Team:Washington/Magnetosomes/Parts

From 2011.igem.org

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(Description of mamAB operon gene functions)
 
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This part consists of the <i>mamI</i> gene from <i>Magnetospirillum magneticum</i> strain AMB-1, fused to  superfolder <i>gfp</i> on pGA1C3. MamI is a membrane-localized protein that is essential for magnetosome vesicle formation, and is also known to bind the MamK filament. Since it localizes to the membrane, MamI may be useful in maximizing the flux of biosynthetic pathways as a membrane-linker protein.
This part consists of the <i>mamI</i> gene from <i>Magnetospirillum magneticum</i> strain AMB-1, fused to  superfolder <i>gfp</i> on pGA1C3. MamI is a membrane-localized protein that is essential for magnetosome vesicle formation, and is also known to bind the MamK filament. Since it localizes to the membrane, MamI may be useful in maximizing the flux of biosynthetic pathways as a membrane-linker protein.
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=='''The Gibson Assembly Toolkit'''==
=='''The Gibson Assembly Toolkit'''==
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This is a low copy plasmid backbone (replication origin pSC101) that confers ampicillin resistance. It has an insert with a LacI-repressible promoter driving GFP expression. It is identical to pSB4A5 except for its bglBrick prefix and suffix, and is optimized for Gibson Assembly. It is also notable that though we searched in multiple BioBrick distributions from different years, we could not find any that could be sequence-verified as pSB4A5 (the Vf2 sequence reads all suggested pSB1A2). We then generated pGA4A5 from pGA4C5 using the ampicillin cassette from pSB1A3.
This is a low copy plasmid backbone (replication origin pSC101) that confers ampicillin resistance. It has an insert with a LacI-repressible promoter driving GFP expression. It is identical to pSB4A5 except for its bglBrick prefix and suffix, and is optimized for Gibson Assembly. It is also notable that though we searched in multiple BioBrick distributions from different years, we could not find any that could be sequence-verified as pSB4A5 (the Vf2 sequence reads all suggested pSB1A2). We then generated pGA4A5 from pGA4C5 using the ampicillin cassette from pSB1A3.
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====Description of <i>mamAB</i> operon gene functions====
 
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{| class="wikitable"
 
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|-
 
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! Gene
 
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! AMB Number
 
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! Cluster Membership
 
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! Member of 28 genes list? (specific*/related**)
 
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! Function Summary (Vesicle chain formation, and/or biomineralization)
 
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! Gene Function
 
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|-
 
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| mamH
 
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| amb0961
 
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| mamAB
 
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| Related
 
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|
 
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|
 
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|-
 
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| mamI
 
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| amb0962
 
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| mamAB
 
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| Specific
 
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| Vesicle, Chain Formation
 
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| >Loss of mamI causes no membrane formation, gene product is localized onto chains
 
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|-
 
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| mamE
 
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| amb0963
 
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| mamAB; mam Islet
 
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| Related
 
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|
 
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| >Membrane-bound serine protease required for magnetite formation; might control the localization of other magnetosome proteins
 
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|-
 
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| mamJ
 
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| amb0964
 
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| mamAB; mam Islet
 
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| Specific
 
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| Chain Formation
 
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| >Proper magnetosome chain organization/assembly
 
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|-
 
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| mamK
 
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| amb0965
 
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| mamAB; mam Islet
 
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| Related
 
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| Chain Formation
 
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| >Required for proper magnetosome chain organization; *bacterial actin-like cytoskeleton protein required for proper alignment of the magnetosomes in a chain, shown to localize the mamI
 
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|-
 
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| mamL
 
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| amb0966
 
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| mamAB; mam Islet
 
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| Specific
 
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| Vesicle, biomineralization
 
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| >Crucial to mangneosome membrane creation, shown to be spread across the cell membrane and sometimes forms lines
 
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|-
 
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| mamM
 
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| amb0967
 
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| mamAB
 
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| Related
 
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|
 
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| >Biomineralization, involved in iron transport, magnetite nucleation, or establishement of the proper chemical enviornment for magnetite synthesis in the magnetosome
 
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|-
 
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| mamN
 
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| amb0968
 
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| mamAB
 
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| Related
 
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|
 
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| >Biomineralization, involved in iron transport, magnetite nucleation, or establishement of the proper chemical enviornment for magnetite synthesis in the magnetosome
 
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|-
 
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| mamO
 
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| amb0969
 
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| mamAB
 
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| Related
 
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|
 
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| >Biomineralization, involved in iron transport, magnetite nucleation, or establishement of the proper chemical enviornment for magnetite synthesis in the magnetosome
 
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|- 
 
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| mamP
 
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| amb0970
 
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| mamAB
 
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| Related
 
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| Biomineralization
 
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| >Loss of mamP causes weak magnetic response, with large but fewer crystals
 
