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1.
PLoS Genet ; 8(8): e1002875, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22912594

RESUMEN

A key challenge in the production of second generation biofuels is the conversion of lignocellulosic substrates into fermentable sugars. Enzymes, particularly those from fungi, are a central part of this process, and many have been isolated and characterised. However, relatively little is known of how fungi respond to lignocellulose and produce the enzymes necessary for dis-assembly of plant biomass. We studied the physiological response of the fungus Aspergillus niger when exposed to wheat straw as a model lignocellulosic substrate. Using RNA sequencing we showed that, 24 hours after exposure to straw, gene expression of known and presumptive plant cell wall-degrading enzymes represents a huge investment for the cells (about 20% of the total mRNA). Our results also uncovered new esterases and surface interacting proteins that might form part of the fungal arsenal of enzymes for the degradation of plant biomass. Using transcription factor deletion mutants (xlnR and creA) to study the response to both lignocellulosic substrates and low carbon source concentrations, we showed that a subset of genes coding for degradative enzymes is induced by starvation. Our data support a model whereby this subset of enzymes plays a scouting role under starvation conditions, testing for available complex polysaccharides and liberating inducing sugars, that triggers the subsequent induction of the majority of hydrolases. We also showed that antisense transcripts are abundant and that their expression can be regulated by growth conditions.


Asunto(s)
Aspergillus niger/genética , Proteínas Fúngicas/genética , Regulación Fúngica de la Expresión Génica , Lignina/metabolismo , ARN Mensajero/biosíntesis , Activación Transcripcional , Aspergillus niger/enzimología , Biomasa , Esterasas/biosíntesis , Esterasas/genética , Proteínas Fúngicas/biosíntesis , Perfilación de la Expresión Génica , Glicósido Hidrolasas/biosíntesis , Glicósido Hidrolasas/genética , Monosacáridos/biosíntesis , Proteínas Represoras/deficiencia , Proteínas Represoras/genética , Análisis de Secuencia de ARN , Transactivadores/deficiencia , Transactivadores/genética , Triticum/metabolismo
2.
Elife ; 52016 11 16.
Artículo en Inglés | MEDLINE | ID: mdl-27849518

RESUMEN

The amphipod crustacean Parhyale hawaiensis is a blossoming model system for studies of developmental mechanisms and more recently regeneration. We have sequenced the genome allowing annotation of all key signaling pathways, transcription factors, and non-coding RNAs that will enhance ongoing functional studies. Parhyale is a member of the Malacostraca clade, which includes crustacean food crop species. We analysed the immunity related genes of Parhyale as an important comparative system for these species, where immunity related aquaculture problems have increased as farming has intensified. We also find that Parhyale and other species within Multicrustacea contain the enzyme sets necessary to perform lignocellulose digestion ('wood eating'), suggesting this ability may predate the diversification of this lineage. Our data provide an essential resource for further development of Parhyale as an experimental model. The first malacostracan genome will underpin ongoing comparative work in food crop species and research investigating lignocellulose as an energy source.


Asunto(s)
Anfípodos/genética , Proteínas de Artrópodos/genética , Genoma , Estadios del Ciclo de Vida/genética , Lignina/metabolismo , Redes y Vías Metabólicas/genética , Anfípodos/clasificación , Anfípodos/crecimiento & desarrollo , Anfípodos/metabolismo , Animales , Acuicultura , Proteínas de Artrópodos/inmunología , Femenino , Regulación del Desarrollo de la Expresión Génica , Ontología de Genes , Secuenciación de Nucleótidos de Alto Rendimiento , Inmunidad Innata , Cariotipo , Estadios del Ciclo de Vida/inmunología , Masculino , Redes y Vías Metabólicas/inmunología , Anotación de Secuencia Molecular , Filogenia , ARN no Traducido/genética , ARN no Traducido/inmunología , Regeneración , Transducción de Señal , Factores de Transcripción/genética , Factores de Transcripción/inmunología
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