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00:02 right. Mhm, mm hmm. , okay. Okay. Hold

00:25 I'm gonna get this thing here There we go. Okay.

00:32 I understand. Mhm. Yeah, we have a whole lot to finish

00:39 Chapter five. So we're likely to here maybe 30 minutes. Okay,

00:44 a little longer. Um, of course the exam is uh,

00:52 tomorrow. Um, the uh, see officers tomorrow. If you have

01:03 . Certainly stopped by or email. , remember there's nothing no blackboard

01:09 There's no smart work this week, , do on sunday. Um,

01:16 finish up in one today and then next monday, start unit Q.

01:20 that material. Uh it will be first thing in the morning.

01:24 uh, I'm not you're not concerned you, you know, you

01:27 to at the moment Word about the . So, but it'll be there

01:32 you tomorrow. Um, and we with Chapter six, which is on

01:38 . Okay, so, uh, see. Um, Let's uh look

01:47 kind of summer topics we talked about Chapter five so far. So,

01:53 when we think we had a small of the chapter, um we talked

01:57 little bit a little bit about zero . So, um, learning

02:01 But Gerald types will have different behaviors you will in the presence of

02:08 Some many many certainly use actively use as part of the metabolism.

02:14 others don't. But then the issue really in oxygen containing environment, uh

02:23 we live in of course, oxygen itself is very reactive. It

02:28 generate the formation of these toxic chemicals as a byproduct of its interaction with

02:34 molecules. And um if you're gonna in this environment you need that

02:40 Right? So related behaviors of bacterial really relate to that protective mechanisms.

02:47 ? Those three enzymes and whether they're uh how many of which are all

02:55 present or just some presents? Are present at the proper levels? Um

02:59 all dictates how the bacteria will grow of oxygen. Okay um so we

03:07 like five different types right? All Arabs and Arabs faculty creative and Arabs

03:15 taller and Arabs and micro profiles. . Uh and then um talk a

03:22 bit about the terminology as it relates controlling microbial growth. And of course

03:30 interest there is pathogens is what we want to target. But obviously all

03:35 will go down. But then the sterilization, conceptualist, inspection,

03:42 Okay. And then a little bit the effects of bacteria cyanobacteria, static

03:48 politic and uh I think oh then last thing was we mentioned was the

03:55 um the reduction of numbers. So there's a bazillion bazillion ways to measure

04:03 efficacy of different antimicrobials. It's it's a popular um science fair project especially

04:10 the younger ages to test this and . Is that the antimicrobial? Um

04:17 the value is one of those Alright so how how much How much

04:22 to get one log of death, death rate, logs of death.

04:27 so uh so today we'll just go some physical chemical agents of control.

04:34 Talk a little bit about um resistance antimicrobials. And uh that's pretty much

04:43 wrap it up. Okay? But start with a I know what I

04:48 hope is a pretty basic clicker Okay. Um It's involves the

04:53 Value calculation. Okay. It doesn't even a calculator. Okay. You

04:59 do this just in your head and your fingers. Okay? So this

05:04 is added to a culture contain 10 the six Cf. You per mil

05:09 . F. U. Is a , see if there's a colony forming

05:13 . Okay. Um think of It sells sells per milk. Um

05:19 the the value of the disinfectant is minutes. Okay, so how many

05:24 cells are looked at for eight minutes exposure. Okay. So remember the

05:28 is the length of time to get log of death. Okay.

05:34 See if you get it quickly come with that one on top of your

05:38 which shouldn't be that difficult. Let's here. Okay, mm hmm.

06:14 . Yeah. Yeah. Okay winding . All right. Yeah. So

06:31 just quickly look at the how do get there uh D. Is

06:37 So we've got um so we're starting that cell cell number and we're gonna

06:45 our disinfectant to that culture at that . So remember one log death every

06:49 minutes. That's our devalue. So it just becomes um you know every

06:54 minutes. Right? Uh We're losing were losing one log every every two

07:00 . So down in the 6th, , 4th, 3rd and second by

07:06 minutes. Okay. Um mm So one of the things the concept

07:12 remember is um in terms of deaths that it's never going to be all

07:19 killed at once. We're gonna Some rate would be very fast

07:25 You can study accumulation of damage it it doesn't occur really equally among all

07:29 in the population. Um Especially if a heavily contaminated area heavily soiled

07:38 Right? You have cells in the may be more susceptible than those morning

07:42 . So different variables will account for . But the point is it's not

07:47 diet once necessary it's going to be kind of a rate. Okay.

