Team:TU-Munich/Project/Biodegradation

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==BioDegradation of Xenobiotics==
==BioDegradation of Xenobiotics==
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[[File: TUM13_Pharmaceuticals.png|thumb|right|450px| '''Figure 1''': Concentration of pharmaceuticals in Waste water treatment plant (WWTP) effluents (top) and surface water (bottom)[http://www.blac.de/servlet/is/2146/P-2c.pdf <nowiki>[1]</nowiki>]]]
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[[File: TUM13_Pharmaceuticals.png|thumb|right|450px| '''Figure 1''': Concentration of pharmaceuticals in Waste water treatment plant (WWTP) effluents (top) and surface water (bottom) [[http://www.blac.de/servlet/is/2146/P-2c.pdf BLAC]]]]
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Biodegradation is defined as "a process by which microbial organisms transform or alter the structure of chemicals introduced into the environment" [http://www.epa.gov/oust/cat/tumgloss.htm (U.S. Environmental Protection Agency, 2009)]. We work with this concept by degrading or transforming noxious substances in waste water into non-hazardous compounds.
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Biodegradation is defined as ''"a process by which (microbial) organisms transform or alter the structure of chemicals introduced into the environment"'' [[http://www.epa.gov/oust/cat/tumgloss.htm U.S. Environmental Protection Agency, 2009]]. We work with this concept by degrading or transforming noxious substances in waste water into non-hazardous compounds.
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These substances, such as antibiotics, hormones or pesticides cannot be removed by common waste water treatment plants, but it is possible to inactivate them with existing enzymes from natural catabolic mechanisms in different microorganisms. To utilize these enzymes we integrated them into a plant as a self-sustaining sedentary organism to create a functional water filter system. To illustrate this approach we chose three potent enzymes:
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These substances, such as antibiotics, hormones or pesticides are not removed by common waste water treatment plants because current methods such as active carbon and ozonization are expensive and energy-intensive. But it is possible to inactivate them with existing enzymes from natural catabolic mechanisms in different microorganisms. To utilize these enzymes, we integrated them into a plant as a self-sustaining, sedentary organism to create a functional water filter system. To illustrate this approach, we chose three potent enzymes:
* The [[#Erythromycin Esterase (EreB)|<b>Erythromycin esterase</b>]], which degrades macrolides, a persistant group of antibiotics
* The [[#Erythromycin Esterase (EreB)|<b>Erythromycin esterase</b>]], which degrades macrolides, a persistant group of antibiotics
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* The [https://2013.igem.org/Team:TU-Munich/Project/Biodegradation#Laccase_.28Bacillus_pumilus.29 <b>Laccase BPUL</b>], which degrades several noxious substances, for example the artificial hormone ethinyl estradiol, the main ingredient of contraception pills
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* The [https://2013.igem.org/Team:TU-Munich/Project/Biodegradation#Laccase_.28Bacillus_pumilus.29 <b>Laccase BPUL</b>], which degrades several noxious substances, for example the artificial hormone ethinyl estradiol, the main ingredient of contraceptive pills
* The [[#Catechol Dioxygenase (xylE)|<b>Catechol-2,3-dioxygenase</b>]], catalyzing the degradation of aromatic pollutants, which occur in pesticides and insecticides
* The [[#Catechol Dioxygenase (xylE)|<b>Catechol-2,3-dioxygenase</b>]], catalyzing the degradation of aromatic pollutants, which occur in pesticides and insecticides
[[File:TUM13_biodegradation.png|thumb|left|300px |'''Figure 2''': Principle of biodegradation]]
[[File:TUM13_biodegradation.png|thumb|left|300px |'''Figure 2''': Principle of biodegradation]]
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[[File:TUM13_antibiotics.png|thumb|right|400px|'''Figure 3''': Causality chain of increasing antibiotic use]]
[[File:TUM13_antibiotics.png|thumb|right|400px|'''Figure 3''': Causality chain of increasing antibiotic use]]
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The discovery of antibiotics in the early 20th century has revolutionized the fight against infectious diseases. Due to their success thousands of '''tons of antibiotics''' have been produced, consumed and excreted, since antibiotics are designed to circulate through the body for a long time and therefore up to 75% leave the organism unaltered. As a result microbes are '''exposed to strong selective pressure''' to which these numerous and extremely adaptable organisms react by developing '''resistance mechanisms'''.   
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The discovery of antibiotics in the early 20th century has revolutionized the fight against infectious diseases. Due to their success, thousands of tons of antibiotics have been produced, consumed and excreted into the environment. Since antibiotics are designed to circulate through the body for a long time, up to 75% of the administered doses leaves the organism unaltered. As a result, microbes are exposed to a '''strong selective pressure''' to which these extremely adaptable organisms react by developing '''resistance mechanisms'''.   
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However, antimicrobial effectiveness is a precious, limited resource, that we can no longer do without. Accordingly, in 2000 a [http://www.who.int/infectious-disease-report/2000/ World Health Organization report] focused on antibiotic resistance as one of the '''most critical human health challenges of the next century''' and called for “a global strategy to contain resistance”. In numbers, the WHO estimates that resistant pathogens affect 2 million Americans each year, of which 14,000 die as a result. In the EU antimicrobial resistance is responsible for 25,000 deaths every year and the annual treatment and social costs have been estimated at some €1.5 billion [[http://www.ecdc.europa.eu/en/publications/Publications/0909_TER_The_Bacterial_Challenge_Time_to_React.pdf ECDC/EMEA joint technical report 2009]]. These numbers will only rise if nothing is done to prevent precious antibiotics from becoming effectless. [[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2937522/ Davies and Davies, 2010]]
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However, antimicrobial effectiveness is a precious, limited resource, that we can no longer do without. Accordingly, in 2000 a [http://www.who.int/infectious-disease-report/2000/ World Health Organization report] focused on antibiotic resistance as one of the '''most critical human health challenges''' of the next century and called for “a global strategy to contain resistance”. The WHO estimates that resistant pathogens affect 2 million Americans each year, of which 14,000 die as a result. In the EU, antimicrobial resistance is responsible for 25,000 deaths every year and the annual treatment and social costs have been estimated at some €1.5 billion [[http://www.ecdc.europa.eu/en/publications/Publications/0909_TER_The_Bacterial_Challenge_Time_to_React.pdf ECDC/EMEA joint technical report 2009]]. These numbers will rise if nothing is done to prevent precious antibiotics from loosing their effect on microbes. [[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2937522/ Davies and Davies, 2010]]
===Current Solutions===
===Current Solutions===
[[File:TUM13_research.png|thumb|right|400px|'''Figure 4''': Timeline of developments since the discovery of antibiotics]]
[[File:TUM13_research.png|thumb|right|400px|'''Figure 4''': Timeline of developments since the discovery of antibiotics]]
[[File:TUM13_antibiotics timeline.png|thumb|right|400px|'''Figure 5''': Development of new antimirobial agents over the years]]
[[File:TUM13_antibiotics timeline.png|thumb|right|400px|'''Figure 5''': Development of new antimirobial agents over the years]]
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The obvious approach to minimize selective pressure on microorganisms is to deal with the problem of carefree, often precautionary overuse of antibiotics, not only in humans but also and especially in animal breeding, by only '''using them when absolutely necessary'''.  
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The obvious approach to minimize selective pressure on microorganisms is to deal with the problem of carefree, often precautionary '''overuse of antibiotics''', not only in humans but especially in animal breeding, by only using them when absolutely necessary.  
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Furthermore '''research on new antibiotics''' should be hugely intensified to create alternative agents and keep pace with the formation of antimicrobial resistance. Unfortunately antibiotic development has slowed dramatically over the past 25 years because as a short-course and very effective therapy they have a much lower rate of return on investment  than other drugs and therefore are financially not viable for pharmaceutical companies (per approved agent development costs are estimated to be $400-$800 million). For example in 2004 only 5 new antibacterial agents were under development by the largest pharmaceutical companies, barely beating the 4 new molecular entities to treat erectile dysfunction. [[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2937522/ Davies and Davies, 2010]]
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Furthermore research on '''new antibiotics''' needs to be hugely intensified to create alternative agents and keep pace with the formation of antimicrobial resistance. Unfortunately, antibiotic development has slowed dramatically over the past 25 years, since as a short-course and highly effective therapy, they have a much lower rate of return on investment  than other drugs and are therefore financially not very viable for pharmaceutical companies. The development costs per approved agent are estimated to be between $400-$800 million. In 2004, only 5 new antibacterial agents were under development by the largest pharmaceutical companies, barely beating the 4 new molecular entities to treat erectile dysfunction. [[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2937522/ Davies and Davies, 2010]]
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These two options are difficult to accomplish due to the '''increasing need of antibiotics''' with a growing world-wide population and the fact that finding new antibiotics is a costly, long-term and extremely difficult project. Therefore we focus on a third option to fight the spread of antibiotic resistance by developing a cheap, innovative water-filter that will prevent continuous inflow of the drugs into surface water and therefore reduce the selective pressure on microbes.
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These two options are difficult to accomplish due to the '''increasing need of antibiotics''' with a growing world-wide population and the fact that finding new antibiotics is a costly, long-term and extremely difficult project. Therefore we focus on a third option to fight the spread of antibiotic resistance: The development of a cost-effective water-filter that will prevent continuous inflow of the drugs into surface water and thus reduce the selective pressure on microbes.
===Our Solution: EreB===
===Our Solution: EreB===
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In our search for a suitable enzyme we looked at antibiotic concentrations in waste water. There have not yet been many investigations on this topic, one of the main surveys was executed by the [http://www.blac.de/servlet/is/2146/P-2c.pdf German national committee for chemical safety (BLAC)] of 202 effluent samples from 34 waste water treatment plants (WWTP). The result was that the main detectable antibiotics are the macrolides Erythromycin, Roxythromycin and Clarithromycin, the Sulfonamide Sulfamethoxalol as well as the Fluoroquinolone Ciprofloxacin. Most concentrations are about 100 ng/l, but maximum concentrations reached more than 3 µg/l. The often prescribed ß-lactam antibiotics, such as penicillin, were not detectable probably due to their fast degradation. Another important conclusion of the study is that the main source of antibiotic input into the aquatic environment is municipal waste water. Similar results were found in other countries (see Table 1).
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In our search for a suitable enzyme we looked at antibiotic concentrations in waste water. There have not yet been many investigations on this topic, but one of the main surveys was executed by the [http://www.blac.de/servlet/is/2146/P-2c.pdf German national committee for chemical safety (BLAC)] of 202 effluent samples from 34 waste water treatment plants (WWTP). The result was that the main detectable antibiotics are the macrolides Erythromycin, Roxythromycin and Clarithromycin, the Sulfonamide Sulfamethoxalol as well as the Fluoroquinolone Ciprofloxacin. Most concentrations are about 100 ng/l, but maximum concentrations reached more than 3 µg/l. The often prescribed ß-lactam antibiotics, such as penicillin, were not detectable probably due to their fast degradation. Another important conclusion of the study is, that the main source of antibiotic input into the aquatic environment is municipal waste water. Similar results were found in other countries (see Table 1).
{|cellspacing="0" border="1" right
{|cellspacing="0" border="1" right
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|+ '''Table''' 1: Antibiotics in WWTP effluents
