Team:SHSBNU China/Project
Project
I. Background
Each year, seven lakh tons of dyes are produced in factories, and a large amount of them were discharged in waste stream without proper treatment. These emissions could lead diseases of human beings or even due irreversible harm the ecosystem. Our team sets our goal to come out with a system that could effectively decompose azo dyes.
Azo dyes’ pollution
First, we researched about previous ways to decompose azo dyes. There are three existing ways to decompose azo dyes: Chemical method, photocatalytic method, and microbiological method. First, chemical method uses carbon-based sorbents to adsorb synthetic dyes. However, it is energy consuming to make such substance. Consequently, this method is too expensive for smaller business owners, so they would never use such method. Second, photocatalytic method involves several catalysis and require special lighting equipment. The reaction tends to be very slow due to most dyes were designed to tolerate strong lights. Thus, this method is time consuming. Third, microbiological decomposition process is relatively cheap and this method does generate any toxic by-products. Nevertheless, bacteria cell that could flow every in the treatment apparatus is still an issue. We decided to improve the on-going microbiological method. We need to create a system that holds all the cells in one piece and could decompose azo dyes.
Focusing on that, we soon located our first key component of our system: The Biofilm. Biofilm is a network of individual cells which act not only as a net that holds everything in one piece, but also as a shield for individual cells to the harsh environment condition. As we all know, bacteria cannot grow as well in medias as in harsh environments like flowing sewage water.
The typical biofilm we researched on is formed by gene csgA on the genome of E. coli MG1655 wild type. Cells were stuck together by a kind of fiber protein known as curli fiber that is assembled by CsgA protein on the cell’s surface. By the way, csgA was a previous iGEM part and we mead improvements to it. We also read about adding the sequence of SpyTag after csgA gene could produce curli fiber with SpyTags on them.
Figure of csgA - SpyTag
We are now confidence that we can fix anything we want to the surface of a biofilm. But we now need a substance that could decompose the azo dyes. After some more researching, we found laccase, a kind of blue multi-copper oxidases, has strong ability to oxidize and decompose azo dyes. Gene cotA, initially found in Bacillus subtilis, can produce protein with high laccase activity. Gene cotA has a very low translation rate in natural hosts. However, when cotA is produced in specialist strains like BL21 – DE3 (after T7 promoter), it shown up a relatively high rate. As mentioned, laccase belong to multi-copper oxidases, so that CotA protein still need to combine with Cu2+ to become active laccase. The solution is quiet simple, we can just ultrasonic cells and mix whatever is left with 0.1 mM/L of CuSO4.
Up till now, we have designed a biofilm with SpyTag and have located a kind of powerful enzyme. In order to fix our powerful enzyme to the biofilm, we added a SpyCatcher sequence after the cotA gene. So that these proteins could fix onto the curli fibers of the biofilm csgA - SpyTag using isopeptide bonds. These bonds are covalent bonds which is relatively hard to broke.
cotA - SpyCatcher
Signal peptides - CotA
We then came out with another solution of how to get CotA protein out of the cells. By adding signal peptide sequence ahead of cotA – SpyCatcher sequence, we could let the cells secrete CotA – SpyCatcher protein in to the media. Then we can let CotA – SpyCatcher combine with Cu2+.
Project Overview
References:
Esther Forgacsa, T. C. t., Gyula Oros. (2004). Removal of synthetic dyes from wastewaters: a review. Environment International, 30(7), 955, 959, 961.
II. Description
Synthetic dyes, which are widely used in many industries and researches, cause various environmental and health problems. Xintang, a village in China, where textile industries are located, have been heavily polluted with indigo blue dye. After enduring such bad environment, many villagers, unfortunately but inevitably, get heart disease as well as leukemia. (Guang etal., 2013)
Biological degradation of dyes is economic and environmentally friendly methods comparing to chemical degradation, so this year, our team aims to use CotA, a laccase coding gene, to deal with synthetic dyes containing effluents. CotA is a polyphenol oxidase which has capability to decolorize a wide range of dyes. Comparing to chemical process which has high expense and take tedious steps, CotA laccase is eco-friendly. It is proven that laccase decompose dye efficiently even in harsh condition with 3.5% salinity and pH 11.6 (Piscitelli etal., 2010, p. 252), which shows potential for dye decomposition.
However, bacteria are not capable to grow in harsh environment. We learn that previous researchers have reported that biofilm is able to be engineered to display proteins with different functions, which ameliorates the drawback. CotA laccase is fussed with Spycatcher to attach covalently to biofilm containing Spytag. Biofilm is a layer adhered by large amounts of microorganisms to the surface, and organic substances such as enzyme are trapped in it. It maximumly protect bacteria and enzyme in wide range pH environment, lowering the impact of acidic sewage water to laccase activity, enhancing reaction efficiency of laccase. We successfully attach CotA laccase to biofilm and prove the effectiveness of laccase to decompose dyes eventually.
To further improve the efficiency of discoloration, we come up with the idea to construct a filter which holds a large amount of laccase while letting water to get pass. We design to attach CotA laccase to biofilm which cover polyhydroxyalkanoates plastic beads to fill the filter. When processing sewages, the velocity of flow will be controlled to be appropriate, at which the treating efficiency as well as the stability of biofilm are both optimized.
Reference:
Alessandra Piscitelli, C. P., Paola Giardina, Vincenza Faraco and Sannia Giovanni. (2010). Heterologous laccase production and its role in industrial applications. Bioeng Bugs, 1(4), 252.
Guang, L. G. J. M. L. (2013). The denim capital of the world: so polluted you can’t give the houses away. Retrieved fromhttps://www.chinadialogue.net/article/show/single/en/6283-The-denim-capital-of-the-world-so-polluted-you-can-t-give-the-houses-away