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00:05 All right. What is that? folks. Welcome. Let's uh

00:34 say sent this email out this So the same information you've been seeing

00:42 week biker quiz. Blackmore quiz opens africa passes. Okay. Um,

00:57 little cover, basically what we've been about since last week. So chapter

01:03 , Chapter 3, Part one mm . The three part 1 and chapter

01:11 how probably should get most of chapter , chapter three part one today.

01:18 And smart work. Do sunday turning are uploaded as you know, um

01:25 be uploaded again after today, but of course the for the first two

01:32 , but so the clock starts next . Okay. Um so the point

01:37 seeing now we're gonna will disappear. I guess Tuesday after last Tuesday once

01:43 next those begin loaded up because right the period just to see that they

01:50 is working in your secret points basically what the use of this is for

01:54 first couple of weeks. Okay, couple of things. The uh flipped

02:02 . So the class, um you the details of this illness, but

02:06 it really is, it's just your are the one preparing ahead of time

02:11 the for that particular material which in case, its natural growth growth growth

02:19 , growth media, um growth phases growth growth problems. So,

02:27 it's just one of the folders folder class folder and that will have um

02:36 video video, which covers that second parts uh this semester I put a

02:42 bit more into part one part. didn't videos from last semester so I

02:46 have an updated in terms of putting one thing content is the same,

02:51 just kind of spread out in one electorate and Like 15 minutes of another

02:56 . But it's all explained for Let's go to the end there isn't

03:00 a folder? Um The same Wonderful. I can just put them

03:05 there as well operative in there as . So it's all on one thing

03:09 you. Okay so I'm gonna do you know, however you do,

03:14 starting to read the book um what need for your coming here. I

03:18 read the relevant pages with Elektra video and take notes during the video

03:24 however you want to do it. your goal is to try to as

03:27 you can as best you can master material. Okay, so in

03:32 Oh a lot of thicker questions covering Chapter 4.1. Okay. And then

03:42 between, in between questions is you have slides that are kind of

03:46 Okay, that's kind of what to here is kind of what this

03:49 Blah Blah Blah. Some explanatory right? But it's heavily different questions

03:55 that material. To test your how did your study in battle in terms

04:01 trying to master that, that particular for that particular subject matter. Okay

04:08 that's what that's about. Um the again that's not until next thursday,

04:15 a week from today um let's see casa schedule. That's weird. Okay

04:24 so that opens next a week from . Okay. There were a week

04:32 tomorrow, so it wasn't until a away. Okay. But the schedule

04:37 opens a couple two weeks before the date. Okay. So the thing

04:44 just to make sure that you're registered casa, right? You have to

04:48 sure we are anyway, but if if you're not familiar with casa just

04:54 to the again everything's explained the Okay if you have any doubts,

04:58 but just go to the website and . I think you still have to

05:02 a finger stance and you have to in person. So the point is

05:05 all that done right soon arrived So you don't have any issues uh

05:12 for the exam because we have to it for a time, a time

05:16 , reserve a seat in order to the right, so uh over two

05:25 to you can sign up for Um I think that's all the administrative

05:32 . Any questions? Right? I think it's always if I'm not

05:39 like midnight so like at 12 AM Friday, is that right? Yeah

05:47 and furious. Um as I understand . So uh you know, I

05:56 it's like concert tickets in my you know first come first serve kind

06:01 thing. So um Okay so let's just briefly. So so again we're

06:15 uh Tuesday next Tuesday covering um which different. The structures of appropriate

06:23 Is it made of or the features functions etcetera? Um variations among different

06:32 types because no no one species is have all the different structures we're talking

06:39 be talking about but certainly they don't many of them but there's gonna be

06:43 variations. Some will have uh Granules or food storage Granules, other types

06:50 little inclusions. We call them somewhat house. Some won't. So there

06:55 be some variations of course. But uh we're gonna go through all of

07:00 out there. Okay. And so kind of didn't overview it at the

07:04 of last time and just kind of the bacterial cell or parks and then

07:08 go into some more, go into detail as we go through today and

07:13 . Um One thing to keep in back of your head the term violence

07:18 throughout last time. So those are features a a pathogenic microbe disease causing

07:26 would have that enables him to cause . I mentioned that friendly I pillai

07:35 . These are things that enable uh certainly non pathogens can have pillai and

07:44 through the pathogens without without those particular they don't cause disease. Like E

07:49 0157. Always mentioned this in the of Chipotle right implicated a bunch of

07:59 the task three. There's a number outbreaks wanted to usually it's like lettuce

08:03 of some sort that chipotle uses that's tainted with E. Coli 0157.

08:10 that the real X. Factor for among a number of rooms factors for

08:15 one. It's uh appropriately is important attachment to the intestinal wall.

08:22 Uh huh. Less mutants that cause of that particular. So um yeah

08:29 really hammer on this particularly in the quarter of the course in the context

08:34 clinical microbiology but it doesn't hurt to about putting the back of your head

08:42 . The uh okay so the one I bring this up again when I

08:47 I hear the term western chemical nature what's going on beyond that cytoplasmic membrane

08:56 having to see variations of what can out there. There's something that have

09:02 the gram negative gram positive. So so um there's something I don't

09:09 that smart variations of it. So but collectively we say what's the cell

09:15 looked like and positive. Looking at gram negative. Something that's right so

09:20 that's what that refers to. Okay um all right so real quick this

09:26 kind of this is for the coli not most of these values are gonna

09:32 similar for most other bacteria there will some variations but this is looking in

09:38 of components of bacterial cells. So the informational molecules D. N.

