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00:02 Testing. Testing. No, that testing. Hey folks,

00:16 Uh Everybody hear me. Everybody hear . Ok, back there.

00:19 All right. Um, welcome. anybody know? Is there a class

00:24 here before me? Ok. That's I'm 20 years. I never come

00:28 a class where the projector has been and I'm ready to go. So

00:33 get used to that. All So, um, what's everybody doing

00:40 ? Ok. Uh, it's gonna like this for the next three

00:43 So, uh, I have to with it. One thing I hate

00:47 than anything is wet feet. So I brought my big boots but

00:54 it wasn't running too hard. So who? So, uh, has

01:00 , uh, in the last 24 enrolled in this course? Ok.

01:06 . Nobody. Ok. Well, you're there and you're too shy to

01:10 , um, you'll have access to the material. If you just,

01:14 enrolled today or yesterday, it takes couple of days a day or two

01:18 get uh, canvas access. but once you do, uh everything

01:23 there for you. Ok. Um see. So remember the clickers,

01:31 ? So they're still just only for if you will. Um just to

01:37 sure that your system is working You're using it, it responds and

01:42 seeing your points because I am uploading though they don't count for anything until

01:47 Monday. Uh Again, just kind make sure everything's working that you're that

01:52 seeing your points on canvas and you be confident that, ok, when

01:56 starts for real, that you're OK. So uh once we get

02:03 next week, the points being collected week, this week will be,

02:08 be deleted. Ok? But until then, just make sure that

02:13 seeing your points if you have an clicker. Ok? It may tell

02:17 when you so remember to session right? That's what you wanna put

02:21 . Um It may tell you to user ID. Just ignore that.

02:26 ? Just ignore it. You don't to uh if you got an active

02:31 clicker, you're good. OK? What else? So, OK,

02:37 the first thing is coming up, ? So this week, well,

02:40 , Friday through Monday, first weekly , which basically all these weekly quizzes

02:44 cover the stuff we've talked about here previous Monday and Wednesday. Ok.

02:50 for us that'll be chapter one Um And then the first smart work

02:55 due. Ok? Uh Next Ok. So remember, um we

03:01 already write the, the CT A if you're part of that too.

03:07 , uh, do what you have do to, I guess, I

03:09 know if you have to go to bookstore, they just email you or

03:12 have you. But, um, get that squared away. Ok.

03:17 , any questions about anything, any , right? Ok. So this

03:22 is really about, um, before I say that, um,

03:26 got a, all the lecture notes each of these chapters we cover has

03:31 condensed it here but they have like list of learning objectives. So think

03:36 that as kind of OK, we're to start this chapter. What should

03:40 know about this? That's kind of list of things to know.

03:43 once you're done. OK. Um we're gonna go through these, not

03:47 today, but we're gonna go through good chunk of these today. Consider

03:51 week kind of um some of it likely a stuff you already know.

03:57 learned an intro bio um some stuff not. Uh the uh this is

04:04 or less kind of the who, , why when and where microbes.

04:08 the one thing that uh I changed up in terms of orders of topics

04:12 things over the years. But one that's always a constant is this is

04:15 the first thing. OK. So kind of get you uh maybe uh

04:21 head into what, OK, what's microbe? Right? You may have

04:24 ideas of what that is, but then, like I said,

04:28 course is 99.9% prokaryotes and viruses. . So I think I said the

04:36 time, if you, if there's you come away with at the end

04:39 the semester, um, at least away with the fact that micros,

04:45 particular bacteria are really critical for your on this planet. Ok.

04:51 The only thing is that make news are all the and your uh whatever

05:03 is occurring, it's all the bad always get the news, right?

05:06 that's few and far between, So you leave here, hopefully,

05:11 know, wow, I didn't know could do all these kinds of things

05:14 of course, those activities they do you, OK, in many

05:19 both directly and indirectly, right? , uh so again, kind of

05:25 , a little bit of historical Uh we to um not too

05:30 uh don't worry about having, you , dates of events or things like

05:34 . Ok. So always as a , um your first exam is for

05:40 good while, but that exam review , you know, download that thing

05:44 you haven't already because that's gonna be , that's your guide. OK.

05:48 , what's gonna be covered? Um So we start, so we're

05:55 do, we have a few quicker here. So again, it doesn't

05:58 . So if you have it, it, OK. And so not

06:04 biology is a huge field, Ecology, um immunology. Um um

06:12 biology. So, it's a huge , obviously, right? But if

06:17 characterized as microbiology, it's this What would be that thing? You

06:24 , if I see that, this guy must be a microbiologist.

06:28 would that thing probably be? What that thing? Probably be? You

06:34 see it and go, yeah, think this guy is a microbiologist.

06:38 would that be? What would you a what? Well, what you

06:45 see with your, with your naked , what you can see with it

06:49 a piece of equipment? Absolutely. , right? I forgot to bring

06:54 microscope with me. Uh I was of those kind of oddballs. Uh

06:59 sure you've all written like in was it sixth grade social studies

07:03 What do you want to be when grow up? Right. And uh

07:07 was such a nerd, I wrote , right? And so I am

07:12 . I didn't know I'd be doing specifically. I'd be doing more

07:14 which I did. But uh I have my microscope in like 1973

07:22 Um Not very good quality resolution. uh yeah, anyway, so that's

07:27 of what spurred my interest. So so of course, the microscope and

07:32 microscope in itself um really influences um influence the um classification taxonomy of

07:44 right? Kept changing because advancements in microscope. OK. Uh There's a

07:51 you'll learn about in lab in a of weeks called uh resolution.

07:58 And that's really the ability to distinguish points that are really close together.

