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# appu88

Member Since 25 Jan 2013
Offline Last Active Jan 25 2013 11:16 PM

### Homework

25 January 2013 - 11:18 PM

Serial Dilution Activity

Many applications require the determination of microbial numbers. Those applications can be either clinical or in a research setting. Clinical applications include determination of antibiotic efficacy and as well as therapy. Research applications include determination of the effectiveness of antimicrobial chemicals, radiation, etc. The viable count is most common or standard method used to quantitate bacteria. With this method only microbes that are alive and able to reproduce can be counted. Since microbes grow into such large numbers it is extremely difficult to perform this without diluting the microbial culture first. A key concept here is the ability of microbes such as bacteria and fungi to form visible colonies when grown on solid media. This can also be used to count viruses but instead they form plaques on cell culture. A microbial colony is defined as a group of genetically identical cells that originated from one cell on solid media. From that definition we can deduce that in order to grow an isolated colony, one cell should be placed on the solid medium. This also means that one colony reflects the existence of one cell and so can be used to count how many cells were placed on the medium. E.g. if there are 20 colonies on a plate then you must have placed 20 cells to create these 20 colonies. These cells are therefore referred to as colony forming units or CFUs for short. From the number of colonies and the dilution of the growth on a plate we are able to count the number of microorganism in an original culture. The equation for that:
Concentration of culture in CFU/ml = number of colonies on a plate multiplied by the serial dilution on that same plate
In this exercise you were browsing through a refrigerator in a microbiology lab and you found a tube with a solution labeled "B. subtilis: 2 x 108 cfu/ml". Now being the skeptic professional that you are, you want to double check the accuracy of the concentration of this culture. Describe how you would embark on this mission, how would you set up the dilutions, which plates would you chose, etc.

Thanks
Appu