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Biochemical engineering fermenters

They do, but the examination must be thorough, factual and not simply wordy. The feedstocks are important, but just as critical is the energy balance. So too are the new tools available to the fermentologist in biogenetics, biochemistry, and biochemical engineering. Fermentation technology has not stood still. But, renewable sources do not necessarily mean economically viable sources. Market surveys plus past experience can help us in our assessments. in the latter cate-... [Pg.321]

B. Atkinson and F. Mavituna, Biochemical Engineering andBiotechnology Handbook, 2nd ed., Macmillan Pubhshers Ltd., Basingstoke, UK, 1991. An exceptional collection of information on all aspects of fermentation with an exhaustive and up to date bibhography. [Pg.185]

J. E. Bailey and D. F. Ohis, Biochemical Engineering Fundamentals, 2nd ed. McGraw-HiU Book Co., Inc., New York, 1986. A very good treatise describing the apphcation of basic engineering principles to fermentation technology. [Pg.185]

H. C. Vogel, Fermentation and Biochemical Engineering Handbook, Noyes Publishing, Inc., Park Ridge, N.J., 1983. [Pg.185]

BIOCHEMICAL ENGINEERING TABLE 24-2 Comparison of Ethanol Fermenters... [Pg.2138]

The term fermentation is often used loosely by biochemical engineers. Biochemists have a more focused perspective (anaerobic) catabolism of an organic compound in which the compound serves as both an electron donor and acceptor and in which ATP is produced. [Pg.853]

Producing the kilograms of tPA necessary to satisfy the world s therapeutic needs requires the special skills possessed by modern biochemical engineers. Sophisticated engineering of the fermentation vessels, culturing conditions, and media compositions is required to culture thousands of liters of mammalian cells. In addition, new extremes of purity must be achieved in order to assure the safety of proteins derived from mammalian cells. The cost of the starting materials and the capacity constraints of the present-day equipment require that yields from each fermentation batch be as high as possible. [Pg.34]

Technology for very large (400,000-gallon) continuous fermenters was developed and is being practiced in the United Kingdom. This development pushes biochemical engineering to hmits not yet explored in the United States. [Pg.39]

Several areas are receiving much of the research attention. Approaches that integrate product recovery with the fermentation in a three-phase fluidized bed bioreactor reflect general research trends in biochemical engineering (Yabannavar and Wang, 1991 Davison and Thompson, 1992). The successful use of three-phase biofluidization has also been demonstrated for recombinant protein systems, where it may have some benefit in improving plasmid stability (Shu and Yang, 1996). [Pg.634]

Bauer, W. and Kunz, B., Solid-state fermentation in food industry, in Chmiel, H., Hammes, W.P. and Bailey, J.E., (eds.). Biochemical engineering, Gustav Fischer Verlag, Stuttgart, 1987, 228-241. [Pg.221]

Andreotti, R. E., "Laboratory Experiment for High Yield Cellulose Fermentation," II International Course-ciim-Symposium on Byconversion and Biochemical Engineering, New Delhi, India (1980). [Pg.90]

You are a biochemical engineer in a pharmaceutical company. Your company is a major producer of penicillin. Currently, what kind of fermenter is your company using for penicillin production Why ... [Pg.172]

D. C. Wang et al., Fermentation and Enzyme Technology, Wiley, New York, 1979. T. J. Bailey and D. Ollis, Biochemical Engineering, 2nd ed., McGraw-Hill, New York, 1987. [Pg.394]

Bhave RR. Cross-flow filtration. In Fermentation and Biochemical Engineering Handbook—Principles, Process Design, and Equipment, 2nd edition, eds., Vogel HC and Tadaro CL, WiUiam Andrew/Noyes, West Woods, New Jersy, 1997, pp. 271-347. [Pg.579]

Additional complexity can be included through cell population balances that account for the distribution of cell generation present in the fermenter through use of stochastic models. In this section we limit the discussion to simple black box and unstructured models. For more details on bioreaction systems, see, e.g., Nielsen, Villadsen, and Liden, Bioreaction Engineering Principles, 2d ed., Kluwer, Academic/Plenum Press, 2003 Bailey and Ollis, Biochemical Engineering Fundamentals, 2d ed., McGraw-Hill, 1986 Blanch and Clark, Biochemical Engineering, Marcel Dekker, 1997 and Sec. 19. [Pg.31]


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