Difference between revisions of "Part:BBa K1523021"
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<partinfo>BBa_K1523021 short</partinfo> | <partinfo>BBa_K1523021 short</partinfo> | ||
− | nahR, encoding a LysR-type transcriptional regulator, is highly conserved among naphthalene-degrading bacteria isolated from a coal tar waste-contaminated site and in extracted community DNA | + | nahR, encoding a LysR-type transcriptional regulator, is highly conserved among naphthalene-degrading bacteria isolated from a coal tar waste-contaminated site and in extracted community DNA. It contains a kind of HTH LysR DNA-binding domain. |
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+ | NAH7 plasmid specify catabolism of naphthalene and salicylate under positive regulation by gene nahR. A 1.75-kb fragment (PstI-HindIII) cloned into the pCP13 derivative of vector RK2 complemented in trans five nahR mutations. The fragment sequence contained a 1,122-base-pair open reading frame with a predicted sequence of 374 residues that was rich in basic amino acids with regions similar to known DNA-binding proteins. Clones from the nahR gene region were expressed in mexicells. Plasmid pY1923, carrying the 1.75-kb PstI-HindIII fragment, expressed a protein of Mr ca. 35,000 which bound to the upstream region of gene nahR in a gel electrophoresis DNA-binding assay. Other clones expressed proteins of currently unknown function; pY1311, with the 1.1-kb HindIII fragment, produced a polypeptide with an Mr of 23,000, and pY1812, with the 1.2-kb PstI-SphI fragment, produced a polypeptide (Mr 41,000) which appeared to be a fused nahR-lacZ product. | ||
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+ | Operons repressed by nahR can be regulated positively by nahR when '''salicylate''' appears. | ||
Revision as of 15:41, 31 October 2014
nahR coding sequence,encoding a LysR-type transcriptional regulator
nahR, encoding a LysR-type transcriptional regulator, is highly conserved among naphthalene-degrading bacteria isolated from a coal tar waste-contaminated site and in extracted community DNA. It contains a kind of HTH LysR DNA-binding domain.
NAH7 plasmid specify catabolism of naphthalene and salicylate under positive regulation by gene nahR. A 1.75-kb fragment (PstI-HindIII) cloned into the pCP13 derivative of vector RK2 complemented in trans five nahR mutations. The fragment sequence contained a 1,122-base-pair open reading frame with a predicted sequence of 374 residues that was rich in basic amino acids with regions similar to known DNA-binding proteins. Clones from the nahR gene region were expressed in mexicells. Plasmid pY1923, carrying the 1.75-kb PstI-HindIII fragment, expressed a protein of Mr ca. 35,000 which bound to the upstream region of gene nahR in a gel electrophoresis DNA-binding assay. Other clones expressed proteins of currently unknown function; pY1311, with the 1.1-kb HindIII fragment, produced a polypeptide with an Mr of 23,000, and pY1812, with the 1.2-kb PstI-SphI fragment, produced a polypeptide (Mr 41,000) which appeared to be a fused nahR-lacZ product.
Operons repressed by nahR can be regulated positively by nahR when salicylate appears.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 57
Illegal PstI site found at 250
Illegal PstI site found at 469 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 57
Illegal PstI site found at 250
Illegal PstI site found at 469 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 323
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 57
Illegal PstI site found at 250
Illegal PstI site found at 469 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 57
Illegal PstI site found at 250
Illegal PstI site found at 469
Illegal NgoMIV site found at 491
Illegal NgoMIV site found at 646 - 1000COMPATIBLE WITH RFC[1000]