Difference between revisions of "Part:BBa K1884011"

(Usage)
(Usage)
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===Usage===
 
===Usage===
  
For testing the efficiency of paromoycin, we formulated six gradient concentrations of paromoycin solution and add 200ul each into six different beakerflask which contain 200ml LB solid medium, then we put the competent cell into six different LB plate. there is a photograph to show several monoclonal colony growing on a LB plate which has the best selected abilty of Paromoycin resistance.<b>(Fig 1)</b>
+
For testing the efficiency of paromoycin, we formulated six gradient concentrations of paromoycin solution and add 200ul each into six different beakerflask which contain 200ml LB solid medium, then we put the competent cell into six different LB plate. there is a photograph to show several monoclonal colony growing on a LB plate which has the best selected abilty of Paromoycin.<b>(Fig 1)</b>
  
Conbined with another resistant device(BBa_K1884012), we are able to screen the green algae which  
+
Conbined with another resistant device(BBa_K1884012), we are able to screen the green algae which has paromoycin resistance and Hygromycin B resistance. we added 200ul paromoycin solution and hygromycin B solution into 200ml TAP solid medium, then we put the green algae without cytoderm into TAP plate. there is a photograph to show several colony growing on a TAP plate which has the best selected efficiency of paromoycin and Hygromycin B.<b>(Fig 2)</b>
  
  

Revision as of 20:28, 16 October 2016


RBCS2 Promoter+Paromomycin+RBCS2 Terminator

We provided Paromomycin resistance under the RBCS2 promoter(BBa_K1884010)

Biology

RBCS2 promoter

Paromoycin is a protein synthesis inhibitor in nonresistant cells by binding to 16S ribosomal RNA. This broad-spectrum antibiotic soluble in water, is very similar in action to neomycin. Antimicrobial activity of paromomycin against Escherichia coli and Staphylococcus aureus has been shown.

RBCS2 terminator is Chlamydomonas reinhardtii RuBisCO small subunit 2 terminator which obtained from the pOpt_mVenus_Hyg expression plasmid provided by Chlamydomonas Resource Center.


Usage

For testing the efficiency of paromoycin, we formulated six gradient concentrations of paromoycin solution and add 200ul each into six different beakerflask which contain 200ml LB solid medium, then we put the competent cell into six different LB plate. there is a photograph to show several monoclonal colony growing on a LB plate which has the best selected abilty of Paromoycin.(Fig 1)

Conbined with another resistant device(BBa_K1884012), we are able to screen the green algae which has paromoycin resistance and Hygromycin B resistance. we added 200ul paromoycin solution and hygromycin B solution into 200ml TAP solid medium, then we put the green algae without cytoderm into TAP plate. there is a photograph to show several colony growing on a TAP plate which has the best selected efficiency of paromoycin and Hygromycin B.(Fig 2)





Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]