237 research outputs found

    Farmer groups enterprises and the marketing of staple food commodities in Africa:

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    "There are some apparently successful cases of collective marketing with staple food commodities (grains and root crops), but these are less common than cases involving higher value agricultural products. These can be attributed to the benefit/cost ratio to participants being generally higher for collective marketing of the higher-value crops. Some of the costs are ‘hidden', in the sense that they are borne by individuals in time spent in attending meetings, and not shown in the financial statements of the enterprises concerned. Examining a series of cases, the paper advocates an approach to the marketing of staples which involves analyzing the value chain and identifying those activities which on the one hand, best lend themselves to individual initiative, and those where on the other hand, group approaches are more likely to prosper. Dual purpose food marketing involving village storage in anticipation of both external market opportunities and local lean season shortages usually falls into the former category. Collective initiatives have a higher probability of success when they complement agricultural intensification and involve bulking substantial quantities of produce for quality-conscious commercial buyers. Prospects for successful collective marketing are moreover greater where there is a history of collective endeavor, where focused on simple activities like bulking and distribution of inputs, where primary groups are small and homogenous in terms of interests and objectives, where they can establish lasting relationships with strong trade counterparties, where supported by effective training (especially re attitudes, numeracy, and business skills), where they can access effectively managed storage and inventory credit services, and where there is framework of law enforcement. The immediate poverty alleviation and programmatic priorities of funding agencies often undermine the effectiveness of promotional activities in support of collective marketing. This problem may be addressed by instituting systems of independent review and peer review processes, and involving open discussion of pros and cons of individual and collective approaches." authors' abstractCollective marketing, Producer organization, Staple food, Village storage, Inventory credit, Microfinance, Disbursement-driven,

    Fluorescence photophysics, characterisation and application of labelled glucose/galactose binding protein

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    There is currently a pressing need for reliable, minimally-invasive, continuous glucose monitoring for the treatment of diabetes mellitus. One promising glucose sensor is bacterially-derived glucose binding protein (GBP). In this project, the modified triple mutant H152C/A213R/L238S-GBP (mGBP) was investigated for viability as a functioning glucose sensor. Labelling the protein with the environmentally-sensitive dye BADAN produced repeatable, nearly linear, changes in both fluorescence intensity and fluorescent lifetime measurements. The robustness of the GBP-BADAN sensor response was tested and the results showed no interference from the sugars fructose and lactose- while it was also shown that alterations in temperature and pH level had deleterious effects on the sensor function. The dyes Texas Red and iodoacetamide nile red (IANR) were attached to the GBP binding site to investigate the possibility of producing an alternative, longer-wavelength sensor system than when using BADAN. The ostensibly environment-insensitive Texas Red dye produced a protein-dye complex with no discernible response to glucose, but a significant response was observed for the GBP labelled with IANR: a 2-exponential lifetime decay relative amplitude change of 18% was recorded. These data provided further evidence for the proposed mechanisms of labelled GBP, while showing proof-of-concept for a long-wavelength fluorescence lifetime based glucose sensor. Finally, methods of protein encapsulation were examined. Silica sol gels derived from both tetramethyl orthosilicate (TMOS) and tetraethyl orthosilicate (TEOS) precursors were found to be ineffective environments for the GBP-BADAN sensor, as the fluorescence response was significantly impaired. Encapsulation in a hydrogel produced using 9-fluorenylmethoxycarbonyl (FMOC-YL) was also examined, and this arrangement was found to provide an environment where both mGBP-BADAN and mGBP-IANR could function. mGBP-IANR in the FMOC-YL hydrogel was found to have a binding constant of 41.99 (±3.78)mM. It was concluded that mGBP-IANR in an FMOC-YL hydrogel could potentially provide a route to a functioning glucose biosensor.There is currently a pressing need for reliable, minimally-invasive, continuous glucose monitoring for the treatment of diabetes mellitus. One promising glucose sensor is bacterially-derived glucose binding protein (GBP). In this project, the modified triple mutant H152C/A213R/L238S-GBP (mGBP) was investigated for viability as a functioning glucose sensor. Labelling the protein with the environmentally-sensitive dye BADAN produced repeatable, nearly linear, changes in both fluorescence intensity and fluorescent lifetime measurements. The robustness of the GBP-BADAN sensor response was tested and the results showed no interference from the sugars fructose and lactose- while it was also shown that alterations in temperature and pH level had deleterious effects on the sensor function. The dyes Texas Red and iodoacetamide nile red (IANR) were attached to the GBP binding site to investigate the possibility of producing an alternative, longer-wavelength sensor system than when using BADAN. The ostensibly environment-insensitive Texas Red dye produced a protein-dye complex with no discernible response to glucose, but a significant response was observed for the GBP labelled with IANR: a 2-exponential lifetime decay relative amplitude change of 18% was recorded. These data provided further evidence for the proposed mechanisms of labelled GBP, while showing proof-of-concept for a long-wavelength fluorescence lifetime based glucose sensor. Finally, methods of protein encapsulation were examined. Silica sol gels derived from both tetramethyl orthosilicate (TMOS) and tetraethyl orthosilicate (TEOS) precursors were found to be ineffective environments for the GBP-BADAN sensor, as the fluorescence response was significantly impaired. Encapsulation in a hydrogel produced using 9-fluorenylmethoxycarbonyl (FMOC-YL) was also examined, and this arrangement was found to provide an environment where both mGBP-BADAN and mGBP-IANR could function. mGBP-IANR in the FMOC-YL hydrogel was found to have a binding constant of 41.99 (±3.78)mM. It was concluded that mGBP-IANR in an FMOC-YL hydrogel could potentially provide a route to a functioning glucose biosensor

