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00:01 Okay. All right so um we going to go through, I've got

00:15 in the last couple of hours I notified and I have to go to

00:18 committee meeting. So we're gonna go . So it's good news, bad

00:23 , bad news would be expected to in here and here. My golden

00:26 for an hour and 20 minutes. news. No I didn't um any

00:34 . Um So we're gonna go through gonna go through all depend on,

00:43 that's what we can and so the part will have will be what we

00:47 other control mechanisms, stranger response, factor regulations etcetera. That will do

00:53 thursday. Okay so get up through of the trip to find out from

01:00 we'll also mentioned really has something back up on stuff like that. A

01:04 of animations then we are done. um so this week uh you know

01:11 . Okay remember that's one of those longer kind of things. A little

01:15 comprehensive. So that will be up smart work kind of a little

01:21 Chapter 19 Sunday, two days Chapter 10. Okay. Uh of

01:27 the exam is later next week. . Um Oh and I posted and

01:34 sent a lengthy email somewhat on that yesterday about the midterm grade. So

01:40 read that if you haven't seen seen email, read it gives you a

01:44 by blow details of how that thing calculated. Just just refer to the

01:48 , exactly how it's done. Okay The quicker grade for the midterm I

01:55 go to the exercise because I don't spend that much time capital, everybody's

02:00 and all that stuff. So I said okay the grade for the mid

02:05 grade for the midterm grade was quicker . You got divided by the number

02:09 sessions you attended. That's it. so. Okay so um so yeah

02:20 can't and you have one more exam uh before you before you decide what

02:29 gonna drop or not, you're going get another third exam that you can

02:33 there into that grade. The email tells you how to do that.

02:37 so bottom line read the email that yesterday that gives you the detailed

02:43 Okay. Um Alright so let's go the whoa there we go. So

02:54 kind of rehashing stuff we've been talking last month. Overriding theme here of

03:01 is regulation gene regulation Makarios. Um to this we looked at like the

03:08 in structure again of bacteria uh things few other things about um the regular

03:17 the plasmids and stuff. And then time the congregation and transformation and trans

03:25 and transposition. So all these mechanisms horrible technology transfer. Now we're zeroed

03:30 on the actual control mechanisms. Talking kind of overview fashion initially. So

03:39 remembering the uh the levels at which control expression of course going to be

03:48 where how how it occurs. So many of these points along the

03:52 whether it's DNA itself um can manipulate of D. N. A.

03:57 nucleotides and effective expression. You can manipulate the our next limericks. We're

04:05 let it transcribing not transcribing. You manipulate the transcript that's me alter the

04:12 of it. You can alter Mess, mess with the riders on

04:16 , you can alter proteins, you modify them, you can just you

04:20 just degrade them. Any of those of these steps will lead to uh

04:26 gene expression obviously. Okay and so we went to different types of terminology

04:31 conduction, repression, repression, co active after repressor. So remember that

04:39 it is um this definition does not . Right? What changes is one

04:47 the conditions which bring each of these about. Right. So as we'll

04:52 lactose and it really in a nutshell this diagram I looked at the top

04:56 here is actually how lactose opera operates terms of control. The bottom part

05:01 how the different opera operates. Okay it's all about repressors interacting with regulatory

05:09 and are examples. We'll look at sequence. Okay. And uh the

05:15 which make it active. Okay. be the absence of a special molecule

05:22 this case. The inducer when it's present, professors active. Okay,

05:27 of inducer in activates the repressor. uh so the inducer then promotes

05:35 Okay Oxford situation down here. refreshing occurring by the presence of the

05:42 pressure. So now the molecule binds the pressure. Now they're pressured

05:46 Right, completely opposite of what's going up here. And so uh this

05:50 how the trip to find corporal We'll talk about in a second.

