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00:34 What goodness. That's good. Okay. Um So weekly quiz opens

01:21 Through Monday. So that will be will cover we're gonna finish six.

01:29 we'll go back to last. Um we? Yeah because we started talking

01:36 viruses last Thursday. So we'll cover as well. So basically I have

01:41 . Not every single thing but there'll questions about Chapter six and then the

01:48 bit of 13 will do today. , so we'll start on that and

01:54 finish that next Tuesday. Okay. let's see what smart workers do.

02:02 that's kind of a part 12316 is monday. The part two on

02:09 And uh I think that's it. um I had an email today.

02:15 haven't looked at it yet. That uh Lincoln there to the uh how

02:21 study part of the day one So if you understood, take a

02:26 at that. If you have Um let me know. Okay um

02:32 today um let's um um recap a bit from last time. Alright so

02:45 went through bacterial viruses. So time put this in the perspective. So

02:52 looking at the virus, you looking at viral life cycles.

02:56 So all begins or ends of recognition behind you. The host getting entry

03:04 carrying out the cycle. So the viruses we saw lighting types uh basically

03:11 mod is but um replicate inside. lots of viral particles burst out filled

03:19 . That's kind of their effect uh that. But they have this other

03:26 dormant stage. If you will um they genome goes into the host

03:34 it kind of sits there while the is replicating no problems with that.

03:39 then eventually if it's going to make particles that have to go through life

03:45 so less so ginny isn't a permanent . It's it's, you know,

03:51 it'll vary. And so again to the particles we have to go in

03:56 cycle but it has both those apartment 13. Remember it was one of

04:02 uh that's it does not does not a profile page, but it will

04:10 make viral particles a low rate. that enables it to not kill the

04:18 . Okay. But the host is feeling super great figure the host is

04:23 a flu alright function as well, still can still can replicate right at

04:27 low, a little rain of Okay, so um uh so kind

04:37 its strategy is to always have a , right while it's um replicating how

04:44 sell, it comes out of the , right parts of the cell,

04:48 the host cell, it was So it always has a host

04:52 Um so just a different strategy. was the host defenses, restriction,

05:03 altering mutation to alter the surface protein the virus recognizes. Okay, um

05:13 the CRISPR system kind of pseudo quasi system if you will. Okay,

05:20 uh, hantavirus. So we started really was kind of looking at the

05:26 encoding mechanisms. Right? So we're look at uh developed the types are

05:31 the coronavirus is uh virus types and uh how they uh different from bacteria

05:39 . Right? They the the entry the cell can be the whole

05:45 right? As you see over Okay. Or here. And so

05:54 uh mechanism diffusion of, you then I'm sort of specifically a license

06:09 or something refuses to kind of digest capsule, releasing the uh the mechanisms

06:21 are similar as a testicle coming in a testicle into the cell, but

06:26 is going to the nucleus close. then just gonna quote in the in

06:36 outside like this. Okay, so more or less catches us up with

06:43 time with any questions. Okay, let's look at uh it's kind of

06:53 little repetitive, but I'm just gonna you the basics of what animal viruses

06:58 here. So, we go from then to eventually copying genome assembling the

07:07 particles uh envelope. So this can through this budding process, which basically

07:16 this membrane here. So, number , uh for an envelope virus,

07:22 see the viral particles, viral proteins red. Right? And so these

07:28 made typically in the gold. So migrate to the surface and that's how

07:34 end up in the host membrane. , then here's the capsule structure of

07:41 virus and the genome inside it. . And so as it exits basically

07:48 happens is it's kind of crude drawing . Okay, so that membrane is

07:55 pinched off, right? Like. so here's our so it goes from

08:01 to that and eventually it just pinches . And we have an envelope virus

08:08 you see here. Okay, let's to the process for the virus.

08:12 uh that's what we cut. That is the budding process. Okay,

08:19 you also hear the term shed? , shedding virus? Okay, dog

08:31 hair, right, losing his A cell can shed virus when you

08:37 that term. That means the virus of viruses are basically coming out of

08:41 cell and shedding virus is okay. it can be synonymous. You know

08:47 happening budding is cause budding is occurring viruses are being released from the

08:53 And you can say the host is viruses. So you'll hear that term

08:57 well. Um but again, it relates to the exit of the

09:02 Okay. And so um it could from buddy, because the budding process

09:10 leave the will leave this host host intact at the hotel still can be

09:20 as a virus. Uh Right. you know, but if this is

09:27 , this process is occurring in a rate but there's types that are

09:35 right? That may lice the cell together. So you can have the

09:41 of of different outcomes here. so the and so this is kind

09:48 recapping the basics of RNA and DNA . Right. So this is generally

09:57 viruses. But there are exceptions. one of those is the flu virus

10:03 virus doesn't actually carry part of its cycle in unlike most other RNA

10:10 it actually does that. Um it so and there are DNA viruses that

10:18 do. Uh but somehow so you're see some variations here and there.

