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00:19 Testing testing testing. All right. we go. Hello folks, nice

00:31 cold outside. Huh? Um uh let's see. Alright, we're in

00:42 red box. Um day did the , whoever came up with that.

00:53 It looks like wait, if he the shadow there was more bad

00:57 right? We didn't see a Everything's good. Anyway, so today

01:03 finished a chapter three finally um started growth. Okay, so different aspects

01:15 growth starting with program, what do need to grow? Um then uh

01:25 guess I call it different ways to then. How do you want to

01:32 a little bit of calculations? Nothing . Ok. Uh There'll be a

01:39 of calculations to do on the Go through by blow, take you

01:45 it. I don't think we're gonna any issues with it, but you

01:49 be allowed to have a calculator with in the examples, only a couple

01:54 problems to solve, but you'll have catheter use if you want any time

02:00 . And uh Castle is always alerted it. Always tell them ahead of

02:04 . Don't mess with people they bringing because they're allowed to so uh so

02:11 obviously we'll email you all this Remember it's uh still two weeks from

02:20 . So but the schedule opens up and it's been posted on top.

02:26 that that's the case. This is . Right? So again this is

02:31 opens basically at 12 a.m. midnight uh morning, 11:59 This evening. I

02:39 want to look at it. Um for those of you that want

02:44 get a specific time. I don't where the time stops are but generally

02:48 once pretty much throughout the whole right? Nine through six or something

02:53 that anyway over two days. So be aware of that. Um And

03:01 made some I just modified a couple things on the blackboard. So this

03:06 chapter five. What is a It's not uh It's right right after

03:11 becomes viruses part one which will be of those type things. And I'll

03:15 the videos for those. Um that's the six on the 16th. So

03:21 a ways away in so but a before then I'll post the videos for

03:27 . Um but that's unit too. anyway we got to finish up you

03:31 one uh so we basically have four we got plenty of time. So

03:36 definitely finish all we're supposed to cover . So um And uh this mature

03:44 thing culture is one of my favorite in the future. I've worked in

03:47 for like 12 years and biotech growing growing bacteria. So it's the one

03:52 I know something about. Okay much anything else I'm here but I do

03:56 that um And the metabolism stuff I'd to talk about that. That's unit

04:04 um let me touch on some some and stuff. Certainly getting the

04:10 Okay. But first let us okay summery kind of all the stuff you

04:19 so previously. Right. Put all parts of the cell cell.

04:26 This dude right here. Um So was familiar with these things.

04:34 It's pretty much chronologically how you went all the future. So we have

04:41 are basically when I call structures. These are features not in all bacterial

04:52 but many have these kind of I say these certainly these off directly or

05:04 . Two metabolism, my metabolic adaptations byproducts of metabolism. So one way

05:13 another kind of directly indirectly related to , metabolic differences between cells. As

05:18 see the last one of course is is about motion. Obviously this can

05:25 about these are about motion and So we'll look at look we're getting

05:31 the nuts and bolts of that. , is there anything over here anybody

05:39 a question about? Yeah. So you can't think of question now let

05:48 know and I'll be glad to help it. Alright, question 1st

05:55 Should look at this session 94 Which is below is false. We're

06:05 cover these terms in the next couple slides here. Right ph bi carb

06:11 zones, twitching positive taxes, magneto man there is a false there is

06:30 false answer here let's get the wrong . There we go. Okay It

06:59 cut down from 10. Yeah. mechanisms are not food. Okay.

07:23 They can influence a type of Okay. But they're not a food

07:30 . Okay. The compass. A for the bacteria that has so.

07:35 right so um so obviously that B. C. D. Are

07:40 true. Okay so let's look at in more detail. Alright so the

07:46 ones we look at our relate to synthesis um Auto trophy. Okay and

07:55 um the so again fresh in memory pro carrier world can be two

08:07 Right? Photo props of course. light energy to chemical energy. Um

08:14 probes uh take a chemo autotrophs. ? They provide energy from the observation

08:24 minerals inorganic ammonia, hydrogen sulfide, . Um Iron and white.

08:34 So in both cases these processes generate . Right? Energy in the form

08:43 N. A. D. And . T. P. Right?

08:50 the role that's the role of this of the trophy in is to produce

08:56 because they're gonna use that to do . That's the nature of an auto

09:01 . You C. 02 and Two fixation takes a tremendous matter.

09:09 one of the structures involved with Well okay you're so don't I remember

09:18 about pro cariocas here. Right? don't have those that photosynthesize don't have

09:24 classes. Yeah in the context Right. We're not talking about your

09:32 or canal but we're talking about coins even the highly golden membranes.

09:43 stuffed full of uh. Right And photosynthetic pigments. Right? That's what

09:51 coins are in a core class that happened to reside inside the program.

09:58 , photosynthetic type. They're just parts its membrane. Right? It's looking

10:05 highly folded stuffed full of these photosynthetic . Okay. We call that.