09:45 . R. N. A. proteins. Um Right so I'm just

09:50 collectively comprised about a quarter of uh cell into in terms of total

09:56 Wait okay now in terms of component see water right. One of the

10:02 gonna be the most abundant obviously. because in any living thing water makes

10:07 the most uh of the components. so but right after that would be

10:12 proteins already D. N. A because that's what does the work have

10:17 seller or the thousands of proteins it um cell envelope so there it can

10:24 comprise that these variations Variations in cell structure um other things rounding out so

10:34 5%. So of that 30 the water component. The last for many

10:42 are all kinds of organic inorganic calcium ions, potassium chloride et

10:51 Uh quality beans are molecules charged molecules different functions. Some buying two

10:57 N. A. Staying alive and other kind of self signaling functions.

11:04 But they are a common molecule in the and so we look at the

11:11 line um we can compare it to of caucus in the context of it's

11:20 of black cancer mature that makes up wall And for here it's any Colin

11:27 .8% of the cell wait staff has called gambits and more than twice as

11:35 as high as that. And why that be? Because staff is a

11:49 . Okay, now this stuff's on membrane structure. I'm not gonna spend

11:55 much time on because I had just before about the basic structure of

11:59 Right? The fluid mosaic model. fossil that could buy a layer that

12:05 of course is a universal uh type in all cells and bacteria are

12:12 But they do have um and you , again, it's also the by

12:18 fossil lipids, here's the core structures glycerol fatty acids are linked to it

12:24 uh bacteria. It's industrial vintages. . And then you handle phosphate as

12:32 of the structure and then some sort chemical group ahead group, it's

12:36 Okay, so basically fossil living And of course there's uh degree of

12:43 ability with water. Right? So have a hydrophobic portion fatty acids hydra

12:48 here to come together when the lipid layer. Okay, now it gives

12:52 membrane the functionality or the programs. ? Approximately 50 50 60 40 proteins

13:01 foster olympics. Okay, lots of as well gives the membranes function.

13:05 can be enzymes uh they can be type proteins uh make it on the

13:13 between cells a lot of different Okay, um now, what is

13:19 to appropriately membrane uh kind of analogous cholesterol in our membranes to kind of

13:26 uh get some integrity to the membrane it bacteria and other periods have popular

13:35 they're called similar in that steroid structure cholesterol is Okay, but popping noise

13:41 you need to prepare. It's kind but but serving the same function as

13:45 does in our brains. Okay. let's see. So looking at some

13:53 um let's say adaptations to certain You'll see some changes here in these

14:00 components. And archaea, archaea, of the files and some of those

14:06 be hyper thermal funds. Right? adaptions to uh high temperatures.

14:12 So either linkage, uh it is a little more stable than estrogen.

14:18 that serves you will see that in types in their membrane molecules. Uh

14:26 so therefore men are called had the of what's called a a turbine

14:32 Don't worry so much about it. they have a little bit different structure

14:37 than a fatty acid type fossil infrastructure these in these thermal filling types and

14:44 form uh So here's glycerol ether and will come together and form longer molecules

14:52 you see here. Okay. And can span 60 cars long in some

14:57 . Right. But the other thing noticing the structure they kind of they

15:01 packed together. Right. The hydrophobic occurring. Okay. Uh so you

15:09 up here in bacterial fossil lipids and acids. Very common that we

15:13 Right. And so you can have bonds to introduce a kink in the

15:19 . Right? Uh Not always whether system trans or just completely saturated.

15:27 saturated don't have double bonds on the saturated new uh bacteria and archaea can

15:34 the cyclic economy protein. This also to to kind of maintain the structure

15:42 the fox flip it and keep it of the strength. So it's kind

15:46 plain water molecule. The cycle program helps keep the change straight.

15:52 And so you can imagine you can configurations of these fatty acids where some

15:58 very straight, right? And packed ? And the demographic proportion of those

16:04 are right? Like the like the you see here the unsaturated and that

16:12 structurally changes the member. So the thing here is um and then in

16:21 want to be psychic structures as well . But the key here is uh

16:29 . So maintaining an optimal pork um lipids types like saturated chain unsaturated.

16:43 . Somebody had a little kink in ability to adjust the membrane if you

16:47 . Okay, the membrane fluidity. remembers the psychopathic membrane that keeps everything

16:53 . Right? Uh Foster lipids give that selective permeability. Right. Someone

17:01 , proteins you have more functions, ? That they will have specific

17:07 That Okay, But it's all about the membrane and optimal fluidity.

17:15 To make proteins happy and to not stuff just leave them to reach out

17:20 begin. Right? And all of all about getting a proportion ratio of

17:28 to unsaturated fatty acids in the bacterial . Okay. Now, what is

17:37 Kia down here, we're specifically talking these high temperature lines that we're having

17:41 very long uh ether molecules. They increase the length to make them longer

17:50 you have more hydrophobic interactions. And so this is all about annotation

17:56 . Yeah, higher temperature. But too, bacteria can be thermal files

18:02 they could be subject to the the of the right where they live,

18:07 ? Where temperatures can can flush. ? And so in response to

18:13 they'll adjust their membrane components ratios of um saturated unsaturated molecules all to keep

18:21 membrane happy and functioning, right? membrane is not just possible. It's

18:26 appropriate for everybody that has to be Okay. And so that's what this

18:31 is meant to address here. so here's the code of life.

18:36 uh it's also called rose it between and 39 740 Um optimal territory.