08:08 . This is your microscope have good resolving power, good enough resolution that

08:13 can those two points can be super together, right? With a naked

08:18 , they look like a blur, with a microscope, good resolution,

08:21 can the two points can be really and still be seen as two distinct

08:26 , right? That's really good right? So think of a

08:29 right, you got a cell and able to see organelles, individual organelles

08:34 that tiny cell. And it's a image that's all due to a large

08:39 resolution. OK? And that's what improved through um the the centuries uh

08:47 course, magnification as well, The magnification of electron microscope, six

08:54 , right? 100,000 X. What you, right. So um and

08:58 that really electron microscope is what kind them that was in the thirties that

09:03 of brought about the oh, now can see what the e Karyo cell

09:07 a prokaryote cell are all about, ? Being able to see those fine

09:11 which I and there's even some weird microscopes as you see here 16

09:17 right? And that was Van Leeuwenhoek's . And so incredibly, you could

09:22 like uh somewhere around three or 400 magnification with that which seems insane.

09:28 um in any case, so certainly microscope is what defines a microbiologist for

09:34 most part. OK. Although all kinds of disciplines use various microscopes as

09:39 . But um so life in a of ways, OK. Um Both

10:01 , socially, culturally, et right? So, um but for

10:07 most of human civilization, um it unknowingly not knowing that micro did these

10:14 that brought us like how to make everything from bread, to make cheese

10:20 beer and wine and other things um these were unknown what was doing

10:26 But obviously, we know it was . OK. And so certainly the

10:30 guys and their devastation of populations. and so certainly using microbes as the

10:40 , right? So you may recall Hersey Chase experiment um Retro bio um

10:48 Griffith experiment. Uh these are all of leading to the DNA was a

10:54 of, of, of he right? And it was bacteria and

11:01 used as models to study these And so it's how we figured out

11:05 like DNA replication and protein synthesis. are all, were you started using

11:11 and, and, and uh in as, as models for these

11:15 OK. So, um now in of historical and being able to see

11:21 things, um so hook versus la band labeled hook, OK. Um

11:29 know, it's always about OK. did this first? Right.

11:32 that goes to hook, but he his microscope is rather not great in

11:39 of magnification. 30 X, And so that's uh he looked at

11:46 macroscopic life under the microscope, looking a flea or a or plant tissue

11:53 this tissue or that tissue, more of in that context, right?

11:57 Van Leel Hook's microscope, much greater . OK. And he was the

12:03 to see bacteria. So he gets , you get the name um father

12:08 microbiology. OK. And so uh was also kind of uh eccentric.

12:15 but I don't know, I know about grinding lenses, but apparently

12:19 that's how you get these very good and magnification in particular is grinding of

12:26 , right? So, um and was apparently a master at that

12:31 but that was very secretive about So he didn't let the people know

12:33 he was doing, but nonetheless, produced these images of certainly over here

12:40 different bacterial types. OK. uh what he called animal cures,

12:47 . And so we'll leave this story a little bit later. But you

12:51 , when you begin to see this world where it takes, took up

12:57 pond water, you look at maybe it's a little cloudy or

12:59 but you put it on the Now you see all these things swimming

13:04 there in many cases, are different and shapes and you know what the

13:08 is this stuff, right? And you'd be OK where this stuff come

13:12 that leads us down to another story talk about soon. OK. So

13:17 now it's, um, let's look this question here. OK, so

13:22 have to read through these. It's of OK, what, what are

13:26 things they can do that microbes can ? I've been talking about, they're

13:31 great, but what's so great about ? Some of the, some of

13:35 things are here. OK. So goal here is to find the true

13:41 . OK. So with these take each choice in a box and

13:48 go. OK. Is this, I think this is true or false

13:51 mark it as such? OK. then go through B and C and

13:58 . OK. Same, same thought , true or false. Then if

14:03 tally up, if you're, if all true or they're all false or

14:07 have you. OK. Um And and see, well, is there

14:13 choice where I can pick nothing? . Or all of them depending on

14:18 question. OK. Don't be afraid pick none are true if that's the

14:24 . OK. Right. It 10 . All right. Let's count down

14:44 . OK. Here we go. right. So we have.

14:54 So uh microbes are ubiquitous. So that's the term we always see

15:03 to microbes. OK? And it's the opposite of what that's saying

15:09 OK. It's not that their locations limited. It's that they're everywhere.

15:12 , ubiquitous means they're all over the . OK. Um So a is

15:18 true. OK. Uh B uh the other way around your microbes are

15:25 and on you actually outnumber yours by X. Not 100 X. So

15:29 , your microbiome, right? Your , fungi, viruses living on your

15:36 that aren't your cells outnumber your own about 10 X. OK. Um

15:41 microbe supply uh 50% more than 50% earth's oxygen. So those are your

15:51 types, right? In the Um What it called cyanobacteria and

15:57 Um Way more than 10% or Similarly uh this one is 90%.

16:07 So nitrogen, this is one we'll on a little bit later uh nitrogen

16:14 . OK? That's where, what see down here. That's what's right

16:19 . So the nitrogen cycle. So remember molecules that need in are

16:25 what's an N using molecule big one your muscles, make them yourselves.

16:32 these things all the time. The PRO genes. OK. Proteins,

16:42 acids both have nitrogen. Uh It's essential element. Every living thing needs

16:47 have N OK. And um we are part of that group too.

16:53 so it's, you have to have in usable forms, right? We

16:58 take just nitrogen gas and use that make our molecules. We gotta take

17:04 um A we use things like OK. Um But who transforms that

17:12 or bacterial activity in the soil Ok. In various forms.

17:18 So um very critical to, to here on this earth is that

17:24 Ok. Especially for plants, plants great, right? Just give them

17:28 sun, give them some water. And CO2 from the atmosphere, they're

17:33 to go, but they can't make like uh nitrogen sources to grow on

17:39 phosphorus sources. That's why you supply , right? When you're growing crops

17:44 . OK. Of course, they on that. I give them bacteria

17:48 give them their nitrogen, right? very critical to all, all levels

17:52 life. OK. Um And certainly is also uh so is also incorrect

18:02 it's actually the other way around. only really aware of a small fraction

18:06 what's out there. OK. but there's ways to, to,

18:10 identify those. OK. So basically answer is none of these are

18:14 OK. So, um so let's at a definition. It's kind of

18:22 getting into the definition of a OK. So we got various choices

18:28 . OK. So which would you a microbe? All right. ABC

18:32 or F? OK. Mhm. . Count number 1210. Uh

19:24 Oops, sorry about that. I here. There we go. And

19:29 answer was there we go. Yeah, it's a virus.

