Team:USP-UNESP-Brazil/Associative Memory/Introduction

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===Objectives===
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=Introduction=
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The objective of this Project is to build an associative memory network using E.coli populations. This system will recognize a given visual pattern and answer it in a previously determined way, demonstrating how a systemic memory storage can be designed using synthetic biology.
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==Objectives==
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===Background===
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The goal of this project is to build an associative memory network using ''E.coli'' populations that should be able to memorize a given pattern and reproduce it when exposed to a similar one. This is a demonstration of systemic memory storage in synthetic biology.
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Synthetic biology is a powerful tool for the construction of mechanisms capable of executing routines for processing and storing information ''in vivo'', in similar ways to what is done ''in silico''. For example, Quian et al. [http://www.nature.com/nature/journal/v475/n7356/full/nature10262.html?WT.ec_id=NATURE-20110721] built a biological system capable of recognizing one person in a group of four people by identifying patterns. In this associative memory network, four neurons made of DNA molecules parts associated a sequence of four answers “yes” or “no”. Each pattern represented one person and could be remembered each time that the right sequence was inserted.
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==Background==
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The final goal of this project is to build an associative memory network in a populational system of E.coli, that is able to  recognize visual patterns as input. This system, therefore, demonstrates perception, storage and processing of information done by a synthetic biological system.  In order to make it, nine different populations will be prepared, representing each one a “neuron” of the network.  Each neuron will communicate with the whole network through quorun sensing signalling, which defines the Hopfield associative memory architecture. In the interaction, a neuron can inhibit another one, leading its production of GFP to a halt, or excite it, stimulating its production of GFP.
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Synthetic biology is a powerful tool for the construction of mechanisms capable of executing routines for processing and storing information ''in vivo''. The final goal of this project is to build an associative memory network in a system of ''E.coli'' populations. In our design, a population of bacteria represents a “neuron” of the network.  Each neuron communicates with the whole network through quorum sensing molecules (QSM), interacting in a repressive or excitatory way. Once all "neurons" are connected, a so called Hopfield associative memory architecture is defined. A similar idea was developed by Quian et al. [http://www.nature.com/nature/journal/v475/n7356/full/nature10262.html?WT.ec_id=NATURE-20110721] using DNA strand displacement cascades. They implemented a Hopfield associative memory with four fully connected artificial neurons that, after training in silico, remembered four single-stranded DNA patterns and recalled the most similar one when presented with an incomplete pattern.  
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The inhibition or excitement of GFP production will be based on a transcriptional regulation mechanism. The communication between bacterial populations will occur by means of quorum sensing substances and the information (inhibiting or exciting) will be defined by which transcriptional regulator the substance will promote. In summary, at the moment when the connections between the neurons are defined, we the system should return a predetermined response pattern.
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This interaction between "bacterial neurons" is based on a transcriptional regulation mechanism. The populations communicate by using quorum sensing substances and the transmitted information (inhibiting or exciting) is defined by which transcriptional regulator the substance promotes. "Activating" a population stimulates its GFP production, while "repressing" the population inhibits it. The result is that from the moment the connections between neurons are defined, the system should return a predetermined response pattern, that should be observed due to GFP production.
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===Application===
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==Application==
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In addition to be one of the first Hopfield Network model made in vivo, this project shows different lineages of bacteria communicating with each other, establishing balance through their systemic memory. This could be useful in the production of bioproducts, such as biofuels - for instance, a biosystem producing some compound inside a reactor could regulate itself according to specific parameter changes, such as temperature or nutrient concentration - it would perform that by communicating within its network and restoring the pattern stored in its ystemic memory. In the future, self-controlled biosystems will be possible, cheap and ecologically friendly alternatives for the industry.
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In addition to be one of the first Hopfield Network models made ''in vivo'', this project shows different strains of bacteria communicating with each other, establishing balance and exhibiting systemic memory. This could be useful in the production of bioproducts, such as biofuels. For instance, a biosystem producing some compound inside a reactor could regulate itself according to specific parameter changes, such as temperature or nutrient concentration - different combinations of parameters would turn the system into producing one composite or another, and it would perform this self-regulation by communicating within its network and restoring patterns stored in its systemic memory.
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Latest revision as of 02:30, 27 September 2012