18:47 Here we're going at 32. Uh so it looks like that at

18:53 . Okay. And then you see proportion of saturated unsaturated there. You

18:59 to 42. You're cranking up the . Yeah. Um And so

19:04 You called me remember and will adjust that. Okay. And so what

19:09 it look like throwing the adjustment? the most likely scenario? What what

19:13 it will do? In other we're gonna be a higher or lower

19:17 from saturated fatty acids. Ok. remember what what elevated temp will

19:23 Right, kinetic energy. Right. interesting got that real quick. Um

19:36 , again, it's all about keeping membrane happy, not letting stuff week

19:39 and week out. Right. And you know, just in the reporting

19:45 saturated unsaturated. Okay, So when gets hot, Okay, It's what

19:51 want to do one. Yeah. . So, remember that human,

20:02 at 32° here. Okay, then elevated temperature, the membrane will will

20:12 to come apart, like kinetic energy bouncing around. So it's going to

20:19 to do something to adjust and counteract . Okay, so uh let's see

20:26 we got. Okay. Oops. . Alright. Who chose?

20:37 Yes. Why don't you do Because I feel like when he it's

20:45 . Right? So you do So what was it going to?

20:52 need to have because changed to have spacing in between or you want

21:03 Yes. You want your answer is . It's hey, Okay, So

21:11 , this happens every single time. , so membrane is at 032.

21:18 it gets hot, these things are wanna we're gonna win a space.

21:25 tends to go that way. Because so you you gotta you want

21:29 those changes to straighten out because that's interactions that keep them together.

21:36 because temperatures to do this. Right stuff. Right. So it increased

21:46 proportion of saturated, like what's happening a Okay to keep that membrane

21:54 Right for the little front here here 42. Okay, getting hotter,

22:06 coming apart. Let's get it back , increase the level of saturation.

22:12 that's what increases the hydrophobic actions between change this. You'll have some of

22:20 . It's always a report. But you should it should have more

22:25 this, right? Because that's what keep it together. The elevated

22:33 If you're creating more of this at temp stuff coming in going out.

22:41 , I can't control it very So increased saturation. Well, hard

22:47 maintain that number now. What would want to to be be can happen

22:52 what conditions? Oh we're going once going down there freezing temperatures. Right

23:00 the absence occurred. Right then you actually freeze And so you want to

23:05 that by putting a few more cakes your chains unsaturated more. Okay,

23:11 about this. All of that. second thoughts, it's possibly changing.

23:16 , that's little bit it happens to extremes, you know, even what's

23:21 on like from 31 to 33 to and then saturates non saturation.

23:28 It's never really all just one of other of course, unless it's a

23:33 period of certain temple. Okay. many questions about that. Yeah.

23:41 ahead. Yeah. They always always reactions and they have they can synthesize

23:50 popular without the bonds. So you have, they grow so fast.

23:56 can bring us about fairly quickly. carry it so it's actually computed to

24:07 too. But they do but you ask the variety of things and not

24:12 not just introducing and but also increasing decreasing also affected. So that can

24:22 is what that's another thing. What multiple things going on increasing and

24:29 Not all influences. I will then hold together but not so much.

24:36 somebody else. Yeah the saturated was lacking double bonds so century ones are

24:46 ones that strength unsaturated have the beds trans. Uh This is this is

24:55 mailbox creating the spacing. Okay go . Is this particular change in saturated

25:04 unsaturated presence? Only change would like availability also triggered something like this.

25:15 Yeah question I'm gonna say it could other than temperature. So things like

25:21 concentrations can affect can affect can affect . So I'm sure there'll be some

25:26 of counteraction to that as well. yeah other things that can um affected

25:32 of the temperature for sure. But things like that uh that would change

25:39 charge on some of the polar groups can have an influence. So yeah

25:42 would I would say thank you not . Sure. Yeah. Yeah.

25:48 you say that the cholesterol or the noise also helps. Yeah they

25:54 They certainly contribute to that. They're gonna obviously being very hydrophobic. They're

25:59 help to pack those uh saturated fatty together as well. So certainly contribute

26:05 other. Yes. Yes. It will be a little bit of

26:14 defeated the more for me than a the patriot here as you get

26:19 Okay. Um yeah. And you , this isn't just unique to procure

26:26 either. I mean, if you yourself. Dude, this is

26:31 Any questions? Okay, So here's question. Just kind of meant to

26:38 a few birds at one stone here terms of concepts. Okay, so

26:44 aquatic bacteria maintains an intracellular sodium iron of 0.1 millimeter. You see the

26:51 drawn there inside the pond Uh pond sodium ions of .05 million Mueller.

27:00 . So substantially less. So evidently miners are entering the cell by mm

27:08 . But Okay. So this is of the again, um career itself

27:15 you know, any microbes, protozoa . How do you have in their

27:20 environment? I decided to, you , all kinds of conditions. Physical

27:27 um capture. No, of Other adjustments are made to to maintain

27:35 salvage concentrations. Okay. Because that fluctuate as well. Oh, mm

27:52 . Yeah. Okay. See um picked B. You're No, you're

28:27 . Why isn't active transport? The outside the diffusion requires some energy.

28:43 . Exactly. So it's all about this the concentration gradient, Right.

28:50 molecules diffuse freely without energy when they down the controversial. The tendency as

28:59 drawn here, the tendency is would for set your mind to go this

29:04 . Okay. But it's not it's that's because that's high low. So

29:08 but they're actually the seller is holding to them okay, are taking them

29:12 , in fact. Okay. And um and that's an important thing because

29:19 , it could be set up with the selling to selling needs to set

29:22 sets of braids are all passive, ? Or they would come in and

29:27 doesn't work out. Okay. So coming passively some don't don't have to

29:33 active transport. Okay. Um The so again the concentration breaking.

29:41 And so um making a concentration It is an important thing for all

29:47 . Okay. Um the probably I'm you've gone through the whole actual potential

29:55 neurons and uh sort of a Right? That's all about concentration

30:01 Okay. And uh that those gradients about the generation of action potential.