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|+ '''Table''' 1: Antibiotics in WWTP effluents, [[http://www.umweltbundesamt.at/fileadmin/site/publikationen/REP0258.pdf environmental agency austria]], [[http://antibiotics.toku-e.com/a/ antimicrobial index]]
! align="center";| Antibiotic
! align="center";| Antibiotic
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! align="center";| max. concentration [µg/l] found in different countries<sup>[http://www.umweltbundesamt.at/fileadmin/site/publikationen/REP0258.pdf <nowiki>[4]</nowiki>]</sup>
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! align="center";| max. concentration [µg/l] found in different countries
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! align="center";| min MIC50<sup>[http://antibiotics.toku-e.com/a/<nowiki>[6]</nowiki>]</sup>[µg/l]
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! align="center";| min MIC50[µg/l]
|-
|-
|Ciprofloxacin (fluoroquinolone)
|Ciprofloxacin (fluoroquinolone)
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Now we compared the concentrations of the most frequent antibiotics found in WWTP effluents to the [http://en.wikipedia.org/wiki/Minimum_inhibitory_concentration minimum inhibitory concentration] (MIC50) at which the growth of at least 50% of bacterial strains are inhibited. The MIC50 depends on the species. In the table the smallest MIC50 over all species is given, indicating the level at which the contamination seriously affects the microbiological system and therefore carrying out a certain stress which gives resistant individuals an increased selective advantage.
Now we compared the concentrations of the most frequent antibiotics found in WWTP effluents to the [http://en.wikipedia.org/wiki/Minimum_inhibitory_concentration minimum inhibitory concentration] (MIC50) at which the growth of at least 50% of bacterial strains are inhibited. The MIC50 depends on the species. In the table the smallest MIC50 over all species is given, indicating the level at which the contamination seriously affects the microbiological system and therefore carrying out a certain stress which gives resistant individuals an increased selective advantage.
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[[File:TUM13_EreB_modelled_structure.png|thumb|left|400px| '''Figure 6''': Ester hydrolysis of EreB [http://pubs.acs.org/doi/abs/10.1021/bi201790u?mi=0&af=R&pr... <nowiki>[9]</nowiki>]]]
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[[File:TUM13_EreB_modelled_structure.png|thumb|left|400px| '''Figure 6''': Ester hydrolysis of erythromycin by EreB [[http://pubs.acs.org/doi/abs/10.1021/bi201790u?mi=0&af=R&pr... Morar et al., 2012]]]]
Our conclusion from these data was that macrolides are a hazardous antibiotic class, from which several representatives are found in WWTP effluents and surface water in concentrations relatively close to their MIC50. Macrolides are important and clinically relevant agents used to treat infectious diseases, first introduced into clinics in 1952 as an alternative to penicillin. Today they are mainly applied for treatment of respiratory diseases, including pneumonia, the leading cause of childhood deaths worldwide. The drug functions by inhibiting protein biosynthesis when it binds to the exit tunnel of the 50S ribosomal subunit which leads to abortion of the growth of nascent peptide chains.
Our conclusion from these data was that macrolides are a hazardous antibiotic class, from which several representatives are found in WWTP effluents and surface water in concentrations relatively close to their MIC50. Macrolides are important and clinically relevant agents used to treat infectious diseases, first introduced into clinics in 1952 as an alternative to penicillin. Today they are mainly applied for treatment of respiratory diseases, including pneumonia, the leading cause of childhood deaths worldwide. The drug functions by inhibiting protein biosynthesis when it binds to the exit tunnel of the 50S ribosomal subunit which leads to abortion of the growth of nascent peptide chains.
Macrolides can be enzymatically inactivated with the macrolide esterases EreA and EreB, from which we chose EreB as our model enzyme since it has a broader degradation spectrum than EreA and is not metal-dependent.  
Macrolides can be enzymatically inactivated with the macrolide esterases EreA and EreB, from which we chose EreB as our model enzyme since it has a broader degradation spectrum than EreA and is not metal-dependent.  
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EreB is a cytoplasmic protein, originally discovered in ''E. coli'' on an exogeneous plasmid, that belongs to the hydrolase superfamily catalyzing the opening of the macrolactone ring, that is characteristic for macrolides. After the enzymatic opening of this cyclic ester bond a non-enzymatic hemiketal formation takes place followed by condensation and dehydration. The only co-substrate needed by the enzyme for hydrolysis is water which also makes it a suitable candidate for our moss-filter.
EreB is a cytoplasmic protein, originally discovered in ''E. coli'' on an exogeneous plasmid, that belongs to the hydrolase superfamily catalyzing the opening of the macrolactone ring, that is characteristic for macrolides. After the enzymatic opening of this cyclic ester bond a non-enzymatic hemiketal formation takes place followed by condensation and dehydration. The only co-substrate needed by the enzyme for hydrolysis is water which also makes it a suitable candidate for our moss-filter.
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More information on the enzyme can be found for example in a very detailed recently published paper by [[http://pubs.acs.org/doi/abs/10.1021/bi201790u?mi=0&af=R&pr... Wright et al., 2012]], [http://130.113.155.235/thewrightlab/ who's group] also generously provided us with the plasmid DNA.
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More information on the enzyme can be found for example in a very detailed recently published paper by [[http://pubs.acs.org/doi/abs/10.1021/bi201790u?mi=0&af=R&pr... Wright et al., 2012]], [http://130.113.155.235/thewrightlab/ whose group] also generously provided us with the plasmid DNA.
==Catechol Dioxygenase (xylE)==
==Catechol Dioxygenase (xylE)==
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=== Catechol: A growing concern ===
=== Catechol: A growing concern ===
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As ever more third world countries around the globe experience a rapid industrialization without establishing proper environmental practices as well as big companies outsourcing their production facilities in order to avoid expensive sewage treatment the problem of water pollution is more urgent then ever. The Ministry of Environment and Forests, Government of India and EPA, USA have listed Phenol and phenolic compounds as priority pollutants [[http://www.neeri.res.in/project_details.php?PID=261&DIV=38 Ministry of Environment and Forest]] [[http://water.epa.gov/scitech/swguidance/standards/criteria/health/phenol_index.cfm EPA]]. In this context, a derivative of benzene, the phenolic compund catechol, or 1,2-dihydroxybenzene, has been deemed to be a very toxic pollutant [[http://www.epa.gov/ttnatw01/hlthef/pyrocate.html Informations about Catechol by the EPA]]. According to the U.S. National Library of Medicine´s Hazardous Substances Data Bank (HSDB) the widespread use of catechol in pharmaceutical and agricultural products as well as in the rubber, chemical, photographic, dye and oil industries poses a risk of water contamination through various waste water streams [[http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+1436 HSDB about Catechol]].
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As ever more third world countries around the globe experience a rapid industrialization without establishing proper environmental practices as well as big companies outsourcing their production facilities in order to avoid expensive sewage treatment the problem of water pollution is more urgent then ever. The [http://www.neeri.res.in/project_details.php?PID=261&DIV=38 Ministry of Environment and Forest], Government of India and [http://water.epa.gov/scitech/swguidance/standards/criteria/health/phenol_index.cfm EPA] have listed phenol and phenolic compounds as priority pollutants. In this context, a derivative of benzene, the phenolic compund [http://www.epa.gov/ttnatw01/hlthef/pyrocate.html catechol, or 1,2-dihydroxybenzene], has been deemed to be a very toxic pollutant. According to the U.S. National Library of Medicine´s Hazardous Substances Data Bank (HSDB), the widespread use of catechol in pharmaceutical and agricultural products as well as in the rubber, chemical, photographic, dye and oil industries [http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+1436 poses a risk of water contamination] through various waste water streams.
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|Behavior, Biochemistry, Enzyme(s), Hormone(s), Mortality, No Effect Coded, Physiology  
|Behavior, Biochemistry, Enzyme(s), Hormone(s), Mortality, No Effect Coded, Physiology  
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|Phytoplankton
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|Phytoplancton
|Behavior, Biochemistry, Cell(s), Intoxication, Mortality, Physiology, Population  
|Behavior, Biochemistry, Cell(s), Intoxication, Mortality, Physiology, Population  
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|-
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|Zooplankton
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|Zooplancton
|Feeding Behavior, Mortality, Population  
|Feeding Behavior, Mortality, Population  
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Due to its physical properties and the localization of its artificial contamination effects of catechol are most severe in aquatic environments [ref]. This allows our water based moss filter to target the problem at its roots. It is shown that catechol pollution has dramatic consequences for aquatic life ranging from disturbances in an organisms biochemistry all the way to anomalies in whole populations.
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Due to its physical properties, the contamination effects of catechol are most severe in aquatic environments. Our water based moss filter targets the problem at its roots. It is shown that catechol pollution has dramatic consequences for aquatic life, ranging from disturbances in individual organisms biochemistry all the way to anomalies in whole populations.
=== Current Solutions ===
=== Current Solutions ===
Today catechol can be treated by a variety of methods including treatment by bioregenerated anaerobic granular activated carbon (GAC), anaerobic biological treatment using upflow anaerobic fixed-film fixed-bed reactors as well as upflow anaerobic sludge blanket (UASB) reactors, with the latter being the most promising one.  
Today catechol can be treated by a variety of methods including treatment by bioregenerated anaerobic granular activated carbon (GAC), anaerobic biological treatment using upflow anaerobic fixed-film fixed-bed reactors as well as upflow anaerobic sludge blanket (UASB) reactors, with the latter being the most promising one.  
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Despite their decent efficiency these methods lack the applicability where they are most needed, rural areas in third world countries most affected by the pollution of the surrounding oil and gas industries. The aforementioned technologies all need skilled technicians, a constant supply of water and electricity and of course money to maintain them.
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Despite their decent efficiency, these methods lack the applicability where they are most needed: Rural areas in third world countries are the most affected by the pollution of the surrounding oil and gas industries. The aforementioned technologies all need skilled technicians, a constant supply of water and electricity and of course money to maintain them. All those factors got us to look deeper into a simpler and more cost-effective way to address those problems: Phytoremediation.
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These are all factors that got us to look deeper into a simpler and more cost-effective way to address those problems: Phytoremediation.
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=== Our Solution: A new approach with old methods ===
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=== Our Solution: A new approach using old methods ===
Further research into this topic showed that catechol was already a popular target for phytoremediation were it was degraded by ''Arabidopsis thaliana'' [[http://www.ncbi.nlm.nih.gov/pubmed/16935988 Liao et al., 2006]].
Further research into this topic showed that catechol was already a popular target for phytoremediation were it was degraded by ''Arabidopsis thaliana'' [[http://www.ncbi.nlm.nih.gov/pubmed/16935988 Liao et al., 2006]].
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After already establishing a whole new chassis and a new effector in our project we decided that we would tackle at least one problem in the original spirit of iGEM, that is taking an existing part and implement it into your own system. To do this we selected an <nowiki>RFC</nowiki> 25 - ready brick [http://parts.igem.org/Part:BBa_K648011 BBa_K648011], which was originally designed as reporter construct, and implemented it in our moss filter.
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Next to establishing a whole new chassis and a new effector in our project, we decided to tackle at least one pollutant by taking an existing part and implement it into your own system. We therefore selected the <nowiki>RFC</nowiki> 25 - ready brick [http://parts.igem.org/Part:BBa_K648011 BBa_K648011] originally designed as reporter construct, and implemented it in our moss filter.
   