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|-
 
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| mamA
 
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| amb0971
 
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| mamAB
 
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| Related
 
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|
 
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| >Required for magnetosome activation; activation of vessicles
 
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|-
 
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| mamQ
 
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| amb0972
 
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| mamAB; mam Islet
 
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| Related
 
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|
 
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| >ORF; formation/maintenance of magnetosome membranes
 
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|-
 
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| mamR
 
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| amb0973
 
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| mamAB
 
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| Specific
 
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| Chain formation, Biomineralization
 
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| >ORF; plays a role in controlling both particle number and size of magnetite cyrstals
 
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|-
 
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| mamB
 
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| amb0974
 
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| mamAB
 
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| Related
 
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| Vesicle, Biomineralization
 
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| >Indirect role in magnetosome membrane invagination and biomineralization; magnetosome compartment formation
 
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|-
 
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| mamS
 
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| amb0975
 
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| mamAB
 
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| Specific
 
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| unknown function
 
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| N/A
 
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|-
 
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| mamT
 
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| amb0976
 
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| mamAB
 
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| Specific
 
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| Biomineralization
 
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| >Magnetite crystal growth; participates in different steps during magnetite synthesis
 
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|-
 
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| mamU
 
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| amb0977
 
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| mamAB
 
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| Related
 
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| unknown function
 
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| N/A
 
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|-
 
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| mamV
 
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| amb0978
 
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| mamAB
 
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| unknown function
 
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| N/A
 
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|
 
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|-
 
-
|}
 

Latest revision as of 00:11, 29 September 2011


iGEM Toolkits: Parts Submitted


The iGEM toolkits group submitted a total twenty-two parts to the registry:

  • 10 magnetosome gene groups from mamAB operon
  • 3 superassemblies of the mamAB operon from the set of 10 gene groups
  • 2 sfGFP-mamK and sfGFP-mamI gene fusions
  • 5 Gibson Assembly (pGA) vectors


Magnetosome Toolkit Favorite Parts

BBa_K590015 sfGFP_mamK_pGA1C3

This part consists of the mamK gene from Magnetospirillum magneticum strain AMB-1, fused to superfolder gfp on pGA1C3. MamK has been reported to be essential for proper magnetosome formation in magnetotactic bacteria; its bacterial actin-like cytoskeleton protein is required for proper alignment of the magnetosomes in a chain. Beyond magnetosome alignment, the MamK filament could act as a scaffold for protein localization or to alter cell morphology.

BBa_K590016 sfGFP_mamI_pGA1C3

This part consists of the mamI gene from Magnetospirillum magneticum strain AMB-1, fused to superfolder gfp on pGA1C3. MamI is a membrane-localized protein that is essential for magnetosome vesicle formation, and is also known to bind the MamK filament. Since it localizes to the membrane, MamI may be useful in maximizing the flux of biosynthetic pathways as a membrane-linker protein.


The Gibson Assembly Toolkit

BBa_K590010 pGA1A3_pLacGFP

This is a high copy plasmid backbone (replication origin pMB1) that confers ampicillin resistance. It has an insert with a LacI-repressible promoter driving GFP expression. It is identical to pSB1A3 except for its bglBrick prefix and suffix, and is optimized for Gibson Assembly.

BBa_K590011 pGA1C3_pLacGFP

This is a high copy plasmid backbone (replication origin pMB1) that confers chloramphenicol resistance. It has an insert with a LacI-repressible promoter driving GFP expression. It is identical to pSB1C3 except for its bglBrick prefix and suffix, and is optimized for Gibson Assembly.

BBa_K590014 pGA3K3_pLacGFP

This is a medium copy plasmid backbone (replication origin p15A) that confers kanamycin resistance. It has an insert with a LacI-repressible promoter driving GFP expression. pGA3K3 is identical to pSB3K3 except for its bglBrick prefix and suffix, and is optimized for Gibson Assembly.

BBa_K590012 pGA4C5_pLacGFP

This is a low copy plasmid backbone (replication origin pSC101) that confers chloramphenicol resistance. It has an insert with a LacI-repressible promoter driving GFP expression. It is identical to pSB4C5 except for its bglBrick prefix and suffix, and is optimized for Gibson Assembly.

BBa_K590013 pGA4A5_pLacGFP

This is a low copy plasmid backbone (replication origin pSC101) that confers ampicillin resistance. It has an insert with a LacI-repressible promoter driving GFP expression. It is identical to pSB4A5 except for its bglBrick prefix and suffix, and is optimized for Gibson Assembly. It is also notable that though we searched in multiple BioBrick distributions from different years, we could not find any that could be sequence-verified as pSB4A5 (the Vf2 sequence reads all suggested pSB1A2). We then generated pGA4A5 from pGA4C5 using the ampicillin cassette from pSB1A3.