19:36 So the RSV virus in terms of definition OK. Um The uh number

19:47 criteria gotta have a microscope to see , right? That's typically the criteria

19:52 is it's not uh B and C D and E and F don't fit

19:58 fit the criteria. OK. So um they're not multi cellar animals.

20:05 the water bear dust might, these animals. Where's the animal kingdom?

20:10 . Uh Onion skin, onion, tissue, right? These are um

20:17 of a larger entity, right? , microbes think microorganisms think um ourselves

20:25 , although not always. Um but live in the environment on their

20:30 They're not part of a tissue or . OK. Um That's kind of

20:37 we define them. OK. Bacterial and a colony. So a bacterial

20:43 arises from a single cell. Grows and all neighbors, you

20:47 get millions and millions and then becomes . OK? But the colony is

20:52 a microbe, it's made up of , but the colony itself is not

20:57 a microbe. OK? And bacterial , these are very common in uh

21:01 biofilms, right? Biofilms are all a surface. OK? And massive

21:08 on a surface that actually gets so , it then expands three dimensionally off

21:13 the surface. OK? Um But comprised of, it itself is not

21:19 micro but is of course like a comprised of bazillions of microbes.

21:26 So the only one that fits here the virus as a microbe.

21:31 Um And so So this, let's at this question. So the,

21:36 the first one is by definition, next is kind of having a feel

21:41 uh the types of microbes. Uh What, what, what,

21:47 groups that we know of fit the in the micro group, but then

21:54 of characterizing based on size, So size is kind of how a

21:57 you can kind of differentiate the the groups. OK. So here we're

22:04 at something that's uh one by 10 , OK? With no organelles.

22:09 that's gonna kind of need you to a choice here. OK. Or

22:16 , right? OK. Let's see we got. OK. So if

22:48 picked um uh G, you pick , you pick G what, what

22:59 the two? So you pick you of the above. What are the

23:03 choices you? Yeah. So what the two correct ones you answered

23:12 You answered G, so what are two? Yep. And what's the

23:20 one? Bacterium? And which No, anybody else? Yeah.

23:31 . IQ so uh these two, . Uh So the micron range is

23:39 proops. OK. And so we'll here at uh kind of the size

23:45 . So, um again, right? Are um think of them

23:53 you threw them out in nature, be able to survive typically.

23:57 Not part of a, a larger like a uh tissue or an

24:03 Um They certainly are cells most of , there's a group that's not that

24:07 talk about. Uh, they're gonna different morphologies, shapes, forms.

24:14 , they, uh uh but they're not multi, not animals

24:20 OK. And so basic size right? The 1 to 10 microns

24:26 cars, 20 or above generally. there's some gray areas in between.

24:30 for the most part they fit these categories when you get to like um

24:36 a micron. Now you're in the realm, right? Nanometers.

24:41 So uh I mean you shouldn't have kind of that basic feel for.

24:46 . This is what fits each Um And so the uh so in

24:52 of size limits, could you could have a cell that's like one

24:58 Big one nanometer is the cell, there be a cell that's that big

25:05 worked? Why not? Right. it wouldn't because so here's one

25:15 right? So a cell that big at the stuff you put inside of

25:20 cell, right? Lipids, Proteins, things are ribosomes. These

25:26 are gonna be bigger than a So you wouldn't be able to fit

25:30 of a cell, right? Uh that's that small. OK. So

25:34 gonna be a science limitation. Um So the, so the,

25:41 this kind of gets into OK, gonna look at, we define a

25:46 , you kind of get the size for each type and then it's

25:49 What are the representative types of OK. So you want to be

25:53 with the different groups and, and fits in what? Ok.

26:10 There may be a couple of terms may or may not throw you but

26:13 , I haven't seen it in a , maybe you forgot, but it's

26:16 term um counter to that is Ok. Um, that's something

26:29 as we get into metabolism next we're gonna talk about that a

26:34 OK. All right. So, know, why don't you know these

26:54 of basic things, size and representative and whatnot, but we're looking for

27:00 outside earth, right? Mars, have you, these are the kind

27:04 things you're looking for, right? gonna be microbes and you're trying to

27:09 what's this similar to these are gonna things that are gonna be helpful knowing

27:13 stuff, right? Um All Let's count down here from 76.

27:28 . Um All right. Let's go algae. Heterotrophic euka. Now,

27:34 are photosynthetic algae are mostly photosynthetic OK. Uh Autotrophs. OK.

27:43 similar to archaea that they both lack nucleus. That's true. OK.

27:49 Viruses type of cell. That's OK. So viruses, that's

27:53 that's the, they're not cells. they're a cellular. OK. Um

27:59 Kia, they're, these are what call extremo files. They're kind of

28:03 in more extreme conditions, right? temp um extremes of uh hot or

28:11 temperature, um high salt conditions. some cases, it just depends,

28:17 kind of, that's what we call . Extremophiles. OK. Uh protozoans

28:22 not sort of synthetic fungi. They're type of protozoan, they're a heterotrophic

28:27 . OK. Um So Eu that's correct. All right. They

28:33 to eu Caria, a Kia and um bacteria. And so our Kia

28:40 Eu Caria do have similarities in common each other. That bacteria don't.

28:45 . So, uh so it is two make this correct answer.

28:51 Um So again, representative types, ? So the cellar and a cellular

28:57 . OK. So uh there's your groups. So you notice that and

29:03 are kind of the um the kingdom if you will. OK. Um

29:08 you don't see animal, that plant , animal, animal kingdom, plant

29:12 don't have representatives that we call OK? But these four do

29:18 as you see here. So uh yeast and moles, not, not

29:23 fun job, not all fungal types microbes, but a good number are

29:29 yeast and certain moles. OK. The proteins are microbes. Uh the

29:36 , spiral gyra is photosynthetic amoeba is protozoan heterotrophic uh bacterium, right?