   
====Catecholdioxygenase====
====Catecholdioxygenase====
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[[File:Catechol_degredation_mechanism.jpg|thumb|right|200px|'''Figure 8''': Mechanism of catechol degradation in the enzymes active site [http://www.sciencedirect.com/science/article/pii/S0969212699800069 Akiko et al. (1999)]]]
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[[File:Catechol_degredation_mechanism.jpg|thumb|right|200px|'''Figure 8''': Mechanism of catechol degradation in the enzymes active site [[http://www.sciencedirect.com/science/article/pii/S0969212699800069 Akiko et al., 1999]]]]
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The enzyme we used to degrade catechol is catechol-2,3-dioxygenase, or metapyrocatechase, from ''Pseudomonas putida''. This enzyme is a homotetramer with a non heme ferrous ion at each subunit´s active site. It belongs to the class of oxidoreductases and catalyzes an extradiol cleavage of catechol, forming the brown 2-hydroxymuconate semialdehyde which can be detected photometrically at wavelenghts of around 380-400 nm and can therefore act as a reporter of the reaction.
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The enzyme we used to degrade catechol is the catechol-2,3-dioxygenase, or metapyrocatechase, from ''Pseudomonas putida''. It is a homotetramer with a non heme ferrous ion at each subunit´s active site. It belongs to the class of oxidoreductases and catalyzes an extradiol cleavage of catechol, forming the brown 2-hydroxymuconate semialdehyde which can be detected photometrically at wavelenghts of around 380-400 nm and can therefore act as a reporter of the reaction.
====Goals====
====Goals====
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By doing this we hope to eliminate many existing problems with the practical application of catecholdegredation when using bacteria as a chassis. Namely the facts that bacteria, other than plants, are neither self-sustaining nor easy to handle for non-experts. Combined with our [https://2013.igem.org/Team:TU-Munich/Project/Killswitch red-light inducible kill-switch] we wanted to create a system which could be used nearly everywhere and by anyone and be as cheap as possible. This way we could ensure that our system would be where it is most needed and would be affordable for every community.
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We hope to eliminate many of the practical application problems of catechol degredation using bacteria as a chassis. These are e.g. that bacteria, are in contrast to plants neither self-sustaining nor easy to handle for non-experts. Combined with our [https://2013.igem.org/Team:TU-Munich/Project/Killswitch red-light inducible kill-switch], we wanted to create a system which could be used nearly everywhere and by anyone and be as cheap as possible, therefore ensuring our system to be usable where it is most needed and affordable for every community.
==Laccase (''Bacillus pumilus'')==
==Laccase (''Bacillus pumilus'')==
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===The Problem: Endocrine Disruptors in the Environment===
===The Problem: Endocrine Disruptors in the Environment===
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The concentration of Estrogens in ground water rises steadily [[http://www.ingentaconnect.com/content/wef/wefproc/2005/00002005/00000005/art00020 Okayasu et al. (2005)]], because of the increasing receipt of contraceptics based on synthetic estrogens. Ground water, cleaned by standard sewage plants, is still contaminated with microelements like Estrogens and painkillers like Diclofenac in low concentrations, causing severe endocrine disorders in animals and humans. Known consequences -  until now - are for example reduced fertility and feminization of animals living in an aquatic environment. Further on, Estrogens belong to the chemical class of Polycyclic aromatic hydrocarbons, which are charaterized by a low biodegradability and a high bioaccumulation rate.
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The concentration of Estrogens in ground water rises steadily [[http://www.ingentaconnect.com/content/wef/wefproc/2005/00002005/00000005/art00020 Okayasu et al., 2005]] due to the increasing use of contraceptics based on synthetic estrogens. Ground water cleaned by standard sewage plants is still contaminated with micropollutants like Estrogens or Diclofenac in low concentrations, causing severe endocrine disorders in animals and humans. Known consequences include reduced fertility and feminization of animals living in an aquatic environments. Estrogens belong to the chemical class of Polycyclic aromatic hydrocarbons, which are charaterized by a low biodegradability and a high bioaccumulation rate.
===Current Solutions: Ozonation, Nitrification and Denitrification===
===Current Solutions: Ozonation, Nitrification and Denitrification===
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Possible solutions to degrade Estradiol are widely spread and very ineffective until now. Researchers are continuously trying to find an effective way to degrade or biodegrade this chemical compound for example by using Ozonation, Nitrification and Denitrification.
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Possible solutions to degrade Estradiol are widely spread and very ineffective until now. Researchers are continuously trying to find a effective ways to (bio)degrade this chemical compound e.g. by Ozonation, Nitrification and Denitrification.
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Using and comparing Nitrification (aerobic conditions) and Denitrification (anaerobic conditions) [[http://www.ncbi.nlm.nih.gov/pubmed/18254398 Dytczak et al. (2008)]] the researchers concluded that '''denitrification did not work''' either but the nitrification rate seemed to be at 22%. The Nitrification rate correlated with the amount of used biomass.  
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Comparing Nitrification (aerobic conditions) and Denitrification (anaerobic conditions) [[http://www.ncbi.nlm.nih.gov/pubmed/18254398 Dytczak et al., 2008]] researchers concluded that '''denitrification did not work''' either, but the nitrification rate seemed to be at 22%, correlating with the amount of used biomass.  
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Further on the was described, where Estradiol was degraded by varying the concentration of Ozon and the pH value [[http://www.ncbi.nlm.nih.gov/pubmed/16387433 Zhang et al. (2006)]]. As described in the paper by Zhang et al., '''small molecules appeared as byproducts''', which have been responsible for a rapid shrinkage of the pH value. This means that byproducts during degradation are acidic, which may '''harm the environment''' in a significant way. Another experimental proven way of ozonating Estradiol is the use of Manganoxid and oxalic acid [[http://www.ncbi.nlm.nih.gov/pubmed/23530323 Jiang et al. (2013)]], which seems to be a promising alternative for degrading Estradiol nearly completely. Nevertheless this method will also cause accumulation of byproducts.
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Furthermore, they described the degradation of estradiol with varying ozon concentrations and pH values [[http://www.ncbi.nlm.nih.gov/pubmed/16387433 Zhang et al., 2006]]. As described in the latter paper, '''small molecules appeared as byproducts''' causing rapid pH decrease. The degradation byproducts are therefore acidic, which may significantly '''harm the environment'''. Another experimentally proven promising alternative for nearly complete Estradiol degradation is its ozonation using mangan oxide and oxalic acid [[http://www.ncbi.nlm.nih.gov/pubmed/23530323 Jiang et al., 2013]]. This method nevertheless causes accumulation of byproducts.
===Bielefeld 2012 Solution: BPUL Laccase===
===Bielefeld 2012 Solution: BPUL Laccase===
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[[File:17_Beta_Estradiol_Laccase.png|thumb|right|400px|'''Figure 9:''' Mechanism of Estradiol degradation in the enzymes active site.]]
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All derivates of estrogen are polycyclic aromatic hydrocarbons, which are hard and not cost effectively removable by standardized purification methods in sewage plants. One possible biodegradation solution of these polycyclic aromatic hydrocarbons -envisioned by the 2012 iGEM Team Bielefeld- is the laccase, a well characterized and widely used protein, that is stable in many varying environmental conditions. Its substrate spectrum allows a broad range of applications, including biodegrading estradiol, estrone, ethinyl estradiol, diclofenac, naphthalene and anthracene.  
 +
[[File:17_Beta_Estradiol_Laccase.png|thumb|left|435px|'''Figure 9:''' Mechanism of estradiol degradation in the enzymes active site]]
 +
[[File:17_Beta_Ethinylestradiol_Laccase.png|thumb|right|435px|'''Figure 10:''' Mechanism of 17-Beta-Ethinylestradiol degradation in the enzymes active site]]
 +
 +
[[File:Diclofenac.png|thumb|left|435px|'''Figure 11:''' Mechanism of diclofenac degradation at the enzyme´s active site]]
-
All derivates of Estrogen are Polycyclic aromatic hydrocarbons, which are hard and non cost effective removable by standardized purification methods in sewage plants. One possible sollution to biodegrade these Polycyclic aromatic hydrocarbons envisioned by the 2012 iGEM Team from Bielefeld is the Laccase, which is a well characterized, widely used and solid protein while environmental conditions are varying. Its substrate spectrum promises a broad range of applications, especially biodegrading Estradiol, Estrone, Ethinyl estradiol, Diclofenac, Naphthalene and Anthracene.
 