10:27 for most, right, they kind fit both of these modes here,

10:32 fact. Um, so let's we're gonna look So now I'm just gonna

10:39 at examples. First DNA virus, a couple of different parties viruses and

10:45 retrovirus. And then that will pretty close up the chapter on viruses.

10:50 , so let's look at the data , papilloma virus. Very common.

10:56 . T. E. Also cause , cervical cancer. Um, there's

11:01 vaccine for it. So it is was actually I've seen signs around campus

11:08 I think I emailed you all a of course looking for volunteers, a

11:14 at the Medical Center volunteers for let I can't remember the exact specifics relating

11:21 the PPV virus. And so uh basis by getting people vaccinated, you

11:27 , women especially uh there is an vaccine. So, but anyway,

11:34 this is an example of not typical viruses virus. Right. Humans of

11:44 ourselves are typically parts of tissues right ? Parts of tissues, parts of

11:52 . And so because of that cells the tissues may have different states right

12:00 make differentiated different types of cells. skin cells cells Skin skin of course

12:14 very thick with layers of cells. and you are sloughing off the upper

12:22 of skin cells continuously. Okay. now P. P. P.

12:29 . P. Okay effect basil cells . And those are the underlying cell

12:38 obey themselves, differentiate into crowded Okay. Um basal cells are not

12:47 growing when you get the signal to growing. Um Then of course they

12:53 into sites. So as you see from lower layer of skin to upper

13:00 . Okay so um this being the layer of skin. Okay so of

13:11 is not visible basal cells without deeper but anyway so the virus and it's

13:19 of linked toward its kind of replication tied to differentiation of the cell

13:29 Okay so in basal cells they can the type that can integrate they can

13:35 a pro virus. So when we about the process of a viral genome

13:39 into a chromosome, when it's animal used to turn pro virus material types

13:45 the land that we call. Pro pro page pro page pro virus

13:50 Similar integrated. But one is specific bacterial viruses. One for animal

13:56 So they can form pro virus here this stage of sepsis. Okay.

14:05 in doing so they integrate into the and that's what can lead to potential

14:12 cell types because they integrate themselves into functioning genes in the cell are responsible

14:21 normal growth and repair themselves. I'm sure we all know. That's what

14:27 know uh that's what viruses do The cancer is a state of uncontrolled

14:34 and not be able to repair mistakes the D. N. A.

14:38 occur during the cell cycle replication. . And so um and that happens

14:45 viruses that cause cancer by the integrated these all the normal growth and repair

14:51 sets the cells off to be growth tumors. That so and that's what

14:58 can do. That's what the that's the cervical cancer caused by PPB.

15:03 how they do that. Okay. so not all P. P.

15:09 borrowers. I love the fact that the control that there may be genetic

15:15 to this as well. Okay. um as the cell begins to

15:22 Okay now remember that this is a of virus that needs the okay remember

15:34 right mitosis. Okay that that nucleus divides. Right? And so yeah

15:43 replication going on in their memories. that's why so as as the skin

15:50 type goes this way right? It's and now the PPV virus can then

15:58 to copy its genome replicate and then the host and that's what you see

16:04 here. So these cells are in shedding HPV um uh virus system.

16:13 so again get tired because they need and that's really only available when the

16:18 are actively dividing and that's and that's begins to their process of replicating themselves

16:26 host time. So um if HPV also cause like you'll see almost like

16:36 unaffected skin as well as how they themselves. Okay um now at least

16:43 just diagram that shows just such a type. And so we see um

16:50 need a virus it carries out coding right um realize I'm supposed to

17:00 Right so you're gonna have so again that the virus is right. They

17:08 you care and excel right transcription occurs the translation outside piece. Okay so

17:15 the virus part of the process can out here. Right so you see

17:22 transcription of the viral genome the R. Exit. That's what happens

17:29 you create sell. And then they then parts come back into the are

17:38 then once again exit. So this going back and forth transcription translation assembling

17:46 because that's very typical for a N. A virus. You have

17:50 going on in different parts to sell not to mention they're not including in

17:56 . Um Goldy. Okay so those lead to us uh borrow envelope proteins

18:06 end up on the surface and so . So again very common for virus

18:11 kind of action happening everywhere in the . Everything. Okay. Um Any

18:19 about? Yeah. I would assume pre cancer should refer to cells that

18:37 the pro virus in them. But the they're not yet activated to begin

18:47 yet. And so the it's when get into the out of the basal

18:54 into the next stages where the cells , that's where the cancer will

18:59 So it's a pre pre cancer would that stage. It's integrated but not

19:05 to sell. Not yet growing because it's one of the boroughs when these

19:08 occur. So that's that's what I call it. Um Good point.