29:43 Coli, right? Archia, you have an Archia up here. But

29:48 nonetheless, those are the microbes in cellular group. OK. Then in

29:52 cellular group um just continue here. these types, these types. So

29:57 of the, not just the basic of each group here. OK.

30:04 uh The, the course, the characteristic of a pro Caro is lacking

30:09 nucleus, right? And you lacking , right? They can't have specialized

30:14 in them, but they're not of membrane bound variety like an organelle.

30:20 . Uh We'll get more into the and bolts of the prokaryote cell in

30:25 three, which is a ways away . OK. Um um You're already

30:30 with eukaryotic functions, I'm sure the , uh multiple chromosomes, et

30:36 OK. So your aay types are categories here. OK. And we'll

30:41 about viruses in unit two. But they have um uh three differences

30:49 OK. So your viruses that you know, you're familiar with like

30:53 flu COVID, what have you? But basically a protein sac with a

30:59 inside DNA RN A, it can have other variations, but that's the

31:04 basic structure. But your vids and are way different. OK. The

31:11 a vid only is made of RN . That's it. Nothing else.

31:16 are only a protein, that's Nothing else. OK. So viruses

31:21 , you know, a little step a step up from that in terms

31:25 complexity. OK. So, um again, they're a sailor, they

31:31 , you can't, uh a virus live, they all require a

31:35 they don't live outside of a OK? Um So just a quick

31:40 about a Kia, right? Um can kind of loosely group, all

31:45 them into one of these three groups thermo files. Methos Halo files,

31:51 files, heat, loving, loving right? Heat loving. Um

31:56 can have hyper themo files in that . OK? Above 80 right?

32:01 boiling water. OK? Um Methano obviously produce methane. OK. Very

32:10 in uh landfills um with treatment et cetera. Um but it's a

32:17 archa metabolism. You don't see it any other group. OK. Halo

32:24 . Uh These you find in natural of water that are very s uh

32:28 salty, great salt lake, Red . Uh but also in uh companies

32:34 manufacture salt, they'll have pools of water, uh evaporate water, evaporates

32:41 get highly concentrated salt and you can these bacteria in there. OK?

32:46 have a very unique um photosynthetic um we'll talk about later. Uh It's

32:53 nothing like a plant or a plant the size. OK? Um So

33:00 the uh viruses again this, they're kind of on the border on

33:05 edge of a, what's a, alive or is it dead?

33:10 And so generally, uh you can both sides, but they're alive in

33:19 , let's say when they're inside their because that's when they're replicating and they

33:23 over the host as a replication OK? Uh When they're outside the

33:30 , they can be viable, they're reproducing. I'm sure the virus is

33:35 on that doorknob over there. On door handle or on the countertop,

33:39 , in the air. Ok. they are, um, they can't

33:44 anything really unless they get into their cell and begin to replicate. And

33:49 we notice them when we begin to symptoms, like a running out or

33:53 or what have you. Right. , there's, right now there's a

33:58 of respiratory viruses going around, like , um, RSV, um,

34:06 , right? Three of these circulating . Ok. Uh All you

34:10 very similar symptoms in many cases. . So um uh but again,

34:16 know, they're alive quote when they're the cell and they're host replicated right

34:21 and their viability, you know, virus sitting here on this countertop um

34:27 remain viable. It depends on the type and the conditions, right?

34:30 can remain viable for days or right? All it has to do

34:36 encounter the host cell, which may by touching, I touch myself.

34:40 have you then it can proliferate, ? Others have a short lifespan when

34:46 outside of the house. Just OK. So the point is they're

34:51 cells and because they don't have the of a cell, right? Cells

34:54 self-replicating. They can take in, uh take in food, right?

34:59 energy. Uh viruses can't do You can't throw glucose at a virus

35:05 go grow, grow, won't OK. They rely on, on

35:09 host of their functions. Ok. they're not, they're not completely,

35:16 , um, um, devoid of anything by themselves because they, they

35:20 have viral components that and parts and that they carry with them. But

35:26 really mainly only for the replication and into the cell. Ok. We'll

35:31 more about that in the next Ok. Now, having just gone

35:37 the definition, right, the microscope see it. They, um,

35:43 have different size ranges, right? , microbes are in the uh bacteria

35:49 the micron range, 1 to 10 , 20 to 5020 to 100 virus

35:56 much tinier, right? Um But with anything in biology, not everything

36:03 into a nice box, OK? always gray areas, OK? So

36:09 gray area here is is we do what are classified as microbes be you

36:17 , visible to the naked eye. ? And that generally has to do

36:22 a type a type of metabolism they that causes this OK? And these

36:30 Thom Margarita, OK. And my got excited when she saw the name

36:37 my on the notes and go It's not a Margarita and it's,

36:41 a type of bacteria, OK? um and don't worry about we'll get

36:47 metabolism next week, but just for this is, this is why they

36:51 get so big. This is what , here's an example of it over

36:55 on the right. OK. That uses this as energy H two S

37:04 . Hydrogen sulfide and it breaks it , oxidizes. We'll learn about that

37:08 the next coming weeks. And when gets oxidized electrons are let go.

37:17 they're given to this process over OK. And so nitrate takes those

37:23 becomes reduced to nitrite. OK? going big. Whoop. What's that

37:28 ? OK. Well, this part the middle, OK. What we

37:34 electron transport chain. OK? For , you substitute something like glucose here

37:45 back here you put in 02, what you do and that's your

37:50 right? You're aerobic. OK? And in the middle part, you

37:55 a lot of energy. OK? But for this guy, it doesn't

37:59 02, it's anaerobic. So it nitrate. OK? And so what

38:03 does is a mechanism to kind of new uh have um an energy production

38:11 available at all times. It can , nitrate. Nitrate is a

38:16 OK? And it can store that nitrate and that's what kind of cause

38:23 to expand in size gets so OK. So it has that kind

38:27 as a reserve kind of like a tank, right? We fill a

38:29 tank with 02 for us to be to breathe underwater. It's got this

38:35 that it fills up with ni nitrate it can use that to breathe

38:40 OK. Um The bubble algae similarly up with water and get huge

38:47 Um microbial communities, right? so this is where a a microbe

38:52 course, is invisible, generally the eye, OK? Um But when

38:57 put bunches and bunches of them they can be visible, right?