10:11 . So the course by folding it . Right, the membrane you can

10:18 a lot of surface area. You a lot of areas of packet full

10:23 these photosynthetic pigments. Jack. Um box zones. Right? So these

10:32 the the light portion right, relates fill voids. Right? This part

10:39 it relates to that car boxy Okay. So uh so one of

10:47 enzymes we'll learn about later is this called? Was the short name?

10:53 name is um Close by phosphate. Don't worry so much about that.

11:02 if you see ribis co you C. Two fixation. Okay.

11:06 it's the end actually combined SEO to with a private carbon intermediate.

11:12 That's the actual fixation reaction involves Biscoe the most abundant enzyme on planet

11:21 When you think about all the things photosynthesize plans to algae etcetera.

11:26 So but in bacteria that are you find that enzyme packed into the protein

11:36 um structures. Okay. That you right here. Right, That dark

11:44 . Right. Is a car boxy . Okay. So just packed full

11:49 enzymes and bacteria are vigorously fixing 02. They'll they'll have those structures

11:54 ? To help fix the 02. so you'll see them in photo photo

11:59 trucks and in chemo water trucks. ? It's possible that both types of

12:05 and both and likely have these Okay. Um Alright. Gas

12:12 So I mentioned gas vacuums here because talked about we are talking to someone

12:20 also photo water close. Okay. so the structures that they will have

12:25 and they can also have gas gas again can produce a type of motion

12:32 it's a bubble that fills fills up air and so we can regulate how

12:38 air is A. So it's gonna a feature of a aquatic um photosynthetic

12:47 . So it kind of allows us shift that water column to get to

12:53 appropriate depth or absorb light. It's a bacterial photo trophy vary the

13:02 of life they absorbed and so this kind of helped me get to the

13:05 depth for that. Okay um Any about these. Okay So let's flip

13:14 storage grants all these on this slide types of energy storage uh particles if

13:23 will. Okay so and they're all repeating units. Okay so many dramatic

13:33 . Another term you may see here a volume 10 um same thing but

13:40 are polymers of foster. Okay. is to be a quick energy store

13:46 by just clipping off one of the to ADP deformity P. Okay.

13:52 somewhat analogous to create team that we . Right have very similar purpose.

13:58 . Quick store of energy. So uh it is it tends to

14:04 prevalent in certain types of others. is one of those. And so

14:11 stated with methylene blue. And hence see the very dark structures here.

14:16 are all packed full of these meta grains they call it because of it

14:22 under a microscope given kind of a appearance. So again, just an

14:29 store. Right. You're familiar with from plants and starch. Right?

14:33 have glycogen in your muscles. polymers of glucose basically. Right.

14:38 um again you hide realize it get glucose and you can go metabolized and

14:45 energy. Okay. Uh you see as both starch and some types can

14:51 like so both types can be Okay, so for granted. So

14:55 this one is actually is not um a store. I can be.

15:03 you can have differentiation in social metabolism types of this particular one. You

15:08 the yellowish blobs in the south These types of. That's true.

15:17 It's actually regardless of the yellow blocks sulfur, elemental sulfur. Right?

15:25 super soluble. Um And so it up as these yellow blocks. It's

15:29 byproduct of the it can oxidize Two S. Right. And produce

15:37 sulfur. There are types that can use this and convert to more oxidized

15:45 compounds as well. And and those don't accumulate the sulfur S.

15:51 In their cells. Using this type is the reaction is elemental sulfur and

15:59 accumulates in the cell. Okay, basically a byproduct of metabolism um

16:05 H. B. Inclusion. So falls in the lipid category. The

16:10 is kind of the repeat unit here bacillus, what's very common soil

16:15 You see the white blobs and it are the PhD graduates chock full of

16:23 . Okay. At one time I kept up with it, but this

16:28 actually exploited as a biotechnology product. ? And when you do that,

16:34 you're doing is you're basically taking the or whatever the microbe is, right

16:38 producing the material you make it produce than ever. Would you do that

16:43 different ways? Very to increase expression the genes that make this material.

16:50 can grow them in certain ways to production of this material. But they

16:57 to this was developed for use in biodegradable grocery bags, right? The

17:04 you get your Kroger's or H. . B. Whatever the plastic bags

17:09 are biodegradable and made it out of PHP material. Okay. And uh

17:17 was only one problem with it. weren't very good put groceries in it

17:21 the bag. So they have to mix in like the biological material with

17:27 of the non biological material to make more back a little bit better stability

17:32 it. But that's kind of the of the whole thing. You want

17:35 completely biodegradable, but I'm not sure they've improved upon that or not.

17:39 don't think I don't see seeds in grocery stores yet. But for

17:45 biotech people majors out there, it may be the kind of stuff that

17:49 do right? Growing bacteria for others commercial purposes. Right? So what

17:55 did for 12 years and I ended here. Right? So because companies

18:00 up and they failed, right? happened to me like four times in

18:03 row. I said enough. So , oh, that's a story for

18:11 different time. Let's uh look at question. We're looking at it.

