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00:17 welcome. Yeah, you don't have whole lot to do today to finish

00:25 this last chapter. Um So um got the exam one this week.

00:34 look at if you have any questions what's going to be on it.

00:38 you already downloaded the exam one review that's going to be content. Um

00:46 about stuff. Still you can email office hours, um can't make office

00:53 out of our so um uh let's . There's nothing no blackboard quizzes this

01:01 , there's no smart work Um do today, which is the last bit

01:06 Chapter five just do today, but next sunday. Um uh So the

01:13 is really just the exam. so today is the end of unit

01:19 will start the next one on thursday that material is all up, all

01:23 you to stuff is up. Um So you'll see in there um

01:32 probably want to hear this now, I think well it carries over over

01:37 , 2 days um Two half days guess. The the 30 dang it

01:46 remember now, it's next. Not week from this thursday really?

01:53 Um And then the following Tuesday, it's like it's a ways away

02:01 But it's one of those foot classes the subclass beyond chapter 13 which is

02:06 . Okay, beginning some metabolism. anyway, just so you heads up

02:10 that offer courses in the course So um but you're not worried about

02:15 right now. I realized that you more concerned about exam one. So

02:21 , so uh let's uh see, we've covered Chapter five, we went

02:28 a row tolerance. Last time we through levels of terminology that the sterilization

02:34 accept this etc. A little about antimicrobial. So you're back to the

02:40 bacterial allergic uh electrostatic agents. Um value and what that means actually we're

02:50 have so we're gonna finish up with um just an example of some physical

02:55 agents of control. Um and uh little bit of discussion around that.

03:02 so let's start with a question. is super super easy. Okay.

03:11 the the value thing. Right? remember that um The value is the

03:20 of time it takes to kill 90% the population on one log. Right

03:25 talk about logs of death. We're at my criminal control of growth.

03:31 So knowing that definition. So we a culture that's at 10 of the

03:39 cf. You per meal. Which colony forming units. Okay. Think

03:43 it as cells per mill. And value is two minutes of the

03:50 Okay. So we have this effective it. That's our devalue. and

03:56 many viable cells are we left After eight minutes of eight minutes of

04:07 . Mhm. Oh timer's on. this 1? Okay. 876543 two

05:37 time attack. There we go. . Okay. Yes You won.

05:49 are correct. Okay, so here's the problem. So starting out with

05:57 many cells. One log of death two minutes. So mm hmm.

06:08 two minutes. We're at 10 in fifth. One log another two

06:11 Another log. So a lot of every two minutes. Right? Don't

06:16 don't don't eat 10 of a Okay. So why don't you

06:21 Okay. So uh so just as little recap, we'll come back to

06:27 question in this second. Well, do it now. Heck with

06:30 We'll summarize here in a second. do this one. Okay. So

06:35 , so we have a growing culture a grand positive electric. Okay.

06:40 we added disinfectant at mid log. ? So kind of in the middle

06:46 log face, right? Uh for exposure. And so we then took

06:54 sample of that uh culture. Following the four our exposure. And

07:02 put it into fresh media. Fresh with no disinfectant, right? Just

07:07 granted. Just call it nutrient All right. So it's a nutrient

07:11 . Mid log growing bam. It it with disinfectant. Four hours then

07:17 it take some of that culture out fresh medium with no disinfectant and monitor

07:25 . Okay, so this is the half here. Okay, So we're

07:31 that the subculture, Right? So have a tube called initial for exposure

07:37 . There are two called subculture. was a sample of that previous

07:41 You're not going into fresh medium. disinfectant. Okay. So different.