39:02 biofilm, right? So biofilm is a microbe, it's made up of

39:08 of them. OK? Uh it's all about a surface, a

39:12 , a shower curtain, your right? These can all be surfaces

39:16 biofilms. OK. Um The and , the tissues, tissues,

39:22 muscle tissue, skin tissue, these um individually, we don't refer to

39:27 as microbes. OK? They're part a tissue. Uh If they're not

39:30 of that tissue, they really don't . OK. Um And then micro

39:36 , we call them multicellular, the bear um and others. OK.

39:42 So uh basically single cells, those cells can have arrangements and chains and

39:49 and whatnot. OK. Um So a little bit about uh uh

39:57 we get, how we come to grouping of Ar Kea, right?

40:01 there's two groups to what the takeaway is mainly is that in prokaryotes,

40:08 two groups of them, right? the main thing here. There's two

40:12 of prokaryotes. This wasn't known until about the seventies, late seventies,

40:18 eighties. OK. Um The before go on any questions about anything,

40:25 can always feel free just to shout or what have you. I

40:29 I want to make sure, I any hands they come up as

40:32 OK. So don't feel free to questions. Um OK. So in

40:39 , invariably it comes down at some to classifying, identifying, classifying,

40:46 into a group taxonomy, classification type . OK. And certainly with the

40:51 that too is the case. we have because we have this framework

40:58 classification of microbes. It's uh obviously a critical certainly from a diagnostic medical

41:06 standpoint, right? We're trying to what, what kind of disease,

41:10 disease someone may have. You wanna already a a catalog of,

41:15 Here's what we know, here's how classify them and how we can identify

41:19 . So, you know, from standpoint, it's important to have something

41:22 this. OK. So the thing um we rely on for the longest

41:29 . Um We classify them based on what they look like. Um Here's

41:35 form and shape and here's the kind metabolisms they can do, right?

41:40 so those are very similar in those were grouped in, in grouped

41:46 Um And so we kind of come relationships that way. OK.

41:51 we still do that, but the is number one, if we can

41:58 sequence DNA sequencing, OK? And DNA sequences. So I remember that

42:05 doing that each, each nucleotide is a point of comparison, right?

42:14 you, you, you and nowadays pretty easy, especially with pro cars

42:19 aren't so huge, you can sequence things pretty rapidly and so you can

42:23 and compare and now you have a base pairs, many different differences to

42:29 with, right? So it's, pretty much the standard to, to

42:34 that, but then you still do other stuff. So look like

42:38 shape metabolism and that kind of Ok. So, um so

42:44 microbes, if you remember from intro , what's his name? Uh

42:51 the Laan system, um everything uh either considered the animal plant right?

42:58 , of course, it changed uh time, but the micros are put

43:03 one group or the other. If was photosynthetic, it was put in

43:07 plant group. OK? If it , let's put in the al

43:11 OK. So fungi and algae are in the plant group. My fungi

43:16 I have no idea but it was . So just focusing on the microbes

43:21 . So in mid 18 hundreds, guy Heckle and again, it just

43:28 with advancements in microscopy, like better magnification improves resolution improves OK. And

43:38 uh all micros are put into this called bro, OK. Taking out

43:43 planting animals and put them in that . OK. Then um cours and

43:52 periods. So that distinction came about really in large part to the advancement

43:59 our development of electron microscope, which occurred like in the thirties,

44:04 . And so now we could oh, we got this group of

44:08 which tend to be smaller. We see organelles, we don't see a

44:13 , we don't see a nucleus, don't see these things. OK.

44:15 these guys must be something completely different what we call eukaryotes. OK.

44:21 that's where that division comes in. . And so, um and so

44:27 and protozoans are put in protist pro . Uh basically kingdom mora now just

44:33 only pro periodic cells, right? so uh so when that split occurred

44:39 it was Moro when I was studying stuff, OK. And it changed

44:45 when I became a graduate student. um in any case, so you

44:49 to mold, have a different, was like in the sixties, they

44:52 , somebody had the sense to OK, they're not plants, if

44:56 Easter MS are more closer to us they eat the same things we

45:00 OK. So they were putting their group called obviously, you know,

45:04 . OK. So, uh just focusing on, so we only

45:09 mention of animals and plants here at beginning, right? And we're taking

45:14 out of those groups into their own . OK. So where we stood

45:19 this point then was this was in seventies, early eighties. Um Mora

45:25 all the prokaryotes. OK. So is where our k our key bacteria

45:30 in. All right. So going to uh comparing organisms based on

45:39 sequences. OK. So Woes and , I don't know if you George

45:47 in the biochemistry department, our biochemistry were part of this group and using

45:55 they decided to use a specific sequence DNA. The segment that codes for

46:03 the um um 16 is RN OK. And the um so remember

46:13 ribosome rights where protein synthesis occurs. . The unit is comprised of two

46:20 , they come together during protein synthesis carry that out. Um It's made

46:25 of a bunch of proteins and uh A sequences. OK. And so

46:34 an example of in terms of um the RNAs are the end

46:41 So most genes are protein coding, get a protein at the end.

46:46 with these kind of genes, the product is the RN A.

46:50 And so your uh ribosome RN A RN A, remember that's transfer RNAs

46:56 involved in protein synthesis. So those A molecules that's the end product.

47:00 you do have genes that, that's they code for and that's it,

47:03 stops there. OK? And so 16 S um is one in the

47:11 unit. OK. So it's a size. I'm like maybe 1500 base

47:18 . It's gonna be the sequence rather . But more importantly, this term

47:23 , right? So the ribosome, think think put on your evolution hat

47:31 . Um This uh OK. This gonna this is gonna be a really

47:37 analogy. The best one I can up with kind of describe this.

