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cells where the whole metabolic machinery is often required for their specific application)
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1. Reactions involving single enzymes (bioconversions) 2. Reactions involving multienzyme systems with or without cofactors 3. Reactions involving a complete metabolic pathway yielding primary or secondary metabolites
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areas 1.when the desired enzymes are intracellular and the extracted, purified enzymes become unstable after immobilization 2. when the microorganism does not contain interfering enzymes or when such enzymes can be inactivated without loss of desired catalytic activity 3. when substrates and products do not have a high molecular mass and can diffuse through the cell membrane
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massaggregation Cell bi- or multifunctional can be induced reagents by low such molecular as glutaraldehyde, diazotized diamines, or toluene diisocyanate
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cell growth monolithic ceramic matrix has been developed for large-scale cell cultures. For adherent cell growth, the scalability is almost linear and depends on the available surface area. Ionic Binding. Ionic binding is a special case of physical adsorption where charged microbial cells can electrostatically interact with the ions on a carrier surface to form stable complexes. Synthetic ionexchange resins, modified cellulose derivatives, or inorganic materials can be used as carriers. Cell adsorption is mainly affected by factors such as pH, ionic strength, surface charge, cell age, or composition of the carrier surface.
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Covalent Binding
Cells can also bind to the functional groups of the carrier surface by covalent bonds.
This technique is frequently used for enzyme immobilization but has only limited use in whole-cell immobilization because the toxicity of the coupling agents often results in loss of cell viability or enzyme activity
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Lattice Entrapment. retention of cells within the network of a polymer matrix. forms pellets high viable cell density (e.g., polyacrylamide gel, alginate gel, kcarrageenan, and photo-cross-linkable resins)
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Polyacrylamide Gel.
free-radical polymerization in an aqueous acrylamide monomer solution containing the cells at low temperature. The degree of cross-linking determines the porosity and mechanical properties of the pellets. The major disadvantage of the method is the toxicity of the acrylamide monomer, the cross-linking agent (e.g., methylenebisacrylamide [110-26-9]), and the polymerization initiator (e.g.,tetramethylethylenediamine [110-18-9]) which can decrease cell viability and enzyme activity], Hydroxyethyl methacrylate [868-77-9] .....less toxic alternative to acrylamide With acrylamide monomers, optimal results are achieved in isotonic buffered solution at low temperature (4 12 C) by keeping exposure time to a minimum (3 4 min).
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Alginate [9005-38-3]
is extracted from seaweed and is a linear copolymer of b-D-mannuronic acid and a-Lguluronic acid linked by 1,4-glycosidic bonds. It forms a gel in the presence of multivalent ions, usually calcium or aluminum. The controlled entrapment of cells is simple and generally nontoxic. Various cell types can be immobilized with negligible loss of viability.
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-Carrageenan [11114-20-8]
sulfonated polysaccharide extracted from seaweed. It consists of b-D-galactose 4-sulfate and 3,6-anhydro-D-galactose units. Only the sodium salt of k-carrageenan is soluble in cold water. Induction of gelation with potassium ions can be performed under very mild conditions without the use of chemicals that decrease enzyme activity. Another advantage of this technique is that the immobilized cell biocatalysts can be tailor-made into pellets, sheets, beads, etc.
one-step procedure
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Photo-cross-linkable resins
Active groups (e.g., vinyl groups) are coupled to polyethylene or poly-(propylene glycol) oligomers of controlled chain length to prepare prepolymers. The prepolymers
are then mixed with the cell culture, and cross--linking is initiated with UV radiation
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2. prepolymers do not contain toxic monomers 3. the network structure of the gels can be adapted as required 4. optimal physicochemical gel properties can be achieved by selecting suitable prepolymers
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The supply of oxygen and nutrients to the cells and the removal of carbon dioxide from the cells occur by diffusion and may be insufficient.
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Microencapsulation
entrapped in hollow spheres where they can be cultured. Different capsule diameters (from 20 nm to 2 mm) and controlled membrane porosity can be achieved In larger microcapsules, however, radial concentration gradients of nutrients or oxygen can result in a necrotic core
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Coimmobilization of Biocatalysts
galactosidase and Saccharomyces cerevisiae for the conversion of cellobiose to ethanol Yeast cells or dead mycelia have been employed for direct coupling of enzymes to cell walls in food-processing applications bioproduction of hydrogen gas with hydrogenase and chloroplasts Coimmobilization results in a fivefold increase in hydrogen production compared with the system employing two separately immobilized catalytic species.
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Economic Aspects
25 % of the world pharmaceutical market is already covered by biotechnologically manufactured products. In the chemical industry, this fraction is approaching 10 %. According to market growth projections, U.S. biotechnology industry sales will increase from about $ 400106 in 1987 to $ 2.5109 by 1990, and more than $ 25109 by 2000 . The world biotechnology market in the year 2004 is predicted to be
$ 75109
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Immobilized Enzymes.
The total market for industrial enzymes is about $ 400106 and is growing by about 15 % each year. Enzyme immobilization has not initiated the expected revolution in the enzyme industry Soluble use-and-discard enzymes have, by far, the most dominant market share. Only one immobilized enzyme product, immobilized glucose isomerase, is used in amounts > 50 t a year; 1500 1750 t are used worldwide annually. The three other major immobilized enzymes are aminoacylase (about 5 t/a), lactase (< 5 t/a), and penicillin G acylase (3 4 t/a) .Other immobilized enzymes are also available but
are used in even smaller amounts: glucoamylase, hydantoinase, invertase, nitrilase, RNAse, and penicillin V acylase.
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Immobilized microorganisms
multiple enzyme reactions especially where cofactor regeneration is essential. Recombinant Escherichia coli can be used for the production of relatively simple peptide hormones with pharmaceutical applications
such as human insulin, human growthused factor, human interferons immobilized biocatalyst is reportedly foror the conversion . A An hepatitis B surface antigen vaccine prepared in recombinant yeast was approved for marketing, and many other products from genetically engineered microorganisms and yeast are in the clinical test stage (interferons, lymphokines, hormones, enzymes, and vaccines.
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hybridoma or recombinant DNA techniques, mammalian cells can often be persuaded to produce and secrete useful quantities of these compounds Tissue plasminogen activator (TPA) recombinant E. coli or yeast or in glycosylated form in mammalian cells. The first three months' sales in the United States were almost $ 60106. Worldwide sales are projected to reach about $ 500106 in the next few years. . Monoclonal antibodies 100 monoclonal antibodies are offered, with annual sales of nearly $ 500106. Generally, the economics of microbial systems are more favorable than those of mammalian cell culture systems for recombinant proteins. When the use of recombinant microbial systems is impossible or impractical, cell culture systems will gain a market position if the products are high-value biologicals (> $ 100/g).
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Immobilized Plant Cells. Plant cell cultures can also be used for the production of metabolites
such as pharmaceuticals, chemicals, flavors, and fragrances. The first product obtained from mass plant cell cultures was shikonin [517-89-5], a red pigment composed of eight naphthoquinone molecules. Shikonin is produced by a two-stage fermentation process and is a high-value chemical ($ 4000/kg) with a limited annual market capacity of ca. 15 kg. Immobilized plant cell systems will be used mainly for products of cells in the stationary growth phase. The release of intracellularly stored products by intermittent permeabilization of immobilized cells can be a great economic advantage, allowing reutilization of the biomass. The continuous immobilized plant cell process in combination with strain selection and improved product leakage allows production of plantderived chemicals in the range of $ 20 25/kg. However, in the present industrial state of technology for plant cell cultures, a relatively small number of products have both high value per weight and sufficient market size.
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