RESUMEN
The methane production and the microbial community dynamics of thermophilic anaerobic co-digestion (AD) of corn stover, swine manure and effluent were conducted at total solid (TS) content of 5%, 10% and 15%, the carbon to nitrogen ratio (C/N) of 20, 30 and 40 and the effluent volumetric percentage (EVP) of 20%, 40% and 60%. For batches with 5% TS, the highest methane yield of 238.5-283.1 mL g-1 volatile solid (VS) and the specific methane productivity of 138.5-152.2 mL g-1 initial VS were obtained at the C/N ratios of 20 and 30. For the mixtures with 10% and 15% TS, the highest methane yield was 341.9 mL g-1 VS and 351.2 mL g-1 VS, respectively, when the C/N ratio of 20% and 60% EVP conditions were maintained. Co-digestion of swine manure with corn stover caused an obvious shift in microbial population, in which the archaeal population changed from 0.3% to 2.8% and the bacterial community changed from 97.2% to 99.7%. The experimental batches with the highest relative abundance of the archaeal population (2.00% of total microbial population for 5% TS, 1.74% for 10% TS and 2.76% for 15% TS) had the highest rate of methanogenesis subsequently enhancing methane production (283.08 mL g-1 VS for 5% TS, 341.91 mL g-1 VS for 10% TS and 351.23 mL g-1 VS for 15% TS). The results of microbiome analysis enabled understanding the key populations in biomethane generation.
Asunto(s)
Reactores Biológicos/microbiología , Estiércol/análisis , Metano/biosíntesis , Microbiota , Residuos Sólidos/análisis , Zea mays/química , Anaerobiosis , Animales , Archaea/crecimiento & desarrollo , Bacterias Anaerobias/crecimiento & desarrollo , Biocombustibles/análisis , Carbono/análisis , Modelos Teóricos , Nitrógeno/análisis , PorcinosRESUMEN
Microorganisms regulate their interactions with surfaces by altering the transcription of specific target genes in response to physicochemical surface cues. To assess the influence of surface charge and surface chemistry on the transcriptional oxidative stress response, we evaluated the expression of three genes, oxyS, katE, and sodB from the Gram-negative bacterium, Escherichia coli, after a short exposure to GaN interfaces. We observed that both surface charge and surface chemistry were the factors regulating the transcriptional response of the target genes, which indicates that reactive oxygen species (ROS) generation and the ROS response at the GaN interfaces were affected by changing surface properties. The changes in transcription did not correlate to the surface charge in all cases, indicating that there was an influence from multiple interfacial properties on the interactions. Alteration of the bacterial morphology also was a critical factor in these transcriptional responses to the surface cues. When compared to wild-type E. coli bacteria, bacteria missing either flagella or curli exhibited altered transcriptional profiles of the three oxidative stress genes when exposed to GaN materials. These results indicate that the bacterial flagella and curli modulated the oxidative stress response in different ways. The results of this work add to our understanding of the interactions of microbes at interfaces and will be useful for guiding the development of electronic biointerfaces.
RESUMEN
Due to the widespread occurrence of multidrug resistant microbes there is increasing interest in the use of novel nanostructured materials as antimicrobials. Specifically, metallic nanoparticles such as silver, copper, and gold have been deployed due to the multiple impacts they have on bacterial physiology. From this, many have concluded that such nanomaterials represent steep obstacles against the evolution of resistance. However, we have already shown that this view is fallacious. For this reason, the significance of our initial experiments are beginning to be recognized in the antimicrobial effects of nanomaterials literature. This recognition is not yet fully understood and here we further explain why nanomaterials research requires a more nuanced understanding of core microbial evolution principles.