基于Cell处理器的异构多核架构及软件显式管理的多级存储层次,使其面临编程困难和性能难以有效发挥等问题.现有基于Cell/B.E.的编程模型多侧重于支持类似于流处理的"批量访存"(bulk data transfer)应用,传统非规则访存应用性...基于Cell处理器的异构多核架构及软件显式管理的多级存储层次,使其面临编程困难和性能难以有效发挥等问题.现有基于Cell/B.E.的编程模型多侧重于支持类似于流处理的"批量访存"(bulk data transfer)应用,传统非规则访存应用性能较低.通过扩展Cell/B.E.访存库增强协处理单元的自主作用,以协处理单元为中心建立Cell计算平台上的MPI和弱一致性Pthread分层并行编程运行时支持.分层的运行时支持结构及扩展后的Cell/B.E.访存库使模型具有更好的效率和可扩展性,并且提高了非规则应用的性能;模型中的MPI方便了大量传统并行应用向新架构的移植及开发,而弱一致性Pthread则为MPI提供高效的任务运行时管理支持及为系统级用户提供对架构全面控制的编程接口.实验结果表明,提出的运行时支持技术不仅可适应不同应用的要求,同时借助访存库中的剖分优化机制可有效地挖掘Cell/B.E.架构性能.展开更多
Previous researches showed that the expression level of E-Cad in most infiltrating cancer cells was reduced or negative. This study explored whether 4HPR restrained the infiltration of bladder cancer cells through reg...Previous researches showed that the expression level of E-Cad in most infiltrating cancer cells was reduced or negative. This study explored whether 4HPR restrained the infiltration of bladder cancer cells through regulating the expression of E-Cad. The infiltrating bladder cancer cells T24 were cultured, and then treated by a proper dosage of drug. Their viability was a determined by MTT method. Western blotting and RT-PCR were adopted to detect the changes of E-Cad gene expression at both protein and mRNA levels. Moreover, immunofluorescent staining and confocal fluorescence microscopy were employed for the observation of the expression of E-Cad. The result showed that, at both mRNA and protein levels, the expression level of E-Cad in T24 cells treated by 4HPR was significantly higher than that of control group, while the β-Cat expression was also relocated from the cell nucleus to cytoplasm. Our findings suggested that the regulatory function of 4HPR on infiltration of bladder cancer cells T24 is at least partly achieved by regulating the expression of E-Cad.展开更多
The effects of E-cadherin-transfected neural stem cells（NSCs） transplantation for spinal cord injury（SCI） in rats were investigated. Sixty SD rats were randomly divided into model control group, NSCs group, empty ...The effects of E-cadherin-transfected neural stem cells（NSCs） transplantation for spinal cord injury（SCI） in rats were investigated. Sixty SD rats were randomly divided into model control group, NSCs group, empty plasmid group and E-cadherin overexpression group（n=15 each）. The animal SCI model was established by using the modified Allen＇s method. NSCs were cultured. Rats in NSCs group were subjected to NSCs transplantation. E-cadherin gene eucaryotic expression vector and pcDNA3.1-E-cadherin were respectively transfected into cultured NSCs, serving as empty plasmid group and E-cadherin overexpression group respectively. At 7th day after transplantation, neurological function of all rats was assessed by Tarlov score. After rats were sacrificed in each group, the number of BrdU and Nestin positive cells was counted by immunohistochemistry. Immumofluorescence method was used to detect the expression of neurofilament protein（NF） and glial fibrillary acidic protein（GFAP）. As compared with model control group, the Tarlov score and the number of of BrdU and Nestin positive cells, and the expression of NF and GFAP in NSCs group, empty plasmid group, and E-cadherin overexpression group were increased significantly（P〈0.05）, and those in the E-cadherin overexpression group were increased more significantly than the other transplantation groups（P〈0.05）. It was suggested that E-cadherin could be conductive to nerve regeneration and repair probably by promoting the proliferation and differentiation of NSCs.展开更多
