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      Site News
    
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            <syn:updateBase>2009-12-28T16:17:26Z</syn:updateBase>
        

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        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/dont-destroy-research"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/what-does-determine-the-speed-of-protein-production"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/the-spike-of-the-virus"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/dna-sequencing-is-now-improving-faster-than-moores-law"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/gut-bacteria-can-control-diabetes"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/orange-sweet-potato-a-hit-in-mozambique-1"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/quasi-science-prevents-an-environmentally-friendly-agriculture-and-forestry"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/gamers-help-protein-3d-structure-modeling"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/synthetic-organization"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/chemical-evolution-of-a-bacteriums-genome"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/farewell-symposium-for-andreas-engel"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/the-3d-architecture-of-the-bacterial-chromosome"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/lifeexplorer-illustrates-the-front-page-of-molecular-microbiology"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/the-eukaryotic-ribosome-has-revealed-its-structure"/>
      
      
        <rdf:li rdf:resource="http://www.fourmentinguilbert.org/postings/bacteria-self-assemble-in-a-composite-material-for-civil-engineering"/>
      
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  <item rdf:about="http://www.fourmentinguilbert.org/postings/dont-destroy-research">
    <title>Don't destroy research</title>
    <link>http://www.fourmentinguilbert.org/postings/dont-destroy-research</link>
    <description>An appeal from scientists at the publicly funded Rothamsted Research.</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p><span style="text-align: left; float: none;">“On 27th May 2012 protesters are planning to destroy our Chemical Ecology group’s scientific research because it uses genetically modified wheat. Growing wheat has an environmental toll of extensive insecticide use to control aphid pests. The research, which is non-commercial, is investigating how to reduce that by getting the plants to repel aphids with a natural pheromone. We are appealing for protesters to call off the destruction and discuss the work.”<span class="Apple-converted-space">&nbsp;</span></span><br style="text-align: left;" /><strong style="text-align: left;">John Pickett, Scientific Leader of Chemical Ecology, Rothamsted Research</strong></p>
<p><br /><strong style="text-align: left;"></strong></p>
<p><span style="text-align: left; float: none;">“As scientists, we know only too well that we don’t have all the answers. But if the work is destroyed, we’ll lose years of work and we will never know whether it could reduce the environmental impact of wheat growing. Please sign our petition and oppose the destruction of our research.”&nbsp;<span class="Apple-converted-space">&nbsp;</span></span><br style="text-align: left;" /><strong style="text-align: left;">Gia Aradottir, Postdoctoral Researcher, Insect Biology, Rothamsted Research</strong></p>
<p>&nbsp;</p>
<p>More information at: <a class="external-link" href="http://www.senseaboutscience.org/pages/rothamsted-appeal.html">http://www.senseaboutscience.org/pages/rothamsted-appeal.html</a><br /><strong style="text-align: left;"></strong></p>
<p><strong style="text-align: left;"><br /></strong></p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>admin2</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2012-05-04T12:23:00Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/what-does-determine-the-speed-of-protein-production">
    <title>New Layer of Genetic Information Discovered</title>
    <link>http://www.fourmentinguilbert.org/postings/what-does-determine-the-speed-of-protein-production</link>
    <description>By measuring the rate of protein production in bacteria, a team at University of California, San Francisco (UCSF) discovered that slight genetic alterations could have a dramatic effect. This was true even for seemingly insignificant genetic changes known as “silent mutations,” which swap out a single DNA letter without changing the ultimate gene product. To their surprise, the scientists found these changes can slow the protein production process to one-tenth of its normal speed or less.</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>As described today in the journal&nbsp;<em>Nature</em>, the speed change is caused by information contained in what are known as redundant codons — small pieces of DNA that form part of the genetic code. They were called “redundant” because they were previously thought to contain duplicative rather than unique instructions.</p>
<p>This new discovery challenges half a century of fundamental assumptions in biology. It may also help speed up the industrial production of proteins, which is crucial for making biofuels and biological drugs used to treat many common diseases, ranging from diabetes to cancer.</p>
