Difference between revisions of "Part:BBa K3724013"
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<partinfo>BBa_K3724013 short</partinfo> | <partinfo>BBa_K3724013 short</partinfo> | ||
− | + | <i>rib d</i> encodes the riboflavin biosynthesis protein rib D which converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)-pyrimidinedione 5'-phosphate in the riboflavin biosynthesis pathway in <i> Shewanella oneidensis MR-1</i>. This gene makes up a component of the riboflavin synthesis gene cluster ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K3724015 BBa_K3724015]). | |
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===Usage and Biology=== | ===Usage and Biology=== | ||
+ | <i>Shewanella oneidensis MR-1</i> are gram-negative bacteria at the center of studies of microbial reduction due to their ability to transfer electrons extracellularly to reduce materials such as graphene oxide (GO) [1]. Such characteristics have made <i>S. oneidensis MR-1</i> an organism of interest in microbial fuel cells for bioelectricity generation and potential applications in bioremediation [2]. | ||
+ | Two extracellular electron transfer pathways have been identified in the reduction of GO by <i>Shewanella oneidensis MR-1</i>. These are indirect electron transfer, mediated by secreted electron shuttles, and direct extracellular electron transfer (DET) which involves direct contact with the extracellular material [3]. | ||
+ | <i>rib d</i> encodes the riboflavin biosynthesis protein rib D which converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)-pyrimidinedione 5'-phosphate. | ||
+ | This protein is essential for the production of riboflavin in the riboflavin biosynthesis pathway of <i> S. oneidensis MR-1 </i>. It has been proposed that flavins may act as electron shuttles in the reduction of extracellular material by <i>S. oneidensis MR-1</i> [4]. Therefore, this gene was used in the construction of the riboflavin synthesis gene cluster ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K3724015 BBa_K3724015]) to increase the production of riboflavin in <i>S. oneidensis MR-1</i> for increased rate of reduction of graphene oxide. | ||
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<partinfo>BBa_K3724013 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3724013 SequenceAndFeatures</partinfo> | ||
+ | ===References=== | ||
+ | |||
+ | [1] Wang, G.; Qian, F.; Saltikov, C. W.; Jiao, Y.; Li, Y. Microbial Reduction of Graphene Oxide by Shewanella. Nano Research 2011, 4, 563–570. <br> | ||
+ | [2] Schwalb, C.; Chapman, S. K.; Reid, G. A. The Tetraheme Cytochrome Cyma Is Required for Anaerobic Respiration with Dimethyl Sulfoxide and Nitrite in Shewanella Oneidensis. Biochemistry 2003, 42, 9491–9497. <br> | ||
+ | [3] Lin, T.; Ding, W.; Sun, L.; Wang, L.; Liu, C.-G.; Song, H. Engineered Shewanella Oneidensis-Reduced Graphene Oxide Biohybrid with Enhanced Biosynthesis and Transport of Flavins Enabled a Highest Bioelectricity Output in Microbial Fuel Cells. <br> | ||
+ | [4] Kouzuma, A.; Kasai, T.; Hirose, A.; Watanabe, K. Catabolic and Regulatory Systems in Shewanella Oneidensis MR-1 Involved in Electricity Generation in Microbial Fuel Cells. Frontiers in Microbiology 2015, 6. <br> | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Latest revision as of 03:15, 22 October 2021
Riboflavin biosynthesis protein RibD
rib d encodes the riboflavin biosynthesis protein rib D which converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)-pyrimidinedione 5'-phosphate in the riboflavin biosynthesis pathway in Shewanella oneidensis MR-1. This gene makes up a component of the riboflavin synthesis gene cluster (BBa_K3724015).
Usage and Biology
Shewanella oneidensis MR-1 are gram-negative bacteria at the center of studies of microbial reduction due to their ability to transfer electrons extracellularly to reduce materials such as graphene oxide (GO) [1]. Such characteristics have made S. oneidensis MR-1 an organism of interest in microbial fuel cells for bioelectricity generation and potential applications in bioremediation [2]. Two extracellular electron transfer pathways have been identified in the reduction of GO by Shewanella oneidensis MR-1. These are indirect electron transfer, mediated by secreted electron shuttles, and direct extracellular electron transfer (DET) which involves direct contact with the extracellular material [3]. rib d encodes the riboflavin biosynthesis protein rib D which converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)-pyrimidinedione 5'-phosphate. This protein is essential for the production of riboflavin in the riboflavin biosynthesis pathway of S. oneidensis MR-1 . It has been proposed that flavins may act as electron shuttles in the reduction of extracellular material by S. oneidensis MR-1 [4]. Therefore, this gene was used in the construction of the riboflavin synthesis gene cluster (BBa_K3724015) to increase the production of riboflavin in S. oneidensis MR-1 for increased rate of reduction of graphene oxide.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 7
Illegal BsaI.rc site found at 1169
References
[1] Wang, G.; Qian, F.; Saltikov, C. W.; Jiao, Y.; Li, Y. Microbial Reduction of Graphene Oxide by Shewanella. Nano Research 2011, 4, 563–570.
[2] Schwalb, C.; Chapman, S. K.; Reid, G. A. The Tetraheme Cytochrome Cyma Is Required for Anaerobic Respiration with Dimethyl Sulfoxide and Nitrite in Shewanella Oneidensis. Biochemistry 2003, 42, 9491–9497.
[3] Lin, T.; Ding, W.; Sun, L.; Wang, L.; Liu, C.-G.; Song, H. Engineered Shewanella Oneidensis-Reduced Graphene Oxide Biohybrid with Enhanced Biosynthesis and Transport of Flavins Enabled a Highest Bioelectricity Output in Microbial Fuel Cells.
[4] Kouzuma, A.; Kasai, T.; Hirose, A.; Watanabe, K. Catabolic and Regulatory Systems in Shewanella Oneidensis MR-1 Involved in Electricity Generation in Microbial Fuel Cells. Frontiers in Microbiology 2015, 6.