30:09 ? And so um so a concentration can serve as a form of potential

30:17 . That's so can do something. . And they do as well.

30:21 , Okay, so this transporter system is active transport because we're we're pushing

30:28 up to the gradient, we're trying stuff it in to an area that

30:32 is high in sodium mines. And that's gonna take energy.

30:37 So it's like we have a was brilliant. Dave reference anybody know where

30:43 phone booth is. Okay. So it was weird to be a thing

30:49 the 50s uh like a college prank . I got stuff everybody in a

30:54 booth. Don't ask me why. so imagine a phone with a full

30:57 people trying to put more in. right. It's gonna take a lot

31:00 energy to do that. Okay, are going the other way.

31:03 so um anyway, so when we at transport of molecules, simple

31:10 So simple versus facilitated is basically um movement is down gradient, so it

31:17 require energy. Okay. In remember that a passive process, even

31:23 it doesn't require energy to move the and in fact will release energy.

31:31 . As a result, so things so the difference here is the obvious

31:36 . Things require help getting in to the membrane and some don't.

31:41 and it's all about the chemical nature the module, is it? How

31:46 polar or non polar isn't? So things like gasses, oxygen

31:51 02. These things pretty much freely across the membrane watermarks. Modern molecules

31:58 actually diffuse, although under stress of stress so many too rapidly. Water

32:08 and it will have specific transport proteins it, but generally not as

32:13 but water monsters do pass across from freely because they're small, even though

32:18 are of course polar, they're small to do that. But things that

32:22 larger are more polar. Don't I'm getting through that hydrophobic membrane

32:29 Okay so they need help. That's facilitated transport is. So both of

32:32 processes the movement of the molecule is the gradient. Okay. The and

32:40 osmosis is reserved for a while. . So in terms of hyper tonic

32:46 time. Right? So these are correlate each other. So if a

32:54 is in hyper tonic solution surrounding the it's hyper tonic then obviously inside its

33:03 . Right H. Y. O. Right. And vice

33:06 Right. It's a hippo tonic solution you can assume inside the cell of

33:12 climb. So that's how they relate each other. So the key with

33:15 is that that water flow to the of high salt. Okay so a

33:23 viable bacteria and archaea that like to in super high salt. Water.

33:30 . 25% salt around them. Those are constantly fighting loss of what?

33:40 . And of course they've evolved adaptations counteract that because they do problem these

33:46 uh assault missions which of course is hyper tonic around them. Okay so

33:52 moves to the high salute side. . Um And so the terms also

34:00 porn's that's that specific transport that moves . Okay. Water constantly moves.

34:07 . But when it's a situation where did a rapid movement because of solar

34:11 stress then aqua porn's or formed in membrane bringing about much quicker movement.

34:18 So hyper tonic celery puree that refers is bacteria tend to uh maintain a

34:28 tonic interior. Okay. Which means hyper tonic security. Okay. Which

34:35 having slightly higher salt concentration inside hyper relative to the outside. Okay.

34:42 the reason for that is that the of water helps to maintain cell shape

34:48 . Okay. That combined with a a cell wall. Okay. Um

34:55 to help keep the shape of the . Okay. And integrity of the

34:59 mentioning again here in a second. uh but bacteria tend to do

35:04 Keep themselves slightly hyper tonic. The I upgraded so we just mentioned

35:11 ingredients are sources of potential energy. . And it's you learn anything

35:18 Is that bacteria? Our efficient. . Um And one of the ways

35:27 to whatever wherever they can conserve energy fact. And here's what mechanism where

35:34 can use an ion gradient to help do work for you in other

35:39 Right? So among bacteria and our is used to help movements for jell

35:46 to transport other molecules. Okay so is a source of energy to do

35:52 things. Okay. Not just make teepee which we'll learn. That's one

35:56 the main functions. We'll talk about next unit. But it has a

36:00 of other uses uh ion gradient in a proton gradient. Okay. Very

36:07 . Okay. And so what happens this is active transport. So you're

36:12 energy from being idolized from a So energy released from that is used

36:18 pump protons out. Right? So you've created a gradient and this out

36:26 represents a form of potential energy. can do something with that and create

36:31 with that. Right? Um That um Sorry. Um Okay. The

36:45 if they move down the gradient right other way, don't bring these

36:50 You can use a couple that with requirement processes. Right? And in

36:54 example it's sucrose transport. Okay, here's sucrose low outside, high inside

37:03 source. And as it does as come back across the cell membrane into

37:12 cell energy release. Can be used bring the sucrose in. Alright.

37:17 efficient than just having protocols popped out energy and then very consumed. Close

37:24 an extended https at the transport. eliminate that. And just use the

37:30 from the proton gradient to bring it . Okay. And so this is

37:35 called a Yeah, molecules going in same direction. We call that sim

37:42 . Okay. If they were going sucrose was going the other way,

37:48 would be anti porn. Just the of her growing up. Same work

37:53 . Okay. But he had a here that you have energy releasing process

37:58 being used to bread energy requiring process the harnessing that to bring it in

38:04 this case to close but just as foreshadowing. Right. Chapter Unit

38:13 When we talk about metabolism, uh talked heavily about a couple of energy

38:19 processes with energy required process occurs all time. Right? In one example

38:28 and proton gradients are used a lot do this kind of work.

