Difference between revisions of "Part:BBa K1172305"

Line 3: Line 3:
  
  
[[Image:IGEM_Bielefeld_Riboflavin_6WellPlate.jpg|500px|thumb|center|<p align="justify"> '''Figure 1: From left to right: ''e. coli'' KRX wild type compared to ''e. coli'' KRX with <bbpart>BBa_K1172303</bbpart> under control of a medium constitutive promoter and ''e. coli'' KRX with <bbpart>BBa_K1172303</bbpart> under control of a strong constitutive promoter.]]</p>
+
[[Image:IGEM_Bielefeld_Riboflavin_6WellPlate.jpg|500px|thumb|center|<p align="justify"> '''Figure 1: From left to right: ''e. coli'' KRX wild type compared to ''e. coli'' KRX with <bbpart>BBa_K1172303</bbpart> under control of a medium constitutive promoter (<bbpart>BBa_K525998</bbpart>) and ''e. coli'' KRX with <bbpart>BBa_K1172303</bbpart> under control of a strong constitutive promoter (<bbpart>BBa_K608002</bbpart>).]]</p>
 
<p align="justify">
 
<p align="justify">
This gene cluster consists of four different genes that form a single operon. These genes are pivotal in the riboflavin biosythesis pathway of shewanella oneidensis and are transcribed polycystronic.
+
This gene cluster consists of four different genes that form a single operon. These genes are pivotal in the riboflavin biosythesis pathway of ''Shewanella oneidensis'' and are transcribed polycystronic.
The original operon in ''shewanella oneidensis'' has additional activator and repressor genes. It was observed that these are not sufficient for riboflavin overproduction. Therefore these genes were not isolated from genomic DNA.
+
The original operon in ''Shewanella oneidensis'' has additional activator and repressor genes. It was observed that these are not sufficient for riboflavin overproduction. Therefore these genes were not isolated from genomic DNA.
 
</p>
 
</p>
 
===Usage and Biology===
 
===Usage and Biology===
 
<p align="justify">
 
<p align="justify">
  
Riboflavin, or Vitamin B2 is a redox-active substance that plays an essential role in living cells. As precursor of FMN and FAD it is crucial for diverse energy supplying metabolic processes, e.g. beta-oxidation or oxidative phosphorylation. Riboflavin is water soluble and shows a distinct yellow coloration. For that reason it is although used for food coloration. It is easily detectable through absorbance and fluorescence measurement. Due to its fluorescent properties and non-toxicity it is used to detect leaks or to control cleaning processes.
+
Riboflavin, or Vitamin B2 is a redox-active substance that plays an essential role in living cells. As precursor of flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) it is crucial for diverse energy supplying metabolic processes, e.g. beta-oxidation or oxidative phosphorylation. Riboflavin is water soluble and shows a distinct yellow coloration. For that reason it is also used for food coloration. It is easily detectable through absorbance and fluorescence measurement. Due to its fluorescent properties and non-toxicity it is used to detect leaks or to control cleaning processes.
 
</p>
 
</p>
 
[[File:IGEM Bielefeld 2013 riboflavin.jpg|200px|thumb|left|<p align="justify">'''Figure 2: '''Riboflavin (Vitamin B2) and flavin-coenzymes FMN (flavin mononucleotide) and FAD (flavin adenine dinucleotide).]]</p>
 
[[File:IGEM Bielefeld 2013 riboflavin.jpg|200px|thumb|left|<p align="justify">'''Figure 2: '''Riboflavin (Vitamin B2) and flavin-coenzymes FMN (flavin mononucleotide) and FAD (flavin adenine dinucleotide).]]</p>
  
 
<p align="justify">
 
<p align="justify">
Chemically riboflavin consists of two functional subunits, a short-chain ribitol and a tricyclic heterosubstituted isoalloxazine ring.
+
Riboflavin consists of two functional subunits, a short-chain ribitol and a tricyclic heterosubstituted isoalloxazine ring.
The latter, also known as a riboflavin ring, exists in three redox states and is responsible for the diverse chemical activity of riboflavin. A fully oxidized quinone, a one-electron semiquinone and a fully reduced hydroquinone states are the three stages of riboflavin oxidation. In an aqueous solution, the quinone (fully oxidized) form of riboflavin has a typical yellow coloring. It becomes red in a semi-reduced anionic or blue in a neutral form and is colorless when fully reduced.
+
The latter, also known as a riboflavin ring, exists in three redox states and is responsible for the diverse chemical activities of riboflavin. A fully oxidized quinone, a one-electron semiquinone and a fully reduced hydroquinone state are the three stages of riboflavin oxidation. In an aqueous solution, the quinone (fully oxidized) form of riboflavin has a typical yellow coloring. It becomes red in a semi-reduced anionic or blue in a neutral form and is colorless when fully reduced.
 
