Phenotypic Expression of PCR-Generated Random Mutations in a Pseudomonas putida Gene after Its Introduction into an Acinetobacter Chromosome by Natural …

RG Kok, DM Young, LN Ornston - Applied and environmental …, 1999 - Am Soc Microbiol
Localized sets of random point mutations generated by PCR amplification can be transferred
efficiently to the chromosome of Acinetobacter ADP1 (also known as strain BD413) by …

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

D Metzgar, JM Bacher, V Pezo, J Reader… - Nucleic acids …, 2004 - academic.oup.com
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 …

Reduced mutation rate and increased transformability of transposon-free Acinetobacter baylyi ADP1-ISx

GA Suárez, BA Renda, A Dasgupta… - Applied and …, 2017 - Am Soc Microbiol
The genomes of most bacteria contain mobile DNA elements that can contribute to
undesirable genetic instability in engineered cells. In particular, transposable insertion …

Natural transformation as a tool in Acinetobacter baylyi: Evolution by amplification of gene copy number

I Pardo, SR Bedore, MP Tumen-Velasquez… - Methods in …, 2023 - Elsevier
For many years, the natural competency of Acinetobacter baylyi ADP1 facilitated studies of
bacterial metabolism, biochemistry, and physiology. With the advent of synthetic biology …

Gene amplification involves site-specific short homology-independent illegitimate recombination in Acinetobacter sp. strain ADP1

AB Reams, EL Neidle - Journal of molecular biology, 2004 - Elsevier
A system for studying gene amplification in the bacterium Acinetobacter sp. strain ADP1 was
used to isolate 105 spontaneous mutants. The method selects for the elevated expression of …

Genome plasticity in Acinetobacter: new degradative capabilities acquired by the spontaneous amplification of large chromosomal segments

AB Reams, EL Neidle - Molecular microbiology, 2003 - Wiley Online Library
In Acinetobacter sp. ADP1, growth on benzoate requires regulation of the cat genes by two
transcriptional activators. Here, mutants were obtained from a strain lacking both activators …

Recovery of DNA from the Acinetobacter calcoaceticus chromosome by gap repair

LA Gregg-Jolly, LN Ornston - Journal of bacteriology, 1990 - Am Soc Microbiol
A strain of Acinetobacter calcoaceticus that demonstrates unusually high competence for
natural transformation by linear DNA has proven valuable for analysis of genes and gene …

Random Insertional Mutagenesis in Acinetobacter

B Vosman, R Kok, KJ Hellingwerf - The Biology of Acinetobacter …, 1991 - Springer
Mutant analysis is a powerful tool in the study of biological processes, the more so if it is
combined with the relevant physiological experiments. Two basically different approaches …

Random mutagenesis by recombinational capture of PCR products in Bacillus subtilis and Acinetobacter calcoaceticus

A Melnikov, PJ Youngman - Nucleic acids research, 1999 - academic.oup.com
We describe a general method for random mutagenesis of cloned genes by error-prone
PCR or DNA shuffling that eliminates the need for post-amplification subcloning following …

Expression vectors for Acinetobacter baylyi ADP1

CD Murin, K Segal, A Bryksin… - Applied and …, 2012 - Am Soc Microbiol
Acinetobacter baylyi ADP1 is naturally competent and proficient at homologous
recombination, so it can be transformed without restriction digests or ligation reactions …