RESUMEN
Powdery mildew, caused by Blumeria graminis f.sp. tritici, is one of the most important wheat diseases in many regions of the world. Triticum turgidum var. dicoccoides (2n=4x=AABB), the progenitor of cultivated wheats, shows particular promises as a donor of useful genetic variation for several traits, including disease resistances. The wild emmer accession MG29896, resistant to powdery mildew, was backcrossed to the susceptible durum wheat cultivar Latino, and a set of backcross inbred lines (BC(5)F(5)) was produced. Genetic analysis of F(3) populations from two resistant introgression lines (5BIL-29 x Latino and 5BIL-42 x Latino) indicated that the powdery mildew resistance is controlled by a single dominant gene. Molecular markers and the bulked segregant analysis were used to characterize and map the powdery mildew resistance. Five AFLP markers (XP43M32((250)), XP46M31((410)), XP41M37((100)), XP41M39((250)), XP39M32((120))), three genomic SSR markers (Xcfd07, Xwmc75, Xgwm408) and one EST-derived SSR marker (BJ261635) were found to be linked to the resistance gene in 5BIL-29 and only the BJ261635 marker in 5BIL-42. By means of Chinese Spring nullisomic-tetrasomic, ditelosomic and deletion lines, the polymorphic markers and the resistance gene were assigned to chromosome bin 5BL6-0.29-0.76. These results indicated that the two lines had the same resistance gene and that the introgressed dicoccoides chromosome segment was longer (35.5 cM) in 5BIL-29 than that introgressed in 5BIL-42 (less than 1.5 cM). As no powdery mildew resistance gene has been reported on chromosome arm 5BL, the novel resistance gene derived from var. dicoccoides was designated Pm36. The 244 bp allele of BJ261635 in 5BIL-42 can be used for marker-assisted selection during the wheat resistance breeding process for facilitating gene pyramiding.
Asunto(s)
Ascomicetos , Mapeo Cromosómico , ADN de Plantas/genética , Genes de Plantas , Enfermedades de las Plantas/genética , Triticum/genética , Análisis del Polimorfismo de Longitud de Fragmentos Amplificados , Cromosomas de las Plantas/genética , Cruzamientos Genéticos , Etiquetas de Secuencia Expresada , Ligamiento Genético , Marcadores Genéticos , Variación Genética , Repeticiones de Minisatélite , Enfermedades de las Plantas/microbiología , Triticum/microbiologíaRESUMEN
Flash-induced redox changes of b-type and c-type cytochromes have been studied in chromatophores from the aerobic photosynthetic bacterium Roseobacter denitrificans under redox-controlled conditions. The flash-oxidized primary donor P+ of the reaction center (RC) is rapidly re-reduced by heme H1 (Em,7 = 290 mV), heme H2 (Em,7 = 240 mV) or low-potential hemes L1/L2 (Em,7 = 90 mV) of the RC-bound tetraheme, depending on their redox state before photoexcitation. By titrating the extent of flash-induced low-potential heme oxidation, a midpoint potential equal to -50 mV has been determined for the primary quinone acceptor QA. Only the photo-oxidized heme H2 is re-reduced in tens of milliseconds, in a reaction sensitive to inhibitors of the bc1 complex, leading to the concomitant oxidation of a cytochrome c spectrally distinct from the RC-bound hemes. This reaction involves cytochrome c551 in a diffusional process. Participation of the bc1 complex in a cyclic electron transfer chain has been demonstrated by detection of flash-induced reduction of cytochrome b561, stimulated by antimycin and inhibited by myxothiazol. Cytochrome b561, reduced upon flash excitation, is re-oxidized slowly even in the absence of antimycin. The rate of reduction of cytochrome b561 in the presence of antimycin increases upon lowering the ambient redox potential, most likely reflecting the progressive prereduction of the ubiquinone pool. Chromatophores contain approximately 20 ubiquinone-10 molecules per RC. At the optimal redox poise, approximately 0.3 cytochrome b molecules per RC are reduced following flash excitation. Cytochrome b reduction titrates out at Eh < 100 mV, when low-potential heme(s) rapidly re-reduce P+ preventing cyclic electron transfer. Results can be rationalized in the framework of a Q-cycle-type model.
Asunto(s)
Bacterias/metabolismo , Complejo III de Transporte de Electrones/metabolismo , Fotosíntesis/fisiología , Proteínas del Complejo del Centro de Reacción Fotosintética/metabolismo , Proteobacteria/fisiología , Antimicina A/análogos & derivados , Antimicina A/farmacología , Fenómenos Fisiológicos Bacterianos , Benzoquinonas/farmacología , Grupo Citocromo b/química , Grupo Citocromo b/metabolismo , Grupo Citocromo c/química , Grupo Citocromo c/metabolismo , Complejo III de Transporte de Electrones/antagonistas & inhibidores , Complejo III de Transporte de Electrones/química , Electrones , Inhibidores Enzimáticos/farmacología , Ferricianuros/farmacología , Cinética , Luz , Metacrilatos , Naftoquinonas/farmacología , Oxidación-Reducción , Fenilendiaminas/farmacología , Proteobacteria/metabolismo , Tiazoles/farmacología , Factores de Tiempo , VolumetríaRESUMEN
This work describes the first case of Acquired Immuno-Deficiency Syndrome (AIDS) to be found in Sardinia. The patient was an adult male drug-addict who died following a respiratory inadequacy due to bronchial pneumonia resulting from Pneumocystis carinii (PCP). For diagnostic purposes the emphasis is laid on the importance of morphological research into the parasite, considering the lack of specific evidence regarding serological investigation. Therefore, the various techniques of coloration are examined here. That which stands out for its simplicity of performance and its thoroughness of investigation is the May-Grünwald-Giemsa coloration which also points out other micro-organisms frequently associated with this type of pathology. In conclusion, then, this work indicates the advisability, on behalf of the Services of Anatomy and Pathological Histology to adopt, as routine practice the specific colorations for Pneumocystis carinii (PC), taking into account the considerable diffusion of this parasite in patients with immuno-deficiency.