In this video, we're going to begin our lesson on measuring microbial growth by membrane filtration. Membrane filtration is a process that's used to count the number of viable cells or living cells in liquid cultures with only a few cells, and so a small number of cells are required. Now, in this process of membrane filtration, a known volume of liquid culture is going to be passed through a membrane filter. This membrane filter has really, really small pores in it, even smaller than cells themselves. As a result, the cells will actually get trapped in the membrane filter. Colonies will begin to form after the membrane filter with the trapped cells is transferred to an agar plate and incubated, and counting the colonies that form gives the total number of viable cells or living cells in the original liquid culture.
Let's take a look at this image down below to get a better understanding of membrane filtration of microbes. On the left-hand side over here, what we're showing you is this filter here, and this red sheet that you hear is the membrane filter paper, which has all of those tiny pores in them, which can be used to trap cells. What you do is pour the liquid culture right into the top of this filter here, and the vacuum that's created down below will filter all of the liquid through. However, the cells remain trapped in the membrane filter. You can remove the membrane filter and place it into a petri dish with solid growth media, which will allow for microbial growth to occur. What you'll see here are the actual colonies forming, and these colonies once again represent colony-forming units, and so they represent individual viable cells.
This concludes our brief lesson on measuring growth by membrane filtration. We'll be able to get some practice applying these concepts as we move forward. So I'll see you all in our next video.