38:34 Um Alright, so a couple of of transporters abc and translocation translocation in

38:42 is very common. And so is transporters among makarios. Um so abc

38:50 have a specific molecule lips that binds on you. Okay. And that's

38:57 binding protein is specific for its particular carrying protein if you will, which

39:03 this portion. So they fit together saw you too specific for that particular

39:10 . And you have abc transporters for acids, different sugars, et

39:16 Um uh and again, we're looking an active transport process here. Um

39:22 transportation. So this is a way again, uh molecules in without having

39:29 spend energy. Okay. And what relies on is the fact that molecules

39:36 independent of each other. Okay, uh same kind of mechanism to different

39:42 . So glucose um binds to the and comes in But it's immediately

39:51 Okay, In this case the glucose phosphate. Okay, so the um

39:59 it weren't modified. Right? In words just came as glucose. And

40:02 stayed in the glucose inside itself. even if it were high on the

40:08 , low on the inside. So you had Uh 10 outside and

40:14 . Right. And but the glucose became modified, saved glucose when it

40:18 in then coming in until what five five is using that example. And

40:26 that we know further that change going . But because of being modified

40:30 six phosphate, it keeps coming in long as it happened. Okay.

40:35 uh smart way you're doing the same with mannitol. Same principle.

40:39 So uh very common in terms of transport bacteria. This kind of

40:46 Okay? Um Okay then membrane permanent acid basis. So this is more

40:55 what can be an issue for. we go. Okay. Um So

41:02 acid, weak bases. So this be like acetic acid perhaps.

41:07 So remember that these are only partially dissolved. Okay. And the uh

41:20 we see it's kind of too generic on the left is the weak

41:24 The other one is a weak So in contrast to a strong acid

41:28 hcl um goes all to nothing but and chloride ions. Right? There's

41:39 there's no H C. L. this form left in solutions. All

41:44 in florida. That's a major a acid. Okay. But it only

41:49 associates if it's a weak acid or . Right? So you're always gonna

41:53 You'll have all three species present in solution or all of these presents

42:00 Okay. And so what happens is neutral form which is the weak acid

42:09 . That's the point of that small , small science, they can diffuse

42:14 the membrane then on the other side they can associate that's where your changes

42:22 sell Okay. Whether acidic or Okay. And uh so these are

42:29 that bacteria have to counteract right, the ph gets to hire loans internally

42:35 because that can affect protein function and get your mount to the set and

42:41 we will have things like buffers and primary buffering and most of them think

42:47 cells are medium assets act as buffers counteract the ph ph change. Um

42:54 so, you know, that's surprisingly what this can create is what's called

42:59 we'll talk about this in Chapter What's called a bacterial static effect,

43:04 growth. Right, so a lot your food preservatives are actually this kind

43:11 gasses with bases like citric acid is common. Different foods and it helps

43:16 um uh cataract spoilage food, uh para amino benzoate acid pama.

43:24 see that a lot of different foods this effective, you know, him

43:29 growth. So um now, any questions at this point?

43:40 Through typically through buffers but in living cells buffers for us are typically amino

43:47 and so that's how they kind of the nudity. Huh? The acidity

43:52 it gets too basic. Yeah, weak acid. Yeah. In

44:04 That's correct. Right. Right. could be like ammonia mine or something

44:08 that. Yeah. Right. Um . The so here on out it's

44:16 cell wall or sell so just take stab at this now. This is

44:24 gonna I'm not gonna mention the I just want you to kind of

44:29 let me just redo that whole so I just just answer the best

44:34 your ability. Okay. That will on. It will reappear again.

44:40 , down the brother will look good we'll answer it again. Right.

44:51 , we'll touch on all of these this next section. Lab stuff.

45:21 stuff. I have to keep checking the disaster happened. I haven't Everything's

45:27 . Nothing blew up. Okay. right, let me count down the

45:35 10 nine eight yeah. 65 for . Okay, deep. So f

45:55 was the consensus remember that have 26% that. All right, let's move

46:03 . Uh Okay. Alright. There's different variations that we'll see.

46:10 may not even have a cell wall all. Okay. Many do So

46:15 you look at bacteria versus archaea with Kia really have to sell water

46:22 It's more kind of 50 50 50 60 40 amount archeo species with bacterial

46:31 . It's moreover, I think. been been dumped. Okay. And

46:36 that have kept of light hands can grand positive and negative and can be

46:41 things as well. See Okay the that don't have a cell wall all

46:46 similar small. I think it's only general problem of bacteria that actually have

46:52 have a cell wall. Um So so so all the s layer will

46:59 mention the outer membrane that we see gram negatives. Uh Micro bacteria are

47:04 ones that have cut the light hand they actually have a lot more other

47:08 that make up their envelope. And we'll see the nature of the

47:14 cell envelope. They have effects in of how they grow, how they

47:20 on a on a plate for Um But you know two terms because

47:25 actually might see this on one of professional terms. Okay firm acute and

47:31 bacteria. Okay and so um these of gram stain. So grandpa zits

47:39 locked into the group called. It's taxonomic group. Okay uh So so

47:46 staphylococcus is a classic grand closet. grand negatives are lumped into the program

47:52 which is pretty varied. Okay. Not that similar. You know the

47:59 grand seriously staph and bacillus or not similar but nonetheless they have the same

48:06 reaction. Okay so why the big the big deal about grandpa and gram

48:10 because this was staying that's been around 1910 or 05 or something like that

48:18 it still has utility to this I mean it's how you you

48:22 in terms of identification, it's how kind of broadly group split bacteria into

48:29 groups. But again, it's a that number that don't stand with this

48:34 . But it is it can be point of where you begin in terms

48:37 identification. Okay, diagnostically it can the important um if you have a

48:47 had a script and script throat and it um you look for grand positive

48:54 peroxide enchantments. Okay. Um stds gonorrhea diplo cox it like little bees

49:05 . Okay. Um if you have same kind of in cerebrospinal fluid.