07:49 did different delusions of disinfectant. Repeated experiment using different delusions. No this

07:55 . Okay. And we came up this result. Right. So basically

07:59 . No growth plus its growth. . Just keep it simple. So

08:05 have four different solutions. So at appropriate concentration. Okay, uh this

08:13 would be considered. What? The effect of that disinfectant? Um

08:21 one of the delusions of I had effect. Okay. But certainly at

08:27 And three of them are dead. question is Okay, what was the

08:35 ? Okay, so let me reset . Okay. Right. So one

08:48 time in my culture growing gridlock. it with disinfectant then. Um take

09:00 sample out. So that that is there with disinfectant for four hours and

09:05 take a sample put it in fresh . No disinfectant and see what happens

09:11 terms of growth. So I'm looking growth of both. Okay, mm

09:40 . Thank you. Okay. Timer's . Oops. Sorry about that

10:17 Mm hmm. Yes. Let's Okay. Mhm. Okay. Who

10:43 one of the 107? Anybody who one of those? Okay. So

10:48 why is the electrostatic? Why do think the material status? Um

10:55 So I just like there's no Do you remember when you transfer it

11:02 a new medium without. Mm This impact to grow. So it's

11:07 killing. So. Alright. So it had been bacterial side for example

11:15 and minuses of it back to the . Could you? So it was

11:23 a bacteria static agent. The cell exposed. This effective log didn't uh

11:30 and the question is okay. Did die? Did they? That's why

11:36 have to do the second part. is to take the cells in the

11:39 there that haven't exposed disinfected. And basically checking the state of those cells

11:45 those cells survive treatment. They were growth inhibited Or were they indeed just

11:50 ? Right. And so the subculture is labeled here and tells you that

11:55 know, especially timely this is a of the cells following exposure to

12:01 They're either alive. Which they were they were killed. And that would

12:06 been a negative result in this subculture . Now can you tell um if

12:12 were if it were if this were let's say okay indicating. Could you

12:21 whether it was bacterial static and bacterial ? Just from just from a plus

12:30 minus growth. Could you tell? . Okay. You couldn't tell if

12:35 if you're just relying on the plus the growth. No growth observation.

12:41 . Um Yeah, you can certainly you'd be right in saying again informing

12:46 scenario if it's this and that are results right? Negative, negative.

12:55 growth in attitude. Okay. In scenario you can confuse conclusively say yes

13:01 they're dead. Right? They Okay. There's no growth in

13:04 and even the subculture they weren't able grow because they were killed.

13:09 But you wouldn't be able to tell from that whether it was bacterial silent

13:14 , like you have to do like viable count perhaps. Well not even

13:19 , you have to do some kind microscopic adopter base to see cells just

13:24 , right, because we're meant to , cells are being blown up,

13:29 , nothing visible once the once once agent has acted. Um Okay,

13:36 Any questions about that? Yeah. . Because that that was such a

13:44 , weak delusion. No effect on . You could take almost any kind

13:49 disinfectant and diluted out enough and there be any effect, just not strong

13:56 . Yeah. The other question. , um Alright, so again,

14:03 is just recap Okay, so we at the value in that calculation.

14:10 again, this looking for logs of , right? How long to get

14:13 . Uh just remember that killing uh really no, this has written on

14:20 slide does not really occur that everybody instantaneously upon exposure to treatment rates occurred

14:28 the summary because damage accumulates and all cells can be may vary somewhat and

14:33 they accumulate damage and are finally Okay, so of course various things

14:40 affect the efficacy as we've talked about . So um let's look at some

14:49 actions of how these things work where working on in terms of killing the

14:53 . What you might think. Okay um many of these agents working

14:59 Okay. Um uh detergent type of mimic membrane structures and they tend to

15:09 membranes and so that will of course the cell. Um if it doesn't

15:14 an intact membrane obviously everything leaks out uh soldiers license um certainly proteins are

15:22 um you're 70% hasn't all disinfected it and and alcohol based hand sanitizers which

15:34 guess most of all of them But these uh alcohol denatured proteins again

15:42 themselves denature breakdown proteins. Um as many other types of agents. Um

15:48 another type of compounds you've probably heard . Uh Doctor's office. You'll see

15:53 nine, the kind of the yellowish iodine in there that acts as a

15:58 actually. It's an antiseptic because you use on your skin but it has

16:01 similar effect in terms of the nature of course, remember that the maturation

16:06 proteins is about um destroying that Right proteins are all about three dimensional

16:12 folding that poly peptide change. And nature of that means to basically make

16:17 unraveled right, loses function similarly with acids. Um They can be denatured

16:23 well. The strands unfold nonfunctional but can be worse damaged. You can

16:30 great nucleic acids radiation sort of types radiation can do that um and create