05:54 , so um do be familiar or with these terms. Okay. And

06:00 they mean then last week we went the almost there. So so remember

06:06 can also have uh activators and repressors once you try to stop expression but

06:11 have activators that actively increase expression. . And we saw that with the

06:18 opera on as shown here. So we went through what happens when

06:24 so overriding thing. The opera is about is a cattle bolic apple

06:30 It's about the components of the outrun proteins that are that are coded for

06:37 the opportunity to metabolize license, begin breaking it down. And so again

06:47 the lack of itself technically is will the inducer to buying professor locking

06:58 Yeah, That's step one. This happens in the presence of black

07:03 absence of glucose, glucose has that influence uh if they preferred carbohydrate sources

07:13 . Um and it will override anything of me resource. And so the

07:18 gone and that and that and that with glucose and cyclic GMP.

07:25 Just like a GMP levels rob glucose around but then the glucose goes

07:33 It's like a GMP levels rise and of promoters. Many different types of

07:40 . Others should be utilizing operations are the same control. And so second

07:47 rises that combine the separate protein and becomes an active complex. So remember

07:54 increased the expression means to let's put on the promoter to let you allow

08:02 really tightly bind. Right, make very attractive for our preliminaries to come

08:08 the promoter and generate lots of Right? So that's what that's what

08:13 do they collect at the promoter um provoke, right, high level

08:20 Which equates to last expression. So not just not just uh in

08:25 example, but if you look at and look at other types of eukaryotic

08:30 expression, the same thing. Budget come together at the at the promoter

08:35 bring about high level expression. Um I kind of went through in

08:42 hurry but we went through this last . There any questions about.

08:47 so let's look at um Okay, just do this now real quick.

08:53 look at the animations which are available you as well. Okay. And

08:59 have the option of you can put text on as well to see kind

09:06 the transcript. But nonetheless, so is uh our bacterium hearing black opera

09:14 the different genes of the operas from . Y. A. We don't

09:18 about A. Because that that protein not really involved. The lactose up

09:23 or breakdown. So you don't need worry about it. Remember the lactose

09:28 ? That's the black Y. That's that that has to be.

09:32 remember there's a little little bit tiny of expression always occurring. Okay.

09:39 um the with lactose permeates is the . We have to make a little

09:49 of expression to produce one or two were with black clothes permit. He's

09:54 . So now if it's present in blue dot that's glucose. But if

09:59 is present, potentially it can bring in. Okay. And so um

10:06 move forward a little bit here. so there's opponents. Again, the

10:17 presser is here according to the rough protein. Okay. And uh back

10:25 a sec here. So remember that control the control is this repressor will

10:32 to the operator. Okay. Unless present and the blue coast is

10:42 And so the binding of the repressor combines the lack opera operator and the

10:50 I operator forming this kind of And and that's something that covers up

10:56 promoter promoters cover. So memories can't do anything. So it's kind of

11:01 goes like that can't buy and can't . So essentially it's blocked.

11:08 So we know that in the presence of that win. Um The instances

11:16 which. Mhm. Let's see if show that here at the last

11:24 So there is instances where um come man here we go where it can

11:37 unbound right temporarily. In very rare that's unbound in that situation. But

11:43 those times to get a little bit transcription, this is what allows us

11:47 produce this guy here, which will enable us to see black horses out

11:52 . Okay, we can ramp that greatly in the in the presence of

11:58 . As you see here. Like comes in. Okay. And we're

12:03 break it down right, committed collective is the lack of Z product And

12:11 reform the two sugars like just I cried and then um produce also

12:19 aloe lactose as well. Okay, alot lactose is the actual inducer that

12:25 see there. Okay, so uh that will buy into the repressor and

12:32 falls off. Okay, so and we get lots of expression.

12:39 so again like glucose absent lactose This is what's going on.

12:45 Um and let's see if they show cyclic GMP refreshes the activator complex.

12:53 forms lots of expression. Okay, at the lactose present. Okay,

13:00 induction occurs then. Who goes Okay, now get repression?

13:08 second imperial would drop and don't forget activate a complex. And so we

13:14 get we don't get very good expression occurring glucose is overriding. Okay,

13:20 uh so I also remember that that . Let me go over here.

13:26 will show it. No, they show it in this animation. Remember

13:33 glucose presence of glucose can inhibit lacquer coming into the cell, like interferes

13:39 the lactose permeates. So um so remembering here that um that we need

13:50 have for best expression, high level is lactose is out there, glucose

13:57 not so much lower level of glucose promotes hi second BnP levels which promotes

14:05 activator complex for me. So all together is what brings you highlight expression

14:12 last opera. And so as we to the tryptophan opera now.

