Difference between revisions of "Part:BBa K590004"

 
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<partinfo>BBa_K590004 short</partinfo>
 
<partinfo>BBa_K590004 short</partinfo>
  
AMB#0967,0968; Gene function: biomineralization, involved in iron transport, magnetite nucleation, or establishement of the proper chemical enviornment for magnetite synthesis in the magnetosome
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This part includes genes mamM and mamN, which were extracted from the genome of ''Magnetospirillum magneticum'' strain AMB-1 by [http://2011.igem.org/Team:Washington UW iGEM Team 2011].
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===Usage and Biology===
 
===Usage and Biology===
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The gene numbers of mamM and mamN aer AMB0967 and AMB0968 respectively. The part is 2323bp in length. MamMN was reported to be involved in iron transport, magnetite nucleation, or establishment of the proper chemical environment for magnetite synthesis in magnetosomes.
  
 
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Revision as of 04:07, 16 September 2011

mamMN, from Magnetospirillum magneticum

This part includes genes mamM and mamN, which were extracted from the genome of Magnetospirillum magneticum strain AMB-1 by [http://2011.igem.org/Team:Washington UW iGEM Team 2011].


Usage and Biology

The gene numbers of mamM and mamN aer AMB0967 and AMB0968 respectively. The part is 2323bp in length. MamMN was reported to be involved in iron transport, magnetite nucleation, or establishment of the proper chemical environment for magnetite synthesis in magnetosomes.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 288
    Illegal PstI site found at 74
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 288
    Illegal NheI site found at 1331
    Illegal PstI site found at 74
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 288
    Illegal BglII site found at 361
    Illegal BamHI site found at 1628
    Illegal BamHI site found at 2148
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 288
    Illegal PstI site found at 74
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 288
    Illegal PstI site found at 74
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 477
    Illegal SapI.rc site found at 56