16:36 that's what UV light does to nucleic . So um so these are kind

16:41 three main things. Um And with disinfectants and antiseptics. Antiseptics um other

16:49 , they are working on multiple So that's not necessarily just one of

16:56 . It could be mhm Multiple Right, proteins, The gasses,

17:02 , all of it. Right. in contrast to an antibiotic,

17:09 Antibiotics target have typically have single Right? And the target a component

17:16 protein synthesis. One component of cell synthesis. Okay. Or whatever the

17:22 maybe. But antibiotics don't work like where they have multiple targets in the

17:29 . Okay, so keep that in because at the end we talked about

17:34 . Okay. Resistance to antibiotics, to disinfectants. Antiseptics. Okay.

17:40 that possible? Okay, so we'll that here shortly. Okay, so

17:45 a little bit about some of the types of physical chemical controls,

17:52 Of course. Um the elevation of . Well, the nature proteins um

18:01 killing cells, high temperature and So, it's auto claims.

18:06 Brings a steam under pressure. And so you get to temperatures that

18:12 aren't used to seeing. Okay. of course they will they will rapidly

18:17 them. Especially in those sports. ? So steam penetrates and those spores

18:22 kills them. So autoclaves are effective in that. And your uh standard

18:29 for auto clapping for this either 15 20 minutes. It's common.

18:38 And again, you're you're achieving very temperatures and that moist heat has a

18:44 high killing power. Okay. The can have equivalent um um equivalent the

18:54 seeds to arctic, claiming that we dry heat. So, think of

18:57 as an oven. Okay. It's dry heat sterilization. Um Of course

19:02 gonna be a lower temperature but a longer time. Um But it's not

19:10 steam under pressure. It's more of dry heat that kills. Okay.

19:15 but actually a higher temps, higher attempt longer time autoclave because of

19:20 ability to heat steam to high Very effective incineration. That's what you

19:26 do in lab when you're putting your in the flame, right? That's

19:31 , basically sterilizing the water. Um air is certainly possibly that's what that's

19:40 an oven is basically giving you Hot convection oven. Okay. The um

19:48 . So pasteurization okay, is a that is used by food and beverage

19:58 . Okay? To reduce levels you know, powerful bacteria in the

20:04 . Okay. But um it's not harsh as an autoclave. Okay,

20:11 you're trying to preserve the color the , the flavor of the food and

20:18 can't really preserve those things by putting . Okay, to harsher treatment.

20:24 for food and beverages, there are . Okay, so pasteurization uses milder

20:32 for but for varying temperatures, varying . Excuse me. So you're

20:37 T. L. T. Low long time. Hi temp short

20:42 Okay these uh for milk pasteurization, all about um reducing the numbers of

20:51 come to that in a second. So we talked about before so they

20:58 course are very resistant to heat. um cox C. L.

21:03 Is like second to end those ports terms of resistance. Okay. And

21:08 they use that as a target uh killing those off or reducing their numbers

21:14 . That's there. Then they say achieving optimal pasteurization by doing so

21:20 Um And so low temp, longtime temps short time ultra high temperature uh

21:28 then ultra pasteurization um is like at C for like um 0.5 or something

21:39 that. So what these ultra ultra ? Ultra high temp. Uh Do

21:45 the what the significance of that It allows you to have a dairy

21:52 that can have a long shelf life without refrigeration. Okay. Which is

21:58 helpful to, you know, areas the world that don't have spotted

22:03 And so if you have to have milk that can be kept on the

22:06 at room temp, right? Because this process? Because this process is

22:10 sterilizing that. But it's pretty darn . Okay. Um But again it

22:16 you to have a product of a shelf life for six months. Of

22:19 that's until you open the bottle. then it's typically 10 days, two

22:24 but at that time you can keep for nearly six months uh and it's

22:28 it's fine. Uh There's some uh that with these types of processes.

22:39 and this one or this one is that high temp, even though it's

22:45 damages, maybe some of the helpful milk components. Um I don't think

22:53 ever drank ultra pasteurized. No, it has like a cooked taste to

22:59 a little bit. So um those tout ultra pasteurized milk, you put

23:05 your coffee don't necessarily drink it like your cookies or whatever. So that's

23:10 of different tastes used to, but , you know, the the the

23:16 method used depends on the food manufacturer what their what works best for their

23:22 . Okay. Um Now, so , remember pasteurization is not sterilization?

