by Bio! Mexico
A classical biosensor consists in two main parts: a biological system -e.g. cells, nucleic acids membrane receptors or tissue fragments- which responds to a particular stimulus, and a transduction system, which transforms this biological response into an electrical output. This signal can then be adjusted to a defined scale, so it is possible to acquire quantitative information about the initial stimulus.
The specificity of biological molecules opens to biosensor a wide application spectrum in biomedical and industrial areas. Nevertheless, their calibration remains technically demanding.
Among the most successful biosensor applications are the glucose biosensors based on the activity of the enzyme Glucose Oxidase. This mechanisms are used for the daily monitoring and control of glucose levels in diabetes patients, representing a significant improvement for their life quality because it is known that the progression of diabetic complications is tightly related to the control of the patient glycemic levels.
It is clear that not all biosensor have response time and detection limits suitable for their application for in-line monitoring at industrial level, as the detection of very low pollutant concentrations is needed. Nevertheless, biosensor have a valuable advantage compared with common chemical detection methods, and it is that biosensor are ecologically amenable. Furthermore, the fact that biosensor's detection limit may be not in the adequate range doesn't make biosensor lose their value, as long as they are still useful for pollutant early detection and for mixtures detection.
The main challenge for environmental and industrial biosenors is to lower their detection limit and increase the robustness. And this is a good challenge for Synthetic Biology to accept.
At iGEM, projects centered on biosensors or which at least involve a quorum sensing module, are quite popular. But among these projects, the work of the 2009 Cambridge University team is one of those which deserve a special mention.
In their project, the Cambridge students made two main contributions: a sensitivity tuner system and a set of reporter pigments. Their effort was rewarded with the 2009 iGEM Grand Prize.
The sensitivity tuner system is based on a previous work, also by Cambridge students but from the year 2007. This mechanism is a signal amplifier and consists on a stimuli receptor that responds producing an activator, which in turn produces a more powerful transcriptional response. In this way, it is possible that a very subtle stimulus may elicit a detectable transcriptional response, detectable by a reporter gene.
Sounds familiar? Of course! This means a possible solution for the biosensor's detection limit challenge. The 2009 Cambridge team performed the task of quantitatively characterizing the magnitude of the signal amplification for twelve sensitivity tuner constructions.The British team also adapted the biosynthetic pathway of three visible pigments: carotenoids (orange/red), melanin (brown) and violacein (purple/green).
Up: black box diagram of the sensitivity tuner
and the pigment generator. Down: detailed diagram of the
The dotted strips.
List of iGEM teams which have worked with biosensor or quorum sensing until 2008:
- 2007 Brown UniversityLead sensor/Tristable switch
- 2007 Colombia
- 2007 Freiburg
Protein Ca sensors/Protein light sensors
- 2007 Glasgow
Toluene sensing and electric signal emission
- 2007 Imperial College
Biofilm sensor of AHLs/Temperature sensor for meet
- 2007 Melbourne
Light sensing E. coli with agregation and gas vesicle module
- 2007 Mississippi StateUbiquitin ligase activity assay
- 2007 MIT
- 2007 Naples Oleic acid biosensor for determining olive oil purity
- 2007 NYMU Taipei
Mammalian insulin secretor with glucose sensing module
- 2007 Prairie View
Metal and organic compound biosensor
- 2007 Saint Pettesburg Copper biosensor with Schmitt trigger
- 2007 Southern Utah Cyanide biosensor in Pseudomonas fluorescens
- 2008 Brown University Electricic signal producer-arsenic biosensor
- 2008 Harvard
Electrical signal output by Shewanella oneidensis to enviromental input
- 2008 Illinois G Protein receptor coupling to pathogenous-associated-antigen-specific antibody and GFP downstream coupling/tyrosine kinase receptor coupling to pathogenous-associated-antigen-specific antibody and GFP downstream coupling/GFP fragmentation and binding to antibodies directed to specific multiantigens, where they would complement and fluoresce, in Yeast.
- 2008 Imperial College Light sensing B. subtilis biomaterial pattern generator through motility arrest
- 2008 Johns Hopkins Yeast mate-type biosensor
- 2008 Missouri Miners Ethanol and methanol sensor with AOX promoter coupled to GFP
- 2008 Newcastle U. B. subtilis that detects pathogenic organisms by their quorum sensing mechanisms, and emits fluorescent signal
- 2008 NTU Singapore
Quorum sensing bacteria which also respond with colicin secretion
- 2008 Prairie View
Cation biosensor, which emits positive signal when cations are present, and negative when anions are.
- 2008 Purdue Biosensor for UV radiation, combining the SOS pathway promoter with a lacZ gene.
- 2008 TU Delft Temperature sensing E. coli through a RNA effector
- 2008 U. of Alberta
biosensor/plant biobricks/butanol synthesis
- 2008 U. of Sheffield
E. coli biosensor of V. cholerae through quorum sensing
- 2008 Utha State
E. coli PHB biosensor that would aid in monitoring the PHB production in culture
- 2009 Brown
Hystamine biosensor in Staphylococcus epidermidis chassis
- 2009 Cambridge
Biosensor with input sensitivity tuner module and three different colour output depending on input strength/ biobricks for six pathways for different coloured outputs
- 2007 Missouri
Biological timer and an ethanol Yeast biosensor
- 2007 Penn State
Xylose metabolism modification/Radiation biosensor
- 2007 Valencia
Promoter biosensor callibrator
- 2008 BCCS Bristol
Structure and material organizationby bacteria, using chemotaxis, enviromental sensing and cell-cell communication
- 2008 Beijing
Polychlorinated biphenyls- and -dioxins sensing and degrading E. coli
- 2008 Caltech
Quorum sensing of pathogenic population by a strain of E. coli capable of oxidative burst/b-galactosidase secreting E. coli in the gut for lactose intolerance/folate secreting E. coli/ Multipotent E. coli
- 2008 Turkey
Metal sensing and carrying E. coli
- 2008 UNAM-IPN
Horizontal gene transfer sensor/turing pattern generator circuit
- 2009 Br. Columbia
Module that receives input and transform it on a signal that varies according to input concentration from green to red output
- 2007 Turkey
Tricolor pulse oscilator/subpopulation differentiation and competing mechanism/metal bacterial intake and taxis
- 2008 Heidelberg
E. coli biosensor and chemotaxis directed to pathogenic organisms through quorum sensing mechanism, and bacteriocidal production through another quorum sensing mechanism
- 2008 NYMU Taipei
E. coli intented to attach and sense pH in the small-intestine and respond with removal of urea and guanidine, and also regulate phosphate balance.
- 2008 Tokyo Tech
- 2008 U. of Lethbridge PCB
E. coli biosensor with chemotactic and degradation modules. Also, riboswitch and SELEX