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{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
 
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!align="center"|[[Team:UChicago|Home]]
 
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!align="center"|[[Team:UChicago/Team|Team]]
 
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!align="center"|[https://igem.org/Team.cgi?year=2013&team_name=UChicago Official Team Profile]
 
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!align="center"|[[Team:UChicago/Project|Project]]
 
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== '''Project Overview''' ==
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Each year, over two billion pounds of feather waste is produced as a byproduct of commercial poultry processing. Most of this waste is chemically treated or steam pressure-cooked into nutrient-poor animal feed (1). Nonetheless, recent research has shown that feather keratin can be used to produce biodegradable plastics (2), fertilizers (3), detergents (4), and pharmaceuticals (5). However, traditional methods of keratin degradation rely on chemicals such as sulfides and limes which are energetically costly and pose serious environmental and health concerns. Therefore, researchers have turned to feather-degrading bacteria as an alternative to traditional chemical methods (6). Although keratin-degrading bacterial strains were isolated from poultry waste nearly two decades ago and some keratin-degrading proteases (keratinases) have been identified, keratinase production in heterologous hosts has been stymied by poor protease expression. By developing an efficient process for the digestion of keratin, we would not only drastically reduce the cost of disposal but also allow the keratin to be used in products like animal feed, fertilizers and biodegradable plastics. Our final product would be a one-step continuous process in which feather waste could be continually added to <i>B. subtilis</i> cultures.
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== '''Overall project''' ==
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[[File:Feather_degradation_schematic.jpg|frame|A simple schematic of our project]]
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Tell us more about your project.  Give us background.  Use this is the abstract of your project.  Be descriptive but concise (1-2 paragraphs)
 
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<p>The goal of our project is to make the tanning industry more environmentally sustainable by making an enzymatically based hide de-hairing system. Ideally, our de-hairing system will involve the expression of a temperature optimized keratinase in <i>B. subtilis</i>. Our experiment is divided into several parts:</p>
 
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<b>Expression of keratinase in <i>B. subtilis</i>.</b> First, we isolated the keratinase gene from <i>B. licheniformis</i> by using specially designed primers. Then, we attached constitutive promoter veg to the gene in order to optimize expression. <b>Optimization of keratinase activity</b>. The keratinase protein works optimally at 50ºC; however, heating is cost prohibitive as it means that the protein must first be isolated and purified in large amounts in order to be used for de-hairing. Optimization of protein activity at optimal B. subtilis growth conditions would reduce the cost in time and money of a keratinase based de-hairing system by allowing the B. subtilis to be cultured right on the hide. The strategy we will be using to optimize the protein is directed evolution as not enough is known about the biophysical properties of the protein. <b>Creation of a keratin-dependent <i>B. subtilis</i> strain</b>. We also want to make a B. subtilis strain that can only survive if it has a source of keratin. We would do this by knocking out amino acid synthesis genes for several amino acids that can be obtained from keratin. This way, it would be unlikely that it could escape into the environment.
 
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== Project Details==
 
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In order to improve keratinase expression in Bacillus subtilis, a host suited to industrial use, we decided to build a BioBrick for the best characterized and most efficient keratinase gene. The keratin-degrading bacterial strain that is best characterized in the literature is Bacillus licheniformis PWD-1. The keratinase, called KerA, responsible for this bacterium’s activity was isolated and characterized by Shih et al. along with its signal peptide and promoter (7). The DNA sequence of kerA is 1458 bases long and codes for a serine protease. Like many secreted proteases in the Bacillus genus, KerA has a signal peptide, which is cleaved before KerA crosses the single plasma membrane of B. licheniformis. Additionally, the kerA promoter is activated when keratin is the sole source of carbon and nitrogen. Shih et al. successfully transformed B. subtilis with kerA and expressed it with its own promoter as well as with P43, a constitutive promoter, and a combination of the two in a high copy number backbone. All transformants expressed keratinase activity in the presence and absence of keratin (8).
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Building on the success of Shih et al., our team designed a BioBrick to improve kerA expression in a heterologous host. We purchased two gBlocks from IDT to assemble the kerA DNA sequence, which included the signal peptide. In order to increase the level of KerA produced in B. subtilis, we planned to use BioBrick part BBa_K143053, which includes Pveg, a constitutive promoter. Moreover, a high copy number backbone with an origin of replication for B. subtilis is needed for the largest production of KerA. Since the current B. subtilis plasmids in the iGEM registry are single copy plasmids that integrate into the genome, our team designed a high copy number backbone compatible with B. subtilis based on pUB110 (9).
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=== Part 2 ===
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We also wanted to determine if KerA expression in E. coli BL21-DE3 was comparable to that of B. subtilis. Unlike the members of the Bacillus genus, E. coli has two membranes. The kerA signal peptide could allow transport across the inner membrane but not the outer membrane, trapping KerA in the periplasm, where the amino acid modifications could render the keratinase inactive. Moreover, it is possible that E. coli does not contain the cellular machinery necessary to cleave the kerA signal peptide, producing an inactive form of the enzyme. Thus, we designed an alternate kerA BioBrick that was missing the signal peptide. To optimize expression of the keratinase in E. coli, we would have used a constitutive E. coli promoter BioBrick and a high copy number backbone.
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== Sources ==
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(1) El-Nagar, K., Saleh, S. M., & Ramadan, A. R. (2006). [http://www.tx.ncsu.edu/jtatm/volume5issue2/articles/El-Nagar/El_nagar_Full_171-05.pdf Utilization of feather waste to improve the properties of the Egyptian cotton fabrics.] Jour. of Textile and Apparel Technology and Management, 2, 1-12.
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(2) Jin, E., Reddy, N., Zhu, Z., & Yang, Y. (2011). [http://pubs.acs.org/doi/abs/10.1021/jf1039519 Graft polymerization of native chicken feathers for thermoplastic applications.] Journal of agricultural and food chemistry, 59(5), 1729-1738.
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=== The Experiments ===
 