19:20 would say it's a pre cancerous You still want a vaccine because doesn't

19:25 all this altar that way. You have some viruses that will be

19:29 So I think yes you want a regardless of what stage. But but

19:35 right. The the effectiveness will might affected by that fact but still do

19:42 vaccinated. Yeah, that makes Okay. Okay so okay so it's

19:53 take us in this is our segue our Okay, so take a look

19:57 this. This goes back to the plus minus. That was ranting and

20:01 about last time. Right sense antisense non coding etcetera. Okay, so

20:10 virus possessing a single plus sense RNA its genome. What first have to

20:19 this into a minus. Anti sense and translate from this minus into

20:26 True or false. Let me get . Sorry, you can't see the

20:31 here. Okay, 26296996. So what I'm mulling that over.

20:51 me get my problem here. Yeah. Oh, good. Good

21:18 . Nice. Alright, let me pause it for so So yeah.

21:25 , go ahead and answer now. bet here it is. Mhm.

21:37 uh here's my pure protein bar. this? A source of?

21:48 it is. But ultimately it's a of coming attractions coming toward the end

21:52 the class. Yes, electron. let's put that in the back of

21:58 head. I'll revisit this problem again . Okay. Um Let me speed

22:07 . So 10 countdown from 10. . 8765. Mhm. 21.

22:20 , dramatic pause. Here we Okay. 50 50. So that's

22:30 right answer. Um It is. answered drumroll. Be false. I

22:41 to be. I'm not saying you're , but you want to be.

22:47 . Why'd you have to be? that's a wow correct. Had to

23:00 read that myself. I was in first place. But you're referring to

23:07 to this? Of course. Let's go through the example here.

23:11 so this is our virus. So sort of that's the first half of

23:22 is right. Like because that's um that minus is not not translatable.

23:35 , So we have to go another . Uh So remember what I said

23:44 time, you know, in in that. All right. So,

23:48 is a virus, right? Infecting host. Right. So happens to

23:56 one of those. And then I what the Endgame is. Right.

23:59 of viruses. And so remember each of these has a genome.

24:11 Which is in this case will be plus R. N. A.

24:14 don't write this down. You're gonna this in the next slide anyway.

24:18 So, you're gonna have all these have plus RNA genomes, right?

24:23 all gonna have these these Right. those proteins. Right? Caps

24:29 And maybe has spikes sticking out of . Right. So, you have

24:32 make all that stuff, right? come from scratch. So, you

24:35 to make all that. That's what on in here, right inside the

24:40 . Making all this stuff. You make viral proteins. You got copies

24:44 the loans. We gotta slap it together. Right. So, so

24:50 . Yes, of course, it be easy to if this were the

24:55 . Alright, If this worked this . Right. If you could do

25:02 , of course, that would be easiest stuff, but it doesn't

25:06 Alright. Doesn't happen because that's just way to pay gasses work.

25:11 When you copy a strand, you're copy that you're going to get a

25:14 of the complementary strand? Just a or if it's a minus A plus

25:18 plus and minus. So that's why have to go this route?

25:24 A Because that's the way to play work. B because you want to

25:28 lots of copies of that and then for the purpose of stuffing in to

25:37 captions as we assemble them plus um to translate from to make the proteins

25:44 it needs. Okay, so that's this happens this way. Okay,

25:50 let's look at um here. So , this is more kind of just

25:59 of stuff we talked about. So the RNA virus genomes can have different

26:04 depending on the viral type. It can be a template for translation

26:09 for um synthesizing A. M. . N. A. Remember the

26:17 Marnie is the plus so a template make that. Right? So basically

26:24 doing that to that. Right? so then of course the retrovirus.

26:30 ? That's totally different. Animal uh . Sorry, that uh D.

26:38 . A. So it's already template one to make DNA. Uh

26:42 Um so let's look at each of um Individually 1 2 3 back.

26:53 is the plus single stranded type. . Um Alright, so I just

27:00 some examples of types but just for . Right? Totally must not all

27:07 these types. And so and so I drew it like this for that

27:11 reason I just mentioned. Right, is a type of virus that's infecting

27:15 is what we're gonna get out of . Right? So how did this

27:21 ? Well we uh virus specific they get this from the host. Right

27:33 a proliferator. Our D. A. Um So I got into

27:43 we get lots of these and then will be used to make a lot

27:49 so while while sitting here so these themselves these minus RNA strands by themselves

27:58 no use for the virus other than template. So many more of the

28:06 . Okay so again some of these be used to translate the protein and

28:13 well the package into the right so that's what it's about for plus so

28:23 minus so we have a lot of etcetera so same same same.

