(Difference between revisions)
(DNA nanocar factory)
(Artificial virus factory)
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In conclusion, these kinds of DNA structures can be suitable, reversible and metastable DNA fuels and a new kind of cargo delivery machine.
In conclusion, these kinds of DNA structures can be suitable, reversible and metastable DNA fuels and a new kind of cargo delivery machine.
== Artificial virus factory ==
== B.Artificial virus factory ==

Revision as of 00:08, 28 October 2008


Biosynthetic Bottum-up approach

A.DNA nanocar factory

The field of artificial molecular machines and motors is growing at an astonishing rate and is attracting a great deal of interest in nanoscience. Research in the last decade has shown that species made of components like DNA or proteins are more attractive candidate. Our aims is to build by a bottom-up approched DNA nanocars that have the properties to produce energy in vitro. Our system is more efficient than a classic system because the FIFO order is very important: the first part will bind by complementarity with part 2 this new part will make the binding site for part 3.


Fig.1:biosynthesis by sequential expression of 3 DNA origami

If we add in vitro a complementary miRNA to the red regions (fig.2), the competition of the miRNA will open the DNA strands by broken the hdrogen backbound this processes deliveres minimun ten time more energy than ATP biodegradation (winfree, the instability of the miRNA may make this processe reversible. In conclusion, these kinds of DNA structures can be suitable, reversible and metastable DNA fuels and a new kind of cargo delivery machine.

B.Artificial virus factory

We can also produce a lot of differentes kinds of self-assembly structures like virus:



Fig2: genetic organization of HIV virus

HIV can be produce by sequential expression of 3 genes gag,env and pol (Fig.2)those genes will be cleaved by protease P10 and than the subunits of the virus will self-assembled into mature virus. In our case, we will expressed gag p10 and finaly Pol (without Pol to avoid pathogenicity) the FIFO in this case will be essential.

If you ask us why?

For 3 main reasons :

First, when they genes 1 and 2 will be expressed the protease P10 will cleave gag that will self-assembled.

Than when 123 will be expresse Pol will get cleaved and self assembled with they products of gag and P10.

Finaly, when 23 get activate we will increase the quantity of subunits delivered from the clivage of Pol.

In conclusion, our sytem will be very useful for the developpement of new drugs against HIV or in new kind of vectors in genetic therapy.

Metabolic engineering of polyhydroxyalkanoate biosynthesis pathways

Human overpopulation combined with the current lifestyle urges the rational, efficient, and sustainable use of natural resources to produce environmentally friendly plastic materials such as polyhydroxyalkanoic acids (PHAs), whose production/degradation cycle reduces undesirable wastes and emissions. Our study is a new metabolic strategy to generate PHA-hyperproducer strains, that have the properties to be a sequential metabolic pathway, we believe the sequential expression may increases the production of purified PHA.

Our strategy consists on replacing the RFP,CFP and YFP genes by the PhaA ,PhaB and PhaC genes in our final system (containing oscillation,FIFO,synchronisation modules).

This strategy is more efficient than a constitutive activation for 3 main reasons:

  • First, in this application the NADPH, which is a cellular metastable fuel, is used by the PhaB to synthesize bioplastic. This molecule is very important for many metabolic pathways in bacteria. A NADPH recuperation step is then needed to ensure other metabolic activities to go on. We can then make the hypothesis that if the PhaB is always activated the bacteria will get exhausted and die quickly (4-5 days). In our system, the bacteria will have a NADPH recuperation step, this is why we hope bacteria will live more than in an usual chemoreactor.
  • Secondly, we hope by the order of the FIFO to make a synchronized and sequential turn-over of the enzymatic expression in order to increase the rate of the PHA biosynthesis.
  • Third, as the quality of the bioplastic increases with time, we could predict the quality of the final product since we would know the duration of a production cycle thanks to the periodicity of our system.