Team:LMU-Munich/Project/Description

Overall project

Metals and especially heavy metals are highly prescribed in concentrations in the drinking water ordinance. Qualifying and quantifying these by standard chemical methods is costly and complicated.

Bacteria sense metals in their surrounding in order to change their expression profile or react in order to adapt and accomodate to their environment.

Using these sensors from (mostly) bacteria we create biosensors by linking them to the expression of a reporter (e.g. green glowing by the green fluorescent protein GFP). To not only qualify but also to quantify the metals, it is also necessary to measure the output by given input (metal concentration) for each of these biosensors. Afterwards one can determine the metal concentration by measuring the output.

The quantification needs heavy high-tech machinery ... something not always given ... especially in free field. So a qualification of metals with an easy-to-see output is also needed.

In the end our team hopes to have not only a set of metallsensors for precise quantification of a group of (heavy) metalls, but also an outdoor kit for qualifying metalls in more remote areas. With these it might be more easy and cheaper to determine the content of metals in our drinking water.

Project Details

This year’s project by the iGEM-team from Ludwig-Maximilians-University in Munich uses natural biosensors to detect the concentration of different metals. We have the vision to develop a set of bacterial metal sensors for easy qualitative and quantitative measurement of toxic metals just by reading the output after adding the water test sample.

We use two different kinds of metal sensors. The ones in the first category work with reporter genes that lay downstream of an inducible promoter. The respective promoter is activated or deactivated by a specific metal-sensitive protein which binds to DNA dependent on the presence of that metal. As a consequence of this statistical event, there is a concentration-dependent transcription of the reporter gene, which is either GFP, luxAB or lacZ´.

The second kind of metal sensors directly uses the characteristics of special proteins to obtain a measurement of the metal, e.g. by analyzing the activity of an enzyme that needs a special metal ion as a cofactor. For easy handling and compatibility we use the E. coli strain DH5α.

Reporter genes

GFP: The well-known green fluorescent protein is detectable after excitation with UV-light without addition of further molecules. The output is not very sensitive because GFP is directly measured in contrast to luxAB and lacZ’, which use an enzymatic multiplying response.

luxAB: These two genes from Vibrio lux-Operon catalyse the light-emitting oxidation of luciferine. Therefore, very expensive luciferin has to be added to the bacteria, or they have to be cotransformed with a plasmid containing luxCDE, an enzyme cascade producing luciferin out of fatty acids.

lacZ´: lacZ‘ codes the β-subunit of β-galactosidase, an enzyme that catalyses the reaction from X-Gal (5-bromo-4-chloro-3-indolyl- beta-D-galactopyranoside) to a blue insoluble indigo-dye (5,5'-dibromo-4,4'-dichloro-indigo). As only the β-subunit is used, the E.coli strain has to contain the α-subunit and must not contain the whole enzyme. These requirements are fulfilled e.g. in DH5α.

Promoter-based Sensors

All genes are transcriptionally fused to the reporter gene, which means that approximately 50 nucleotides from the originally transcribed gene still remain with the promoter to ensure correct read-off. Downstream of this short open reading frame, the reporter gene with its own ribosome binding site is added.

pnikA: The nik-operon from E. coli codes for a nickel-influx system, which is constantly active, unless the concentration of nickel inside of the bacteria is too high. In this case, the regulator NikR binds Ni(II)-Ions and attaches to the NikR-operator site, which is located in the promoter sequence of nikA, called pnikA. So with rising nickel concentration, the activity of pnikA is reduced. Since nikR originates from E.coli, it’s sufficient to clone the promoter pNikA from E.coli K12 MG1655 gDNA using Phusion polymerase, primer A and B and 50°C annealing temperature. The linear response is fulfilled for a concentration range from 1-400 nM. This Regulator works under anaerobic conditions.

source(s):
- [http://www.ncbi.nlm.nih.gov/pubmed?term=coordinating%20intracellular%20chivers Coordinating intracellular nickel-metal-site structure-function relationships and the NikR and RcnR repressors] Iwig JS, Chivers PT
- [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1236639/?tool=pubmed Complex transcriptional control links NikABCDE-dependent nickel transport with hydrogenase expression in Escherichia coli] RoweJS, Starnes GL, Chivers PT
- [http://www.ncbi.nlm.nih.gov/pubmed/10787413 Regulation of high affinity nickel uptake in bacteria] Ni2+-Dependent interaction of NikR with wild-type and mutant operator sites. Chivers PT, Sauer RT
- [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC93426/?tool=pubmed Isolation and characterization of the nikR gene encoding a nickel-responsive regulator in Escherichia coli] de Pina K, Desjardin V, Mandrand-Berthelot MA, Giordano G, Wu LF

prcnA: The rcn-operon from E. coli codes for a nickel- and cobalt-efflux system. If the repressor RcnR has Ni(II)-ions bound, it cannot attach to DNA and the prcnA-promoter is active. In the absence of nickel or cobalt, the rcnR binds to the rcnR operator and blocks the nikA-promoter pnikA. Since the regulator originates from E. coli and is not coded on the plasmids, E. coli must be used as reporter organism. The promoter was cloned using Phusion polymerase, primer C and D and 50°C annealing temperature. The linear response is fulfilled for a concentration range from 0.5-60 µM.

source(s):
- [http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2958.2006.05369.x/pdf Nickel homeostasis in Escherichia coli – the rcnR-rcnA efflux pathway and its linkage to NikR function] Iwig JS, Rowe JL, Chivers PT
- [http://www.ncbi.nlm.nih.gov/pubmed?term=coordinating%20intracellular%20chivers Coordinating intracellular nickel-metal-site structure-function relationships and the NikR and RcnR repressors] Iwig JS, Chivers PT

pars: The pars-promoter from Escherichia coli is regulated by the repressor arsR, which can bind As(III)- and Sb(III)-ions. Without these ions, the arsR binds to the pars-promoter, deactivating it. In the presence of As(III) or Sb(III), the repressor leaves the DNA, by this means enabling the promoter to work. For less leakiness of the repressed promoter, a second arsR-binding site was used.

Since the regulator arsR does not exist in E. coli, it is coded on our plasmids. The pars-promoter with two binding sites has been multiplied via PCR with Phusion polymerase and primers E and F at an annealing temperature of 50°C. arsR with a constantly active promoter was cloned from BBa_K3562 and fused using 3A-assembly.

Bacillus subtilis based promoter constructs:

PaseR: The pase-promoter from Bacillus subtilis is regulated by the repressor aseR, which can bind As(II)- and As(III)-ions. In presence of these ions the repressor is releaved from the aseR binding site next to the Promoter PaseR. The promoter region was amplified from genomic DNA of Bacillus subtilis subtilis W168, which is used as a laboratory wildtype of the gram-positive model organism. For the amplification the Primers XXXX and XXXX where used in a phusion PCR according to the standard PCR protocol displayed on this wiki.

source(s):

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The Experiments

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Results

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