Literature DB >> 15514111

Acinetobacter sp. ADP1: an ideal model organism for genetic analysis and genome engineering.

David Metzgar1, Jamie M Bacher, Valérie Pezo, John Reader, Volker Döring, Paul Schimmel, Philippe Marlière, Valérie de Crécy-Lagard.   

Abstract

Acinetobacter sp. strain ADP1 is a naturally transformable gram-negative bacterium with simple culture requirements, a prototrophic metabolism and a compact genome of 3.7 Mb which has recently been sequenced. Wild-type ADP1 can be genetically manipulated by the direct addition of linear DNA constructs to log-phase cultures. This makes it an ideal organism for the automation of complex strain construction. Here, we demonstrate the flexibility and versatility of ADP1 as a genetic model through the construction of a broad variety of mutants. These include marked and unmarked insertions and deletions, complementary replacements, chromosomal expression tags and complex combinations thereof. In the process of these constructions, we demonstrate that ADP1 can effectively express a wide variety of foreign genes including antibiotic resistance cassettes, essential metabolic genes, negatively selectable catabolic genes and even intact operons from highly divergent bacteria. All of the described mutations were achieved by the same process of splicing PCR, direct transformation of growing cultures and plating on selective media. The simplicity of these tools make genetic analysis and engineering with Acinetobacter ADP1 accessible to laboratories with minimal microbial genetics expertise and very little equipment. They are also compatible with complete automation of genetic analysis and engineering protocols.

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Year:  2004        PMID: 15514111      PMCID: PMC528786          DOI: 10.1093/nar/gkh881

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  25 in total

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Journal:  Nucleic Acids Res       Date:  2003-01-01       Impact factor: 16.971

3.  Artificially ambiguous genetic code confers growth yield advantage.

Authors:  V Pezo; D Metzgar; T L Hendrickson; W F Waas; S Hazebrouck; V Döring; P Marlière; P Schimmel; V De Crécy-Lagard
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-26       Impact factor: 11.205

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Review 5.  Genetic engineering using homologous recombination.

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7.  Genetic code ambiguity. Cell viability related to the severity of editing defects in mutant tRNA synthetases.

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10.  Mutational analysis of the critical bases involved in activation of the AreR-regulated sigma54-dependent promoter in Acinetobacter sp. strain ADP1.

Authors:  Rheinallt M Jones; Peter A Williams
Journal:  Appl Environ Microbiol       Date:  2003-09       Impact factor: 4.792

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  69 in total

1.  Genomics-driven reconstruction of acinetobacter NAD metabolism: insights for antibacterial target selection.

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Review 2.  Essential biological processes of an emerging pathogen: DNA replication, transcription, and cell division in Acinetobacter spp.

Authors:  Andrew Robinson; Anthony J Brzoska; Kylie M Turner; Ryan Withers; Elizabeth J Harry; Peter J Lewis; Nicholas E Dixon
Journal:  Microbiol Mol Biol Rev       Date:  2010-06       Impact factor: 11.056

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Journal:  Antimicrob Agents Chemother       Date:  2006-08-28       Impact factor: 5.191

4.  Naturally transformable Acinetobacter sp. strain ADP1 belongs to the newly described species Acinetobacter baylyi.

Authors:  Mario Vaneechoutte; David M Young; L Nicholas Ornston; Thierry De Baere; Alexandr Nemec; Tanny Van Der Reijden; Emma Carr; Ingela Tjernberg; Lenie Dijkshoorn
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5.  Genetic code ambiguity confers a selective advantage on Acinetobacter baylyi.

Authors:  Jamie M Bacher; William F Waas; David Metzgar; Valérie de Crécy-Lagard; Paul Schimmel
Journal:  J Bacteriol       Date:  2007-07-06       Impact factor: 3.490

Review 6.  Global challenge of multidrug-resistant Acinetobacter baumannii.

Authors:  Federico Perez; Andrea M Hujer; Kristine M Hujer; Brooke K Decker; Philip N Rather; Robert A Bonomo
Journal:  Antimicrob Agents Chemother       Date:  2007-07-23       Impact factor: 5.191

7.  Bacterial natural transformation by highly fragmented and damaged DNA.

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Journal:  Proc Natl Acad Sci U S A       Date:  2013-11-18       Impact factor: 11.205

8.  Natural competence in Thermoanaerobacter and Thermoanaerobacterium species.

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Journal:  Appl Environ Microbiol       Date:  2010-05-14       Impact factor: 4.792

9.  FLP-FRT-based method to obtain unmarked deletions of CHU_3237 (porU) and large genomic fragments of Cytophaga hutchinsonii.

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Journal:  Appl Environ Microbiol       Date:  2014-07-25       Impact factor: 4.792

10.  Predicting the pathway involved in post-translational modification of elongation factor P in a subset of bacterial species.

Authors:  Marc Bailly; Valérie de Crécy-Lagard
Journal:  Biol Direct       Date:  2010-01-13       Impact factor: 4.540

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