18:19 any questions about the storage management. . All right. So one thing

18:25 think about is with these structures that going through, can there be commonality

18:32 like this basket? Right. Maybe structures were looking at uh be similar

18:40 they're all involved in emotions. Any of motion. Right? As long

18:44 the cell is going from point A point B. It could be multiple

18:49 to do that. Good time to when they get timer gets that

19:24 Okay. Alright, let's count down five 432. Hey, what's

19:41 O. Can be a kind of , right, jell o Obviously can

19:46 way emotion stylus. That's the Military pilots can be involved in that

19:53 . Black girl can just mentioned kind moving up and down water on magnetic

19:59 . It's like a compass accepted towards north or south depending on what hemisphere

20:05 . So yeah like I said because any type of motion. Alright then

20:13 can certainly all 40s fit that. let's look at these little closer

20:20 So okay so the And next week gratitude. Actually somebody actually acquired some

20:33 these and grew them in this liquid in this jar. And a big

20:39 . I see you're probably familiar You're probably using chemistry lamp. Maybe

20:45 magnetic stirs. Right? And so can see that the fact we put

20:51 magnetic stirrer on one side of the and after a few hours you see

20:56 kind of dark with the cell particles were attracted to the magnet. All

21:00 . Very very strange. Um But what is this about? Okay so

21:07 relates to their metabolism? Right. so so depending on what hemisphere in

21:15 and south. Right. The magneto particles acting like a compass inside the

21:22 . Okay. It's gonna attracted to north of the northern hemisphere and in

21:28 south in the southern hemisphere. And the movement is towards the people

21:34 . So it's like like here's the like that going down towards as you

21:40 here, right here and here. so what's what's going on? So

21:47 term here? Micro era. Filic aerobic. Okay, so these are

21:53 that metabolize in the absence of oxygen very low levels of options because we'll

22:00 about options. Actually check five coming bacterial have materials will have different behaviors

22:10 citizens for oxygen, right? And categorize them and really like before five

22:18 groupings based on their behavior towards Okay. And these are two of

22:22 anaerobic micro flow. Okay, so and a robe uses oxygen at atmospheric

22:31 . 2021% 02 micro era filed much 5%. 25%. Something like

22:39 Okay, too much. It's toxic So and so again these are we're

22:46 about aquatic bacteria here in this And they uh so depth typically uh

22:59 column 02 levels varied by depths. . Not always. There's times when

23:06 have an underwater current coming through as in oxygen. But you know the

23:10 of thumb as you go further down depth of the ocean, the less

23:16 there is. Okay. And so kind of the idea. So being

23:20 anaerobic or micro profile, they're gonna for levels of oxygen but or

23:26 Right? The highest level is gonna at the top. Right? For

23:29 , mixing in with the water creating . So we're gonna go further down

23:33 kind of find the optimal level of . And I think that's what this

23:38 taxes, right, taxes movement, , Movement based on magnetic magnetism.

23:43 ? So magneto tactic movement makes it down and toward the pole because it

23:48 be guiding into a depth of optimal which for these guys is less than

23:56 or none right? Or very Let's say okay, so so

24:01 it's not nothing to do with being food source. Right? It's all

24:04 kind of orienting itself in its Okay, now pillow stocks we talked

24:14 earlier in the context of the poles the cell. Right? But so

24:24 tend to be more numerous on the attachment is kind of the function of

24:30 we see uh instrumental in biofilm So that typically those are about the

24:40 right. It's very critical to their to attach and start the biofilm process

24:48 also something attacks okay, but tend be less in number and more specialized

24:56 . Okay, um example that shows is conjugation, right? That we

25:03 sex pilots is used for conjugation, is what's going on here.

25:08 bridging the two cells and Jack material change into two cells. Right?

25:13 talk about conjugation later. But there's pilots that can we'll also talk about

25:19 which is the uptake of D. . A. From the environment.

25:25 there are certain types that can do by using a pilot to grab onto

25:29 and bring it into the cell. . Um there's also a kind of

25:33 weird putting motion, right? Look that here in a second.

25:39 um the uh stop as we mentioned . Right? It can switch between

25:48 a stop or on the end of cell. So remember recall that this

25:53 a function of the environment that was . It was a nutrient rich nutrient

25:59 talk can allow it to stick and in that nutrient rich environment until it's

26:05 longer favorable. This was just a and swims away to look for a

26:10 favorable environment. Okay, so um let's look at briefly this twitching

26:18 Okay, so um so the twitching is a feature of carriers that are

26:28 a surface. Okay, This is a surface phenomenon, like forming a

26:34 . In fact, you often see this feature of twitching in cells that

26:40 beginning to form a biofilm. But not always. Right. But

26:44 point is it's not a surface again the surface here. Okay. And

26:49 um here's an example. So we kind of follow the positioning,

26:58 So we're starting here. Right? , bad term extend. So the

27:03 can elongate all you're doing is just on the monitors, right, pilling

27:10 the monitor and you stack those together and the pilots gets longer you diploma

27:18 , you chop them off and then shorter. So it can ultimately by

27:22 longer and diploma rising, making it , right. And that's really the

27:29 of this whole movement. So you here the pilots prelim arises,

27:33 extending and then will attach check then it diploma rises. Okay And so

27:46 see now how this gets shorter but it's attached right, we see the

27:52 movement going this way. Right? it started here and then ended up

28:00 here. Okay so motion. So is they call it twitching because it

28:07 kind of a turkey jerky movement. ? It sends out a pilot's then

28:13 kind of bumps along the surface and extends again. So it kind of

28:18 start, stop start motion almost. they use the term of twitching

28:24 Okay so again it's all about being the surface. What is this?