Summary: To investigate whether the change of E-cadherin (ECD) expression plays a role in the injury and repair of airway epithelial cells (AEC) caused by smoking, porcine AECs were cultured by using an enzyme-dispers...Summary: To investigate whether the change of E-cadherin (ECD) expression plays a role in the injury and repair of airway epithelial cells (AEC) caused by smoking, porcine AECs were cultured by using an enzyme-dispersed method. After exposure of the AECs to cigarette smoke extract (CSE), the ECD expression in the cells was detected by using immunocytochemistry and in situ hybridization. The results showed that ECD was distributed on the plasma membrane at the cell junctions of AECs. After exposure to 20 % CSE, the membranous ECD expression was decreased, the cytoplasmic ECD expression was increased (P<0.01) as the exposure time went on. But the content of ECD mRNA in the AECs did not chang. It suggests that the change of ECD ex- pression is regulated at the posttranslational level and plays a role in the injury and repair of AEC caused by smoking.展开更多
Objective: To prove the molecular mechanisms of Mahkota Dewa(Phaleria macrocarpa) in suppressing proliferation of human retinoblastoma cells through suppression of cell cycle's gene-regulators expression.Methods: ...Objective: To prove the molecular mechanisms of Mahkota Dewa(Phaleria macrocarpa) in suppressing proliferation of human retinoblastoma cells through suppression of cell cycle's gene-regulators expression.Methods: In this study, the molecular mechanism of anti-tumor effect of fractioned extract of Phaleria macrocarpa(DLBS1425) in human retinoblastoma cells Y-79 was investigated by measuring the tumor cells viability, the assessment of population profiles of tumor cells in the cell cycle, and the mRNA concentration of p16, p21, p53, cyclin D,cyclin E, and E2 F.Results: DLBS1425 showed an inhibition effects towards proliferation of Y-79 cell line.Inhibition of proliferation was shown by suppression of cell cycle progression.DLBS1425 downregulated cyclin E, a G1 phase regulator gene of cell cycle, in dosedependent manner without affecting p53–p21 pathway.In the other word, DLBS1425 inhibits cell proliferation through suppression of cyclin E independently towards conventional proliferation pathway.Conclusions: Our results suggest that DLBS1425 is a potential anticancer agent which targets genes involved in cell proliferation in human retinoblastoma cells which make it pharmacologically ideal for the prevention and/or treatment of retinoblastoma cancer.展开更多
To explore the effect of NF κB on bcl x gene transcription in extended drug resistance leukemia cell line HL 60/E6, drug resistant subline HL 60/E6 was derived by intermittently exposing HL 60 cells to 6 ng/ml ...To explore the effect of NF κB on bcl x gene transcription in extended drug resistance leukemia cell line HL 60/E6, drug resistant subline HL 60/E6 was derived by intermittently exposing HL 60 cells to 6 ng/ml epirubicin. Indirect immunofluorescence was used to demonstrate the location of NF κB RelA in HL 60/E6 cells. FCM analysis and RT PCR were used to detect the efficiency of liposome mediated ODN transfection and the change of bcl x L mRNA levels after 5 μmol/L phosphorothioate (PS) derivatized antisense (AS) oligodeoxynucleotide (ODN) directed to RelA was transferred into HL 60/E6 cells. The results showed that RelA remained persistently active and located at the nuclei of HL 60/E6 cells,but in the cytoplasm of HL 60 cells, the efficiency of liposome mediated ODN transfection was significantly higher than that of null ODN ( P <0.01 in 4 h, 6 h, 12 h, 24 h). Exposure of HL 60/E6 cells to 5 μmol/L AS PS ODN directed to RelA led to a maximal 40 % decline of bcl x L mRNA levels within 8 h. The inhibition rate of bcl x L mRNA was (15±1.79) %, (28±2.34) %, (40±3.47) %, (20±1.54) % in 4 h, 6 h, 8 h, 15 h, respectively, but it was less than 15 % in control group. It was concluded that NF κB was involved in regulating bcl x transcription. It was suggested that NF κB was an important factor for drug resistance in leukemia cells.展开更多