28:33 So here's our we were infected with we produce in the end. So

28:41 we've got to have lots of copies the genome and of course lots of

28:45 approaches. So uh again we produce of friends. Okay and so you

28:55 think okay well we can stop right we've got lots of templates to make

29:01 right translate but that's only part of flavor, right? Because it's so

29:09 it is, that's the hand that genome inside of. Okay so we

29:15 do that. Okay then we have do this part because it's a minus

29:24 virus. So that's why we do you might think it's some kind of

29:29 process to get to the game. that's how it has to be

29:36 Um And so this this diagram is to show this I think this is

29:46 uh really just the main thing here the events are currently outside,

29:54 Not yet. Not part of It's all outside the nucleus synthesis

30:02 Alright then, um the copy of culturing strands and then back in plus

30:11 translation of uh proteins, proteins and assembly. So uh pretty much previous

30:23 but now um any questions about either it's one of those things you kind

30:32 think just kind of look at it be drawn out yourself. Right,

30:37 you're having problems with it, but it's easy enough just to put on

30:41 piece of paper that this Right, then see if you can carry out

30:49 . Okay, so um so with retrovirus. Okay, um well,

30:58 see if you can answer this question . Pretty simple, I think Takes

31:04 into our next one and last Oops. Okay, let's count down

31:40 3 to one. It's um it a retrovirus. Okay, so it's

31:54 its own transparent, right? They need an independent. Okay, so

32:06 , so retrovirus life cycle. Um , so they have a plus single

32:14 RNA genome um and the indian of eventually they will do this.

32:22 But their way is a little So we diverse transcriptase the virus makes

32:34 again relationship. Right? We're now plus minus. Right? Even though

32:44 are the ones DNA. The same still apply. Okay so copy plus

32:49 . N. A. We're gonna a minus D. N.

32:53 Okay. Um is used to make second copy of the right now.

33:00 have a remember this is going to the host. We're gonna form a

33:04 virus here. Okay. And so but when it does but it does

33:15 it will translate proteins uh sample viral . So they are unique in having

33:28 state here. We're just gonna integrate the promise. Okay and it can

33:38 in that state. Okay and still all of this. Okay. It

33:45 have to be doesn't have to pop of the chromosome to do this.

33:51 can stay in the chrome zone and this. Okay so we see that

33:58 . Okay so here is a retrovirus uh here's our virus. Find it

34:10 specific. They act very specific immune cell T. Helper cell specifically.

34:19 think it's a t. Helper type . Right okay. And but these

34:27 of helper cells T helper cells direct the hola response. So if you're

34:33 those you're really really um damaging the system response or at least that

34:40 Okay you've got to get these antibodies so forth. So many case.

34:47 the release the transcripts from the virus we get into D. N.

34:55 . D. N. A. and then the genome in fact so

35:02 I said it can be in this and they can just stop right

35:08 Okay and do nothing. Right? can just remain that's what we call

35:14 latent state. Okay. Where it's kind of hanging out. Uh This

35:19 of course very analogous to right? we don't don't use that term in

35:26 following anti viruses that do this. don't that's the term only we use

35:31 like land of age and bacterial viruses the life. I wouldn't use that

35:36 for for this although it's obviously looks similar. Okay so um so again

35:43 can remain in this state here just this for months weeks weeks months

35:51 Okay. It's not detectable. A who gets uh blood test will be

35:59 negative in that state. It's not you begin to get some production of

36:06 . Okay. So it can be for large state and then carry out

36:11 transcription. Right? And then translation somebody off and they can do this

36:21 a lower rate but the cell is they can reproduce the cell phone copy

36:28 . Uh But surely releasing these Okay so uh so it's not until

36:39 get enough enough virus built up. . It's what they call viral

36:48 viral load builds up until it becomes . So it's at that point where

36:57 having negative uh of course like I uh for several months several years and

37:11 uh progresses and of course during this this assembly is replicated. Okay so

37:18 have more more cells with this genome it. All right. And so

37:26 doing this viral production of a little . So obviously the virus accumulating in

37:32 body. Okay. And at some it uh obviously damages the uh the

37:39 effects of a disease. Okay. so uh no but you know in

37:45 developed countries like ours right we have for for H. I.

37:51 A. C. T. Has around for a long time. It

37:56 affects the reverse transcriptase Function. Uh like a series of like nine or

38:03 different medications that are given to a and uh personally along both you know

38:12 life. Um but we don't not in the world has access to those

38:20 um because HIV is is endemic in of the world epidemic in parts of

38:26 world and uh they don't have access the drugs. So that's a whole

38:31 discussion uh involving politics and pharma pharma etcetera. So um anyway the point

38:43 it is it can be not curable definitely treatable and uh just to be

38:49 to have uh Access to health So that's a whole other conversation I'm

38:55 with my 93 year old 93 year mother and seeing all the offensive healthcare

39:00 it's frankly pathetic. So and she's . She's not like um in terms

39:07 insurance care, so plus veterans so you know that it's still I'm

39:15 just like oh my God, so probably may be dealing with some of

39:19 yourself. So it's uh something's gotta faced for sure. Uh Any questions

39:26 not gonna tangent there. Okay, off my soap box. Okay.

