Literature DB >> 2832693

Maintenance of the cellobiose utilization genes of Escherichia coli in a cryptic state.

B G Hall1, P W Betts, M Kricker.   

Abstract

The genes for cellobiose utilization are normally cryptic in Escherichia coli. The cellobiose system was used as a model to understand the process by which silent genes are maintained in microbial populations. Previously reported was (1) the isolation of a mutant strain that expresses the cellobiose-utilization (Cel) genes and (2) that expression of those genes allows utilization of three beta-glucoside sugars: cellobiose, arbutin, and salicin. The Cel gene cluster has now been cloned from that mutant strain. In the course of locating the Cel genes within the cloned DNA segment, it was discovered that inactivation of the Cel-encoded hydrolase rendered the host strain sensitive to all three beta-glucosides as potent inhibitors. This sensitivity arises from the accumulation of the phosphorylated beta-glucosides. Because even the fully active genes conferred some degree of beta-glucoside sensitivity, the effects of cellobiose on a series of five Cel+ mutants of independent origin were investigated. Although each of those strains utilizes cellobiose as a sole carbon and energy source, cellobiose also acts as a potent inhibitor that reduces the growth rate on glycerol 2.5-16.5-fold. On the other hand, wild-type strains that cannot utilize cellobiose are not inhibited. The observation that the same compound can serve either as a nutrient or as an inhibitor suggests that, under most conditions in which cellobiose will be present together with other resources, there is a strong selective advantage to having the cryptic (Cel0) allele. In those environments in which cellobiose is the sole, or the best, resource, mutants that express the genes (Cel+) will have a strong selective advantage. It is suggested that temporal alternation between these two conditions is a major factor in the maintenance of these genes in E. coli populations. This alternation of environments and fitnesses was predicted by the model for cryptic-gene maintenance that was previously published.

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Year:  1986        PMID: 2832693     DOI: 10.1093/oxfordjournals.molbev.a040406

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  11 in total

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Authors:  S P Otto; V Walbot
Journal:  Genetics       Date:  1990-02       Impact factor: 4.562

2.  Central role of the cell in microbial ecology.

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3.  Effect of Increased beta-Glucosidase Activity on Virulence of Erwinia amylovora.

Authors:  T K Kerppola; T Serwold-Davis; D C Gross; M L Kahn
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4.  Mechanisms of activation of the cryptic cel operon of Escherichia coli K12.

Authors:  L L Parker; B G Hall
Journal:  Genetics       Date:  1990-03       Impact factor: 4.562

5.  Cellobiose-6-phosphate hydrolase (CelF) of Escherichia coli: characterization and assignment to the unusual family 4 of glycosylhydrolases.

Authors:  J Thompson; S B Ruvinov; D I Freedberg; B G Hall
Journal:  J Bacteriol       Date:  1999-12       Impact factor: 3.490

6.  Functional genes for cellobiose utilization in natural isolates of Escherichia coli.

Authors:  B G Hall; W Faunce
Journal:  J Bacteriol       Date:  1987-06       Impact factor: 3.490

7.  A fourth Escherichia coli gene system with the potential to evolve beta-glucoside utilization.

Authors:  L L Parker; B G Hall
Journal:  Genetics       Date:  1988-07       Impact factor: 4.562

8.  Characterization and nucleotide sequence of the cryptic cel operon of Escherichia coli K12.

Authors:  L L Parker; B G Hall
Journal:  Genetics       Date:  1990-03       Impact factor: 4.562

9.  Wild-type Escherichia coli grows on the chitin disaccharide, N,N'-diacetylchitobiose, by expressing the cel operon.

Authors:  N O Keyhani; S Roseman
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-23       Impact factor: 11.205

10.  Mapping and molecular cloning of the phn (psiD) locus for phosphonate utilization in Escherichia coli.

Authors:  B L Wanner; J A Boline
Journal:  J Bacteriol       Date:  1990-03       Impact factor: 3.490

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