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Chemical waste in water?!

Water is the source of all life and it covers 71% of the Earth’s surface. How could its importance be more highlighted than its nickname "the blue planet"? Healthy drinking water is an important aspect and essential for mankind. However, the growing industrialization, the production of chemical agents and the increasing consumption of pharmaceuticals are some of the causes of rapidly increasing pressure on the aquatic environment as well as on the availability and quality of safe and clean water. The continuous release of pharmaceuticals into the environment and their negative effects on biological systems are not proven. The measured environmental concentrations are responsible for the fact that water pollution is one of the main environmental worries of our society. According to a survey of March 2012 from the Public Opinion Analysis sector of the [http://www.europarl.europa.eu/meetdocs/2009_2014/documents/envi/pr/909/909091/909091en.pdf European Commission],

• 68 % of Europeans think that water quantity and quality problems are serious.
• 80 % believe that chemical pollution is a threat to the water environment.
• 62 % feel that they are not sufficiently informed about problems facing groundwater, lakes, rivers and coastal waters in their countries.

The birth control pill is a widespread contraception method. However, large amounts of the active compounds, i.e. modified estrogens, leave the body via the urine. According to the Federal Environment Agency in Germany (Umweltbundesamt, UBA) several hundred tons of analgetics, antibiotics, beta blockers, X-ray contrast agents, anti-epileptic drugs, poly aromatic hydrocarbons pesticides etc. enter the waste water and end up p in rivers, lakes and consequently in drinking water.

Main sources of micro-contaminants are: Domestic wastewater (e.g. analgetics, estrogen, other pharmaceuticals), hospital sewage (e.g. antibiotics, X-ray contrast agents and drugs), industrial wastewater (e.g. polycyclic aromatic hydrocarbons) and agriculture effluent (e.g. pesticides)

The most human-derived substances which can be detected in the surface water possess at least one aromatic ring structure. Due to the aromatic structures, these substances are not effectively degraded in the sewage treatment plants with conventional methods. This means that a high proportion of these substances is being released into the environment. According to the Rhine Westphalian Institute of Water Research gGmbH (IWW) environmental concentrations of [http://www.umweltbundesamt.de/chemikalien/veranstaltungen/ws-monitoring-arzneimittel/11_vortrag-abstract_bergmann.pdf 247] human and veterinary drugs can be detected in the environmental sewage effluent, the surface water, the groundwater, the drinking water and the sewage sludge. These substances include:

Sweeteners: Acesulfam, Sucralose

Antibiotics: Clarithromycin, Sulfamethoxazol, N4-Acetylsulfamethoxazol , Carbamazepin

Analgetics: Diclofenac, Ibuprofen

Benzotriazole: Benzotriazol, 4-Methylbenzotriazol, 5-Methylbenzotriazol,

Beta-Blocker: Metoprolol, Sotalol

X-Ray contrast agents: Amidotrizoeacid, Iomeprol, Iopamidol, Iopromid

Subsequently to the wastewater treatment, the concentrations of these substances and their corresponding metabolites are below their therapeutically effective concentration so that these agents are classified as concepts micro-contaminants. But the impacts of the micro-contaminants on the environment are already evident. For example [http://toxsci.oxfordjournals.org/content/106/1/93.short Shved et al. 2008] has shown that 17a-Ethinylestradiol in an environmentally relevant concentration is able to influence fish growth and reproductive functions of bony fishes.

The long-term consequences of an increasing estrogen concentration for human beings are still largely unknown. Nonetheless, declining sperm counts and thereby increasing infertility in men living in industrial nations may well relate to this hormonal pollution. In addition, [http://bmjopen.bmj.com/content/1/2/e000311.full testicular and prostate cancers] as well as osteoporosis could be a consequence of overly high concentrations of estrogen in the human body. At the moment only the acute and short term effects are obvious, but the long term effects of continuous exposure of micro-contaminates to ecosystems and the effects that occur even below therapeutic levels in non-target organisms are not [http://www.umweltbundesamt.de/chemikalien/veranstaltungen/ws-monitoring-arzneimittel/16_vortrag-abstract_knacker.pdf predictable].