-
[[File:Diclofenac.png|thumb|left|450px|'''Figure 10:''' Mechanism of Diclofenac degradation in the enzymes active site.]]
 
-
[[File:17_Beta_Ethinylestradiol_Laccase.png|thumb|right|400px|'''Figure 11:''' Mechanism of 17-Beta-Ethinylestradiol degradation in the enzymes active site.]]
 
-
<br>
 
-
<br>
 
-
<br>
 
====General Information on Laccases====
====General Information on Laccases====
-
Laccases are implicated in a wide spectrum of biological activities and, in particular, play a key role in morphogenesis, development and lignin metabolism in fungi, bacteria and plants. For example, they are necessary to degrade lignin in Basidiomycetes and synthesize complex polymers like Melanin in Ascomycentes. Laccases belong to the [http://www.chem.qmul.ac.uk/iubmb/enzyme/ enzyme class of Oxidoreductases (EC 1.10.3.2)]. They are also known as monophenolic Oxidases, because of their substrate specifity. It is widely believed that Laccases are the simpliest representatives of the ubiquitous blue multi-copper oxidase family. Laccases are extracellular enzymes consiststing usually of 15-20 % carbon-hydrogen. Their molecular weight ranges deglycated from 60 to 80 kDa. Further on Laccases can occur as monomers, dimers, trimers and tetramers.
+
Laccases are implicated in a wide spectrum of biological activities and, in particular, play a key role in morphogenesis, development and lignin metabolism in fungi, bacteria and plants. For example, they are necessary to degrade lignin in ''Basidiomycetes'' and synthesize complex polymers like melanin in ''Ascomycentes''. Laccases belong to the [http://www.chem.qmul.ac.uk/iubmb/enzyme/ enzyme class of Oxidoreductases (EC 1.10.3.2)]. They are also known as monophenolic Oxidases, because of their substrate specifity. It is widely believed that laccases are the simpliest representatives of the ubiquitous blue multi-copper oxidase family. Laccases are extracellular enzymes consiststing usually of 15-20 % carbon-hydrogen. Their molecular weight ranges deglycated from 60 to 80 kDa. Further on, laccases can occur as monomers, dimers, trimers and tetramers.
====Active site and catalyzed reaction====
====Active site and catalyzed reaction====
-
[[File:Laccase_Copperoxidase.gif|thumb|right|435px|'''Figure 12:''' Model of the active site of the Laccase as a Metalloprotease.]]
+
[[File:Laccase_Copperoxidase.gif|thumb|right|435px|'''Figure 12:''' Model of the active site of the laccase metalloprotease]]
-
The specific blue copper ions in the active site of Laccases are essential for the enzyme mediated radical oxidation of phenolic groups. In general, Laccases catalyze the linked oxidation of many aromatic and phenolic substances while the phenolic group is oxidized to a radical and oxygen is reduced to a hydrate.
+
The specific blue copper ions in the active site of laccases are essential for the enzyme mediated radical oxidation of phenolic groups. In general, laccases catalyze the linked oxidation of many aromatic and phenolic substances while the phenolic group is oxidized to a radical and oxygen is reduced to a hydrate.
-
The active site of the enzyme includes a four-copper-ion-cluster which can be detected by using Spectroscopy. The cluster consists of one type 1 blue copper-ion, one type 2 and two type 3 copper-ions. In this reaction the electron from the oxidation is transfered to the other three copper ions. These ions form a trinuclearic cluster, which transfers electrons to the terminal electron acceptor oxygen. In the end, molecular oxygen is reduced, by receiving four electrons, to water.
+
The active site of the enzyme includes a four-copper-ion-cluster which can be detected by using spectroscopy. The cluster consists of one type 1 blue copper-ion, one type 2 and two type 3 copper-ions. In this reaction the electron from the oxidation is transfered to the other three copper ions. These ions form a trinuclearic cluster, which transfers electrons to the terminal electron acceptor oxygen. In the end, molecular oxygen is reduced, by receiving four electrons, to water.
====Possible applications of Laccases====
====Possible applications of Laccases====
-
Due to their ability to oxidize phenolic and nonphenolic lignin related compounds, as well as highly recalcitrant environmental pollutants, Laccases possess a high potential as a bioremediation agent in synthetic biology. Waste water from hospitals, textile and paper industry, as well as in sewage treatment plants can be detoxified. Possible substrates may be natural and synthetic Estrogens, Xenoestrogens and polycylic aromatic hydrocarbons. Laccases may also be used to degrade high polymeric Lignin to make use of the polymer for energy generation. Carcinogenic, mutagenic aromatic hydrocarbons and estrogens, xenoestrogens and polycyclic aromatic hydrocarbons can be oxidized and detoxified by laccases, too. In addition to   that, Laccases can oxidize up herbicides, pesticides in soil.
+
Due to their ability to oxidize phenolic and nonphenolic lignin related compounds, as well as highly recalcitrant environmental pollutants, laccases possess a high potential as a bioremediation agent in synthetic biology. Waste water from hospitals, textile and paper industry, as well as in sewage treatment plants can be detoxified. Possible substrates may be natural and synthetic estrogens, xenoestrogens and polycylic aromatic hydrocarbons. Laccases may also be used to degrade high polymeric lignin to make use of the polymer for energy generation. Carcinogenic, mutagenic aromatic hydrocarbons and estrogens, xenoestrogens and polycyclic aromatic hydrocarbons can be oxidized and detoxified by laccases, too. In addition to that, laccases can oxidize up herbicides, pesticides in soil.
-
====Laccase BPUL from Bacillus Pumilus [http://parts.igem.org/Part:BBa_K863000?title=Part:BBa_K863000 BBa_K863000]====
+
====Laccase BPUL from ''Bacillus Pumilus'' [http://parts.igem.org/Part:BBa_K863000?title=Part:BBa_K863000 BBa_K863000]====
-
In this project, we used the BPUL Laccase from Bacillus Pumilus [http://parts.igem.org/Part:BBa_K863000?title=Part:BBa_K863000 BBa_K863000], which was established and well characterized by the [https://2012.igem.org/Team:Bielefeld-Germany iGEM Team of Bielefeld in 2012 ]. The Laccase, which was prepared and sent to the Parts Registry by the team of Bielefeld was fused to a Histag and a Ribosome Binding Site. The molecular weight of this Laccase is 58.6 kDa. Comparing the enzyme activity between 25°C and 10°C, you can see that it is influenced marginal, but it slightly decreases. Its pH optimum is reached at pH 4 to 5. The differences in activity varying the concentration of CuCl2, differ minimal. An optimum is reached at 0.6 mM. An increase of the Concentration of CuCl2 decreases the enzyme activity of the Laccase. The lower the used concentration of MeOH and Acetonitrile was, the higher the enzyme activity was detected. Bielefeld established many different Laccases in iGEM 2012, but we chose this one, because it seemed to be the most effective one, they have characterized.
+
In this project, we used the BPUL laccase from ''Bacillus pumilus'' [http://parts.igem.org/Part:BBa_K863000?title=Part:BBa_K863000 BBa_K863000], which was established and well characterized by the [https://2012.igem.org/Team:Bielefeld-Germany iGEM Team of Bielefeld in 2012]. The laccase, which was prepared and sent to the Parts Registry by the team of Bielefeld was fused to a histag and a ribosome binding site. The molecular weight of this Laccase is 58.6 kDa. Comparing the enzyme activity between 25°C and 10°C, you can see that it is influenced marginal, but it slightly decreases. Its pH optimum is reached at pH 4 to 5. The differences in activity varying the concentration of CuCl2, differ minimal. An optimum is reached at 0.6 mM. An increase of the concentration of CuCl2 decreases the enzyme activity of the laccase. The lower the used concentration of MeOH and acetonitrile was, the higher the enzyme activity was detected. Bielefeld established many different Laccases in iGEM 2012, but we chose this one, because it seemed to be the most effective one, they have characterized.
==References:==
==References:==
<!-- Kopiervorlagen -->
<!-- Kopiervorlagen -->
 +
[[http://www.epa.gov/oust/cat/tumgloss.htm U.S. Environmental Protection Agency, 2009]] EPA definition of BioDegradation
 +
 +
[[http://www.blac.de/servlet/is/2146/P-2c.pdf BLAC, 2003]] Report on pharmaceuticals in the environment
 +
 +
