In this study,conductive polymer polyaniline(PANI)is employed to modify the anodes of benthic microbial fuel cells(BMFC).Four electrochemical methods are used to synthesize the polyaniline anodes;the results show that...In this study,conductive polymer polyaniline(PANI)is employed to modify the anodes of benthic microbial fuel cells(BMFC).Four electrochemical methods are used to synthesize the polyaniline anodes;the results show that the PANI modification,especially the pulse potential method for PANI synthesis could obviously improve the cell energy output and reduce the anode internal resistance.The anode is modified by PANI doped with Fe or Mn to further improve the BMFC performance.A maximum power density of 17.51 mW/m2 is obtained by PANI-Fe anode BMFC,which is 8.1 times higher than that of control.The PANI-Mn anode BMFC also gives a favorable maximum power density(16.78 mW/m2).Fe or Mn modification has better effect in improving the conductivity of polyaniline,thus improving the energy output of BMFCs.This work applying PANI composite anode into BMFC brings new development prospect and could promote the practical application of BMFC.展开更多
[Objective] This study aimed to develop a PCR assay for detecting Xanthomonas campestris pv. mangiferaeindicae(Xcm) in culture and in planta. [Method] Primers(Xcm HF and Xcm HR) were designed based on the partial sequ...[Objective] This study aimed to develop a PCR assay for detecting Xanthomonas campestris pv. mangiferaeindicae(Xcm) in culture and in planta. [Method] Primers(Xcm HF and Xcm HR) were designed based on the partial sequence of hrp B gene from xanthomonads to develop a PCR assay for Xcm. Furthermore, specificity and sensitivity of the primer pairs were analyzed in detection of genomic DNA and cell from Xcm. [Result] Amplication was positive only with genomic DNA from positive control ATCC11637 and 12 Xcm strains; no PCR products were amplified with genomic DNA from ten other xanthomonads and seven other bacterial species. The sensitivity of detection was 2.4 pg/μl genomic DNA, and 1.8 × 104CFU/ml cells. The primers also worked well for pathogen detection in direct PCR assays of Xcm colonies grown on liquid medium and in PCR assays of total DNA from leaf, branch and fruit lesions. [Conclusion] A PCR assay was successfully established for rapid detection of Xcm in culture and in planta.展开更多
基金Project(HIT.NSRIF.2014128)supported by the Fundamental Research Funds for the Central Universities,ChinaProject(2014M551257)supported by the China Postdoctoral Science FoundationProject(WH20150208)supported by the Subject Development Foundation of Harbin Institute of Technology at Weihai,China
文摘In this study,conductive polymer polyaniline(PANI)is employed to modify the anodes of benthic microbial fuel cells(BMFC).Four electrochemical methods are used to synthesize the polyaniline anodes;the results show that the PANI modification,especially the pulse potential method for PANI synthesis could obviously improve the cell energy output and reduce the anode internal resistance.The anode is modified by PANI doped with Fe or Mn to further improve the BMFC performance.A maximum power density of 17.51 mW/m2 is obtained by PANI-Fe anode BMFC,which is 8.1 times higher than that of control.The PANI-Mn anode BMFC also gives a favorable maximum power density(16.78 mW/m2).Fe or Mn modification has better effect in improving the conductivity of polyaniline,thus improving the energy output of BMFCs.This work applying PANI composite anode into BMFC brings new development prospect and could promote the practical application of BMFC.
基金Supported by Fundamental Scientific Research Fund of Chinese Academy of Tropical Agricultural Sciences(2014hzs1J007-2)
文摘[Objective] This study aimed to develop a PCR assay for detecting Xanthomonas campestris pv. mangiferaeindicae(Xcm) in culture and in planta. [Method] Primers(Xcm HF and Xcm HR) were designed based on the partial sequence of hrp B gene from xanthomonads to develop a PCR assay for Xcm. Furthermore, specificity and sensitivity of the primer pairs were analyzed in detection of genomic DNA and cell from Xcm. [Result] Amplication was positive only with genomic DNA from positive control ATCC11637 and 12 Xcm strains; no PCR products were amplified with genomic DNA from ten other xanthomonads and seven other bacterial species. The sensitivity of detection was 2.4 pg/μl genomic DNA, and 1.8 × 104CFU/ml cells. The primers also worked well for pathogen detection in direct PCR assays of Xcm colonies grown on liquid medium and in PCR assays of total DNA from leaf, branch and fruit lesions. [Conclusion] A PCR assay was successfully established for rapid detection of Xcm in culture and in planta.