<p><span id="internal-source-marker_0.5204017294801508">To know more:</span></p>
<p><span id="internal-source-marker_0.5204017294801508"><a class="external-link" href="http://www.ucsf.edu/news/2012/03/11794/new-layer-genetic-information-discovered">http://www.ucsf.edu/news/2012/03/11794/new-layer-genetic-information-discovered</a></span></p>
<p><span id="internal-source-marker_0.5204017294801508"><a class="external-link" href="http://www.nature.com/nature/journal/vaop/ncurrent/full/nature10965.html">http://www.nature.com/nature/journal/vaop/ncurrent/full/nature10965.html</a><br /></span></p>
<p>&nbsp;</p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2012-03-30T13:58:57Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/the-spike-of-the-virus">
    <title>The spike of the virus</title>
    <link>http://www.fourmentinguilbert.org/postings/the-spike-of-the-virus</link>
    <description>Wherever there are bacteria (digestive tracts, contaminated water,...) you will find a group of virus called bacteriophages.</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>These
 viruses infiltrate bacteria by drilling into the bacterial outer 
membrane. Once completely through all of a bug's defenses, the phages 
inject their DNA, which essentially turns the bacterium into 
phage-producing factories. Eventually, the microbes become filled with 
so many viruses that they burst, releasing a new horde of phages into 
the environment.</p>
<p><br />Scientists
 have long known that bacteriophages have a knack for infiltrating 
bacteria and that some begin their attack with a protein spike. But the 
tip of this spike is so small that no one knew what it was made of or 
exactly how it worked. Now a team of researchers has found a single iron
 atom at the head of the spike, a discovery that suggests phages enter 
bacteria in a different way than surmised: Forcefully rather than 
softening first the membrane. "It's like driving a nail or stake through
 the membrane of the bacteria." says virus experts.<br /><br />Read the complete article at:</p>
<p><a class="external-link" href="http://news.sciencemag.org/sciencenow/2012/02/bacteria-killing-viruses-wield-a.html?ref=hp">http://news.sciencemag.org/sciencenow/2012/02/bacteria-killing-viruses-wield-a.html?ref=hp</a></p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2012-03-02T09:16:04Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/dna-sequencing-is-now-improving-faster-than-moores-law">
    <title>DNA Sequencing is Now Improving Faster Than Moore's Law!</title>
    <link>http://www.fourmentinguilbert.org/postings/dna-sequencing-is-now-improving-faster-than-moores-law</link>
    <description>Two leading manufacturers of DNA sequencing instruments announce that they would introduce new machines this year capable of sequencing an entire human genome in a single day for a cost of $1,000 per genome.</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>&nbsp;</p>
<p>The speed of genome sequencing has far better than doubled every two years since 2003, when the first whole human genome was completed in 13 years’ time at a cost of $3.8 billion.<br /><br />The parallel with Moore’s law indicates that, just as revolutionary computing and digital electronics applications have transformed society over the past four decades, innovations spurred by widely available gene sequencing could soon do the same. In cancer research for instance, widespread access to DNA sequencing will enable patients or oncologists to share the genomic details of their cancer over time, helping researchers more quickly identify links between mutations and various therapeutic responses.<br /><br />Article source:</p>
<p><a class="external-link" href="http://www.forbes.com/sites/techonomy/2012/01/12/dna-sequencing-is-now-improving-faster-than-moores-law/">http://www.forbes.com/sites/techonomy/2012/01/12/dna-sequencing-is-now-improving-faster-than-moores-law/</a></p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2012-01-16T09:48:47Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/gut-bacteria-can-control-diabetes">
    <title>Gut Bacteria can control Diabetes</title>
    <link>http://www.fourmentinguilbert.org/postings/gut-bacteria-can-control-diabetes</link>
    <description>Insulin resistance is the harbinger of metabolic syndrome.</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>Insulin resistance is when the body cannot use insulin effectively. As a result, blood sugar and fat levels rise. Therein lies the path to morbid obesity, diabetes, stroke, and heart problems.</p>
<p>A group of Brazilian researchers have taken a strain of mice normally known to be immune to insulin resistance, and made them insulin resistant (pre-diabetic) by changing their gut bacteria. They then gave the mice antibiotics, and by changing their gut bacteria again, reversed the process, curing them of the disease. Their research shows just how influential the bacteria living in our gut can be on our health."</p>
<p>&nbsp;</p>
<p>More information:</p>
<p><a class="external-link" href="http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001212">http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001212</a></p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2012-01-13T10:02:14Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/orange-sweet-potato-a-hit-in-mozambique-1">
    <title>Orange sweet potato a hit in Mozambique</title>