[[http://www.who.int/infectious-disease-report/2000/ World Health Organization, 2000]] Infectious Diseases Report
 +
 +
[[http://www.ecdc.europa.eu/en/publications/Publications/0909_TER_The_Bacterial_Challenge_Time_to_React.pdf ECDC/EMEA joint technical report 2009]] The bacterial challenge: time to react
 +
 +
[[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2937522/ Davies and Davies, 2010]] Origins and Evolution of Antibiotic Resistance. ''Microbioly and Molecular Biology Reviews'', 74(3): 417–433
 +
 +
[[http://www.umweltbundesamt.at/fileadmin/site/publikationen/REP0258.pdf Clara, Gans, Humer et al, 2010]] Federal austrian environmental agency report on antibiotics in the ground water
 +
 +
[[http://www.blac.de/servlet/is/2146/P-2c.pdf German national committee for chemical safety (BLAC) report, Rohweder, 2003]] Antibiotics in the environment
 +
 +
[[http://antibiotics.toku-e.com/a/ The antimicrobial index]]
 +
 +
[[http://www.watereuse.org/files/images/91051.pdf Sedlak, Pinkston, Huang, 2005]] Occurrence survey of pharmaceutically active compounds, WateReuse foundation
 +
 +
[[http://faculty.tamucc.edu/plarkin/4292folder/Ab%20resistance%20-%20enzymatic.pdf Wright, 2005]] Bacterial resistance to antibiotics: Enzymatic degradation and modification, ''Advanced Drug Delivery Reviews'', 57: 1451–1470
 +
 +
[[http://pubs.acs.org/doi/abs/10.1021/bi201790u?mi=0&af=R&pr... Morar et al., 2012]] Mechanism and Diversity of the Erythromycin Esterase Family of Enzymes, ''Biochemistry'', 51(8): 1740–1751
 +
 +
[[http://cid.oxfordjournals.org/content/46/2/155.long Spellberg et al. 2008]] The Epidemic of Antibiotic-Resistant Infections: A Call to Action for the Medical Community from the Infectious Diseases Society of America, ''Clinical Infectious Diseases'', 46(2): 155-164
 +
 +
[[http://www.neeri.res.in/project_details.php?PID=261&DIV=38 Ministry of Environment and Forest]]
 +
 +
[[http://water.epa.gov/scitech/swguidance/standards/criteria/health/phenol_index.cfm EPA]] about Phenolderivatives
 +
 +
[[http://www.epa.gov/ttnatw01/hlthef/pyrocate.html EPA]] about Phenol
 +
 +
[[http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+1436 HSDB]] about Catechol
 +
 +
[[http://www.ncbi.nlm.nih.gov/pubmed/16935988 Liao et al., 2006]] The key role of chlorocatechol 1,2-dioxygenase in phytoremoval and degradation of catechol by transgenic Arabidopsis
 +
 +
[[http://www.ncbi.nlm.nih.gov/pubmed/12126701 Mayer, Staples, 2002]] Laccase: new functions for an old enzyme, ''Phytochemistry'', 60(6):551-65
 +
 +
[[http://www.ncbi.nlm.nih.gov/pubmed/15036303 Claus, 2004]] Laccases: structure, reactions, distribution, ''Micron.'', 2004;35(1-2):93-6
 +
 +
[[http://www.ncsu.edu/bioresources/BioRes_04/BioRes_04_4_1694_Madhavi_Lele_Laccase_Properties_Applications_Review_567.pdf Madhavi and Lele, 2009]] Laccase properties, use, ''Bioresources'', 4(4), 1694-1717
 +
 +
[[http://www.ingentaconnect.com/content/wef/wefproc/2005/00002005/00000005/art00020 Okayasu et al., 2005]] Degradation of Free Estrogens and their Conjugates in Wastewater Treatment Process, ''Proceedings of the Water Environment Federation, Technology 2005''  291-297(7)
 +
 +
[[http://www.ncbi.nlm.nih.gov/pubmed/18254398 Dytczak, Londry, Oleszkiewicz, 2008]] Biotransformation of estrogens in nitrifying activated sludge under aerobic and alternating anoxic/aerobic conditions, ''Water Environ Res.'' 2008 Jan;80(1):47-52
 +
 +
[[http://www.ncbi.nlm.nih.gov/pubmed/16387433 Zhang et al., 2006]] Degradation of 17-ethinylestradiol in aqueous solution by ozonation, ''Journal of Hazardous Materials'' 291–298
-
[[http://www.rsc.org/chemistryworld/2013/03/antibiotic-resistance-ticking-time-bomb Antibiotic resistance is a `ticking time bomb`]] Stafford, N. (2013). Antibiotic resistance is a `ticking time bomb`. ''Advancing the chemical sciences''.<br>
+
[[http://www.ncbi.nlm.nih.gov/pubmed/23530323 Jiang et al., 2013]] Degradation of 17beta-estradiol in aqueous solution by ozonation in the presence of manganese(II) and oxalic acid. ''Environ Technol.'' 2013 Jan-Feb;34(1-4):131-8
-
[[http://www.who.int/infectious-disease-report/2000/ WHO report 2000]] World Health Organization Report on Infectious Diseases (2000).<br>
+
-
[[http://www.ecdc.europa.eu/en/publications/Publications/0909_TER_The_Bacterial_Challenge_Time_to_React.pdf ECDC/EMEA joint technical report 2009]] The bacterial challenge: time to react. ECDC/EMEA joint technical report (2009).<br>
+
-
[[http://www.umweltbundesamt.at/fileadmin/site/publikationen/REP0258.pdf report on antibiotics in ground water, 2010]] Clara M., Gans O., Humer F., et al (2010). Antibiotics in ground water. Federal austrian environmental agency report. Vienna<br>
+
-
[[http://www.blac.de/servlet/is/2146/P-2c.pdf report on antibiotics in the .environment, 2003]] Rohweder, U. (2003). Antibiotics in the environment. German national committee for chemical safety (BLAC).<br>
+
-
[[http://antibiotics.toku-e.com/a/ The antimicrobial index]]<br>
+
-
[[http://www.watereuse.org/files/images/91051.pdf Occurrence survey of pharmaceutically active compounds (2005)]] Sedlak, D., Pinkston, K., Huang, C. (2005). Occurrence survey of pharmaceutically active compounds. WateReuse foundation.<br>
+
-
[[http://faculty.tamucc.edu/plarkin/4292folder/Ab%20resistance%20-%20enzymatic.pdf Wright, 2005]] Wright, G. (2005). Bacterial resistance to antibiotics: Enzymatic degradation and modification. ''Advanced Drug Delivery Reviews'', 57: 1451–1470.<br>
+
-
[[http://pubs.acs.org/doi/abs/10.1021/bi201790u?mi=0&af=R&pr... Wright et al., 2012]] Morar, M., Pengelly, K., Koteva, K. and Wright, D. (2012). Mechanism and Diversity of the Erythromycin Esterase Family of Enzymes. ''Biochemistry'', 51(8): 1740–1751.<br>
+
-
[[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2937522/ Davies and Davies, 2010]] Davies, J. and Davies, D. (2010). Origins and Evolution of Antibiotic Resistance. ''Microbioly and Molecular Biology Reviews'', 74(3): 417–433.<br>
+
-
[[http://cid.oxfordjournals.org/content/46/2/155.long Spellberg et al. 2008]] Spellberg et al. (2008). The Epidemic of Antibiotic-Resistant Infections: A Call to Action for the Medical Community from the Infectious Diseases Society of America. ''Clinical Infectious Diseases'', 46(2): 155-164.<br>
+
-
[[http://www.neeri.res.in/project_details.php?PID=261&DIV=38 Ministry of Environment and Forest]]<br>
+
-
[[http://water.epa.gov/scitech/swguidance/standards/criteria/health/phenol_index.cfm EPA about Phenolderivatives]]<br>
+
-
[[http://www.epa.gov/ttnatw01/hlthef/pyrocate.html EPA about Phenol]]<br>
+
-
[[http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+1436 HSDB about Catechol]]<br>
+
-
[[http://www.ncbi.nlm.nih.gov/pubmed/16935988 Liao et al., 2006]] Liao Y, Zhou X, Yu J, Cao Y, Li X, Kuai B. (2006).<br> The key role of chlorocatechol 1,2-dioxygenase in phytoremoval and degradation of catechol by transgenic Arabidopsis.<br>
+
-
[[http://www.ncbi.nlm.nih.gov/pubmed/12126701 Mayer AM, Staples RC, 2002]] Mayer AM, Staples RC (2002). Laccase: new functions for an old enzyme. ''Phytochemistry'', 60(6):551-65.<br>
+
-
[[http://www.ncbi.nlm.nih.gov/pubmed/15036303 Claus H.2004]] Claus H. (2004). Laccases: structure, reactions, distribution. ''Micron.'', 2004;35(1-2):93-6.<br>
+
-
[[http://www.ncsu.edu/bioresources/BioRes_04/BioRes_04_4_1694_Madhavi_Lele_Laccase_Properties_Applications_Review_567.pdf Madhavi and Lele (2009)]] Madhavi and Lele (2009). Laccase properties, use. ''Bioresources'', 4(4), 1694-1717.<br>
+
-
[[http://www.ingentaconnect.com/content/wef/wefproc/2005/00002005/00000005/art00020 Okayasu et al. (2005)]] Degradation of Free Estrogens and their Conjugates in Wastewater Treatment Process. ''Proceedings of the Water Environment Federation, Technology 2005''  291-297(7)<br>
+
-
[[http://www.ncbi.nlm.nih.gov/pubmed/18254398 Dytczak MA, Londry KL, Oleszkiewicz JA (2008)]] Biotransformation of estrogens in nitrifying activated sludge under aerobic and alternating anoxic/aerobic conditions. ''Water Environ Res.'' 2008 Jan;80(1):47-52.<br>
+
-
[[http://www.ncbi.nlm.nih.gov/pubmed/16387433 Zhang et al. (2006)]] Degradation of 17-ethinylestradiol in aqueous solution by ozonation. ''Journal of Hazardous Materials'' 291–298<br>
+
-
[[http://www.ncbi.nlm.nih.gov/pubmed/23530323 Jiang et al. (2013)]] Degradation of 17beta-estradiol in aqueous solution by ozonation in the presence of manganese(II) and oxalic acid. ''Environ Technol.'' 2013 Jan-Feb;34(1-4):131-8.<br>
+
<!-- Ende des Inhalts -->
<!-- Ende des Inhalts -->