23:30 . David reduces microbial numbers, especially target one. Um And although ultra

23:38 temp ultra pasteurization can get close, it's not it's still not sterilization.

23:45 . Um Alright, so not everything hot temperatures or very hot temperatures in

23:56 of reducing numbers. So um depends the nature of the material.

24:04 And so uh cold temperature for is used obviously for refrigeration, cold

24:10 doesn't kill. Cold attempt slows down , right? It can slow down

24:16 growth, but it doesn't kill, , we use it for obviously for

24:22 preservation of foods too, You so spoiled so quickly obviously, but

24:28 a lab to preserve microbes, we have a -80 freezer. All

24:36 strains used in lab are kept in there, you have to put it

24:41 like a an antifreeze or antifreeze Ice crystals that form can actually cause

24:46 . So try to minimize that by agents to your culture essentially antifreeze to

24:53 that from happening and they can remain . I've had cultures in there since

24:59 that I revived this past week and grew right up. Okay, so

25:06 very convenient method for that. The one thing is there is a particular

25:14 which we'll talk about that toward the of the semester hysteria that actually grows

25:19 refrigeration temperature. It's something that you to be aware of uh listeriosis.

25:25 There was a blue belt ice cream out in Brenham. I was like

25:31 567 years ago I had some batches the ice cream, make people

25:38 There's a couple of fatalities due to . And so this can grow refrigeration

25:45 . Uh And so obviously we're ice manufacturer, you're doing your thing and

25:50 temps. And so it was the was traced to dirty uh where they

25:56 holding the ice cream before they dispensed . The kind of the fixtures and

26:01 weren't very clean and so that's where traced the listeria ah contamination to.

26:10 but uh I'll say to the rest the story a story for later

26:14 but that it is, it is something to be aware of um

26:21 So not all liquids can well behaved will not are not really the student

26:28 any kind of heating type of So you have to um So the

26:33 maybe an option. There's a couple media we have in latin that we

26:37 that direction. Say don't you have sterilize it or you have to not

26:44 anything just boil it and then pour out. So it just depends on

26:48 ingredients in the product. So uh . Of course you can not only

26:53 liquids, you can filter air. , so your HEPA filters consult the

26:58 . Um technically all of the the itself can exclude microbes for sure.

27:07 You might say, okay, well go through sterilized and I use the

27:11 myself. But technically it's not because can't keep viruses out. Okay.

27:18 generally that's not a problem. But nonetheless, you know, it's

27:23 not because I just can't technically get there. Okay. But it is

27:29 for a lot of different uh products and liquids. The uh okay,

27:38 radiation radiation relies on basically two So we call non ionizing and ionizing

27:46 radiation has has been approved for use and on foods, many frozen foods

27:54 irradiated. Um It's gonna be with gamma radio. Typically very high energy

28:03 UV light. So let's just look the two types of radiation. So

28:06 ionizing radiation UV in arrangements um 200 300 nanometers. Remember the smaller the

28:16 of like the more high energy. . And so the damage that UV

28:20 does, it's an altar bases and gas IDs cause mutations. Okay.

28:27 But the thing about UV lights, it's not penetrate very well.

28:33 A shirt can stop Petri additionally can it. Right? So um it's

28:39 used for surface disinfection. Okay? now the ionizing radiation um can I

28:50 very high so we can actually break and take acids. Um of

28:55 it's a lethal effect. Um And used for, like I said for

28:59 foods are rated with gamma rays. and it can be quite effective of

29:08 . Um It's more for solid. wouldn't use it for um liquid liquids

29:17 racism can penetrate liquid very well. just gonna be more surface or solid

29:23 of. Okay, I think even Petrie not partridges, but pipette boxes

29:31 pipette tips that are in boxes, like that. Other types of lab

29:35 . Medical equipment, things like Um The chemical agents. Okay.

29:42 disinfectant. So phenolic compounds, iodine . These are all things that damage

29:50 . Uh membrane lipids take assets. have a varied effect. Okay.