14:17 so let's look at a question that to that. Okay, so it's

14:23 about the trip trip to Panama Uh I'll refer to this trip

14:29 Just abbreviate, but it means the thing. Okay, so these four

14:35 then, which is possibly true. trying. Mhm. Yeah,

15:20 Okay. Ship. Okay, here we go. I'm not

15:36 Just give it a shot. the majority is correct. It

15:49 This is correct. Okay. Um metabolic pathway for the what? A

15:57 man metabolism synthesis, synthesis of trip . Okay, um and the answer

16:10 a co oppressor. The tryptophan operation he expressed. Okay, as we'll

16:19 the repression of the opposite occurs when is absent. Okay, so remember

16:28 is to block expression. The repression the opposite we allowed expression.

16:34 so we're gonna go through all these right now. Okay, so

16:39 this opera is bio synthetic unlike the opera. Okay um this is a

16:46 the works in a similar fashion to other in the elastic pathways.

16:51 so the products of the pathway um for enzymes that make a trip to

16:59 . Okay. And so should define of basically kind of self regulates the

17:06 process. Okay, as I mentioned , this there is another mechanism that

17:12 on top of this is a trip fan. You can actually interfere with

17:17 enzyme and that too will stop So that's a post translation in

17:24 Were messing with the protein itself. . And so um the uh regulation

17:34 repressor protein produced by the regulatory green Okay. And so the apolo

17:41 Okay. Is the form that is active, it's inactive. Okay,

17:47 to make it active we need to the co repressor present and the core

17:52 is okay, so when low or to defend president, you get

18:00 Okay. If crypto fan is present such then it becomes active.

18:08 So then the question is when does cell accumulate When to sell Cuban trip

18:14 fans And when this trip to fans not so high levels in the

18:17 Okay. All high the fans. you know, acid middle class issues

18:22 proteins, protein synthesis is greatest during . Okay. So if the cells

18:29 actively growing. Okay, it'll likely to defend and the other amino acids

18:34 fast as it's made. Especially if in log phase. Like crazy.

18:41 uh That's a high, high demand protein synthesis. So you're gonna have

18:46 crank out tryptophan and it's going to used probably as fast as made.

18:51 , So the levels of tryptophan in cell, what we call intracellular levels

18:56 gonna be really loved. Okay. for good reason because needs to meet

19:03 demand. And you're gonna when you making tryptophan right? Which means turn

19:07 opera on. Right. So but soon as gross begins to slow

19:14 Okay, that's when this can Okay, so uh so we will

19:23 up in the cell and then of if it's free like this, it's

19:27 to bind that repressor. And so come together to form the active complex

19:33 that binds to the operator blocks Right? So this is um this

19:40 course is repression down here. And this would be the repression up

19:48 . Okay. Depression. Depression. . And the presidents of tryptophan or

19:56 is what influences what what state you're . Okay. Am I going to

19:59 repressed? Well, there must be of different events. My dear request

20:04 not be there. It's being Okay. Um And that's that's the

20:10 . Right? Remember this is the of lactose opera for the presence of

20:16 uh promoted expression here. The presence tryptophan. An impressive expression.

20:25 Um Now we're gonna look at an method on top of this here in

20:31 second called the attenuation mechanism. but what you're seeing here controls

20:43 of the control occurs through this. . Um but you can still get

20:49 little bit of expression and when you want it. So what the mechanism

20:56 helps you clamp down on that? . To really shut it off is

21:01 attenuation mechanism which we'll talk about in few minutes. Okay. But that

21:07 relies on this here. Okay. sequence this leader sequence called trip

21:16 Okay this is part of the you the turn their attention. Okay so

21:23 little pieces involved in that process. uh So the the. Okay so

21:33 this point any questions about japan We're gonna get a couple of questions

21:38 . Let's look at this. This here. Okay. When we took

21:42 family present growth typically tied to growth all the amino acids and proteins involved

21:47 are gonna be used for protein It's growth that's going to determine for

21:51 most part. Okay. Okay, here is an example here. This

21:57 a clicker question. It's just a I don't answer any questions. So

22:03 e coli which is which is which ferment lactose. You can use lactose

22:09 plus it synthesizes trip to fan. . Is grown in a minimal

22:16 Recall that from Chapter four. Um minimal medium containing both lactose and tripped

22:23 . Okay, no glucose is Okay, sands, glucose.

