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1.
Chemosphere ; 238: 124597, 2020 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-31450106

RESUMEN

In this study, we focused on the proportion of particular bacterial groups and changes in microbial community structure in relation to the anammox process parameters and the feeding medium strategy in the Sequencing Batch Reactor (SBR). In order to present an insight into the microbial dynamics while feeding medium shift from synthetic wastewater to landfill leachate, fluorescent in situ hybridization (FISH), Real Time PCR, PCR - DGGE (Polymerase Chain Reaction-Denaturing Gradient Gel Electrophoresis) and Reverse Transcription PCR-DGGE analysis were used. Feeding medium change has the strongest impact on relative abundance of denitrifiers and representatives of Planctomycetes. The relative abundancy of specific genes for all investigated nitrogen removal bacterial groups dropped after landfill leachate implementation. However, anammox consortium were able to adapt to the new reactor operating conditions and time for adaptation was estimated at the level of 90 days.


Asunto(s)
Compuestos de Amonio/metabolismo , Reactores Biológicos/microbiología , Planctomycetales/metabolismo , Aguas Residuales/química , Contaminantes Químicos del Agua/metabolismo , Electroforesis en Gel de Gradiente Desnaturalizante , Desnitrificación/fisiología , Hibridación Fluorescente in Situ , Nitrógeno/metabolismo , Oxidación-Reducción , Planctomycetales/genética
2.
Methods Mol Biol ; 1728: 137-145, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29404995

RESUMEN

The incorporation of noncanonical amino acids has given protein chemists access to an expanded repertoire of amino acids. This methodology has significantly broadened the scope of protein engineering allowing introduction of amino acids with non-native functionalities, such as bioorthogonal reactive handles (azides and alkynes) and hydrophobic fluorinated side chains. Here, we describe the efficient residue-specific replacement of methionine by azidonorleucine in an engineered green fluorescent protein using a bacterial expression system to introduce a single reactive site for the strain-promoted azide-alkyne cycloaddition.


Asunto(s)
Aminoácidos/genética , Biosíntesis de Proteínas , Ingeniería de Proteínas , Proteínas/genética , Secuencia de Aminoácidos , Aminoácidos/química , Aminoacil-ARNt Sintetasas/química , Aminoacil-ARNt Sintetasas/metabolismo , Azidas/química , Cromatografía de Afinidad , Expresión Génica , Genes Reporteros , Modelos Moleculares , Norleucina/análogos & derivados , Norleucina/química , Norleucina/genética , Conformación Proteica , Proteínas/química , Proteínas/aislamiento & purificación , Proteínas/metabolismo
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