Only for 70 of the [http://www.umweltbundesamt.de/chemikalien/veranstaltungen/ws-monitoring-arzneimittel/11_vortrag-abstract_bergmann.pdf 247] substances sufficient information exist for an ecotoxicological assessment. To assess the risk, the Federal Environment Agency (UBA) published a recommendation for not or only partially assessable micro-contaminants, defined as “risk for your healthy value" [http://www.umweltbundesamt.de/chemikalien/veranstaltungen/ws-monitoring-arzneimittel/3_vortrag-abstract_vietoris.pdf GOW]. Some of these recommended values already have been exceeded by several agents, like Diclofenac (up to 10,5µg mL-1) and Ibuprofen up to 9,79 µg mL-1).

Detailed concentrations in sewage effluent and surface water of Diclofenac and some other substances can be found here. The increasing amounts of some micro-contaminants, prompted the European Commission to add [http://www.europarl.europa.eu/meetdocs/2009_2014/documents/envi/pr/909/909091/909091en.pdf 15 new priority substances] to the list of priority hazardous substances:

• six ingredients of pesticides (Aclonifen, Bifenox, Cypermethrin, Dicofol, Heptachlor und Quinoxyfen),
• six ingredients of biocides (Cybtryn, Dichlorvos und Terbutryn),
• two industrial chemicals (Perfluoroctansulfonat (PFOS) und Hexabromcyclododecan (HBCDD)),
• three pharmaceutical agents (Diclofenac, 17a-Ethinylestradiol (EE2) und Estradiol (E2)) and
• Dioxin and dioxin like polychlorinated Biphenyls (dl-PCB).

This list defines priority substances in the field of water policy, namely chemicals presenting a significant risk to or via the aquatic environment. Beside these 15 substances the European commission plans to [http://www.europarl.europa.eu/meetdocs/2009_2014/documents/envi/pr/909/909091/909091en.pdf increase the priorization of other substances] such as Anthracen, brominated diphenylether, Naphthalene and Polycyclic Aromatic Hydrocarbons.

Nonetheless, there are currently no legally binding limits for concentrations of pharmaceutically active compounds in surface water, groundwater or drinking water. Consequently the increasing consumption of pharmaceuticals lead to an increasing pressure on the aquatic environment and on the availability and quality of healthy and clean water. This is the problem the our iGEM team wants to take care of. The idea of the Bielefeld iGEM team is to developing a biological filter using immobilized laccases to purify municipal and industrial wastewater from synthetic estrogens and other micro-contaminants.

Our Focus

The following substrates are our focus for possible degradation because they have remarkable features. Ethinyl estradiol which can cause unimageble damages to the environment for example. For more information about the substrates we used look at the chemical waste in water tab.

Estradiol:

Figure 1: Structure of Estradiol. Source of the figure

Estradiol is a natural human hormone secreted not only in women but also in men. Its importance in women metabolism is that after reaching puberty this hormone provides being a woman. In men on the other hand Estradiol has been detected to have influence on sperm ejaculation.^[1] This hormone has particularly effect on female characteristics for example in breast development, changing body shapes or texture of bones. During the menstrual cycle, Estradiol levels fluctuates indicating its importance in sexual development.^[2]
Since Estradiol is easily degradable by many sorts of enzymes we thought it would be a good substrate to start from. Its structural similarity to the hardly to degradable synthetic Ethinyl estradiol could make it a good indicator for higher potential.

UV-light detection: 230 nm Extinction, 310 nm Emission
Molecular Mass: 272,39 g * mol^-1
Chemical structure: C₁₈H₂₄O₂

Estrone:

Figure 2: Structure of Esteron. Source of the figure

Estrone is one of several natural estrogens. Like Estradiol it is important in several female development steps. It has been said that Estrone disordered people has a higher potential for breast cancer ([http://toxnet.nlm.nih.gov/cgi-bin/sis/search/r?dbs+hsdb:@term+@rn+53-16-7 HSDB]). Our focus is to characterize the activity of the laccases regarding several substrates similar to estradiol like estrone.

