Literature DB >> 16347906

Colonial and Cellular Polymorphism in Xenorhabdus luminescens.

R E Hurlbert1, J Xu, C L Small.   

Abstract

A highly polymorphic Xenorhabdus luminescens strain was isolated. The primary form of X. luminescens was luminescent and nonswarming and produced a yellow pigment and antimicrobial substances. The primary form generated a secondary form that had a distinct orange pigmentation, was weakly luminescent, and did not produce antimicrobial substances. Both the primary and secondary forms generated a set of colony variants at frequencies that exceeded normal rates for spontaneous mutation. The variant forms include nonswarming and swarming forms that formed large colonies and a small-colony (SC) form. The primary and secondary forms generated their SC forms at frequencies of between 1 and 14% and 1 and 2%, respectively. The SC forms were distinct from their parental primary and secondary forms in colony and cellular morphology and in protein composition. The cellular morphology and protein patterns of the nonswarming and swarming colony variants were all very similar. The DNA fingerprints of all forms were similar. Each SC-form colony reverted at high frequency to the form from which it was derived. The proportion of parental-type cells in the SC-form colonies varied with age, with young colonies containing as few as 0.0002% parental-type cells. The primary-to-secondary switch was stable, but all the other colony forms were able to switch at high frequencies to the alternative colony phenotypes.

Entities:  

Year:  1989        PMID: 16347906      PMCID: PMC184266          DOI: 10.1128/aem.55.5.1136-1143.1989

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  18 in total

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Review 5.  GABAergic neurons.

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Journal:  Parasitology       Date:  1966-05       Impact factor: 3.234

7.  Unique phenotype of opaque cells in the white-opaque transition of Candida albicans.

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Authors:  B Slutsky; M Staebell; J Anderson; L Risen; M Pfaller; D R Soll
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  15 in total

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2.  A Phosphopantetheinyl transferase homolog is essential for Photorhabdus luminescens to support growth and reproduction of the entomopathogenic nematode Heterorhabditis bacteriophora.

Authors:  T A Ciche; S B Bintrim; A R Horswill; J C Ensign
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3.  Influence of Osmolarity on Phase Shift in Photorhabdus luminescens.

Authors:  K C Krasomil-Osterfel
Journal:  Appl Environ Microbiol       Date:  1995-10       Impact factor: 4.792

4.  Toxicity of Irradiated Media for Xenorhabdus spp.

Authors:  J Xu; R E Hurlbert
Journal:  Appl Environ Microbiol       Date:  1990-03       Impact factor: 4.792

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6.  In vitro and In vivo characterization of a small-colony variant of the primary form of photorhabdus luminescens MD (Enterobacteriaceae)

Authors: 
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7.  Cloning, organization, and expression of the bioluminescence genes of Xenorhabdus luminescens.

Authors:  S Frackman; M Anhalt; K H Nealson
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8.  Transcriptional analysis of a Photorhabdus sp. variant reveals transcriptional control of phenotypic variation and multifactorial pathogenicity in insects.

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9.  Insertional inactivation of genes encoding the crystalline inclusion proteins of Photorhabdus luminescens results in mutants with pleiotropic phenotypes.

Authors:  S B Bintrim; J C Ensign
Journal:  J Bacteriol       Date:  1998-03       Impact factor: 3.490

10.  Polyclonal Antisera To Distinguish Strains and Form Variants of Photorhabdus (Xenorhabdus) luminescens.

Authors:  L Gerritsen; J M van der Wolf; J van Vuurde; R Ehlers; K C Krasomil-Osterfel; P H Smits
Journal:  Appl Environ Microbiol       Date:  1995-01       Impact factor: 4.792

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