BBa_K1702005 1 BBa_K1702005 Trans-zeatin biosynthesis under control of the lac promoter 2015-09-16T11:00:00Z 2015-09-17T03:35:57Z This piece was synthesized based on sequences from Kamada-Nobusada, Tomoe and Sakakibara, Hitoshi. "Molecular basis for cytokinin biosynthesis." Phytochemistry 70:444-449. and from KEGG (kegg.jp). Synthesized tzs gene (from Agrobacterium tumefaciens C58) and LOG (Oryza satifa), both codon optimized for E. coli as a biobrick. The tzs gene encodes for the enzyme which converts 4-hydroxy-3-methyl-2-(E)-butenyl diphosphate into zeatin riboside 5'-phosphate. The LOG gene produces N6-dimethylallyladenine by removing the phosphoribosyl group from N6-(delta2-isopentenyl)-adenosine 5'-monophosphate. Hydroxylation of the N6-dimethylallyladenine produces biologically-active trans-zeatin. Under control of the lac promoter in DH5alpha E. coli cells, expression of the trans-zeatin biosynthesis pathway is induced by lactose or its analog IPTG. false false _2121_ 22741 22741 9 false The piece was synthesized with the two genes back-to-back (i.e. as an operon) and expression can be induced using lactose or IPTG. false Olivia Smith, Adriana Collings component2467153 1 BBa_J04500 component2467154 1 BBa_K1702004 annotation2467154 1 BBa_K1702004 range2467154 1 229 1709 annotation2467153 1 BBa_J04500 range2467153 1 1 220 BBa_B0034 1 BBa_B0034 RBS (Elowitz 1999) -- defines RBS efficiency 2003-01-31T12:00:00Z 2015-08-31T04:07:20Z Released HQ 2013 RBS based on Elowitz repressilator. false true _1_ 0 24 7 In stock false Varies from -6 to +1 region from original sequence to accomodate BioBricks suffix. <p>No secondary structures are formed in the given RBS region. Users should check for secondary structures induced in the RBS by upstream and downstream elements in the +50 to -50 region, as such structures will greatly affect the strength of the RBS. Contact info for this part: <a href="mailto:(bchow@media.mit.edu)">Brian Chow</a> true Vinay S Mahajan, Voichita D. Marinescu, Brian Chow, Alexander D Wissner-Gross and Peter Carr IAP, 2003. annotation23325 1 conserved range23325 1 5 8 BBa_J04500 1 BBa_J04500 IPTG inducible promoter with RBS 2005-06-08T11:00:00Z 2015-08-31T04:08:14Z Davidson Synth-Aces Released HQ 2013 R0010.B0034 false true _16_ 0 326 16 In stock false false Kristen DeCelle component1508149 1 BBa_R0010 component1508159 1 BBa_B0034 annotation1508149 1 BBa_R0010 range1508149 1 1 200 annotation1508159 1 BBa_B0034 range1508159 1 209 220 BBa_R0010 1 LacI promoter (lacI regulated) 2003-01-31T12:00:00Z 2015-05-08T01:14:14Z The Plac insert was PCR'd from the MG1655 strain of E.coli K12. Released HQ 2013 Inverting regulatory region controlled by LacI (<bb_part>BBa_C0010</bb_part>, <bb_part>BBa_C0011</bb_part>, etc.) <p> The pLac regulatory region is a 243 base-pair sequence with standard BioBrick prefix and suffix sections on its ends. It contains two protein binding sites: CAP, which is generally present in E.coli and is