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(3) Hadas, A., & Kautsky, L. (1994). [http://link.springer.com/article/10.1007%2FBF00748776 Feather meal, a semi-slow-release nitrogen fertilizer for organic farming.] Fertilizer research, 38(2), 165-170.
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(4) Riffel, A., Lucas, F., Heeb, P., & Brandelli, A. (2003). [http://www.ncbi.nlm.nih.gov/pubmed/12677362 Characterization of a new keratinolytic bacterium that completely degrades native feather keratin.] Archives of Microbiology, 179(4), 258-265.
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=== Part 3 ===
 
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(5) Tiwary, E., & Gupta, R. (2010). [http://www.ncbi.nlm.nih.gov/pubmed/20597544 Extracellular expression of keratinase from Bacillus licheniformis ER-15 in Escherichia coli.] Journal of agricultural and food chemistry, 58(14), 8380-8385.
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(6) Williams, C. M., Richter, C. S., Mackenzie, J. M., & Shih, J. C. (1990). [http://aem.asm.org/content/56/6/1509 Isolation, identification, and characterization of a feather-degrading bacterium.] Applied and Environmental Microbiology, 56(6), 1509-1515.
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(7) Lin, X., Kelemen, D. W., Miller, E. S., & Shih, J. C. (1995). [http://www.ncbi.nlm.nih.gov/pubmed/7747965 Nucleotide sequence and expression of kerA, the gene encoding a keratinolytic protease of Bacillus licheniformis PWD-1.] Applied and environmental microbiology,61(4), 1469-1474.
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(8) Lin, X., Wong, S. L., Miller, E. S., & Shih, J. C. H. (1997). [http://www.ncbi.nlm.nih.gov/pubmed/9366094 Expression of the Bacillus licheniformis PWD-1 keratinase gene in B. subtilis.] Journal of Industrial Microbiology and Biotechnology, 19(2), 134-138.
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(9) Boe, L. A. R. S., Gros, M. F., te Riele, H. E. I. N., Ehrlich, S. D., & Gruss, A. (1989). [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC210059/ Replication origins of single-stranded-DNA plasmid pUB110.] Journal of bacteriology, 171(6), 3366-3372.
== Results ==
== Results ==
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Latest revision as of 02:54, 26 October 2013




Project Overview

Each year, over two billion pounds of feather waste is produced as a byproduct of commercial poultry processing. Most of this waste is chemically treated or steam pressure-cooked into nutrient-poor animal feed (1). Nonetheless, recent research has shown that feather keratin can be used to produce biodegradable plastics (2), fertilizers (3), detergents (4), and pharmaceuticals (5). However, traditional methods of keratin degradation rely on chemicals such as sulfides and limes which are energetically costly and pose serious environmental and health concerns. Therefore, researchers have turned to feather-degrading bacteria as an alternative to traditional chemical methods (6). Although keratin-degrading bacterial strains were isolated from poultry waste nearly two decades ago and some keratin-degrading proteases (keratinases) have been identified, keratinase production in heterologous hosts has been stymied by poor protease expression. By developing an efficient process for the digestion of keratin, we would not only drastically reduce the cost of disposal but also allow the keratin to be used in products like animal feed, fertilizers and biodegradable plastics. Our final product would be a one-step continuous process in which feather waste could be continually added to B. subtilis cultures.