07:51 question on the D. Value Mhm. Um So let's uh look

07:57 another question. This relates to the of bacteria. Asylum material static bacterial

08:03 . Okay so uh so this one walk you through this a growing culture

08:11 a grand positive okay bacterium had a added at mid lock. Right?

08:16 it's growing the mid log phase had following before our exposure growth was checked

08:24 it's just really basic visual plus Okay. Um Loop. Full of

08:30 was subculture to fresh nutrient medium lacking . Okay. Growth was checked.

08:39 . The experiment was repeated using four of disinfected. So according to the

08:45 below which you'll see in a This disinfectant is what? So here's

08:50 first part of the experiment. Mid . Get disinfected, you can get

08:54 hours check the growth and then um a look for into broad without disinfectant

09:06 . And then let's see what it like at that point. Okay,

09:11 here are our choices. Okay. what we see then is growth so

09:18 which is here. Okay. That and then subculture Just two.

09:28 And here are our choices. All . Okay. Mhm. And minus

09:40 more growth occurred. Plus we see . Okay. Oh, I did

09:59 the polling things. There was no . Just two answers to choose

10:04 Mm hmm. Mhm. Yeah. hmm. Mhm. Okay.

10:57 Right. Yeah. Okay. Alright. So I bet you're

11:11 So um so who picked back? ecstatic. A volunteer. So why

11:21 you think back to your stand? what told you that it's gross.

11:35 . Can you um so the um the growth our lack of growth in

11:46 first tube, I told you that the disinfectant had an effect on

11:52 Okay. Um if there had been even after addition than a plus sign

12:02 you see here. Okay. Thank see here at that concentration of

12:12 there was no effect. Okay. when you do this, you always

12:16 different delusions when you're testing the efficacy these and a septic or disinfected um

12:23 there will be at some point where so dilute, there's so little disinfect

12:27 there's no effect. Okay. Um you have to know what that point

12:32 , Certainly from the economic standpoint, ? What's how much, how much

12:36 of disinfectant can get away with and still works really good. Okay,

12:41 the waste of money, just if get the same effect at 1 to

12:44 64 1 to 64 is 1 to will do the 1 64 right?

12:47 gonna get the same effect. So anyway, so aside from that,

12:53 the purpose of the subculture for them to really test what happened in the

12:58 of disinfectant? Right. What happened my results in the first tube?

13:02 are the state of those cells? . How am I going to test

13:06 while you just take them out? them in a broth that doesn't have

13:09 disinfectant to see if they're they're a . Right, well, they just

13:14 . Okay, so if we had obviously the other result would be if

13:19 subculture was a negative. Right? it was that result? Who is

13:27 in that most have made it I mean that would be a bacterial

13:32 effect, right? Because they were look at them at the initial

13:38 checking the state of them. Well state of them was their dead.

13:42 grew in the subculture. Okay. obviously had a bacterial seidel effect or

13:47 it can you could you tell just a visual of the broad tube.

13:52 it was back to asylum naturalistic. . Maybe. No. Just from

14:02 looking at oh was it back to side and back to your leg?

14:05 . Okay. You have to do a look under the microscope. Are

14:11 seeing actual self disappearing? Okay. indicates bacterial bidding. Right. Remember

14:18 is the operative part of the world . Is that lice the cell break

14:24 up? All right. So um couldn't tell. But you you you

14:30 know it's not even a killing effect the cells are still alive. They're

14:34 gross inhibited. Right? So back the status and that's what we see

14:39 Jack. Um many questions about Okay so uh so what do these

14:51 targets? We're talking about um chemical , radiation treatments or temperature.

15:00 Um What you might think what are what are the main one of the

15:05 in cells that do things? Frankie's Paycheck acids. Right. And

15:10 a membrane that holds the whole thing . Right. You take that and

15:14 are all the targets of different antimicrobial . Okay. We'll see that there

15:21 molecules that are disinfectant or in the category that look like these.

15:27 These are the fossil lipids, And they're called detergent molecules. And

15:32 can mimic um the structure of fossil and by doing so can dissolve

15:38 Right? So there's the churches that do that. Uh There's other types

15:43 alcohol based disinfectants that one of the is to dissolve membranes. Okay.

15:51 The the gram stain right? You 95% ethanol in one of the

15:56 And that kind of destroys the gram outer membrane so it loses the

16:00 Right? So alcohol can have that also has other effects as we'll

16:04 But certainly proteins can be denatured Remember what the nature means? And

16:10 that term both for proteins and Right Because certain proteins are held together

16:16 a certain three dimensional structure. And you d natural you're breaking it that

16:22 peptide down. You're not destroying those . So it loses shape, loses

16:27 similarly with nucleic acids. Um You denature the DNA strands they come apart

16:34 more than that you can physically alter . You can create new patients on

16:38 basis you can uh even break uh the transition of tank acids particularly with

16:45 energy radiation gamma rays. X rays do that. UV light not as

16:51 but it will do it will um the bases and in the D.

16:57 . A. Causing mutations. Okay again these are the prime targets for

17:02 my criminals and you know kind of at the end we're going to talk

17:07 potential resistance resistance to disinfectants and antiseptics um that's not really a common thing

17:17 happen right? Because as you can antiseptics disinfectants uh physical treatments radiation when

17:27 acting on a cell, they're basically on all these things right there in

17:32 with all of these components. Uh They may have maybe more damage

17:37 one type than another but they're affecting all these components. Protein membranes take

17:42 because they're coming into contact with. , the point is multiple targets.

17:48 ? And in contrast with antibiotics um typically target 11 single target like a

17:59 a single amazon. I'm involved in wall synthesis. Like penicillin. Um

18:04 single component involved in protein synthesis. antibiotics target that. But the point

18:09 it's one target. Okay they're not not a varied effect. Like an

18:15 disinfectant or these kind of treatments. um now the um physical agents.

18:26 we're talking about physical agents, temperature . Um So temperature of course um

18:31 temperatures will uh denature proteins um if hack acids life cells obviously. So

18:40 the autoclave uses steam under pressure. so you create temperatures that cells are

18:47 to be used to. Right? it's gonna be fatal to them.

18:51 Steam under pressure. What we call heat that's essential for killing endo

18:55 It that allows it to penetrate into sport coat and killed the spore.

19:03 frankly why we use an auto payment to sterilize media is to kill in

19:07 sports. Okay. Um and standard there uh 15 p. s.

19:15 . 1 21 15 minutes uh is much standard content. It changes only

19:22 terms of the time element, depending how much your auto claiming at the

19:27 . Okay. But the the you have equivalent methods for another, for

19:37 . Okay. Which we call dry sterilization. Right? So the equivalent

19:41 there are higher temp. Okay. longer duration because it's it's a dry

19:48 a hot air dry, like a oven basically. Okay, you don't

19:52 the steam hot steam aspect, but can have a high temp and do

19:57 for a longer time. And you have sterilized. Um Your every time

20:03 try to sterilize the incineration, incineration actually those who've been lab when you

20:11 your loop and you put it in flame Bunsen burner flame to sterilize

20:15 You're that's incineration putting into a flame into the flame is incineration um

20:24 So we've all heard of that of , and that's um and that's

20:30 we use these every context of milk it's used for any food and beverage

20:36 reduce microbial numbers. And generally certainly dairy industry uh the target organism they

20:44 to test their um to test their . Is this organism called taxi

20:54 Okay. So it's not it's not endospore former, but it's like the

21:00 notch down in terms of resistance to . Okay. And so it's used

21:05 a way to test their uh Uh and the additions can be,

21:11 course. Uh These three you see low temp longtime, high attempt short

21:16 . It can be ultra high Mhm. And again, it's all

21:21 preserve the flavor and the taste of product, right? You don't want

21:25 you know um uh You don't want drink autoclave milk. Trust me.

21:31 , it doesn't look nice and it correct, right? Ah So you

21:36 to make conditions that preserved taste, , flavor etcetera. And that's what

21:42 is all about. And to reduce , reduce microbial numbers. Okay.

21:49 And uh but in the process these two uh pasteurization modes. Ultra high

22:00 ultra pasteurization. That's like uh that's close to ultra high temp. Um

22:07 that that's actually getting near not quite very nearest sterilization. Okay. It's

22:14 certainly was developed for uh use in countries where refrigeration can be kind of

22:23 . So you can have ultra pasteurized other high temp milk. And um

22:28 can made on the shelf at room for up to six months.

22:32 But and it's fine. Of Once you open it, then you

22:37 to refrigerate. But uh it's proven beneficial from that standpoint in areas where

22:43 don't have very good refrigeration. So but the I've heard that ultra pasteurized

22:51 for example, can have kind of funny taste to it. It's kind

22:55 like a cooked taste. Okay, , but you know, it's not

23:00 it's it's one of the sacrifices you . Um but you know, whatever

23:04 conditions are within these three parameters or of them, manufacturers will, you

23:11 , of course tailor it to optimize that they uh don't compromise too much

23:19 the outcome of the product. In words, they wanted to to um

23:24 the flavor, the taste, those of things. Okay, um

23:30 uh so the other thing is not , well, as we've seen,

23:35 everything is amenable to the conditions of state. Right? So dairy products

23:40 so you have to reduce the temperature time. Uh Some things are even

23:45 , you can't do any kind of temp at all. Right. Something

23:50 have to be a filter. um which I really hated myself.

23:56 , filter sterilization, I'll come back cold temp in a second. So

24:00 sterilization of course can be used also air. Right? Have two

24:03 filters in there in your house are filtration. Um the of course the

24:11 sizes block um the microbes from getting , but technically, you know that

24:18 , you know, we don't have sizes from filters that will excuse

24:25 that will get that will take out . Okay, but generally we don't

24:32 worry about that so much. But but certainly happy filters can be very

24:38 pore size and pickup vander and all of other part of the particulates as

24:46 . The you know certainly in the the lab there's certain media that we

24:52 auto paper. We have to use filter sterilization for that process. Um

24:58 temp. So cold temp uh doesn't but it does slow down growth.

25:04 ? So obviously refrigeration of food is to um Is there a food and

25:09 the time until spoilage occurs? Um the lab we use uh cold temps

25:17 preserve cultures. All the bacterial strains in lab are maintained for long for

25:24 term storage. So it can be can be used Year after year by

25:28 him in the -80 freezer. And you do that you have to you

25:35 them and then you add some what call it. Antifreeze to it.

25:41 glycerol. It has the same effect antifreeze. Uh Ice crystals are what

25:46 the damage when sold freeze. And you minimize that and and in a

25:52 glycerol can do that for you. you preserve the cells that way.

25:57 I've had cells and therefore five years and they revive quite easily. Um

26:06 listeria because one we'll talk about later the semester. We have a number

26:11 diseases we talked about and listeria actually grow. Yeah refrigeration camp.

26:20 It um and it can be a . So it's a problem for if

26:25 like to eat a lot of your foods like uh deli meats in particular

26:32 , these kinds of things. That where you can get the osteria.

26:35 smoked meats, these kinds of things pregnant women in particular have to be

26:42 of that. Not for their sake for the baby's sake. Uh listeriosis

26:47 occur in and those who like to these kinds of meat parks and

26:52 So they say doctors say don't do while you're pregnant. For that reason

26:57 listeria organism can cross the placenta and the baby. For most of

27:03 Um With healthy immune systems, we very likely ingested Listeria, we just

27:09 know it or just give us a upset. Okay. Um But uh

27:16 the newborns or fetuses it's it's they're more susceptible to that. And then

27:22 was this outbreak I think maybe 78 ago. Blue Bell ice cream factory

27:26 Brenham. Uh Mysterio sis outbreak traced one of the batches of ice cream

27:33 they made. Um There were a fatalities uh in L. A.

27:39 was elderly. It's usually either very . People are very young that succumbed

27:44 the worst effects typically due to the immune systems. But it was traced

27:52 dirty uh not very well cleaned holding . I think that we used used

27:58 dispense it. But then they uh the last step they put it in

28:03 dispense into the tubs and then off the market uh and that the parts

28:09 weren't cleaned very well. Of course manufacture ice cream and cold temps and

28:13 can grow in that. Well if not careful then that can happen.

28:19 Now irradiation. Okay so radiation remember the electromagnetic spectrum and wavelengths of light

28:31 uh lower wavelengths of light have higher . Right so wavelength equates the energy

28:39 of the radiation. So um we're look at U. V.

28:43 203 100 nanometer wavelengths. Um It's energy but not as high energy as

28:50 what we call ionizing radiation Like gamma , X rays. Uh Non ionizing

28:57 UV light. Okay so this can doesn't penetrate very well. Uh Sure

29:03 can stop it. You know it take a lot to stop it.

29:06 it's very good for it's better suited surface disinfection. Okay um We have

29:13 biological hood we work in in prep for micro and that has a UV

29:19 source when we're done in there flip light on, it stays on for

29:22 hour disinfecting the surface um That's what best suited for. It can cause

29:29 by altering bonds in the D. . A. Um The ionizing radiation

29:40 very happy. Okay so you can the difference in wavelength here versus

29:49 Less than 0.1 nanometers. So significantly lower wavelength, much higher energy.

29:55 . Enough energy to break fragment nucleic . Obviously that's going to be

30:03 Okay and so um and II's radiation been approved for sterilization of various foods

30:15 frozen foods, especially frozen meats, and beef and so forth. They

30:19 uh financial radiation uh to kill foodborne foodborne bacteria that maybe there. Um

30:29 it's uh and other non biological materials well. Um You don't want to

30:35 don't use radiation to um uh on liquids. Fisher's gonna be solid material

30:45 they're going to penetrate liquids very well ionizing radiation to a degree. Um

30:53 your chemical agents. Okay so commercial track o saying you see there is

31:00 I think it's no longer in use time. This is this used to

31:06 popular. And hand sanitizers nowadays hand have alcohol, alcohol based alcohol is

31:14 disinfectant. Um But the point here phenolic phenolic have the aromatic rings,

31:22 ? That's the phenolic compounds. And these can be good, phenolic tend

31:26 be more, there's a concept in and then except it's called contact

31:33 right? The amount of time that agent is actually interacting with the surface

31:39 you're trying to get rid of. so finally have have that feature to

31:44 . They. They're kind of sticky in a way. They'll they'll stay

31:48 the surface for a while doing But what they do is of course

31:52 damaged proteins, lipids um uh nucleic as well as iodine and chlorine do

31:58 bleach for example. Uh You may seen beta dying if you work in

32:04 doctor's office um clinic, what have that the yellow, yellowish looking liquid

32:11 for um surgical procedure, pre uh to wipe down the skin where they're

32:18 operate um as well as a hand um alcohol. So it can be

32:24 based is common I. P. . Or isopropyl alcohol. Another

32:29 And there's always the question of what's because we use we have we have

32:36 ethanol lab. We have but we to 70% for use as a disinfectant

32:42 has to do with obviously the water . Okay, so ethanol alcohol in

32:51 do damage by dissolving membranes and denatured . Okay. Uh particularly that.

33:02 the 95% ethanol. It's good. really good at doing the saturation of

33:09 . Okay. But the problem is evaporates quickly. Okay, that's that

33:15 time. Right. It's very low 95% ethanol 70% more water.

33:21 Evaporates less quickly. More contact Okay, so that actually is much

33:27 in terms of as a disinfectant. also a little bit higher. Water

33:33 helps draw ethanol into the cells so can contact the proteins and DNA for

33:38 . Okay, so you know, hand sanitizers are uh will have alcohol

33:44 them. You want to have one has maybe in a range of 62

33:49 or so percent is optimal range. again that water helps and you

33:56 less evaporation to okay um, So we have to mention that

34:02 So, detergent, michael. So is um example of that.

34:08 So here is the our group here very long carbon hydrocarbon chain. So

34:14 looks like a fossil olympic. the short term for these, it's

34:21 uh somebody called co ordinary co ordinary compounds a trade name for that is

34:29 they call squats. Okay, we're . Um and because it looks like

34:37 looks like a fossil, but it membranes, right? Will dissolve

34:40 Uh fell apart. Bless you. Gasses, gas is uh can be

34:52 good, especially um ethylene oxide. . And this can actually be a

34:57 agent in uh in many cases uh use being gas best. Not used

35:04 liquids. Of course, I'm not get good penetration there. But good

35:08 with solid items like uh pipette boxes of pipette tips, for

35:13 You've seen those in lab medical devices are packaged like catheters, et

35:19 Petri dishes. Box bags of Petri are often gas this way and the

35:25 will penetrate rail. Well in there the product, the ethylene oxide itself

35:32 the presence of acid or base. will kind of that ring kind of

35:38 apart and then in that form kind a chain reaction begins to interacting with

35:44 , nucleic acids and causing damage. , so um it's it can be

35:50 good in terms of sterilizing these kinds dry goods if you will. You

35:56 also took maybe a glassware in there well. Uh The issue though can

36:02 um anything that can be quite Okay, so those that sterilize these

36:10 with ethylene oxide had to be careful they're actually looking at some other types

36:14 gasses that with similar effect that a bit safer. But ethnic Knox has

36:18 used for quite some time in this this purpose. Um Okay. Any

36:27 at this point? Yeah. So was the deal with quantity the there

36:34 a short short name for co No, I can't remember the name

36:39 ordinary. Um I mean blah Sorry, I can't remember the full

36:44 but what they are, are they detergent type molecules? That's what's so

36:51 the and you know, your book list has a whole table of list

36:56 different types and I don't expect you need to know that. I'm just

37:00 of giving you here are some of major categories of these kinds of disinfectants

37:07 . There's some of that, you , this is what they look like

37:11 how they work that kind of More overview. So don't don't memorize

37:15 single disinfectant. Antiseptic in the tables your book. For goodness sakes.

37:22 . Um Yeah. Um I guess have to have a you have to

37:27 a sterile solution before you pour it there, right? It doesn't actually

37:31 . No you don't you do You can just pour it in because

37:35 pore size of the filter is what . So you typically Uh .2 microns

37:42 what you use and that will that take out what you need to.

37:47 It's gonna be like I said technically not sterile because viruses aren't taken

37:55 But I don't really worry about viruses the lab. If you're in lab

37:59 using um Yuria broth is one of things we use for biochemical tests and

38:05 inoculate it. See if you can your area, right? So you're

38:09 a broth is not cannot be out it. You have to you have

38:13 sterilize it through a filter. Those sterilized filter, sterilize it.

38:18 And uh and like I said, don't worry about viruses. It's not

38:22 a concern to me. I don't I never see anything growing in it

38:27 unless somebody screwed up afterwards. Or or intentionally. And of course

38:32 want to see rose. But um yeah you don't really worry about that

38:37 it becomes an issue. I have never been in this scenario in 30

38:43 years where I've had an issue with the virus is messing things up.

38:49 I've actually I've never seen that. I'm not saying it doesn't happen.

38:53 sure it does, but I haven't I'm not sure if I answer the

38:58 . Okay, definitely. An You can assume that's not safe.

39:09 . I think the people that use are gonna be like the manufacturing companies

39:13 make these things like Petri dishes and not like that. And they're they're

39:17 ones who can do it like on mass scale kind of a thing.

39:19 sure big chamber whatnot, you Yeah. With all the safety things

39:25 place. Yeah. Yeah. I I wouldn't want to use it.

39:31 But then yeah, I wouldn't be those kind of things anyway that I

39:34 eat for that. We've mainly sterilized liquids and that's it. Pretty

39:40 Exactly. Exactly. Um Any other ? Okay, so resistance.

39:50 So as mentioned um disinfectants, radiation and all these other kinds of

39:59 antibiotic treatments are basically contacting all these in the cell and and having various

40:06 on them. Whether it's proteins, membranes, what have you.

40:10 so you get the picture of you when a when a bacterium is resistant

40:19 a chemical. Right. Right. has that happened? Well, a

40:26 of members of the population already have existing mutation that has um somehow

40:36 Maybe the target for the antibiotic um generated an enzyme that can destroy the

40:45 or something like that change has been that the antibiotic doesn't work on it

40:50 . Okay. It's for antibiotics because single you know I mentioned single targets

40:56 they go after it's obviously not all the rental possibility that bacteria can acquire

41:06 single mutation and then that will enable to counteract the effects. We know

41:11 happens right. It's it's a it's problem and everybody resistance among bacteria is

41:16 issue. And now there's and of there's multi drug resistant. So um

41:21 with antiseptics disinfectants that is not an thing because of the all the molecules

41:29 with in a in a cell in process of killing it. So you

41:33 the bacteria will have to acquire multiple to account for all the damage being

41:39 to it and that statistically it's not . Okay at all. And so

41:45 don't really see resistance to disinfectants occurring except if it's if they're used at

41:55 optimal concentrations. Right. Somebody wants be cheap and say okay I'm supposed

41:59 dilute this at 1 to 10 but going to dilute it 1 200.

42:02 right now as a more dilute The disinfectant may not have the same

42:09 of targets as it once did. maybe it's um only interacts with maybe

42:14 couple uh targets in the in the now because it's so dilute, okay

42:20 where maybe resistance can can occur. . But you know the places where

42:28 this infection is important, you is obviously a hospital in a clinical

42:33 . Okay. And yeah, they a regular kind of they're constantly

42:39 obviously disinfecting. Um but particularly in you know the operating rooms, things

42:47 that. Uh there will be a of cleaning or they'll disinfect one week

42:53 with a detergent type, disinfected and the next time around they'll disinfect with

43:00 an alcohol based disinfectant next time around the finale based the next time around

43:04 they keep changing the chemical nature of type and have a rotating schedule that

43:10 itself even makes it more unlikely that becomes resistant. Okay, so uh

43:17 bottom line is resistance, resistance is really a thing against disinfectants and those

43:23 treatments but obviously is for antibiotics. . Which is why we're constantly looking

43:30 new ones or modifying ones. We to slightly change their effect perhaps.

43:37 . Or using combinations. Mental we do that as well. Um

43:44 the effect, so effects of your that work on cell wall, like

43:52 , ampicillin, amoxicillin, etcetera. They remember these things interfere with the

43:58 a lot of them interfere with the bridging, right? That holds a

44:03 of black can together. Okay, what happens is when that's when the

44:09 that's not a lot to happen. peptidoglycan and kind of is more flexible

44:15 . It's more um um it's like you have a neck All right,

44:22 you're being cutting coming to the net it kind of comes apart.

44:26 So the pepper light can kind of apart that way. And now remember

44:30 is the cell membrane, right? pushing up against the cell wall.

44:34 so as you kind of expand that of light can now it bubbles out

44:39 the cell wall and that's what these you see here little little horns on

44:44 are these actual cytoplasmic membrane pushing through then it slices and then kills the

44:50 . And so working against actively growing . Right? So that's the thing

44:56 that a lot of antibiotics have the effect on rapidly growing cells.

45:03 Uh So for example, cell wall , right. Um that we see

45:10 of that activity occurring during cell Right? Because this would be under

45:18 septum Alright, so while synthesis, where it's occurring, actively occur.

45:28 . And so that southern splits in . Right then it divides again.

45:33 you're gonna see lots of forms of during the long phase. Right?

45:38 growing and see lots of cells in state. And so that's when a

45:43 or these kind of brothers have their effect because there's lots of targets that's

45:48 since uh synthesizing cell wall material, then that penicillin has lots of things

45:53 target to interact with. Okay, contrast like stationary phase. Right,

46:00 it's not really growing. You don't see a lot of cell wall synthesis

46:04 all. It's really trying not to . Okay to to survive. So

46:10 when it's gonna be less effective. not just penicillin, there's other types

46:13 antibiotics that that really works best when cells are actively growing. Okay,

46:19 and it's even a strategy for for pathogen types too um to slow down

46:26 growth in the presence of antibiotics for reason. So they're not as susceptible

46:30 it. Okay. Um there's really such consideration for for disinfectants really,

46:37 antiseptics. Uh They'll just kill whatever's . Right? Just contact with molecules

46:42 kill it. But antibiotics have more we can have more that dependence on

46:47 in terms of effectiveness. Um So so how what are the resistance mechanisms

46:56 resistance? So this kind of we're we're not going into any great

46:59 I mean, what you can probably sit and think of a list

47:03 How how can you become resistant to ? Well, you can simply just

47:07 the antibiotic completely. Right, that's uh resistance to penicillin was one of

47:14 mechanisms is beta lacked. Um They lack thomas's they destroyed the penicillin.

47:20 that's that's one effect. Uh don't the antibiotic in the cell at

47:26 So maybe the antibody goes through some of a specific transport protein. Well

47:31 there's a slight change in the in in the protein And now it doesn't

47:36 enter the cell um If it does in, pump it out.

47:40 That's what anne flux pump is. , so um or alter growth.

47:46 , modified target. Right. So um that's the bank of medicine.