22:30 So um what can you say about cells with respect to lack and trip

22:36 respectively. So we have two columns and Trip operas. So is the

22:41 peron expressed? Damn it. To pen activated. Okay. Yes it

22:50 . Okay. Um We're growing black present. No glucose. That's that's

22:58 that's your crew. Okay. We're gonna be expressing the what about

23:03 trip to yes or no because because tryptophan is present, is present in

23:13 meeting is present, present in the . The seller will take him.

23:18 . And use it. The cells will definitely take it up because why

23:23 energy making it if I've got Like if I was fooling in

23:27 No need to make it. I've it. Okay so no need no

23:30 to synthesize. Okay. Um So the lac operation side, what is

23:37 state of the repression? Thank Uh correct. It's inactive because we're

23:48 lactose is present because absolute were expressing . It's going to be inactive.

23:53 . If it were active it will stopping trying to stop expression.

23:56 so when the trip operation side it's dr And Yes. Right? Because

24:03 are uh tricked fans out there combined repress her and activating. Right?

24:10 So on the right hand side it's the GMP levels are high or

24:16 Yeah because again it's one of the about the lack opera because absent like

24:23 president um inactive repressor and then cycle levels are rising. That will promote

24:30 activator complex for it. Okay so let's see I think. All

24:38 So you do you know be able compare and contrast these 22 operas.

24:46 . Do look at the animations. think they help. Okay we'll see

24:50 in a second for Trip to fancy as well. Yeah. Right.

24:59 would be a trigger. So uh growth. Whether it's running our nutrients

25:04 or or something is stressing it that have caused it to stop growing.

25:08 those are instances where where the amino not just but all the acids are

25:14 be there's gonna be a demand for so if they're being made then they

25:18 accumulate. So everyone to shut that . Right? So growth the state

25:22 the cell is growing. Is it growing? I did not grow because

25:25 made of food or some other That's gonna be a trick. Any

25:30 questions Jack. So that's part Okay so um So in part two

25:40 kind of all we're gonna do in of part two today is just the

25:44 of the Tryptophan opera. Okay and the second part of how that

25:49 Okay so um there's gonna be a tricky. Okay. I would think

25:57 the mechanism we just looked at, know when the pressure's on or off

26:01 what causes it to be on or that can be easier to grasp.

26:06 this um this can be a little tricky because it's unusual in that the

26:12 don't is actually the mechanism that is you're allowing or not allowing transcription.

26:24 . It's not a it's not a person or introduce or anything doing

26:27 It's a it's the rivals and it's the rivals of position on a transcript

26:33 influences whether we get true opera Sounds kind of weird but that's that's

26:40 it works. Right? And it's based on this trip leader sequence I

26:45 earlier. Okay that comes right before that's that's the key thing to remember

26:52 this sequence and words placed. It's before. So this trip E.

26:59 the start of the structural genes. so if we if we if there

27:04 any problems raise Okay, begins to into that region. Okay. And

27:14 . That's gonna be the start of . It's gonna transcribe those genes.

27:18 ? So that's the do or die is there? Okay well we're gonna

27:23 it we're gonna let this happen or . Okay. It's all based on

27:28 positioning of the tribal zones as it's translating the leader sequence. Okay so

27:35 uh and so that is the leader right there. It doesn't code for

27:42 . Alright. It's only there as regulatory element. Okay so it is

27:49 . Okay. It is transcribed before get to the essential information. Okay

27:57 uh so the bigger sequence um has secondary structures that can form. I

28:06 like already they're single stranded but they form different kinds of loops and structures