28:31 If you're a call if you're a um lab one. We had the

28:37 called proteus on the plate produced like weird looking colonies. Right? Colony

28:43 on the plate is what you might looks something like that. But these

28:48 the colony initially appears like that but it kind of has an appearance like

28:55 and then like this then like Right? And this is growth.

29:02 cells are moving on the plate. . And so the plate the

29:08 Okay. And it's what they call behavior but it's on the top of

29:15 order and motility can contribute to Okay so some bacteria do it this

29:23 . Okay so it does represent the of motion. Okay so um questions

29:31 that pill etcetera. Okay so nana , our extensions as you see

29:43 it's attention to those cells and between typically between members of the same

29:50 But they have seen cases where it's between different species. Okay. So

29:55 can imagine what's what's being exchanged. know anything really in in the sight

30:00 class in between the two can be if it's not too big. Okay

30:05 certainly things like proteins but they've seen like M. R. N.

30:09 . I think the resilient changes were resistance has passed as a result.

30:16 it's it's it's characterized well in some and not so much in others.

30:23 So it's kind of a thing that's kind of trying to be figured out

30:26 certainly um if they can connect themselves stuff can pass between. Okay.

30:33 prevalent this is. I can't tell . But I know the syllabus is

30:37 of these that that does that we about earlier in the context of PHP

30:42 . Okay so um it's a it's phenomenon still being figured out.

30:48 But Okay the last part of three , right so obviously this is for

30:59 of the south um is I mentioned motion for the eukaryotic cell. It's

31:09 to be more of a whip like . Right? This is a sperm

31:17 . Right? This thing is going call it undulating, right? Like

31:22 right wing. Okay. And so bacterium does not move like that.

31:28 bacterial flagellum doesn't. Okay, Okay, so bacterial flagellum rotates.

31:35 , move like a propeller propeller. , so you can so you see

31:43 this slide 1234 different types based on in Majella Ajello, singular morphology.

31:54 ? You can have types that have over the perfect of the cell types

32:00 have it just on one end, that have multiple types on one end

32:06 some that have one on one one on the other. Okay.

32:12 that's kind of a real weirdo because only one operates at a time and

32:19 are spinning then it really doesn't go . Or maybe the spins in

32:23 So either one movie or the other of alternate. I don't think it's

32:27 very common type. More common types the other ones. Okay, E

32:32 I think is uh looks like And again, you don't even know

32:36 . So, I'm just throwing out . I need to don't worry about

32:39 species and all that. But the is you can actually use this as

32:44 way to identify certain types. The of morphology. Uh h And

32:53 so this is the itself. So many of these units called come

33:01 to make the polymer and they can't the immune system can respond to

33:07 Right? And so um so much the old policy to ride in the

33:13 negative right? The uh that produces response so can. Right and so

33:22 classified bacteria bacterial types that are disease pathogens typically in the e. Coli

33:32 group. Right? So we have old and an H. Very often

33:36 these types. Okay. Um and it's a way to identify this was

33:43 decades ago. And so if there's foodborne outbreak, things like salmonella and

33:49 . Coli and others we can quickly based on the reaction. We have

33:55 to these different asian oh engines. go okay let's try it on these

34:01 ones and see which one gives a that tells us oh it's echo y

34:06 blah blah blah. That was not a pathogen. Right? But it's

34:10 blah blah blah. That one So it gives me a way to

34:14 , identify what you're dealing with. H owes for the old point.

34:22 . Right, okay. Now the and bolts of how the excuse put

34:29 . This would be a gram negative have this as well. Uh Point

34:36 not proportion that rotates which is the that rotates general other parts of the

34:45 of a cell body etcetera are really anchoring it anchoring in the so the

34:51 here is that the motion is rotational . Okay. And then you can

34:56 motion by rotating in one way or clockwise counterclockwise give you two very different

35:08 . Okay. So if you wanted really swim, so to speak or

35:12 they call run? Right, that's be counterclockwise. Okay. CCW.

35:20 . Means it's going right, so the are kind of cooperating together right

35:27 unison, Right. And that proves a straight line run. Okay,

35:32 course, the alternative is clockwise right? When that happens, the

35:37 kind of just unravel, right, not working together. Okay, and

35:43 this form here, this tumble is or less kind of spinning in

35:50 right, kind of doing this kind action. Okay, referred to counter

35:54 words actually. Okay, so it between the two types. Okay,

36:03 and clockwise. Alright, so what the proportion of those motions?