A simple schematic of our project



In order to improve keratinase expression in Bacillus subtilis, a host suited to industrial use, we decided to build a BioBrick for the best characterized and most efficient keratinase gene. The keratin-degrading bacterial strain that is best characterized in the literature is Bacillus licheniformis PWD-1. The keratinase, called KerA, responsible for this bacterium’s activity was isolated and characterized by Shih et al. along with its signal peptide and promoter (7). The DNA sequence of kerA is 1458 bases long and codes for a serine protease. Like many secreted proteases in the Bacillus genus, KerA has a signal peptide, which is cleaved before KerA crosses the single plasma membrane of B. licheniformis. Additionally, the kerA promoter is activated when keratin is the sole source of carbon and nitrogen. Shih et al. successfully transformed B. subtilis with kerA and expressed it with its own promoter as well as with P43, a constitutive promoter, and a combination of the two in a high copy number backbone. All transformants expressed keratinase activity in the presence and absence of keratin (8).


Building on the success of Shih et al., our team designed a BioBrick to improve kerA expression in a heterologous host. We purchased two gBlocks from IDT to assemble the kerA DNA sequence, which included the signal peptide. In order to increase the level of KerA produced in B. subtilis, we planned to use BioBrick part BBa_K143053, which includes Pveg, a constitutive promoter. Moreover, a high copy number backbone with an origin of replication for B. subtilis is needed for the largest production of KerA. Since the current B. subtilis plasmids in the iGEM registry are single copy plasmids that integrate into the genome, our team designed a high copy number backbone compatible with B. subtilis based on pUB110 (9).


We also wanted to determine if KerA expression in E. coli BL21-DE3 was comparable to that of B. subtilis. Unlike the members of the Bacillus genus, E. coli has two membranes. The kerA signal peptide could allow transport across the inner membrane but not the outer membrane, trapping KerA in the periplasm, where the amino acid modifications could render the keratinase inactive. Moreover, it is possible that E. coli does not contain the cellular machinery necessary to cleave the kerA signal peptide, producing an inactive form of the enzyme. Thus, we designed an alternate kerA BioBrick that was missing the signal peptide. To optimize expression of the keratinase in E. coli, we would have used a constitutive E. coli promoter BioBrick and a high copy number backbone.

Sources

(1) El-Nagar, K., Saleh, S. M., & Ramadan, A. R. (2006). [http://www.tx.ncsu.edu/jtatm/volume5issue2/articles/El-Nagar/El_nagar_Full_171-05.pdf Utilization of feather waste to improve the properties of the Egyptian cotton fabrics.] Jour. of Textile and Apparel Technology and Management, 2, 1-12.


(2) Jin, E., Reddy, N., Zhu, Z., & Yang, Y. (2011). [http://pubs.acs.org/doi/abs/10.1021/jf1039519 Graft polymerization of native chicken feathers for thermoplastic applications.] Journal of agricultural and food chemistry, 59(5), 1729-1738.


(3) Hadas, A., & Kautsky, L. (1994). [http://link.springer.com/article/10.1007%2FBF00748776 Feather meal, a semi-slow-release nitrogen fertilizer for organic farming.] Fertilizer research, 38(2), 165-170.


(4) Riffel, A., Lucas, F., Heeb, P., & Brandelli, A. (2003). [http://www.ncbi.nlm.nih.gov/pubmed/12677362 Characterization of a new keratinolytic bacterium that completely degrades native feather keratin.] Archives of Microbiology, 179(4), 258-265.


(5) Tiwary, E., & Gupta, R. (2010). [http://www.ncbi.nlm.nih.gov/pubmed/20597544 Extracellular expression of keratinase from Bacillus licheniformis ER-15 in Escherichia coli.] Journal of agricultural and food chemistry, 58(14), 8380-8385.


(6) Williams, C. M., Richter, C. S., Mackenzie, J. M., & Shih, J. C. (1990). [http://aem.asm.org/content/56/6/1509 Isolation, identification, and characterization of a feather-degrading bacterium.] Applied and Environmental Microbiology, 56(6), 1509-1515.


(7) Lin, X., Kelemen, D. W., Miller, E. S., & Shih, J. C. (1995). [http://www.ncbi.nlm.nih.gov/pubmed/7747965 Nucleotide sequence and expression of kerA, the gene encoding a keratinolytic protease of Bacillus licheniformis PWD-1.] Applied and environmental microbiology,61(4), 1469-1474.


(8) Lin, X., Wong, S. L., Miller, E. S., & Shih, J. C. H. (1997). [http://www.ncbi.nlm.nih.gov/pubmed/9366094 Expression of the Bacillus licheniformis PWD-1 keratinase gene in B. subtilis.] Journal of Industrial Microbiology and Biotechnology, 19(2), 134-138.


(9) Boe, L. A. R. S., Gros, M. F., te Riele, H. E. I. N., Ehrlich, S. D., & Gruss, A. (1989). [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC210059/ Replication origins of single-stranded-DNA plasmid pUB110.] Journal of bacteriology, 171(6), 3366-3372.


Results

Check out our BioBrick designs.