RESUMEN
A unique method was developed and applied for monitoring methanogenesis pathways based on isotope labeled substrates combined with online membrane inlet quadrupole mass spectrometry (MIMS). In our study, a fermentation sample from a full-scale biogas plant fed with pig and cattle manure, maize silage, and deep litter was incubated with 100 mM of [2-(13)C] sodium acetate under thermophilic anaerobic conditions. MIMS was used to measure the isotopic distribution of dissolved CO2 and CH4 during the degradation of acetate, while excluding interference from water by applying a cold trap. After 6 days of incubation, the proportion of methane derived from reduction of CO2 had increased significantly and reached up to 87% of total methane, suggesting that synthrophic acetate oxidation coupled to hydrogenotrophic methanogenesis (SAO-HM) played an important role in the degradation of acetate. This study provided a new approach for online quantification of the relative contribution of methanogenesis pathways to methane production with a time resolution shorter than one minute. The observed contribution of SAO-HM to methane production under the tested conditions challenges the current widely accepted anaerobic digestion model (ADM1), which strongly emphasizes the importance of the acetoclastic methanogenesis.
Asunto(s)
Acetatos/metabolismo , Reactores Biológicos/microbiología , Espectrometría de Masas/métodos , Membranas Artificiales , Metano/biosíntesis , Anaerobiosis , Animales , Biocombustibles , Calibración , Dióxido de Carbono/metabolismo , Isótopos de Carbono , Bovinos , Hidrógeno/metabolismo , Límite de Detección , Microbiota , Oxidación-Reducción , Estándares de Referencia , Porcinos , Factores de TiempoRESUMEN
We demonstrate here a rapid and cost-effective technique for nanoscale patterning of functional molecules on the surface of a DNA origami. The pattern is created enzymatically by transferring a functionalized dideoxynucleotide to the 3'-end of an arbitrary selected set of synthetic DNA oligonucleotides positioned approximately 6 nm apart in a 70 × 100 nm(2) rectangular DNA origami. The modifications, which are performed in a single-tube reaction, provide an origami surface modified with a variety of functional groups including chemical handles, fluorescent dyes, or ligands for subsequent binding of proteins. Efficient labeling and patterning was demonstrated by gel electrophoresis shift assays, reverse-phase HPLC, mass spectrometry, atomic force microscopy (AFM) analysis, and fluorescence measurements. The results show a very high yield of oligonucleotide labeling and incorporation in the DNA origami. This method expands the toolbox for constructing several different modified DNA origami from the same set of staple strands.
Asunto(s)
ADN/química , Oligonucleótidos/química , Modelos Moleculares , Estructura Molecular , Coloración y Etiquetado , Propiedades de SuperficieRESUMEN
Surplus electricity from fluctuating renewable power sources may be converted to CH4 via biomethanisation in anaerobic digesters. The reactor performance and response of methanogen population of mixed-culture reactors was assessed during pulsed H2 injections. Initial H2 uptake rates increased immediately and linearly during consecutive pulse H2 injections for all tested injection rates (0.3 to 1.7LH2/Lsludge/d), while novel high throughput mcrA sequencing revealed an increased abundance of specific hydrogenotrophic methanogens. These findings illustrate the adaptability of the methanogen population to H2 injections and positively affects the implementation of biomethanisation. Acetate accumulated by a 10-fold following injections exceeding a 4:1 H2:CO2 ratio and may act as temporary storage prior to biomethanisation. Daily methane production decreased for headspace CO2 concentrations below 12% and may indicate a high sensitivity of hydrogenotrophic methanogens to CO2 limitation. This may ultimately decide the biogas upgrading potential which can be achieved by biomethanisation.