    <link>http://www.fourmentinguilbert.org/postings/orange-sweet-potato-a-hit-in-mozambique-1</link>
    <description>Mozambique, like many poor countries, has a high prevalence of vitamin A deficiency, which can erode the immune system and cause blindness. Pregnant woman and young children in low-income countries are often hit the hardest, according to the WHO, and 600,000 children are estimated to die from a lack of vitamin A each year.</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>&nbsp;</p>
<p align="LEFT">
Scientists
have been working on the sweet potato for years, in the hope
of&nbsp;battling deficiencies in vitamin A&nbsp;that afflict around
200 million of the world's poor. A programme aiming to persuade
Mozambican villagers to switch from eating white and yellow sweet
potato to a biofortified orange version, which contains more of a
precursor of vitamin A,&nbsp; has proved successful, with two-thirds
of the targeted households adopting the new variety.</p>
<p align="LEFT">
For
three years, the&nbsp;biofortified sweet potato was created using
conventional techniques to introduce six varieties to the Zambezia province.</p>
<p align="LEFT">
The
study, published in the&nbsp;<em>British Journal of Nutrition</em>&nbsp;last
month (10 October) showed that the varieties were welcomed. It
did not assess whether eating orange sweet potato caused levels of
vitamin A to rise in the blood,&nbsp;though a previous, much smaller
study in the same area had demonstrated this connection. "There
has been a growing body of evidence to show that betacarotene [a
precursor of vitamin A] in orange sweet potato is bioavailable and
converted to vitamin A in the body," said Christine Hotz, former
coordinator of HarvestPlus Nutrition, which led the research.
HarvestPlus&nbsp;said that new, more
drought-tolerant, orange-fleshed sweet potato varieties will be
distributed to 120,000 households over the next two years.</p>
<p align="LEFT"><br /><br /></p>
<p align="LEFT">
The
complete article is available at:</p>
<p align="LEFT"><a class="external-link" href="http://www.scidev.net/en/health/nutrition/news/orange-sweet-potato-a-hit-in-mozambique-say-inventors.html">http://www.scidev.net/en/health/nutrition/news/orange-sweet-potato-a-hit-in-mozambique-say-inventors.html</a></p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2011-12-06T11:12:45Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/quasi-science-prevents-an-environmentally-friendly-agriculture-and-forestry">
    <title>Quasi-science prevents an environmentally friendly agriculture and forestry</title>
    <link>http://www.fourmentinguilbert.org/postings/quasi-science-prevents-an-environmentally-friendly-agriculture-and-forestry</link>
    <description>At the end of this month, the world’s population will reach 7 billions; 1 billion are hungry, and 1 billion more are malnourished. In the next decades, there will be more humans. Limited land and water, costly energy for fertilizer, and climate change will ensure that more of them are hungry.
Science and technology can contribute greatly to the solution. Why then is Europe regulating one part of the solution- GM (genetically modified) crops- as if they are a hazard?</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>&nbsp;</p>
<p>&nbsp;</p>
<p>41 leading Swedish plant
scientists urge politicians and environmental groups to take the
necessary steps to change the relevant legislation so that all
available knowledge can be used to develop sustainable agricultural
and forest industries. Endorsed by British plant scientists, they
have issued an important statement, expressing dismay, bewilderment
and anger that legislation of GM crops in the EU is not based on
science, ignores recent evidence, blocks opportunities to increase
agricultural sustainability, and sustains the dominance of
multinationals.</p>
<p>&nbsp;</p>
<p>To know more:</p>
<p>&nbsp;</p>
<p><a class="external-link" href="http://www.plantsci.org.uk/news/leading-plant-researchers-call-science-based-gm-regulation">http://www.plantsci.org.uk/news/leading-plant-researchers-call-science-based-gm-regulation</a></p>
<p>&nbsp;</p>
<p><a class="external-link" href="http://www.plantsci.org.uk/sites/default/files/Debate%20article.pdf">http://www.plantsci.org.uk/sites/default/files/Debate%20article.pdf</a></p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2011-10-21T09:47:35Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/gamers-help-protein-3d-structure-modeling">
    <title>Gamers help protein 3D structure modeling</title>
    <link>http://www.fourmentinguilbert.org/postings/gamers-help-protein-3d-structure-modeling</link>
    <description>One of the goals of computational biology is to predict the complete high-order structure of a protein from its amino acid sequence. Often reasonably good structures can be produced by modeling a new protein according to an already-known structure of a homologous protein, one with a similar sequence and presumably a similar structure. However, these structures can be inaccurate, and obviously this method will not work if no homologous structure is known.</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>&nbsp;</p>
<p align="LEFT">
Foldit is an online
game developed by the research team of Dr. David Baker that attempts
to address this problem by combining an automated structure
prediction program called&nbsp;ROSETTA with input from human players
who manually remodel structures to improve them.
Even
though most of the players have little or no advanced biochemical
knowledge, Foldit has already had some striking results improving on
computational models. A
paper in&nbsp;<em>Nature
Structural &amp; Molecular Biology</em>
details some interesting new successes from the Foldit players.</p>
<p align="LEFT">&nbsp;</p>
<p align="LEFT">
Does
this prove that gamers know more about folding proteins than
computers do? Some of them might, but Foldit doesn’t really use
human expertise. Rather, the game uses human intelligence to identify
when the ROSETTA program has gone down the wrong path and figure out
how to push it over the hump.
When
the human intelligences aren’t daring enough, or trust the system
too much, Foldit doesn’t do any better than completely automated
structural methods. When the human players are encouraged to
challenge the computational results, however, the results can be
striking. As Baker’s group are clearly aware, further development
of the program needs to be oriented towards encouraging players to go
further afield from the initial ROSETTA predictions.</p>
<p align="LEFT">&nbsp;</p>
<p align="LEFT">
The complete article
by Michael W. Clarkson is at:</p>
<p align="LEFT"><a class="external-link" href="http://conflux.mwclarkson.com/2011/09/foldit-pmv-pr/?utm_source=feedburner&utm_medium=feed&utm_campaign=Feed%3A+ConformationalFlux+%28Conformational+Flux%29">http://conflux.mwclarkson.com/2011/09/foldit-pmv-pr/?utm_source=feedburner&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+ConformationalFlux+%28Conformational+Flux%29</a></p>
<p align="LEFT">&nbsp;</p>
<p align="LEFT">
The paper describing
Foldit players results is available directly from David Baker's lab:</p>
<p align="LEFT"><a class="external-link" href="http://www.cs.washington.edu/homes/zoran/NSMBfoldit-2011.pdf">http://www.cs.washington.edu/homes/zoran/NSMBfoldit-2011.pdf</a></p>
<p align="LEFT">&nbsp;</p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2011-09-22T18:09:08Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/synthetic-organization">
    <title>RNA as an assembly line</title>
    <link>http://www.fourmentinguilbert.org/postings/synthetic-organization</link>
    <description>Delebecque and coworkers describe in Science the design and construction of self-assembling RNA scaffolds that spatially organize enzymes in bacterial
cells. </description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<p>Internal organization in cells ranges from the simple colocalization of molecules in complexes to the compartmentalization of metabolic pathways within organelles.</p>
<p>Delebecque and coworkers designed and assembled multidimensional RNA structures and used them as scaffolds for the spatial organization of hydrogen-producing pathway.</p>
<p>RNA scaffolds served as docking sites to promote protein-protein interactions in cells and concentrate proteins and their products.</p>
<p>Several arrangements of organelle-like structures are generated and their effectiveness to increase hydrogen biosynthesis is measured.</p>
<p>This study is another demonstration that component spatial organization is key in the design of biosynthetic pathways. 3D modeling with a tool like LifeExplorer can help as it allows to construct, visualize and simulate cellular processes in a realistic way.</p>
<p><a href="http://www.sciencemag.org/content/333/6041/470.short">http://www.sciencemag.org/content/333/6041/470.short</a></p>]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>damien</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2011-07-27T13:00:12Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/chemical-evolution-of-a-bacteriums-genome">
    <title>Escherichia chlori</title>
    <link>http://www.fourmentinguilbert.org/postings/chemical-evolution-of-a-bacteriums-genome</link>
    <description></description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>Marlière
and coworkers evolved the
genetic program of an E. coli bacterium in order to replace one of the four DNA acid base by a chloro molecule analog.</p>
<p>This experiment is opening the road to