Latest revision as of 02:40, 29 October 2013


BioDegradation of Xenobiotics

Figure 1: Concentration of pharmaceuticals in Waste water treatment plant (WWTP) effluents (top) and surface water (bottom) [BLAC]

Biodegradation is defined as "a process by which (microbial) organisms transform or alter the structure of chemicals introduced into the environment" [U.S. Environmental Protection Agency, 2009]. We work with this concept by degrading or transforming noxious substances in waste water into non-hazardous compounds. These substances, such as antibiotics, hormones or pesticides are not removed by common waste water treatment plants because current methods such as active carbon and ozonization are expensive and energy-intensive. But it is possible to inactivate them with existing enzymes from natural catabolic mechanisms in different microorganisms. To utilize these enzymes, we integrated them into a plant as a self-sustaining, sedentary organism to create a functional water filter system. To illustrate this approach, we chose three potent enzymes:

  • The Erythromycin esterase, which degrades macrolides, a persistant group of antibiotics
  • The Laccase BPUL, which degrades several noxious substances, for example the artificial hormone ethinyl estradiol, the main ingredient of contraceptive pills
  • The Catechol-2,3-dioxygenase, catalyzing the degradation of aromatic pollutants, which occur in pesticides and insecticides
Figure 2: Principle of biodegradation

Erythromycin Esterase (EreB)

The Problem: Antibiotics in the environment

Figure 3: Causality chain of increasing antibiotic use

The discovery of antibiotics in the early 20th century has revolutionized the fight against infectious diseases. Due to their success, thousands of tons of antibiotics have been produced, consumed and excreted into the environment. Since antibiotics are designed to circulate through the body for a long time, up to 75% of the administered doses leaves the organism unaltered. As a result, microbes are exposed to a strong selective pressure to which these extremely adaptable organisms react by developing resistance mechanisms.

