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A convenient technique to compare the efficiency of promoters in Escherichia coli.
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Molecular characterization of malQ, the structural gene for the Escherichia coli enzyme amylomaltase.
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3
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A technique for integrating any DNA fragment into the chromosome of Escherichia coli.
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Indirect effects of the 3'-5' cyclic adenosine monophosphate binding protein (CAP) on the transcription of the malPQ operon in Escherichia coli.
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Comparison of the malA regions of Escherichia coli and Klebsiella pneumoniae.
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The maltodextrin system of Escherichia coli: glycogen-derived endogenous induction and osmoregulation.
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8
The mac promoters: functional hybrid promoters activated by the malT product and repressed by the lacI product.
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9
Three adjacent binding sites for cAMP receptor protein are involved in the activation of the divergent malEp-malKp promoters.
Proc Natl Acad Sci U S A. 1991 Jan 1;88(1):229-33. doi: 10.1073/pnas.88.1.229.
引用本文的文献
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Lysine represses transcription of the Escherichia coli dapB gene by preventing its activation by the ArgP activator.
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2
Interactions between the 2.4 and 4.2 regions of sigmaS, the stress-specific sigma factor of Escherichia coli, and the -10 and -35 promoter elements.
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3
Regulation of osmC gene expression by the two-component system rcsB-rcsC in Escherichia coli.
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4
Regulatory architecture of the iron-regulated fepD-ybdA bidirectional promoter region in Escherichia coli.
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An Escherichia coli host strain useful for efficient overproduction of cloned gene products with NaCl as the inducer.
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6
CRP induces the repositioning of MalT at the Escherichia coli malKp promoter primarily through DNA bending.
EMBO J. 1994 Oct 3;13(19):4558-67. doi: 10.1002/j.1460-2075.1994.tb06777.x.
7
Analysis of E. coli promoter sequences.
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8
A human villin cDNA clone to investigate the differentiation of intestinal and kidney cells in vivo and in culture.
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9
Cloning and expression in Escherichia coli of the Klebsiella pneumoniae genes for production, surface localization and secretion of the lipoprotein pullulanase.
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DNA-protein recognition: demonstration of three genetically separated operator elements that are required for repression of the Escherichia coli deoCABD promoters by the DeoR repressor.
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Genetic regulatory mechanisms in the synthesis of proteins.
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Gene regulation at the right operator (OR) of bacteriophage lambda. II. OR1, OR2, and OR3: their roles in mediating the effects of repressor and cro.
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Point mutations that reduce the expression of malPQ, a positively controlled operon of Escherichia coli.
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Vectors bearing a hybrid trp-lac promoter useful for regulated expression of cloned genes in Escherichia coli.
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Use of deletions created in vitro to map transcriptional regulatory signals in the malA region of Escherichia coli.
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Transcription from efficient promoters can interfere with plasmid replication and diminish expression of plasmid specified genes.
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Construction of improved M13 vectors using oligodeoxynucleotide-directed mutagenesis.
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Repression is relieved before attenuation in the trp operon of Escherichia coli as tryptophan starvation becomes increasingly severe.
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Decay of mRNA in Escherichia coli: investigation of the fate of specific segments of transcripts.
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