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00:02 Welcome folks uh in this module we're chapter 13 which will cover energetic and

00:10 . So we're gonna talk a little about microbial metabolism and um go into

00:17 little bit about how microbes get energy about the basics of energetic sex.

00:26 including the concepts of delta G. free energy and how um the breakdown

00:36 organic material the energy from that's captured is used to make a T.

00:40 . S. Of course this is for any living thing to be able

00:47 take in nutrients to produce energy and that to do the work of the

00:51 . And so we'll be describing this looking at respiration, fermentation and um

00:59 and all that goes with that. as we get into chapter 14 we'll

01:03 more about respiration. Um and then go into little troves and photosynthesis.

01:11 , so 1314 are heavily of course describing microbial metabolism. Alright, so

01:20 start with kind of example, we previously about microbial growth and so we

01:26 how fast bacteria can grow and if envision, say a single cell of

01:32 an inoculation to a medium that very we'll get the number of cells as

01:38 go into log phase. Right? many more cells. Um So high

01:44 density. So this represents of course substantial increase in biomass. Um It

01:52 that a lot of energy is needed do this to create um uh representing

01:59 replication which of course requires DNA replication of course requires protein synthesis to be

02:06 to generate this biomass. So all is a energy expensive process. And

02:12 has to be uh something fueling right? And because life is carbon

02:19 , right? Uh the central nucleic acids, carbohydrates, lipids,

02:27 proteins are all based on carbon as talked about before. When we try

02:31 grow microbes, we have to supply H O M. P.

02:34 And C. Is carbons the number . Because that's what all the molecules

02:40 are based on. So of course has to be for header tropes,

02:46 ? Um metabolism is about the breakdown complex organic materials as you see there

02:53 it's again about the carbon. so breaking these down for a head

02:58 trophy if it can serve dual So it serves the source of carbon

03:04 also can be broken down and energy be captured. And that energy is

03:08 to do the work that living cells to do. Okay. Whether it's

03:12 move um um to to reproduce as see here. So it's essential.

03:21 and that's what we're looking at here metabolism in this chapter. The chemical

03:26 . Right? So obviously we uh the the energy of molecules comes from

03:31 chemical bonds in those molecules and as break molecules down through metabolism, we

03:37 release energy. Of course, uh quite obvious that an explosion,

03:42 is obviously a tremendous release of But obviously um living things cannot it's

03:49 practical uh way for living things to energy obviously. So because you know

03:56 most life most of them things um occur at moderate tempo, conditions of

04:04 and pressure uh etcetera. So um course enzymes are used to carry out

04:11 kind of metabolic reactions and and energy is not all. So the explosion

04:16 see there that's basically energy released all once. And so that's not efficient

04:21 living things. So basically what happens a series of reactions are carried out

04:26 energy is captured in incremental steps. . Rather than as an all in

04:31 um being that because basically it's more that way and we'll see how that

04:38 . So as we uh look at of the variations of contam bill is

04:45 okay so we see here uh um forehead a trophy of course which uses

04:54 organic carbon. Um we can see classes here. So the differentiation between

05:01 and fermentation. Okay so both are processes. No utilize complex organic carbon

05:11 fermentation. It's anaerobic. So no used. It will will lead to

05:17 formation of of um simpler organic Um So we call these um it's

05:26 incomplete oxidation. You can still see there's energy left in those molecules like

05:32 , acetate fermentation provides and products that small organic acids organic alcohols but there

05:40 still energy left in those molecules. hence we call these incomplete oxidation.

05:46 um respiration uh is a is a oxidation. Okay so we can break

05:55 down all the way to see Two and water. You can't break

05:59 . 02 down. In fact it released from the hetero proof. Um

06:04 the process though we produce lots of 80 P. And these other energy

06:10 molecules in A. D. And F. A. D.

06:14 . Um So um in fermentation you you do That process does provide a

06:19 . Okay. Uh just not in same amounts. Okay so there's there's

06:27 very wide Disparity in the amount of p produced um from fermentation compared to

06:38 to respiration as well. See um the redox reaction. So um the

06:49 process of breaking down this organic material through respiration or fermentation is done through

06:56 reactions. Oxidation reduction reactions and energy captured at certain points along the

07:02 either in the form of producing a directly or through the production of these

07:11 carriers and A D. H. F. A. D.

07:13 Two that should actually be to So um and respiration also involves the

07:25 of an electron transport system. And and that serves to um the

07:32 energy captures in the form of an reduction reactions are about transfer of

07:37 And so really respiration is about is that capturing energy from molecules by oxidizing

07:44 capturing those electrons handing them off to carriers and A. D.

07:49 D. N A D F A . And then taking these production transport

07:55 where they ultimately are handed off to terminal except er it's aerobic respiration.

08:01 gonna be one oxygen if it's something than auction. It's anaerobic respiration.

08:07 . But the key is for respiration electron transport system. Okay. And

08:12 was an aerobic, it would be like uh nitrate being reduced to

08:19 Okay, so um so we're looking you know, different redox reactions,

08:25 of electrons and then ultimately getting lots energy production from that process.

08:32 So you can see you know from doesn't involve these processes of electron transport

08:38 so forth. And it's one of main reason why fermentation doesn't yield as

08:43 energy as the respiration. Okay. Now Photo trophy will talk about in

08:51 14 but it's worth mentioning here, for comparative purposes. The photo does

08:58 , right? They have they can light energy to make a teepee.

09:02 kind of facilitate their metabolism but the term is heavy. So it must

09:07 on metabolism in order to provide its source. Okay. Um and as

09:15 previous slide shows a number of different uh sources can be used um for

09:22 not just sugars, carbohydrates but certainly proteins. And we'll look at aromatic

09:27 as well. So bacteria have the to to utilize these what are often

09:33 compounds as as a catatonic source for . So um but we'll talk about

09:42 14 here looking at inorganic energy So, little trophy methanol genesis.

09:49 are chemo autotrophs as well as photo of course to use light energy.

09:53 so just to refresh your memory, , Auto Trophy relies on C.