However, antimicrobial effectiveness is a precious, limited resource, that we can no longer do without. Accordingly, in 2000 a World Health Organization report focused on antibiotic resistance as one of the most critical human health challenges of the next century and called for “a global strategy to contain resistance”. The WHO estimates that resistant pathogens affect 2 million Americans each year, of which 14,000 die as a result. In the EU, antimicrobial resistance is responsible for 25,000 deaths every year and the annual treatment and social costs have been estimated at some €1.5 billion [ECDC/EMEA joint technical report 2009]. These numbers will rise if nothing is done to prevent precious antibiotics from loosing their effect on microbes. [Davies and Davies, 2010]

Current Solutions

Figure 4: Timeline of developments since the discovery of antibiotics
Figure 5: Development of new antimirobial agents over the years

The obvious approach to minimize selective pressure on microorganisms is to deal with the problem of carefree, often precautionary overuse of antibiotics, not only in humans but especially in animal breeding, by only using them when absolutely necessary.

Furthermore research on new antibiotics needs to be hugely intensified to create alternative agents and keep pace with the formation of antimicrobial resistance. Unfortunately, antibiotic development has slowed dramatically over the past 25 years, since as a short-course and highly effective therapy, they have a much lower rate of return on investment than other drugs and are therefore financially not very viable for pharmaceutical companies. The development costs per approved agent are estimated to be between $400-$800 million. In 2004, only 5 new antibacterial agents were under development by the largest pharmaceutical companies, barely beating the 4 new molecular entities to treat erectile dysfunction. [Davies and Davies, 2010]

These two options are difficult to accomplish due to the increasing need of antibiotics with a growing world-wide population and the fact that finding new antibiotics is a costly, long-term and extremely difficult project. Therefore we focus on a third option to fight the spread of antibiotic resistance: The development of a cost-effective water-filter that will prevent continuous inflow of the drugs into surface water and thus reduce the selective pressure on microbes.

Our Solution: EreB

In our search for a suitable enzyme we looked at antibiotic concentrations in waste water. There have not yet been many investigations on this topic, but one of the main surveys was executed by the German national committee for chemical safety (BLAC) of 202 effluent samples from 34 waste water treatment plants (WWTP). The result was that the main detectable antibiotics are the macrolides Erythromycin, Roxythromycin and Clarithromycin, the Sulfonamide Sulfamethoxalol as well as the Fluoroquinolone Ciprofloxacin. Most concentrations are about 100 ng/l, but maximum concentrations reached more than 3 µg/l. The often prescribed ß-lactam antibiotics, such as penicillin, were not detectable probably due to their fast degradation. Another important conclusion of the study is, that the main source of antibiotic input into the aquatic environment is municipal waste water. Similar results were found in other countries (see Table 1).

Table 1: Antibiotics in WWTP effluents, [environmental agency austria], [antimicrobial index]
Antibiotic max. concentration [µg/l] found in different countries min MIC50[µg/l]
Ciprofloxacin (fluoroquinolone) 0.14 (D), 0.18 (USA), 0.74 (N) 3
Clarithromycin (macrolide) 1.00 (D), 0.30 (CH) 2
Erythromycin (macrolide) 1.10 (D), 0.17 (USA), 0.29 (CH), 2 (China) 4
Roxythromycin (macrolide) 1.00 (D), 0.28 (China) 15
Sulfamethoxalol (sulfonamide) 4.00 (D), 1.40 (USA) 60
Trimethoprim (diaminopyrimidine) 1.50 (D), 1.20 (USA), 1.30 (N) 120

Now we compared the concentrations of the most frequent antibiotics found in WWTP effluents to the minimum inhibitory concentration (MIC50) at which the growth of at least 50% of bacterial strains are inhibited. The MIC50 depends on the species. In the table the smallest MIC50 over all species is given, indicating the level at which the contamination seriously affects the microbiological system and therefore carrying out a certain stress which gives resistant individuals an increased selective advantage.

Figure 6: Ester hydrolysis of erythromycin by EreB [Morar et al., 2012]

Our conclusion from these data was that macrolides are a hazardous antibiotic class, from which several representatives are found in WWTP effluents and surface water in concentrations relatively close to their MIC50. Macrolides are important and clinically relevant agents used to treat infectious diseases, first introduced into clinics in 1952 as an alternative to penicillin. Today they are mainly applied for treatment of respiratory diseases, including pneumonia, the leading cause of childhood deaths worldwide. The drug functions by inhibiting protein biosynthesis when it binds to the exit tunnel of the 50S ribosomal subunit which leads to abortion of the growth of nascent peptide chains. Macrolides can be enzymatically inactivated with the macrolide esterases EreA and EreB, from which we chose EreB as our model enzyme since it has a broader degradation spectrum than EreA and is not metal-dependent.

Figure 7: Degradation mechanism of erythromyine. The ester hydrolysis catalyzed by the erythromycine esterase B is followed by a hemiketal formation and a condensation. Hence the educt and the product have the same molecular mass.

EreB is a cytoplasmic protein, originally discovered in E. coli on an exogeneous plasmid, that belongs to the hydrolase superfamily catalyzing the opening of the macrolactone ring, that is characteristic for macrolides. After the enzymatic opening of this cyclic ester bond a non-enzymatic hemiketal formation takes place followed by condensation and dehydration. The only co-substrate needed by the enzyme for hydrolysis is water which also makes it a suitable candidate for our moss-filter.

More information on the enzyme can be found for example in a very detailed recently published paper by [Wright et al., 2012], whose group also generously provided us with the plasmid DNA.

Catechol Dioxygenase (xylE)

Catechol: A growing concern

As ever more third world countries around the globe experience a rapid industrialization without establishing proper environmental practices as well as big companies outsourcing their production facilities in order to avoid expensive sewage treatment the problem of water pollution is more urgent then ever. The Ministry of Environment and Forest, Government of India and EPA have listed phenol and phenolic compounds as priority pollutants. In this context, a derivative of benzene, the phenolic compund catechol, or 1,2-dihydroxybenzene, has been deemed to be a very toxic pollutant. According to the U.S. National Library of Medicine´s Hazardous Substances Data Bank (HSDB), the widespread use of catechol in pharmaceutical and agricultural products as well as in the rubber, chemical, photographic, dye and oil industries poses a risk of water contamination through various waste water streams.

Table 2: Impact of catechol on aquatic ecosystems
Organism group Observed effects of catechol on
AquaticPlants Biochemistry, Cell(s), Population
Crustaceans Mortality
Fish Behavior, Biochemistry, Enzyme(s), Hormone(s), Mortality, No Effect Coded, Physiology
Phytoplancton Behavior, Biochemistry, Cell(s), Intoxication, Mortality, Physiology, Population
Zooplancton Feeding Behavior, Mortality, Population

Due to its physical properties, the contamination effects of catechol are most severe in aquatic environments. Our water based moss filter targets the problem at its roots. It is shown that catechol pollution has dramatic consequences for aquatic life, ranging from disturbances in individual organisms biochemistry all the way to anomalies in whole populations.

Current Solutions

Today catechol can be treated by a variety of methods including treatment by bioregenerated anaerobic granular activated carbon (GAC), anaerobic biological treatment using upflow anaerobic fixed-film fixed-bed reactors as well as upflow anaerobic sludge blanket (UASB) reactors, with the latter being the most promising one. Despite their decent efficiency, these methods lack the applicability where they are most needed: Rural areas in third world countries are the most affected by the pollution of the surrounding oil and gas industries. The aforementioned technologies all need skilled technicians, a constant supply of water and electricity and of course money to maintain them. All those factors got us to look deeper into a simpler and more cost-effective way to address those problems: Phytoremediation.

Our Solution: A new approach using old methods

Further research into this topic showed that catechol was already a popular target for phytoremediation were it was degraded by Arabidopsis thaliana [Liao et al., 2006]. Next to establishing a whole new chassis and a new effector in our project, we decided to tackle at least one pollutant by taking an existing part and implement it into your own system. We therefore selected the RFC 25 - ready brick BBa_K648011 originally designed as reporter construct, and implemented it in our moss filter.

Catecholdioxygenase

Figure 8: Mechanism of catechol degradation in the enzymes active site [Akiko et al., 1999]

The enzyme we used to degrade catechol is the catechol-2,3-dioxygenase, or metapyrocatechase, from Pseudomonas putida. It is a homotetramer with a non heme ferrous ion at each subunit´s active site. It belongs to the class of oxidoreductases and catalyzes an extradiol cleavage of catechol, forming the brown 2-hydroxymuconate semialdehyde which can be detected photometrically at wavelenghts of around 380-400 nm and can therefore act as a reporter of the reaction.