49:14 , that's meningitis. Typical. so there are certain uh for certain

49:19 diseases that can be diagnostic uh to the grandstanding morphology and depending on where

49:25 sample and the patients coming from, that can give you a pretty idea

49:28 what it maybe you're dealing with. . But nonetheless, so uh the

49:35 wall in general of course, is , I don't think of it as

49:41 a brick wall in the movie because not it's it's flexible. Okay.

49:47 it certainly does provide integrity to the protection, but it is it is

49:51 porous. Okay, you have the to kind of the two. Um

49:58 kind of the selected barrier of the . Not not the cell wall so

50:02 correct, but um Okay, So we have kind of analogous to

50:10 D. N. A. Right talk about the sugar, phosphate

50:14 Right? And everything the type of of past. So this is a

50:20 backbone of the glucosamine. And moronic dc. There. Okay. And

50:28 are linkages in between uh what we cross bridges. Okay, so the

50:34 pepper look like, can it kind gives it away? It's part protein

50:37 part sugar. Okay. Probably mostly . But there are the linkages are

50:44 linkages. Okay now uh so this obviously this would be a so we'll

50:53 like around a rod shaped cells can curly or something. Okay synthesized as

51:00 continuous strand. Okay, around the . And um but again back to

51:07 osmotic pressure. Right? So it to keep itself um slightly hyper tonic

51:13 comes in and then it presses that against the cell wall. Alright,

51:17 that's so collectively this all helps to the shape of the center.

51:22 maintain the shape of the cell so structurally. Okay, the linkages.

51:30 , so the amino acids you see uh Alani glycemic acid, di amino

51:39 unique is a little bit different amino . It's not like one of the

51:42 20 amino acids. You only see in this Pepsi with left hand structure

51:47 it can vary this this these amino in this peptide can vary from species

51:52 species. There's some that have all same in terms of their in their

51:58 amino acids. But it can vary . But this is this is a

52:02 common sequence but there can be The linkage here you see between the

52:09 acid Okay, residues are coming together link up. Okay. And so

52:16 occurs like this at the Alan nine ? But then the terminal align the

52:22 one exits. Right. It gets off. Now you have the complete

52:27 bridge. Okay so the the cross is important. So you see the

52:33 up here again. So you have sugars coral and bonded together. So

52:40 then the cross bridges and that's critically . Without those cross bridges you lose

52:47 becomes too flexible. And so the remember the psychopathic membranes underneath there.

52:54 so we will begin to bulge Okay and can gradually lice and that's

53:00 effect of interfering with the cross Okay. And that's what the number

53:06 an inbox do penicillin, methicillin, interfere with different aspects of of the

53:13 wall synthesis. Right? Kind of acts on on the cross bridging specifically

53:18 cross bridging. And so the cell bulges through and license and the cell

53:23 . Okay. Um Vanco Myerson has little bit different action. It's um

53:32 it will bind to reality by into terminal Mallonee. Okay so it will

53:39 in here. Okay V for my my son by their. And now

53:48 enzyme that brings about the cross vision buy. Right? So they can

53:52 cross version that way. Okay. , of course we're all familiar with

53:58 bacteria that are resistant to these So with penicillin is basically buys penicillin

54:05 break to the park destroyed. That's what does Vancouver business is a

54:12 different. So bacteria that are resistant that will. So basically, we're

54:19 showing you how Bank of my son . What would be probably obvious logical

54:23 as to what a resistant type might like. But what what would it

54:28 ? So and again, right with there and resistant types obviously don't.

54:36 has no effect on them. And they have a mutation that does

54:41 Okay, doesn't destroy banker Myerson. does something else. Any idea.

54:50 hmm. The landing site by doing ? Yeah. Right. So we

54:59 a mutation that would put a different sitting down. I think I've read

55:06 uh they accepted lactic acid has been to intensive alley. So the bank

55:11 doesn't recognize that. And so I no effect on it. Um and

55:17 binding still occurs because it's it's it's the terminal it's it's the link.

55:23 sorry. The bonding occurs here at molecule before this terminal one.

55:30 But there are molecules that can be there that will allow itself to make

55:35 wall but not but be have no with the bank bank of mine is

55:39 . Okay. And And so like said, there's a there's a bunch

55:43 different antibiotics that had this as a . So there's there's multiple enzymes involved

55:49 synthesizing. So wall and those are potential targets, right? Because uh

55:55 I'm obviously live antibiotics and found them that work on different aspects of brain

56:01 wall synthesis. But of course it's war between them and us right to

56:05 evolve. And uh and so we not only try to look for new

56:10 , but that's that list is getting but but to chemically modify what we

56:16 have to hopefully have a little bit the bacteria cannot yet respond to

56:23 Okay. Yeah. Work mm Well, it's all about so there

56:30 be like any, you know uh all Koreans would be involved. There

56:36 be in the population education already That be able to counteract. There's kind

56:42 many four basic ways of resistance. either a galaxy and then sign that

56:51 just totally destroy the enzyme altogether. is alter the target, which is

56:57 the resistance resistance to Bank of that alternative target. Another way is

57:03 uh invitation in a existing transport pump then is specific from the antibiotic and

57:11 it out. Okay, that's another . So, um so first in

57:18 important. Mhm. I figure out that time. Well, number

57:28 because they grow so fast. that's that's what evolution is all

57:32 Like you can grow fast and produce quickly lost and then you can you

57:37 get the potential is there? But but again it's not the The antibiotic

57:44 is not creating change okay because in competition is already you know knowing how

57:51 bacteria grow, giving a single you know 1% of them we signed

57:56 different genetic or just becomes spontaneous mutation it grows back. Right? So

58:01 that sub population maybe something that's already a variation that makes it resistant.

