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Phased culture techniques

In terms of in situ adsorption, although none of the solid adsorbents for non-aqueous phase tested to date are entirely satisfactory for the selective separation of secondary metabolites formed by plant cells, the result obtained so far have been encouraging enough to stimulate the search for more selective solid adsorbent material. The most important advantages of the two-phase culture techniques are that it increases productivity by removing the feedback regula-... [Pg.99]

Figure 6.50. Experimental setup for obtaining asynchronous cultures (DCSTR and CSTR) and synchronous (phased) cultures (a), characterization of overall growth conditions (b), and illustration of growth of individual cells (c). A comparison of the different approaches shows clearly that in the DCSTR and CSTR, cells in the populations are randomized at all stages, while cells adjust their growth rate to the dosing interval and become synchronized to it in the phased culture technique (Dawson 1980a). Figure 6.50. Experimental setup for obtaining asynchronous cultures (DCSTR and CSTR) and synchronous (phased) cultures (a), characterization of overall growth conditions (b), and illustration of growth of individual cells (c). A comparison of the different approaches shows clearly that in the DCSTR and CSTR, cells in the populations are randomized at all stages, while cells adjust their growth rate to the dosing interval and become synchronized to it in the phased culture technique (Dawson 1980a).
Human osteoblast-like MG63 cells were cultured on the macroporous chitosan scaffolds reinforced with hydroxyapatite or calcium phosphate invert glass were fabricated using a thermally induced phase separation technique. [Pg.171]

Having produced and selected a desirable strain, the breeder must then produce sufficient numbers of plants to test for trait stability and determine optimal conditions for commercial production. Unlike annuals that produce abundant seed, perennials with long generation times such as forest trees are a challenge to the plant breeder. For species such as conifers, advances in tissue-culturing techniques have transformed production processes in both the development and the marketing phases. [Pg.1487]

Biopolymer Extraction. Research interests involving new techniques for separation of biochemicals from fermentation broth and cell culture media have increased as biotechnology has grown. Most separation methods are limited to small-scale appHcations but recendy solvent extraction has been studied as a potential technique for continuous and large-scale production and the use of two-phase aqueous systems has received increasing attention (259). A range of enzymes have favorable partition properties in a system based on a PGE—dextran—salt solution (97) ... [Pg.80]

The most widespread biological application of three-phase fluidization at a commercial scale is in wastewater treatment. Several large scale applications exist for fermentation processes, as well, and, recently, applications in cell culture have been developed. Each of these areas have particular features that make three-phase fluidization particularly well-suited for them Wastewater Treatment. As can be seen in Tables 14a to 14d, numerous examples of the application of three-phase fluidization to waste-water treatment exist. Laboratory studies in the 1970 s were followed by large scale commercial units in the early 1980 s, with aerobic applications preceding anaerobic systems (Heijnen et al., 1989). The technique is well accepted as a viable tool for wastewater treatment for municipal sewage, food process waste streams, and other industrial effluents. Though pure cultures known to degrade a particular waste component are occasionally used (Sreekrishnan et al., 1991 Austermann-Haun et al., 1994 Lazarova et al., 1994), most applications use a mixed culture enriched from a similar waste stream or treatment facility or no inoculation at all (Sanz and Fdez-Polanco, 1990). [Pg.629]

CSPs and chiral mobile phase additives have also been used in the separation of amino acid enantiomers. Another technique that should be mentioned is an analysis system employing column-switching. D-and L- amino acids are first isolated as the racemic mixture by reverse-phase HPLC. The isolated fractions are introduced to a second column (a CSP or a mobile phase containing a chiral selector) for separation of enantiomers. Long et al. (2001) applied this technique to the determination of D- and L-Asp in cell culture medium, within cells and in rat blood. [Pg.27]


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