UV-light detection: 230nm Extinction, 310nm Emission
Molecular Mass: 270,36g * mol ^-1
Chemical structure: C₁₈H₂₂O₂

Ethinyl estradiol:

Figure 3: Structure of Ethinyl Estradiol. [http://www.tcichemicals.com/eshop/en/eu/commodity/E0037/ Source of the figure]

Ethinyl estradiol is the synthetic variation of the natural estradiol. Its structure is constructed so that it is not easily degradable with human enzymes. Birth control pills contain ethinyl estradiol that passes via excretion into wastewater which reaches sewage plants and from there lake water where fishes and other organisms live. This causes several disorders in the natural metabolisms of the organisms such as the feminization of fish.^[3] The increase of ethinyl estradiol in wastewater in the past years has made ethinyl estradiol to a potential problem in the future. But not only fishes also humans are affected from this problem because the wastewater from sewage seeps into groundwater and from there into drinking water. Therefore the degradation or filtration of ethinyl estradiol will become more important in cleaning water. Activated carbon or ozonation treatment of wastewater could solve this problem but it is too expensive in practice. Such an activated carbon treatment in England would cost around $10,3 Milion for 250.000 people.^[4]

UV-light detection: 230nm Extinction, 310nm Emission
Molecular Mass: 296,4g * mol^-1
Chemical structure: C₂₀H₂₄O₂

Diclofenac:

Figure 4: Structure of Diclofenac. Source of the figure

Diclofenac is used to reduce inflammation. As an analgesic it reduces pain in certain conditions and reaches through wastewater lakes and drinking water. Since this chemical, like Ethinyl estradiol is not filterable in sewages without activated carbon or ozonation treatment.^[5] Diclofenac and Ethinyl estradiol are getting [http://europa.eu/rapid/pressReleasesAction.do?reference=IP/12/88&format=HTML&aged=0&language=EN&guiLanguage=en more attention] from the [http://ec.europa.eu/environment/water/index_en.htm European Commision for Water]. Besides there is a precise example in the [http://www.schlossholtestukenbrock.de/060/sr_seiten/artikel/112120100000015850.php sewage plant Schloß-Holte], where a concentration of 1900ng/L Diclofenac was detected. For more information about the risks read the [http://www.umweltbundesamt.de/chemikalien/veranstaltungen/ws-monitoring-arzneimittel/3_vortrag-abstract_vietoris.pdf GOW]. Molecular Mass: 296,148g * mol^-1
Chemical structure:C₁₄H₁₀Cl₂NO₂Na

Ibuprofen:

Figure 5: Structure of Ibuprofen. Source of the figure

Ibuprofen is as well as Diclofenac used in pain treatments like in the case of rheumatism. The World Health Organization ([http://www.who.int/en/ WHO]) has set Ibuprofen on the [http://www.who.int/medicines/publications/essentialmedicines/Updated_sixteenth_adult_list_en.pdf list of essential medicine]. According to a medicine study, people who take regularly Ibuprofen have a higher risk getting kidney cancer.^[6]

UV- light detection: Extinction 224nm, Emission 290nm
Molecular Mass: 206,3g * mol^-1
Chemical structure: C₁₃H₁₈O₂

Naproxen:

Figure 6: Structure of Naproxen. Source of the figure.

Naproxen is also used in pain treatment. Besides its helpful side, Naproxen can also cause several side effects such as hoarseness or nausea.^[7] Naproxen reaches lake water through the wastewater.

UV- light detection: Extinction 232nm, Emission 272nm
Molecular Mass: 230,3g * mol^-1
Chemical structure: C₁₄H₁₄O₃

Naphthalene:

Figure 7: Structure of Naphthalene. [http://en.wikipedia.org/wiki/File:Naphthalene-2D-Skeletal.svg Source of the figure]

Commonly used as an intermediate for some chemical synthesis of insect repellents or fungicides in the industy. From industrial use naphthalenes reaches sewage water and from there lake. Naphtalene may destroy red blood cells when overdosed in blood. This would be fatal for fishes in lakes. It is already shown that the laccase from E. coli which we produced as well is able to degradate naphtalene.^[8] That is why we used naphtalene to test the activity of the expressed laccases.

UV-light detection: Extinction 275nm, Emission 350nm
Molecular Mass: 128,17g/mol
Chemical structure: C₁₀H₈

Acenaphthene:

Figure 8: Structure of Acenaphthene. [http://de.wikipedia.org/w/index.php?title=Datei:Acenaphthene.svg&filetimestamp=20070113040401 Source of the figure]

This chemical is a polycyclic aromatic hydrocarbon (PAH) consisting of naphthalene with an ethylene bridge and is used in the preparation of pesticides and pharmaceuticals. It reaches the ground water the same way as the other chemicals. The effects on organisms are not yet clearly defined. But the E.coli Cue0 laccase is able to degradate acenaphten.^[8]

UV-light detection: Extinction 275nm, Emission 350nm
Molecular Mass: 154,21g * mol^-1
Chemical structure: C₁₂H₁₀