09:58 . Right? So that's the 02 as a carbon source for

10:01 And that of course is built into organic carbon. Okay. Um and

10:08 that the energy so that's gonna be very energy required process to do

10:12 And that comes from with a Photo comes from light energy is the conversion

10:18 light energy to chemical energy provides that for the process. For little

10:24 it'll be through the energy coming from oxidation of inorganic sources. So,

10:31 but that will leave for chapter So for now I just want to

10:37 through so you see at the bottom , the respiration process. So we'll

10:41 through through this two at one level chapter 13 that will dive a little

10:47 deeper into it in chapter 14 as . I think it's worth kind of

10:53 showing you up front kind of what's involved in this process. So we'll

10:58 through this uh bagram on the next here. Remember? It's it's redox

11:05 are an essential part of this. , so begin with respiration an important

11:13 structure is the membrane the membrane is respiration, the reactions of respiration are

11:21 occurring within or around or near. , um the reason for that is

11:28 membrane is essential into creating a or creating a proton gradient here and that

11:35 gradient requires the compartmentalization if you will you can you can push molecules to

11:44 side of the membrane and thereby create gradient. So membrane is essential.

11:48 respiration also in photosynthesis will see this it's really electron transport chain uh is

11:55 it's in the membrane. And so essential for respiration for the synthesis.

12:01 as we'll see, it's not essential fermentation. Okay. But certainly for

12:07 photosynthesis. It is. And so as mentioned electron transport system components are

12:14 within the membrane the source. a source of electrons. Right?

12:21 for ahead of trove, um the organic source. Right? So,

12:26 be looking at glucose of course, as an example, but it could

12:30 any kind of organic carbon source. It serves dual purposes. It's it's

12:35 a carbon in the form of a source, right to make carbon based

12:40 but also serves as the energy the electron source. Um For

12:45 for the respiration process. Okay, the source is going to be a

12:49 that's going to be reduced. Reduced means it's going to be electron

12:53 . Let's call it that. And as we oxidize that reduced

12:58 It becomes oxidized. And those electrons are given up. Okay, so

13:02 the electron sources organic or inorganic that your your chemo organic trophy head a

13:09 versus your chemo autotrophs slash with a . Right? So that's there because

13:15 rely on inorganic sources. So but , our focus here in 13 Chapter

13:20 is on organic. So the metabolism so the electron source that becomes will

13:29 oxidized. Right? And in the those electrons are handed off to the

13:34 carriers and N A. D. one of the major ones. And

13:39 the N A. D then becomes as a result of picking up those

13:43 and it carries them to the electron chain. And so there's a series

13:48 molecules that are part of this system in the membrane that alternately accept and

13:57 uh receive and donate electrons uh in flow of electrons ends with a terminal

14:06 er which an aerobic respiration can be . And so this maintains an electron

14:12 as we'll see the components of the transport system are arranged such that we

14:17 from molecules that are that um readily up electrons right, are really strong

14:24 . We call them readily give up and flow to progressively molecules that are

14:33 better and better at grabbing electrons. what we call strong except er so

14:39 line them up as strong donors. to strong except ear's and auction is

14:45 the strongest um and so it it that flow going in this direction and

14:52 diagram left to right. So um again the terminal except er the nature

14:57 that, the chemical nature of that tells us is an aerobic respiration.

15:01 an 02. Or is it something ? Is it nitrate sulfate, iron

15:06 or or another type ammonia? Not ammonia but um um some other

15:15 of oxidized form in any case so we accept er is an oxidized form

15:22 it's it's that's a form that they receive electrons. So the terminal sector

15:26 becomes is oxidized then becomes reduced by electrons at the end of the terminal

15:33 er becomes oxygen becomes reduced to Okay. And so some of these

15:40 of the electronic transport system can so as electrons are transferred energy is

15:47 . So having carrying electrons. Is means you're carrying energy. And if

15:53 donate those electronic you can release And so at a couple of points

15:57 transport system, uh that energy released electronic transfer is coupled to the pumping

16:05 protons. Okay. And this is the grading comes in. Right?

16:10 is why it's important to have this in a membrane because now you can

16:15 one side from the other and you pump protons across and you create a

16:19 . Right? That's a form of energy. Okay. Um those those

16:25 protons are concentrated on one side, bumping into one another and and and

16:32 charged and being having a concentration They'll gladly move down their gradient and

16:38 energy. They're also drawn in by charge that's inside the cell because the

16:44 of the cell is is has a negative charge. And those positive protons

16:49 attracted to that. So you have forces. And this is what we

16:53 the proton motive force. The force to the charge attraction bringing them in

16:59 well as the concentration difference that will them in. Right? And that

17:03 is harnessed through an HTTPS. And they flow through uh that energy release

17:09 used to produce a T. S. Okay. And that's what

17:14 call oxidative phosphor relation. This this of 80 P. Generation tied to

17:22 , the the oxidation and transfer electrons are the energy from which is used

17:28 pump protons. So collectively we call oxidative phosphor relation. If it were

17:33 by light, if this process were by light, we call it photo

17:37 relation and would involve very similar components an A. T. P.

17:42 . And that's what we see in , it's photo phosphor relation. But

17:46 driving force there is light. Um So um so in a nutshell

17:53 this is respiration. Okay. Um again the basics are as we can

18:00 here A. And B. A. Is the electron source.

18:04 have to have electronic source fueling the . Right? We have to have

18:09 terminal accept er That is very good receiving electrons that sets up a electron

18:16 . That energy from electron transfer. used to pump protons out, creating

18:20 gradient. We capture that through oxidative relation. Right? So um having

18:25 sources critical um that helps maintain the gradient uh that then helps maintain a

18:33 production. So law goes hand in . Right? So it's again students

18:37 reactions, right? Oxidation reaction reactions electrons are transferred ultimately then handed down

18:44 electron transport system. Okay. And what we're doing here in terms of

18:51 sex is we're combining energy requiring processes, processes with energy releasing

19:01 And so in this diagram alone, we can see that, you

19:06 the the transfer of electrons and electron system. That's that's energy releasing

19:11 We're using that energy to pump protons because pumping protons out remember, is

19:16 active transport process. Right? Going low concentration to high requires energy and

19:22 energy is coming from the transfer of . So there were coupling energy releasing

19:27 energy requiring process. Um The the of a tps through that 80 piece

19:33 place. Those are protons going down gradient which releases energy and then that's

19:39 to form a T. P. . The A. T.

