WEBVTT

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 Hello Mr. Dr. Peters, please introduce yourself in two or three sentences.

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 What is your personal background?

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 Yes, my name is Dr. Peters and I am a biologist.

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 So I am a full-blown biologist, but because of the activity at Enemer

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 I slipped into biotechnology and also because of my family background.

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 I am a farmer and I have always been interested in the practical application of biology.

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 And that doesn't go away when I look back at the time at Enemer.

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 And also the time before the studies, it was always about making something meaningful out of it.

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 It was never pure research.

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 So it was basically a practical approach.

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 Yes, exactly, I always had a practical approach.

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 We founded the company Enemer in 1997 from the University of Kiel.

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 There was a working group that dealt with the production of nematodes.

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 So the name Enemer was also used for entomopathogenic nematodes, that is, nematodes that kill insects.

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 And that was the core topic that we dealt with as a company.

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 We are currently producing these nematodes as one of the three largest producers in the world.

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 And we have growth rates of 10 to 15 percent per year, because it is a biological process

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 that works very well and is also relatively inexpensive and can replace chemical processes.

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 And since we produce these nematodes in bioreactors, we have already said from the beginning

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 that we have to produce the nematodes at certain times, but we have empty times.

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 That means we can use these bioreactors for other microorganisms and were therefore always open

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 to new ideas that either come from the area of biological plant protection or from other areas.

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 So we were always open to anything.

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 So you can say that the focus of Enemer is basically biological problem solutions.

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 In any case, we are not a company that knows its way chemically or could offer chemical solutions.

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 On the contrary, we are actually a fundamental building block in the replacement of chemical substances in plant protection.

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 Not only with the nematodes, but also simply because we have built up such a large capacity in the meantime

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 so that we can develop new microbiological products for plant protection for many companies

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 and are a partner in order to produce them.

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 That is actually our main mission, that we want to contribute to this change

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 from chemical plant protection to biological plant protection.

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 How would you say from the gut feeling is the relationship between actual development and production of new products/production of existing products?

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 If you look at it from a financial point of view, it is about 10% of the revenue that we invest in research.

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 But it is relatively efficiently invested money.

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 That means we get to the point where we produce a new product every one or two years.

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 So almost every year something new is added.

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 Now we have already thrown the keyword "new products" at me.

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 There was a time when Harald Meyer came to you.

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 Do you still remember what the framework conditions were?

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 Yes, I still remember quite well, because companies are always calling.

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 Some of them you know, some of them you don't.

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 And some of them are pretty strange crosses.

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 You know right away on the phone that it's not worth it.

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 That's a pretty crazy idea.

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 That wasn't quite the case here.

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 We thought we had heard something about it, that you can use microorganisms to clean waste.

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 And we thought, let's hear about it.

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 As a result, this has developed into a fairly fruitful cooperation.

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 You never know before, but we are usually very open to a first conversation.

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 Then tell us, Liebhausan has also developed over time.

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 What was the status quo like you started?

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 What was the challenge then?

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 What was the product you were working with at the time?

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 So when we started or when we were involved,

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 first of all, it was about a bacterium that was to be produced.

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 The bacterium produces lipases and splits fat.

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 But it turned out pretty quickly.

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 That's why Mr. Mayer tested it and found that there was actually no bacterium in the product

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 that was produced at the time.

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 And that it was instead a fungus.

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 But it worked very well.

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 And that's when I became aware of it and thought, that's actually something new.

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 And it is interesting to continue to pursue this.

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 Because it is a lucky case that is partly based on ignorance.

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 But as it often is, ignorance paired with a certain curiosity

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 often leads to something very, very interesting to be discovered.

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 So if it had been a microbiological company,

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 they would probably have worked so cleanly that it would not have come to a contamination.

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 That's how it came to the contamination.

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 But the contamination itself was the sixth in the lottery in a way.

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 I didn't know that.

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 That actually means that the samples you got from lipases,

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 as they were back then, the microbacterial samples,

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 they took them apart and found out,

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 okay, these are not the micro-bacterias that do the main job,

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 but it is basically polluted by a fungus trace.

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 Yes, we saw it.

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 And Mayer then saw it too.

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 He sent it away to a company that examines professional transparency samples.

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 And then they said, Meier, that's something really interesting that you have there.

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 And then I also took a closer look when we had the name of this germ.

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 And said, yes, that is indeed a very interesting germ.

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 Because in any case it is completely harmless.

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 It is also used in food technology, the same way.

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 At the same time, it is a germ that separates excellent fat.

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 And in addition, it is also relatively easy to produce in artificial media.

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 And everything else has resulted in the development that it is still relatively sustainable.

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 We have noticed that over time, that it can be done for a long time

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 and with relatively representative effort.

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 That was another plus point of this product.

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 What is the challenge in the production of the germ?

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 The challenge is actually that we had to switch

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 from bacterial production, which usually grows much faster than fungi,

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 to a fungus production.

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 That means we had to adapt something.

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 We had to adjust the nutrient medium, adjust the temperature conditions,

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 so that we could produce this fungus in a large amount in a short time.

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 The medium that we got at the beginning,

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 from LipoBug, was of course cut into the bacterium.

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 And then we first had to do optimization work

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 to optimize this for the fungus.

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 Where are the strengths of the fungus as it is today?

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 The fact that it is a fungus and not a bacterium has different advantages.

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 On the one hand, there are often antibiotics in the waste water.

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 And the antibiotics, as the name suggests, suppress bacteria growth.

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 Fungi, on the other hand, are completely immune to antibiotics.

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 That is a big advantage.

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 And another advantage is that these fungi

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 are generally classified as less harmful than bacteria,

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 when it comes to the entire microbial community in the chlorophyll,

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 in the biological chlorophyll level.

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 The fungi are there simply because they grow a little slower,

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 they are less able to balance each other than when certain bacteria are added.

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 What are the technical framework data of LipoBug?

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 Where can I use it?

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 In what temperature areas?

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 How does the water quality have to be?

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 What does it look like?

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 The temperature area is an important point.

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 LipoBug is next to a germ.

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 And if the temperatures rise over a longer time, over 50-60 degrees,

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 then you kill this germ and it can no longer multiply in the process.

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 The enzymes themselves are still capable of working,

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 but they just can't be reproduced.

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 And that's actually the principle of LipoBug.

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 So temperatures possibly below 60 degrees.

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 Then it is important that the water does not contain strong antifungal substances.

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 As I said, antibiotics are not a problem now,

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 but often the disinfectants have a wide effect.

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 That means that it is sometimes chlorophyll or pericelic acid.

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 And these substances would also kill the fungus.

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 That means that if you decide for the biology and the biology works,

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 you should make sure that you do not kill the biological substances.

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 In many cases, a mixture of chemical and biological measures is not possible.

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 Are there any safety-relevant things with production, transport, storage, use?

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 Or is it actually something that you just ...

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 In the end, there are no safety-relevant concerns.

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 As I said, the whole thing is an organism that is also used in food technology.

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 There are many cheeses, for example.

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 It is also actually brought up specifically to make common beer sustainable, for example.

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 Therefore, it is a completely harmless germ and there are no chemicals in the product.

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 The whole food media are ultimately organic.

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 It is soy, oil, yeast extract.

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 Therefore, there are no concerns in the use,

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 neither for the user nor for those who might see the waste at the sewer.

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 Or for someone who uses it in the kitchen and puts it in the drain.

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 So it is completely out of the question.

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 At the moment, the focus is on waste water.

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 What would you say, what areas are still being offered?

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 Well, waste water is defined as the waste water that falls into the sewer system.

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 But in the end, the waste water of course falls earlier,

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 somewhere where liquid is poured into a drain with fat.

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 And these are often large or small kitchens.

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 Ideally, lipasanF® would actually already be used at this point,

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 because then all the lines from the kitchens to the sewer itself would be kept clean,

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 there would be less waiting.

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 And lipasanF® would then also do its work in the sewer itself.

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 So in an ideal world, at some point the sewer would no longer have any problems,

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 because all running rivers would already be treated with lipasanF®.

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 But at the moment, we have started with the kitchens,

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 with the marketing, and now we can roll it up backwards.