Phenanthrene:

Figure 9: Structure of Phenanthrene. [http://de.wikipedia.org/w/index.php?title=Datei:Phenanthren_-_Phenanthrene.svg&filetimestamp=20070308185106 Source of the figure]

Its name comes from phenyl and anthracene. Phenanthere is used in some explosives and drugs. There is not much information about the effects or interactions in water or with organisms in water but the E.coli laccase CueO was able to degrade this chemical.^[8]

UV-light detection: Extinction 275nm, Emission 350nm
Molecular Mass: 178,23g * mol^-1
Chemical structure: C₁₄H₁₀

Anthracene:

Figure 10: Structure of Antracene. [http://de.wikipedia.org/w/index.php?title=Datei:Anthracene_structure.png&filetimestamp=20070610032248 Source of the figure]

Anthracene is used in producing dyes but the consequences for human or other organisms are not yet cleared. Because the E.coli laccase CueO was able to degrade other polycyclic aromatic hydrocarbons we decide to test Anthracene with the laccases we produced.

UV-light detection: Extinction 260nm, Emission 430nm
Molecular Mass: 178,24g * mol^-1
Chemical structure: C₁₄H₁₀

References:

[1] Sharpe RM, Skakkebaek NE (1993). "Are oestrogens involved in falling sperm counts and disorders of the male reproductive tract?" The Lancet 341(8857):1392-1395.

[2] Sonya S. Dasharathy et al. (2011). "Menstrual Bleeding Patterns Among Regularly Menstruating Women." American Journal of Epidemiology 175(6):536-545.

[3] Kidd KA et al. (2007). "Collapse of a fish population after exposure to a synthetic estrogen PNAS 104(21):8897-8901.

[4] Owen R, Jobling S (2012). "Environmental science: The hidden costs of flexible fertility." Nature 485(7399):441

[5] Beltrán FJ et al. (2009). "Diclofenac remocal from water with ozone and activated carbon." Journal of Hazardous Materials 163(2-3):768-776.

[6] Bloomberg, http://www.bloomberg.com/news/2011-09-12/commonly-used-pain-pills-increase-kidney-cancer-risk-in-study.html on www.bloomberg.com Sept. 13, 2012

[7] PubMed Health, http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0000526/ on http://www.ncbi.nlm.nih.gov/ Sept. 14, 2012

[8] Zeng J, Lin X et al. (2011). "Oxidation of polycyclic aromatic hydrocarbons by the bacterial laccase CueO from E. coli." Appl Microbiol Biotechnol 89(6): 1841-1849.

Laccase - Our Teammate

In the last few years a lot of attention has been drawn to Laccases due to their ability to oxidise both phenolic and nonphenolic lignin related compounds as well as highly recalcitrant environmental pollutants. This makes them very useful for applications concerning several biotechnological processes. This includes the detoxification of industrial effluents, for example from the paper and pulp, textile and petrochemical industries. Laccases are also valuable as a tool as a tool for medical diagnostics and as a bioremediation agent to clean up herbicides, pesticides and certain explosives in soil. Furthermore these enzymes are also used as catalysts for the manufacture of anti-cancer drugs and even as ingredients in cosmetics^[1]. Their capacity to remove xenobiotic substances and produce polymeric products makes them a useful tool for bioremediation purposes. In our project laccases are used as cleaning agents for a water purification system.

Laccases are copper-containing polyphenol oxidase enzymes (EC 1.10.3.2) that can be found in many plants, insects, microorganisms and mainly in fungi. These enzymes fulfill several functions in different metabolic pathways. One the one hand these enzymes are necessary to degrade lignin in Basidiomycetes and on the other hand to synthesize complex polymers like Melanin in Ascomycentes. In general, laccases are extracellular enzymes and consists usually of 15-20 % carbon-hydrogen. The molecular weight of the deglycated protein ranges from 60 to 80 kDa. These enzymes can occur as monomers, dimers, trimers and tetramers. The first crystal structure of a laccase from the organism Trametes versicolor was published in 2002 ^[2]. The structure is illustrated in the video at the end of this text.

