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00:04 Okay. Okay folks. Welcome. let's get started. Oh okay.

00:31 um jesus christ mm hmm. Um yeah, come on my computer

01:01 the computer died all this stuff So anyway, exam to check so

01:14 to I'm starting to put the they posted on blackboard but it's very similar

01:21 the first exam. Um So another now which for some is okay.

01:26 I stay in course or do I the course? I don't tell you

01:29 do that. But what I can , just give you the information to

01:32 you make to help you make that whether you want to or not.

01:36 . So um a midterm grade will calculated. It will come out sometime

01:43 week. Okay. It will include up to this point and just doing

01:48 scores Quizzes on blackboard, uh clipper , you know everything. Alright.

01:55 it'll be a uh you can use to evaluate. Okay. Uh believe

02:01 drop date is April 20th. So um anyway again I don't usually

02:12 um my opinion but um you I can only give you information

02:19 And so if you make a my eye on this side toward the

02:24 of, well you're doing great. got to figure out How to to

02:31 because you dropping the tape again, gonna be in the same book.

02:35 me, I've seen this over and for 17 years. Okay. So

02:43 that's why I say can we stick out and try to improve. Make

02:47 her goal to you know do as you can and get help for God's

02:52 . Okay If zero people come to hours literally nobody comes to office

03:00 Okay so you can leave the house can lead you can lead a horse

03:02 water you can't make him drink. so again I'm here for the resource

03:08 you need it. Um So okay santa will be available to view uh

03:17 tomorrow. Um And uh certainly looking questions let me know. Okay uh

03:26 see so today we're gonna continue with three so we'll finish up eight.

03:31 into nine, finished with a chunk that and then 10 ft class.

03:36 would probably be some more than the Tuesday because 4.2 I'll give you all

03:44 10 1 10 1 is kind of intro. Here's how the basics of

03:49 regulation in bacteria and then we'll kind apply that in the next part.

03:54 is um uh Ron Ron. If looked that far ahead or not uh

04:03 do this week backward quiz. Um will cover uh last week seven and

04:11 talking about 7888 789. Okay the says it also includes 10.1 but I'm

04:21 gonna do that. It's just gonna 78 and nine on Blackwater quiz.

04:25 I'll send out another reminder email thursday To repeat that again. Okay so

04:34 there's already like there's like six questions think on the backboard quiz. Um

04:38 work that's due next sunday. So 21 22 is an assignment 78 I

04:46 both those are kind of rather So um anyway so that's coming

04:54 The other thing here is um the er for exam three which is April

05:04 That opens on Friday of this week four. Okay so that's when you

05:11 first time here for that. Okay um let's see, I think any

05:22 . Yeah. Alright so let's go and start with clicker question is going

05:30 relate to most of it. The think we talked about all that.

05:36 mean I've been super specific on a of these things but uh we're gonna

05:42 fish all this up today uh for minutes probably. So someone of a

05:47 for some of these. Okay, we're just true. Some gene

05:54 Okay so remember the operation structure, , bacteria and what that entails.

06:05 And then the have certain elements, of the process, G expression,

06:15 factors you may recall. Okay. , anybody, I assume everybody who

06:33 the whole Oscars fiasco thing. I that in real time and I said

06:40 is a joke or it's just reel it was real when I saw Will

06:45 was mountain, I didn't realize how that guy was, I guess how

07:00 was Will smith justified? No, yes defending defending the honor of his

07:08 . I did laugh at the general know but but in hindsight. Um

07:19 don't know if you you know the G. I. Jane Demi moore

07:24 you shave your head. Alright. fast. That's my error. That's

07:30 your. Alright. Let's see what are. Um um um um um

07:37 um um um Somebody did some Okay. Uh Let's see. Is

07:43 correct? All the true operator serves the site for sigma factor binding is

07:51 mm hmm. Is that true? operator doesn't site for sigma factor about

07:58 . For service as a site not operator can I? Uh So that's

08:05 false. Okay. An operator possesses promoters. True. One promote as

08:16 opera in one promoter, multiple structural . Multiple genes under control of one

08:22 structural genes have a single operation. for enzymes of different metabolic pathways.

08:27 wouldn't make any sense because an opera all about being efficient. They're gonna

08:31 kind of common pathway. So you it Expression of us of the whole

08:36 at one time. Um A single transcript will contain information for all structural

08:44 of that opera. That is That's that policy. Histrionic message.

08:49 . Some of the factors buying to shining del Garneau sequence. So you

08:52 not have known that unless you looked . That's Ribas own binding site.

08:59 . Not a sigma factor. My . So that's what we'll go through

09:06 . So um so d is the answer. Alright. What's your

09:14 13 If you answered. D who it? Who was a deep person

09:20 you guess? Or did you know ? You do it stone cold.