assocciated with cell health and availability of glucose., and LacI, the Lac inhibitor <bb_part>BBa_C0010</bb_part> which binds in an dimerized cooperative manner to inhibit the transcription of the protein that follows. In the presence of lactose or IPTG, an analog of lactose, LacI is unable to correctly bind and inhibit transcription. This allows <bb_part>BBa_R0010</bb_part> to be used as a inverter or as a detector of lactose or IPTG. false true _1_ 0 24 7 In stock false <P> <P><P> LacI binds to this regulator. This part is incompatible with species containing active LacI coding regions. Lactose and IPTG disable the operation of LacI and this regulator. This part is incompatible with environments containing lactose or lactose analogs. true annotation1961227 1 start range1961227 1 173 173 annotation1961223 1 CAP binding site range1961223 1 89 126 annotation1961222 1 BBa_R0010 range1961222 1 1 200 annotation1961225 1 -10 range1961225 1 161 166 annotation1961226 1 LacI binding site range1961226 1 166 200 annotation1961224 1 -35 range1961224 1 137 142 annotation1961221 1 end of LacI coding region (inactive) range1961221 1 1 88 BBa_K1702004 1 BBa_K1702004 trans-zeatin biosynthesis pathway 2015-09-16T11:00:00Z 2015-09-17T03:16:37Z The genes were synthesized based on sequences based on Kamada-Nobusada, Tomoe and Sakakibara, Hitoshi. "Molecular basis for cytokinin biosynthesis." Phytochemistry 70:444-449. March 2009. and found on KEGG (kegg.jp). Synthesized tzs gene (from Agrobacterium tumefaciens C58) and LOG (Oryza satifa), both codon optimized for E. coli as a biobrick. The tzs gene encodes for the enzyme which converts 4-hydroxy-3-methyl-2-(E)-butenyl diphosphate into zeatin riboside 5'-phosphate. The LOG gene produces N6-dimethylallyladenine by removing the phosphoribosyl group from N6-(delta2-isopentenyl)-adenosine 5'-monophosphate. Hydroxylation of the N6-dimethylallyladenine produces biologically-active trans-zeatin. false false _2121_ 22741 22741 9 false The piece was synthesized with the two genes functioning as an operon. false Olivia Smith BBa_R0010_sequence 1 caatacgcaaaccgcctctccccgcgcgttggccgattcattaatgcagctggcacgacaggtttcccgactggaaagcgggcagtgagcgcaacgcaattaatgtgagttagctcactcattaggcaccccaggctttacactttatgcttccggctcgtatgttgtgtggaattgtgagcggataacaatttcacaca BBa_B0034_sequence 1 aaagaggagaaa BBa_J04500_sequence 1 caatacgcaaaccgcctctccccgcgcgttggccgattcattaatgcagctggcacgacaggtttcccgactggaaagcgggcagtgagcgcaacgcaattaatgtgagttagctcactcattaggcaccccaggctttacactttatgcttccggctcgtatgttgtgtggaattgtgagcggataacaatttcacacatactagagaaagaggagaaa BBa_K1702005_sequence 1 