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Microbial Growth Kinetics

Microbial Growth Kinetics. Lecture 2 Tahir. Fermenters. Fermentation Process. Fermentation Technology. -> Fermentation: from latin -> ” fervere ” -> to boil (describing the anaerobic process of yeast producing CO 2 on fruit extracts) -> Nowadays: more broad meaning!!!!

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Microbial Growth Kinetics

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  1. Microbial Growth Kinetics Lecture 2 Tahir

  2. Fermenters

  3. Fermentation Process

  4. Fermentation Technology -> Fermentation: from latin -> ”fervere” -> to boil (describing the anaerobic process of yeast producing CO2 on fruit extracts) -> Nowadays: more broad meaning!!!! The five major groups of commercially important fermentations: -> Process that produces microbial cells (Biomass) as a product -> Process that produces microbial enzymes as a product -> Process that produces microbial metabolites (primary or secondary) as a product -> Process that produces recombinant products (enzymes or metabolite) as a product -> Process that modifies a compound that is added to the fermentation – transformation process

  5. Growth: basic concepts Precursors Anabolism = biosynthesis Catabolism= reactions to recover energy (often ATP)

  6. Fermentation Respiration Oxidant = terminal e--acceptor No added terminal e--acceptor ATP: (e--transport) oxidative phosphoryl. ATP: substrate level phosphorylation Glucose Glucose • 2 ATP • 2 NADH 2 Pyruvate • 2 ATP • 2 NADH 2 Glyceraldehyde-3-P CO2 2 Acetyl-CoA 2 Pyruvate • CO2 • GTP • NADH, FADH Citric acid cycle Regeneration of NAD+ Acetaldehyde +2 CO2 2 Lactate + 2 H+ Acetate + Formate ATP H2O O2 in 2 Ethanol H2 + CO2 Cytoplasmic membrane H+ H+ H+ H+ H+ H+ out 1 Glucose  2 ATP 1 Glucose  38 ATP Slow growth/low biomass yield Fast growth/high biomass yield

  7. Major functions of a fermentor 1) Provide operation free from contamination; 2) Maintain a specific temperature; 3) Provide adequate mixing and aeration; 4) Control the pH of the culture; 5) Allow monitoring and/or control of dissolved oxygen; 6) Allow feeding of nutrient solutions and reagents; 7) Provide access points for inoculation and sampling; 8) Minimize liquid loss from the vessel; 9) Facilitate the growth of a wide range of organisms. (Allman A.R., 1999: Fermentation Microbiology and Biotechnology)

  8. Microbial Growth Kinetics • Fermentation can be carried out as: • Batch • Continuous • Fed-batch processes Mode of operation is to a large extent dictated by the type of product being produced.

  9. Biotechnological processes of growing microorganisms in a bioreactor

  10. Batch Culture

  11. Growth cycle of yeast during beer fermentation From: Papazian C (1991), The New Complete Joy of Home Brewing.

  12. Alternate modes of energy generation (H2S, H2, NH3) (in autotrophs) Fermentation Fermentation

  13. Fermentation Technology -> Process that produces microbial cells (Biomass) as a product mainly for -> baking industry (yeast) -> human or animal food (microbial cells)

  14. Fermentation Technology

  15. Fermentation Technology -> Process that produces microbial enzymes as a product mainly for -> food industry

  16. Fermentation Technology -> Process that produces microbial metabolites (primary or secondary) as a product

  17. Fermentation Technology -> Process that produces microbial metabolites (primary or secondary) as a product

  18. Fermentation Technology -> Process that produces microbial metabolites (primary or secondary) as a product

  19. Fermentation Technology -> Process that produces microbial metabolites (primary or secondary) as a product

  20. Continuous cultures

  21. Fed-Batch Culture A fed-batch is a biotechnologicalbatch process which is based on feeding of a growth limiting nutrient substrate to a culture. The fed-batch strategy is typically used in bio-industrial processes to reach a high cell density in the bioreactor. Mostly the feed solution is highly concentrated to avoid dilution of the bioreactor. The controlled addition of the nutrient directly affects the growth rate of the culture and allows to avoid overflow metabolism (formation of side metabolites, such as acetate for Escherichia coli, lactic acid in cell cultures, ethanol in Saccharomycescerevisiae), oxygen limitation (anaerobiosis).

  22. Batch culture versus continuous culture Continuous systems: limited to single cell protein, ethanol productions, and some forms of waste-water treatment processes. Batch cultivation: the dominant form of industrial usage due to its many advantages. (Smith J.E, 1998: Biotechnology)

  23. Advantages of batch culture versus continuous culture • Products may be required only in a small quantities at any given time. • Market needs may be intermittent. • Shelf-life of certain products is short. • High product concentration is required in broth for optimizing downstream processes. • Some metabolic products are produced only during the stationary phase of the growth cycle. • Instability of some production strains require their regular renewal. • Compared to continuous processes, the technical requirements for batch culture is much easier.

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