09:25 . Good. All right. Um so let's look at just as a

09:32 of summary of everything here. Okay we talked last time of course about

09:38 know our our focus is called pro genomes. And so here's our bacteria

09:45 you can actually um slowly uh lice gently and and the and the chromosome

09:50 slowly spool out of it like you there. But so thanks to

09:57 Right so genome size um half a to five million is about the range

10:05 the appropriate genome. They can have chromosomes and the dish. I mean

10:11 in addition to the larger chromosome and represents the entire genome, refugee

10:17 all of the D. N. . In the organism. And plasmas

10:21 certainly contribute to that. Um The so go to the opera again.

10:29 . So here is um uh So opera itself is the promoter. Okay

10:39 operator structural genes. So this part the opera. Okay so once you've

10:43 it all operator works in conjunction, regulatory proteins partly control methods.

10:49 We'll go more into that next week thursday. Um Again the product is

10:56 to be a transcript of continuing a piece of RNA containing the coding information

11:04 three or however many genes that And the opera generally isn't bigger than

11:15 . This kind of seven is kind the high range. OK um We'll

11:22 about it next week has five genes part of the operation. But again

11:27 just it's one continuous message that gets into its subsequent proteins. Typically part

11:34 will be part of a common Okay. Um let's see what else

11:41 . I mean regular. Excuse me now we're evolving multiple operations and we're

11:49 them. Kind of coordinate coordinate way they all are part of a bigger

11:55 function. So we use nitrogen metabolism an example last time. So operations

12:01 in different aspects of that. The kind of control that so they can

12:06 the utilization and allotment of 19 comments we usually many different things makes sense

12:13 control all together. So it's not energy being efficient. Um and the

12:22 can occur through the sigma factors or sigma factors which will start off with

12:28 are how the race that brings about transcription is guided to the front of

12:35 genes. So you want to make that commemorates is going here. Okay

12:42 don't want to just plop them down . So oriented and signal factors helped

12:48 that. So then we finished with about plasmas. Right. And so

12:55 plasmas are these autonomous segments of N. A certain piece of

13:00 N. A much smaller than chrome are transferable can be transferable among

13:07 Um Of course they carry multiple genes involved in different functions. Can be

13:15 , tablet, tablet catholic can be resistance. It can be lots of

13:20 things. Okay but it's only gonna a few because obviously plasmids are

13:24 They're only going to carry a few . Exactly. But the fact that

13:29 has the story right, the ori of replication is what enables it to

13:36 autonomous. They can replicate itself. then I think that the hand because

13:41 uh rolling circle replication, right? it can do the conventional replication type

13:49 our chromosomes activity um bi directional replication form and that mechanism. But it

13:58 also be rolling circle replication which we'll today in the context of conjugation.

14:05 as the chromosome I'm sorry the plasma strand, well we'll create will break

14:14 bond living experience and then begin to from that Exposed three prime hydroxy

14:23 And then you go around like this that template but then technology the other

14:31 and that was trying to get shoveled typically it would be another cell.

14:36 it looks something like that cell one to and that so there so now

14:42 the recipient self hands up with a of that plastic and whatever genes are

14:47 . Okay that's that process. The we'll talk about later. Okay so

14:53 kind of the highlights uh from last . Um so what we'll pick up

15:01 with. Okay. Only in terms so again, number seven and eight

15:09 stuff. Okay. But we're only at a small portion of each chapter

15:16 I'm not gonna expect you to be to translate hey transcript using genetic code

15:22 and those kind of things you probably . Okay. But this is

15:27 here's the overview and here's some things precarious. Okay. And of course

15:33 arctic summer I used to think particular it is a benefactor. Okay,

15:38 again, just mentioned that that's what molecules so they can do the

15:46 Right. Um need to promote A rider zone needs mechanism as well

15:59 align it in front of the um to be translated. Okay. They

16:05 arrived his own binding site. These a certain effect. Okay. And

16:12 um when you look at precarious, was done, done this for years

16:22 . Um just saying, okay, line up these promoter sequences from lots

16:26 bacteria that we've sequenced. And is anything similar. Okay, let me

16:32 flash forward real quick. I'll come to this and so let's look at

16:37 bunch of promoter sequences and what they . There's some hm ology Right.

16:45 a couple of areas -35 -10. , what that refers to is those

16:52 the basic distances upstream from the start transcription, which is plus one mm

17:02 . Okay, so that's plus one and then you go minus numbers and

17:13 the promoter. So they find that is, you know, a lot

17:16 commonality among different promoters factor of motors the -25-10. Okay. And hence

17:25 name -35. See that's what sigma sigma seven. Right. So there's

17:33 , you might think that there are sisters. About 3000 on average,

17:40 to 5000 genes in the but you , okay, there must be 3-5000

17:49 factors in front of the genes. , well no, you have the

17:56 model because that means that means you one promoter and multiple genes. So

18:01 lowers the number. But even then may still be around, you may

18:04 , oh, this is gonna be the hundreds that you have from the

18:07 factors but you don't have maybe 8 10, 12, maybe once.

18:13 that's it. Okay, so a very common one is Sigmund 70

18:22 60% or more of jeans utilizes. . Um, and there are others

18:31 will briefly mentioned here. And so are what we call consensus sequences.

