BBa_K917012 1 BBa_K917012 pLac promoter plus napC quinol dehydrogenase gene 2012-09-23T11:00:00Z 2015-05-08T01:13:46Z pLac gene comes from E. coli BL21 genomic DNA napC was cloned from Escherichia coli JM109 chromosome. This part consists of the standard registry lac promoter (BBa_J33207) plus Escherichia coli tetraheme quinol dehydrogenase napC with native RBS (BBa_K917003). false false _1182_ 0 13804 9 In stock true no special notes false Jakub Krakowiak component2195981 1 BBa_K917003 component2195977 1 BBa_J33207 annotation2195977 1 BBa_J33207 range2195977 1 1 600 annotation2195981 1 BBa_K917003 range2195981 1 609 1239 BBa_J33207 1 BBa_J33207 lac promoter and lacZ 2006-10-26T11:00:00Z 2015-08-31T04:08:46Z The DNA was amplified from E. coli BL21 genomic DNA using primers based on published sequence (Genbank accession J01636, gi:146575). The annotation shown here is based on that associated with this Genbank entry. The sequence shown here is derived by sequencing the construct. This part (submitted in pSB1A2) consists of the lac promoter and lacZ' gene, encoding the N-terminal 76 amino acid residues of LacZ, sufficient to complement the lacZ-delta-M15 mutation for blue-white selection on Xgal plates. A SacI site has been introduced at the 3' end, overlapping the XbaI site of the Biobrick prefix. This is designed to be used as a cloning vector for making new biobricks. PCR primers can be designed with a SacI site in one primer and an SpeI site in the other. This removes the necessity for an excessively long non-complementary tail on one primer bearing either the full biobrick prefix or suffix. The PCR product can then be digested with SacI and SpeI for insertion into this plasmid, replacing the Plac-lacZ' cassette. Recombinant plasmids will then be white on IPTG/Xgal plates, whereas any that still contain the original insert will be blue. We have used this strategy to prepare several biobricks, including BBa_J33204, which contains the xylE gene encoding catechol-2,3-dioxygenase. (For making biobricks that contain lacZ', BBa_J33204 can be used in the same way; in this case, clones with plasmids that still contain xylE will turn yellow on addition of a drop of 10 mM catechol.) false false _63_ 0 837 63 It's complicated true Note that the SacI site overlaps the SpeI site. The Biobrick prefix ends ...TCTAGAG. When this is added to the CTC at the start of the sequence shown here, the SacI site, GAGCTC, is generated. false Chris French annotation1907859 1 -10 range1907859 1 320 325 annotation1907858 1 lacZ' range1907858 1 370 600 annotation1907857 1 rbs range1907857 1 359 362 annotation1907856 1 LacI binding site range1907856 1 332 352 annotation1907860 1 -35 range1907860 1 297 302 annotation1907854 1 SacI range1907854 1 1 3 annotation1907855 1 CAP binding site range1907855 1 248 285 BBa_K917003 1 BBa_K917003 E coli quinol dehydrogenase napC 2012-08-09T11:00:00Z 2015-05-08T01:13:46Z Escherichia coli JM109 chromosomal DNA This part consists of Escherichia coli