</p>
 
</p>
  
 
<p align="justify">
 
<p align="justify">
Secreted into the medium, it can be effectively used by some bacteria for electron transfer. Presence of riboflavin in anaerobic cultures leads to higher current flow in a microbial fuel cell, which made riboflavin overproduction a suitable target for optimisation of our MFC.
+
Secreted into the medium, it can be effectively used by some bacteria for electron transfer. Presence of riboflavin in anaerobic cultures leads to higher current flow in a Microbial Fuel Cell, which makes riboflavin overproduction a suitable target for optimisation of our MFC.
 
<br>
 
<br>
 
We have shown that cloning of the riboflavin cluster from a metal-reducing bacterium ''Shewanella oneidensis MR-1'' in ''E. coli'' is sufficient to achieve significant riboflavin overproduction detectable both in supernatant and in cells.
 
We have shown that cloning of the riboflavin cluster from a metal-reducing bacterium ''Shewanella oneidensis MR-1'' in ''E. coli'' is sufficient to achieve significant riboflavin overproduction detectable both in supernatant and in cells.
Line 27: Line 27:
  
 
<!-- -->
 
<!-- -->
 
 
<br><br><br><br><br><br>
 
<br><br><br><br><br><br>
 
<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>

Revision as of 15:26, 28 October 2013

Riboflavin synthesis gene cluster from s. oneidensis under control of a medium Anderson promoter


Figure 1: From left to right: e. coli KRX wild type compared to e. coli KRX with BBa_K1172303 under control of a medium constitutive promoter (BBa_K525998) and e. coli KRX with BBa_K1172303 under control of a strong constitutive promoter (BBa_K608002).

This gene cluster consists of four different genes that form a single operon. These genes are pivotal in the riboflavin biosythesis pathway of Shewanella oneidensis and are transcribed polycystronic. The original operon in Shewanella oneidensis has additional activator and repressor genes. It was observed that these are not sufficient for riboflavin overproduction. Therefore these genes were not isolated from genomic DNA.

Usage and Biology

Riboflavin, or Vitamin B2 is a redox-active substance that plays an essential role in living cells. As precursor of flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) it is crucial for diverse energy supplying metabolic processes, e.g. beta-oxidation or oxidative phosphorylation. Riboflavin is water soluble and shows a distinct yellow coloration. For that reason it is also used for food coloration. It is easily detectable through absorbance and fluorescence measurement. Due to its fluorescent properties and non-toxicity it is used to detect leaks or to control cleaning processes.

Figure 2: Riboflavin (Vitamin B2) and flavin-coenzymes FMN (flavin mononucleotide) and FAD (flavin adenine dinucleotide).

Riboflavin consists of two functional subunits, a short-chain ribitol and a tricyclic heterosubstituted isoalloxazine ring. The latter, also known as a riboflavin ring, exists in three redox states and is responsible for the diverse chemical activities of riboflavin. A fully oxidized quinone, a one-electron semiquinone and a fully reduced hydroquinone state are the three stages of riboflavin oxidation. In an aqueous solution, the quinone (fully oxidized) form of riboflavin has a typical yellow coloring. It becomes red in a semi-reduced anionic or blue in a neutral form and is colorless when fully reduced.

Secreted into the medium, it can be effectively used by some bacteria for electron transfer. Presence of riboflavin in anaerobic cultures leads to higher current flow in a Microbial Fuel Cell, which makes riboflavin overproduction a suitable target for optimisation of our MFC.
We have shown that cloning of the riboflavin cluster from a metal-reducing bacterium Shewanella oneidensis MR-1 in E. coli is sufficient to achieve significant riboflavin overproduction detectable both in supernatant and in cells.







Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 1176
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Part uses

For overproduction of riboflavin, the BioBrick BBa_K1172303 was combined with promoters of different strenghts.

Device: BBa_K1172303

under control of accordant promoter.

Promoters used RBS / Activity
BBa_K1172304 BBa_K525998 “T7 induced" strong / very strong
BBa_K1172305 BBa_K608006 “Anderson 0.33” medium / medium
BBa_K1172306 BBa_K608002 “Anderson 0.77” strong / strong



Since the regional in Lyon, we were able to combine BBa_K1172303 with other BioBricks from our project.

Device: Combination of BBa_K1172303

with accordant parts

Part 1 of the new device Explanation
BBa_K1172588 BBa_K1172502 Combination of oprF from p. fluorescence under control of T7 promoter and the rib-gene-cluster from s. oneidensis
BBa_K1172599 BBa_K1172501 Combination of the coding sequences oprF from p. fluorescence and the rib-gene-cluster from s. oneidensis



Results

This part was used to characterize the riboflavin synthesis gene cluster from shewanella oneidensis (BBa_K1172303). Please look at the Parts Registry page for BBa_K1172303 for results and detailed information.