47:41 say you wanted to, you want want to investigate the history of

47:48 Ok. And you wanted to go back in time and, and pick

47:52 characteristic that, you know, would constant throughout. Ok. Um And

47:58 we're talking transportation, think of anything used for transportation or to carry

48:04 right? What's probably a feature that could point to go? Yeah,

48:09 can go way back in time with thing because the early transportation things have

48:13 . What would that be? That's of a clue wheel, right?

48:19 wheel. So they probably had uh horse drawn wagons and or whatever,

48:25 know, uh the wheel would have something very early on, but you

48:28 see today airplanes have wheels, Land on it, right? So

48:32 can uh cars obviously have wheels, , right? So that's a feature

48:37 can go back and go, I can trace back evolution of transportation

48:42 that characteristic way back because they all it, right? And then see

48:47 it evolved over time, right? , um so think of that as

48:53 ribosome, ribosome was 16 inch ribosome A, if you in evolution,

48:58 evolve at different rates, they change change slightly over time. Ok.

49:06 The, you, you can't do much of that tinkering with the,

49:10 the, with the ribosome RN right? So we do do great

49:15 um can affect the function. And you have a, a functioning

49:21 you're dead, right? Because that's gotta make proteins, right? If

49:25 have AAA structure that can't function to that, then that life of that

49:30 , that organism is, that's OK. So changes accumulate slowly and

49:37 specific parts of the vibes. And so we can use that as

49:42 measure of going back in time. . And then you can, where

49:48 can tie that to fossil evidence to specific times on things. OK.

49:56 when this was done, so this done really just initially, the project

50:00 just focusing on carriers, OK. so when they did this and this

50:06 just showing you kind of a two drawing of the actual 16 S.

50:12 so when I, what I'm saying I'm referring to the, the DNA

50:17 codes for this RN A OK. so we look at the sequence,

50:21 the arrows that you see there, are, what are the areas that

50:29 at in terms of changes? Here. And so it's those areas

50:37 accumulate changes more rapidly than the other because they don't really so much because

50:41 you do you affect the function, . So uh so, so you

50:47 even from the two dimensional drawing, can see, right? But there's

50:51 difference uh in these two groups, ? So within Procar, they

50:55 hmm, we're, we're seeing this Procar group. OK. Um Based

51:02 this information and it turns out that I look, look at the

51:05 at the types that were showing these guys are Kia, right?

51:12 they tended to be found, you , when you can grow them,

51:16 tend to be found in these weird , right? High, high temperature

51:20 methano agains or what have you, . So they, they knew they're

51:24 to something and then they found this proal group. OK. So there's

51:29 groups of Procans, OK? The and the archaea. OK.

51:36 um they're not kind of, they're like exclusive that you don't ever find

51:44 together because you do find them You'll have Ar Kea, then you'll

51:49 bacteria in the neighborhood as well, not able to fully handle the extreme

51:57 that the Ar Ka are in. there are the they, they'll be

52:01 the vicinity of each other. And there's cases where gene transfer occurs

52:06 two groups. OK? And um mentioned earlier about that when they,

52:11 have those halo files of salt loving have this weird kind of photosynthesis and

52:18 actually have acquired that as well that in the same ecological niches as

52:23 OK. So there can be this of transfer between the two.

52:28 Nevertheless, the point here is that and this also brought about this uh

52:34 to this point, it was all so I can remember genus species,

52:40 class order phylum kingdom, right? was all the names. Now we

52:46 domain. OK. So the main the biggest, most inclusive,

52:52 So we have Eu Caria, which us obviously um then Archia and

52:59 OK. So three domains, Three groups. OK? But make

53:04 mistake, right? Ar Ka are , they have the the hallmark of

53:09 , right? No nucleus, um a single circular chromosome. OK?

53:17 organelles. OK. So they have proal features. So, but there

53:23 some similarities that um they have a for sure, I just mentioned but

53:30 with eukaryotes that bacteria lack lack these . OK. So, and it's

53:38 , not every IKEA have these similarities EY but many do OK? And

53:46 may or may not remember the intron gene structure. We'll talk a little

53:52 about that way later, but that's to you. Caro is a structure

53:56 , and, and some genes in have this structure. Uh the,

54:02 RN A uh polymerase. Um some the Ramos components are similar more similar

54:07 eukaryotes than prokaryote. So they, have those features. OK. So

54:13 that reason, it's not that uh terms of life evolving on this

54:18 bacteria were the first OK, followed thereafter by IKEA and then E car

54:26 OK. So um but again, home here is this creation of domains

54:33 that there's two pro period groups. . Um All right. And so

54:42 is uh so throughout the 1st 22 years on this planet was strictly occupied

54:54 pro carriers, right? So 1st billion years a verse origin was Procar

55:04 . Then came eukaryotic cells um then multicellular eukaryotes more complex than coming out

55:13 the water on the land. And you know, evolving. So these

55:18 origins are um what, what is um how did you carry like cells

55:25 ? Right. And so this endosy . So endosy biosis is of course

55:32 relationship between two organisms. Um but endosymbiont is a very intimate, they're

55:39 associated with each other. OK. so this is believed how this would

55:45 occurred. You would have some kind a pre eukaryotic cell um that would

55:51 been characterized by lots of membrane folding the formation of a nucleus,

55:56 And then endoplasmic reticulum. So if recall bic cell have lots of membrane

56:01 structures in it, right? And uh it's thought that uh it would

56:06 engulfed the bacterial cell Procar cell. if it would have been a uh

56:15 uh heterotrophic cell type, right? you see here, the prote ofac

56:21 um this would have given the cell own power source, so to

56:28 evolved into mitochondria. OK. Uh it then engulfed a for a synthetic

56:34 , OK, it then would have into chloroplast. OK. And

56:41 Ok. Well, what's the evidence that? Well, the evidence is

56:45 we can, those, those organ actually have DNA in them.

56:51 Fragments of DNA in them. And that DNA actually does have

56:56 too different modern day bacterial species. . That's pretty strong evidence that those

57:04 were once a cell that, that was part of a symbiotic

57:08 Ok. Over, over time, course, that that cell would have

57:14 a lot of functions because it's not of its larger entity. So what

57:18 left is what we see now, of DNA, there's even ribosomes and

57:24 in there. So some of the for photosynthesis for respiration are actually coded

57:32 in the organelle by some of those , not all but some OK.