28:14 things. Okay so and and all that is just complementary base pairing native

28:20 18 A. D. U. . To C. Okay. And

28:24 for this uh leader sequence that's there are multiple regions that can do

28:31 . And so you see two of there. Right. The one and

28:33 they call it? One and Right and 23 and four. And

28:36 also a two and 3 regions. . And that one is actually what

28:43 call the anti attenuate. Er Okay all any three of those performances all

28:54 under that. Okay, if you just a plop plop plop that leader

29:01 into a buffer by itself, you assume secondary structure and the most energetically

29:08 one. That forms is actually the . Alright. That would form if

29:13 just like do something but we influence influences which ones form is that this

29:22 ? Tenuously loop Or this one. . Which one forms is all about

29:28 the rivals um is at? so because it covered up, it's

29:33 big it's a big complex, it's little cover up part of that transcript

29:39 then where it stops kind of is which loop forms. That's how it

29:46 as kind of a sensor here. , so, so some of the

29:51 that are involved with this, are the TRS remember? Arriba zones

29:57 course translate and they translate? Um translate by the, you know,

30:09 tr N. S. Right? , right? Charged and uncharged.

30:12 charged ones contain their video action, ones. Do not right. Remember

30:19 each code on here, particularly if have a bigger transfer our name that

30:24 the code on, through the anti on, but then it brings with

30:28 and then we don't ask specific for code. Okay. But you can

30:34 but you only form your form charged by combining and uncharged with together.

30:43 . And so um so for this it's about what's the prevalence of

30:51 Tryptophan trn A's right, these how much of these guys are around

30:58 to these guys uncharged? One strip that, so you combine that with

31:09 These two things. One to stop on. Okay. And two adjacent

31:16 cartoons. Okay. And so you the positioning, one is positioned here

31:21 the other position here, so whether the riding zone is going to stop

31:29 one of those two places. Depending on where it stops, determines

31:34 you form the continuous loop for the attention. Okay, that's what I

31:40 by the positioning of the Robinson, what controls the whole thing.

31:45 and there's factors that determine where where it stalls we call it

31:50 Okay so again the stem loop structures former audience inspiring? Where's the on

32:00 transcript? Right. And that's controlled these two points. Is it the

32:07 or is it gonna stop? Their stop putting and that's going to determine

32:12 luke forms? Okay so let's look here. Alright, so high trip

32:19 fan. Love it. Okay so the attenuation mechanism, The the the

32:28 code pressure, that mechanism we saw , you know that's the majority of

32:33 control 95% of. Okay but this actually stops a little bit, a

32:39 bit that doesn't that that one doesn't . Okay. But um so many

32:45 high triglyceride levels. Okay you're a trip to fan, you likely have

32:51 of, do you have lots of ? Lots of uncharged. There's lots

33:00 trips to find around. You can more or less charged to urinate.

33:09 has to be all right, we more, of course we have more

33:14 to fan around and then that's when this onto the T. R.

33:20 . I have lots of lots of er if you have lots of,

33:25 so what that means is um when environment zone was on the computer sequence

33:32 it's translating. Okay, where is ? Black spot? It's gonna spark

33:39 the usual spot at the stop code . Okay the normal stop coding,

33:45 gonna go past the triple coupons. And so by stopping at that location

33:53 ? That you see here, that up any ability to make it 3-3

34:00 the anti anywhere. Okay. So what's promoted now is 234.

34:09 And so also notice the the distance . Okay. Between so remember you

34:17 the RNA polymerase running ahead, Transcribing? Right? So this is

34:22 RNA polymerase here, so it's transcribed . What's out in front?

34:28 And now remember this this area here the danger point. Okay. That's

34:36 you want to stop it. If want to stop it, you don't

34:38 it to go into structural genes. so that's and so that's where the

34:45 takes place. Okay so the hairpin that forms the 34. The itinerary

34:51 is in close contact with that memory knocks it off. As you see

34:56 . Just well then being knocked off you don't you don't go any

35:02 Right? Which is what you want you ever sell around, you don't

35:06 to make more tryptophan. So you want that plumbers to go into the

35:11 trip. E. E. C. B. A.

