Difference between revisions of "Team:British Columbia/Description"
| Line 109: | Line 109: | ||
</style> | </style> | ||
| − | <div class="tab-pane" id="a"><p>In order to create our pro-bee-otic, | + | <div class="tab-pane" id="a"><p>In order to create our pro-bee-otic, bacteria specific to <i>Apis mellifera</i> were chosen: the β-proteobacteria, <i>Snodgrassella alvi</i>, and the γ-proteobacteria, <i>Gilliamella apicola</i>. By using microaerophilic bacteria that are unique to the honey bee gut, a specificity is acquired and the chances of pests acquiring the engineered imidacloprid resistant strains are decreased. However, due to the small amount of existing literature on <i>G. apicola</i> and <i>S. alvi</i>, an aspect of the project revolved around discovering methods of culturing the bacteria, inducing competence, and transforming them with a compatible plasmid.<br />Click <a href="https://2015.igem.org/Team:British_Columbia/Growing">here</a> to read more.</p></div> |
| − | + | ||
| − | <div class="tab-pane" id="b">Microbial strains able to degrade imidacloprid were isolated from soil environments, however the specific enzymes involved in the degradation pathway have not been characterized yet. | + | <div class="tab-pane" id="b">Microbial strains able to degrade imidacloprid were isolated from soil environments, however the specific enzymes involved in the degradation pathway have not been characterized yet. Functional metagenomic approaches were desugbed to screen large-insert environmental fosmid libraries obtained from Dr. Hallam lab for the imidacloprid-degrading phenotype. <br />Click <a href="https://2015.igem.org/Team:British_Columbia/Screening">here</a> to read more.</div> |
Revision as of 17:53, 13 September 2015
Project Description
According to the U.S. Department of Agriculture, bees pollinate 80% of our flowering crops, which constitute one third of everything we eat. From an economic standpoint, a study done at Cornell University estimates that honeybees pollinate $14 billion worth of seeds and crops per year in the United States alone. Unfortunately, global bee populations have been under attack since the early 1990s; in 2015, US beekeepers reported that 42% of their colonies died within the past year.
Honeybee Colony Collapse Disorder (CCD) refers to a phenomenon in which adult working bees disappear from the colony, leaving behind the queen bee and resulting in its eventual collapse. CCD remains a major concern across North America and Europe. Though the mechanisms by which CCD occurs are still unknown, neonicotinoids (a widely-used class of pesticides) has been implicated.
UBC’s 2015 iGEM team aims to create a strain of engineered honeybee intestinal bacterium capable of degrading the neonicotinoid pesticide imidacloprid, alongside an antifungal agent to eliminate N. apis. In doing so, we plan to render inoculated honeybees resistant to common field doses of imidacloprid, allowing its sustained use while reducing the risk of CCD.
Gilliamella apicola is a bacterium that natively resides in the midgut of the bee. We believe that by engineering G. apicola to metabolize imidacloprid into harmless organic compounds as well as to produce gastrodianin, a potent antifungal agent, we can create a strain of G. apicola capable of conferring resistance to imidacloprid, significantly reducing the risk of CCD once stably introduced into the bee gut.
Imidacloprid is known to be naturally degraded in the environment to 6-chloronicotinic acid (6-CNA). Though 6-CNA displays a significantly lower lethal dosage than imidacloprid, it remains bioactive to a small degree. As such, we plan to investigate downstream enzymes that further degrade 6-CNA, and use this novel pathway in G. apicola to degrade imidacloprid to a completely non-toxic product in the bee gut.
Click to view more on each subgroup.
In order to create our pro-bee-otic, bacteria specific to Apis mellifera were chosen: the β-proteobacteria, Snodgrassella alvi, and the γ-proteobacteria, Gilliamella apicola. By using microaerophilic bacteria that are unique to the honey bee gut, a specificity is acquired and the chances of pests acquiring the engineered imidacloprid resistant strains are decreased. However, due to the small amount of existing literature on G. apicola and S. alvi, an aspect of the project revolved around discovering methods of culturing the bacteria, inducing competence, and transforming them with a compatible plasmid.
Click here to read more.
Click here to read more.
Three cytochrome P450 enzymes (CYPs), CYP6CM1vQ, CYP6G1 and HUMCYPDB1, have been found to degrade imidacloprid into less toxic metabolites. In an attempt to synthesize E.coli, and further, G.apicola, to be able to degrade imidacloprid, we are constructing four vectors containing these genes. In addition to the CYP genes, each vector contains a pelB signal sequence and a AgCPR reductase to i) target the CYP to the inner membrane and ii) to recycle NADPH. Three vectors will contain one CYP gene and the fourth will contain all three CYP genes. In addition, we will optimize the genes for heterologous expression in E. coli through i) N-terminal truncations and/or ii) codon optimization.
Time permitting, we will optimize, demonstrate and characterize the in vivo detoxification of imidacloprid in E. coli through i) titrating cofactor or cofactor precursor concentrations (heme/heme precursors, NADPH), and ii) measuring detoxification kinetics during relevant growth and resting conditions. Click here to read more.
6-CNA is one of the byproducts of imidacloprid and is toxic, though to a lesser degree than imidacloprid. To degrade 6-CNA, it will be converted to a central metabolite in the TCA cycle, fumaric acid hence benefiting the host with the vector. In an attempt to synthesize E.coli, and further, G.apicola, to be able to degrade 6-CNA, CCH2, NIC C, NIC X, NIC D, NIC F and NIC E will be assembled into a vector via standard assembly. The vector contains each gene with a Ptac promoter, however only one of the genes will contain a Lac I repressor.
First the level of protein expression of CCH2 of the soluble and insoluble fraction at five temperatures (16 °C, 20 °C, 25 °C, 30 °C, 37 °C) will be tested to see the optimal temperature for expression and to check correct protein length. To test the degradation efficiency of CCH2, a resting cell assay as described in literature will be done. The quantity of 6-CNA will be validated via Gas chromatography- mass spectroscopy to determine how long degradation takes. To test degradation of 6-CNA, 6-CNA will be used as a sole carbon source with the assembled vector, the control without CCH2. Any growth by the vector with CCH2 plus the NIC cluster and no growth with the assembly missing CCH2 confirms that the pathway is functioning. Click here to read more.
UBC iGEM 2015