Mutational analysis of the critical bases involved in activation of the AreR-regulated sigma54-dependent promoter in Acinetobacter sp. strain ADP1.
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Toxicity caused by hydroxycinnamoyl-coenzyme A thioester accumulation in mutants of Acinetobacter sp. strain ADP1.Deletion mutations caused by DNA strand slippage in Acinetobacter baylyi.The generation of successive unmarked mutations and chromosomal insertion of heterologous genes in Actinobacillus pleuropneumoniae using natural transformationHydroxycinnamate (hca) catabolic genes from Acinetobacter sp. strain ADP1 are repressed by HcaR and are induced by hydroxycinnamoyl-coenzyme A thioesters.Acinetobacter sp. ADP1: an ideal model organism for genetic analysis and genome engineering.When coupled to natural transformation in Acinetobacter sp. strain ADP1, PCR mutagenesis is made less random by mismatch repair.Chromosomally located gene fusions constructed in Acinetobacter sp. ADP1 for the detection of salicylate.Characterizing the regulation of the Pu promoter in Acinetobacter baylyi ADP1.Vibrio fischeri DarR directs responses to d-aspartate and represents a group of similar LysR-type transcriptional regulators.
P2860
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P2860
Mutational analysis of the critical bases involved in activation of the AreR-regulated sigma54-dependent promoter in Acinetobacter sp. strain ADP1.
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name
Mutational analysis of the cri ...... Acinetobacter sp. strain ADP1.
@en
type
label
Mutational analysis of the cri ...... Acinetobacter sp. strain ADP1.
@en
prefLabel
Mutational analysis of the cri ...... Acinetobacter sp. strain ADP1.
@en
P2860
P1476
Mutational analysis of the cri ...... Acinetobacter sp. strain ADP1
@en
P2093
Peter A Williams
P2860
P304
P356
10.1128/AEM.69.9.5627-5635.2003
P407
P577
2003-09-01T00:00:00Z