Objective: To explore the activities of Composite Artemisia Capillaris Tablet (复方茵陈片, CACT) against hepatitis B virus replication in vitro . Methods: By means of radioimmunoassay (RIA), Dot blot and Southern blo...Objective: To explore the activities of Composite Artemisia Capillaris Tablet (复方茵陈片, CACT) against hepatitis B virus replication in vitro . Methods: By means of radioimmunoassay (RIA), Dot blot and Southern blot, the surface and e antigen production of 2.2.15 cells, HBV DNA in 2.2.15 cell culture medium and that in 2.2.15 cells were examined respectively. Results: HBsAg, HBeAg values of 2.2.15 cells treated by CACT were lower than those of the control, the HBV DNA quantities in culture medium and in 2.2.15 cells decreased as compared with those cells with no treatment by CACT given to them. Conclusion: CACT could inhibit HBV DNA replication, showing its potential antiviral activity in hepatitis B treatment.展开更多
Objective Cucurbitacins are the highly oxygenated tetracyclic triterpenes,which are predominantly found in the Cucurbitaceae family but are also present in several other families of the plant kingdom.A number of compo...Objective Cucurbitacins are the highly oxygenated tetracyclic triterpenes,which are predominantly found in the Cucurbitaceae family but are also present in several other families of the plant kingdom.A number of compounds of this group have been investigated for their cytotoxic,hepatoprotective,anti-inflammatory,cardiovascular and anti-diabetic activities.In China,the cucurbitacin preparation,which contains mostly cucurbitacin B and cucurbitacin E,has been clinically used for the treatment of the primary liver carcinoma.It has been previously reported that cucurbitacin E could produce cytotoxicity against a variety of cancer cells,and various mechanisms were implicated in its cytotoxic effect.The present study is to investigate the effect of cucurbitacin E on hepatoma cells in vitro and in vivo and to study their potential mechanisms of action.Methods The MTT assay was used to assess the viability of human HepG2 and BEL7402 hepatoma cells in vitro after treatment with different concentrations of cucurbitacin E.The cell cycle distribution was determined by flowcytometric analysis after propidium iodide(PI)staining.The cell cycle-related proteins were detected using western blotting analysis.Implanted mouse hepatoma H22 model was built to evaluate the growth inhibitory effect of cucurbitacin E in vivo in mice.Results Our studies found that cucurbitacin E(10-300 nM)produced anti-proliferative effect on human HepG2 and BEL7402 hepatoma cells in vitro without cytotoxicity.According to flowcytometric analysis,cucurbitacin E arrested the cell cycle at G2/M phase in both HepG2 and BEL7402 hepatoma cells after 24 h treatment.Cucurbitacin E induced the decrease in the level of CDK1 protein and the increase in the level of p21 protein,but had no effect on the levels of cyclin A,cyclin B1 and Cdc25C protein.In in vivo anti-tumor experiment,cucurbitacin E had significant inhibitory effects on the growth of mouse H22 hepatoma cells.Conclusions Cucurbitacin E inhibited the proliferation of hepatoma cells in vitro and in vivo,at least in part,through induction of cell cycle arrest at G2/M phase,which was mediated by concomitant upregulation of p21 and downregulation of CDK1.We consider that cucurbitacin E may be useful in the treatment of liver cancer.展开更多
Objective To report a protocol using biotin-labelled PrP protein in cell free conversion assay instead of isotope. Methods A hamster PrP protein （HaPrP） was expressed in E. coli and purified with HIS-tag affinity ch...Objective To report a protocol using biotin-labelled PrP protein in cell free conversion assay instead of isotope. Methods A hamster PrP protein （HaPrP） was expressed in E. coli and purified with HIS-tag affinity chromatograph. After being labelled with biotin, HaPrP was mixed with PrP^sen preparation from scrapie strain 263K. Results Protease-resistant bands were detected after four-day incubation. Conclusion The new conversion model provides a reliable, easily handling, and environment-friendly method for studies of prion and transmissible spongiform encephalopathies.展开更多
In order to evaluate supplemented vitamin E and selenium in terms of safety,we investigated individual and combined effects of vitamin E and selenium at different concentrations on proliferation of a normal baby hamst...In order to evaluate supplemented vitamin E and selenium in terms of safety,we investigated individual and combined effects of vitamin E and selenium at different concentrations on proliferation of a normal baby hamster kidney fibroblast cell line(BHK-21/C13) and ots polyoma virustransformed counterpart (BHK-21/PyY).The results showed that vitamin E(α-tocopherol);at the concentration of 7 μmol/L,stimulated BHK-21/C13 and BHK-21/PyY growth by 11 % and 16% respectively;selenium(sodium selenite),up to 0.1 μmol/L, had no effect on growth of both cell lines ;co-supplementation of vitamin E and selenium at the same concentrations as above increased BHK21/C13 growth rate by 78%,while BHK-21/PyY cell line remained unaltered. The results suggest that co-supplemcntation of vitamin E and selenium at low concentrations is better than separate sup plementotion of them in safety.展开更多
A mediator microbial fuel cell (MFC) was constructed by using E. coli as biocatalyst and new methylene blue as electron mediator. E. coli cells were carried out in anaerobic growth prior to inoculating them into the M...A mediator microbial fuel cell (MFC) was constructed by using E. coli as biocatalyst and new methylene blue as electron mediator. E. coli cells were carried out in anaerobic growth prior to inoculating them into the MFC in order to pre-adapt bacterial metabolism in an anaerobic environment, the electricity generation of MFC was tested, its maximum power density reached 263.94 mW/m2 with the corresponding current density 1287.50 mA/m2, the internal resistance of MFC was 200Ω, and capability of the MFC was even better than those reported so far. Moreover, on-electrode taming method was adopted to improve electrochemical activity of E. coli, namely a combination of E. coli taming and electricity generation simultaneously in the same MFC without scraping off the biofilm of MFC, after the 4th on-electrode taming, the tamed E. coli MFC showed a 54% improvement in peak current density, being 612.50 mA/m2, and a 64% improvement in the maximum power output, being 166.67 mW/m2, compared with that of parental E. coli MFC. And the maturation time of tamed biofilm was obviously reduced to 240 min, quickening up 1 times compared with that of parental E. coli biofilm.展开更多
文摘基于Cell处理器的异构多核架构及软件显式管理的多级存储层次,使其面临编程困难和性能难以有效发挥等问题.现有基于Cell/B.E.的编程模型多侧重于支持类似于流处理的"批量访存"(bulk data transfer)应用,传统非规则访存应用性能较低.通过扩展Cell/B.E.访存库增强协处理单元的自主作用,以协处理单元为中心建立Cell计算平台上的MPI和弱一致性Pthread分层并行编程运行时支持.分层的运行时支持结构及扩展后的Cell/B.E.访存库使模型具有更好的效率和可扩展性,并且提高了非规则应用的性能;模型中的MPI方便了大量传统并行应用向新架构的移植及开发,而弱一致性Pthread则为MPI提供高效的任务运行时管理支持及为系统级用户提供对架构全面控制的编程接口.实验结果表明,提出的运行时支持技术不仅可适应不同应用的要求,同时借助访存库中的剖分优化机制可有效地挖掘Cell/B.E.架构性能.
基金supported by a grant from the National Natural Science Foundation of China(No.30972975)
文摘Previous researches showed that the expression level of E-Cad in most infiltrating cancer cells was reduced or negative. This study explored whether 4HPR restrained the infiltration of bladder cancer cells through regulating the expression of E-Cad. The infiltrating bladder cancer cells T24 were cultured, and then treated by a proper dosage of drug. Their viability was a determined by MTT method. Western blotting and RT-PCR were adopted to detect the changes of E-Cad gene expression at both protein and mRNA levels. Moreover, immunofluorescent staining and confocal fluorescence microscopy were employed for the observation of the expression of E-Cad. The result showed that, at both mRNA and protein levels, the expression level of E-Cad in T24 cells treated by 4HPR was significantly higher than that of control group, while the β-Cat expression was also relocated from the cell nucleus to cytoplasm. Our findings suggested that the regulatory function of 4HPR on infiltration of bladder cancer cells T24 is at least partly achieved by regulating the expression of E-Cad.
文摘The effects of E-cadherin-transfected neural stem cells（NSCs） transplantation for spinal cord injury（SCI） in rats were investigated. Sixty SD rats were randomly divided into model control group, NSCs group, empty plasmid group and E-cadherin overexpression group（n=15 each）. The animal SCI model was established by using the modified Allen＇s method. NSCs were cultured. Rats in NSCs group were subjected to NSCs transplantation. E-cadherin gene eucaryotic expression vector and pcDNA3.1-E-cadherin were respectively transfected into cultured NSCs, serving as empty plasmid group and E-cadherin overexpression group respectively. At 7th day after transplantation, neurological function of all rats was assessed by Tarlov score. After rats were sacrificed in each group, the number of BrdU and Nestin positive cells was counted by immunohistochemistry. Immumofluorescence method was used to detect the expression of neurofilament protein（NF） and glial fibrillary acidic protein（GFAP）. As compared with model control group, the Tarlov score and the number of of BrdU and Nestin positive cells, and the expression of NF and GFAP in NSCs group, empty plasmid group, and E-cadherin overexpression group were increased significantly（P〈0.05）, and those in the E-cadherin overexpression group were increased more significantly than the other transplantation groups（P〈0.05）. It was suggested that E-cadherin could be conductive to nerve regeneration and repair probably by promoting the proliferation and differentiation of NSCs.
基金This project was supported by a grant from National Natural Science Foundation of China !(39570288).
文摘Summary: To investigate whether the change of E-cadherin (ECD) expression plays a role in the injury and repair of airway epithelial cells (AEC) caused by smoking, porcine AECs were cultured by using an enzyme-dispersed method. After exposure of the AECs to cigarette smoke extract (CSE), the ECD expression in the cells was detected by using immunocytochemistry and in situ hybridization. The results showed that ECD was distributed on the plasma membrane at the cell junctions of AECs. After exposure to 20 % CSE, the membranous ECD expression was decreased, the cytoplasmic ECD expression was increased (P<0.01) as the exposure time went on. But the content of ECD mRNA in the AECs did not chang. It suggests that the change of ECD ex- pression is regulated at the posttranslational level and plays a role in the injury and repair of AEC caused by smoking.
基金Supported by The Dexa Laboratories of Biomolecular Sciences(DLBS),PT.Dexa Medica,Cikarang,West Java,Indonesia,Grant No.135/MP/DLBS/2016
文摘Objective: To prove the molecular mechanisms of Mahkota Dewa(Phaleria macrocarpa) in suppressing proliferation of human retinoblastoma cells through suppression of cell cycle's gene-regulators expression.Methods: In this study, the molecular mechanism of anti-tumor effect of fractioned extract of Phaleria macrocarpa(DLBS1425) in human retinoblastoma cells Y-79 was investigated by measuring the tumor cells viability, the assessment of population profiles of tumor cells in the cell cycle, and the mRNA concentration of p16, p21, p53, cyclin D,cyclin E, and E2 F.Results: DLBS1425 showed an inhibition effects towards proliferation of Y-79 cell line.Inhibition of proliferation was shown by suppression of cell cycle progression.DLBS1425 downregulated cyclin E, a G1 phase regulator gene of cell cycle, in dosedependent manner without affecting p53–p21 pathway.In the other word, DLBS1425 inhibits cell proliferation through suppression of cyclin E independently towards conventional proliferation pathway.Conclusions: Our results suggest that DLBS1425 is a potential anticancer agent which targets genes involved in cell proliferation in human retinoblastoma cells which make it pharmacologically ideal for the prevention and/or treatment of retinoblastoma cancer.
