RESUMEN
Mucor circinelloides transformants prototrophic to leucine and resistant to carboxine (Leu(+) Cbx(r)) have been obtained by treatment of protoplasts with plasmid constructs containing homologous leuA gene and adjacent autonomously replicating sequences (ARS) element combined with the Cbx(r)(carboxine-resistance) gene of Ustilago maydis and ARS sequences from this basidiomycete (plasmid pGG37) or from the 2 mu plasmid of Saccharomyces cerevisiae (plasmid pGG43). The presence in the same plasmid molecule of the M. circinelloides leuA gene and adjacent ARS element together with heterologous ARS elements produced an increase in the transformation frequency of about 65-120%. The presence of autoreplicating plasmid molecules in the transformants was demonstrated by mitotic stability experiments, by Southern analysis, and by the rescue of plasmids from transformed bacterial cells.
Asunto(s)
Replicación del ADN/genética , Farmacorresistencia Fúngica/genética , Técnicas de Transferencia de Gen , Vectores Genéticos/genética , Mucor/genética , Transformación Genética/genética , Carboxina/farmacología , Genes Dominantes , Genes Fúngicos , Leucina/metabolismo , Mucor/efectos de los fármacos , Plásmidos/genética , Ustilago/genéticaRESUMEN
NAD-dependent alcohol dehydrogenase (ADH) activity was detected mainly in the cytosol of aerobically cultured mycelium and in anaerobically grown yeast cells of Mucor circinelloides. ADH levels were about 2.5-fold higher in yeast cells than in mycelium; zymogram analysis suggested that the same ADH enzyme is produced in both developmental stages. The enzyme, named ADH1, was purified to homogeneity from yeast cells, using ion-exchange and affinity chromatography. The active ADH1 appears to be a homomeric tetramer of 37,500-kDa subunits. Km values obtained for acetaldehyde, ethanol, NADH and NAD+ indicated that in vivo the enzyme mainly serves to reduce acetaldehyde to ethanol. Amino acid sequences of internal peptides obtained from the purified ADH1 were used to design oligonucleotides that allowed the cloning of the corresponding cDNA by RT-PCR, and the characterization of the genomic DNA sequence. The adh1 ORF is interrupted by two small introns located towards the 5'-end. M. circinelloides adh1 encodes a protein of 348 amino acids, which display moderate to high overall identity to several hypothetical ADH enzymes from the related zygomycete Rhizopus oryzae. adh1 mRNA is expressed at similar levels in aerobic mycelium and anaerobic yeast cells. During exponential growth under aerobic conditions, the level of adh1 transcript was correlated with the glucose concentration in the growth medium.
Asunto(s)
Alcohol Deshidrogenasa/química , Alcohol Deshidrogenasa/genética , Mucor/enzimología , Mucor/genética , Acetaldehído/química , Secuencia de Aminoácidos , Secuencia de Bases , Northern Blotting , Southern Blotting , Sistema Libre de Células , Cromatografía de Afinidad , Cromatografía por Intercambio Iónico , Clonación Molecular , Medios de Cultivo/metabolismo , Citosol/metabolismo , ADN/química , ADN Complementario/metabolismo , Electroforesis en Gel de Poliacrilamida , Etanol/química , Fermentación , Proteínas Fúngicas/química , Regulación Fúngica de la Expresión Génica , Biblioteca de Genes , Genes Fúngicos , Intrones , Cinética , Datos de Secuencia Molecular , Peso Molecular , NAD/química , NAD/metabolismo , Sistemas de Lectura Abierta , Péptidos/química , Filogenia , Isoformas de Proteínas , ARN Mensajero/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Rhizopus/metabolismo , Especificidad por Sustrato , Factores de TiempoRESUMEN
Chromium is a highly toxic non-essential metal for microorganisms and plants. Due to its widespread industrial use, chromium (Cr) has become a serious pollutant in diverse environmental settings. The hexavalent form of the metal, Cr(VI), is considered a more toxic species than the relatively innocuous and less mobile Cr(III) form. The presence of Cr in the environment has selected microbial and plant variants able to tolerate high levels of Cr compounds. The diverse Cr-resistance mechanisms displayed by microorganisms, and probably by plants, include biosorption, diminished accumulation, precipitation, reduction of Cr(VI) to Cr(III), and chromate efflux. Some of these systems have been proposed as potential biotechnological tools for the bioremediation of Cr pollution. In this review we summarize the interactions of bacteria, algae, fungi and plants with Cr and its compounds.
