Home LiteratureArticle Details
PMID: 16535129 Published · ppublish English Journal Article

Impact of Field Release of Genetically Modified Pseudomonas fluorescens on Indigenous Microbial Populations of Wheat.

Applied and environmental microbiology ·Vol. 61 ·No. 9 ·1995-09-00 ·Pages 3443-53

De Leij F, Sutton EJ, Whipps JM, Fenlon JS, Lynch JM

Abstract

In a field release experiment, an isolate of Pseudomonas fluorescens, which was chromosomally modified with two reporter gene cassettes (lacZY and Kan(supr)-xylE), was applied to spring wheat as a seed coating and subsequently as a foliar spray. The wild-type strain was isolated from the phylloplane of sugar beet but was found to be a common colonizer of both the rizosphere and phylloplane of wheat as well. The impact on the indigenous microbial populations resulting from release of this genetically modified microorganism (GMM) was compared with the impact of the unmodified, wild-type strain and a nontreated control until 1 month after harvest of the crop. The release of the P. fluorescens GMM and the unmodified, wild-type strain resulted in significant but transient perturbations of some of the culturable components of the indigenous microbial communities that inhabited the rhizosphere and phylloplane of wheat, but no significant perturbations of the indigenous culturable microbial populations in nonrhizosphere soil were found. Fast-growing organisms that did not produce resting structures (for example, fluorescent pseudomonads and yeasts) seemed to be most sensitive to perturbation. In terms of hazard and risk to the environment, the observed microbial perturbations that resulted from this GMM release may be considered minor for several reasons. First, the recombinant P. fluorescens strain caused changes that were, in general, not significantly different from those caused by the unmodified wild-type strain; second, perturbations resulting from bacterial inoculations were mainly small; and third, the release of bacteria had no obvious effects on plant growth and plant health.

Authors & Affiliations
5 authors, click to expand affiliations / ORCID
De Leij F
Sutton E J
Whipps J M
Fenlon J S
Lynch J M
References (7)
7 references, click to expand
  1. Metabolism of benzoate and the methylbenzoates by Pseudomonas putida (arvilla) mt-2: evidence for the existence of a TOL plasmid.
    J Bacteriol. 1974 Oct;120(1):416-23 PMID: 4418209
  2. A broad-host-range shuttle system for gene insertion into the chromosomes of gram-negative bacteria.
    Gene. 1988 Nov 15;71(1):75-84 PMID: 2850977
  3. Rapid determination of bacterial ribosomal RNA sequences by direct sequencing of enzymatically amplified DNA.
    FEMS Microbiol Lett. 1989 Nov;53(1-2):171-6 PMID: 2482222
  4. Detection of Plasmid Transfer from Pseudomonas fluorescens to Indigenous Bacteria in Soil by Using Bacteriophage phiR2f for Donor Counterselection.
    Appl Environ Microbiol. 1991 Dec;57(12):3482-8 PMID: 16348599
  5. Amplification of bacterial 16S ribosomal DNA with polymerase chain reaction.
    J Clin Microbiol. 1990 Sep;28(9):1942-6 PMID: 2095137
  6. Evaluation of methods for detecting ecological effects from genetically engineered microorganisms and microbial pest control agents in terrestrial systems.
    Biotechnol Adv. 1992;10(2):149-78 PMID: 14544532
  7. Isolation and characterization of a human cDNA clone encoding a novel DNA topoisomerase II homologue from HeLa cells.
    FEBS Lett. 1990 Jun 18;266(1-2):115-7 PMID: 2163884
Article Info
Journal
Applied and environmental microbiology
Abbr.
Appl Environ Microbiol
ISSN
0099-2240
Published
1995-09-00
Pages
3443-53
Language
English
Region
United States
NLM ID
7605801
PMCID
PMC1388583
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com