57:37 the fact that the organelles, so mitosis, right, the the nucleus

57:43 and so too do these, these or class mitochondria? Uh But

57:48 don't take that to mean that you pull a mitochondria out of the cell

57:55 put it on a Petri dish and will grow, it won't.

57:59 But as part of the mi mitosis , those organelles do duplicate.

58:05 So all that pretty strong evidence of origins of, of eukaryotic cells.

58:12 . Um Now, uh let's see . So, OK, genomes,

58:19 kind of talked about this a little in the context of um you

58:23 they're, they're, they're small compared our genomes, which are pretty,

58:27 big, multiple chromosomes, single circular , easily manipulable with the techniques we

58:35 um which has allowed us to uh hundreds of thousands of different prokaryote

58:41 And in the process to find all of unique metabolism, that's one thing

58:47 peres you'll find in them, the to do all types of metabolisms that

58:54 don't, we can't even begin to try to do OK. From

58:59 metabolism to producing all kinds of different . So, uh and even degrading

59:06 different types of things. So, diversity of metabolism is one of the

59:11 that characterizes proios. OK. And in that we've, you know,

59:16 where biotechnology came in to exploit these to figure out. OK? Here's

59:22 cool enzyme, let's uh let's commercialize , right? So that's where biotech

59:27 in and, and then uses those . We'll talk about some of that

59:31 . But um but one of the is also the um uh this meta

59:39 . OK. So what this really is you see meta genomes, that's

59:45 way to basically in a show The show um how you can maybe

59:53 types that you can't culture in the . Right? Again, I think

59:57 only maybe 3 to 5000 str strains you can actually culture in the

60:03 OK. There's thousands of others that can't, right? So, number

60:09 , why is that? Why can't culture it, well, in

60:15 OK. Obviously these things are all in, in concert with each

60:21 Uh, fighting, fighting with right? Cooperating with others.

60:27 Um The, the products of one would be used by another. Um

60:34 don't know all the mm feeding relationships on there. So we, we

60:41 not know what it's required to grow on their own. Right. So

60:45 why, you know, we have really coached everything that's out there because

60:50 not, it's not easy to We don't know all the nutritional requirements

60:54 them. OK. So how do find it out? Well, you

60:57 an environmental sample and you basically just all the DNA. That's OK.

61:04 any anything that's in that dirt if it's a dirt, soil

61:08 right? We will blow it blow up the cells, get all

61:13 DNA, OK? Then we use techniques of a common uh DNA

61:19 We'll take those fragments, we'll put in a vehicle to kind of allow

61:26 to grow it and work with That's what the vector will do for

61:30 . Uh We then put it into cell, right? The cell will

61:35 it for us. It will, can grow it and it will make

61:38 of it for us. OK? that's what we use that for the

61:41 coli there. And then what we in the end is a bank of

61:48 . OK? Each containing a different of that DNA that was in our

61:55 . OK. So what we call library, right? Meta genomic

61:59 So now our it say 1 g of dirt and we did this,

62:04 got all the genes that are in soil now at our disposal,

62:11 In the, in this form. . So with all the information we've

62:17 over decades that are on, it's , right? So now this becomes

62:22 the bioinformatics. This is where they guys come in, right? All

62:27 databases and you go OK. This what I got in my library.

62:32 are sequences. What's it matching up in terms of microbial sequences we've

62:39 we figured out, right? There's match up with E coli or

62:44 right? So, or is it unique? So this is how we

62:48 see what's in there without having to in the lab? OK. And

62:54 we can find be un cultural, ? By doing these kinds of

62:59 OK. And it's proven to be , especially from uh if you wanted

63:03 study my ecology, right? What the bacterial types in, in this

63:10 soil in this particular environment? If gonna go in there and try to

63:15 and coach everything on a plate, been doing that for decades,

63:19 If you have this technique now you get representation of what's out there,

63:25 ? Very fairly quickly, right? can give you an idea of the

63:30 in that particular environment? OK. Now the any questions about that?

63:40 . Questions. So, so as mentioned earlier, um kind of going

63:47 to discovery of microbes, Van Ley hope, right? So 16 hundreds

63:53 completely different, obviously belief system, very superstitious. Um You're now seeing

64:00 invisible world pop up in front of eyes, you're going oh my

64:04 what is this, is this something the devil or what's going on

64:07 Ok. So of course, origins these things become of, of,

64:13 importance. So why, where are things coming from? What is this

64:16 ? OK. And so this takes down the pathway of, of

64:22 which may seem crazy to us Um But was a thing for quite

64:27 long time, right? Um A goose, right? So these

64:34 apparently, I, I've never seen barnacle, a goose barnacle, which

64:38 of plant tree, I guess. so of course, uh ponds or

64:43 are frequented, lakes are frequented by land on it, right? And

64:47 see these trees which I guess, don't know if they were high or

64:51 , but it appeared to them like were yeet or something. It would

64:54 into the water from these plants. made, they made the connection,

64:59 , these come from these, these using these barnacles nuts, right?

65:05 do you produce mice? There's a , sweaty underwear. Uh take

65:11 take husks of wheat. Put it a jar. Wait 21 days.

65:14 . Then you get mice. Sounds pretty cool. Um, muddy

65:20 gets right to frogs and we'll see here in Houston. Right in your

65:24 . Right. You see frogs jump over the place. Uh, if

65:27 today. Certainly by the end of week with all this rain, rain

65:29 . Right. If you didn't know , you go. Oh rain,

65:33 frogs. There we go. So again, this is these kind

65:37 beliefs held for a lot longer than would think. OK. So these

65:42 all examples of what these are examples , I'll give you a hint.

66:16 not, it's not how the world naturally operates if you know that.