29:57 tobacco sand is what used to be A lot of your hand Sanitizer because

30:02 said they discontinued because material can resistant it. Okay. And most of

30:07 hand sanitizers nowadays have like the alcohol in there, which is much

30:13 effective. Um The beta dying I that that's kind of the yellow uh

30:22 seen a doctor's office or using surgical setting the uh iodine is an effective

30:30 as well. Uh The Alcohol, 95%, which is 70%.

30:38 And there's other words, many different of alcohol. So we're just gonna

30:42 uh isopropyl alcohol. It can just sm all where it gives the two

30:47 more common ones. Um And people , well what would be much better

30:55 better proportion, 75% and 95%,, is more effective disinfectant. Okay.

31:02 has to do with the The couple things. one is um the

31:08 Alright, so Alcohol works by denatured . So if you do take 90

31:15 ethanol and apply it okay it will to destroy proteins. But then it

31:22 of dissipates. Okay, because it's more evaporates much more quickly. There

31:28 were some more water. Right? 70%, it's a thing that's called

31:34 contact time. Alright, so 95% has a very low contact time because

31:39 evaporates quickly. So it can be in terms of geometric proteins, but

31:44 last long. Okay. And those actually survive survive. Okay, but

31:51 . It's much better. And water less water makes it makes it have

31:56 higher contact time. It can penetrate . And and the more water in

32:01 70% kind of draws the ethanol molecules the cell as well where they can

32:07 proteins and being to destroy them. , so um so anyway, so

32:13 I said, hand sanitizer that they want to get. I don't think

32:16 want to get below 60% like 62 , 80 in that range is kind

32:24 what you want to get the maximum . Okay. We use 70% in

32:29 lab. Um detergents look look like you see here um where uh that

32:39 mimic where the our our group Yeah. Is this So it looks

32:44 much like a fossil limit. Because the fossil looking structure to

32:49 And so these then dissolve membranes. . And in doing so, break

32:56 the membrane and break the cell Um Gasses can be effective sterile.

33:05 okay. These are often used for preconditions, um medical equipment, um

33:13 and so forth. Okay, so can penetrate really well. Exactly.

33:19 , we were all solid type items were sterilizing using gas. Gas is

33:26 not gonna be good on link with liquids very well but they can penetrate

33:31 nooks and crannies of plastic. Where fact, and so it works kind

33:36 like this chain reaction you see. here's ethylene oxide in the presence of

33:43 base. Okay, it will then and began to interact with proteins.

33:51 at acids causing dance. Thanks. he said it could be it's quite

34:00 is used but um the danger it be explosive. So there are looking

34:10 there are some other equivalent equivalent gasses been looked at the kind of

34:16 I mean oxide for that reason hazard the person using it. Um

34:25 okay, resistance. So he told to talk about that. All

34:33 Um the I think your book party a table of all different types of

34:39 and disinfectants. I don't expect you memorize what every single one is.

34:43 kind of like kind of give you examples of different categories, you kind

34:47 just stick with that. Um The just so as I mentioned earlier,

34:57 uh this effectiveness epic will have multiple . Right? Memory programs in the

35:05 , basically all proteins are going to susceptible to the agent. Okay,

35:10 acids. Right, so multiple multiple . Okay, resistance uh to enter

35:17 programs. The 4th based on acquiring . Okay. In education somehow counteracts

35:24 effect of the antimicrobial. Okay, that process on on from the viewpoint

35:32 the let's say bacterium who's becoming resistant um if it's becoming resistant to antibiotics

35:41 the resistance to disinfectants, that's a different body. Okay. Antibiotics typically

35:49 With the new Target one component of process. Whether it's a particular enzyme

35:55 in sylvan synthesis, right? Or a component of working senses or what

36:02 ? Okay. Typically single targets. . So what is the resistance if

36:08 bacteria becomes resistant? Well it typically a mutation singular and that will enable

36:14 to counteract the effect. Okay. of course does happen. We're all

36:20 of that. Multi drug resistant types um resistance to disinfectants and antiseptics that's

36:28 likely. Okay. Because we have acquire multiple mutations to kind of write

36:35 single effect that can happen when disinfectants antiseptics do their thing. Okay.

