Fósforo na alimentação de pacu (Piaractus mesopotamicus)

Objetivou-se avaliar o uso de fósforo na dieta de juvenis de pacu (Piaractus mesopotamicus) sobre a qualidade da água, o desempenho zootécnico, o rendimento corporal e a composição química da carcaça. Foram utilizados 100 juvenis com peso médio inicial de 25,9±1,32 g, distribuídos em delineamento inteiramente ao acaso, em 20 tanques de fibra de vidro, com cinco tratamentos e quatro repetições. Os peixes foram alimentados quatro vezes ao dia, às 8; 11; 14 e 17 h, com dietas extrusadas contendo 0,40; 0,55; 0,70; 0,85 e 1,0% de fósforo total. Não foram observadas diferenças nos parâmetros de qualidade de água, com exceção da concentração de ortofosfato na água, que apresentou aumento linear. Os parâmetros de desempenho zootécnico, rendimento corporal e composição química da carcaça não diferiram entre os níveis de suplementação de fósforo na dieta. A utilização de 0,40% de fósforo total atende às exigências de fósforo de juvenis de pacu (Piaractus mesopotamicus), além de disponibilizar menor concentração de ortofosfato da água.The objective of the present research was to evaluate phosphorus in diet for pacu (Piaractus mesopotamicus) juveniles on water quality, livestock performance, body yield and carcass chemical composition. A total of 100 juveniles, 25.9±1.32 g average weight were randomly assigned into 20 fiberglass tanks, with five treatments and four replications. The fish were fed four times a day (8 and 11 a.m.; 2 and 5 p.m.), with extruded diets containing 0.40; 0.55; 0.70; 0.85 and 1.0 % total phosphorus. No differences were observed in water quality parameters, except for the concentration of orthophosphate in water, which presented linear increase. The parameters livestock performance, body yield and carcass chemical composition showed no differences for the levels of supplementation of phosphorus in diet. The use of 0.40% total phosphorus meets the requirements of phosphorus for pacu (Piaractus mesopotamicus) juveniles, in addition to releasing lower concentration of orthophosphate in water

Sequencing and promoter analysis of the nifENXorf3orf5fdxAnifQ operon from Azospirillum brasilense Sp7

A 40-kb DNA region containing the major cluster of nif genes has been isolated from the Azospirillum brasilense Sp7 genome. In this region three nif operons have been identified: nifHDKorf1Y, nifENXorf3orf5fdxAnifQ and orf2nifUSVorf4. The operons containing nifENX and nifUSV genes are separated from the structural nifHDKorf1Y operon by about 5 kb and 10 kb, respectively. The present study shows the sequence analysis of the 6045-bp DNA region containing the nifENX genes. The deduced amino acid sequences from the open reading frames were compared to the nif gene products of other diazotrophic bacteria and indicate the presence of seven ORFs, all reading in the same direction as that of the nifHDKorf1Y operon. Consensus sigma54 and NifA-binding sites are present only in the promoter region upstream of the nifE gene. This promoter is activated by NifA protein and is approximately two-times less active than the nifH promoter, as indicated by the ß-galactosidase assays. This result suggests the differential expression of the nif genes and their respective products in Azospirillum

Partial characterization of nif genes from the bacterium Azospirillum amazonense

Azospirillum amazonense revealed genomic organization patterns of the nitrogen fixation genes similar to those of the distantly related species A. brasilense. Our work suggests that A. brasilense nifHDK, nifENX, fixABC operons and nifA and glnB genes may be structurally homologous to the counterpart genes of A. amazonense. This is the first analysis revealing homology between A. brasilense nif genes and the A. amazonense genome. Sequence analysis of PCR amplification products revealed similarities between the amino acid sequences of the highly conserved nifD and glnB genes of A. amazonense and related genes of A. brasilense and other bacteria. However, the A. amazonense non-coding regions (the upstream activator sequence region and the region between the nifH and nifD genes) differed from related regions of A. brasilense even in nitrogenase structural genes which are highly conserved among diazotrophic bacteria. The feasibility of the 16S ribosomal RNA gene-based PCR system for specific detection of A. amazonense was shown. Our results indicate that the PCR primers for 16S rDNA defined in this article are highly specific to A. amazonense and can distinguish this species from A. brasilense