36:12 so it's all about are we having counterclockwise vs clockwise if we are,

36:18 means that cell is has some kind purposeful movement towards something. Okay.

36:26 So you see, if you track , it can be something like this

36:30 would have a higher proportion of clockwise . More clockwise means more kind of

36:38 meandering around if you will. so all these little points here that

36:46 that these are all tumbles. and it's mixed in with some of

36:55 straight line runs in between. so a mixture of counterclockwise and

37:03 Okay, just happens to be more because it's kind of going all over

37:07 . Okay. No, really, directions going direction list. Okay,

37:14 , so what's going on here is influences is the presence of attractive.

37:19 ? This is a chemo taxes movement on credits and chemicals that can be

37:25 . Okay. And the detection occurs receptors right? So here's the receptors

37:32 again general rolls off criterium cells in are rod shaped, Okay, there's

37:41 very few species that are even overwhelmingly are killed in the motel are rod

37:52 , right? And it's that at one pole there is a difference in

37:57 , right? You can have receptors one end, You could have just

38:02 the other end. But regardless the here is can detect chemicals in the

38:08 , what's going to be something that's be caught on for the move to

38:11 . Right? 200 acids, These are things that they can use

38:18 grow. Okay, so so if bind these if they so think of

38:25 part over here this random walk as maybe trying to see if it accidentally

38:33 into some kind of nutrient chemical. . And if it does then those

38:39 sites will fill up and increase the of counterclockwise rotations because that's what binding

38:51 receptor by a chemo attractive will lead expectations more of them. So if

38:58 encounters more and more of this chemo receptors get full right and you have

39:06 and more runs going toward that attractive this. Okay, so you see

39:13 much more straight line activity going on these tumbles. The proportion of rotation

39:22 much greater because it's encountering chemo It's binding to the cell and that's

39:28 motion into that. Whatever chemical is it can use it take it in

39:37 . Okay that's really the difference between two. So again it just boils

39:43 to the proportions of park wise, clockwise versus clockwise right? And the

39:57 of more counterclockwise more runs through a presumably because it's binding that chemical and

40:05 and it's moving toward it. not so much present. It's kind

40:10 just more more tumbles more clockwise rotations sending it in a random direction that

40:16 will run into some kind of attracted . Any questions? Yeah. No

40:31 it's chemo attractive. So it's gonna a so it's gonna be carbohydrates,

40:37 acids, nutrients so can use those gonna be what it's gonna bind

40:44 Hey that's my cube. Good or . Okay I hope it's good.

40:55 like I get that. All Um Alright. Chapter four. So

41:03 three and 124. Okay so I'm gonna go step by step. So

41:07 bottom line here is Um in part is kind of okay, here's what

41:17 in all honesty it's kind of what needs to grow. Okay we're focused

41:22 period. So um so we put things together. Reconnecting medium. Alright

41:29 can make different types of media classified in different ways, we look at

41:34 um the will relate to its metabolic . We'll explore that and then um

41:46 at media types and then that's part . Then we'll finish up part one

41:53 time into quantitative growth and then grow in the last part. Part two

42:01 actually relatively short. It covers um and then does sports. Okay so

42:08 so let's start with you. Do not yet. Okay so um.

42:22 . The so in terms of growth . So of course growth needs soldered

42:29 dividing version. Right? We'll look the concept of generation. Alright.

42:35 generation time. It's something we'll talk next time in the context of quantitative

42:42 of growth. Okay. But generation can be you can think of it

42:47 as okay this is one generation, ? 11 cell dividing make too.

42:53 . But you also look at it terms of how was the time frame

42:58 go from a population at this Okay. To win it doubles.

43:10 . That time frame the same Both of those mean the same

43:13 generating right? Generation time. That's we look at how fast our generation

43:19 being produced over time. Right? for 20 generations you collect the optimal

43:30 in eight hours. 8-10 hours. takes us 400 years to do

43:39 Right? So that's we're talking about terms of fast growth. Right?

43:43 so of course that takes you can't put it in water and home is

43:48 to do that. Okay, you to provide nutrients of course.

43:53 And so uh it's so growing, growing in general. Why do we

44:00 this? Well if you're a uh lab where you just you may just

44:07 using very commonly e coli shoot as vehicle to do your incompetent DNA

44:14 right. Have a plasmid genes and e coli as a as a means

44:20 grow those assets for you. Um you probably care that much about

44:29 detailed what the are and things like . You know, rose on a

44:33 type of media, you just cannot . Next day you got themselves and

44:37 you go, right, that's most in that way. But you

44:42 um my experience is not so much it's if your industrial industrial mode and

44:50 commercializing uh micro for for enzyme or protein you want or what have

44:58 You gotta make bucket fulls of Little flask is not enough. So

45:03 you really have to understand how it because you have to grow the high

45:07 density. So you really gotta get there. What's going on?

