Literature DB >> 2604401

Survival of Pseudomonas putida UWC1 containing cloned catabolic genes in a model activated-sludge unit.

N C McClure1, A J Weightman, J C Fry.   

Abstract

The possibility of the accidental or deliberate release of genetically engineered microorganisms into the environment has accentuated the need to study their survival in, and effect on, natural habitats. In this study, Pseudomonas putida UWC1 harboring a non-self-transmissible plasmid, pD10, encoding the breakdown of 3-chlorobenzoate was shown to survive in a fully functioning laboratory-scale activated-sludge unit (ASU) for more than 8 weeks. The ASU maintained a healthy, diverse protozoal population throughout the experiment, and the introduced strain did not adversely affect the functioning of the unit. Although plasmid pD10 was stably maintained in the host bacterium, the introduced strain did not enhance the degradation of 3-chlorobenzoate in the ASU. When reisolated from the ASU, derivatives of strain UWC1 (pD10) were identified which were able to transfer plasmid pD10 to a recipient strain, P. putida PaW340, indicating the in situ transfer of mobilizing plasmids from the indigenous population to the introduced strain. Results from plate filter matings showed that bacteria present in the activated-sludge population could act as recipients for plasmid pD10 and actively expressed genes carried on the plasmid. Some of these activated-sludge transconjugants gave higher rates of 3-chlorobenzoate breakdown than did strain UWC1(pD10) in batch culture.

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Year:  1989        PMID: 2604401      PMCID: PMC203135          DOI: 10.1128/aem.55.10.2627-2634.1989

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  32 in total

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Authors:  C Winstanley; J A Morgan; R W Pickup; J G Jones; J R Saunders
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Authors:  G Stotzky; H Babich
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5.  Plasmid coding for transferable drug resistance in bacteria isolated from cultured rainbow trout.

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Authors:  R V Miller; C M Ku
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7.  Isolation of indigenous wastewater bacterial strains capable of mobilizing plasmid pBR325.

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8.  Reasons for possible failure of inoculation to enhance biodegradation.

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9.  Specific-purpose plasmid cloning vectors. II. Broad host range, high copy number, RSF1010-derived vectors, and a host-vector system for gene cloning in Pseudomonas.

Authors:  M Bagdasarian; R Lurz; B Rückert; F C Franklin; M M Bagdasarian; J Frey; K N Timmis
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10.  Survival of selected bacterial species in sterilized activated carbon filters and biological activated carbon filters.

Authors:  Y Rollinger; W Dott
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  36 in total

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2.  Plasmid donor affects host range of promiscuous IncP-1beta plasmid pB10 in an activated-sludge microbial community.

Authors:  Leen De Gelder; Frederik P J Vandecasteele; Celeste J Brown; Larry J Forney; Eva M Top
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3.  Survival in soils of an herbicide-resistant Pseudomonas putida strain bearing a recombinant TOL plasmid.

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4.  Mobilization of the genetically engineered plasmid pHSV106 from Escherichia coli HB101(pHSV106) to Enterobacter cloacae in drinking water.

Authors:  C H Sandt; D S Herson
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5.  Survival and function of a genetically engineered Pseudomonad in aquatic sediment microcosms.

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6.  Isolation and screening of plasmids from the epilithon which mobilize recombinant plasmid pD10.

Authors:  K E Hill; A J Weightman; J C Fry
Journal:  Appl Environ Microbiol       Date:  1992-04       Impact factor: 4.792

7.  Adaptive plasmid evolution results in host-range expansion of a broad-host-range plasmid.

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8.  Evaluation of aquatic sediment microcosms and their use in assessing possible effects of introduced microorganisms on ecosystem parameters.

Authors:  I Wagner-Döbler; R Pipke; K N Timmis; D F Dwyer
Journal:  Appl Environ Microbiol       Date:  1992-04       Impact factor: 4.792

9.  Exogenous isolation of mobilizing plasmids from polluted soils and sludges.

Authors:  E Top; I De Smet; W Verstraete; R Dijkmans; M Mergeay
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10.  Resolving genetic functions within microbial populations: in situ analyses using rRNA and mRNA stable isotope probing coupled with single-cell raman-fluorescence in situ hybridization.

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