Descripción
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The transcriptional activation of the NifA-dependent promoter of the Rhizobium leguminosarum hydrogenase structural genes hupSL (P1) has been studied through gel retardation analysis and detailed mutagenesis. Gel retardation analysis indicated the existence of a physical interaction between NifA and the promoter. Extensive mutagenesis followed by in vivo expression analysis showed that three sequences of 4 bases each (170 ACAA 167, 161 ACAA 158, and 145 TTGT 142) are required for maximal stimulation of in vivo transcription of the P1 promoter. The arrangement of these upstream activating sequences (ACAA N5 ACAA N12 TTGT) differs from the canonical 5ACA N10 TGT 3 UAS structure involved in NifA-dependent activation of nif/fix genes. Mutant promoter analysis indicated that the relative contribution of each of these sequences to P1 promoter activity increases with its proximity to the transcription start site. Analysis of double mutants altered in two out of the three enhancer sequences suggests that each of these sequences functions in NifA-dependent activation of the P1 promoter in an independent but cooperative mode. The similarities and differences between cis elements of hup and nif/fix promoters suggest that the structure of the P1 promoter has adapted to activation by NifA in order to coexpress hydrogenase and nitrogenase activities in legume nodules. | |
Internacional
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Si |
JCR del ISI
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Si |
Título de la revista
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JOURNAL OF BACTERIOLOGY |
ISSN
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0021-9193 |
Factor de impacto JCR
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4,013 |
Información de impacto
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Volumen
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190 |
DOI
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10.1128/JB.00107-08 |
Número de revista
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9 |
Desde la página
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3185 |
Hasta la página
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3191 |
Mes
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MAYO |
Ranking
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