45:11 now, just from an academic you probably grow cells to isolate

45:17 N. A. Sequence or whatever can do it. Or I say

45:21 is what you grow and you depending on what you're trying to

45:25 you may want to know more about it grows. You don't care so

45:30 . You just know if I plop in this video I get themselves what

45:33 need but sometimes maybe even more you more information. So any of those

45:38 gotta know about what is the organism is required for those at the most

45:43 whatever you do you have to understand . Right? So once you do

45:47 then you go because you have to is that uh you're growing them kind

45:54 I'm gonna say unnaturally to a degree ? Because you're dealing with your culture

46:02 ? And you're not in fairness just one particular species okay completely devoid of

46:09 competition right? Occurring in your flat not competing with other species or other

46:17 or any time by themselves. So course they're gonna grow too high

46:21 Okay obviously nature is not that wait a competition out there nutrients are limited

46:27 their and so yeah you may there be spurts of growth here and

46:32 But pretty much everybody's like competing with other. Right? So that's gonna

46:38 you know that you get lots of . Of course you can control everything

46:42 lab control ph control auction loaders the so there's no wonder you can grow

46:49 till they're like climbing out of the so to speak. Okay so that's

46:54 we'll look at here. Okay it begins or ends with this right?

47:00 . H. O. N. . S. Not true really true

47:04 you? You got yes. So is our this is our question.

47:14 so for most bacteria increasing amount of nutrients to X. And a growth

47:24 typically able to almost a two X in cell yield what nutrient would this

47:33 be? Ignore the question in the . Okay. Don't look at this

47:40 one. Okay. There Everybody knows one. I predict 100% correctness.

48:08 gonna say 99%. 10 54. . All right. Uh almost that

48:35 certainly 95%. It's carbon Carbone because are carbon based life forms and carbon

48:51 life forms because our molecules are based the most part of that structure.

49:01 ? Carbohydrates, libyans, do cake , proteins. Right. All have

49:08 carbon skeleton you can call and then make different types but just adding different

49:14 . Right. And nitrogen and phosphorus what happened right to make various

49:21 Uh So so we gotta fueling ourselves right at the carbon to make these

49:31 frameworks to make our multiples. Okay what let me just erase this one

49:38 . So what is um Okay so of these is It's not a question

49:46 of these is A B. D. E. Anybody. Uh

49:57 all essential because um you have to it to them. You have to

50:04 these things you have to provide. what you do. Okay. And

50:11 pro carry attacks should be better than . Right? In what you provide

50:17 forms right? You can provide them basic forms of C. H.

50:22 . M. P. S. others or and I'm being a little

50:30 cryptic. Right? But you'll see I mean to go on for.

50:34 the forms of these elements. Um Well we will defer, okay

50:42 bacteria can be very very basic in of the forms they need and they

50:47 just kind of mix up from scratch more complex forms of these. Okay

50:53 the so can't can't make carbon It has to get it as

50:57 02 or something more on class. ? The same for the other elements

51:02 . So um the essential essential nutrients the ones you have to supply the

51:09 for them to grow. They won't . Right? Uh So macro micro

51:16 . So from my experience I I of classify these based on the amounts

51:22 ? You know you know grants for adding something grams per liter. I

51:27 it a macro nutrient. Okay if micro grams or less per liter

51:33 But the thing is they don't need supply a lot right because they're not

51:39 may be a second to the cell grow but they don't need to be

51:41 in high quantum's certainly macronutrients. These for sure. Um Those four are

51:52 macron interests politically added in large part carbon. That's that's gonna be the

51:57 influence in terms of growth and you we had a lot of that.

52:02 ? We want to get themselves. , so let's look at some examples

52:07 . So we just mentioned this and remember the you know the form of

52:13 carbon. Right? Is that this or that form that's needed? You

52:19 ? Again, carbon dioxide is an but it's just the most simplest.

52:26 can't take C. 02 and break down. You can only build up

52:30 . Okay, of course you can down more complex sources, carbohydrates,

52:35 can break those down breakdown facts Okay, so then we have these

52:41 ones and I'm sure oxygen right? there used proteins etcetera where phosphates

52:49 right? Where sulfur is used with couple of you know assets but there's

52:53 a few other sulfur containing compounds are but um cat ions, right?

53:00 magnesium, iron I would consider it's the toward the macro inside the micro

53:10 you do add iron in relatively substantial but not not as much to do

53:15 carbon. For sure. Okay, certainly things like potassium magnesium, these

53:19 very common and irons in mineral You typically call mural salt is kind

53:24 the term here. Okay, so parts of enzymes and things like

53:29 Okay, um now micronutrients you see by these all certificate like code factors

53:38 enzyme um uh nickel also there's a that use W. W. Is

53:49 tungsten. Yeah tungsten. Okay and you're a graph of finding is part

53:55 an enzyme typically. Uh So but in fact um you would and all

54:07 these are added as some kind of right off the shelf. Plop it

54:13 . Okay you don't really add these a chemical off the shelf there typically

54:20 in the water. You use that dissolve your stuff. Trace contaminants from

54:25 and things like that. I've never to add any of these in the

54:29 medium. I just know they're there trace contaminants in the water so you

54:33 really bother with having to physically add but you certainly do physically add these

54:39 other ones. Okay so um okay factors. So growth factors is kind

54:49 a term they use um something in to typically the C. H.