Goals

We hope to eliminate many of the practical application problems of catechol degredation using bacteria as a chassis. These are e.g. that bacteria, are in contrast to plants neither self-sustaining nor easy to handle for non-experts. Combined with our red-light inducible kill-switch, we wanted to create a system which could be used nearly everywhere and by anyone and be as cheap as possible, therefore ensuring our system to be usable where it is most needed and affordable for every community.

Laccase (Bacillus pumilus)

The Problem: Endocrine Disruptors in the Environment

The concentration of Estrogens in ground water rises steadily [Okayasu et al., 2005] due to the increasing use of contraceptics based on synthetic estrogens. Ground water cleaned by standard sewage plants is still contaminated with micropollutants like Estrogens or Diclofenac in low concentrations, causing severe endocrine disorders in animals and humans. Known consequences include reduced fertility and feminization of animals living in an aquatic environments. Estrogens belong to the chemical class of Polycyclic aromatic hydrocarbons, which are charaterized by a low biodegradability and a high bioaccumulation rate.

Current Solutions: Ozonation, Nitrification and Denitrification

Possible solutions to degrade Estradiol are widely spread and very ineffective until now. Researchers are continuously trying to find a effective ways to (bio)degrade this chemical compound e.g. by Ozonation, Nitrification and Denitrification.

Comparing Nitrification (aerobic conditions) and Denitrification (anaerobic conditions) [Dytczak et al., 2008] researchers concluded that denitrification did not work either, but the nitrification rate seemed to be at 22%, correlating with the amount of used biomass.

Furthermore, they described the degradation of estradiol with varying ozon concentrations and pH values [Zhang et al., 2006]. As described in the latter paper, small molecules appeared as byproducts causing rapid pH decrease. The degradation byproducts are therefore acidic, which may significantly harm the environment. Another experimentally proven promising alternative for nearly complete Estradiol degradation is its ozonation using mangan oxide and oxalic acid [Jiang et al., 2013]. This method nevertheless causes accumulation of byproducts.

Bielefeld 2012 Solution: BPUL Laccase

All derivates of estrogen are polycyclic aromatic hydrocarbons, which are hard and not cost effectively removable by standardized purification methods in sewage plants. One possible biodegradation solution of these polycyclic aromatic hydrocarbons -envisioned by the 2012 iGEM Team Bielefeld- is the laccase, a well characterized and widely used protein, that is stable in many varying environmental conditions. Its substrate spectrum allows a broad range of applications, including biodegrading estradiol, estrone, ethinyl estradiol, diclofenac, naphthalene and anthracene.

Figure 9: Mechanism of estradiol degradation in the enzymes active site
Figure 10: Mechanism of 17-Beta-Ethinylestradiol degradation in the enzymes active site
Figure 11: Mechanism of diclofenac degradation at the enzyme´s active site


General Information on Laccases

Laccases are implicated in a wide spectrum of biological activities and, in particular, play a key role in morphogenesis, development and lignin metabolism in fungi, bacteria and plants. For example, they are necessary to degrade lignin in Basidiomycetes and synthesize complex polymers like melanin in Ascomycentes. Laccases belong to the enzyme class of Oxidoreductases (EC 1.10.3.2). They are also known as monophenolic Oxidases, because of their substrate specifity. It is widely believed that laccases are the simpliest representatives of the ubiquitous blue multi-copper oxidase family. Laccases are extracellular enzymes consiststing usually of 15-20 % carbon-hydrogen. Their molecular weight ranges deglycated from 60 to 80 kDa. Further on, laccases can occur as monomers, dimers, trimers and tetramers.

Active site and catalyzed reaction

File:Laccase Copperoxidase.gif
Figure 12: Model of the active site of the laccase metalloprotease

The specific blue copper ions in the active site of laccases are essential for the enzyme mediated radical oxidation of phenolic groups. In general, laccases catalyze the linked oxidation of many aromatic and phenolic substances while the phenolic group is oxidized to a radical and oxygen is reduced to a hydrate. The active site of the enzyme includes a four-copper-ion-cluster which can be detected by using spectroscopy. The cluster consists of one type 1 blue copper-ion, one type 2 and two type 3 copper-ions. In this reaction the electron from the oxidation is transfered to the other three copper ions. These ions form a trinuclearic cluster, which transfers electrons to the terminal electron acceptor oxygen. In the end, molecular oxygen is reduced, by receiving four electrons, to water.

Possible applications of Laccases

Due to their ability to oxidize phenolic and nonphenolic lignin related compounds, as well as highly recalcitrant environmental pollutants, laccases possess a high potential as a bioremediation agent in synthetic biology. Waste water from hospitals, textile and paper industry, as well as in sewage treatment plants can be detoxified. Possible substrates may be natural and synthetic estrogens, xenoestrogens and polycylic aromatic hydrocarbons. Laccases may also be used to degrade high polymeric lignin to make use of the polymer for energy generation. Carcinogenic, mutagenic aromatic hydrocarbons and estrogens, xenoestrogens and polycyclic aromatic hydrocarbons can be oxidized and detoxified by laccases, too. In addition to that, laccases can oxidize up herbicides, pesticides in soil.

Laccase BPUL from Bacillus Pumilus BBa_K863000

In this project, we used the BPUL laccase from Bacillus pumilus BBa_K863000, which was established and well characterized by the iGEM Team of Bielefeld in 2012. The laccase, which was prepared and sent to the Parts Registry by the team of Bielefeld was fused to a histag and a ribosome binding site. The molecular weight of this Laccase is 58.6 kDa. Comparing the enzyme activity between 25°C and 10°C, you can see that it is influenced marginal, but it slightly decreases. Its pH optimum is reached at pH 4 to 5. The differences in activity varying the concentration of CuCl2, differ minimal. An optimum is reached at 0.6 mM. An increase of the concentration of CuCl2 decreases the enzyme activity of the laccase. The lower the used concentration of MeOH and acetonitrile was, the higher the enzyme activity was detected. Bielefeld established many different Laccases in iGEM 2012, but we chose this one, because it seemed to be the most effective one, they have characterized.

References:

[U.S. Environmental Protection Agency, 2009] EPA definition of BioDegradation

[BLAC, 2003] Report on pharmaceuticals in the environment

[World Health Organization, 2000] Infectious Diseases Report

[ECDC/EMEA joint technical report 2009] The bacterial challenge: time to react

[Davies and Davies, 2010] Origins and Evolution of Antibiotic Resistance. Microbioly and Molecular Biology Reviews, 74(3): 417–433

[Clara, Gans, Humer et al, 2010] Federal austrian environmental agency report on antibiotics in the ground water

[German national committee for chemical safety (BLAC) report, Rohweder, 2003] Antibiotics in the environment

[The antimicrobial index]

[Sedlak, Pinkston, Huang, 2005] Occurrence survey of pharmaceutically active compounds, WateReuse foundation

[Wright, 2005] Bacterial resistance to antibiotics: Enzymatic degradation and modification, Advanced Drug Delivery Reviews, 57: 1451–1470

[Morar et al., 2012] Mechanism and Diversity of the Erythromycin Esterase Family of Enzymes, Biochemistry, 51(8): 1740–1751

[Spellberg et al. 2008] The Epidemic of Antibiotic-Resistant Infections: A Call to Action for the Medical Community from the Infectious Diseases Society of America, Clinical Infectious Diseases, 46(2): 155-164

[Ministry of Environment and Forest]

[EPA] about Phenolderivatives

[EPA] about Phenol

[HSDB] about Catechol

[Liao et al., 2006] The key role of chlorocatechol 1,2-dioxygenase in phytoremoval and degradation of catechol by transgenic Arabidopsis

[Mayer, Staples, 2002] Laccase: new functions for an old enzyme, Phytochemistry, 60(6):551-65

[Claus, 2004] Laccases: structure, reactions, distribution, Micron., 2004;35(1-2):93-6

[Madhavi and Lele, 2009] Laccase properties, use, Bioresources, 4(4), 1694-1717

[Okayasu et al., 2005] Degradation of Free Estrogens and their Conjugates in Wastewater Treatment Process, Proceedings of the Water Environment Federation, Technology 2005 291-297(7)

[Dytczak, Londry, Oleszkiewicz, 2008] Biotransformation of estrogens in nitrifying activated sludge under aerobic and alternating anoxic/aerobic conditions, Water Environ Res. 2008 Jan;80(1):47-52

[Zhang et al., 2006] Degradation of 17-ethinylestradiol in aqueous solution by ozonation, Journal of Hazardous Materials 291–298

[Jiang et al., 2013] Degradation of 17beta-estradiol in aqueous solution by ozonation in the presence of manganese(II) and oxalic acid. Environ Technol. 2013 Jan-Feb;34(1-4):131-8