18:36 there is such a commonality homologous between different types of mothers. They are

18:41 common in this way, You can the -25 -10. A consensus there

18:46 a consensus among all these promoters and have this very similar sequence. Okay

18:51 they're often high in 80 base Okay remember goes back to the 18

19:04 bonding is 200 months GCS three. remember where transcription is going to occur

19:10 pull the strands apart. So it of makes sense to have maybe a

19:14 bit more Concentration of 18 base pairs energy to pull it apart than

19:20 Okay. Um now um so you change. And one of the things

19:28 in um biotechnology uh we're often trying get engineer bacteria to either uh make

19:40 produce the protein of some sort It's a commercial value. Welcome to

19:44 lots of a particular protein or Maybe an enzyme that can have some

19:50 of catalytic activity you want and you to mass produce it. Uh Force

19:55 to make lots of it because when go now from from the academic lab

20:00 industrial lab very often we're talking about and quantities of stuff, okay we're

20:07 to commercialize the process stuff won't do need buckets of stuff. Okay so

20:13 means making bacteria will produce these things they wouldn't normally do. So that's

20:19 you have to go in there and with. Okay fiddle with them gross

20:23 , prison with them D. A manipulate. Okay and one of

20:28 things to do is to tinker with regions. Right? So you can

20:34 based changes and erase this. You make basic changes in the promoter and

20:43 can lead to either up or So down means a decrease in expression

20:51 for. And what has changed is crossed up uh It's called a

21:01 Up right increasing expression. Okay. you often do this um if you

21:08 out the if you discover the promoter the june you're working with and you

21:12 that perfectly mass produced, high quality one of the things you can try

21:16 do is fill it with the Make it more making up reputation.

21:23 . Um The terms promoter strength. high versus uh weak expression.

21:33 Let me let me flip ahead Okay, I'll come back to this

21:36 . I'm skipping over. It's not big deal. So it's something about

21:39 high and low promoter strength. Or region this week. Okay.

21:49 um so your hand will hold what call basil expression. Okay. Which

21:58 just means that you see that you a choice and it's that's what you

22:06 . Okay. That can in many . Getty was called fatal oppression very

22:12 . That's that's insignificant. It doesn't not even enough. So do

22:17 Okay. Maybe a handful approaches. . And so what the have to

22:27 is okay if it needs the right expression then that's where you involve different

22:33 of uh components. Okay, so level expression may require one or more

22:40 these. Okay, this is where control elements? That's right. Um

22:46 like activators, transcription factors. Different regulatory proteins. So they can

22:52 all right at that promote. Alright really right. You can even have

23:00 in bacteriophages as well. You can do it as well. Is to

23:06 having the D. N. Scan itself loop around and create secondary

23:12 at the side of the motor and them bring everything. Okay so you

23:17 inform us that we call it a transcription complex. Okay. So when

23:24 when all these parts come together, know high level expression. Okay.

23:30 times more for more than you get base depression. Okay. And so

23:36 a dynamic situation. It's rarely that just all one or the other.

23:40 can be you know none to a to maybe somewhere in between. It

23:47 depends on what are the collection of bankers you have to bring this about

23:54 these can fluctuate in some cases, on Okay. Um that will determine

24:06 know the conditions around the cell and the cell to determine you know and

24:10 agent so determined the levels of Okay um and so collecting these parts

24:19 the promoter. Right. It's about the affinity of the preliminaries for that

24:29 . Okay so I can remember is know buying you know you can you

24:36 almost write a paper saying biology is about binding things happen in biology because

24:42 life. Whether the proteins binding proteins binding substrate proteins binding DNA

24:50 That's really what causes everything to Are these bindings right. And but

24:56 lot usually universal. They're almost always . Okay. But you know,

25:06 you can influence how how much is and how much is off.

25:11 And that's kind of what this is . So, if we have all

25:15 confusion factors and already there at the high level it happens because now we've

25:21 a site but they're very high affinity the generals colonels combined really well now

25:29 that equates to kind of drive And create lots of transcripts. Lots

25:36 protein. Okay, so it's really influencing that binding to the promoter.

25:43 . He's gonna be finding not so on more off less transcription or it's

25:49 be more bond less off. Higher transcription. So that's that's what

25:56 the idea is here. Okay, . By making that promoter uh really

26:03 that are the primaries, so to . Okay. Um and so and

26:09 is I know you can't necessarily fathom important this is maybe at this

26:16 but it's so hugely important because, know, just thinking in your own

26:22 from zero to you know, if born like that whole process,

26:28 is all about that. All Turning genes on and off at different

26:33 timing. Right? Making sure that sequence occurred properly. So that you

26:40 up with two arms here and two here for example. All right.

