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Name: | pspG | ||||||||||
Synonym(s): | yjbO | ||||||||||
Gene(s): | pspG, pspH Genome Browser M3D Gene expression COLOMBOS | ||||||||||
Note(s): | pspG is physically unlike the psp operon but is coconserved and coregulated with the psp operon genes by σ54, PspF, IHF and PspA Lloyd LJ,2004. Based on DNA microarray analysis, the mechanism of bacterial inactivation by carvacrol and citral was studied Chueca B, Pérez-Sáez E, Pagán R, García-Gonzalo D,2017. Treatment by both compounds caused membrane damage and activated metabolism through the production of nucleotides required for DNA and RNA synthesis and metabolic processes Chueca B, Pérez-Sáez E, Pagán R, García-Gonzalo D,2017. A total of 76 and 156 genes demonstrated significant transcriptional differences by carvacrol and citral, respectively. Genes upregulated by carvacrol treatment included the multidrug efflux pump genes acrA and mdtM, genes related to the phage shock response, pspA, pspB, pspC, pspD, pspF, and pspG, and genes whose products are important for biosynthesis of arginine (argC, argG, artJ) and purine nucleotides (purC, purM). Genes upregulated by citral treatment included purH, pyrB, and pyrI. On the other hand, mutations in several differentially expressed genes confirmed the roles of ygaV, yjbO, pspC, sdhA, yejG, and ygaV in mechanisms of inactivation by carvacrol and citral Chueca B, Pérez-Sáez E, Pagán R, García-Gonzalo D,2017. Based on DNA microarray analysis, the mechanism of bacterial inactivation by carvacrol and citral was studied Chueca B, Pérez-Sáez E, Pagán R, García-Gonzalo D,2017. Treatment by both compounds caused membrane damage and activated metabolism through the production of nucleotides required for DNA and RNA synthesis and metabolic processes Chueca B, Pérez-Sáez E, Pagán R, García-Gonzalo D,2017. A total of 76 and 156 genes demonstrated significant transcriptional differences by carvacrol and citral, respectively. Genes upregulated by carvacrol treatment included the multidrug efflux pump genes acrA and mdtM, genes related to the phage shock response, pspA, pspB, pspC, pspD, pspF, and pspG, and genes whose products are important for biosynthesis of arginine (argC, argG, artJ) and purine nucleotides (purC, purM). Genes upregulated by citral treatment included purH, pyrB, and pyrI. On the other hand, mutations in several differentially expressed genes confirmed the roles of ygaV, yjbO, pspC, sdhA, yejG, and ygaV in mechanisms of inactivation by carvacrol and citral Chueca B, Pérez-Sáez E, Pagán R, García-Gonzalo D,2017. |
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Evidence: | [COMP-AINF-SINGLE-DIRECTON] Automated inference that a single-gene directon is a transcription unit | ||||||||||
Reference(s): | [1] Lloyd LJ., et al., 2004 | ||||||||||
Promoter | |||||||||||
Name: | pspGp | ||||||||||
+1: | 4262816 | ||||||||||
Sigma Factor: | Sigma54 Sigmulon | ||||||||||
Distance from start of the gene: | 24 | ||||||||||
Sequence: |
gggcgttttgctgttaaatcaatagattatttttggcatgattcttgtaatgccagcaagAgatttcatatttgggagagc -24 -12 +1 |
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Note(s): | Although the transcriptional start site position was not determined experimentally it was inferred by Lloyd LJ,2004, based on footprinting with the RNA polymerase and the identification of its -12 and -24 σ54 recognition boxes. | ||||||||||
Evidence: |
[COMP] [COMP-AINF] [EXP-IDA-RNA-POLYMERASE-FOOTPRINTING] |
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Reference(s): |
[2] Huerta AM., et al., 2003 [1] Lloyd LJ., et al., 2004 |
Type | Transcription factor | Function | Promoter | Binding Sites | Growth Conditions | Evidence | Confidence level (C: Confirmed, S: Strong, W: Weak) | Reference(s) | |||
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LeftPos | RightPos | Central Rel-Pos | Sequence | ||||||||
proximal | IHF | activator | pspGp | 4262771 | 4262783 | -38.5 | ttttgctgttAAATCAATAGATTatttttggca | nd | [COMP] | nd | [1] |
Type | Transcription factor | Function | Promoter | Binding Sites | Growth Conditions | Evidence | Confidence level (C: Confirmed, S: Strong, W: Weak) | Reference(s) | |||
---|---|---|---|---|---|---|---|---|---|---|---|
LeftPos | RightPos | Central Rel-Pos | Sequence | ||||||||
proximal | PspF | activator | pspGp | 4262721 | 4262737 | -87.0 | tcaccaaaaaGTAGTCAAATTCACCACgccctgcgca | nd | [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] | W | [1] |
Reference(s) |
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