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Industrial-scale Production (industrial-scale + production)

Distribution by Scientific Domains

Life Sciences	50%
Chemistry	50%

Selected Abstracts

Interspecific Effects of Artifically Propagated Fish: an Additional Conservation Risk for Salmon

CONSERVATION BIOLOGY, Issue 6 2002
Phillip S. Levin
We tested the hypothesis that hatchery-reared steelhead salmon ( Oncorhynchus mykiss) released into the Snake River Basin negatively affect the survival of wild Snake River steelhead and chinook ( O. tshawytscha) salmon. Because climatic conditions can influence salmon survival, we included an index of the El Niño,Southern Oscillation ( ENSO) as a covariate in our analyses. Based on time series of hatchery releases and rates of smolt-to-adult survival, we demonstrate that the survival of wild chinook salmon is negatively associated with hatchery releases of steelhead. The state of the ( ENSO) did not affect the strength of this relationship. We observed no relationship between survival of wild steelhead and steelhead hatchery releases. Our results suggest that industrial-scale production of hatchery fish may hinder the recovery of some threatened salmonids and that the potential interspecific impact of hatcheries must be considered as agencies begin the process of hatchery reform. Resumen: Por más de 120 años, las granjas han liberado números enormes de salmones del Pacífico para compensar las numerosas agresiones humanos a sus poblaciones, sin embargo, los impactos ecológicos de este esfuerzo masivo son poco entendidos. Evaluamos la hipótesis de que la trucha cabeza de acero ( Oncorhynchus mykiss) criada en granjas y liberada en la cuenca del Río Snake afecta negativamente la supervivencia de truchas cabeza de acero y salmones chinook ( O. tshawytscha) silvestres. Puesto que las condiciones climáticas pueden influir sobre la supervivencia del salmón, incluimos un índice de la Oscilación del Niño del Sur como covariable del análisis. En base a series de tiempo de las liberaciones de las granjas y las tasas de supervivencia hasta adulto de peces migrantes al mar, demostramos que la supervivencia del salmón chinook silvestre está negativamente correlacionada con las liberaciones de truchas cabeza de acero de las granjas. El estado de la Oscilación del Niño del Sur no afectó el grado de correlación. No observamos relación alguna entre la supervivencia de las truchas silvestres y las liberaciones de las granjas. Nuestros resultados sugieren que la producción a escala industrial de peces de granja puede obstaculizar la recuperación de algunos salmónidos amenazados y que el impacto interespecífico potencial de las granjas debería ser considerado en cuanto las agencias inicien el proceso de reforma de las granjas. [source]

Biofuels in China: past, present and future

BIOFUELS, BIOPRODUCTS AND BIOREFINING, Issue 3 2010
Cheng Zhong
Abstract Energy security and environmental stress force China to seek and develop biofuels as a substitute of fossil energy. Meanwhile, China has great potential to provide a large quantity of feedstocks for biofuel production due to its vast amount of non-food crops, such as tuberous crops, sweet sorghum, cellulosic biomass, and algae. Recently, the study and the industrial-scale production of biofuels, particularly, fuel ethanol and biodiesel, have progressed remarkably in China as a result of government preferential policies and funding supports. We have briefly reviewed the historical development of biofuels in China with special emphasis on current feedstock utilization and process technology development. The bottlenecks of utilizing various feedstocks have also been analyzed and the prospects for future biofuel development in China have been explored. Biorefineries integrating reliable, low-cost and sufficient non-food feedstock supplies with highly efficient, environmentally friendly process technologies could sustain a bright future for biofuel development in China. Copyright © 2010 Society of Chemical Industry and John Wiley & Sons, Ltd [source]

Study of Protein Splicing and Intein-Mediated Peptide Bond Cleavage under High-Cell-Density Conditions

BIOTECHNOLOGY PROGRESS, Issue 3 2003
Shamik Sharma
Protein splicing elements (inteins), capable of catalyzing controllable peptide bond cleavage reactions, have been used to separate recombinant proteins from affinity tags during affinity purification. Since the inteins eliminate the use of a protease in the recovery process, the intein-mediated purification system has the potential to significantly reduce recovery costs for the industrial production of recombinant proteins. Thus far, the intein system has only been examined and utilized for expression and purification of recombinant proteins at the laboratory scale for cells cultivated at low cell densities. In this study, protein splicing and in vitro cleavage of intein fusion proteins expressed in high-cell-density fed-batch fermentations of recombinant Escherichia coli were examined. Three model intein fusion constructs were used to examine the stability and splicing/cleavage activities of the fusion proteins produced under high-cell-density conditions. The data indicated that the intein fusion protein containing the wild-type intein catalyzed efficient in vivo protein splicing during high-cell-density cultivation. Also, the intein fusion proteins containing modified inteins catalyzed efficient thiol-induced in vitro cleavage reactions. The results of this study demonstrated the potential feasibility of using the intein-mediated protein purification system for industrial-scale production of recombinant proteins. [source]

Protein Engineering Strategies for Selective Protein Purification

CHEMICAL ENGINEERING & TECHNOLOGY (CET), Issue 11 2005
M. Hedhammar
Abstract When producing and purifying recombinant proteins it is of importance to minimize the number of unit operations during the purification procedure. This is accomplished by increasing the selectivity in each step. Due to the high selectivity of affinity chromatography it has a widespread use in protein purification. However, most target proteins lack a suitable affinity ligand usable for capture on a solid matrix. A way to circumvent this obstacle is to genetically fuse the gene encoding the target protein with a gene encoding a purification tag. When the chimeric protein is expressed, the tag allows for specific capture of the fusion protein. In industrial-scale production, extension of the target protein often is unwanted since it might interfere with the function of the target protein. Hence, a purification scheme developed for the native protein is desired. In this review, different fusion strategies used for protein purification are discussed. Also, the development of ligands for selective affinity purification of native target proteins is surveyed. [source]