transfer vector to construct a recombinant baculovirus containing hSCE gene. DNA dot blotting and RNA dot blotting demonstrated that the hSCE gene was contained in the recombinant virus and transcribed. The recombinant baculovirus was infectious to BmN cells and to silkworm. SDS-PAGE analysis showed a specific band of expressed product in the extract of infected cells and in the heamolymph of infected larvae. Bioactivity of the recombinant hSCE was determined with W-1 cell line and MTT colorimetric method in synergy with interlukin-3 (IL-3). These results revealed that the hSCF gene was over-expressed in cultured cells and lavae of silkworm.
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Lei Huang,Zhinan Xu,Yijuan Xiang,Jin Cai,Ling Jiang,Zhengbing Lv,Yaozhou Zhang 한국화학공학회 2011 Korean Journal of Chemical Engineering Vol.28 No.12
The effects of three main sugars in cane molasses were investigated systematically to prepare a cost-effective medium for butyric acid bioproduction. Additionally, 30 g/L corn steep liquor was screened out as the suitable nitrogen source. In the batch fermentation of free cells, when 60 g/L glucose was the only carbon source, 21.28 g/L butyric acid was achieved after 30 h cultivation. Similar product concentration, productivity and yield were obtained when 60 g/L fructose was applied. The utilization of sucrose would bring about lower productivity (0.29 g/L·h) and product concentration (18.15 g/L), but the yield of butyric acid/sucrose (0.34 g/g) is almost the same as that from glucose or fructose (0.35 g/g). Finally, the sugar mixture (15 g/L glucose, 20 g/L fructose and 35 g/L sucrose) was employed to produce butyric acid in a fibrous-bed bioreactor (FBB), and 40.11 g/L butyric acid was produced with one simple fed-batch strategy.
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