39:32 right, so let's look at some offenses. Right, so again,

39:36 is common what we saw before. , so that's any life form,

39:42 virus potentially. Right? Just kind having to take from that affects the

39:48 or whatever the molecule is that allows virus to get in right bank it

39:52 . Okay, um RNA interference, talk a little bit more about this

39:59 you know, three but it is way very widespread is using RNA molecules

40:06 control expression. Okay, we can it in this way right to counteract

40:14 infection by interfering with viral expression. RNA is right in a very brief

40:21 . Alright, this is an R. N. A. Let's

40:25 there can be interfering RNA is in complementary right? So we call it

40:31 R. N. A. Okay, let's say and it short

40:38 typically and they'll buy into a complementary . And in doing so remember arriba

40:45 have to be on here to Right? And if you have any

40:50 right there, you have a ribbon trying to translate. Okay, there

40:57 just be a physical block but we get around that sequence. Right?

41:03 you don't get any expression in some , this binding of an RNA I

41:10 another protein to come in and just of chop it up. So that

41:15 of two ways it can happen to the expression destroy it or just kind

41:20 physically blocking translating. Okay. And very we're talking about this in three

41:28 that is certainly a mechanism. And lastly, this is all not last

41:34 second to last. We have the system. Okay, so the immune

41:39 , adaptive immunity antibodies. Right. these are why shaped things here that

41:46 can buy into a virus vaccinations about we can introduce an antibody response by

41:54 a vaccine to create the same Uh And then lastly again, this

41:59 something we'll talk about in the last as well as this one here to

42:05 on so interfere on uh this. what it does and don't worry so

42:15 about the show you here, cause gonna revisit this at the end.

42:18 more more more so now it's just interfering with the defense that can produce

42:24 um molecules that will counteract it viral . But just for now, just

42:30 show you that what it does, it works is it um will it

42:38 infected with the virus is the one produces the interference. Okay, so

42:44 see that there's an environment affection induces then that diffuses into outside the cell

42:56 and then kind of diffuses outside the and whatever other cells in the area

43:03 have a receptor for it. All . Find it. Okay. And

43:09 it in and it acts like a as a transcription activator for activates transcription

43:17 specific antiviral proteins. But then interfere with it gets affected and then

43:24 can interfere with the virus life blocking it from damaging it. And

43:30 it's a protective mechanism protects those cells the area in the vicinity that aren't

43:36 infected. So it's likely that this will this cell will go away be

43:44 but any themselves. So, um . Is those that have a for

43:53 that hospitalized you give you can't give interference. That's an option as an

44:00 . Okay. And it does have does have efficacy in that in that

44:07 . Um Okay, so just another defense that we have. We have

44:11 of course. Right. Um All . Any questions that wraps up Chapter

44:18 , I'm always gonna do a 1 year. Chapter 13. Remember my

44:23 . Right, okay, So, so a couple of things to get

44:29 the tablet, which is basically the of this game. So two is

44:35 . Okay, so 13 to 14 metabolism. Okay. Again, I'm

44:43 gonna expect you to memorize the 80 reactions that occur nor the enzymes of

44:49 . There's a couple. Uh but from that, don't bother memorizing

44:56 Okay, the way I approach this in stages and four stages.

45:02 And it's no wonder what goes in out of those stages before then.

45:09 kind of one diagram you'll see a . Is this? So, I

45:14 a little box. I put T. C. Alright. Or

45:21 . T. S electron transport chain try and transport system. Okay.

45:26 don't have uh something like this exposed y here and uh a to be

45:34 . Okay, So, we see a lot in this section simplified way

45:41 doing something, right? You may what it is, maybe that's

45:44 but it's um it involves this, , involves these. Not not sure

45:51 bars, but there's a constituent's Uh Okay. If you don't,

45:58 will. Okay. So what I'm to say is I'm trying to I'm

46:02 I'm not going to be down in weeds on this stuff. Hopefully keep

46:07 more. Here's the basics, Because you should know the basics.

46:11 is one of those things, like should know what D. N.

46:14 . Is, right. Everybody should where the gene is. One of

46:16 things when you graduate from college. go, somebody puts a microphone in

46:20 face like and goes, what's uh the D. N. A.

46:24 don't know if you probably remember jay used to have, you know,

46:28 Fallon hosted tonight show. Right. hope some of you know that jimmy

46:33 is uh So jay Leno used to this man on the street interviews or

46:40 on the street person on the street . Right. Random people. And

46:45 go, what is the capital of ? And people would just nobody would

46:50 anything. It's so ignorant. don't be one of those people.

46:54 , so you put a microphone in face and say, what's respiration?

46:58 ? Know what it is. They're Harvard graduates. And you go,

47:02 my God, they know everything, ? They ask him what's photosynthesis?

