A convenient technique to compare the efficiency of promoters in Escherichia coli
- PMID: 3162159
- PMCID: PMC321922
- DOI: 10.1093/nar/13.16.5919
A convenient technique to compare the efficiency of promoters in Escherichia coli
Abstract
We describe a technique which allows one to insert any promoter in front of the chromosomal malPQ operon. This can be done easily by using only one plasmid, one strain, and two simple selections. Properties of the final chromosomal fusion are such that the level of amylomaltase, the product of the malQ gene, measures quantitatively the efficiency of the inserted promoter. This method was utilized to compare the efficiency of four well-known promoters: lacZp, trp, tac, lambdaPR and three malT activated promoters: malPp, malkP and malEp.
Similar articles
-
Molecular characterization of malQ, the structural gene for the Escherichia coli enzyme amylomaltase.Mol Microbiol. 1988 Jul;2(4):473-9. doi: 10.1111/j.1365-2958.1988.tb00053.x. Mol Microbiol. 1988. PMID: 2845225
-
Essential and nonessential sequences in malPp, a positively controlled promoter in Escherichia coli.J Bacteriol. 1985 Mar;161(3):1201-8. doi: 10.1128/jb.161.3.1201-1208.1985. J Bacteriol. 1985. PMID: 3156124 Free PMC article.
-
A technique for integrating any DNA fragment into the chromosome of Escherichia coli.Gene. 1984 Jul-Aug;29(1-2):231-41. doi: 10.1016/0378-1119(84)90183-5. Gene. 1984. PMID: 6092225
-
Indirect effects of the 3'-5' cyclic adenosine monophosphate binding protein (CAP) on the transcription of the malPQ operon in Escherichia coli.Biochimie. 1985 Jan;67(1):145-8. doi: 10.1016/s0300-9084(85)80241-8. Biochimie. 1985. PMID: 2986727
-
Comparison of the malA regions of Escherichia coli and Klebsiella pneumoniae.J Bacteriol. 1986 Dec;168(3):1220-7. doi: 10.1128/jb.168.3.1220-1227.1986. J Bacteriol. 1986. PMID: 2946664 Free PMC article.
Cited by
-
A human villin cDNA clone to investigate the differentiation of intestinal and kidney cells in vivo and in culture.EMBO J. 1986 Dec 1;5(12):3119-24. doi: 10.1002/j.1460-2075.1986.tb04618.x. EMBO J. 1986. PMID: 3453110 Free PMC article.
-
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.EMBO J. 1986 Aug;5(8):2015-21. doi: 10.1002/j.1460-2075.1986.tb04458.x. EMBO J. 1986. PMID: 3019678 Free PMC article.
-
Genes of the Escherichia coli pur regulon are negatively controlled by a repressor-operator interaction.J Bacteriol. 1990 Aug;172(8):4555-62. doi: 10.1128/jb.172.8.4555-4562.1990. J Bacteriol. 1990. PMID: 2198266 Free PMC article.
-
Cloning, characterization, and expression of the dapE gene of Escherichia coli.J Bacteriol. 1992 Aug;174(16):5265-71. doi: 10.1128/jb.174.16.5265-5271.1992. J Bacteriol. 1992. PMID: 1644752 Free PMC article.
-
Continuous production of restriction endonucleases: continuous two-stage cultivation with E. coli JM103; continuous cell disintegration and purification by affinity chromatography.Appl Microbiol Biotechnol. 1992 Nov;38(2):220-5. doi: 10.1007/BF00174472. Appl Microbiol Biotechnol. 1992. PMID: 1369142
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials