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00:01 Yeah. Okay, testing. Alright. Welcome folks for raising the

00:27 . Um So today is that foot and I got a few years ballads

00:36 people going, what's so special about class, nothing other than, it's

00:40 a way to change stuff up. ? So it doesn't count for like

00:45 not super sized, they count count 100 points extra, anything like that

00:49 another class just delivered for me. . A few more questions than normal

00:54 guess. But you know, I think it's something not to wig out

00:58 . Okay. But you you know kind of I think assess uh would

01:06 somewhat higher studying one in preparing for . Okay, so um so like

01:13 said, we'll intersperse this with different Important important things to take away.

01:20 so but we do have to finish for the last part of Chapter

01:24 Right? That's where we'll start. not email uh detailing this stuff.

01:32 cost of schedule is open now so can go in to reserve a seat

01:38 quiz too. Um in smoking available class. So that covers topics in

01:48 temperatures report to basically what we talked on some of the stuff we talked

01:53 on Tuesday and M today. Um so I wait until I get

02:01 that Chapter four stuff. So let's is there anything else here?

02:06 not yet. We gotta tucker three . So let me go to

02:10 All right, so ah what are left with what kind of infrastructure structures

02:20 themselves, you know that um We with Mhm metabolic kind of late

02:29 The combat zone and dial up Boyd's gas HVAC you als um and that

02:37 of every storage molecules. No I . Starch does monochromatic Granules of phosphate

02:45 uh manuals sulfur Granules was kind of byproduct of metabolism. So and then

02:54 we um didn't get yet. So what we're gonna start with. Medina

03:00 . The last thing we talked about so um pilar so these are made

03:06 the same material. Okay same structurally material. The pylon monitors make them

03:13 . The difference is from reality tend be more numerous. Um As you

03:18 see here this is uh this is the of surrounding that bacteria there uh

03:26 be shorter. More numerous pillai um to have more specialized functions memorized by

03:33 all the attachments. So can of pillai as well in different ways and

03:40 it can be associated with the type motility as well. See called this

03:43 motility still I can't have a straight function. You can have a you

03:48 have a sex pilot involved in congregation bring cells together and transfer of genetic

03:56 . We'll talk about that later. They can there's also specialized functions where

04:02 is used to rub onto DNA fragments the cell and bring them in.

04:07 called transformation. Okay so again with pillai there could be less numerous of

04:14 with more specialized functions in some Okay, But where more numerous tend

04:19 be shorter and certainly. Okay. they both can be careless backwards for

04:26 certain pathogens. Right? Um those lacking these presents factors will not cause

04:33 are much reduced in terms of coffee . Um the uh so I'm pushing

04:41 chills just talking about that for a . So the utility number one,

04:48 pilots, # two. It's all surface. Okay, so where as

04:55 pendulum, as we'll see shortly, after this, um this movement of

04:59 bacterium in the matrix, you acquis matrix. Okay, and all

05:04 mentions, of course, um a motility is all about on the

05:09 Okay. And involved in pinas that glamorize add more pilin monomers, make

05:18 longer, and then Diploma rise. them out, make them shorter.

05:22 it alternates between Stanley that pilots. , then, attachment comes in where

05:30 looking at the pilots here, it's arising. So you see it's extending

05:35 in this direction. It's gotten larger and we'll attach at a point on

05:40 surface. Okay, So if you at the this cock, see the

05:45 movement is of course in this Okay. And so as the pilots

05:52 arises, gets longer, attaches, diploma rises, get shorter and then

06:00 subsequently draws itself goes emotion. Tour attachment point. Okay, so it's

06:05 about on the surface and they collect because it's not necessarily a smooth kind

06:10 motion. Okay, It's not a kind of motion. Okay, so

06:17 I think if it's it's kind of crazy analogy but think of a trying

06:21 row a boat on land, Whether it's yours or the pill,

06:25 right and you're words are going forward around, then you moved as well

06:31 the polite shortens. Not a great , but the point is that detaches

06:40 it's kind of a perky jerky or . They call it motility for that

06:44 , but it's all on the all about being on the surface.

06:48 um you can combine, you legitimate Caroline motion in the matrix and

06:54 on the surface it just depends on bacterial type. Um but the uh

07:01 we talked really about and so the on the right, let me just

07:05 complete the thought. So the picture the right here. Okay,

07:09 explaining the same thing. So the , I can extend in different

07:14 right? Depending on motion where it's to analyze this can be driven

07:19 you know, a attractive types of that will draw one way or the

07:25 that bind to receptors. We'll see in motion without using a Okay,

07:32 , but the difference between the the jello motion. This motion is

07:36 is on the surface. Okay. now we we talked about the stock

07:45 um in the context of the having on one end of the cell versus

07:51 other? Asymmetry? Asymmetry in terms a rod shaped cell for example.

07:57 so this is a stock. Uh is a function of the nutrient

08:04 The self finds itself. So you switch between between a stock which holds

08:09 place and therefore it's all about nutrient . Uh If it's in a nutrient

08:21 area it will want to stay in until the nutrients are exhausted. Uh

08:26 the artist will switch to the mode go elsewhere to find just kind of

08:31 drives this. Okay. Um Any questions about that pillow in february

08:37 motion? Yeah. You try to it back to me. So what

08:44 this involve? # one and number . Thank you. What's the pilot's

08:52 to Surface Collins and surface are two . So when it's attached to the

08:59 , what's the house the motion The pilots is like this and then

09:06 , right length shorts. How is doing? How's it shortening?

09:12 Diploma Rising. Taking units out. . How's it how's it going?

09:16 arising, adding us to it. alternates and the motion is attached then

09:23 rised draws the salt to it. move again. Problem arise make it

09:30 attached again. And so it Memorization, decriminalization is how tell the

09:36 lengthens and shorts and the cells attached it. So it's gonna go that

09:41 . Right? The cells attached to pilots pilots attached to a surface

09:45 they're gonna draw go along with Okay. Does that make sense?

09:51 . Yeah. Is it similar to elements, movement? Not like a

09:56 contraction kind of a thing. Not because that involves minus and acting,

10:02 them across each other. And not not really only in the sense that

10:07 have a protein binding and it will some kind of movement. But this

10:11 this is going to be different. . Any other questions? Yeah.

10:20 . Uh I've seen values of, , I don't describe in terms of

10:30 like um like a few millimeters per something like that. So you can

10:37 if you're in a lab you saw may have seen the proteus on a

10:43 . It's kind of swarms all It doesn't really form a really good

10:46 from the movement that's actually due to kind of twitching motion. And so

10:53 , the motion is it's it's certainly is I can't I don't know exactly

11:00 I don't need to see. You , it in terms of millimeters per

11:03 . And my dad, so there is certainly noticeable. Yeah,

11:08 Yes, suit typical movement toward a source or something like that. That

11:12 this any other way. Yeah. let's look at so nanotube eagles don't

11:19 much to say about this other than found in a few bacterial species,

11:24 relatively new phenomenon that it wasn't aware this when I was studying microbiology but

11:30 back in the Stone Age, but there are types but so this is

11:36 that can perform uh um extensions of cytoplasm and connect with other members of

11:42 population, right? He didn't do . So exchanging material molecule, It's

11:49 I think they've documented for. Even genetic material have been transferred this

11:54 Okay. Um There is this phenomenon um psychopathic streaming. We see new

12:02 cells. I don't know what they those tubules though that was traveling through

12:06 nonetheless kind of somewhat similar to Okay. Um the end there can

12:13 connections between different species as well from cytoplasm connect with each other.

12:19 so uh for jell o Okay, the last part of Chapter three is

12:25 fragile emotions. Um you made of with gelatin protein that are connected together

12:36 the motion unlike the eukaryotic cell, so you're eukaryotic from john. Oh

12:42 firm. For example, the motion kind of a whip like motion like

12:47 . Okay, bacterial motion is much than propeller. Alright, biscuits

12:53 Okay. And the john the arrangements uh can be there depending on the

13:04 . So you may have some that just one flagellum shown here. Uh

13:10 may have a cluster at one end all around the cell as you see

13:17 or one of and which is not that common. And you might

13:22 okay, well how is that thing swim? It was one at both

13:26 , what they might be opposing each and it turns out that either one

13:29 functioning or the other is functioning not at the same time but that's not

13:34 type that's really that common. More to see things like this, this

13:40 this type here. Okay. Um so we talked about before in the

13:47 of the LPS layer program negatives. the H engine related to the

13:57 again um you know technically any any that's motorbikes, pendulum has an

14:02 And again but it's really only was for uh and it really worked out

14:08 like your e coli and Samuel and like enteric pathogens where they use this

14:14 a way to identify. So the saw that no 1570 coal line identified

14:21 that particular. Oh police accurate variant the H engine. There can be

14:28 numbers of others and identified by the slab. Um and the last sequence

14:35 the for that type. And you give me that give me a logical

14:40 and you can identify with antibodies Service . Okay. Um so the point

14:48 H. And okay now the Well the structure the structure is a

14:57 that is inserted into the membrane and rotor portion or rather the hook portion

15:06 is what's attached into the basil body is then inserted into the membrane the

15:13 is actually where the rotation occurs and again the propeller like action. So

15:19 rotation can be two orientations right, ready to rotate clockwise and rotate

15:25 Okay. And that uh that's essentially difference in the types of motion is

15:32 one way or the other and that you two types of motions.

15:37 It is of course energy requiring and we mentioned about the proton pumps earlier

15:45 I on grading too, you can the stored energy to do things.

15:50 that's one of the things that many that nine grand is used for us

15:54 move a foot jell o The energy that movie, the jello uh to

15:59 motion. Okay, so that or can either move counterclockwise or clockwise and

16:07 rotation promotes straight line movements. we're called runs. Okay, so

16:16 counterclockwise rotation produces a purposeful let's say motion towards something. Okay. Um

16:29 it's all about binding to a Okay, so chemo attractants for

16:35 All right, these are things that move towards them. Okay, and

16:40 the movement is influenced by binding to molecules. You have receptors for attractants

16:48 one pole. Okay. And you'll attractive molecules that if they had the

16:56 for will bind. Right, and binding will promote so these are attractive

17:06 . Little triangles that will promote Okay, and that reinforced the counterclockwise

17:16 . Okay, now the it's influenced how much is there? Okay and

17:23 how much these receptors are bound with molecules because it becomes a a phenomenon

17:32 mhm amount or proportion the proportion of . Okay, two tumbles and tumbles

17:42 the clockwise clockwise tumble, counterclockwise Alright so a tumble means it's almost

17:50 spinning in place. Okay that's kind how to think about. So that's

17:55 jello in this example here when you're they kind of all around rather than

18:01 in a unified motion as you see here. Okay so they kind of

18:07 and it's kind of spinning in place ? Okay so when we look it's

18:12 about the ratio is the proportions of to tumbles. Okay. And so

18:18 it's infamous by of course the levels a is attractive present and how

18:23 Okay so if you look at what call a random walk, okay this

18:31 really a just um a non purposeful , right? So it's it's moving

18:38 in the straight line briefly that So the points um would be a

18:45 , okay and then the these would runs so they alternate randomly between runs

18:54 tumbles. Okay so it'll run for bit then it will tumble and spin

18:59 then go in one direction. So idea is that presumably the bacterium is

19:04 to find something favorable out there. it goes okay let me let me

19:10 this way randomly let me randomly go the direction then I'll spin and be

19:15 off in a different direction and maybe doing this I'll run into something,

19:20 , so that's probably kind of what idea is here, that there's an

19:23 out there, don't know where it's , but if I just go in

19:26 directions here and there or whatever, accidentally run into it, okay?

19:30 when it does happen okay then there's more purposeful movement motion right from point

19:38 . To point B. And so don't completely eliminate the tumbles.

19:46 but you do increase the frequency of as you can see here initially and

19:51 is attracted so low level, concentration level of attractant too high level

20:06 high I'm going this way. Okay and as it gets it senses it

20:15 to the receptors been rich and receptors promotes more clockwise rotations less tumbles and

20:21 it keeps going more and more encounters and more and that produces more and

20:26 uh run run motions and so that of course that's what we want to

20:33 . Getting this really high concentration of which presumably attractive is going to be

20:38 type molecules. All right, so will enable it to then get into

20:43 area of lots of nutrients and then energy source etcetera. Okay, so

20:48 it's all about movement. The proportions to tumbles right more more tumbles we

20:56 real signature tumbles and runs then it's kind of casually going here and there

21:03 to find attractive but if you see of of ones tunnels and it's likely

21:11 detected something is is going toward Okay. Something favorable. Okay.

21:17 Pente clockwise runs clockwise topics and it's comes by by them to uh

21:24 Okay. Any questions about that? on the previous slide only happened when

21:37 it promotes those but you get more those if you have more attractive

21:41 So it's about levels of how much are all the receptors being bound or

21:47 ? So that's that's the frequency of many receptors being bound determines how how

21:53 runs occur running can still happen. can but yeah but then but then

22:03 you have the tumbles are more Right. Right. So correct.

22:08 correct. The parts of the cell are technically attractive. No so magnetic

22:14 are only a specialized species. Okay it's not that has nothing to do

22:23 so that's strictly just magnetic attraction. . Oh sure sorry about that.

22:34 about that. Yes. Absolutely. Is there a bench to having more

22:43 gel? Um I don't I think um There's varieties have different types.

22:51 I can't tell you which one is common though. I'm not I'm not

22:54 don't know that answer but but I I don't think there's a difference in

22:58 more or less. I don't think there is maybe somebody studied that.

23:07 , different. Yes. All Um, well, I don't know

23:15 you see it. You have So, we have now two bits

23:18 different species. You would have to then um, I mean isolate and

23:25 those organisms. I mean, it be obvious. I'm not sure if

23:29 answering a question. Right? Yeah. Um so in the

23:37 mm hmm. If it's constantly there's likely not very little if anything

23:48 there that's promoting it to run. it's probably very little attractive out

23:52 At least that it can bind Yeah, the other one.

23:59 what's the difference between like and like uh, a sex pilot is gene

24:10 ? Um, it's part of the process, um, that we'll talk

24:16 . But now to Bill, I know. I don't even know if

24:20 is now the mechanism that promotes nanotube . I don't know if it's a

24:29 thing or Exactly. The second pilot an actual protein structure. Yes.

24:40 , I yeah, there there can two fortresses can connect and share

24:46 It makes sense that they possibly seriously . But in conjugation requires replication of

24:55 of the and typically transfer plasmids in . He had a copy detachment synthesized

25:02 pilots was all part of the Whereas nanotube information don't know the exact

25:09 and then it's not maybe more, . Okay. The and the chances

25:15 exchanging genetic material. I don't know if that would happen, very frequently

25:20 at all because it's not an orchestrated . Like congregation is Okay. Is

25:26 makes sense? Yep. Any other ? What? Alright, so let's

25:35 we have to remember we had a that preceded this section at the end

25:38 time that covered some of the latter of the part to stuff. So

25:43 of that here and then uh this . Okay, so let's look at

25:54 question here. All right. So so we looked at this before last

26:04 . So ph be boxy zones, chemo taxes. Um Making those

26:13 So uh waldron uh talking about Um So while you're reading an

26:19 so it's positive cuba taxes. So there are molecules that are more exclusively

26:26 the context of attractants. You can't repellants, repellants or molecules that

26:32 present will be noxious or toxic to cell and would run away. So

26:37 can have kind of worked the opposite too. But a negative chemo taxes

26:43 movement away from Yeah, this is about positive chemo taxes. Movement towards

27:01 . Yeah, I know it would less likely maybe. I mean if

27:13 connecting to selves together and transferring stuff a random class would just accidentally be

27:21 through maybe. But I think it being a regulated process of what goes

27:33 my congregation is pretty well control that . So I think part of chances

27:39 less. No. Alright. mm hmm. Mhm mm hmm.

28:12 543 two one europe mm hmm. . So the magnetism, that's the

28:24 one. Alright. So magnetism is not um about food or energy for

28:30 compass orient that sell the magnetic field towards south or north depending on what

28:38 itself. Okay. Okay. Um on chapter three could all this

28:50 Right? So um uh quiz backward will cover more of this. But

28:59 just what we talked about on So areas involving I guess more on

29:06 right side here. Several skeletal elements blah blah blah. That's of the

29:12 on the blackboard quiz this week is what's. Right, okay. Um

29:18 then then then the material from Chapter We'll talk about today. Okay So

29:25 one thing I just I did do the end here was to uh switch

29:33 uh this part. I put the stuff which involved calculations at the

29:39 We're probably not gonna get to it . That's fine. But we're gonna

29:43 about everything that's above here. Uh so we're gonna do calculations stuff until

29:51 next Tuesday is not that complicated. look through. And uh we'll do

29:55 of those problems on Tuesday. Um we're gonna focus on growth requirements blah

30:02 blah. So I actually have like little flow chart here. So let's

30:05 a look at that. So um looking at growth requirements for bacteria which

30:13 course um It depends on the nutritional , how to grow it and what

30:18 need to add to the medium. physical chemical factors, right. Different

30:23 ingredients elements etcetera, physical factors, . Uh Other things to consider their

30:33 requirements. Of course. Growth putting together in the growth medium formulation.

30:40 grows media type. Okay complex with media. We'll talk about that.

30:46 um And then there's different categories selective differential enrichment medium, general purpose,

30:55 high yield medium. These are all . What are you trying? Why

30:58 you why are you growing them? for what purpose? And so you

31:02 employ different of these media types. . Um The growth media form is

31:10 liquid solid. Now a semi Of course the most common types of

31:17 and liquid and there are roles for of those uses for both of

31:21 Um Then what we'll talk about next . Cell numbers growth rate growth we'll

31:28 talk about batch growth curve. Right the phases of growth like black log

31:36 death based. Okay. Um But talk more about how you produce numbers

31:41 quantitative these things next time. Okay uh let's start here with this

31:54 So for most bacteria increasing the amount this nutrient to a growth medium will

32:01 lead to a significant increase in cell . Which nutrient would this be?

32:08 so I'm gonna go and put the on. I already know you know

32:13 answer is this slam dunk. All right. 1 1.11 .2.

32:45 . Here we go. Cute. 78%. Say carbon. Um That's

32:59 . Okay somebody so happy you've got . It's good. Okay so the

33:07 is then why why why carbon why why the cells of carbon,

33:18 They have many saturates. Okay if can't manufacture it, what does that

33:23 it? What kind of nutrient does make it? Okay so so back

33:29 the white farmer is carbon skeletons. so biomolecules of life. Right,

33:40 acids, carbohydrates, proteins, fats all built around a carbon frame and

33:46 you add different elements to that to it very small molecules. Okay

33:51 So um life depends on this. ? Uh There has been uh I

33:57 a star trek episode where they had based life okay. Where everybody had

34:02 S instead of the sea there. . Um But it's what we are

34:08 carbon based life. We have to these molecules uh two to build our

34:15 . Right? We break stuff We take those building blocks and we

34:19 new biomolecules. Okay so in any growth anything really? But you know

34:27 talking about bacteria of course you want get lots of bacteria growing. You

34:31 have carbon in there. Yeah you the other stuff too. But carbon

34:35 the biggest so C. H. . M. P. S.

34:39 ? Um essentially these these are your nutrients the things that are carbon um

34:46 phosphorus. So macronutrients I say are of I use the term these are

34:55 grams per leader. These are in or less per leader micronutrients more or

35:04 less of them. Machinations of course more. Right The special interests cannot

35:09 made. Right? So carver's essential so you can't make carbon right?

35:13 you have to give it to them ? Um And then they can do

35:17 thing with um Now I didn't mention said see in yes you don't have

35:25 add a church to approach me. is that for the water? Right

35:33 it's also part of carbon market. . Your sugar to a carbon

35:41 It's gonna a just come along with . So too is old. Right

35:45 there's generally parts of of hydrocarbon molecules you didn't give right as food

35:52 Okay or there are other parts of molecules that you supply to them.

35:58 um Okay here's another question. Alright this kind of addresses a couple of

36:05 here. Um So take your time read it. So each of the

36:11 represents the chemical composition of various growth which one is chemically defined what we

36:20 synthetic. Okay or minimal medium uh for growth of a hetero trophic

36:27 So the operative words are involved can defined and header proof. Mhm.

36:34 which of those? Oh let me that again. Okay, so which

36:39 those fits? Okay. So not here write and read. So supplying

36:51 to remember certain things require sio They can't eat things like fats or

36:56 and things like that. Why? here four we put it directly in

37:06 medium and something like this incarnate That uh that will be converted to

37:11 two. So that's another way of theo too. Okay. Mm

37:35 So chemically combined for minimal medium or . I mean the same thing.

37:46 right. Let me put timer Mm hmm mm hmm hmm hmm hmm

38:04 hmm hmm hmm hmm hmm hmm hmm hmm hmm hmm hmm. Okay,

38:12 hmm. Thank you. Okay. . Here we go. 10.

38:30 . So between A. And It seems like um okay um let's

38:42 with which are the chemically defined media chemical to find. We're not saying

38:50 going on? The find media are . And D. Correct Because why

39:00 can quantify everything correct? You can't can't you quantify? And when these

39:04 the media, right? So you're complex media have things like this and

39:11 it's next question. Pep tone used extract. Um you see here as

39:19 uh here as well. Okay. these are we call comp complex

39:27 So even if you have a bunch ingredients like this. Right? You

39:33 sucrose and you see all this other . Right. And you have even

39:38 complex nutrient that makes that media a meeting like and so a complex medium

39:47 know the you can be given a and periodic chart. You can calculate

39:55 all the ends of carbon hydrogen auction polluted and everything right? But you

40:01 believe it has a pep Toni yeast because although and what pep Toni is

40:07 basically a beef product that's been treated enzymes I think. Right you can

40:13 any kind of meat right treated with or you boil it to kind of

40:20 it down, make it make it able to use it and to dissolve

40:24 in the medium to use it. but it's essentially meat or plant.

40:30 can be like soy products, soy can be a complex nutrient but you

40:35 it contains all. It contains C . O. M. P.

40:38 . Yes. You don't know the proportions right. Of what's in

40:45 That's what we call it. A medium. Right? But with a

40:49 example the chemical formulas for glucose and , phosphate and ammonium chloride and sodium

40:56 . The mag sulfate and trace and trace metal. They'll be defined with

40:59 . No and we can know exactly the proportions of are of all the

41:08 . Okay that's what is a defined . Hence the term defined.

41:13 Um So A. And D. fit that fit that description.

41:20 The other ones have either one or of these complex nutrients of Pepito East

41:25 . Okay. Um So now the is fine. Okay A. And

41:36 . Okay. Now the question is one of those two will the hetero

41:44 ? Hey. So because the carbon here. All right. It is

41:55 form like that. Okay. Just , the art professor professor. All

42:01 . You're gonna be sick of hearing say article pedagogy if you're But um

42:12 2nd you know how cultural heritage. . But we don't know what before

42:18 . Right. Anyway, so um the although hetero carbon, what's the

42:28 form? What's the form of the ? Okay so the correct answer is

42:32 Okay. Petra Trophy wife will grow that. And that's a defined medium

42:38 . Is the key. There is right source of C. 02 as

42:47 . But then Sulfur is H. s. That's a. You don't

42:52 aren't familiar that but that's so much now. But when we talk about

42:56 Trophy which we have, that's what is for energy. Okay.

43:04 So we're gonna mention define media here in a second. Let's look at

43:10 one. So you can again defining types. Right. So photo tropes

43:19 chema tropes photo trove. So energy . Right defining by an energy source

43:26 source. Right? Electronic sector. . So let's look at which one

43:32 Little Trophy. Okay. So you've your choice of A through G.

43:39 . A. B. C. . E. F. G.

43:43 one is little trophy? Mhm. . Remember what little troughs can and

44:20 do mm hmm. Mhm. Yes. The timer going. So

45:03 not you're not answering the bottom one . You're answering the little trophy.

45:08 let me pause it. Which box ? Little Trophy there? Took it

45:17 . All right. Which one is problem is that? Let the

45:24 Which box represents Little Trophy? A G. Are your choices? Here

45:34 go? Okay. 876. And okay. Alright. See

45:56 Uh look at the Mhm. I . Okay. Who answered the they

46:06 to be resolved? Why do you to me? Mhm. All

46:20 And yeah, that's that's right. right. You're right, correct.

46:29 you C. 02. They don't organic carbon. They use things like

46:35 . Two as an energy source and two west and whatnot. Right?

46:43 , uh to um So what would . What would that represent you?

47:46 , timer's going. Mhm. I . Okay. So um Yeah,

48:20 is That is correct. Um The organic comments obviously. And we breathe

48:34 . Okay, so we are any about what is appropriate? Is

48:39 Yeah. So look at her It says so can you explain

48:49 Why for the first one? Why do you need to see what

48:55 up, grow up, grow Train tree. Yeah. So you

49:03 , all organisms energy source like that cool for a little pro um carbon

49:12 . That's where it's like C. . Okay. Um So here are

49:22 categories. Okay, chemo autotrophs. photo any question. Alright. Um

49:36 . And here we are again. the uh and you can combine these

49:41 . Right? Hetero hetero auto Hello? Is it seo two or

49:48 more complex? Glucose. Uh Fats have you? Energy source? Um

49:57 gonna be light or right. Non chemical oxidation or like Robin oxidation.

50:06 electrons right? Uh left organized. the uh little trough. Right?

50:14 something like uh let's change it up something like And they will oxidize that

50:24 will take the electrons from that and use the electron transport chain.

50:31 And eventually they can become reduced. ? So these these can be used

50:36 some cases oxygen. So there's little that can use oxygen. Those that

50:41 . Right. And so this is we'll talk about, you know,

50:45 . Okay. But the thing is we, for example, can use

50:52 , right? C six H 12 . Right? Break that down to

50:58 CO two and water. All And so we're getting carbon units from

51:04 to make biomolecules. Right? We're getting an energy source on this because

51:09 will produce a tps. Right? we are you know, hetero coasts

51:15 the two for one. They're carbon is also an energy source. Break

51:20 down. Make building blocks and make more organic molecules. And then in

51:25 process you breaking it down and release catches a teepee. But the chemo

51:31 lot of stuff gets energy here, ? Because that will produce a

51:35 P. S. Okay. But , Right? Where's the carbon coming

51:44 ? So it uses the energy of gps from that process of breaking down

51:48 organic molecules. And that energy is to fix CO two co two fixation

51:52 a lot of energy. And so photo of using light energy to help

51:58 you to fixation. Right? So another pro it's all about Okay,

52:03 got you. C. 02. . And so c. 0.

52:08 . It is very small. So you compare that to glucose,

52:13 ? You gotta take those C. . T. Let's build them

52:16 They energy. Right? So for truth um if you're having to make

52:23 organic molecules using Sio two, you've to have an energy source applying that

52:27 so it can be light. It be chemical oxidation uh questions mm

52:35 So uh what kind of growth medium this in the box? That that

52:51 about that? Okay. Hey, running? Okay. 10 seconds.

53:43 . So uh yeah, it's gonna a complex medium. So again,

53:51 addition of these complex histories pepto beef tripped. Oh, soy extract

53:58 Right. These are all components that C. H. O.

54:03 P. S. We just don't the relative proportions types necessarily. Alright

54:10 um here's a question. So this a terminology. So oxide trophy.

54:16 right so we're bacterium known to be distance. It was rolled on this

54:26 . Thanks Christine's amino acid. Our means something. Right? The question

54:35 what? So it's not a type questions so just somebody throw it at

54:39 . What do you got anybody? or no. No. Okay you

54:52 um Yes. Y yes you're a because oxygen is included in there.

55:02 also like he said it needed He grows on amino acids which is

55:06 in so what's, so what does Mr but randy randomly got for me

55:19 think you know what's that? What's ? Trust me. Bye bye.

55:25 so it's the hospitals can or can't ethnicity. Yeah. Right so it's

55:31 grow you have to do what? a five minute meeting. Right?

55:38 um so is it being supplied to ? Yes. Yeah I grew up

55:49 decision is the actual big supplier at complex nutrients the effects track headstone.

55:57 again just think of these things think pepperoni beef extract, its meat everything

56:04 , muscle tissue and whatnot. So gonna have always in real assets and

56:10 in there. Okay so um as as you got that complex nutrient

56:20 Um So again the obstacle. Term it's deficient, right? History or

56:26 oxygen is deficient in that pathway. can't make that amino acid for

56:32 Okay. He has a crime where sufficient or won't grow, wow.

56:38 , um, you could supply institution . Okay. Also supplied through one

56:45 these complex nutrients. Any questions on ? Yeah, My priority five.

56:57 on. Very acid is no longer credible media. It's like medium plus

57:08 disagree with that. But I don't with him about it. But that's

57:12 a lot. Absolutely. It's microbiologist invented it. So we invented those

57:18 . So yeah, he's that I disagree with that. Yeah.

57:26 , because you know what if you're the amino acid, you know what

57:29 , you know what the name as is and the and the atoms in

57:32 , you can absolutely quantify it. Alright. Any other questions?

57:39 not, not just it wasn't to , is it to that other

57:41 Okay. Yeah. Go ahead. . Mm hmm. Because you know

57:55 those complex differences are just lower though again, people that meet right here

58:00 the ground beef, you're getting all things in, right? Because you're

58:04 ground ground up towel and all the with kids in there are gonna be

58:09 that. Now the qualities that you have. No, but it's it's

58:14 gonna have a lot of those in . So that's why we're doing like

58:18 studies and you want to be You want to add this to the

58:22 you want to control that for some then you wouldn't want to have complex

58:26 . You wanna mil million and add into it. You can control

58:31 Okay. Any other questions? Um So can you explain the difference

58:37 selective Yeah, selective, selective. you are adding a chemical to the

58:45 ? Yeah. Species and growing very to gram negative, gram positive.

58:53 you add chemicals to prevent gram negatives growing and knowing that our grand positive

58:58 are types that give reverse as well destruction. Being just wanted. That's

59:04 trying to limit anything color reactions. you can find out something about

59:10 So great comment or something like headed many. Sure. And to see

59:16 supplying sugar and the ph indicator in color yellow and city city. So

59:26 see growth yet. Use the sugar that's producing this yellow color. So

59:32 using a other type of differences between types. Tell me something about your

59:42 . The other question. Okay, here's another medium question. Okay,

59:52 we have three media types. So a complex and to define media.

60:01 , so which meeting would a chemo growth? Go on. There are

60:07 lot of these terms that we There's overlap. Okay, thank

60:13 Uh it's just different terms to being same thing. Hi. So let's

60:23 open up. Mm hmm. Chemo tropes of chemo chemical chemical oxidation.

60:48 these organic sources. Right. the media and matching matching up what

61:09 what? Always into the carbon That's perfect carbon source then other

61:26 Thank you. You're a chemo organic . Okay. You're a chemo organic

61:49 . All right. So if you're chemo organic trophy, are you going

61:56 grow on uh A Yeah, complex . It's got the C.

62:04 O. M. P. In there. Okay. Um Are

62:08 going to grow on B. Key ? Gastro Yeah, organic glucose.

62:15 . You're gonna go and see? . Okay. C. 02.

62:20 right. I hear. So let's uh endure the clicker questions over the

62:28 . What would the chemo autotrophs go . All right. Mhm.

62:34 Is correct. So is for a right. c. 0.

62:42 Okay. Um A. And Are what? A. Mhm.

62:49 Lexapro for growing what C. A head or a trophy. So

62:55 trophy or kmart down through the same . Okay. Role on the

63:01 A. Right. Uh Okay. . M. D. C.

63:13 . PEI NB. And all these you're seeing when you posted after class

63:18 , so um so yeah. trip Tony yeast extract. Remember.

63:32 think it has meat. Absolutely. meat. I'm meat. We're

63:42 I'm okay. Um Yes. So I just put this in just

63:51 to mention quickly that there was a uses primary use for planes we call

63:59 the solid media is you know, the key step in obtaining a pure

64:04 . Okay, assuming the organisms cultural , excuse me. I said

64:13 Um and tangos. I said the and subculture and do work with

64:18 But a plate. Solid media has be a part somewhere in eventually attending

64:24 culture. Because allows individual alliance for , cells that are in this liquid

64:30 . And of course you can't see the naked eye, but you want

64:33 be able to see what's in there put it on the plate.

64:37 Yeah. You can see under a . But you can't you can't,

64:43 know, separate the mouth and grow up individually on this in a sample

64:46 that. So you need to put on a plate and then see what

64:50 got. And then go from there get a pure culture liquid media is

64:57 primarily for large quantities. You can stuff. Lots of cells. You

65:02 a pure culture inoculate a liquid medium you get tons of cells that you

65:07 for various purposes. But it's just DNA and sequencing or isolate proteins.

65:13 happens if you want mass quantities of for different reasons to use liquid

65:18 And I need you use something, gonna test your flask or you can

65:24 up to 100,000 liters if you wanted . Okay. But the point is

65:28 liquid. What you used to get quantities themselves to do things with.

65:34 . Um Okay, enrichment culture. look at this. Mm hmm.

65:41 this isn't a good proportion. Just about it and throw something happened.

65:48 What would grow on this medium is uh media components. Okay. And

65:54 a hint, Jack. Something in diagram. The hint. Uh any

66:10 . What's is there something missing? missing? Is there something missing from

66:15 media? Remember what you need in growth needs? Right, okay.

66:23 . So remember the C. O. M. P.

66:27 Right. And thanks. Right, is missing. Okay. So what

66:35 grow on this? But something will to grow on this. Mhm.

66:39 , we're all in this will be guys. Okay. We called nitrogen

66:45 into fixers. Not that not that expect you to notice for this exam

66:50 just an example of an enrichment So enrichment culture is it broke me

66:57 you, my components into to favor growth of one type over enough.

67:06 the soil sample, you're gonna have of things in there. But when

67:10 have put that grow generally you're hetero types often are the ones that really

67:17 fast and grow everything. Okay, let me try to monitoring the medium

67:23 get what you want to throw. is an example of something that's very

67:28 , right? Because that would be would certainly enrich for natural fixing bacteria

67:34 the soil of putting on this. not that militated or something this

67:41 So but again you can you can this to to you know again what

67:46 of metabolic type are you trying to grow or find? Then you can

67:51 the medium to that particular metabolic type then that will favor the growth of

67:56 over others. So that's what enrichment about. Okay so it's a subtle

68:02 between selective enrichment. They may see very similar work but with selective media

68:08 are actively putting inhibitory molecules to prevent from growth. Richmond doing I'm just

68:17 ch oh and ps you know putting ones of those in my medium to

68:22 growth of certain types. I'm not inhibitory chemicals to actually hit something.

68:28 so like putting antibiotics in immediately we that so that you're actually putting something

68:33 there to prevent something from growing. so no little bit of difference

68:38 But again there was being towards things stop something from growing or not just

68:46 playing the C. H. M. P. S. Into

68:49 combination that will favor one type or um Question um Fastidious. Let me

69:00 mention that real quick. So fastidious . Um Are you know it when

69:07 have one because you've got a Recipe a meeting that's like 100 ingredients

69:13 Right? They of course have to C. H. O.

69:15 P. S. But they often make a lot of stuff so you

69:18 lots of vitamins in there typically. and what we call gross factors.

69:23 factors are our components that you may necessarily know what's in there but you

69:29 what helps their growth like blood. example adding blood to a medium is

69:32 used patterns you know what's in blood a lot of stuff in there that

69:37 them grow but you know they grow and you just add it. So

69:39 call those things growth factors. So types, you typically had lots of

69:44 vitamins and amino acids and stuff because deficient a lot of out of

69:51 Okay. That's what we call fastidious . Very exacting requirements. Okay.

69:59 The status is often used in the of humans. We say another person's

70:03 are typically very annoying. Okay and go back to the fastidious would be

70:08 annoying because you're wearing lots of stuff and having to put this all

70:12 Um Okay so bacterial growth so we're gonna go into but just to show

70:21 magnitude growth and it can occur relatively . Right? So of course bacteria

70:26 binary fission which produces um exponential growth cells very quickly. Um 20

70:35 You see you can grow in 8 10 hours. It was back e

70:39 for example under optimal conditions. Uh worry about these equations will mention that

70:44 time. But generation time is something you'll hear next lecture uh doubling time

70:51 often used the same thing. So time of course to produce a generation

70:57 we use generation time as a measure growth. Okay, so when we

71:01 at what's called batch growth. So a question that relates to the batch

71:09 . So take a look at So bad growth refers to you.

71:15 a container. Okay. Scientific, a shake flask. Yeah. And

71:23 plug media. Yeah. You Right? So that that badge,

71:30 ? You inoculate and you follow Yeah. And then we'll go through

71:35 cycle that you see there and then and that's it. You don't do

71:40 else to it. That's what we a batch batch growth. Okay,

71:45 all your Oh, that was my . Let me uh let me go

71:50 the podium. His name. so um, it's not working.

72:04 right, give me a second. got batteries. Thank you. Testing

72:21 . There we go. Okay, um sorry. Okay, so

72:41 batch growth. So again, we're kind of taking samples out just to

72:45 growth, which we do with the centimeter. You measure the cloudiness,

72:49 cloudy is getting anybody growth growth, you're not doing any other manipulations to

72:54 batch. Okay, so uh let's they wouldn't answer this the but the

73:06 phases of growth have different features. . And uh different characteristics as it

73:16 along. Okay. Yeah. go ahead and answer and go in

73:41 . So uh phases 1234. So is lag phase. Okay um evacuate

73:51 you first add cells. The cells to acclimate to their surroundings.

73:56 Um becoming turning genes on turning genes , adjusting to the surroundings. No

74:04 occurring yet. But once it does will then begin to take off and

74:08 phase. Okay and so uh in phase rapid increase. Right? Exponential

74:18 uh sales actually increased in size. . Lots of cells dividing obviously.

74:24 but eventually beginning to here. So is a log lag stationary phase is

74:38 we plateau growth equals growth rate death . Okay so it's not dying yet

74:47 it's very limited growth. They're very . Okay um Actually that's kind of

74:53 smaller right because now it's in survival right? And to become a smaller

74:57 less to keep up with let's be able to survive. The hope being

75:04 will come in and I'll be able grow again. Okay But eventually it

75:09 reach a point where uh nutrients are and now death rate exceeds growth

75:16 Okay so here this is true uh changes occur both into obviously but also

75:27 death phase. Okay So that's true well. Okay and then and face

75:34 face what we talked about Chapter five we're trying to add antiseptics and disinfectants

75:38 kill to kill cells. Okay. But this battery just died again.

75:46 So uh changes in cell size occur two and three. That's also true

75:54 and log a little bit smaller in . And this is also true.

76:03 the ceiling acts um. Ah when actively growing cultures as most most act

76:13 , yeah, better acting on Okay, So we'll leave it

76:17 folks. Pick it up on Thank

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