36:42 just statistically it's not likely. When it is like when it is

36:49 is if it's not used with disinfectant antiseptic using the proper concentration when it's

36:57 out. Okay. And the targets not be as many. Okay,

37:05 that's menu when resistance might occur. ? So not using that chemical at

37:13 proper concentration, maybe you're trying to corners to save money and say well

37:19 me do this out tenfold more and I can stretch it further.

37:24 That's when you can make perhaps set chances for resistance then to that

37:32 Now um of course the hospitals. is like all the time.

37:38 But it's surgical operating rooms, et . What have you? Okay.

37:43 they do it in a way that more so makes it less likely for

37:47 to occur because they'll use different categories disinfectants. Okay. And they'll switch

37:55 on a on a biweekly basis or when they clean up that one time

38:00 use the alcohol based perspectives next time based the next time based.

38:07 So they keep changing it up on regular routine and that that also makes

38:13 even less likely for resistance to Ah Now antibiotics have just mentioned because

38:21 are typically single target uh types they is resistance can occur but you know

38:28 anybody does work like uh ones that with cell wall synthesis. Okay.

38:36 that kind of similar for example, will interfere with the cross bridging that

38:43 between and within the people I can then that then that um people like

38:49 you can kind of destabilize. So you don't have the connections holding

38:53 together right now. Kind of expand little bit. And that's when the

38:59 . Remember there's the membrane is pressing against it. Right? And so

39:04 that kind of thing collapses someone, that set of plastic member can bold

39:09 out. Alright, bubble out and and then lice eventually. Okay,

39:14 that's how um you see kind of bulging on the micrografx for some of

39:19 bulging parts sticking out. That's that's coming through the people of like handler

39:24 kind of falling apart. Okay, um and then this thing about antibiotics

39:31 actively growing cells versus slow growing Okay, so that's about penicillin for

39:39 , works on ah enzymes involved in wall surfaces. Well, several synthesis

39:47 its most active during log phase. . Let me see all kinds of

39:53 during this process of dividing. And so that's when you see lots

39:57 cell wall synthesis. Remember when cells ? Like so that there's many cells

40:06 that state in law phase. So is where. Right. The septum

40:12 where the cell wall synthesis is We have lots of cells in log

40:17 that are in kind of that And the civil sympathies going, they're

40:20 be highly susceptible, especially for grant . Right. Um The grand negatives

40:28 to be not as susceptible to these of cell wall synthesis antibiotic types that

40:35 to do with their outer membrane, kind of restrict movement of these

40:39 Okay. But the Grand positive when growing rapidly there's lots of targets for

40:46 pedestal to attack in that state. . Um but uh but slow

40:53 Right. There's not as many And the slow growing cells aren't gonna

40:57 as susceptible. Okay. Um Mhm. Resistance. So what are

41:07 ways they become resistant? Okay. , okay. Um you can probably

41:15 up with a list on your own basically it's let me show you I

41:19 out a graphic that I have in I use my other class in the

41:24 again. Just just for illustrative Right. So you can have you

41:29 block entry of the antibiotics. So doesn't commit. Maybe it goes through

41:34 particular transport protein or maybe their mutation that then that is not able to

41:39 that antibiotic in. So it's resistant it. Maybe it can inactivate uh

41:47 activate the antibiotic. That's what the resistance. Beta lacto. He just

41:54 destroyed the penicillin. Okay um a to pump out the antibiotic.

42:00 E flux needs to pump out. alteration of target molecule. That's what

42:08 resistance. Right man commission latches onto that amino acid that's part of that

42:14 the cross bridge forms. And if a change in that target that bank

42:22 can't bind and it's resistant to Right? So again all these uh

42:29 that uh but it can be one more of these, it doesn't have

42:33 be just one, it can be because that um it's it's members of

42:40 population will be present. That will one of these changes one or more

42:45 these changes in them already. And the presence of being about

42:50 Well then favor those types to Right? Evolution 101. Right,

42:56 the changes already present and the president barnicle allowed them to proliferate over there

43:03 of narcissists. Okay so that's that's that mechanism works. Right? Um

43:11 biological control it's called so taking right? Or probiotics? Um uh

43:21 your microbiome let's say. Okay so can be effective especially if you've been

