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The development of projects to promote agricultural activity is of great importance today, as it responds to national priorities. To this end, it is necessary to diversify and make financial products more efficient in order to cover the investment and working capital needs of such projects. However, even when there are funds for the promotion of agricultural activity, there are limitations in their management, which limits the implementation of development project ideas in the state and nonstate sectors. In view of this problem, the main objective of this article is to design a procedure for the management of the Agricultural Development Bank that will contribute to the implementation of projects associated with agricultural production. The main research method used was the inductiondeduction, which is applied for the design of the proposed procedure and the formulation of actions to facilitate its implementation. The proposed procedure represents a support tool in the management of the Agricultural Development Fund from the financial institutions at the municipal level and has a set of suggestions that will facilitate its application, which are variable according to the criteria of the actors who implement it. [ABSTRACT FROM AUTHOR]

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Copyright of Retos: Nuevas Perspectivas de Educación Física, Deporte y Recreación is the property of Federacion Espanola de Asociaciones de Docentes de Educacion Fisica and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Cuadernos de Psicología del Deporte is the property of Cuadernos de Psicologia del Deporte and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Cultura, Ciencia y Deporte is the property of Cultura, Ciencia y Deporte and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The following article presents the analysis of a wireless cellular network's capacity, typically from a fixed wireless application environment, in which through a simulation model with discrete events, the capacity of the network is determined under non-ideal conditions, represented by the power control error model and the human voice activity factor model. [ABSTRACT FROM AUTHOR]

The sequence of the genome of Vibrio cholerae N16961 is deposited in a database of The Institute for Genomic Research (TIGR). In that database, genes VCA0260 and VCA0261 are annotated as two independent and overlapped genes, which are predicted to encode two hypothetical proteins of 11.9 kDa and 7.3 kDa of molecular weight, respectively. In a previous proteomic study of V. cholerae C7258 cells, one spot up-regulated under anaerobic culture revealed a correspondence with predicted polypeptides from genes VCA0260 and VCA0261. This finding suggested that genes VCA0260 and VCA0261 constitute a single gene encoding a single protein. Here, it is described PCR amplifications, cloning and nucleotide sequencing of regions spanning both genes from V. cholerae strains C7258 and N16961. Nucleotide sequencing of both regions showed the existence of a guanine nucleotide preceding the stop codon of VCA0261, which is absent in the published sequence. The presence of this guanine changes the reading frame of ORF VCA0261 to the same as VCA0260, resulting in a predicted larger ORF coding for a protein of 18.7 kDa of molecular weight. Production of this protein was co-rroborated by expression, purification and sequencing by mass spectrometry of the peptide synthesized from cloned regions in Escherichia coli. Thus, VCA0260 and VCA0261 genes constitute a single gene (VCA0261-VCA260) encoding a single protein. A mutant of V. cholerae C7258 with the gene VCA0261-VCA0260 deleted from its chromosome was constructed. In the presence of copper, growth of the VCA0261-VCA0260 mutant was affected compared to the growth of wild type strain, suggesting that the protein coded by VCA0261-VCA0260 gene is involved in copper homeostasis in V. cholerae. On the other hand, this protein does not seem to play an important role during the colonization process in the presence of 10 µmol/L of copper, in an infant mouse model of cholera colonization. [ABSTRACT FROM AUTHOR]