tetraheme quinol dehydrogenase napC with native RBS. NapC is located in the inner membrane and acts as part of E coli electron transport system. false false _1182_ 0 13804 9 In stock true Part obtained by PCR amplification of E coli JM109 gene false Jakub Krakowiak annotation2179463 1 Start codon range2179463 1 14 16 annotation2179465 1 RBS range2179465 1 3 8 annotation2179464 1 Stop codon range2179464 1 614 616 BBa_J33207_sequence 1 ctcatgttatatcccgccgttaaccaccatcaaacaggattttcgcctgctggggcaaaccagcgtggaccgcttgctgcaactctctcagggccaggcggtgaagggcaatcagctgttgcccgtctcactggtgaaaagaaaaaccaccctggcgcccaatacgcaaaccgcctctccccgcgcgttggccgattcattaatgcagctggcacgacaggtttcccgactggaaagcgggcagtgagcgcaacgcaattaatgtgagttagctcactcattaggcaccccaggctttacactttatgcttccggctcgtatgttgtgtgaaattgtgagcggataacaatttcacacaggaaacagctatgaccatgattacggattcactggccgtcgttttacaacgtcgtgactgggaaaaccctggcgttacccaacttaatcgccttgcagcacatccccctttcgccagctggcgtaatagcgaagaggcccgcaccgatcgcccttcccaacagttgcgcagcctgaatggcgaatggcgctttgcctggtttccggcaccagaagcggtgccggaaagctggctggagtga BBa_K917003_sequence 1 ataagaggttattatgggaaattctgaccgtaagcctggtctgattaagcgcctgtggaaatggtggcgtacccccagccgtctggcgctggggacgctgctgttgatcggttttgttggcggcatcgtcttctggggtggctttaacaccgggatggaaaaagccaataccgaagagttctgcattagctgccacgaaatgcgcaacacggtgtatcaggaatacatggattccgtgcactacaacaaccgtagcggcgtccgtgcgacctgtccggattgtcacgttccgcacgagtttgtgccgaagatgatacgcaagctcaaagcaagtaaagagctgtatggtaaaatttttggcgttattgacacgccgcagaaatttgaagctcatcgtctgacgatggcacagaatgagtggcggcgcatgaaggacaataactcgcaggagtgccgtaactgtcacaacttcgagtatatggatacaaccgcccagaaatcggttgccgcgaagatgcatgaccaggcggtgaaagatgggcaaacctgtattgattgccataaagggatagcgcacaagctgcccgatatgcgtgaagtcgagccaggtttttaacagggttattgcgtg BBa_K917012_sequence 1 ctcatgttatatcccgccgttaaccaccatcaaacaggattttcgcctgctggggcaaaccagcgtggaccgcttgctgcaactctctcagggccaggcggtgaagggcaatcagctgttgcccgtctcactggtgaaaagaaaaaccaccctggcgcccaatacgcaaaccgcctctccccgcgcgttggccgattcattaatgcagctggcacgacaggtttcccgactggaaagcgggcagtgagcgcaacgcaattaatgtgagttagctcactcattaggcaccccaggctttacactttatgcttccggctcgtatgttgtgtgaaattgtgagcggataacaatttcacacaggaaacagctatgaccatgattacggattcactggccgtcgttttacaacgtcgtgactgggaaaaccctggcgttacccaacttaatcgccttgcagcacatccccctttcgccagctggcgtaatagcgaagaggcccgcaccgatcgcccttcccaacagttgcgcagcctgaatggcgaatggcgctttgcctggtttccggcaccagaagcggtgccggaaagctggctggagtgatactagagataagaggttattatgggaaattctgaccgtaagcctggtctgattaagcgcctgtggaaatggtggcgtacccccagccgtctggcgctggggacgctgctgttgatcggttttgttggcggcatcgtcttctggggtggctttaacaccgggatggaaaaagccaataccgaagagttctgcattagctgccacgaaatgcgcaacacggtgtatcaggaatacatggattccgtgcactacaacaaccgtagcggcgtccgtgcgacctgtccggattgtcacgttccgcacgagtttgtgccgaagatgatacgcaagctcaaagcaagtaaagagctgtatggtaaaatttttggcgttattgacacgccgcagaaatttgaagctcatcgtctgacgatggcacagaatgagtggcggcgcatgaaggacaataactcgcaggagtgccgtaactgtcacaacttcgagtatatggatacaaccgcccagaaatcggttgccgcgaagatgcatgaccaggcggtgaaagatgggcaaacctgtattgattgccataaagggatagcgcacaagctgcccgatatgcgtgaagtcgagccaggtttttaacagggttattgcgtg 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