47:51 ? That's what happened. Bank of and resistance. Right, sobakam binds

47:55 that that terminal amino acid on the where links up with the the creative

48:02 bridge. Right. So bank of sitting there then you're not gonna get

48:05 bridge formation occurring. Right? So do you become resistant? Well you

48:09 change the target. Right, so the bank of missing. Can't buy

48:13 now you don't get the effect. it becomes resistant. Right? Or

48:17 can alter growth as I just mentioned ? If it's an antibiotic depending on

48:21 works really best when the cells are going well then just don't grow so

48:25 . Right? Oh so that stop being kind of a a non growing

48:31 when you buy it goes away then grow these are all strategies that we

48:38 resistant types have. Okay. Which why it's a constant battle to keep

48:43 with it. Okay. Um Biological control. So probiotics. Um

48:54 uh your microbiome, right? Microbiome a is a balance really of of

49:01 Brazilians of bacteria you have. Uh And when uh when you're in

49:06 healthy state, right? When that is compromised. Okay. Maybe you

49:13 were on antibiotics for an infection or . Right. That's going to change

49:17 balance of your microbes, especially in gut. Um The uh and so

49:26 can restore that balance. Okay. There are certain diseases infectious diseases that

49:34 when that imbalance occurs. Um We'll about it later. But an organism

49:40 Clostridium difficile. Okay. You don't to write this down but I'm just

49:46 abbreviate. See the fi style you have heard of that. It is

49:53 uh it causes a severe diarrhea um be fatal. Often see it in

50:00 and nursing home settings or very young . It but it arises when um

50:11 gut microbiome is out of whack due particularly due to already being an antibiotic

50:16 something else. And that upsets the . And then that's when those are

50:20 kept in check when you're when you're . But when you're compromised then that

50:26 emerge and it can cause this gastrointestinal . Um There was a student of

50:32 look past it said he had helicobacter but that's the bacteria that causes

50:40 And one of the treatments for that to to prescribe probiotics to kind of

50:46 it out of there right competitive competition it. So so there's different context

50:52 that where that certainly is beneficial. get my probably actually the yogurt.

50:57 I don't buy pills but my wife she takes them um does anybody here

51:03 probiotics? Yeah I think it Yes but she's afraid to go off

51:11 she said I'm not gonna do Something bad is gonna happen sometimes.

51:15 you you know if you think it good then then why my question?

51:21 South anybody else have a good or experiences with had before you have,

51:31 it? But you're not on it ? So just wasn't it was it

51:34 didn't see much of a factor. We do. Yeah. That's really

51:42 me I like like throughout the Yeah. I think you know I

51:52 see it being detrimental to you. think I see it only being a

51:57 . Um I don't think so. don't think so. I haven't looked

52:04 any long term data but I don't don't see that as a case because

52:08 gonna be it's gonna be once you the pill and they get into your

52:12 like hey Brazilians are gonna be killed anyway as you get down there.

52:16 if you're gonna buy them and get get the ones with the highest levels

52:21 once they're there they're going to be it's it's there's gonna be a competition

52:25 what's there it's a dog eat dog right in your gut. So but

52:30 mean I think that they but but already gonna be types that are already

52:35 . Right so you're just gonna enhance there anyway. So I don't see

52:39 being a negative a I haven't researched a lot. But I don't know

52:46 you take if you can like take number of pills like say in a

52:51 or something like 10 times what you're to take. Will that cause

52:56 I mean, I wouldn't be surprised . But you know, if you

52:59 the prescribed those for my wife and it before five years honey. So

53:08 seen or heard of the issues. uh anyway, so we'll see.

53:14 any of them questions. Okay. I think that um yeah that is

53:24 it. That's the end of unit ru five year one. And if

53:28 want one uh any questions so Mm hmm. It does not work

53:40 what? Um Good question. So I don't think so. I think

53:47 Yeah. Because in the sport's gonna in a dormant state. I don't

53:50 think it could penetrate in those I never thought of that. That

53:52 a good good question. Yeah. don't think it would. Yeah.

54:03 , we just. Did you use flicker? You've got tenants?

54:07 you can't. Oh, how do mean? Yeah. If you if

54:14 enter anything in any of those clear you've got tenants. Yeah. Uh

54:24 answer now. Yeah. Yeah. sometimes if you mhm. Yeah.

54:34 hmm. It's just like body It could be. Yeah. I

54:45 so. Did that happen to But they changed it up?

54:53 Okay. Yeah. It could very be because whatever it was, it's

54:58 responding to it and then switch. . For sure. Especially if you

55:02 isolate and see what it is to specific, then that can be,

55:08 . Yeah. Wait. Yeah. . I thought that. Okay.

56:11 happened? Yeah, it was Thank you. Thank you. Thank

56:31 for the growth problems and stuff. I noticed there's a

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