Laccases are able to oxidize a broad range of substrates due to the contained copper-cluster, by reducing oxygen to water. The active site of the enzyme includes a four-copper-ion-cluster, which can be distinguished by spectroscopic analyses. This cluster consists of one blue copper-ion (type 1), one type 2 and two type 3 copper-ions. Because of the blue copper-ion, the laccases belong to the big family of the blue copper proteins. This specific blue copper ion is essential for the enzyme mediated radical oxidation of the phenolic groups. In this reaction the electron from the oxidation is transferred to the other three copper ions. These ions form a trinuclearic cluster, which transfers electrons to the terminal electron acceptor oxygen. By receiving four electrons the molecular oxygen is finally reduced to water.

Structure of the Laccase from Trametes versicolor

The vidoe was done with the [http://jmol.sourceforge.net/ Jmol-software] in combination with the data from the [http://www.rcsb.org/pdb/explore/explore.do?structureId=1GYC RCSB Protein Data Bank]

References

[1] Susana Rodríguez Couto & José Luis Toca Herrera;Industrial and biotechnological applications of laccases: A review; 2006; Biotechnology Advances 24 500–513

[2] O. V. Morozova, G. P. Shumakovich, M. A. Gorbacheva, S. V. Shleev, and A. I. Yaropolov, “Blue” Laccases ,Biokhimiya, 2007, Vol. 72, No. 10, pp. 1396-1412.

Laccase-donators

Arabidopsis thaliana

Picture of A. thaliana found at [http://de.wikipedia.org/wiki/Acker-Schmalwand/ wikipedia.de]

Arabidopsis thaliana (A. thaliana), or commonly known as thale cress, is a small flowering plant which is an established model organism. We have chosen this little plant as representative for higher eukaryotes and not only because there is a lot of research going on at Bielefeld University with this organism. A. thaliana has a small genome with 125 Mb total and was sequenced completely in year 2000. Besides the sophisticated annotation of genes there is also a large number of mutant lines available. The research on A. thaliana is progressing fast and researchers from all around the world are working with this model organism because of its rapid life cycle of six weeks and its simple growth conditions, just to name a few examples. The Arabidopsis community is therefore huge and progress in understanding the cellular and molecular biology of this flowering plant is documented well and available. For our project we were interested in the laccase(s) of A. thaliana. We did some research at [http://www.arabidopsis.org/servlets/Search?type=general&search_action=detail&method=1&show_obsolete=F&name=laccase&sub_type=gene&SEARCH_EXACT=4&SEARCH_CONTAINS=1/ TAIR]^[1] and found 22 laccases or laccase-like genes. Stunned by the amount of laccase genes we decided to concentrate on just one which does not encode a laccase-like protein. We have chosen gene [http://www.arabidopsis.org/servlets/TairObject?type=sequence&id=123870/ AT5G48100.1] from A. thaliana Col-0 and moved on with further research. In the next step we used the [http://bar.utoronto.ca/efp/cgi-bin/efpWeb.cgi/ eFP Browser]^[2] to see where our chosen laccase is expressed. We found out that it is expressed in the seeds and therefore available in the siliques as it is indicated in the following picture:

Laccase gene expression in A.thaliana seeds and siliques of different developmental stages. Expression is visualized in different red colors (see bar on the right).

With this bioinformatic research we set the basis for the following laboratory work on a laccase from a higher eukaryote.

Bacillus halodurans

Bacillus pumilus

Escherichia coli

electron microscopic recording of [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia_coli] found at [http://wikipedia.org wikipedia.de]

Another laccase which catched our attention is the enzyme [http://www.ncbi.nlm.nih.gov/protein/85674340 CueO] from Escherichia coli. The bacterium naturally occurs in human and animal intestine. In laboratory it’s a model organism and the most widely used organism in molecular genetics. The about 1-6 µm long bacterium has a laccase with a high potential for our approach. It is described that the laccase [http://www.ncbi.nlm.nih.gov/protein/85674340 CueO] from E. coli W3110 is able to oxidize different PAHs (polycyclic aromatic hydrocarbons). An oxidation activity for the crude laccase was measured for fluorene, acenaphthylene, phenanthrene and benzo[a]anthracen (Zeng, Lin et al., 2011). The laccase has a predicted molecular weight of 53%nbsp;kDa. Our aim is to produce and characterize this laccase with regard to the plan to develope a degradation system using immobilized laccases. After blasting this laccase we found out that E. coli BL21(DE3) has this laccase, too. Therefore we isolated the laccase CueO from E. coli DE(BL21) because this strain is available in our lab. For consistently names we call this laccase ecol in our wiki. For further information about our characterization of CueO look here.