58:07 that's where it starts. That's withdraw . Right? And so um so

58:13 when if that member is that say one cell is resistant in that population

58:20 it will preferentially grow prepared to its mental population. And then that's how

58:26 takes hold. Yeah that's the important is making is that. And understandably

58:32 saying ok well it's the antibiotic or . That's that is the thing causing

58:37 not right that the presence of them who's not listening to grow more that's

58:43 that's what that's the concept. Questions exactly. So so it's when

58:51 were used haphazardly right that they're out and now because there there are those

58:57 are resistant we'll grow more. Alright then you can spread that to

59:04 Um Okay so synthesis of pepper like okay here with me and so we're

59:12 talk about M. R. B. In the part two of

59:15 material. It's kind of what's it's the equivalent of a bacterial side of

59:21 . So you know in ourselves we a very extensive side of skeletons.

59:25 , properly going through ourselves the bacteria have a set of skeleton not as

59:33 or complex as ours. One of components of that is involved in cell

59:40 synthesis. And there's a differentiation between shaped cells and round of toxoid

59:48 Okay but this part of it is same right? This part of the

59:53 is the same. What's different? this part? Okay and in a

59:57 shaped cell? Okay. It'll have M. R. E.

60:02 Baylor skeletal element throughout the length of cell. And on each of the

60:09 that's kind of a scaffold where the the soul since it's making parts are

60:13 top of it guiding it. And so petra glycogen is synthesized as

60:20 strand, continuous strand. Okay and it will in a rod shaped cell

60:26 form from different starting points along the of skeleton and then connect up uh

60:33 a circular set sell similar thing but only one one scaffold if you will

60:40 set of skeletal development in the middle the cell around which the sentences

60:45 Okay um The uh So here you kind of some different examples rod shaped

60:52 ah circular cell. Uh Then you some of our called that that differentiate

61:00 terms of Synthesis occurring at one pole the other. Okay as in these

61:06 , you see it occurring here um and that type of soul. Since

61:11 leads to the cells that kind of these non uniform morphology is kind of

61:18 or somewhat um uniform morphology is just the way they grow more and one

61:24 in the other. It kind of them some weird shapes and things.

61:26 talk more about that next time but there are some variations. But the

61:32 the thing is is that when when cell wall synthesis broken? The most

61:40 most active? Most of it's going during when? Yes, so direct

61:49 between cell grows and the degree of . Uh So synthesis. Okay.

61:58 bacteria Yeah they grow like crazy but aren't there aren't necessarily always growing like

62:03 . Okay and so the level of synthesis correlates to how fast it

62:09 Exactly so little or none. If just kind of states that are doing

62:12 . Not growing at all to high the third exponential growth. Keep that

62:19 the back of your head. We'll to a clicker question coming up.

62:24 so cell wall synthesis versus growth. um Okay so there's your classic gram

62:32 gram positive. Okay grandpa sails of , forgot gram negative pink.

62:38 Alright so side by side is actually obvious in terms of Yeah but they're

62:45 different, different looking. Okay so with the get your brains uh and

62:55 really differentiate that. So, in grand negative, there's multiple layers.

63:00 ? So we intend to use the but but they're the same thing when

63:04 get a possible negative. It's the . Okay, the deposit doesn't have

63:10 those layers. Right? It has cell membrane. Dennis has a

63:13 Alright. Uh as we see so, here's the Grand positive.

63:18 ? Very thick peptidoglycan. Tycho acids kind of like and if you're familiar

63:25 the construction, but rebar it's like and cement, right, helps reinforce

63:30 cement. This helps reinforce the electric hand cell wall having these strands of

63:37 gasses going through them. Okay. beyond that, you have a gram

63:43 negative. There's not there's really not else for grandpa. That's it.

63:48 negative is more complex to see the of peptidoglycan is much less. All

63:54 . But you do have a an , that kind of curve in

63:58 Okay. Um talk more about that . The gram negative has um the

64:07 bits sell law connected to an outer through these little proteins. You see

64:17 ? Um And so the um I remember the outer membrane of course is

64:25 lipid nature. Right? What they LPS lippo policy Sacha. Right,

64:30 this is a carbohydrate. These long , there's of course a lipid

64:36 as they say, Liberal Party Saccharine . Right. Um obviously much different

64:42 the grand positive. Okay the of they're gonna be in the outer

64:49 There'll be proteins that help bring solute in like it's pouring. Okay,

64:56 also notice that in the outer membrane halves of the other membrane so this

65:06 this you can look much different. the two halves of the er membrane

65:12 different because the other half calves molecules don't see on the internet, like

65:16 big part of the GOP s lay here. Okay um so look just

65:25 on the Grand positive for a I really don't think that's the last

65:31 as much to it as there is . So type of assets don't need

65:36 worry about the structure of the Taiko . I just put it in there

65:39 to show you what these things look . But again they span the wind

65:45 you will on the wall and I to help reinforce it because there is

65:50 could be several layers of this so kind of need some help along with

65:53 cross bridging the S layer is um issue with studying the escalator is cells

66:04 are in culture on a plate tend lose it after a while.

66:10 it's kind of like a neck of covering the cell. Um poorest but

66:19 is some evidence to suggest it may sunday and adhesion for some selves adhering

66:26 the surface or other selves and may some role in virulence factor.

66:33 it's kind of some evidence but but because the complication of consistently studying because

66:41 loses in culture has been kind of . But they certainly have got an

66:46 ray group electron micro graphs of what looks like if you see here.