caatacgcaaaccgcctctccccgcgcgttggccgattcattaatgcagctggcacgacaggtttcccgactggaaagcgggcagtgagcgcaacgcaattaatgtgagttagctcactcattaggcaccccaggctttacactttatgcttccggctcgtatgttgtgtggaattgtgagcggataacaatttcacacatactagagaaagaggagaaatactagagtactagatgctgctgcatctgatctatggtccgacgtgtagtggcaaaacggatatggctattcaaatcgcacaggaaacgggttggccggtggtggcactggatcgtgttcagtgctgtccgcaaatcgctaccggcagtggtcgcccgctggaaagtgaactgcaatccacccgtcgcatttatctggatagccgtccgctgacggaaggcatcctggacgcggaatctgcccatcgtcgcctgatttttgaagttgactggcgcaaatctgaagaaggtctgattctggaaggcggtagcatctctctgctgaactgcatggccaaatcaccgttttggcgttcgggcttccagtggcacgtcaaacgtctgcgcctgggtgatagtgacgcatttctgacgcgtgctaaacaacgcgtggcagaaatgttcgctatccgtgaagatcgcccgtccctgctggaagaactggcggaactgtggaattatccggcggcacgtccgattctggaagatatcgacggctaccgctgtgcgattcgttttgcccgcaaacatgatctggcgatttcacagctgccgaacatcgacgccggtcgtcatgtcgaactgattgaagcaatcgctaatgaatacctggaacacgcgctgtcgcaggaacgcgatttcccgcaatggccggaagatggtgctggtcaaccggtctgcccggtcacgctgacgcgcattcgctgaaggaggaattaaccatggcgatggaagcagcagcagaacgctcggcaggcgcaggtgcagcagcaacggcagccccggaatcaggcggtggtggcgcaggtgaacgtcgctcccgttttcgtcgcatctgcgtgtattgtggtagcgcaaaaggccgcaaagcttcttaccaggatgcggccgtcgaactgggtaaagaactggtggaacgtggcatcgacctggtttatggcggtggctcaattggtctgatgggcctggtttcgcatgcagtccacgatggtggccgccatgtgatcggtgttattccgaaaagcctgatgccgcgtgaagtgaccggtgaaccggtcggcgaagtgcgtgcagtttctggtatgcacgaacgtaaagcggaaatggcccgctttgcagatgctttcattgcgctgccgggtggctatggtaccctggaagaactgctggaagtgatcacgtgggcccaactgggcattcataaaaaaccggtgggtctgctgaacgttgatggcttttacgacccgtttctgagtttcatcgatatggccgtttccgaaggtttcattgcagaagacgctcgtcgcattatcattagcgcaccgacggcacgtgaactggtcctgaaactggaagaatatgttccggaatacgaagtcggcctggtgtgggacgaccaaatgccgcactcgttcgcaccggacctggaaacccgtatcacctcatcctaa BBa_K1702004_sequence 1 tactagatgctgctgcatctgatctatggtccgacgtgtagtggcaaaacggatatggctattcaaatcgcacaggaaacgggttggccggtggtggcactggatcgtgttcagtgctgtccgcaaatcgctaccggcagtggtcgcccgctggaaagtgaactgcaatccacccgtcgcatttatctggatagccgtccgctgacggaaggcatcctggacgcggaatctgcccatcgtcgcctgatttttgaagttgactggcgcaaatctgaagaaggtctgattctggaaggcggtagcatctctctgctgaactgcatggccaaatcaccgttttggcgttcgggcttccagtggcacgtcaaacgtctgcgcctgggtgatagtgacgcatttctgacgcgtgctaaacaacgcgtggcagaaatgttcgctatccgtgaagatcgcccgtccctgctggaagaactggcggaactgtggaattatccggcggcacgtccgattctggaagatatcgacggctaccgctgtgcgattcgttttgcccgcaaacatgatctggcgatttcacagctgccgaacatcgacgccggtcgtcatgtcgaactgattgaagcaatcgctaatgaatacctggaacacgcgctgtcgcaggaacgcgatttcccgcaatggccggaagatggtgctggtcaaccggtctgcccggtcacgctgacgcgcattcgctgaaggaggaattaaccatggcgatggaagcagcagcagaacgctcggcaggcgcaggtgcagcagcaacggcagccccggaatcaggcggtggtggcgcaggtgaacgtcgctcccgttttcgtcgcatctgcgtgtattgtggtagcgcaaaaggccgcaaagcttcttaccaggatgcggccgtcgaactgggtaaagaactggtggaacgtggcatcgacctggtttatggcggtggctcaattggtctgatgggcctggtttcgcatgcagtccacgatggtggccgccatgtgatcggtgttattccgaaaagcctgatgccgcgtgaagtgaccggtgaaccggtcggcgaagtgcgtgcagtttctggtatgcacgaacgtaaagcggaaatggcccgctttgcagatgctttcattgcgctgccgggtggctatggtaccctggaagaactgctggaagtgatcacgtgggcccaactgggcattcataaaaaaccggtgggtctgctgaacgttgatggcttttacgacccgtttctgagtttcatcgatatggccgtttccgaaggtttcattgcagaagacgctcgtcgcattatcattagcgcaccgacggcacgtgaactggtcctgaaactggaagaatatgttccggaatacgaagtcggcctggtgtgggacgaccaaatgccgcactcgttcgcaccggacctggaaacccgtatcacctcatcctaa igem2sbol 1 iGEM to SBOL conversion Conversion of the iGEM parts registry to SBOL2.1 Chris J. Myers James Alastair McLaughlin 2017-03-06T15:00:00.000Z