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Bioreactors efficient recovery from

Initially fermentation broth has to be characterised on the viscosity of the fluid. If the presence of the biomass or cells causes trouble, they have to be removed. Tire product is stored inside the cells, the cells must be ruptured and the product must be freed. Intracellular protein can easily be precipitated, settled or filtered. In fact the product in diluted broth may not be economical enough for efficient recovery. Enrichment of the product from the bioreactor effluents for increasing product concentration may reduce the cost of product recovery. There are several economical methods for pure product recovery, such as crystallisation of the product from the concentrated broth or liquid phase. Even small amounts of cellular proteins can be lyophilised or dried from crude solution of biological products such as hormone or enzymes.2,3... [Pg.170]

The economic feasibility of a bioreaction process clearly depends on the characteristics of the associated bioseparation process, especially in the usual case when the product is present at low concentration in a complex mixture. For example, the existence of an extremely efficient and low-cost separation process for a particular compound could significantly lower the final concentration of that compound required in the bioreactor to achieve a satisfactory overall process. After noting that special approaches and processes are needed for efficient recovery of small molecules (ethanol, amino acids, antibiotics, etc.) from the dilute aqueous product streams of current bioreactors, I shall discuss further only separations of proteins. These are the primary products of the new biotechnology industry, and their purification hinges on the special properties of these biological macromolecules. [Pg.427]

Mori and Inaba (1990) applied a PV technique to attain both high productivity and efficient recovery of EtOH from a fermentation broth. The manbrane bioreactor consisted of a jar fermenter and a PV systan for the direct production of EtOH from uncooked starch with a thermophilic anaerobic bacterium, Clostridium thermohydrosulfuricum. From the four types of EtOH-selective monbranes tested, microporous PTFE membrane, the pores of which were impregnated with silicone rubber, was chosen for its large flux, high EtOH selectivity, and high stability. During... [Pg.309]

In this review, we focus on the use of plant tissue culture to produce foreign proteins that have direct commercial or medical applications. The development of large-scale plant tissue culture systems for the production of biopharmaceutical proteins requires efficient, high-level expression of stable, biologically active products. To minimize the cost of protein recovery and purification, it is preferable that the expression system releases the product in a form that can be harvested from the culture medium. In addition, the relevant bioprocessing issues associated with bioreactor culture of plant cells and tissues must be addressed. [Pg.16]

Cabral and coworkers [253] have investigated the batch mode synthesis of a dipeptide acetyl phenylalanine leucinamide (AcPhe-Leu-NH2) catalyzed by a-chymotrypsin in a ceramic ultrafiltration membrane reactor using a TTAB/oc-tanol/heptane reverse micellar system. Separation of the dipeptide was achieved by selective precipitation. Later on the same group successfully synthesized the same dipeptide in the same reactor system in a continuous mode [254] with high yields (70-80%) and recovery (75-90%). The volumetric production was as high as 4.3 mmol peptide/l/day with a purity of 92%. The reactor was operated for seven days continuously without any loss of enzyme activity. Hakoda et al. [255] proposed an electro-ultrafiltration bioreactor for separation of RMs containing enzyme from the product stream. A ceramic membrane module was used to separate AOT-RMs containing lipase from isooctane. Application of an electric field enhanced the ultrafiltration efficiency (flux) and it further improved when the anode and cathode were placed in the permeate and the reten-tate side respectively. [Pg.165]


See other pages where Bioreactors efficient recovery from is mentioned: [Pg.547]    [Pg.49]    [Pg.251]    [Pg.65]    [Pg.334]    [Pg.38]    [Pg.327]    [Pg.224]    [Pg.659]    [Pg.102]    [Pg.277]    [Pg.180]    [Pg.49]    [Pg.250]    [Pg.49]    [Pg.259]    [Pg.36]    [Pg.41]    [Pg.480]   
See also in sourсe #XX -- [ Pg.427 ]




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