RESUMEN
Arthrinium phaeospermum is the major pathogen responsible for the significant stem disease "blight" in B. pervariabilis × D. grandis. The interacting proteins of the key pathogenic factor ApCtf1ß, BDUbc and BDSKL1, have previously been obtained by two-hybrid, BiFC, GST pull-down yeast assays. However, the functions of these interacting proteins remain unknown. This study successfully obtained transgenic plants overexpressing BDUbc, BDSKL1, and BDUbc + BDSKL1 via Agrobacterium-mediated gene overexpression. qRT-PCR analysis revealed significantly increased expression levels of BDUbc and BDSKL1 in the transgenic plants. After infection with the pathogenic spore suspension, the disease incidence and severity index significantly decreased across all three transgenic plants, accompanied by a marked increase in defense enzyme levels. Notably, the co-transformed plant, OE-BDUbc + BDSKL1, demonstrated the lowest disease incidence and severity index among the transgenic variants. These results not only indicate that BDUbc and BDSKL1 are disease-resistant genes, but also that these two genes may exhibit a synergistic enhancement effect, which further improves the resistance to blight in Bambusa pervariabilis × Dendrocalamopsis grandis.
Asunto(s)
Bambusa , Queratoconjuntivitis , Agrobacterium , Bioensayo , Plantas Modificadas Genéticamente , Saccharomyces cerevisiaeRESUMEN
We introduce a high-performance microbial fuel cell (MFC) that was operated using a 0.1 M bicarbonate buffer as the cathodic electrolyte. The MFC had a 136.42 mW/m(2) maximum power density under continuous feeding of 5 mM acetate as fuel. Results of the electrode potential measurements showed that the cathode potential of the bicarbonate-buffered condition was higher than the phosphate-buffered condition, although the phosphate condition had less interfacial resistance between the membrane and electrolyte. Therefore, we posit here that the increased power of the bicarbonate-buffered MFC may be caused by the higher cathode potential rather than by the interfacial membrane-electrolyte resistance.
Asunto(s)
Bicarbonatos/metabolismo , Fuentes de Energía Bioeléctrica , Electricidad , Electrodos/microbiología , Acetatos/metabolismo , Tampones (Química) , MembranasRESUMEN
The interface resistances between an anion exchange membrane (AEM) and the solution electrolyte were measured for low buffer (or ionic strength) of electrolytes typical of microbial fuel cells (MFCs). Three AEMs (AFN, AM-1, and ACS) having different properties were tested in a flat-plate MFC to which 5-mM acetate was fed to the anode and an air-saturated phosphate buffer (PB) solution was fed to the cathode. Current density achieved in the MFCs was correlated inversely with independently measured membrane-only resistances. However, the total interfacial resistances measured by current-voltage plots were approximately two orders higher than those of the membrane-only resistances, although membranes had the same order as with the membrane-only resistance. EIS spectra showed that the resistances from electric-double layer and diffusion boundary layer were the main resistances not the membrane's resistance. The electric-double layer and diffusion boundary layer resistances of the AEMs were much larger in the 10 mM PB electrolyte, compared to 100 mM PB. EIS study also showed that the resistance of diffusion boundary layer decreased due to mechanical stirring. Therefore, the interface resistance that originates from the interaction between the membrane and the catholyte solution should be considered when designing and operating MFC processes with an AEM. The AEMs allowed transport of uncharged O(2) and acetate, but the current losses for both were low during normal MFC operation.