Asunto(s)
Cromo/farmacología , Contaminantes Ambientales/toxicidad , Secuencia de Aminoácidos , Bacterias/efectos de los fármacos , Biodegradación Ambiental , Cromo/análisis , Cromo/química , Cromo/farmacocinética , Cromo/toxicidad , Microbiología Ambiental , Contaminantes Ambientales/análisis , Eucariontes/efectos de los fármacos , Hongos/efectos de los fármacos , Datos de Secuencia Molecular , Plantas/efectos de los fármacosRESUMEN
Arsenic resistance determinants from 42 environmental bacterial isolates (32 Gram negative) were analyzed by DNA: DNA hybridization using probes derived from Escherichia coli and Staphylococcus plasmid or chromosomal arsenic resistance (ars) genes. In colony hybridization assays, 11 and 1 Gram negative strains hybridized with the E. coli chromosome and plasmid probes, respectively. No hybridization was detected using a probe containing only the arsA (ATPase) gene from E. coli plasmid or with a Staphylococcus plasmid ars probe. From Southern hybridization tests of some of the positive strains it was concluded that homology to ars chromosomal genes occurred within chromosome regions, except in an E. coli isolate where hybridization occurred in both the chromosome and a 130-kb plasmid. Our results show that DNA sequences homologous to E. coli ars chromosomal genes are commonly present in the chromosomes of environmental arsenic-resistant Gram negative isolates.
Asunto(s)
Arsenicales/farmacología , Bacterias/genética , Proteínas Bacterianas , ADN Bacteriano/genética , Farmacorresistencia Microbiana/genética , Bombas Iónicas , Complejos Multienzimáticos , Factores R/genética , Microbiología del Suelo , Adenosina Trifosfatasas/genética , Arseniatos/farmacología , ATPasas Transportadoras de Arsenitos , Arsenitos/farmacología , Bacterias/efectos de los fármacos , Cromosomas Bacterianos/genética , Escherichia coli/genética , México , Hibridación de Ácido Nucleico , Contaminantes del Suelo/farmacología , Transactivadores/genéticaRESUMEN
The dimorphic fungus Yarrowia lipolytica grows to form hyphae either in rich media or in media with GlcNAc as a carbon source. A visual screening, called FIL (filamentation minus), for Y. lipolytica yeast growth mutants has been developed. The FIL screen was used to identify three Y. lipolytica genes that abolish hypha formation in all media assayed. Y. lipolytica HOY1, a gene whose deletion prevents the yeast-hypha transition both in liquid and solid media, was characterized. HOY1 is predicted to encode a 509-amino-acid protein with a homeodomain homologous to that found in the chicken Hox4.8 gene. Analysis of the protein predicts a nuclear location. These observations suggest that Hoy1p may function as a transcriptional regulatory protein. In disrupted strains, reintroduction of HOY1 restored the capacity for hypha formation. Northern blot hybridization revealed the HOY1 transcript to be approximately 1.6 kb. Expression of this gene was detected when Y. lipolytica grew as a budding yeast, but an increase in its expression was observed by 1 h after cells had been induced to form hyphae. The possible functions of HOY1 in hyphal growth and the uses of the FIL screen to identify morphogenetic regulatory genes from heterologous organisms are discussed.
Asunto(s)
Proteínas Fúngicas , Genes Fúngicos , Genes Homeobox , Proteínas de Homeodominio/genética , Saccharomycetales/genética , Secuencia de Aminoácidos , Secuencia de Bases , Clonación Molecular , Cruzamientos Genéticos , Eliminación de Gen , Expresión Génica , Prueba de Complementación Genética , Proteínas de Homeodominio/biosíntesis , Datos de Secuencia Molecular , Morfogénesis/genética , Mutación , Hibridación de Ácido Nucleico , Proteínas Recombinantes/biosíntesis , Secuencias Reguladoras de Ácidos Nucleicos , Saccharomyces cerevisiae/genética , Saccharomycetales/citología , Análisis de Secuencia de ADN , Homología de Secuencia de Aminoácido , Factores de Transcripción/genéticaRESUMEN
We designed PCR primers by comparison of the deduced amino acid sequences of several ornithine decarboxylase (ODC) genes. They were used to amplify fragments homologous to these genes from several dimorphic fungi. These were sequenced and the deduced amino acid sequences were compared with the corresponding regions of ODCs from different sources. Fungal ODCs fell into a compact group, well separated from the ODCs of other taxa. Sequence homology among fungal enzymes corresponded to their taxonomic position. Interesting patterns of amino acid conservation in ODCs from fungi, distinct from other organisms, were detected.
Asunto(s)
Hongos/enzimología , Ornitina Descarboxilasa/química , Secuencia de Aminoácidos , Datos de Secuencia Molecular , Ornitina Descarboxilasa/genética , Reacción en Cadena de la PolimerasaRESUMEN
Three allyl-alcohol-resistant mutants were isolated in the dimorphic fungus Mucor rouxii and characterized with regard to their alcohol dehydrogenase (ADH) activity in vitro and in vivo as well as their ability to execute the morphological alternatives of dimorphism under different environmental stimuli, either in the absence or in the presence of oxygen. These studies indicated that fermentation and yeast-cell development are independent events and that ADH activity is essential for growth of the fungus in the absence of oxygen. Heterokaryon construction and analysis indicated that in the three mutant strains the corresponding genetic alterations are recessive nuclear mutations which behave as allelic in complementation tests.
