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  • 1
    ISSN: 1365-2958
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: TOL plasmid PWWO of Pseudomonas putida contains two operons that specify a pathway for the degradation of aromatic hydrocarbons. The ‘upper’ operon encodes enzymes for the oxidation of toluene to benzoate and xylenes to toluates, whereas the meta-cleavage operon specifies the further oxidation of benzoate and toluates. Transcription of the upper pathway operon (s positively regulated by the XylR protein, which is activated by toluene/xylenes and their alcohol catabolic products, in combination with the NtrA protein, a sigma factor. Expression of the meta-operon is positively controlled by the XylS protein which is activated by meta-pathway substrates, and is Independent of NtrA protein. Expression of the meta pathway is also Induced by toluene/xylene-activated XylR protein via a cascade regulatory system in which this protein in combination with NtrA protein stimulates transcription from the xylS gene promoter. Hyper-production of XylS protein in turn provokes high level expression of the meta-operon, which is independent of meta-pathway substrates. The two promoters, which are activated by the XylR and NtrA proteins, the upper pathway promoter and the xylS gene promoter, exhibit three regions of homology centred at –12(5′–TTGCTÃG–3′), –24(5′ -TGGCPuT –3) and –45(5′-TTAAATÃGPuPuGCGPuTc-3′), with respect to their principal transcription initiation points. The possible physiological significance of activated XylR-protein-induced expression of the meta-operon through amplification of XylS protein levels is considered.
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  • 2
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Microbiology 47 (1993), S. 139-166 
    ISSN: 0066-4227
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1365-2958
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: Stimulation of transcription from the Pseudomonas TOL plasmid xylS gene promoter (Ps) and the upperpathway operon promoter (Pu) is dependent on the positive regulator protein XylR activated by an effector molecule such as 3-cholorotoluene, and on RpoN, an RNA polymerase sigma factor. Mutational analysis of the Ps and Pu promoters showed that upstream activator sequences located between -110 and -218bp upstream of the main transcription initiation point are required for regulated expression from these promoters. A search for homologous nucleotide sequences in the -110to -218bp region in Pu and Ps revealed conserved sequences that may act as putative recognition sequences for the XylR protein. Ps and Pu exhibit another well-conserved region at around 50 bp, which is homologous to corresponding sites in other RpoN-dependent promoters and may constitute a binding site for integration host factor (IHF).
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  • 4
    ISSN: 1573-0972
    Keywords: Dodecylbenzenesulphonate ; Pseudomonas aeruginosa ; surfactant biodegradation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract A bacterium able to grow at the expense of some isomers in a commercial surfactant preparation consisting of branched-chain dodecylbenzenesulphonate was isolated (W51), and it was identified as a Pseudomonas aeruginosa strain. A faster growing derivative was selected (W51D) after enrichment in batch culture under microaerobic conditions, using the surfactant as the sole source of carbon and energy. Strain W51D is the first microorganism reported to degrade at least 70% of a branched-chain alkylbenzenesulphonate mixture and to be resistant to high concentrations of this surfactant. The ability to degrade the surfactant was shown to be transferred by conjugation to other P. aeruginosa strains and to an Escherichia coli strain.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    World journal of microbiology and biotechnology 9 (1993), S. 433-443 
    ISSN: 1573-0972
    Keywords: Alginate ; gene expression ; negative regulators ; positive regulators ; promoters ; Pseudomonas ; TOL plasmid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Gene regulation studies in pseudomonad bacteria are mainly restricted to Pseudomonas aeruginosa and Pseudomonas putida. Constitutive promoters exhibit DNA sequences similar to the σ 70-dependent constitutive promoters of Escherichia coli. The TOL meta-cleavage pathway operon promoter and the nah operon promoters are the best characterized σ 70-dependent promoters, which exhibit-10 regions rich in As and Ts and non-conserved-35 regions. The DNA binding motif recognized by the respective positive regulators lies between-40 and-80. Another set of positively controlled promoters exhibit upstream activator sequences located between-100 and-500. Transcription stimulation from some of these promoters also involves σ 54 and/or IHF protein. In this class of promoters, DNA binding is required to establish open complexes. Promoters for the utilization of histidine (hut) are under negative control by the HutC protein. hut promoters exhibit-10/-35 consensus regions and an overlapping operator sequence between-15 and-50. Repression of hut promoters seems to be achieved through steric hindrance of RNA polymerase. Another set of promoters are controlled by catabolite repression, which seems to be cyclic-AMP independent.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 83 (1996), S. 201-213 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 83 (1996), S. 201-213 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-2048