26:43 all indifferently controlled. So um we now to the world of g

26:52 It will literally blow your mind because go, oh my God, this

26:55 complicated. How can it possibly But it does. But of course

27:00 know when things up works are that can be glaringly visible as

27:05 Okay. But anyway, so I'm a tangent here but there isn't any

27:10 about that. Makes sense? So . Okay, so um like I

27:17 , controlling gene expression is probably one the most important things because again,

27:23 be wasteful depending with lots of other out there if you're a bacteria.

27:29 let me go back just to um couple things I skipped over. So

27:34 This is just to show that all that 60, 70 is what's used

27:38 expression of most genius. You do others behind these specialized functions. Um

27:46 shock and uh shock and um jeans temperature sensitive. So uh temperature high

27:57 can be bad of course. Um Vienna RNA proteins to denature. And

28:04 you want to bring expressed proteins that kind of minimize that effect.

28:10 So you do have heat specific genes are controlled by a certain factor um

28:18 and chemo taxes. Right? And all of that details has as

28:22 own singular factor uh stationary phase dress genes. So these are for other

28:30 beyond heat that are triggered again. are all kind of survival genes are

28:36 on by the search signal factor that activated at that time. And then

28:41 talked about the nitrogen regularly on. so it has its own same effect

28:46 control. That's a control those nitrogen operations if you will by a common

28:53 factor. Okay so um and one to the body. This is just

29:02 the same effect as Uh if it's same 70 it recognizes the -25

29:09 And the simple fact there's a transient of the off off its sole purpose

29:17 I hope we get to that promoter . Okay and find that sequence.

29:24 ? And in doing so then you um transcription. So this comes

29:30 Single handed comes off and transcription. they can go and find another.

29:37 guiding that. Yeah. Um I think so here. Alright so this

29:48 kind of summarize everything I think that been talking about in this chapter

29:54 Most of it. So yeah here the uh bacterial structure. Gene

30:00 Okay uh here's the D. A. Here is the promoter.

30:03 is showing of minus 25 minus Okay so sense strand plus strand,

30:09 coding strand in the template strand to operation promoter to structural genes uh

30:18 Check so one continuous message. Place a strong message. So within

30:26 each second transfer for this gene and gene will have their own elements.

30:32 . Start, start stop pulling on one. Right? Um These leader

30:38 can be involved in some aspects of . We'll see that later.

30:43 This is translatable. And the next that happens is to get the

30:49 Alright. The complete My until the s inappropriate to then find its

30:57 Right? So just like a single has its sights suddenly. Okay.

31:02 so that brings in front of the to then this little tape um expression

31:09 translation in this program. So. . And so that shine Del

31:13 Just named for the for the two that that discovered this. Okay.

31:17 its fur so china gonna site is . N. A. Right single

31:24 binds D. N. A. , so make sure you've got that

31:29 your head. So things like the the promoter sequence. This is

31:33 N. A. Okay. Um of binding sites are already are

31:40 Okay. Um and then of course already talked about before the information.

31:49 , this all occurs, transcription translation virtually simultaneously because there's no separation of

31:55 process and bacteria. Um Alright. questions so I'm gonna roll on to

32:06 nine. Okay so here we're gonna at um He may look at A

32:17 we all have the color in our as you may you know, different

32:24 . Happy because we know E. like all the bacteria archaea replicate like

32:34 . All right. Um 100 You would think. Okay they're all

32:39 all the same right? They're all . It's all binary vision binary vision

32:44 genetically identical dollars. That's not the . Might collect and hold as identical

32:52 yours. Okay even within the same then it's not gonna be identical.

32:58 so this variation it was very Okay Yeah evolution 101 variation is what

33:10 accident. Yeah If if everybody in work genetic control genetically identical. Okay

33:19 Any kind of interaction with your Everybody's trying to behave descent because you're

33:28 . Same day that so that can good or bad. It was something

33:36 . And then maybe there's nobody capable surviving because they all have the same

33:41 of genius. But if you have in population right now you may have

33:47 there that can survive different conditions. because you have variation built in why

33:55 so important variations. So important. so bacteria are no different. They

34:00 have other ways to get this creation the fact they don't replicate reproduce

34:07 Luck for us. That's what gives surprises. Not all of. Alright

34:14 a sexual reproduction but bacteria can generate for sure as well. Okay so

34:20 transmission is passengers currently vertical transmission. how you will hear now what you're

34:32 capable of. I don't think it's transmission. Okay you can't inherit genes

34:38 the person next to you. Because you can't congregate like a

34:43 Okay. But bacteria can do Right? And so members of the

34:48 can transfer genes in certain different mechanisms that's carried out transformation, conjugation,

34:57 deduction and transposition are all mechanisms for . Ok so here is a

35:05 So the big big blue blob. , are all the polite genes.

35:12 are aware of even sequence city collect decades. Okay so we have a

35:20 they have this information, what do call it? So we have to

35:25 date. I'm not sure what data here but we're aware of Almost a

35:30 over 10,000 different ecologies. Yeah kids been found before. So An average

35:40 has about almost 5000 half that. . Um It's like if there are

35:50 genes for a particular human trait in jeans when you ever have You have

35:58 10. Alright, that too. so you collect will not have no

36:12 called them at all. 10 will their collection of them roughly half.