35:14 That's because that's gonna make the cell and you don't want to do

35:17 You want to talk before then. . It all ties back to lots

35:25 charged. Should uh T RNA. ? So you have lots of

35:36 you don't stall at the strip club you would stall here. Right?

35:42 would stall there if you didn't have had very little or no charged tr

35:52 what happens in the next as we'll here? Right low to defend

35:57 You have these guys. Right? uncharged ones. Okay. The uncharged

36:06 , So they don't have unlike this . Right? These are the charged

36:10 here. Okay. So they don't the trip to found. Okay,

36:15 when this thing with that T. . N. A. Plopped down

36:19 a trip code on there's no trip find any lasted there. Right?

36:24 can't Right? That's where you make bonds. Right? So you have

36:29 two of these uncharged trip tr sitting and no tryptophan there to link

36:36 So it's going to stall? It at that point. Okay. And

36:41 those adjacent trip cotton's come before Right? So it's all about

36:47 Right? So they're gonna so the person is going to stall here.

36:52 . And now that two region isn't up anymore. Right? It was

36:58 . Here is number two right Alright, covered in that scenario,

37:02 defend, but in low it's And so the anti itinerary. The

37:07 , right? That can form. . And so now note the

37:12 All right, between that loop and implementation running ahead of it.

37:18 Much farther away, so it can't . Right? So it keeps

37:23 Okay. And we transcribed structural Right? So it um it promotes

37:31 the expression of the genes. And it's all it's kind of all one

37:36 leads to another, right? So level of crypto fan, right?

37:41 is what's controlling things. So low fan um less charge T. RNA

37:50 more of these? Okay. I on going down the transcript gets to

37:58 trip to code on and there's two a row. Right? Well there's

38:03 a lot of charge T. Trip . R. A. So it's

38:07 that guy, right? So it's plug in, right? But there's

38:11 real answer to The link together. it's going to stall the whole

38:16 right? And that's what enables the loop to form, right? Anti

38:22 . So you get expression of those which is what you want because your

38:26 trip to things. Okay. Um the opposite is that it's high.

38:32 ? You have lots of the They're gonna blow right past these two

38:37 codacons because many lessons are there on T. R. D.

38:40 So they can be linked to linked and extend the chain. Right?

38:45 then it's and then so it will stop at the usual normal spot,

38:51 arrival zone would stop that to stop on it. Okay. And that

38:56 happens to be Where it covers up two regions. So 3344 um Taylor

39:04 and that's what that knocks off diploma . Okay so let's um look

39:13 Mhm. Okay. Okay so here's trip to fan opteron there's our shut

39:27 . Okay so there's the opera and structural genes you see the leader sequence

39:35 . Okay so of course transcript codes the enzymes that make crypto fan as

39:40 see. And the let's see how thing. Okay so there's our oppressor

39:49 ? The core oppressor if present will and then that will bind. Make

39:54 active repressor, binds the operator, what they call a holo repressor.

40:00 so it will bind to the There we go. No uh that

40:06 this is the this is the majority the control, is this what you're

40:09 there? Okay um and then of in the mechanism so here is our

40:21 sequence. Okay let's speed this up little bit. Okay so we're going

40:30 transcribe the leader sequence you see there a different stem loop structures that can

40:36 . Okay. 23. Okay or the 12 and and a 12.

40:46 the stem loop continue later. And that's so let's kind of go through

40:52 mechanisms kind of give you an overview first let's go through. Okay

40:58 Which are okay so now e The code in here. Okay so

41:13 code on the trip Cardin's and and levels of tryptophan. Okay we think

41:23 kind of there we go. So an expression of leader sequence.

41:31 there we go, write his own . Remember, drivers on binding site

41:37 there we get the attenuated loop performs it goes through this trip code

41:44 it doesn't stop until the stop code . Okay. And that's enough during

41:49 loop is in proximity to the primaries knock it off. Okay. And

41:54 we go. So in the low scenario, right? There's our leader

42:03 , there's a rebel zone. It's stall at those trip codacons,

42:07 But the proximity of the loop to preliminaries is far away so it's not

42:11 to interfere with it and it can ahead and transcribe. Okay, the

42:16 genes. Okay, keeps going. , so again this is just a

42:24 an additional safeguard to either really clamp or make sure we get some

42:30 Okay um so let's look at. , is there any questions? This

42:37 this is one of the mechanisms you have, it really does look at

42:40 animation to kind of get in Yeah, so those shapes and forms

42:45 things like that. Yeah. So you were to take that um That

42:53 trans that leader sequence and just with else around and put it in a

42:58 , it would most of the time the 23 actually that's the most energetically

43:04 loop that forms but because we have on going on there translated.

