Team:UniSalento Lecce

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Why? ... An overview
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Why NickBusters?
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<h3>Sense it!</h3>
<h3>Sense it!</h3>
<p style="font-size: 14px">Population #1 feels the danger and calls up for help! When sensing nickel in the environment, this population turns red, then releases a QS molecule, recruiting population 2! </p>
<p style="font-size: 14px">Population #1 feels the danger and calls up for help! When sensing nickel in the environment, this population turns red, then releases a QS molecule, recruiting population 2! </p>
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<a href="#">Read more &raquo;</a>
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<h3>Store it!</h3>
<h3>Store it!</h3>
<p style="font-size: 14px">Population #2 receives the QS signal, which activates the adsorption of nickel; then amplifies the QS signal, inducing further bacteria to accumulate the heavy metal. </p>
<p style="font-size: 14px">Population #2 receives the QS signal, which activates the adsorption of nickel; then amplifies the QS signal, inducing further bacteria to accumulate the heavy metal. </p>
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<a href="#">Read more &raquo;</a>
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from bacteria to higher forms of life. However, as all the heavy metals, even a small amount of Nickel higher
from bacteria to higher forms of life. However, as all the heavy metals, even a small amount of Nickel higher
than the essential dose could be toxic, leading to various noxious effects <a href="#biblio" style="color: #8ac101">[1-2]</a>: then the need to remove its
than the essential dose could be toxic, leading to various noxious effects <a href="#biblio" style="color: #8ac101">[1-2]</a>: then the need to remove its
-
excess from many substrates. Nowadays <b>bacteria-mediated bioremediation</b> from inorganic substances seems to be a considerably relevant frontier in microbic biotechnologies <a href="#biblio" style="color: #8ac101">[3]</a>.
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excess from many substrates. Nowadays <b>bacteria-mediated bioremediation</b> from inorganic substances seems to be a considerably relevant frontier in microbial biotechnologies <a href="#biblio" style="color: #8ac101">[3]</a>.
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Our project aims to develop a living system, in an easy monitorable bacterial platform, who would work as a
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Our project aims to develop a living system, in an easily monitorable bacterial platform, who would work as a
<b>Nickel detector</b> and a <b>Nickel remediation</b> system. The whole system is based on genetic parts from the
<b>Nickel detector</b> and a <b>Nickel remediation</b> system. The whole system is based on genetic parts from the
pathogen <i>Helicobacter pylori</i>, whose evolution led to a stronger reliance on Nickel ions for host interaction
pathogen <i>Helicobacter pylori</i>, whose evolution led to a stronger reliance on Nickel ions for host interaction
and pathogenesis.
and pathogenesis.
<b>Sensing</b> relies on nickel regulator <i>NikR</i> from <i>H. pylori</i> (<i>HpNikR</i>): though homolog of <i>E.coli NikR</i>, it has a
<b>Sensing</b> relies on nickel regulator <i>NikR</i> from <i>H. pylori</i> (<i>HpNikR</i>): though homolog of <i>E.coli NikR</i>, it has a
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stronger dependance on Nickel ions and a wider range of regulated elements, being a rare case of pleiotropic
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stronger dependence on Nickel ions and a wider range of regulated elements, being a rare case of pleiotropic
regulator in bacteria.
regulator in bacteria.
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As <i>HpNikR</i> could contemporaneously activate and repress gene expression <a href="#biblio" style="color: #8ac101">[4-5-6]</a>, we thought of developing
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As <i>HpNikR</i> could contemporaneously activate and repress gene expression <a href="#biblio" style="color: #8ac101">[4-5-6]</a>, we thought to develop
a synthetic gene cluster under <i>HpNikR</i> - regulated promoters. With a <b>double regulation</b>, one of the promoters
a synthetic gene cluster under <i>HpNikR</i> - regulated promoters. With a <b>double regulation</b>, one of the promoters
-
being activated while the other being repressed, the system allows to follow up Nickel sensing as a
+
being activated while the other gets repressed, the system allows to follow up Nickel sensing as a
fluorescence signal from fluorescent proteins. Thus, adding bacteria to a nickel containing medium results in
fluorescence signal from fluorescent proteins. Thus, adding bacteria to a nickel containing medium results in
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<b>switching off a basal occuring green fluorescence</b> and in <b>switching on a red fluorescence signal</b>.
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<b>switching off a basal occurring green fluorescence</b> and in <b>switching on a red fluorescence signal</b>.
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The Nickel <b>storage</b> system is even taken from our pathogenic friend: <i>Hpn</i> protein is a Nickel binding protein,
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The Nickel <b>storage</b> system is even taken from our pathogenic friend: <i>Hpn</i> protein is a Nickel-binding protein,
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whose role is to store the Nickel ions inside the cell and to supply them to other proteic interactors, from
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whose purpose is to store the Nickel ions inside the cell and to supply them with other protein interactors, from
Nickel dependent heat shock proteins to pathogenesis factors as urease <a href="#biblio" style="color: #8ac101">[7]</a>. <i>Hpn</i> can be expressed in a
Nickel dependent heat shock proteins to pathogenesis factors as urease <a href="#biblio" style="color: #8ac101">[7]</a>. <i>Hpn</i> can be expressed in a
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heterologous model system (<i>E.coli</i>), increasing bacterial resistance to toxic dose of Nickel ions and allowing
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heterologous model system (<i>E.coli</i>), increasing bacterial resistance up to a toxic dose of Nickel ions and allowing
Ni++ intracellular accumulation <a href="#biblio" style="color: #8ac101">[8]</a>.
Ni++ intracellular accumulation <a href="#biblio" style="color: #8ac101">[8]</a>.
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We thought to split the <b>sense and store machineries in two different bacterial populations</b>, making them
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We thought to split the <b>sensing and storing machineries into two different bacterial populations</b>, making them
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communicate through Quorum Sensing <a href="#biblio" style="color: #8ac101">[9]</a>: we used the <i>LuxI/LuxR</i> system from <i>Alivibrio fischerii</i>. The first
+
communicate with each other through Quorum Sensing <a href="#biblio" style="color: #8ac101">[9]</a>: we used the <i>LuxI/LuxR</i> system from <i>Alivibrio fischerii</i>. The first
population senses nickel concentration in medium ( and translates it in a fluorescence signal), then activating
population senses nickel concentration in medium ( and translates it in a fluorescence signal), then activating
<i>Acyl-Homoserine-Lactones</i> (<i>AHLs</i>) production. The second population receives the <i>QS</i> signal and sums it up to the nickel detection signal (as in an AND gate), activating <i>Hpn</i> (the storage protein) expression and <i>AHLs</i> signal amplification.
<i>Acyl-Homoserine-Lactones</i> (<i>AHLs</i>) production. The second population receives the <i>QS</i> signal and sums it up to the nickel detection signal (as in an AND gate), activating <i>Hpn</i> (the storage protein) expression and <i>AHLs</i> signal amplification.
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Latest revision as of 14:43, 4 October 2013



