<td><b>Registry Code</b></td>

     <td><b>Name</b></td>  

     <td><b>Role</b></td>

     <td><b>Description</b></td>

     <td><b>Length (bp)</b></td>

     <td>BBa_K1819003</td>

     <td>RoxA</td>  

     <td>Protein coding</td>

     <td>Rubber oxygenase A (Rox A) from <i>Xanthomonas sp.</i> strain 35Y- catalyzes oxidative C-C cleavage of

   poly(cis-1,4-isoprene)</td>

     <td>1954 (bp)</td>

     <td>BBa_K1819001</td>

     <td>Lcp</td>  

     <td>Role</td>

     <td>Latex clearing protein (Lcp) from <i>Streptomyces sp.</i> strain K30

   cis double bonds</td>

     <td>1138</td>

     <td>BBa_K1819000</td>

     <td>Linker-GFP</td>  

     <td>Reporter part</td>

     <td>Is a GFP coding sequence with an N-terminal linker, which is 5’-flanked by NdeI restriction site</td>

     <td>750</td>

     <td>BBa_K1819002</td>

     <td>TAT signal</td>  

     <td>Signalling part</td>

     <td>Twin-arginine translocation signal</td>

     <td>147</td>

     <td>BBa_K1819004</td>

     <td>GFP_I13507</td>  

     <td>Composite part</td>

     <td>RFP regulation through promoter tetR (part R0040), dependent of tetracycline</td>

     <td>2499</td>

     <td>BBa_K1819005</td>

     <td>J23101 + linkerGFPTerm</td>  

     <td>Characterization circuit</td>

     <td>Constitutive promotor from Anderson library (BBa_J23101) assembled to green fluorescent protein attached to linker</td>

     <td>930</td>

     <td>BBa_K1819006</td>

     <td>J23106 + linkerGFPTerm</td>  

     <td>Characterization circuit</td>

     <td>Constitutive promoter from Anderson library (BBa_J23106) assembled to green fluorescent protein attached to linker</td>

     <td>930</td>

     <td>BBa_K1819007</td>

     <td>J23117 + linkerGFPTerm</td>  

     <td>Characterization circuit</td>

     <td>Constitutive promotor from Anderson library (BBa_J23117) assembled to green fluorescent protein attached to linker</td>

     <td>930</td>

     <td>BBa_K1819008</td>

     <td>Pl_I13507</td>  

     <td>Construction promoter test</td>

     <td>Promoter test circuit to analyze the kill switch efficiency</td>

     <td>2725</td>

     <td>BBa_K1819009</td>

     <td>pVeg + GFP_Term</td>  

     <td>Characterization circuit</td>

     <td>This device express GFP under a strong constitutive Bacillus promoter control (pVeg) (BBa_K823003)</td>

     <td>1123</td>

     <td>BBa_S05291</td>

     <td>RBS-OmpA</td>  

     <td>Construction intermediate</td>

     <td>It is composed of a RBS preceding an outer membrane protein A (OmpA), that displays proteins on cell surface.</td>

     <td>484</td>

     <td>BBa_S05307</td>

     <td>GFP_P0440</td>  

     <td>Construction intermediate</td>

     <td>This construction gives the possibility of adding the most suitable promoter in order to regulate GFP transcription and any genetic sequence inserted after RBS and before TetR</td>

     <td>1568</td>

     <td>BBa_S05308</td>

     <td>Linker-GFP_Term</td>  

     <td>Construction intermediate</td>

     <td>It is an intermediate construction of the export test circuit fused to a terminal region</td>

     <td>887</td>