    Keywords: Calvin cycle ; Chloroplast ; Fructose-1,6-bisphosphatase ; Photosynthesis ; Pisum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A positive clone against pea (Pisum sativum L.) chloroplast fructose-1,6-bisphosphatase (FBPase; EC 3.1.3.11) antibodies was obtained from a copy DNA (cDNA) library in λgt11. The insert was 1261 nucleotides long, and had an open reading frame of 1143 base pairs with coding capability for the whole FBPase subunit and a fragment of a putative processing peptide. An additional 115 base pairs corresponding to a 3′-untranslated region coding for an mRNA poly(A)+ tail were also found in the clone. The deduced sequence for the FBPase subunit was a 357-amino-acid protein of molecular mass 39253 daltons (Da), showing 82–88% absolute homology with four chloroplastic FBPases sequenced earlier. The 3.1-kilobase (kb)KpnI-SacI fragment of the λgt11 derivative was subcloned between theKpnI-SacI restriction sites of pTZ18R to yield plasmid pAMC100. Lysates ofEscherichia coli (pAMC100) showed FBPase activity; this was purified as a 170-kDa protein which, upon sodium dodecyl sulfate-polyacrylamide gel electrophoresis, displayed a 44-kDa band. As occurs with native FBPases, this indicates a homotetrameric structure for the expressed FBPase. When assayed under excess Mg2+ (10 mM), the expressed enzyme had a higher affinity for the substrate than the native pea leaf FBPase; this parameter appears to be substantiated by a tenfold higher specific activity than that of the native enzyme. However, when activated with dithiothreitol plus saturating concentrations of pea thioredoxin (Td) f, both FBPase had similar activities, with a 4:1 Td f-FBPase stoichiometry. In contrast to the native pea chloroplast FBPase, theE. coli-expressed enzyme did not react with the monoclonal antibody GR-PB5. It also had a higher heat sensitivity, with 42% residual activity after heating for 30 min at 60°C, conditions which preserved the native enzyme in a fully active state. These results show the existence of some difference(s) in the conformation of the two FBPases; this could be a consequence of a different expression of the genomic and cDNA clones, or be due to the need for some factor for the correct assembly of the oligomeric structure of the native chloroplast enzyme.
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  • 9
    ISSN: 1617-4623
    Keywords: IHF ; Pseudomonas ; Sigma-54 ; TOL plasmid ; XylR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The upper pathway operon of the Pseudomonas putida TOL plasmid belongs to the −12/-24 class of promoters. These promoters exhibit three regions critical for regulated transcription, namely, the −12/−24 site for RNA polymerase/σ54 binding, the −55/−67 region for IHF protein binding, and the -130(UAS2)/−170(UAS1) region, where two sites for XylR binding are located. The XylR-protected G residues located at −131, −139, −160 and −169 were replaced with As, and the activity of the mutant promoters was assayed after fusion to a promoterless lacZ gene. The mutation (G(−169) → A) resulted in a 50% decrease in expression from the promoter (Pu), whereas the other three changes had no significant effect. The XylR recognition sequence UAS2 has a perfect inverted repeat (5′-ATTTN4 AAAT-3′) while UAS1 shows two mismatches (5′-CCTTN4AAAT - 3′). The two Cs (located at −172 and −173), which interrupt the inverted repeat, were changed as follows: C(−172)→ T; C(−173)→A, CC(−172, −173) −AT. Transcription activation from the mutant promoters was measured as β-galactosidase activity after fusion to lacZ; the better the palindromic sequence, the higher the rate of transcription from Pu, with increases in activity of up to 50%. The introduction of one or two full helix turns between the IHF and the XylR binding sites did not significantly affect transcription from Pu; however, the insertion of three helix turns resulted in a drop of 90% in the activity. The non-permissive effect of insertion of three full helix turns between the IHF and XylR binding sites was not evident in an IHF- background. The introduction of a half helix turn between the RNA polymerase/σ54 and IHF sites also resulted in a notable decrease in transcription from Pu; however, the introduction of one full helix turn did not affect transcription from Pu. The introduction of a full helix turn on both sides of the IHF binding site reduced expression from Pu by 75%, whereas the introduction of a half helix turn on both sides decreased expression by more than 90%. Our findings help to elucidate the sequence requirements for expression from Pit and the architectural organization of the Pu promoter.
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  • 10
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