54:58 . M. P. S. things like vitamin right maybe it's deficient

55:02 B. 12 B. One. have you can't make it. So

55:07 have to add it to okay uh can't make any real acid. So

55:12 have to add it to. Right what we called growth factors.

55:15 Um Blood this is very blood and series of fractional blood uh it's kind

55:21 protein fraction of blood but very often add these when you're dealing with pathogens

55:29 microbes bacteria very often you grow them even a blood augur you don't very

55:36 blood has a lot of stuff. ? And so very often it's like

55:40 we know the pathogen goes better off you had blood or serum.

55:45 But you don't necessarily take all the to figure out what is in the

55:48 and serum. That's that's promoting growth it can be very complex. So

55:52 you do is just add the blood the serum. But you know there's

55:56 in it to help it grow. . So anything like that falls in

56:00 category of a growth factor. Something It's really not. You're supplying

56:05 CH one P. S. But still can't grow well enough unless you

56:09 these things and that's the growth Okay. These terms here protocols if

56:15 don't hear protocols so much but I we all are aware of wild

56:20 Okay. Wild type uh taken you the Gillette, you That's right.

56:28 wild type. Right? So the type is I call the wild

56:31 the the member of the species that has all the features of that

56:38 Right? Then you can have variations that wild type. Okay. And

56:45 variation can be an oxygen. so an oxygen is typically just it

56:50 it lacks a it lacks or is in in particular metabolic pathway very often

56:59 in the context of amino acids. ? So something that's an Albanian oxy

57:04 , right? This guy you have add alimony to the meeting or world

57:11 . So even in certain any term right blank obstacle whatever is in the

57:22 in there for us. So that's you have to add that. It's

57:26 in that catholic. So I said hospital, it can't produce history.

57:32 gotta add it to the meeting. that's that's what that term means.

57:37 Okay there's a couple of quick questions here. So before I open

57:48 read the bottom so you start the and reach bottom. Right? So

57:55 organisms. Right? Just start here go down. Right. Just

58:05 Okay so CC energy source is Okay so first And the next

58:16 Right. 2nd. Alright. Alright. So kind of read it

58:22 that fashion. So let's look at of course A. Through G.

58:27 your potential choices. Okay so first is which box represents Chemo? Auto

58:39 , email. Auto Trophy A. G. To choose from.

59:10 Time is on. Got this And we got another one. And

59:21 3rd 1. Just not a Just Alright, I count down from

59:37 to pause, dramatic pause. And we go like. All right if

59:48 answered, let's switch to the next . Alright reveal. Make it more

59:55 . Okay. Okay. Which Oh wait no that's not what hold

60:02 this one. The one the box box represents a plant or algae timer's

60:41 . Hey countdown. Mhm. 87 F. So we had d over

61:02 with the consensus F. Here. Yeah, both of those are

61:09 Okay, so um so a question talking about here is classifying metabolic

61:18 right? If you know that then know what we need to put together

61:21 make it. So um first and the first tier energy source,

61:30 Chemical light that basically defines the uh source. Obviously, right, we're

61:38 use light or we're gonna oxidize some of chemical compounds. Okay, so

61:44 trophy. Photo trophy. Okay Carbon source. Right? That's your

61:51 . Autotrophs autotrophs distinction right? On sides. Okay. So um and

62:02 then it's um the in terms of compounds, right? On this

62:12 right. It's final electronic sector, ? Think of it is. How

62:17 it breathe, sort of? How does it breathe? What does

62:21 breathe with? Okay. And then on the other side, right.

62:29 so it relates to on the on autotrophs side, I'm sorry. On

62:34 side. Right. Um electron right? Can use water or can

62:42 use something else? Okay, so have one more question. It's not

62:46 question. Let's just uh see which represents an aerobic headed trophy? Which

62:51 you see you even e e uh , of course your name.

63:14 Um now this I got to reveal . Alright, so so the one

63:33 we'll find out is you know how role of electrons in this process

63:38 especially when you get the metabolism. really all about that. Okay.

63:44 so um the Arabs using oxygen. , anna robes using other types of

63:54 . Okay, these guys right our we'll talk about this in unit

64:01 . These are fermenting organisms there Okay, don't so much worry about

64:06 now, but we'll talk that's that's they fit in organic compounds. Those

64:11 anaerobic respirators. Okay. Uh anaerobic are different from fermenters. They both

64:19 use auction but they are different. Okay. And then of course over

64:27 , right. A source of Right? Water for plants and algae

64:32 bacteria will learn that other photo trophic have something else, write things like

64:38 two S is very common. All . Not water, but H two

64:43 , donor. Okay, so uh next slide here kind of summarizes

64:49 Okay, this up. And um , source energy and electrons. So

65:02 you can combine terms, right, were an organic growth. Okay.