47:05 could answer the question, insane. , so, don't be one of

47:10 . All right, I'm gonna make not one of those. So,

47:14 the first question. Alright, this kind of just gauging. What do

47:19 remember about metabolism? Because I know had some of it in intro

47:23 Okay. Remember anything. Alright, , there's only certain words,

47:29 Like oxidation may produce the timer oxidation . We mentioned that before. Um

47:38 teepee. Right? Um what else you have oxidation you also have

47:46 These are the terms we're gonna be . Let's see, I look at

47:51 question a while. Let's see if can answer it. I hope

47:56 We're in trouble. Sure. I think I remember? Mm

48:38 Okay, gave you the I gave one of these already. Right,

48:42 this up. What's this for? . Actually these are the answer to

48:49 . Okay, let's proceed 15 14 . Okay, great. The answer

49:18 is okay, so yes auction is to water. Okay, so uh

49:26 , that's yeah, that's this uh little diagram right, electron transport chain

49:35 we have why going to Z The back part here is oxygen for

49:46 treatment electronic sector. I am reduced water. So, um yeah,

49:55 the donut, this is the equivalent the donut, right? Source of

49:58 . Okay, we're gonna oxidize it and get energy from it. Um

50:04 , so 13 focuses on energetic Right? So I'm not gonna get

50:12 on energetic switches, thermodynamics, that alone. And so, um,

50:24 more kind of just the basics of . Okay, Some things we

50:28 we have to know. All And then uh, so, so

50:33 we're focusing on header approach us how eat, right? And so I'm

50:42 you had some part of policies so . So, um, we'll focus

50:51 that in 13 and then in 14 of expand beyond that. So hopefully

50:57 14 there's some things you don't know right? Like anaerobic respiration. Uh

51:03 covered fermentation I'm sure, but we'll through that again. And then um

51:07 little trophy. Okay. And photo , but photo trophy of the

51:13 You may not be aware of We all we all know plant pants

51:16 allergy photos inside. So it's different that. Okay. But anyway,

51:20 start here. So this is kind meant to illustrate, I guess a

51:25 of things. But one of them um, the number of things that

51:30 energy may not be obvious because your don't really show um whether it's DNA

51:39 or protein synthesis, uh, culture right? Takes lots of energy.

51:48 . And uh, energy obviously comes somewhere. Right? And so,

51:55 in order to do this. All . To get lots and lots and

51:58 of cells that of course, number , right. We know this from

52:03 four. Right? C H O P S. Right? We gotta

52:06 these components, particularly your carbon. , so, um so remember that

52:14 us. We get a two for deal with with our carbon service.

52:20 ? We get we get carbon we can put together to make molecules

52:26 we also get energy. That's not case for everything. Okay,

52:32 but it is for us. Uh so I can get I get two

52:36 from this, right? We'll get things. I get fat from

52:38 Okay, that's what I can get electrons from this. Right? Um

52:44 my energy ultimately will be my energy I can get my carbon from

52:49 Okay. Which I then converted to . And then you get this.

52:53 . Anyway, so, um so other thing is this is kind of

53:01 why there's somebody metabolism just remember obviously multiple things can be the carbon and

53:14 source. Okay, That's program. , but typically always the example.

53:22 ? Because um that that's the ancient with that back. Right. And

53:31 still have have held onto that. . It's one of the one of

53:36 many things that are similar to bacteria black policies. We both do it

53:40 much the same way. And so the point here is that,

53:44 know, chemical energy, Right? of course you can you can carry

53:49 by fire fire or light a bomb . Right. And but it's very

53:58 to capture all the energy in a . Okay. So that's why metabolism

54:05 has so many reactions, right? break down profits molecule. And then

54:12 certain stages we capture energy. It's that's more efficient than taking that

54:19 multi one. You can't just gonna a lot of heat. Right?

54:27 so life works at moderate traditions If you have the birth of energy

54:36 all this heat, the selling So, you have to do it

54:39 a way that in the current ambient . Right? And that's of

54:44 we don't talk about this here because learned it earlier. That's the beauty

54:48 enzymes, right? They operate at temperatures, right? They can carry

54:55 these right having to evolve. And which wouldn't work. And so and

55:06 yeah, all these reactions are catalyzed different insects. Right? But you

55:10 to you need to memorize what they . Okay, so, um so

55:17 we're focusing on 13 is how does happen? So we have capitalism of

55:25 complex food source, carbon sources Excuse me, go through different

55:33 Gonna capture some energy and ultimately makes of a T. P.

55:40 Okay. Uh not the soul. a certain energy molecules form but there's

55:48 types as well that we'll talk Okay. And when we form those

55:51 we can do stuff with. And so ultimately it's about, you

55:57 , really about making a DPS but are other molecules that are used.

56:02 in large part is those that dr protein synthesis, DNA replication. It's

56:09 . So, um okay, just the basics of metabolism.

56:15 So hetero tropes, right. That's we are. And so, um

56:21 does the energy come from in the ? Where the where? What's

56:37 Okay, so we're talking about a . So, say something like

56:44 Where the energy comes from in It's a good question, mark.

