Metabolic engineering

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Cellular metabolism can be optimized for industrial use.
Cellular metabolism can be optimized for industrial use.

Metabolic engineering is the practice of optimizing genetic and regulatory processes within cells to increase the cells' production of a certain substance. Metabolic engineers commonly work to reduce cellular energy use (ie, the energetic cost of cell reproduction or proliferation) and to reduce waste production. Producing beer, wine, cheese, pharmaceuticals, and other biotechnology products often involves metabolic engineering.

Cells are complex systems; genetic and regulatory changes can have drastic effects on the cells' ability to survive. Therefore, trade-offs become apparent during metabolic engineering.

Decreasing cellular energy use

Metabolic engineering can be useful in industry. Certain industries use cells to create useful products. Producing the greatest number of those cells is a sought-after goal. The only known method of production, however, may involve oxidizing of carbon compounds. The carbon compounds may be in limited supply. Therefore, engineering cells to reproduce or proliferate more rapidly given the same amount of carbon compounds would mean greater industrial efficiency.

E. coli genes were added to the M. methylotrophus genome.
E. coli genes were added to the M. methylotrophus genome.

The role of Methylophilus methylotrophus in the animal feed industry is an example. M. methylotrophus uses methanol to produce certain proteins used in animal feed. Producing greater masses of proteins using the same mass of methanol would increase efficiency. Windass, et al. (1980) accomplished this by silencing genes in M. methylotrophus and inserting genes from E. coli. This example of metabolic engineering resulted in an organism capable of using a lesser mass of adenosine triphosphate to produce the same mass of glutamate.

References

  • Stephanopoulos, G. N., Aristidou, A. A., Nielsen, J. (1998). "Metabolic Engineering: Principles and Methodologies". San Diego: Academic Press.
  • Domach, M. M. (2004). Introduction to biomedical engineering. Upper Saddle River: Pearson Prentice Hall.
  • Windass, J. D. & Worsey, M. J. & Pioli, E. M. & Pioli, D. & Barth, P. T. & Atherton, K. T. & Dart, E. C. & Byrom, D. & Powell, K. & Senior, P. J. (1980). Improved conversion of methanol to single-cell protein by Methylophilus methylotrophus. In Nature, 287, 396 – 401.

See also

de:Metabolic engineering

Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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