ArticleJournal of bacteriology2004
Reversible phase variation in the phnE gene, which is required for phosphonate metabolism in Escherichia coli K-12.
Article in Journal of bacteriology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed.
- Article
- Phosphate uptake by the phosphonate transport system PhnCDE.BMC microbiology · 2019Article
- Influence of ISAntimicrobial agents and chemotherapy · 2017Article
- Clinical Significance and Pathogenesis of Staphylococcal Small Colony Variants in Persistent Infections.Clinical microbiology reviews · 2016Review
- Utilization of glyphosate as phosphate source: biochemistry and genetics of bacterial carbon-phosphorus lyase.Microbiology and molecular biology reviews : MMBR · 2014Review
- Bacterial genome instability.Microbiology and molecular biology reviews : MMBR · 2014Review
- Directional RNA-seq reveals highly complex condition-dependent transcriptomes in E. coli K12 through accurate full-length transcripts assembling.BMC genomics · 2013Article
- Article
- Catabolism and detoxification of 1-aminoalkylphosphonic acids: N-acetylation by the phnO gene product.PloS one · 2012Article
- Activation of the cryptic PhnE permease promotes rapid adaptive evolution in a population of Escherichia coli K-12 starved for phosphate.Journal of bacteriology · 2012Article
- Alternative pathways for phosphonate metabolism in thermophilic cyanobacteria from microbial mats.The ISME journal · 2011Article
- Phosphorus deprivation responses and phosphonate utilization in a thermophilic Synechococcus sp. from microbial mats.Journal of bacteriology · 2008Article
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Authors and funding
5 authors.
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No grant is acknowledged in the PubMed record.
Abstract
It is known that Escherichia coli K-12 is cryptic (Phn-) for utilization of methyl phosphonate (MePn) and that Phn+ variants can be selected for growth on MePn as the sole P source. Variants arise from deletion via a possible slip strand mechanism of one of three direct 8-bp repeat sequences in phnE, which restores function to a component of a putative ABC type transporter. Here we show that Phn+ variants are present at the surprisingly high frequency of >10(-2) in K-12 strains. Amplified-fragment length polymorphism analysis was used to monitor instability in phnE in various strains growing under different conditions. This revealed that, once selection for growth on MePn is removed, Phn+ revertants reappear and accumulate at high levels through reinsertion of the 8-bp repeat element sequence. It appears that, in K-12, phnE contains a high-frequency reversible gene switch, producing phase variation which either allows ("on" form) or blocks ("off" form) MePn utilization. The switch can also block usage of other metabolizable alkyl phosphonates, including the naturally occurring 2-aminoethylphosphonate. All K-12 strains, obtained from collections, appear in the "off" form even when bearing mutations in mutS, mutD, or dnaQ which are known to enhance slip strand events between repetitive sequences. The ability to inactivate the phnE gene appears to be unique to K-12 strains since the B strain is naturally Phn+ and lacks the inactivating 8-bp insertion in phnE, as do important pathogenic strains for which genome sequences are known and also strains isolated recently from environmental sources.
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