43:11 That's going to influence whatever conforming because it's just covering up covering up the

43:17 regions. For example if it started so that then that enables it physically

43:22 that form. But it would have . That's the most favorable. But

43:26 that's what arrives in really influencing what's on. Okay. Yeah.

43:33 So yeah, this mechanism is wanting kind of have to wrap your head

43:37 but if you think about it you know, you begin with high

43:42 low tryptophan and kind of work your from there. Okay. Hi tryptophan

43:46 what do you have? And you to think of these molecules of the

43:49 levels. The trip to fan uh . R. N. A.

43:55 . Okay. Because that's linked together the amount of truth defend present.

44:00 then that that influences where the riders stopped because they have two choices.

44:07 to trip Cardin's side by side. can stall there or you can just

44:12 . The stock word stops. All on the level of tryptophan which influences

44:19 uncharged Tr N. A. For tryptophan right? Which influences what

44:24 it stops, which influences which Right? So it all connects

44:29 Okay, that's kind of how to about it. But do look at

44:33 the animation. Okay, so let's at the question here. So the

44:39 mechanism that helps block expression. Of the tip opera would include all

44:46 following. Except which of these? me hoping that. So we're looking

44:59 the exception here. Mhm. Okay. Please stop. Mm

46:02 Mhm. Okay. Let's see what get here. Okay. Um,

46:19 the majority the majority was correct with be Yeah. Mhm. Okay.

46:28 whether you um have attenuation if you , you're going to produce that leader

46:34 regardless. Okay. So a is to be a part of it regardless

46:38 if it's blocking or not blocking you're gonna have the leader sequence for

46:42 . Um of course every blank expression all about form in the continuously

46:47 Right? So attenuate means to limit to stop. Okay. Um you

46:52 , you're gonna have high levels of . If you're blocking expression, then

46:56 doing so because you have enough tryptophan . Okay. So, uh,

47:01 the wrappers was gonna stall in this . The rivals was going to stall

47:06 the stop code ons not the right you have lots of trip to fans

47:15 you have lots of charged trip which means you're going to go through

47:19 trip coders and stop at the stop on and that's what promotes the

47:24 Okay. Um Any questions. So the, so this okay,

47:33 one I got about five more So that's um, so this is

47:37 of again, analyzing the different parts the process here. Right? So

47:42 versus high trip level. So synthesize to fan um low. Yeah,

47:53 yes or no. That's what What? Um Hello. All

48:00 As soon as I took the fan uh low interest. Yes, I

48:06 you did anyway, load interesting trip . Yes. You're gonna send a

48:10 trip to family. Okay. Hi levels. No, of course.

48:14 . Transcribed the opera. Low intracellular . Let's see. Yes.

48:24 Low levels need to make need Might be going to transcribe it.

48:29 . Hi adversarial levels. No, strip co repressor repressor complex form under

48:35 levels and high levels. Yeah. . Charge trip transfer RNA is

48:45 Low. Yeah. Yes. grab some stalls at right assaulted trip

48:54 ons stop photons. Okay. Which leader sequence performs anti tenure later.

49:01 these kind of things that kind of to each other under these conditions.

49:05 . Just another way of looking at . So um so again, I

49:11 you to look at the animations, black opera. Uh Turn on the

49:17 . Text with both of those animations that can kind of get you through

49:21 . Um Also listen to me Okay um so I mean, how

49:29 questions are you going to see on on the exam? A total honesty

49:34 maybe like four questions. four or questions times. Okay. Uh 24

49:43 to for lack of a round two the tip off. Some general

49:48 Alright folks. Uh That's it for . We'll see you on

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