Literature DB >> 8380783

Analysis of Pseudomonas gene products using lacIq/Ptrp-lac plasmids and transposons that confer conditional phenotypes.

V de Lorenzo1, L Eltis, B Kessler, K N Timmis.   

Abstract

Novel transposon and plasmid-based broad-host-range expression systems have been developed to facilitate the genetic analysis of gene products of Pseudomonas and related Gram- bacteria. The properties of lacIq/Ptrp-lac were used to construct mini-Tn5 expression vector transposons and RSF1010-derived plasmids for controlled expression and generation of conditional phenotypes. These plasmids were used to hyper-express the XylS regulator of the meta operon of the TOL plasmid of P. putida or the bphB and bphC genes of the polychlorobiphenyl-degrading pathway of Pseudomonas sp. LB400 in different strains of Pseudomonas instead of in Escherichia coli. Specific activity of 2.3 dihydroxybiphenyl dioxygenase (bphC gene product) was increased tenfold when hyperproduced in its native host as compared to E. coli, but under the same in vivo conditions, the XylS regulator formed protein aggregates. The other lacIq/Ptrp-lac-based expression vector presented here, transposon mini-Tn5 lacIq/Ptrc, facilitates the insertion of genetic cassettes containing heterologous genes under the control of lac inducers in the chromosome of target bacteria, as shown by monitoring expression of a lacZ reporter cloned in mini-Tn5 lacIq/Ptrc and inserted in the chromosome of P. putida.

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Year:  1993        PMID: 8380783     DOI: 10.1016/0378-1119(93)90533-9

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  190 in total

1.  Engineering of a stable whole-cell biocatalyst capable of (S)-styrene oxide formation for continuous two-liquid-phase applications.

Authors:  S Panke; V de Lorenzo; A Kaiser; B Witholt; M G Wubbolts
Journal:  Appl Environ Microbiol       Date:  1999-12       Impact factor: 4.792

2.  The pvc gene cluster of Pseudomonas aeruginosa: role in synthesis of the pyoverdine chromophore and regulation by PtxR and PvdS.

Authors:  A Stintzi; Z Johnson; M Stonehouse; U Ochsner; J M Meyer; M L Vasil; K Poole
Journal:  J Bacteriol       Date:  1999-07       Impact factor: 3.490

3.  Insertion mutagenesis and membrane topology model of the Pseudomonas aeruginosa outer membrane protein OprM.

Authors:  K K Wong; R E Hancock
Journal:  J Bacteriol       Date:  2000-05       Impact factor: 3.490

4.  Evaluation of a structural model of Pseudomonas aeruginosa outer membrane protein OprM, an efflux component involved in intrinsic antibiotic resistance.

Authors:  K K Wong; F S Brinkman; R S Benz; R E Hancock
Journal:  J Bacteriol       Date:  2001-01       Impact factor: 3.490

5.  Characterization of SepL of enterohemorrhagic Escherichia coli.

Authors:  A U Kresse; F Beltrametti; A Müller; F Ebel; C A Guzmán
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

6.  Recovery of active medium-chain-length-poly-3-hydroxyalkanoate polymerase from inactive inclusion bodies using ion-exchange resin.

Authors:  Q Ren; B Kessler; B Witholt
Journal:  Biochem J       Date:  2000-07-15       Impact factor: 3.857

7.  Specific adhesion to cellulose and hydrolysis of organophosphate nerve agents by a genetically engineered Escherichia coli strain with a surface-expressed cellulose-binding domain and organophosphorus hydrolase.

Authors:  Aijun A Wang; Ashok Mulchandani; Wilfred Chen
Journal:  Appl Environ Microbiol       Date:  2002-04       Impact factor: 4.792

8.  Export of autotransported proteins proceeds through an oligomeric ring shaped by C-terminal domains.

Authors:  Esteban Veiga; Etsuko Sugawara; Hiroshi Nikaido; Víctor de Lorenzo; Luis Angel Fernández
Journal:  EMBO J       Date:  2002-05-01       Impact factor: 11.598

9.  A new pathway for the secretion of virulence factors by bacteria: the flagellar export apparatus functions as a protein-secretion system.

Authors:  G M Young; D H Schmiel; V L Miller
Journal:  Proc Natl Acad Sci U S A       Date:  1999-05-25       Impact factor: 11.205

10.  Pseudomonas aeruginosa synthesizes phosphatidylcholine by use of the phosphatidylcholine synthase pathway.

Authors:  Paula J Wilderman; Adriana I Vasil; Wesley E Martin; Robert C Murphy; Michael L Vasil
Journal:  J Bacteriol       Date:  2002-09       Impact factor: 3.490

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