19:41 T. P. Formation requires So there again we're coupling energy requiring

19:47 releasing processes. So here and here the in the electronic transfer energy release

19:56 pumping a proton. So doing doing that in both of those

20:01 Right? So it occurs all the in metabolism to to couple these

20:06 energy requiring an energy releasing. So when we look at um Uh

20:14 so this is the overall process going . We're gonna break this down into

20:19 stages. Okay. And and we'll how it all fits together and we'll

20:25 more of this as we get in Chapter 14. Okay. But I

20:28 it's helpful just kind of up see what this process is about.

20:33 . And why it's important in terms membranes, You know, this is

20:36 happens in your mitochondrial membranes, This is what happens in a bacterial

20:42 membrane. Okay. This is where process is occurring. Um It's I

20:48 , it's, you know, for it's obviously is essential for us to

20:51 energy. You know, we so you buy, when you eat

20:55 whatever you eat for lunch today, know that food, you know,

20:59 terms of what your your your cells looking at, It's really the

21:03 right? Because that food is going be broken down by your digestive system

21:06 smaller molecules that then will flow to cells that then will be oxidized.

21:13 then those electrons gained through different reaction will be to support the electron transport

21:20 in your mitochondria, which will then used to produce a proton gradient which

21:24 then be used to to generate a . P. So in essence the

21:28 you eat your body sees you know of the main needs your body sees

21:32 as is a source of electrons of source of carbon as well. Because

21:36 gonna build your molecules using that. um so that's the essence of

21:42 So if we look at bio right? So this is where we

21:45 of see we know from, you , centuries of doing chemistry that chemical

21:52 we know we can lump basically metabolic either in as those that require energy

22:00 go or they release energy. so we look at these in in

22:06 of changes in free energy. The delta G value. So delta

22:13 . We can look at in terms total energy or entropy which is delta

22:19 . Okay. In terms of usable or the free energy which we call

22:25 G. Right? That's the energy that the cell can do something

22:29 Right? Then there's entropy which is of a measure of which is unusable

22:33 measure of disorder. If you will a system conversely you can look at

22:39 as a measure of stability. So more disorder equals more entropy uh

22:46 more order equals less entropy. And so in in uh what we

22:55 X. Organic or inorganic also term and non spontaneously used um negative delta

23:03 . Equates to energy release right? are basically cattle bolic processes uh positive

23:08 G processes and organic processes are those which energy input is required?

23:15 So we can look at whenever um is typically looking at the bio energetic

23:22 a system and what's the what's the G uh positive negative. The amount

23:30 it is negative or positive. What's magnitude of that change changes in the

23:35 looking at is systems versus surroundings. ? And basically you can you can

23:42 uh your system at a number of ways. It can be, it

23:47 be a single cell. The system be uh an organism and a system

23:52 be an ecosystem. You can measure changes and all these at all these

23:58 . And it is and it is particularly in ecosystems. Energy changes are

24:02 uh that information tells us, you , you know, how much life

24:08 be supported at the different different levels an ecosystem. For example, uh

24:12 can tell us how may be efficient particular ecosystem is. So it's an

24:19 parameter. So so here just to this hypothetically say, we're looking at

24:25 cell. Right? So cells are systems they can exchange with their

24:29 That's what an open system means you exchange, we ourselves can exchange nutrients

24:34 with with the environment. Exchange things like that. Right? So

24:39 to a closed system which might be a chemical reaction in a in a

24:44 tube that's closed. Right? Um in a in an open system but

24:51 able to to to exchange with the . So you have a chemical reaction

24:57 plus B. To give C plus . Right? In a closed system

25:02 will A. And B reactions will form C. And D. Product

25:07 then eventually come to equilibrium. And at that point there's no net

25:12 . Okay? But because cells are systems, that same reaction uh you

25:18 , A. And B. Reactors be supplied, you know, through

25:23 with the environment. Right? So can continually fuel the process and provide

25:28 . And B. At the same perhaps products C. And D.

25:32 used for um other metabolic reactions as material. So, you know,

25:40 those open systems that can continue exchange the environment. Right? And so

25:44 fact you don't want organisms don't want come to equilibrium because once they come

25:50 equilibrium, they're no longer living. , so continual exchange with the environment

25:55 what keeps reactions going towards equilibrium but quite getting there because either we keep

26:04 the the reactant for action. And the products go on to to fuel

26:10 processes. So, you know, metabolism which is basically all the chemical

26:15 going on in the body or sell these are all many of them are

26:20 interconnected in some way. And so often the case that the products of

26:25 our service your actions for the next . So um so um so in

26:32 again these energy changes, we can which processes are negative delta G.

26:37 release energy and those that require. cata bolic processes release anabolic processes require

26:44 . And so in terms of factors to delta G. Right? So

26:49 are additives. So we can take this is this is the concept going

26:54 to the combining energy releasing an energy processes. Right? That's what

26:59 That's what we're doing here. We take a a process that may be

27:04 positive delta G. And combine it a negative delta G. And if

27:08 negative delta G exceeds then then overall is a process that may work.

27:16 , for example, the um uh the graph over here, so we

27:23 glucose and uh phosphate to give glucose phosphate. Right? That's a positive

27:30 G process, Right? Plus 13.8 joules promote. Um And so you

27:36 see it's an uphill look at the energy change. It's an uphill process

27:41 energy input. A teepee hydraulic Right? Which we see here.

27:48 an energy releasing process. Right? always use the analogy particularly of a

27:55 being moved uphill, right? That tremendous energy but a rock moving

28:02 gets rolling. Of course it's going be energy releasing. Okay, so

28:08 question then is is this energy releasing of a teepee hydraulic sis can that

28:18 the positive delta G. Of that ? And we combine them as we

28:24 here. Then we see downhill And it's a net uh change.

