Metabolic engineering
You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.
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.
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 engineeringAcknowledgement 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 .