    The impact of a pre-hospital critical care team on survival from out-of-hospital cardiac arrest

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    © 2015 Elsevier Ireland Ltd. Aim: To assess the impact of a pre-hospital critical care team (CCT) on survival from out-of-hospital cardiac arrest (OHCA). Methods: We undertook a retrospective observational study, comparing OHCA patients attended by advanced life support (ALS) paramedics with OHCA patients attended by ALS paramedics and a CCT between April 2011 and April 2013 in a single ambulance service in Southwest England. We used multiple logistic regression to control for an anticipated imbalance of prognostic factors between the groups. The primary outcome was survival to hospital discharge. All data were collected independently of the research. Results: 1851 cases of OHCA were included in the analysis, of which 1686 received ALS paramedic treatment and 165 were attended by both ALS paramedics and a CCT. Unadjusted rates of survival to hospital discharge were significantly higher in the CCT group, compared to the ALS paramedic group (15.8% and 6.5%, respectively,

    NOVEL ROLES FOR TEN-ELEVEN TRANSLOCATION 1 (TET1) 5-METHYLCYTOSINE DIOXYGENASE IN THE CELLULAR RESPONSE TO STRESS

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    Cells maintain exquisite control over gene expression in the struggle to preserve homeostasis. While some genes remain constitutively active to function in energy production or provide mechanical support, other batteries of genes respond only in the context of specific stresses, and must be silenced when homeostasis is achieved. Numerous transcription factors have been identified as responders to stress, whose gene targets aid in maintaining homeostasis. An additional layer of regulation over the relatively static genetic code involves chemical modifications of histones and DNA, particularly in or near gene promoters. Recent advances in the understanding of such epigenetic changes show that methylation at the 5-carbon position of cytosines neighboring guanosines (CpG) is an important player in the regulation of mammalian genes and chromatin architecture. Moreover, methyl groups can be further modified by in a reaction catalyzed by Ten-Eleven Translocation (TET) 5-methylcytosine dioxygenases, whose products were shown to be intermediates in DNA demethylation as well as stable, final products that may have functional relevance. DNA methylation has therefore become increasingly viewed as a dynamic process, yet the proteins regulating epigenetic marks and gene expression remain poorly-understood. Because changes in CpG methylation underlie numerous threats to health, including cancer and neurodegenerative diseases, these proteins are potential targets in developing biomarkers and in drug development. This dissertation explores the role of TET1 in response to cellular stress. Toward this end, an in vitro approach was taken in order to manipulate TET1 levels and measure the response to toxicant-induced stress. Two major roles for TET1 were elucidated. First, reactive oxygen species generated by exposure to the benzene metabolite hydroquinone (HQ) led to genome-wide and gene-specific CpG demethylation in a TET1-dependent manner. Moreover, cytoprotective genes induced by HQ were dependent TET1, suggesting the protein is involved in transcriptional responses to stress. Secondly, a role for TET1 in the response to DNA damage was uncovered and found to be unrelated to catalytic activity, indicating a novel, non-enzymatic role for TET1. Taken together, these data suggest that TET1 represents a heretofore unappreciated interface between the environment and the cellular response to stress. The findings presented are used to support the underlying hypothesis that TET1 is involved in mediating responses to stresses which would be harmful to the genome if left unconstrained. The idea that TET1 plays a protective role linked to disease is strengthened by reports of nearly uniformly low levels of TET proteins and their products in cancers. Highlighting the role of TET1 as a critical protector of the genome may serve as a foundation upon which a better understanding of the role of DNA methylation in disease may be built. Ultimately, unraveling the protein’s functions – both enzymatic and non-enzymatic - will lead to improved prevention and treatment strategies in diseases involving inappropriate DNA methylation
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