Introduction to NickBusters Project

Nickel is one of the most widespread heavy metals in the ecosystem, and it is essential for many organisms, from bacteria to higher forms of life. However, as all the heavy metals, even a small amount of Nickel higher than the essential dose could be toxic, leading to various noxious effects [1-2]: then the need to remove its excess from many substrates. Nowadays bacteria-mediated bioremediation from inorganic substances seems to be a considerably relevant frontier in microbial biotechnologies [3]. Our project aims to develop a living system, in an easily monitorable bacterial platform, who would work as a Nickel detector and a Nickel remediation system. The whole system is based on genetic parts from the pathogen Helicobacter pylori, whose evolution led to a stronger reliance on Nickel ions for host interaction and pathogenesis. Sensing relies on nickel regulator NikR from H. pylori (HpNikR): though homolog of E.coli NikR, it has a stronger dependence on Nickel ions and a wider range of regulated elements, being a rare case of pleiotropic regulator in bacteria. As HpNikR could contemporaneously activate and repress gene expression [4-5-6], we thought to develop a synthetic gene cluster under HpNikR - regulated promoters. With a double regulation, one of the promoters being activated while the other gets repressed, the system allows to follow up Nickel sensing as a fluorescence signal from fluorescent proteins. Thus, adding bacteria to a nickel containing medium results in switching off a basal occurring green fluorescence and in switching on a red fluorescence signal.

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The Nickel storage system is even taken from our pathogenic friend: Hpn protein is a Nickel-binding protein, whose purpose is to store the Nickel ions inside the cell and to supply them with other protein interactors, from Nickel dependent heat shock proteins to pathogenesis factors as urease [7]. Hpn can be expressed in a heterologous model system (E.coli), increasing bacterial resistance up to a toxic dose of Nickel ions and allowing Ni++ intracellular accumulation [8]. We thought to split the sensing and storing machineries into two different bacterial populations, making them communicate with each other through Quorum Sensing [9]: we used the LuxI/LuxR system from Alivibrio fischerii. The first population senses nickel concentration in medium ( and translates it in a fluorescence signal), then activating Acyl-Homoserine-Lactones (AHLs) production. The second population receives the QS signal and sums it up to the nickel detection signal (as in an AND gate), activating Hpn (the storage protein) expression and AHLs signal amplification.




Bibliography

  1. Denkhaus and Salnikow, Nickel essentiality, toxicity and carcinogenity; Critical Reviews in Oncology/Hematology, 42 (2002) 35–56
  2. “Nickel, Elemental” on TOXNET- Databases on toxicology, hazardous chemicals, environmental health, and toxic releases.
  3. Gadd, Metals, minerals and microbes: geomicrobiology and bioremediation; Microbiology, 156 (2010), 609–643
  4. Dosanjh and Michel, Microbial nickel metalloregulation: NikRs for nickel ions; Current Opinion in Chemical Biology, 10 (2006), 123–130
  5. Contreras et al., Characterization of the roles of NikR, a nickel-responsive pleiotropic autoregulator of Helicobacter pylori; Molecular Microbiology, 49 (4) (2003), 947–963
  6. Muller et al., Hierarchical regulation of the NikR-mediated nickel response in Helicobacter pylori; Nucleic Acids Research, 39 (17) (2011), 7564–7575
  7. Seshadri et al., Roles of His-Rich Hpn and Hpn-Like Proteins in Helicobacter pylori Nickel Physiology; Journal of Bacteriology, 189 (11) (2007), 4120–4126
  8. Ge et al., Expression and characterization of a histidine-rich protein, Hpn: potential for Ni2+ storage in Helicobacter pylori; Biochemistry Journal 393 (2006), 285–293
  9. Miller, Bassler, Quorum Sensing in bacteria; Annual Review of Microbiology 55 (2001), 165-99.

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