36:18 then within that equal About four no over 2000 were called for Jeans.

36:27 so these are common to all Alright so these guys here would be

36:33 color has. Okay and what's probably gene that's in that lot of methodology

36:44 black polycystic some inspiration. Genes involved replication of D. N. A

36:52 synthesis. These are all gonna be functions. What every cell has to

36:57 has to replicate that. It's like . So all components are in there

37:01 gonna be of course and all of . Okay. So um and so

37:08 look at E coli K 12 versus . Okay. You see only 57

37:14 a lot more regimes I called over . All right. Um comfort

37:23 Warm pathogen chair. And so it sense that. Ok. Price.

37:29 lot of genes involved in enabling cause . Okay. Virulence factors. And

37:36 um but they will share of Oh and 57 10-K 12 K 12

37:41 benign last spring. It's the one is not harmless but so they're gonna

37:47 certainly common. They're gonna share recordings course maybe some others. But we

37:53 a bacterial genomes in general. Not dissimilar. Okay. Is the level

38:02 um D. N. A. correctional programs much higher in humans.

38:08 superhumans anybody know? Is it Yeah. 2%. Who says 2%

38:22 . It's love. It's like two something percent. Right. We have

38:27 lot of DNA that's called regulation a of the DNA. That's like just

38:32 D. N. A. We're exactly sure what it's for but only

38:36 2.5% is actually used to build the . Right? Um So much more

38:44 that in bacterial then in preparing this used for coding proteins. Okay there's

38:49 gonna be a portion for regulation. is a big part of control expression

38:55 but of that. Um So the thing to remember of course is not

39:01 most genes are all protein killing some because you do go for the the

39:07 chronic can be R. N. . That's what represents these guys.

39:12 there are there are gene but gene is a approach. Okay now.

39:19 so when you look at the genome its entirety e coli about 25% of

39:24 genome required from other microbes. Okay this is part of the horizontal gene

39:32 . Okay so how do we find something like that? Okay and so

39:38 on your genes are going to be I mentioned things like those involved in

39:48 reputation and protein sentences. Um This gonna be your all right. And

39:56 are generally not things that are transferred because it's still gonna hold on.

40:02 not something you want to do that passed along. So flexible gene tour

40:06 that are not so critical function James . Um So back to this question

40:14 how do you how do you find been deduced if a second of material

40:21 . T. A. D. . A. Is but as far

40:23 horizontally parameters are used to that is called percent G. C.

40:30 Um If you do you remember that charged off rule he was the guy

40:42 he's the one that came up with uh knowledge of the percentage of adding

40:47 the percentage of bio means right? is equal to a percentage of science

40:52 . So since that time you see is used actually as a way to

40:59 It's about 34 years old. But that changed once we worked out too

41:04 sequenced DNA. And then that became of this but nevertheless there's a lot

41:08 information on descent. So in bacterial will have in particular G. Percent

41:16 . C. Okay you can kind use it as a taxonomic tool for

41:20 purpose but the video provides about 50.8% . C. Okay so with that

41:28 of mind and look at this is of course on computers with Um you

41:35 scan protozoa bacteria and you know using a significant statistically significant segment of

41:45 Right? Uh you should probably value opposed to 50.8% G. C.

41:51 . Okay um And so you see long stretch that deviates from that.

41:56 maybe 2000 bases but that's about the size of the gene. Okay um

42:03 if you see a long stretch that is is within that region significantly

42:08 Okay so for example something like um erogenous which is a relative of Cola

42:15 the GC content of 54. So that you know maybe that segment That

42:22 second at 2500 bases in this example at that range. Again you might

42:28 that it could have been transferred from . It was easy. That's one

42:35 or the easy way really to um at least provide some elements that maybe

42:42 these these jeans I'm seeing I'm studying transferred horizontally. Okay. And so

42:47 you collapse mentioned this this think about of his genome was acquired this

42:53 I mean that's pretty crazy isn't A of his genome. Okay so

42:58 for technology transfer is all right in of again creates variation but the

43:07 Okay, requiring new jeans. Uh so we were talking about these mechanisms

43:13 get the idea. We're talking about whole scale transfer of crows. Um

43:20 we're not talking about segments but there's congregation. Um Trans deduction. These

43:30 small sectors but nevertheless they represent acquisition new in many cases. Okay so

43:39 so this is just kind of a quickie. Um Here's what these steps

43:44 like. Um So transformation. Okay probably easiest to grasp because we're talking

43:52 taking okay because you get all little say that it's not necessarily as simple

44:00 it sounds okay because there are components . Uh congregation is involved several cell

44:09 . Okay. Uh certainly more complicated transformation to two cells coming together

44:18 This is where can asthma transfer occurs the two. Okay. Um trans

44:23 . That's a virus. Okay so viruses in comedian between the two

44:28 Okay, viral infection occurs um in packaging of viral particles. Host

44:35 N. A. Is inserted rather viral. Yeah that's how the DNA

44:40 transfer to another cell when the virus the new cell. So that's that's

44:46 . Okay. Uh service here viral and it affects another cell. Um

44:54 position. Okay so I think I'm small pig already. Things also based

45:02 has has posed as we do. what they do is they remain in

45:09 organism because they jump around the Okay. But occasionally they can jump

45:15 a ride figure out plasma. Or are other mechanisms by which transposes conform

45:23 transfers for them to sell. I'd say of the four.