xenobiology with modified organisms unable to exchange genetic material with living systems. <br /><br />To go in the details of the paper:</p>
<p><a class="external-link" href="http://onlinelibrary.wiley.com/doi/10.1002/ange.201100535/abstract?systemMessage=Wiley+Online+Library+will+be+disrupted+2+July+from+10-12+BST+for+monthly+maintenance">http://onlinelibrary.wiley.com/doi/10.1002/ange.201100535/abstract?systemMessage=Wiley+Online+Library+will+be+disrupted+2+July+from+10-12+BST+for+monthly+maintenance</a></p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2011-07-04T05:30:00Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/farewell-symposium-for-andreas-engel">
    <title>Farewell Symposium for Andreas Engel</title>
    <link>http://www.fourmentinguilbert.org/postings/farewell-symposium-for-andreas-engel</link>
    <description>Andreas Engel, Professor for Structural Biology and former Chairman of the Biozentrum, retired from service to the Biozentrum and became Professor emeritus in October 2010. On February 11th, 2011, the Biozentrum bade farewell to its long standing member and remarkable researcher with a scientific symposium in his honor.</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>&nbsp;</p>
<p>Andreas
Engel worked and taught at the Biozentrum for over 25 years. He
focused on unraveling the structure and understanding the function of
various membrane proteins. To analyze these proteins, he employed the
techniques of electron crystallography, atomic force microscopy and
scanning transmission electron microscopy.</p>
<p>Andreas
Engel had a great influence on the development of 2D crystallization
of membrane proteins, on the initial work of the 3D structure
determination of the bacterial OmpF porin as well as the elucidation
of the structure of human aquaporin-1. Together with
Peter Agre (Baltimore) and Yoshinori Fujiyoshi (Kyoto) Engel’s work
led to the first understanding of the atomic structure of a water
channel membrane protein. It was in connection to this, that Peter
Agre received the Nobel Prize for Chemistry in 2003, for his
discovery of water channels.</p>
<p>&nbsp;</p>
<p>For more information :</p>
<p><a class="external-link" href="http://www.biozentrum.unibas.ch/bionews/bionews_20110214_engl.html">http://www.biozentrum.unibas.ch/bionews/bionews_20110214_engl.html</a></p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2011-03-30T13:56:32Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/the-3d-architecture-of-the-bacterial-chromosome">
    <title>The 3D architecture of the bacterial chromosome</title>
    <link>http://www.fourmentinguilbert.org/postings/the-3d-architecture-of-the-bacterial-chromosome</link>
    <description>A bacterial chromosome is so long that it must be highly compacted and folded to stand within the cellular space. Genetic studies coupled with fluorescence microscopy showed that it is well organized into isolated domains. These domains also move with order when the chromosome is duplicated and the two new chromosomes are separated each in one half the dividing cell.</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>&nbsp;</p>
<p>But 3D images of the
chromosome within its intact cell were still very difficult to obtain
due to the limitations of the current microscopy technics. The
folding of the chromosome in space, its functional architecture have
thus remained unclear.</p>
<p>A recent study shows such
images. Thanks to a cryo-electron tomographic analysis, of the 3D
architecture of the chromosome of the bacterium <em>Bdellovibrio
bacteriovorus</em>. clearly appears. The salient observation is the
versatile nature of this architecture: The chromosome can take
several but very different shapes (twisted spiral vs. compact)
providing the bacterium with different behaviors.</p>
<p>This study reinforces the
idea of a pivotal role for one particular proteins called MreB. MreB
is more and more thought to be a major actor in several cellular
processes like the elongation, the nucleoid organization, the
chromosome segregation, the chemoreceptor localization.</p>
<p>&nbsp;</p>
<p>&nbsp;</p>
<p>Reference:</p>
<p><strong>Spiral
architecture of the nucleoid in Bdellovibrio bacteriovorus</strong><br />C.
Butan, L.M. Hartnell, A.K. Fenton, D. Bliss, R.E. Sockett,
S.Subramaniam and J.L. S. Milne<br />J. Bacteriology, 2010 Dec 10.</p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2011-02-07T09:26:55Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/lifeexplorer-illustrates-the-front-page-of-molecular-microbiology">
    <title>LifeExplorer illustrates the front page of Molecular Microbiology</title>
    <link>http://www.fourmentinguilbert.org/postings/lifeexplorer-illustrates-the-front-page-of-molecular-microbiology</link>
    <description>The December 2010 issue contains several papers dedicated to bacterial cell division. The journal cover highlights a 3D model of the bacterial division machinery (the divisome) created with the LifeExplorer tool in collaboration with F.-X. Barre and N. Dubarry.</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>&nbsp;</p>
<p>More information:</p>
<p><a class="external-link" href="http://onlinelibrary.wiley.com/doi/10.1111/mmi.2010.78.issue-5/issuetoc">http://onlinelibrary.wiley.com/doi/10.1111/mmi.2010.78.issue-5/issuetoc</a></p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2010-12-10T09:45:00Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/the-eukaryotic-ribosome-has-revealed-its-structure">
    <title>The eukaryotic ribosome has revealed its structure</title>
    <link>http://www.fourmentinguilbert.org/postings/the-eukaryotic-ribosome-has-revealed-its-structure</link>
    <description>Researchers at the Institute of Genetics and Molecular and Cell Biology (CNRS / University of Strasbourg / Inserm) have determined the first atomic structure of an eukaryotic ribosome (yeast ribosome).</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>The
eukaryotic ribosome, currently the largest asymmetric biological
molecule, is an essential machinery of the cell for proteins
synthesis
from genetic information. It interacts with many proteins and
has a key role in various cellular
processes.</p>
<p>In
2009, the Nobel Prize in Chemistry rewarded researchers who first
determined in 2000 the first
structure at atomic resolution of the bacterial ribosome. The
race for revealing the high
resolution structure of the eukaryotic ribosome was then
initiated.</p>
<p>More information
on:</p>
<p><a class="external-link" href="http://www2.cnrs.fr/presse/communique/2042.htm">http://www2.cnrs.fr/presse/communique/2042.htm</a></p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2010-11-30T13:20:00Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>


  <item rdf:about="http://www.fourmentinguilbert.org/postings/bacteria-self-assemble-in-a-composite-material-for-civil-engineering">
    <title>Bacteria self-assemble in a composite material for civil engineering</title>
    <link>http://www.fourmentinguilbert.org/postings/bacteria-self-assemble-in-a-composite-material-for-civil-engineering</link>
    <description>Researchers have designed bacteria that can produce a special glue to knit together cracks in concrete structures.</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<p>&nbsp;</p>
<p>The
genetically modified microbe (Bacillus subtilis) has been programmed
to swim down
fine cracks in concrete. Once at the bottom, the resulting clumping
of bacteria activates the concrete repair process and the cells
differentiate into three types: cells which produce calcium carbonate
crystals, cells which become filamentous —acting as reinforcing
fibers — and thirdly cells that produce a glue that acts as a
binding agent and fills the gap. The whole ultimately
hardens to the
same
strength as the surrounding concrete.</p>
<p><br />Jennifer
Hallinan says that "this could be particularly useful in
earthquake zones where hundreds of buildings have to be flattened
because there is currently no easy way of repairing the cracks and
making them structurally sound."<br />Regarding
potential risks to the environment, the microbe spores start
germinating only when they make contact with concrete — triggered
by the very specific pH of the material — and they have a built-in
self-destruct gene that prevents them from proliferating away from
the concrete target.<br /><br />More
information at:</p>
<p><a class="external-link" href="http://www.msnbc.msn.com/id/40201539/ns/technology_and_science-future_of_energy/">http://www.msnbc.msn.com/id/40201539/ns/technology_and_science-future_of_energy/</a></p>
]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>nathalie</dc:creator>
    <dc:rights></dc:rights>
    <dc:date>2010-11-16T11:15:40Z</dc:date>
    <dc:type>News Item</dc:type>
  </item>





</rdf:RDF>

