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This unit is concerned with the cell nucleus. The different stages of mitosis are pointed out and explained by Stephen Hurry. Michael Pentz briefly takes up the topic of nucleic acid as a short int...roduction to B.S. Cox's experiment in DNA transformation. Cox explains the controls needed to perform the experiment and shows what happened to the controls during the experiment.
Subtitle Number Time In Time Out Subtitle Text
3200:03:21,00000:03:26,000You will notice that there is a substantial bacterial growth on both sides of the plate.
3600:03:21,00000:03:25,000..daughter cells a new nuclear membrane will appear.
3700:03:26,00000:03:30,000Now you can see this if you watch not only this cell but this one…
3300:03:27,00000:03:30,000Cells of both cultures have been able to grow on this medium.
3800:03:30,00000:03:34,000..and this one, all three at the same time, for in these two cells…
3400:03:32,00000:03:35,000Now here is the other plate, the one which contains a medium that has…
3500:03:35,00000:03:39,000..no Tryptophan in it and you will see that there is a growth on only…
3900:03:35,00000:03:40,000..the process is slightly in advance of the process in this big cell.
3600:03:40,00000:03:43,000..one side of the plate, the side where we put…
4000:03:41,00000:03:43,000So let’s see that happen.
3700:03:43,00000:03:46,000..cells from the culture which could make its own Tryptophan.
4100:03:45,00000:03:50,000Now the chromosomes are separating, some of them…
3800:03:46,00000:03:48,000The cells from the other culture on the other side of the plate have been…
3900:03:49,00000:03:53,000..unable to grow, they need that Tryptophan, they can’t make it so they can’t grow.
4200:03:51,00000:03:54,000..fairly reluctantly as if the chromosomes were sticking together.
4000:03:55,00000:04:02,000Well now, what we’re going to try and do is transform these cells,
4300:03:58,00000:04:03,000There they go and the last one. An arrow will appear in a moment…
4100:04:03,00000:04:07,000the ones which cannot make their own Tryptophan into cells which can make Tryptophan.
4400:04:04,00000:04:11,000..simply to show the direction of movement. There it is.
4200:04:08,00000:04:11,000To do this we have to transfer the ability to make Tryptophan…
4300:04:12,00000:04:16,000..from cells which can make it. And as we think that the DNA is…
4500:04:12,00000:04:15,000Now you can begin to see the beginnings of the cell wall…
4600:04:16,00000:04:23,000..forming across the middle, growing inwards from the edges.
4400:04:17,00000:04:21,000..the material which will give the cells this information we have to…
4500:04:22,00000:04:27,000..extract the DNA from these cells, the ones which are able to make their own Tryptophan.
4600:04:29,00000:04:32,000Now this is quite a lengthy process and we haven’t got time to show you the whole of it.
4700:04:29,00000:04:32,000The cell wall’s very distinct now.
4700:04:34,00000:04:38,000We start off by breaking open the cells with an enzyme called Lysozyme.
4800:04:35,00000:04:38,000Here are the last stages in the division of the cell.
4800:04:39,00000:04:42,000And then we go through a chemical procedure which is relatively simple…
4900:04:39,00000:04:42,000In this cell the chromosomes have retreated to the ends of the daughter cells.
4900:04:43,00000:04:50,000..and we end up with a cell extract which contains a solution of DNA and…
5000:04:43,00000:04:46,000A new cell wall is forming between them and…
5100:04:47,00000:04:51,000..in these two cells the final stages can be seen.
5000:04:51,00000:04:56,000..various other cell products and what we want to do is a final stage
5200:04:52,00000:04:55,000Notice that the structure of the chromosomes is being lost and…
5300:04:56,00000:04:59,000..in this lower nucleus, even less of the chromosomes can be seen.
5100:04:57,00000:05:02,000..is remove the DNA from the solution, so that we end up…
5400:05:00,00000:05:03,000And around each, a new nuclear membrane will be forming.
5200:05:03,00000:05:07,000..with a purified DNA solution from these cells.
5500:05:04,00000:05:08,000Daughter cells, each now with their own nucleus and separated…
5300:05:08,00000:05:13,000And to do this we precipitate the DNA out of solution using alcohol.
5600:05:09,00000:05:13,000..by a cell wall, so that we have two cells where we started with one.
5400:05:14,00000:05:26,000We carefully layer alcohol on top of our cell extract and we get…
5500:05:28,00000:05:35,000..two layers of liquid, the cell extract at the bottom and the alcohol layer on top…
5600:05:36,00000:05:41,000..and where the two layers meet, a cloudy precipitate forms and the DNA molecule…
5700:05:42,00000:05:47,000..is a fibre so the precipitate is a fibrous precipitate and…
5800:05:48,00000:05:52,000..we can collect it by spooling it onto a glass rod.
5900:05:56,00000:06:00,000There it is spooled on the glass rod and now we dissolve off…
6000:06:01,00000:06:08,000..the spooled fibres from the glass rod in a sterile dilute salt solution.