45:29 transformation. Conjugation transaction probably won't come to transfer. The transmission does occur

45:38 if you uh to the path this in fact. But in terms of

45:47 communication transaction follow my transformation more No. Um Alright. So what

46:00 transferred? So this is another All right. These are in the

46:05 and they're the particularly acquisitions of of through horizontal gene transfer. That chromosome

46:17 uh we call them islands I guess they are a specific function. Okay

46:22 you see the terms pathogenesis the island fitness island. These are segments that

46:30 a pathway and jeanne's properties. Okay capsule gene the gene for the

46:40 Okay these would be in that class pathogenesis possibly transfer. Okay.

46:48 So we talked about nitrogen fixation symbiotic couldn't be exactly this. Okay um

46:58 we talked about the metabolism of aromatic . So that could that could be

47:04 of the pathway you might see here these can be these types of things

47:07 be transferred. Okay and so um so let's so one of the things

47:21 remember because we're gonna go through the of transfer DNA. Passion here and

47:27 and being taken up and this and . Okay remember that uh combination plays

47:36 big part in one of these Okay so you can have um so

47:43 can be ah say uh layer in D. N. A. Can

47:49 taken up to your transformation for example D. N. A. Can

47:55 how how viruses transfer um passed the of circular but both are forms of

48:05 that can be external to the cell end up in a cell. Okay

48:10 from the viewpoint of the you can use as a food source right?

48:16 on the state of health. Okay could crunch up that that music as

48:20 as organic carbon source. Um Generally it's a single strand. Okay like

48:29 guy that is something certainly bacteria itself gonna be very suspicious of. Okay

48:39 that that's likely gonna think it's environment . Crime. Okay it's not normal

48:45 even ourselves to have the single stranded . N. A. Floating around

48:49 . That's not normal. Okay um extraneous fragments like this for. Okay

48:59 uh that really sets off alarm bells it gets quickly degrading. Okay so

49:04 layered piece like that could be two to integrate. That's where recombination comes

49:12 . Okay plasmas can live external. but they too can integrate as

49:19 Okay and so the combination is a immediately part of the recombination is all

49:28 having some level of form ology complete it's all about complementary base part.

49:38 so if you have enough nucleotides and a complementary to the D.

49:43 A. Is integrated into then it happen. Okay and wreck A.

49:48 that there's multiple components involved? But A. For recombination protein A.

49:55 accommodates a. Is is um that player in all material souls that do

50:02 that they carry every combination. Okay so it it helps align homologous regions

50:11 that causes a donor and recipient to combined. Okay you just have to

50:19 and potentially they can then integrate and certainly when when it integrates into the

50:27 . Now we've got something that has that's the permanent life. Okay and

50:35 the classes to to integrate. Uh so let's look at um this

50:44 So first the first stop is So with the transformation congregation trans deduction

50:51 that world. Okay so the trans okay what's the answer. Everybody hurry

51:00 and pick that one violence showing. . Um Okay so transformation. It's

51:11 about cell cell contact, that's congregation , immediate transaction. Sex pilots

51:21 Those are elements of congregation. Transpose A. That's transposition right at

51:28 end. So each process has it's of features so definitely be familiar with

51:37 . Okay so let's move on. correct answer is easy by the

51:42 Okay give me the fragments in the . Okay. Um Alright so transformation

51:53 It seems it's fairly simple but it be more complicated and it can differentiate

51:59 gram negative and gram positive. Okay so the more complicated process is grant

52:05 . Okay uh likely due to that thick peptidoglycan layer, there's components that

52:14 DNA get into the cell. Um what's called transformers own complex. So

52:22 this will evolve as an example of regular right? There is a regular

52:26 in the grand positives and facilitate Okay quorum sensing. So we saw

52:33 in biofilm information. Okay so quorum sensing is one of those cell death

52:39 things. Alright I have to have cells present too. Two because the

52:45 . Okay um so natural versus artificial . Okay so naturally transformed cells of

52:56 are built to do this but they the capability to do this in

53:01 Okay E coli for example cannot lose . Yes it can only be used

53:09 artificially attached on it. Of course coal ideas. What's used is the

53:15 , genetic recombination. Okay. We it to various aspects for gene cloning

53:21 whatnot. And certainly transformation. We collide as a vehicle to replicate

53:28 Okay. And so the only way can do that to get the plants

53:32 any claims to artificially manipulate. Why? Why that? Well because

53:37 know we collect so well we can it very quickly that it's just it's

53:41 historically just become that role. And so we have officially transforming the

53:48 days. He was using um maybe chloride, potassium chloride and ice on

53:55 . Okay. That create pores in membrane. Um You had the

54:02 N. A heat shock it. how many ice and very wide temperature

54:08 ice and heat shock creates pores in cell where the uh the classes can

54:14 in. Then you put it on and then it kind of closes up

54:19 pores. So it's not very But remember that. But because bacteria

54:25 so much so the high density it have to be super efficient.