28:34 ? So a negative 16.7. So , yes, that's a process that

28:41 by combining a teepee hydrologist with Right. That's what happens in a

28:46 of different metabolic reactions that require A Tps are used because the hydraulic

28:51 will produce so much energy that it the it will make a positive process

28:59 . Okay? So um concentration gradients just saw right in the respiration pumping

29:05 protons, right? So concentration gradients forms of energy storage. So um

29:11 we saw that by the by by energy to create the gradient. We

29:17 get that back and in fact produce tps as protons move down their

29:22 So um concentration gradients are very important cells to do various types of

29:28 So we can use a proton gradient only to make a tps, but

29:32 can also use it to to pump flagellum for movement to um bring other

29:38 in uh into the cell. So very important. Uh And then of

29:45 there's a concentration of reactant and right? If we have an excess

29:49 so there's our A. And B to give products C. And

29:54 If we um have provided excess right reactant um over products, right then

30:05 can uh produce uh a a favorable G. If we have an excess

30:15 of reactant over products. Okay, gonna go I'm gonna flip to a

30:23 slide. So just give me a here. Okay folks. Um So

31:40 just wanted to show um this is is in regards to the uh Changing

31:50 over products. So if we have product to reactant ratio of 1-10,000 you

31:59 see the change in delta G. ? If the products and records are

32:05 , there's really no change uh went ratio of of reaction products or went

32:14 10,000. So 10,000 fold excess or fold excess. You see the change

32:20 delta G. So having a a change right in this um the difference

32:32 uh the two products that can favor negative DELTA G in some cases.

32:39 um so again all these are So combining the nativity uh positive DELTA

32:48 . With a negative DELTA G. negative DELTA G. Is enough.

32:51 can it can allow the reaction to concentration gradients then the concentrations of reactions

32:57 products. So all these can can the delta G. So um

33:03 so kind of overview here of of metabolism and metabolism the how in these

33:17 how these are linked together. So look at examples of cellular respiration,

33:22 , Glucose oxygen to give CO two water. Okay so um multi step

33:30 but in the process we capture energy different steps during this. There needs

33:35 oxidation process. And so that energy right is going to be captured.

33:43 nationalism in contrast as shown by the of sensitive proteins using amino acid building

33:50 uh building stuff that's an apple is so that certainly represents an example of

33:56 . So too would be something like . N. A replication because we're

34:01 a DNA polymer from nucleotide substance. that too is an apple is um

34:09 with either process heat is released and always a feature of of of any

34:17 energetic process. And so he you of course represents the you know,

34:23 increase in entropy. So um and generally is not usable in biological systems

34:29 of course us humans and other Uh use this heat given off by

34:35 metabolism to to um control our body . So we do have a need

34:41 need for that obviously. Um The the the role of A T.

34:49 . And how it links these processes . Um So you have to remember

34:56 a TP itself. Of course there's forms there's a teepee and there's ADP

35:01 phosphate. Right? So eight EP be hydrolyzed to release energy.

35:07 So that's an energy releasing process. teepee formation uses ADP and phosphate to

35:14 a teepee that's energy requiring. Okay each of those processes processes is going

35:22 have a role linking it to metabolism it to an apple. Is um

35:29 we see here. Okay so there's D. P. And phosphate.

35:35 A T. P. Formation. ? So this is what we're looking

35:44 is energy requiring. Right? That this it's going to be an energy

35:54 process. Where does the energy come ? The energy comes from energy released

36:02 the lapses? That energy is used produce a T. P. Okay

36:11 that requires energy, where is it from? It's coming from the energy

36:16 of metabolism. Right. So that's generating energy released from metabolism.

36:25 The glucose to C. O. the energy release is then used to

36:29 a teepee. Okay conversely at S. Then 80 behind your analysis

36:41 energy releasing. Right? We need input. It comes from a

36:53 P. Hydro sis so you can with anabel is um to make that

37:01 go. So that's how they're That's how they're linked. Okay so

37:07 a T. P. Formation form . This that energy to do that

37:18 from metabolism. Okay conversely and metabolism energy input. That comes from a

37:31 hydraulic sis that that process. Okay um and you and cells are performing

37:39 teepee and using a TPS millions of a second. Okay and so when

37:47 look at um you know these processes talking about? Of course energy potential

37:55 conversion of energy. Right. And and then obviously energy capture.

38:02 so redox reaction. So recall Although it's kind of counterintuitive you think

38:08 is getting smaller. And in the of redox it's gain of electrons,

38:14 is loss of electrons. Okay. we look at the process of cellular

38:20 , glucose plus oxygen to give CO and water and energy. Right?

38:25 forget. That is this again, redox redox reactions? So glucose is

38:33 oxidized to SEO to write. And reactions is typically through the movement of

38:43 ions, hydrogen atoms, right? of hydrogen atoms of hydrogen atoms,

38:50 . Right? 1, 1 one electron. And so we can

38:53 how CO2 of course is devoid of Jen's. Right. So glucose has

39:01 up those electrons that process become oxidized CO2. There's always gonna be a

39:06 . So if something's being oxidized giving electrons, something must be capturing those

39:11 . Right? And so in this process, ultimately oxygen is the receiver

39:17 ? That terminal Except er it becomes two water. Right? And you

39:26 see the acquisition of those 12 Right, show up at 12 hydrogen

39:39 represent electrons shows up in water. ? So option has been reduced.

39:46 was the receiver of the of those coming from glucose. Okay. In

39:50 process we generate energy. Right, here again, here's glucose. The

39:55 . Where is the potential energy of ? It comes from uh the arrangements

40:00 the atoms. So potential energy is of energy of position or state in

40:04 to molecules. And so of if we look at the three dimensional

40:08 of glucose, you see that there be various bond angles of these atoms

40:13 the molecule. Um and of course electron clouds around that will kind of

40:20 each other. So, you molecule with lots of bonds like

40:23 there's gonna be some inherent instability in in the molecule and associated energy with

40:31 . Right? So we can capture energy if we can remove some of

40:35 electrons. Okay, that's what redox all about. Right? So,

40:39 metabolism we're gonna break down glucose ultimately C. 02. And you can

40:43 the difference in the two molecules, , C 02 is obviously lacking a

40:48 of different chemical bonds. And so we're breaking glucose down, oxidizing

40:52 we're capturing it in certain steps. ? So, I'm glad causes and

40:57 respiration. Right? So I'm glad , we're breaking down glucose to this

41:02 carbon pyro vein. Right? Actually of those. And in between we're

41:09 to capture energy via electron transfer. ? As H Adams, similarly as

41:16 go from Pirate Bay to C So that encompasses uh Krebs cycle T

41:23 A cycle. And then again, gonna capture more energy via electron

41:27 Okay and so they're gonna be specialized involved in doing this. Okay.