文摘To explore the effect of NF κB on bcl x gene transcription in extended drug resistance leukemia cell line HL 60/E6, drug resistant subline HL 60/E6 was derived by intermittently exposing HL 60 cells to 6 ng/ml epirubicin. Indirect immunofluorescence was used to demonstrate the location of NF κB RelA in HL 60/E6 cells. FCM analysis and RT PCR were used to detect the efficiency of liposome mediated ODN transfection and the change of bcl x L mRNA levels after 5 μmol/L phosphorothioate (PS) derivatized antisense (AS) oligodeoxynucleotide (ODN) directed to RelA was transferred into HL 60/E6 cells. The results showed that RelA remained persistently active and located at the nuclei of HL 60/E6 cells,but in the cytoplasm of HL 60 cells, the efficiency of liposome mediated ODN transfection was significantly higher than that of null ODN ( P <0.01 in 4 h, 6 h, 12 h, 24 h). Exposure of HL 60/E6 cells to 5 μmol/L AS PS ODN directed to RelA led to a maximal 40 % decline of bcl x L mRNA levels within 8 h. The inhibition rate of bcl x L mRNA was (15±1.79) %, (28±2.34) %, (40±3.47) %, (20±1.54) % in 4 h, 6 h, 8 h, 15 h, respectively, but it was less than 15 % in control group. It was concluded that NF κB was involved in regulating bcl x transcription. It was suggested that NF κB was an important factor for drug resistance in leukemia cells.
基金Supported by the Project of Military Science during the 9th Five Year Plan Period (No. 01G19) and the National Natural Science Foundation (No. 39970911)
文摘Objective: To explore the activities of Composite Artemisia Capillaris Tablet (复方茵陈片, CACT) against hepatitis B virus replication in vitro . Methods: By means of radioimmunoassay (RIA), Dot blot and Southern blot, the surface and e antigen production of 2.2.15 cells, HBV DNA in 2.2.15 cell culture medium and that in 2.2.15 cells were examined respectively. Results: HBsAg, HBeAg values of 2.2.15 cells treated by CACT were lower than those of the control, the HBV DNA quantities in culture medium and in 2.2.15 cells decreased as compared with those cells with no treatment by CACT given to them. Conclusion: CACT could inhibit HBV DNA replication, showing its potential antiviral activity in hepatitis B treatment.