54:31 But nevertheless uh your away or if needs in my four years is using

54:38 shot, there is the same There are currently more efficient process than

54:42 chemical withhold chemical transformation. Okay. I think if you were in I

54:49 know if they still do the experiment in bio bio one lab to lab

54:54 did that actually I think the transformations there. But anyway so confidence

55:01 These are these are part of the positive transformation process. The whole part

55:06 the form sensing thing as we'll see in a second. But gram negatives

55:12 there's a little less complicated. So back to remember pilots structure um the

55:22 I am in contact or less numerous have more specialized functions without about sex

55:29 and congregation helps facilitate transferring. Una is a bigger pill I typed for

55:35 code that helps it attach to N. A. And bring it

55:41 . I also saw pillai in twitching . Right? So this is a

55:45 of that will bind to DNA fragments bring them in. Okay. So

55:49 not that complicated. Okay. A gram negatives can do this.

55:55 Um Not in himachal listen, Neisseria both um known pathogens so but we're

56:07 focus mostly on more so on the positives. Okay. And they're mechanism

56:13 so we just talked about artificial transformation that using electricity as we called electrical

56:20 create pores using electric shocks. Um now okay so here's the grand

56:28 processes a streptococcus example. And so so you see. All right one

56:45 different operations. Right? Hence common factor that turns all those on and

56:54 synthesize different components of this transforms um called the complex that brings in the

57:00 . N. A. Okay so that though we have the production of

57:06 competence factors. Alright so the term term competence. So if you see

57:11 term okay in this context Congress refers can information. Yeah. So self

57:21 is ready to take up the N. A. Okay. Um

57:26 so the grand positives is in this . Companies factors are synthesized in the

57:34 and but they have to reach a level to initiate this whole process.

57:41 that's where the quorum sensing comes Okay so um if you have enough

57:49 around then we'll initiate this process. the the complex factors accumulate. Okay

57:57 they reach a threshold level then they'll into the sensor protein comedy. Right

58:04 that ultimately leads to production of sigma . Okay. And then that's its

58:11 is what turns on four problems And so the genes for those codes

58:17 different parts of it transforms us Um And so the question I guess

58:27 why is this a density dependent Okay well you think of a thing

58:34 the growth cycle of a of a bacteria? Right. We follow this

58:42 . Okay. There's time and Okay. Alright. Growth. We've

58:53 that before. Alright so you know didn't point along that line you're going

58:58 have you know a proportion of souls live and so they're dead. Okay

59:04 course the proportion gets more and more , right? As we get to

59:09 phase. Okay. So um for . All right. So in the

59:26 one of those when we're gonna see D. N. A. From

59:29 south and the soul, he alright, so advice is that the

59:38 I'm just guessing that it's likely that is a phenomenon because he has to

59:42 more settles, right? You will likely have more rare reports of dead

59:48 are sliced and now you have N. A. That's available to

59:51 taken up what? Okay. Um if there if not then why go

60:01 all this process for the likelihood of may have been incorrect. Okay.

60:09 , you can't see the is going it's it's an energy producing process requiring

60:15 . Okay, So that's not to the idea why it's time to sell

60:21 more so mentally greater likelihood that maybe have more so than dialyzers and their

60:27 is free to be taken off. . Um The the DNA comes in

60:35 so this is part of the function this complex. It was one strand

60:40 in. Okay. Not both. so one strain is degraded. And

60:46 of course that strand then, but was very it was the coolest thing

60:51 sells very recent mind chromosome. And so that's um that's transformation in

60:59 grand positive at least. Okay. for right. Um he crushes.

61:15 . Thank you. Yeah, I . Okay. Singapore the name the

61:33 not surely order. And I just that when you see if you hear

61:36 term see it think about it means itself is it's confident to take A

61:44 . N. A. And that's only thing that's part of it.

61:47 because you have to get program probably to get this transforms them together and

61:51 was all this kind of set did just say to take it? That's

61:58 . That's that's probably one of that the term. Sure. Yeah.

62:03 for the competence factors when they did they form like a concentration

62:08 Yes. Yes exactly. So That much. Like very similar.

62:15 how biofilm formation occurs as well. that will trigger the expressive of operations

62:24 in formation, et cetera. Um so the conjugation. Mhm. Uh

62:34 will uh evolve. So so contact the indefinitely certain parts evolved.

62:42 So sex pilots is what brings the together um F factors. So remember

62:50 plasma transfers and the platforms that are to transfer ability to pay the f

62:56 . And the facts are simply the segment of the past contain those

63:05 That's an eight um taxes. So a gene for a sex pilots for

63:11 . Okay. Um You're also gonna what we call mating pairs.