41:33 what you see there is metabolism, , breakdown of a complex organic material

41:38 simpler compounds C. 02. Um now in an Apple is um

41:45 of B. C. Co two . Right? Which is what autotrophs

41:49 . So our troops will take 02 and build up to these larger

41:53 molecules co two fixation. And and can see the difference in the two

41:59 . We have to add a bunch Adams to the C. 02 to

42:04 this. So we're gonna have to course supply add electrons to we're gonna

42:08 to reduce C. O. To electrons to build it up into this

42:12 molecule. Okay, so so um let's look at um some of these

42:27 carriers. Okay, so again we're down, right, so we're different

42:33 . We're capturing energy. Uh and then ultimately we're gonna use those those

42:41 specialized carriers that have received these electrons they're going to the electron transport

42:47 And that's where that's where we're gonna our big energy output from energy captured

42:52 of a T. P. Okay, so let's um so the

42:59 current molecules of course a tp. that 80 P. Had draw sis's

43:05 energy. Right? Uh of course um photo relation will generate a tps

43:15 well. Um N. A. . N. A. D.

43:19 . Right? So N A D is the electron carrying form. It

43:22 receive electrons and become reduced, forming A D H. Okay, so

43:28 A. D. H is that that's carrying the electrons? Okay.

43:33 and A D. P and A . P. H are often seen

43:36 bio synthetic processes. Uh these serve as the electron sources for bio

43:42 Very often I will also see F D. F A D H two

43:47 access as hydro assist GDP. It serves as a source of energy.

43:53 see that in protein synthesis as GDP as the energy source source to provide

44:00 . Um so just a closer look N A. D. Briefly.

44:03 any D when you see this written a reaction, um in A.

44:08 becomes reduced to an A. H plus H. Plus, it

44:12 to do with the nature of the nature of the molecule. So,

44:17 N A. D. And we're to focus on the boxed part.

44:21 so we see here, so transfer hydrogen, which represents two electrons to

44:27 that the that that that molecule can two of the electrons in its aromatic

44:34 . Remember aromatic rings have this property residence. So the electrons are kind

44:39 circulate around uh that benzene ring and can provide room for one of the

44:46 regions to bond to it. And um then the remaining proton is

44:57 outside the market. So that's why plus H plus. Right. So

45:02 two hydrogen is the two electrons are up by the N. A.

45:05 . H. One hydrogen forms of and bond the other one. It's

45:11 a proton. Alright. That's not of the molecule. So that's why

45:14 always see the reaction here in D. Plus two hydrogen gives you

45:19 A. D. H. Plus . Okay, so the point is

45:22 accepts two electrons um now generating a . So energy release uh form

45:30 T. P. So we can um of course the formation of A

45:34 . P. Is energy requiring and involves of course the phosphor relation.

45:39 ? So if we're gonna make A . P. S. We have

45:42 phosphoric ADP. So one mechanism is do what's called substrate level phosphor

45:48 We see this in fermentation and we it in respiration at a couple of

45:54 . So it's very simple. All doing here is using a phosphor related

46:00 , a molecule containing a phosphate And we're simply removing the phosphate group

46:06 adding it to a D. To make a teepee. That's all

46:09 is. Alright, so just think it as a straightforward made to make

46:12 A. T. P. And again there's a couple of steps

46:15 respiration where this happens and the fermentation the only way a Tps are formed

46:21 substrate level of phosphor relation. Now phosphor relation is via respiration. Photo

46:29 relation via photosynthesis. Right So both processes rely on the army osmotic

46:36 So we I showed you the diagram respiration. This is what we're talking

46:41 . Okay so this involves the use electron transport chain. It involves production

46:47 a proton gradient. The use of 80 piece in place and the same

46:51 photo fox relation. The same. same general components involved in a teepee

46:56 this electron transport chain. But it's it's a light driven process which is

47:01 differentiates it. Okay but both rely this keamy osmosis. The formation of

47:08 T. P. Is using a gradient supplied by the energy for electron

47:14 And then harnessed or tied to this piece entities to form AT. so

47:22 both both operated phosphor relation. E and for photo phosphor relation as in

47:29 . Okay so a little bit more . Certainly different from substrate level phosphor

47:37 . Okay so um so let's look um real quickly at this data we

47:50 different carbon sources in the left We see different oxidants. Okay and

47:56 we see different delta G values. . All all negative but very magnitudes

48:03 then the impact on biomass. Okay when you're of course growing um bacteria

48:14 culture as we've seen already. We supply them proper nutrients that they

48:20 you inoculate with a few cells they then of course grow and produce lots

48:25 cells along the way. Okay so you already know we need to provide

48:29 source. Right? Carbon source will used as both for um as an

48:34 source as well. Right. And if we look at different carbon sources

48:38 . Right. So this is what looking at in terms of respiration.

48:43 ? So electron source feeds feeds the transfer chain. There's a terminal except

48:47 Right. So what are the equivalent these in the table to the

48:52 Well, the carbon source is electron . Right? Your glucose appropriation it

48:58 etcetera are the um carbon sources slash source. Right in the table the

49:07 is the terminal except er right. the occident is the molecule. The

49:12 is a molecule that becomes reduced so oxidant becomes reduced. Right so this

49:16 going to serve the role terminal Okay so this is what is going

49:22 . Um Now you see for one them there is no such terminal except

49:27 right because the bottom process with ethanol green is fermentation. Right? So

49:34 see in blue is aerobic respiration and is anaerobic respiration and the bottom one

49:41 fermentation. Right? So you see have a nitrate as a terminal except

49:46 here versus oxygen aerobic versus anaerobic. um in terms of of yield we

49:56 that glucose yields the most amount of delta G. Also note that um

50:03 greater a greater negative DELTA G equates the production of more biomass.