65:07 can consider yourself as an organic growth organic sources of electrons. Okay,

65:14 is this? This again? I . Yeah. What is it also

65:29 a source of Mhm. Basic source get down to some atomic levels.

65:38 of source of electrons. Williams These folks, I mean, doesn't

65:56 very sexy, like steak and baked and sour cream and baked potato sauce

66:05 some kind of gravy on your Right. If you're a carnivore.

66:16 , okay. Um but almost natural when it goes to your body,

66:26 are looking me Okay. Yeah, looks very nice. You know,

66:34 eyes see that but inside your body it all goes down to electrons.

66:41 , so that will will get deeper that as we go along. But

66:47 so when you two. But the here is can combine, right,

66:52 organic trove and chemo autotrophs are essentially same thing. Okay, chemo with

66:57 trove. Chemo autotrophs, same Okay, these are two very different

67:04 . Yeah, photo ties them together use light energy. But the operative

67:10 No. Really this question, can a photo hetero profuse carbon

67:14 Right. Because the operative term is that trumps trumps it. That's what

67:22 okay. It does not it rules ahead of you use things like glucose

67:34 Things like that. Not so So there are 400. Okay,

67:39 can use light energy but they But they don't think so too.

67:43 , we'll talk about those next uh you get to but anyway, so

67:49 , so putting together these components, ? We know the metabolic nutritional type

67:57 pro for chemo autotrophs or what have that we can put the elements together

68:03 say yes, if there's anything else needs put it in there in the

68:07 medium. So what kind of? we can we can differentiate different types

68:11 growth medium. So what kind of medium is this? You got four

68:19 there, Put the timer on. realize that shooting sound you're gonna hear

68:56 the recording. So when you get like 65 minutes you know what that

69:04 is? Um All right and what got it is okay. Um Why

69:18 be who has to be so why it a complex medium? And what's

69:26 you that? And on this list ingredients, what's telling you? It's

69:34 ? Yeah that's one it's really these these two okay so up to this

69:44 right up here that's a defined medium but because we've added these two complex

69:57 so it doesn't matter if you think it a defined medium as one that

70:02 can give you a periodic chart in calculator. You can tell me exactly

70:07 the most per liter are of every . Okay? And you could write

70:13 above here. Okay. But now add these what we call complex

70:19 Okay we know that pepto contain H. O. M.

70:25 S. It's in there. You pep tone is basically meet uh comes

70:31 a cow beef that's been digested with , beef extract has been I think

70:37 and something else. So these are treatments to like break it down so

70:42 they can be can be used by growing on it. But it provides

70:49 all these complex nutrients like soy soy you can add they contain all of

70:55 . C H. O. P. S. You just don't

70:57 what the proportions are exactly. And that's the nature of a complex

71:02 . Okay, so um now more of this. Right, so here

71:10 three different types of media and um you know, medium by itself.

71:18 know this right? You're just talking C. H. O.

71:20 P. S. And macro micronutrients right to make a medium to be

71:25 medium could be a solid medium. uh There are different uses for

71:30 So complex also called rich medium. ? We'll have so by supplying these

71:36 nutrients. Okay uh listen, here's list of beef extract, there's

71:42 there's milk protein, soy protein. a whole bunch of different types right

71:47 providing everything right there providing preformed So certainly these will have fully formed

71:56 and a bunch of other stuff. You can also add things like East

72:02 rich in B vitamins. Right? supplies a bunch of stuff. The

72:09 is less. So right, so medium shown here. Okay, These

72:17 , right again, you can and cross of course is C6 H

72:25 So you know how much of each is in there. Right, just

72:29 . You know these other ones. is completely complex. Right chloride.

72:37 this is a medium that's defined. one for uh little right? There's

72:49 it has C. 02, As carbon. That's the clear

72:54 These here's the carbon. So carbon remember the carbon defines albuterol predator.

73:05 ? This this is complex carbon As . It's not CO2. But so

73:12 you see something like a trip tone tone, you just think it's meat

73:18 . Right? That state's gonna have , proteins, Right? Those are

73:25 complex carbon sources. Right? So your carbon, Right? Um So

73:30 the carbon here. That's an auto , Right? In this case of

73:35 will roll. You can't grow on . All right. You need to

73:44 added carbohydrate to it, right? fat or whatever, But not see

73:49 you can't grow on you unless you're kind of mutant type. That is

73:54 only one on planet Earth. You do that. Okay, so um

74:01 those in lab nutrient auger. You use that all the time.

74:07 , It's a complex medium. Um Are any questions? Wait,

74:19 going to talk about that next Alright, so don't worry about

74:22 Hey folks, see you every See you next week.

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