56:48 are you getting here? Mhm electrons how are you getting the electrons

56:56 I heard oxidation over there. Oxidizing after that oxidation is loss of electrons

57:03 you're gonna capture electrons. So where those electrons at in the molecule bonds

57:11 bonds. That's where it's coming So you break bonds. You have

57:15 like captures electrons carry electrons carry energy you can go somewhere with that to

57:22 you lots of a T. P . Okay, so it comes from

57:27 molecular bonds. Okay, so redox . Of course electrons redox reactions are

57:33 be what it's about. Whether it's it's metabolism, whether it's photo

57:39 Okay. Little trophy. It's all redox reactions. Right. Because if

57:44 capture energy through capture electrons, you're oxidizing molecules before oxidizing something. You're

57:53 at the same time reducing something. something you have Michael using electronic they

57:58 to be going somewhere and the one captures those molecules becomes reduced. So

58:03 going on all the time. so both are going to be a

58:07 of the process obviously. Okay, we differentiate respiration fermentation because both use

58:14 know, sugars for example. And and other things. But certainly

58:19 as we saw previously with passage or right we use he look at sugar

58:24 . Right. And so both of have that in common the source but

58:29 differ in terms of what you get terms of energy versus um the end

58:37 you get. Okay, So since fermentation by comparison is pretty simple.

58:43 , because you when you ferment the in this case glucose you do.

58:49 fermentation occurs in the act. so um but produce Michael's like this

58:59 um ethanol acetate things like formic acid ? Like C one C two,

59:07 three, C four alcohol passes. um so look at by comparison.

59:16 at respiration. Okay we go down take glucose for example and go all

59:23 way down and see the water. . So if we look at these

59:27 fuels compared to this, which has energy. One bigger one.

59:38 there's still a lot of energy left these molecules. There are bacteria that

59:42 take ethanol and eat it. Optimizes from bacteria that can use acid

59:47 Okay, so there's lots of energy in these molecules. Okay, that's

59:52 nature of fermentation. Okay. You go all the way down as far

59:57 you can go. Okay in terms product. So um the that's why

60:04 call fermentation and incomplete oxidation because reproducing that still can be further oxidized.

60:11 yeah, that's the improv a Respiration is a complete oxidation because you

60:18 do you can't break down ceo to further. Very stable. Okay?

60:26 and biologically you just don't do You can't do it. Okay.

60:31 you can do is sio two is build it up and used as a

60:35 block to make things like this Blue . You know that's what photosynthesis is

60:42 co two fixation. So that's a energy required process. Right? So

60:48 we're talking about metabolism releasing energy, ? And so um so uh in

60:56 gonna form these types of energy You do form energy over here.

61:00 course uniform 80 P only. Okay the quantity is much less. It's

61:07 like 10, 10 to 1 You form 10 times more a tps

61:12 respiration than you do in fermentation. . Um and then of course the

61:18 involves electric. There's a lot more and components to respiration and fermentation.

61:23 , so you have electron transport That's where you have molecules like oxygen

61:32 it can also create aerobically. I . Okay, so just because it's

61:41 , so we hear the term 02 probably fermentation but there's also respiration that

61:50 occur anatomically. Okay. And remember won't get you as much energy as

61:57 but it gets can get pretty darn . So anaerobic respiration is nothing to

62:01 at. It can be very effective terms of energy production. Okay.

62:07 in fact most most living things on are are microbes and most of those

62:13 either anaerobic or faculty demand of Okay, so they do quite well

62:19 without oxygen especially they can inspire. um and so great because I know

62:26 you're not just mostly gonna be about respiration. That's what you learn I

62:31 beginning in high school and then and on. So but anyway um so

62:37 molecules in the respiration that these are the end of the process.

62:43 These are molecule types that are super electron rabbit molecule's electron grabbers. They

62:55 we love becoming what we call oxidizing , powerful Oxidizing agents and oxidizing agents

63:02 grab electrons and then become the Okay, so that's why we have

63:09 at the very end is because a important part of this is called electron

63:16 . Best to say that until we to the right diagram. So just

63:20 of put that back your head. . So um now what we won't

63:25 about in this chapter? Although we're about this part of it. I'm

63:34 talking about photo the photo part So anything with a photo trophy.

63:41 hair trophy. Uh and little That's all gonna be chapter 14.

63:47 we're not gonna talk about it in context. I'm just bringing it up

63:50 it kind of fits fits here. . And then um as I said

63:55 , right, we know that sugars uh aromatic compounds can be used by

64:02 and archaea. So that's a unique . Right? So we look at

64:06 as well. Okay, um Okay, so again, we're talking

64:12 this in the next chapter. But your autotrophs. Right? So the

64:19 right, where this comes from either ? All right. If you're a

64:28 a photo type. Okay, if a little low well, I should

64:35 it this way. But the dash there with a type then you use

64:47 . Right? You oxidize inorganic iron, ammonia etcetera. Right?