Thermus thermophilus

Electron microscopic recording of [http://en.wikipedia.org/wiki/Thermus_aquaticus Thermus aquaticus] found at wikipedia.de

Thermus thermophilus is a gram-negative eubacterium. It is classified as an organism of the [http://www.bvl.bund.de/SharedDocs/Downloads/06_Gentechnik/register_datenbanken/organismenliste.html?nn=1484542 basic biosafety level 1]. The bacterium is as the name suggests extremely thermophilic and has an optimal growth temperature at about 65 °C. Due to its cell characteristics this organism can grow on temperatures up to 85 °C. This properties are caused by very thermostable proteins which lead to a high interest in many proteins from different Thermus strains for laboratory research. The most famous strain is probably Thermophilus aquaticus which was isolated from water of hot springs. The strain has an interesting polymerase, the widely used Taq polymerase, a very thermostable protein. In our project we are interested in another protein of Thermus thermophilus, called laccase. The first description of the [http://www.ncbi.nlm.nih.gov/pubmed/15999224 Tth-laccase] from T. thermophilus was in year 2005. This multi copper blue oxidase (53 kDa), short laccase, shows an oxidative activity on ABTS and SGZ. Like the most proteins of T. thermophilus this enzyme presents a high stability under harsh industrial conditions. Due to its skills and properties our attention was drawn to this laccase. We decided to isolate the sequence from the strain [http://www.dsmz.de/catalogues/details/culture/DSM-7039 T. thermophilus HB27] and to develope a degradation system against micro-contaminants using this laccase immobilized. More information about the characterization of our produced Tth-laccase (TTHL) you find here.

Trametes versicolor

Picture of Trametes versicolor

Trametes versicolor is a common mushroom which is very widespread all over the world so it is also classified as an organism of the [http://www.bvl.bund.de/SharedDocs/Downloads/06_Gentechnik/register_datenbanken/organismenliste.html?nn=1484542 basic biosafety level 1]. It is described that Trametes versicolor has four genes for different laccase isoenzymes. The substrate specifies were described as mostly similar but with certain variations in the oxidation rate of polymeric substrates. Laccases from Trametes versicolor exhibits a high redox potential and are shown to remove substrates such as phenol and bisphenol A. Furthermore they are able to degrade endocrine disrupters (natural estrogens, 17β-estradiol (E2), estriol (E3),estrone (E1) and the synthetic estrogen 17α-ethinylestradiol (EE2)).^[6] For further information about the production of laccases from Trametes versicolor click here and for information about the characterization of [http://www.sigmaaldrich.com/catalog/product/sigma/51639?lang=de&region=DE TVEL0] which we used as reference and positive control click here.

References

[1] The Arabidopsis Information Resource (TAIR), www.arabidopsis.org/aboutarabidopsis.html, on www.arabidopsis.org, Oct 24, 2000

[2] Winter et al. (2007). Arabidopsis eFP Browser at bar.utoronto.ca. PLosOne 2(8): e718.

[3] Ruijssenaars HJ, Hartmans S (2004). A cloned Bacillus halodurans multicopper oxidase exhibiting alkaline laccase activity. Applied Genetics and Molecular Biotechnology 65:177-182

[4] Danesh A, Mamo G, Mattiasson B (2011). Production of haloduracin by Bacillus halodurans using solid-state fermentation. Biotechnology Letters 33(7):1339-44.

[5] Reiss, R., J. Ihssen, et al. (2011). "Bacillus pumilus laccase: a heat stable enzyme with a wide substrate spectrum." BMC Biotechnol 11: 9.

[6] Zeng, J., X. Lin, et al. (2011). Oxidation of polycyclic aromatic hydrocarbons by the bacterial laccase CueO from E. coli. Appl Microbiol Biotechnol 89(6): 1841-1849.

[7] Wallace JG, Zhou Z, Breaker PR (2012). OLE RNA protects extremophilic bacteria from alcohol toxicity. Nucleic Acids Research 40(14):6898-6907.

[8] Miyazaki, K. (2005). A hyperthermophilic laccase from Thermus thermophilus HB27. Extremophiles 9(6): 415-425.

[9] Bourbonnais, R., M. G. Paice, et al. (1995). Lignin oxidation by laccase isozymes from Trametes versicolor and role of the mediator 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonate) in kraft lignin depolymerization. Appl Environ Microbiol 61(5): 1876-1880.

W