50:11 more biomass glucose is a bigger six carbons versus appropriate, which is

50:16 carbon. Right? So it gives more carbon uh thus potentially more

50:23 Okay. Uh contrast. So, we look at um ethanol, for

50:32 , as a carbon source. All , so we look at an aerobic

50:42 and in fermentation, ethanol is the source in all three. Right?

50:48 comparative purposes, we see that using through aerobic cellular respiration uh produces more

50:56 than those anaerobic respiration using ethanol, the difference terrorism isn't great, but

51:01 still better with oxygen. Okay. but both of those, both aerobic

51:07 are definitely much better than fermentation. see the yield of biomass and delta

51:13 . Is much less than that shown respiration. And that's and that's that's

51:19 case because aerobic respiration is simply produces energy, then does fermentation and of

51:27 the the difference difference in in differences biomass that are ultimately produced.

51:32 so, um so, you when when when growing cells, you

51:37 , these are things to consider if in terms of biomass levels, you

51:41 , what's the carbon source? Uh anaerobic respiration um are gonna have an

51:48 , or it can only ferment. these are all things that will impact

51:52 the bio energetic will tell us, know what the ultimate level of growth

51:56 be. Okay. So um so we look through as we go through

52:03 causes. And so aspiration We're not go through every single of the 50

52:09 reactions that occur, right? You to know there's no it in stages

52:14 comes in and out of each So here are the relevant terms to

52:18 . Of course you should know oxidative relation. You should know when we

52:23 when we get to a photo phosphor . But these are the relevant

52:26 And so again it's about knowing the . So in in black colossus we

52:30 from a six carbon glucose, 2 three carbon para baits or producing two

52:35 these. And then Along the way have a net energy yield of 80

52:43 and AD. Pirate bait is the in the road. So we can

52:49 either to fermentation where we get production small organic acids, alcohols or through

52:57 set of core way. Okay. then on to the Krebs cycle.

53:02 we produce some energy, more energy the Krebs cycle. And then finally

53:09 the electron transport chain or where these carriers end up producing more a

53:14 Right? So knowing the stage is . And what happens what comes in

53:19 comes out? All right. And main molecule C c glucose to pirate

53:24 sudoku way Krebs cycle and electron transport . Okay, so that's how we're

53:30 to look at it. And so , in terms of numbers, so

53:33 two pair of eight right to a away. Um And of course as

53:42 oxidize glucose, we're going to lose , lose it as C.

53:46 To write C 02, CO two as well. Um And you

53:53 eventually completely oxidizing glucose as we go respiration. Okay, so um so

54:01 start with black colossus colossus or oxidizing to peru vic acid. Okay.

54:11 initially there is an energy input that to occur. And so even though

54:17 cause this is a negative delta G , even for those who sometimes have

54:23 put energy in. Okay, so of a ball rolling downhill,

54:30 But there may be a little hump have to get over, but once

54:34 get it going it will be a delta G. It does. The

54:41 hump. Maybe put in for a on a hill and we have to

54:46 in a piece of wood and kind wedge it in and then get the

54:49 rolling. So that's a little bit energy expenditure to get the ball

54:53 But once we do it's a surplus get we get a negative delta G

54:58 the process. Okay? And that's going on here with the energy investment

55:04 . So glucose needs load of a . And so we're gonna add some

55:09 to it in the form of a , get a couple of steps,

55:12 ? So as we as we go we form fructose, 16 by phosphate

55:17 phosphate. And then in the phosphor form and then we're going to break

55:23 into two molecules ultimately to glycerol three . Okay. As you said,

55:30 23 carbon molecules that then then we the energy harvest phase. So we're

55:35 get back a surplus of energy Both in the form of A.

55:40 . H. And in the form a Tps. And it's gonna be

55:44 net a net gain of energy. ? So the A. T.

55:49 . Occurring a teepee formation occurring here here is through substrate level of phosphor

55:59 . A false for intermediate right is the phosphate group to make an

56:05 T. P. Okay there and okay. But as well we're gonna

56:12 gonna generate an A. D. . Two. Right? And we're

56:18 use that later on. But also this is a anaerobic process. Does

56:23 require the presence of 02 to Okay. Doesn't rely on that.

56:29 anaerobic 80 P through substrate level phosphor production of two molecules. Para

56:36 three carbon, para bait and A . H. Okay. Now we

56:43 look also at some variations beyond what's the M din Meyerhoff pathway or Emden

56:51 Meyerhoff partners E. M. Okay too. These alternate mechanisms which

56:59 of which is the pathway or D. Pathway for short it's called

57:04 sugar acids pathway. Certain gram negatives it. Um You can see that

57:10 six possible gluconate right? The production that um is a type of

57:16 So glucose looks like this. So what's called Aldo sugar has an

57:21 high group at the end of it there um sugar acid has a carb

57:30 group. Okay. And so these prevalent in in in mucosal secretions of

57:38 intestinal wall. And so of course gut is inhabited by many bacteria and

57:44 gram negatives like E. Coli. so they evolved the pathway to kind

57:49 take advantage of these types of Sugar acids that are prevalent in these

57:54 secretions and so enables them to kind break these down and get energy from

57:58 . Okay um the energy production isn't great. So you form half the

58:06 of a TP through substrate level phosphor and half the amount of N.

58:11 . D. H. In some it can form any DPH depending.

58:15 uh not the same level of energy but nonetheless unable to use a different

58:21 of carbon source. Okay. Different of carbohydrate. The I believe most

58:28 those with the E. D. have that in addition to glenn hollis

58:34 so for example has both the M. P. Glycol is pathway

58:40 in addition have have the E. . Pathway as well. Okay um

58:47 phosphate pathway or pintos phosphate shunt um be a source of energy information again

58:52 as much as with psychosis. Um Any DPH produced domestically user uh bio

59:03 and that's really what the pintos phosphate is. It serves more a role

59:08 bio synthesis for anabel is um uh forms this five carbon ribbon goes by

59:15 intermediate that's used as a building block make things like aromatic amino acids like

59:24 for example. Um nucleotides as The service building blocks for nuclear

59:30 That's primarily its role is bio synthetic it can if needed to serve the

59:35 of providing some energy as well. so so just you know a couple

59:40 alternative pathways to to the E. . P. Pathway. Now um

59:47 in terms of let's look at an again. So we're gonna get into

59:55 right but let's look first at at So we start with like causes no

60:04 whether we're going into respiration or we're to fermentation like cause this is a

60:08 of it. Okay. Of both of course. And the regular energy

60:13 . Any D. H. T. P. Right so whether

60:17 pirate that's formed goes respiration depends on available is an aerobic respiration is oxygen

60:25 . Well then we can go this . Okay maybe it's not option.