66:50 there is some evidence to suggest that species that have these that there may

66:55 some features like adherence violence in some . It's sad. Okay. Um

67:02 for the gram positive, that's it's it's it's it's hallmark. It's that

67:07 peptidoglycan layer and the presence of those colic acids. Those aren't in gram

67:12 gram negative. Don't have psychotic Okay. Because they have a very

67:17 type of like hand layer, they need it. Okay. And so

67:23 the really the focus for the gram is in that outer membrane.

67:29 so because that extra layer we basically the space between the two members in

67:36 out. We call it the plasma . Okay, on the outer membrane

67:43 got this complex of sugars and This LPS layer um it's long repeating

67:52 chain called the old policy Sacha ride underneath it uh this lipid a

68:00 Okay, so this this is really characterizes that LPS we call it.

68:08 . Um the the outer membrane can pose some issues in terms of what

68:18 come in. Right? So antibiotics have when you test antibiotics or any

68:24 kind of chemical agent. Disaffected, have you. You always test gram

68:30 gram negative because they're gonna behave And it has to do with that

68:34 membrane will be resistant to certain types antibiotics coming in. Certain chemicals coming

68:39 . Okay. Where there will be susceptible as a grand positive.

68:45 Um and penicillin is one of those it doesn't easily get into the gram

68:51 . So they tend not to be susceptible to them as as a grand

68:55 would be uh you have to use types of antibiotics. Um Program

69:01 Typically the okay so again inside a thin layer of black man. Do

69:11 have this cross linking here? There's a pep type and then you

69:17 the little protein. So this is unique to the gram negative. You

69:23 see the liberal protein on the gram . Right? It's it's a mechanism

69:26 help hold it hold itself all in in the gram negative. Okay um

69:34 so let me I'm gonna come back that. No you're not. I'm

69:38 do it now. Okay so this Uh huh. It brings about a

69:45 x one of the features of the name. The point of this.

69:49 so the patient has septicemia infection which it's that's a bad infection when it's

69:55 . It's in the blood travels about bodies in the blood. A couple

70:04 the patient experiences fever and neurology and prime accident which inhibits cell wall

70:12 It was provided to stop the infection worst. However, it only works

70:18 a few hours because the symptoms continued . Mhm. Additional testing confirmed that

70:24 Prime maximum was effective. So it well. Did anybody initially work?

70:28 then it didn't work to confirm that didn't work by testing in culture and

70:37 uh but when he had a different I play mixing B then the patient

70:42 . Uh huh. So the key is a couple of things Grand negative

70:51 the scenic and um the fact that pilot mixing work because plenty mixing combines

71:07 has an end endo toxin. so a thing with the gram negative

71:13 the endo toxin effect and that's part the grand negative outer membrane.

71:19 so the club's yellow venogram negative was to prime action but the Prime axinn

71:26 it. Alright then we're supposed Right? But including the sell it

71:32 the cell. Right. I mean of sell basically everything comes out and

71:36 apart. All right. It's a of stuff that falls apart from the

71:40 negative. Is that how the window released? Alright. And supply mix

71:47 be actually combine that and that's what the effect. So the antitoxin is

71:53 of the LPS player specifically this lipid material. Okay, right here and

72:01 only released when they sell license and you release endo toxin and well,

72:07 does that? No toxic effect? , and the toxic effect over stimulates

72:12 immune system. The immune system detects and goes, oh this is this

72:17 an infectious agent. We need to what we do when we have this

72:21 of inflammatory response was don't worry don't worry about so much.

72:25 we'll talk about it in uniform. the bottom line is over all of

72:31 new system and but it's only really worst danger. That's why I said

72:37 was a key because this effect is its worst when it's traveling throughout the

72:43 kill it 20 agents stuff and release toxin, then it can travel throughout

72:49 whole mind and all your immune Selves can theoretically respond to it.

72:54 that body wide effect is too You typically go into shock and canned

72:59 can be fatal. If the infection localized, right, then this effect

73:06 as dangerous not to worry about that . Right? Like that cut on

73:10 finger or whatever. Right? And it remains a localized infection. But

73:14 it gets set to see nick and , then already themselves can be ready

73:20 respond to it and that's too You can't handle it. Okay.

73:25 , so grand, native infections are have to be aware of those in

73:30 context of endo toxin. But really aware of it when if it

73:33 septicemia gets because of local infection can something travels from that area and gets

73:40 your blood. Okay then it's then super dangerous. Okay, so lipid

73:45 material so there's there's a structure to . So you can see the um

73:51 sugar linkage here here. To the policy, correct? Okay, so

73:58 use the term. Oh and For example, he called i.

74:03 . n 57. So later on talk next time about eight engines.

74:10 the problem. So there is a . Um and and so to blame

74:19 40 years ago we realized that this could those are the immune response.

74:26 we've we've come up with ways to genealogical tests to identify it right to

74:32 antibodies to particular o antigens and use to identify certain bacterial types.

74:38 Owen H engines are really sounds like coli is your salmon villas and closely

74:45 types, your enteric bacteria. And used it as a way to identify

74:51 uh an infectious agent in in these using the O. And H.

74:57 . Yeah, the ferocity of the membrane is porous but there certainly are

75:03 specific protein transport proteins in there to allow certain molecules to come in uh

75:10 to be the outer membrane tends to more non specific and more specifically get

75:15 the intermingling. Okay, um para so it's really that's the kind of

75:22 , right? That's where the cell is at the grand name between the

75:26 membrane, we call it. Para plasm. Para pandemic space.

75:32 Um, that sink. Oh You guys have a lap there's a

75:39 . Any questions? Yes. correct. Yeah. Good morning.

75:55 . Just come up after after next ,

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