64:55 light. Okay. That's the energy . Um so we'll focus on

65:02 And uh, oh, another week so. So now our focus is

65:09 really just uh, capitalism. So here's the first question or

65:17 The first one. Here's a question respiration. Okay. Okay. So

65:23 a shot at this one. So does have some specific requirements.

65:34 how's that? So respiration does not . Let's see. Mm hmm.

66:13 predict 95 success. That I was say failure. Have more faith in

66:23 than that. Okay. Let's count from three 21. Yeah, I

66:34 right. I was required. Okay. Um, yeah.

66:40 it may not be obvious. But it's obvious to you because pretty much

66:44 answer correctly is the membrane that they required. They're all hard, but

66:51 of them maybe not so obvious ones that. And this may be

66:57 Um, let's look at this All right. So, it's kind

67:04 again, one of these surprise. , oh, electron flow that was

67:12 earlier. So electron flow. this is very basic terms kind of

67:20 respiration is. This is what goes in you in your okay. And

67:26 of it outside the money Carney. nonetheless, um, you have a

67:31 where you are generating a proton Okay. That's really the crux of

67:38 whole thing. Okay. It's why are alive. Okay. Well,

67:46 kind of dramatic. It's, it's how you're alive. Okay.

67:51 you are sustaining a proton gradient because that is what generates your energy.

67:58 exclusively but pretty good. Part the chunk of it. Okay because remember

68:04 is a thing if we talk about three right? The old uh couple

68:10 energy releasing process with the energy required . And that's what essentially is going

68:15 here. Energy released as protons go . So there's a gradient right?

68:23 . Okay. And as they go the greatest and release energy, the

68:28 released to form A. T. . S. Right? So that

68:34 right is what we're trying to That's what's keeping you alive to be

68:40 . Okay. Um So um that's this is so important maintaining electron flow

68:49 in this case is going this Okay so we gotta keep keep that

68:56 , keep going. Keep so proton going and you keep producing A.

69:01 . P. S. Okay, keep that going. So um what

69:07 we need? How readouts reactions? . That's what fuels this whole

69:13 Okay so this this concept again. know I'm I'm laboring the point but

69:21 for a reason. See this time again in different ways, energy requiring

69:26 . Put those together. Okay so leaving out part of the explanation here

69:35 you don't know what A. And . Is. Alright so I'm gonna

69:38 that as part of the question coming in this one. Okay so um

69:47 me pause that. So we're inside E. Coli that can actually do

69:59 . So this e coli or an aspiring right location For 5:10 minutes.

70:15 you look at this circled area go that's that's telling me it's anaerobic

70:21 Okay. You're not sure thing about you're doing. You're aerobically inspiring.

70:38 would you where would you look to that out? Okay, counting down

71:00 10. Okay. 321. Yeah if you answered C.

71:21 Okay so Um let's answer the next real quick. Okay. Same

71:30 Same responses. Different questions were inside bacteria. This bacterium or little

71:37 Okay. Little trophy. Which location you look at to determine this?

71:45 . Okay. Same diagram. Um Location one. Yeah. Location

72:07 and 3. Right. So basically we're doing, that's how we maintain

72:13 right to have a source of electrons we need to have molecule that will

72:25 them terminal accept her. Okay. so if your aerobic anaerobic b.

72:35 . 2 could be N. And among other things there's other things

72:39 can be it's anaerobic. Right? eternal? Except er Right. That's

72:44 I mentioned that molecule is the one a super electron grabber. Right?

72:50 what we call has the highest reduction . We'll talk about that next

72:54 But oxygen has the highest reduction It draws electrons toward it.

73:01 And so you have that source though well. Okay. To be

73:06 If your like you coach this. , um uh, a little

73:16 Something irrigating iron or these two s happened? Right? So it's the

73:21 becomes oxidized those electrons. They're the of electrons are going to feed that

73:27 . Okay. But that's not enough now. I have to feed

73:32 You have to keep the flow right? Because that's what generates the

73:36 from those electron transfers here or what the energy to pump protons.

73:44 And so you need to have oxygen at the end. If you're a

73:47 or something like nitrate or similar. , trust me, you know,

73:54 , this is correct because if it's a robe, let's say I take

73:59 I have that truck here. Put plastic bag over your head, tie

74:03 off. All right, You do . You're eliminating your terminal except

74:08 see what happens then. Okay, all stops. All stops. No

74:15 protons get about eight minutes, eight . But then it's all right.

74:20 done. No more proton gradient. more. No amount of time flow

74:24 happening. No more proton gradient. . Okay, So trust me,

74:29 uh, that's what happens. So, it's about fueling fueling the

74:34 for electrons making sure you have flow a molecule at the end and that's

74:39 very powerful so called reducing agent and agent becomes uh reduced. Um,

74:46 keeps the flow going. So keep . That's the key. No matter

74:50 you're a real breathe, breathe what breathe and keep doing that.

74:54 then you'll make lots of this, ? So that is, I'm over

75:00 , so that's, that's a good to start. So have a good

75:05 and we'll see you on monday and

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