43:30 a course of antibiotics for some kind infection you may have had. Uh

43:35 good to replenish replenish your gut Okay when your when your microbiome is

43:42 of balance right? For whatever reason can sometimes initiate unwanted types to then

43:50 over. Um And that can be problem. Clostridium difficile style is one

43:56 those that causes severe diarrhea. It be fatal in infants and the elderly

44:03 it arises typically when those people are antibiotics and it kind of changes the

44:09 of bacteria in the gut and then guys begin to emerge. Okay so

44:15 so probiotics do you have can't have roles in terms of maintaining your

44:20 Okay. Um uh anybody take anybody who yeah they help you?

44:33 . Oh okay. Yeah but yeah cause of ulcers. Right?

44:40 Pylori. Right well good. Um my wife takes them. Uh I

44:46 mine through eating yogurt. Okay. But um it's always ask you

44:53 how many how many which pills should buy it with, what concentration should

44:56 be in? I say you get ones with the most because a lot

44:59 the bare die as they get to they're going Okay. But um uh

45:06 certainly there's you know I'm I don't I I just say eat yogurt but

45:14 those cases where probiotics will definitely So it's kind of uh kind of

45:18 out for yourself is it helping me it's not helping me? You know

45:21 think it's one of those kind of . Um But face there so fixed

45:29 is I think the up and coming way to go in terms of controlling

45:35 caribbean numbers because a it's very specific pages. We haven't talked about viruses

45:39 that's common. The pages are very . They have a specific who they

45:45 . Okay And um so you get get rid of any kind of of

45:51 um somewhat of the resistance that can . Although bacteria become resistant to the

45:57 . The page can also adapt and but the the they use that already

46:05 um controlling salmonella salmonella in in the . Also like the E. Coli

46:14 that's found in cow's right doesn't cause . And cows they're the ones that

46:19 it in their gut. And so seen where they've um so there's a

46:25 so it's a no 157 equals 1570 of those our cattle. Okay in

46:31 and in the feces. And so they've I've seen where they've taken a

46:38 where they've taken. So the cows go to slaughter then uh they will

46:42 spray them with a page specific to colon because that's how many times trying

46:50 get the e coli in the food is through the cattle and not using

46:55 sanitary procedures while you're you know doing butchering and whatnot. And you can

47:00 into the food supply. So if then blast it with um fades specific

47:06 that e coli that that can be effective. So it's kind of something

47:11 um on the forefront a lot of going on but I can't see that

47:18 being quite effective I think eventually. The yeah and yes the bacteria can

47:25 resistant to fade for the faith can . But the page can also evolve

47:29 well. Right? Unlike an antibiotic ? Antibiotic why resistant to it.

47:36 the antibiotics not a living thing. not going to evolve and change itself

47:39 them. Right. But the but page can and does so it's

47:45 Yeah. Um Any questions. Yeah don't know if this is true but

47:52 heard that bacteria can kind against both and antibiotics because like for example say

47:58 changed their service cell receptors right? making antibiotics for viruses and vice versa

48:08 maybe using both the best treatment. that makes sense. Using both antibiotics

48:13 face. Yeah that that makes sense . That's that's good. Yes can

48:20 and change with antibiotic. Yeah. on their own. So you that's

48:26 we we've taken like um penicillin and have the number of cases chemically chemically

48:35 and slightly change their structures so that and I can't think. I taught

48:40 head what are some of the synthetic , but we have done that.

48:44 everybody itself, right. So any , Yeah. Is it safe to

48:54 ? All right now, they're only it on in the context of uh

49:01 that are for food. And so you for so for like farmers,

49:09 , um, in farm raised I mean like factory farm raised where

49:15 math production, right? When you a crowded conditions like that disease can

49:20 quite quite quickly in those scenarios and out your product. And so,

49:27 , it's in those contexts right now they're experimenting with the space therapy.

49:32 don't think they've gone to humans Maybe kind of studying that, but

49:36 yet. But right now it's just terms of different types of animals used

49:40 food, you know, questions Okay , that it was all I

49:49 Right? So we've got an you've got another 20, minutes.

50:01 that's all I'm gonna say today. you have any questions, you can

50:03 have any questions about anything? Well enough

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