60:29 it's an anaerobic respiration maybe nitrates Well then it can go this

60:33 Okay and so what that means is going to go through these different stages

60:38 information of a silk away the Krebs electron transport chain. All this become

60:44 a part of respiration, whether it's or aerobic. Okay so of course

60:51 . It's an aerobic right? Doesn't oxygen. Doesn't require any of this

60:56 the process. As you see here the left. All gone.

61:00 So fermentation relies on black colleges for teepee formation. We do for men

61:07 . D. H. Of course black causes is a part of

61:11 So we have to have a continual of N. A. D.

61:17 to supply glycol Asus because in D. Is a reactive in black

61:24 so we have to keep supplying that that we can keep performing in

61:27 D. H. Right so fermentation actually that's the role they serve.

61:32 regenerate the N. A. Needed for black analysis. Okay so

61:37 the gas the fermentation, ethanol fermentation look at both of these uh fermentation

61:43 . Okay so again and psychosis uh casa stage provides the A.

61:51 P. Formation. Okay um and long as you keep supplying glucose or

62:00 other sugar uh and N. D. Plus. Right and of

62:05 ADP and phosphate. So as long you're providing these reactant it will form

62:13 energy. Right? But you have keep resupplying your carbon and your

62:18 A. D. Okay. And see how fermentation reactions do that.

62:23 so um so it's all about recycling N A D H. Okay to

62:30 N A D. So here's black . Okay, glucose to power And

62:37 about all about maintaining redox balance. ? So making sure that you have

62:42 the oxidized form of N A. . Available to accept electrons during black

62:48 to form an A. D. . And then continually resupply regenerating the

62:52 A. D. Right, um, and the lactic acid

62:57 So we see the power of So empire of eight has become reduced

63:05 lacking. So pirates actually receiving You see how molecules are different

63:13 Right? So pirate has accepted electrons become reduced to lactate. And in

63:19 process we regenerate the N A So it keeps going and going.

63:23 right. So in this example is keep supplying glucose. Um we form

63:30 pirate. Then the fermentation reactions will it to lactate. Okay, in

63:36 fermentation again, para bait uh, initially broken down car D. Car

63:43 . Later we call it the esa tal height. Okay, to carbon

63:48 behind then this is where this comes . So N A. D.

63:53 from electrolysis, right? Will be as the talbot gets reduced.

64:02 you see there and they're reduced. you see the addition of electrons in

64:12 form of hydrogen right here and So we've any D H has become

64:19 electrons handed off to a settled behind reducing it to form ethanol. Okay

64:26 and the purpose has been served we've regenerated N. A.

64:30 Which can then keep keep black colleges and keep producing energy because this is

64:34 only way energy is produced. And it has to keep that

64:45 Alright. Once again that substrate level phosphor relation occurring, there's no no

64:50 transport chain, none of that's Right? This is substrate level of

64:54 relation. Not not oxidative relation. , so if we look at so

65:01 we go then the route of respiration the next stop for pyro bait is

65:08 the formation of acidic away. so recall that. So we go

65:14 coast to Prior Bates private oxidation at next stage. So we're going to

65:20 box late. Nice see there and gonna form this to carbon away.

65:26 CO A is a coenzyme called coenzyme and it's derived from this. It's

65:38 from panther authentic acid. If next time you look on your pant

65:46 , I'm not gonna test you on but just to for completeness. So

65:51 authentic as the next time you look a cereal box. Look at the

65:54 and you'll see a bunch of actually bunch of vitamins that are involved in

65:59 like vitamin B one B two. um and Panasonic acids in there as

66:07 . Um and it's a source for CO and Co actually has a self

66:13 group on it. And um it's when you add CO a kind of

66:19 a high energy bond. And so CO a to a molecule kind of

66:23 it. So like glucose needed a uh you need to be energized at

66:29 start of glycol Asus by adding by a couple of a tps. So

66:35 does pyre of eight. So part it kind of is a lower energy

66:38 needs a boost as well. So attaching a CO A two as part

66:44 the process that energizes it and then be more reactive and then that's what

66:50 the Krebs cycle. Okay, so Krebs cycle then is is actually a

66:56 point in metabolism. So the Krebs has a number of intermediates, some

67:01 which are used for anabolic processes. if you ever look at a metabolic

67:05 , you'll see that the Krebs cycle what we call a central point

67:09 There's there's arrows going to and arrows away from it because it supports both

67:17 and and and an apple is um a central point where there are building

67:22 for for things like amino acids nucleotides are in the Krebs cycle and it

67:28 both those purposes both Annapolis. Um metabolism. Okay. And so you

67:34 the energy production in the Krebs cycle in the private oxidation to acetic away

67:41 for N. A. D. . Right? All the A.

67:43 . H. Is being formed as as F. A. D.

67:45 . Two being formed and we have step where we see substrate level of

67:51 relation again. Okay so um so each turn so remember that one block

68:03 formed goes through one turn of the . Okay. One turn of the

68:07 gives you three and A D. . One F. A.

68:10 H. Two and 1 80 Right so but we generate two takeaways

68:15 each glucose that gets oxidized. Okay so for each glucose we're going through

68:23 . Right two turns which means we're double up our value. So six

68:27 A. D. H. Two . A. D. H.

68:29 to 80 P. Per glucose Okay so of course here now we

68:37 have completely oxidized glucose to C. 11 mole of CO two in the

68:42 that you look away process two more of C. 02 during the

68:50 C. A. Cycle right here here. Okay so and as mentioned

69:00 T. C. A cycle of Krebs cycle is a central point of

69:04 . So it's it's it's a term and feet bolic that's what we call

69:15 Krebs cycle. Anti bullet means it both metabolism and it serves an apple

69:21 um by by providing building blocks to various molecules. Okay so um so

69:31 we look at the overall process then we see that um you see the

69:42 energy output if you will. so um so in the area in

69:53 respiration and we see the breakdown of to private information of energy here as

70:00 saw. Right? Uh then electrons transfer redox reactions. So we have

70:06 electrons to any data from N D H. Right? Uh in

70:11 pirates of silicon way step, we that as well. T C A

70:18 more right formation of N A D D H two. We do have

70:22 step of phosphor relation there. So we see in oxygen and this

70:30 what represents oxidative phosphor relation. The process of electron transport, so

70:36 see how the N A. H is. Right? This is

70:39 N A D H FADH two. are all going to be funneled electron

70:49 chain. Right? So through oxidative relation. Right. The A.

70:53 . P synthesis production of a Right. So you can see the

70:58 . Okay, so, again, on a proton gradient to to generate

71:04 A T. P. S. subject frost relation for a T.

71:08 . S. Right. Right. activated false correlation. 34. So

71:19 , huge difference. Right? 34 four. Big difference. Okay,

71:25 more than 90% of a Tps to are coming through oxygen false relations.

71:30 it's very important for us humans to carrying this out. We couldn't rely

71:34 fermentation. The energy output would not enough to sustain our bodies. Okay

71:41 um uh so that's respiration. So get a little more closely at this

71:48 respiration in chapter 14. But you this is kind of the overview of

71:54 that's about. Right? So we a carbohydrate source. But remember,

72:00 know, the same basic thing occurs you're whether you're breaking down proteins,

72:07 , nucleic acids, they'll just funnel different entry points in this pathway overall

72:17 . So for example lipid metabolism will into the silicone way formation. Protein

72:24 breakdown will feed into the T. . A. Cycle for example.

72:28 they'll have different entry points depending on being used as the organic source but

72:33 you're gonna form lots of a Tps . Okay. Um so again this

72:38 a complete contrast to what happened in . None of this is involved in

72:42 other than the substrate phosphor relation from . Okay, so looking at uh

72:51 aromatic compounds as sources of energy uh for particular bacteria are able to do

72:58 . Some bacteria can definitely do this use these aromatic compounds. Um they

73:07 the thing about aromatic compounds is they be quite toxic. Okay and then

73:13 see there which is what's basically would formed from lignin. Uh you see

73:19 the aromatic rings present. Um So compounds in general again can be quite

73:26 . Uh the utility of bacteria that these down it comes from pollutants uh

73:35 these aromatic compounds. What are they whether with sort of contamination or water

73:41 , bacteria have been used in bioremediation to to clean up these pollutants uh

73:49 there are many types of that are to break these things down and use

73:53 as a source of carbon and Okay, so we see these kind

73:58 things certainly in petroleum products are rich aromatic compounds. Um uh things like

74:06 and die dies are contained these aromatic , pesticides. So a number of

74:12 things um contain aromatic compounds. And these things can be very hard to

74:19 because the benzene ring itself, the ring is quite stable. Okay.

74:25 so but they can be can tantalized certain bacteria. And the key to

74:31 breaking them down is to break the . So ring break, which is

74:36 key to the process. Okay. so many of these aromatic the pathways

74:42 break down certain of these aromatic compounds on plasmas in in in because it

74:48 be a few genes in length that that bring about the metabolism of the

74:54 . And it's very often that these be transferred by plasma to from one

74:58 to another. And we've engineered bacteria do this to to be able to

75:04 a variety of these different compounds. And so you see there tara Winkler

75:10 , aniline nitrobenzene that they all frontal to this molecule called catacombs.

75:19 that's kind of the the central um in the processing of of aromatic

75:28 So and that requires the addition of . Right? So addition of oxygen

75:34 the ring is what is what enables to be broken down. So you

75:38 the ring then it can be fairly metabolized and fall into the Krebs

75:44 So you see there benzoate uh is canticle uh the addition of oxygen.

75:53 die oxygenates enzymes. You see the benzoate, di oxygenates aniline dye,

76:01 , nitrobenzene, di oxygen etcetera. are all enzymes and oxygen to the

76:07 and then eventually lead to the So that this system is the product

76:14 is the the of of the ring so cat skull to mutilate. And

76:19 once that happens then we can break further down into components that fall into

76:28 T. C. A. Cycle you see there. Right, So

76:32 is the aerobic pathway is very There's also an anaerobic pathway that can

76:36 this. And pseudomonas species of pseudomonas wrote A caucus are have been used

76:43 bioremediation purposes because the number of these able to to break down these aromatic

76:49 and use them for growth. Um but again, so the bottom line

76:56 breaks of aromatic compounds, breaking the ring. Doing so using dioxin enzyme

77:01 will add oxygen to it. And the products that will funnel into the

77:06 . C. A cycle. And where the energy capture can occur.

77:11 um so again canticle is kind of main molecule to the intermediate that then

77:20 then we break it down to the or other that is now the the

77:27 ring product. And then intermediates to go to T. C.

77:31 Cycle. And then we kind of for A. D. H.

77:34 . H. Two and 80 Okay so uh so in summary then

77:40 again it's it's uh in terms of metabolic pathways overall pathway caused to so

77:48 is to know in stages. So just refer back to refer back

77:52 this diagram here uh it's kind of starting point um And in the terms

78:00 and then doing a little bit about basics of of antibiotic anabolic, how

78:05 teepee hydro sis and um formation have role in the process. Um And

78:19 um let me just go to the here so you know and then knowing

78:36 , knowing the let's go here, we go. The basic principles of

78:47 G. Um What influences delta The uh construction of the energy

78:54 So um so yeah and and again one in stages, you don't need

79:02 know all the individual reactions and all enzymes involved but you know The state

79:08 , what comes in and what comes of each stage. Okay so we

79:11 then continue this in Chapter 14 with little closer look at respiration, kind

79:17 what's involved there, a little bit redox reactions. Um, and so

79:23 is going to be broken up into parts, so we'll have part one

79:26 part two there. Okay, so next time I'll see you in the

79:32

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