66:31 . Alternative. OK. So it spontaneous generation. OK? So BB

66:44 C are the opposite of each OK. So biogenesis is life produces

66:50 , OK. Spontaneous generation is non produces life, OK? Um Mud

66:58 soil giving rise to frogs, That's non life, giving rise to

67:02 . Doesn't, doesn't happen. So even Van Lebel Van Leeuwenhoek

67:08 right? So this vital force is that believed in this thought that any

67:14 of mostly inanimate matter with, with , that was the key and of

67:21 . Those two together can produce OK? And even Van Leeuwenhoek,

67:27 is this drawing of a sperm, ? You see they're in the head

67:31 the sperm, a fully thorn. , he's got his knees, knees

67:38 to his chest and the hands in front. All right. And the

67:43 head right there. So down the of the head, right? Hold

67:49 . So he was uh one of people you called a sperm sperms,

67:56 . His belief and many others along him thought male, right? Gave

68:01 to a fully formed human in his . Ok? And the role of

68:06 woman was simply as I love OK. Yeah, that wouldn't fly

68:12 , obviously, right? So uh just being totally ridiculous, of

68:16 but uh that that was woman. this, right? So obviously crazy

68:22 goes along with the kind of belief had in these times, right?

68:26 um so then of course, if a scientific sort in this time,

68:31 going OK. Is this for Just BS? OK. So those

68:37 kind of more of the inquisitive type thought, OK. I don't know

68:42 this spontaneous generation stuff. Let me to go down various experiments and things

68:47 kind of either prove or disprove it it kind of the division occurs kind

68:53 here where we go OK. Maybe doesn't fit for macroscopic life, this

69:01 generation because this experiment here by you know, you can have uh

69:06 meat carcass, flies are, are flying around it and maggots are

69:12 in the meat and they go Look, here, meat gave rise

69:16 the maggots. No flies landed on meat, laid their eggs. Maggots

69:22 . OK. So very simple experiment just put a cork in it.

69:28 ever let flies land on it and will never see the maggots,

69:33 So then you go uh oh gotta have oxygen, gotta have air

69:38 the force. So let's put some cloth on it. Right? So

69:42 can really pass back and forth. you fulfilled your criteria, right?

69:50 is present, but there's still no generation occurring. So you go

69:56 you settle the issue. Well, and no. Yes for these macroscopic

70:02 forms, but no for microscopic right? Remember by this time this

70:09 , this was well known that they hook et cetera, right? So

70:13 , let's take some broth and literally is stuff just like soup,

70:18 beef, soup, broth. It be what it is. OK?

70:22 you boil it, you want to everything in there. OK? And

70:27 cool it. All right. If do the flask open, of

70:31 stuff's gonna grow in there. We nowadays it's just contamination, right?

70:36 But they literally thought it was the plus the air giving rise to cruising

70:42 . OK? Didn't know any right? So if we do the

70:46 down below, eat broth seal right? But again, because you're

70:53 letting air there spontaneous generation wo are doesn't count no good. Ok.

71:01 So this is where, right, is where pasture comes in to kind

71:05 finally settle all this ridiculousness. Um He has an ingenious way of

71:13 air to be present but not letting uh contaminate. Ok. Um So

71:21 , uh the, the thing here , yes, you can seal

71:25 but you're not getting air in And that's, they said that's part

71:28 the equation, air and inanimate um gives life and it was at the

71:35 to kind of finally put an end this. OK? And so he

71:42 or a number of different hats, was trained as a chemist. If

71:46 had chemistry already, you may have through the uh uh the chirality of

71:51 . He's kind of the one that that. Um But then he quickly

71:55 into with that background. It was to be a microbiologist, um went

72:01 fermentations studying uh uh the French government on him because the French wine industry

72:07 having issues. If you know anything France, they love their wine.

72:12 ? The wine is not, They're not happy. OK? And

72:16 , and this is really the first of attributing these chemical transformations,

72:23 So uh reactants yielding products, You add your reactants, then they

72:36 they combine and form products um equilibrium , et cetera, et cetera.

72:41 But now is the first time where was actually seeing living things, living

72:46 are transforming these chemicals into products. . So the microbes are the

72:53 OK. So that was the first this was ever shown. And that's

72:57 how the germ theory of fermentation comes , right? So, fermentation in

73:01 is uh basically is um metabolism in absence of air. OK. And

73:09 we know of course, in uh uh wine production is grapes,

73:15 Grapes are the source of the right? Or the hydrate source,

73:20 what gets fermented, OK. Um uh are then um or what transformed

73:29 sugar into ethanol. Ethanol, of is what is the alcohol?

73:34 And so you, you don't have oxygen present and you get that

73:40 OK? Uh And what you get is as, as the yeast culture

73:45 , you get more product, And so now they didn't add,

73:51 didn't have, didn't have like uh couldn't go to the store and get

73:54 little packet of yeast and dump it , right? The they didn't even

73:58 even add yeast like that. The source of the yeast here is actually

74:03 what anybody know, because it this has been going on p production

74:09 been going on for centuries, And there was no such thing as

74:12 get yeast off the shelf and dump in the yeast were already there and

74:16 were there on the grapes, on surface of the grapes is where the

74:21 were at and so that's how they more sophisticated. Now, we have

74:26 strains we've isolated and engineered. Uh for, for until then, uh

74:32 was all the yeast that were on were on the grapes themselves. And

74:37 , um and so more yeasts you get more product. OK.

74:42 nowadays, you can buy wine that's that's from the, the wine,

74:54 leads to like wine production, like 9% alcohol. Nowadays is double

74:59 And uh they have yeast strains that handle the high levels of alcohol.

75:06 And so the the off, so off tasting of the wine is due

75:10 the vinegary taste is due to bacterial . So, acidic acid. So

75:16 can ferment sugars into many different products on the species. OK? And

75:22 acid is one of those. And that then brought about the fermentation and

75:29 basically that uh its microbes that account the production of chemicals in this

75:38 they grow as a result, more , more product and he can identify

75:44 types based on the end product, it smelled you go. Oh

75:48 this is bacteria. So and so do this fermentation and so we could

75:53 them in different ways. And so is all what the germ theory of

75:57 is about. OK. So um questions? So we will wrap up

76:08 pasture story and get into medical microbiology next time. OK. Thanks

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