63:17 We call it F. Plus which the transferable plasma and f minus Celso

63:24 recipient. Okay so again these congregations genes. This is what makes the

63:32 , are those collection of genes which called which include T. R.

63:38 . Trade genes. Transfer genes. sex pilots which included sex pilots relax

63:44 . Uh we're gonna see that's a complex that access liberation from the cells

63:49 facilitates transfer. Uh Rory has been transfer for transfer the plaster. That's

63:57 rolling circle replication mechanism. Okay, uh so a number of parts coming

64:04 . And uh so we see that the the fact that the pilot will

64:11 extend militarized and stand quite a ways it can and then they will latch

64:17 to a f minus. So a in particular receptor on the surface that

64:22 recognized by the pilots. And then it attaches there will be a deep

64:28 . So it shortens, right, can see how we're at this distance

64:34 and we've shrunk to this distance. finally to that. Okay, because

64:42 gonna be kind of a fragile connection transferring A. D. N.

64:46 . Across the quietest weather so far obviously, so you bring them once

64:52 contact you, kind of bring them to enable uh that connection to the

64:58 a little longer. So you can . Okay, so um and

65:06 rolling circle reputations what occurs here. , so we see somebody call this

65:11 the green is kind of this relaxes that bridges and sells rolling circle replication

65:21 . And uh that bridge facilitation, transparently of the plants with Vienna into

65:29 cell and then gets copied into the . Okay. Finally we end up

65:35 the plus, the plus and minus had become Yeah, that's the outcome

65:41 of these. Um we call F if minus is that we create and

65:50 another right there. And then that is able to transfer its password to

65:57 cells. Okay. So it kind increases the number of the population.

66:02 of course, obviously whatever genes around plasma, whatever they may be,

66:11 certainly be expressed about that by this cell that's required this. Okay.

66:19 that's you know that this is the basic kind of congregation. Okay.

66:26 the so let's talk about. So the most basic. Here's here's here's

66:31 next one. Okay, this is H. F. R.

66:40 Okay. HFR. So okay. remember this is going to evolve.

66:47 One step up let's say, let's see what we come up with

66:53 . All right. Hit the No. Mm hmm. Okay.

68:00 survey says yes, um effective integrated the chromosome. Okay, so the

68:10 . F. R. We've got frequency of incompetent strain. Okay.

68:19 occurs when so we will contain the forests are already detained the net

68:24 So initially. Okay. And so age of our forms from that plastic

68:31 into the chromosome. Okay. And typically there's common sites where it

68:38 We see this thing called S. . So called insertion sequence. OK

68:45 there'll be some big beautiful apology that ever for recombination. You gotta have

68:49 little bit of cosmology between the Okay. Um and then it becomes

68:55 HFR cell Jack. Now the thing Marcel is it's it's at plus

69:04 It's just the planets that we Okay now and plus cell.

69:11 Plus something like this. Okay. chromosome. Here's plasma. Right?

69:21 that contains those plus genes. So that guy could congregate right mate

69:28 an F minus. And but now guy looks like this. Okay here's

69:36 chromosome and now the F factors in . Okay. In there.

69:46 So what that means is that now entire chromosome can be mobilized in

69:53 Okay. And so um but that ever happens. Okay. Part of

70:02 gets transferred. And so what you here is that section contains those those

70:10 specific genes. Okay. When it copied, okay it will begin.

70:19 transferring. They're okay? And then in the clockwise direction. Okay so

70:27 transferable genes are here at the So when it's conjugated with f

70:33 So HFR contracts with minus, That begins to get a copy and mobilized

70:41 pushed into the recipient self. Okay um how how much DNA gets transferred

70:52 totally dependent on how long do you . Okay so it will take on

71:00 order of nine of nearly two Nearly two hours to be together.

71:07 entire chrome zone. And that rarely happens. This doesn't happen if you

71:12 think about what the force is causing come apart while other cells bouncing into

71:17 rally and move. It's just molecules the water matrix bouncing off of

71:24 Right? Eventually. It's gonna be much to connection breaks. Okay.

71:29 so for that reason when you have and H. F. R.

71:37 minus congregation. Okay. The F cell stays as hef minus.

71:47 It's only because the last portion that transferred into the F. Plus.

71:55 they rarely if ever are together long for that to occur. So the

71:59 minus. So typically always stays as F minus. This doesn't because they

72:04 stick together long enough to transfer all it. And the last part that

72:08 be transferred are these F plus That's what makes it transfer.

72:13 So, um yeah, so it's a bad thing. All right.

72:19 the has inherited. Okay. It pass those on through vertical transmission.

72:26 . But in itself cannot. that's that's specific for special for this

72:36 . F. R. F Mhm. Okay. We're ahead.

72:42 . Okay. Um, crushing. . Um, I'm not sure.

72:51 gonna end here, but now we'll next time with some animations that show

72:55 process. Okay. Thanks folks?

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