文摘Objective Cucurbitacins are the highly oxygenated tetracyclic triterpenes,which are predominantly found in the Cucurbitaceae family but are also present in several other families of the plant kingdom.A number of compounds of this group have been investigated for their cytotoxic,hepatoprotective,anti-inflammatory,cardiovascular and anti-diabetic activities.In China,the cucurbitacin preparation,which contains mostly cucurbitacin B and cucurbitacin E,has been clinically used for the treatment of the primary liver carcinoma.It has been previously reported that cucurbitacin E could produce cytotoxicity against a variety of cancer cells,and various mechanisms were implicated in its cytotoxic effect.The present study is to investigate the effect of cucurbitacin E on hepatoma cells in vitro and in vivo and to study their potential mechanisms of action.Methods The MTT assay was used to assess the viability of human HepG2 and BEL7402 hepatoma cells in vitro after treatment with different concentrations of cucurbitacin E.The cell cycle distribution was determined by flowcytometric analysis after propidium iodide(PI)staining.The cell cycle-related proteins were detected using western blotting analysis.Implanted mouse hepatoma H22 model was built to evaluate the growth inhibitory effect of cucurbitacin E in vivo in mice.Results Our studies found that cucurbitacin E(10-300 nM)produced anti-proliferative effect on human HepG2 and BEL7402 hepatoma cells in vitro without cytotoxicity.According to flowcytometric analysis,cucurbitacin E arrested the cell cycle at G2/M phase in both HepG2 and BEL7402 hepatoma cells after 24 h treatment.Cucurbitacin E induced the decrease in the level of CDK1 protein and the increase in the level of p21 protein,but had no effect on the levels of cyclin A,cyclin B1 and Cdc25C protein.In in vivo anti-tumor experiment,cucurbitacin E had significant inhibitory effects on the growth of mouse H22 hepatoma cells.Conclusions Cucurbitacin E inhibited the proliferation of hepatoma cells in vitro and in vivo,at least in part,through induction of cell cycle arrest at G2/M phase,which was mediated by concomitant upregulation of p21 and downregulation of CDK1.We consider that cucurbitacin E may be useful in the treatment of liver cancer.
基金This work was supported by National Natural Science Foundation of China 30070038 and 30130070, National High-Tech Research and Development Program of China (863 Project) 2001AA215391, and EU Project QLRT 2000 01441.
文摘Objective To report a protocol using biotin-labelled PrP protein in cell free conversion assay instead of isotope. Methods A hamster PrP protein （HaPrP） was expressed in E. coli and purified with HIS-tag affinity chromatograph. After being labelled with biotin, HaPrP was mixed with PrP^sen preparation from scrapie strain 263K. Results Protease-resistant bands were detected after four-day incubation. Conclusion The new conversion model provides a reliable, easily handling, and environment-friendly method for studies of prion and transmissible spongiform encephalopathies.
文摘In order to evaluate supplemented vitamin E and selenium in terms of safety,we investigated individual and combined effects of vitamin E and selenium at different concentrations on proliferation of a normal baby hamster kidney fibroblast cell line(BHK-21/C13) and ots polyoma virustransformed counterpart (BHK-21/PyY).The results showed that vitamin E(α-tocopherol);at the concentration of 7 μmol/L,stimulated BHK-21/C13 and BHK-21/PyY growth by 11 % and 16% respectively;selenium(sodium selenite),up to 0.1 μmol/L, had no effect on growth of both cell lines ;co-supplementation of vitamin E and selenium at the same concentrations as above increased BHK21/C13 growth rate by 78%,while BHK-21/PyY cell line remained unaltered. The results suggest that co-supplemcntation of vitamin E and selenium at low concentrations is better than separate sup plementotion of them in safety.
基金Supported by Natural Science Foundation of China (No.20776091)
文摘A mediator microbial fuel cell (MFC) was constructed by using E. coli as biocatalyst and new methylene blue as electron mediator. E. coli cells were carried out in anaerobic growth prior to inoculating them into the MFC in order to pre-adapt bacterial metabolism in an anaerobic environment, the electricity generation of MFC was tested, its maximum power density reached 263.94 mW/m2 with the corresponding current density 1287.50 mA/m2, the internal resistance of MFC was 200Ω, and capability of the MFC was even better than those reported so far. Moreover, on-electrode taming method was adopted to improve electrochemical activity of E. coli, namely a combination of E. coli taming and electricity generation simultaneously in the same MFC without scraping off the biofilm of MFC, after the 4th on-electrode taming, the tamed E. coli MFC showed a 54% improvement in peak current density, being 612.50 mA/m2, and a 64% improvement in the maximum power output, being 166.67 mW/m2, compared with that of parental E. coli MFC. And the maturation time of tamed biofilm was obviously reduced to 240 min, quickening up 1 times compared with that of parental E. coli biofilm.
