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  • Articles: DFG German National Licenses  (2)
  • Rhodobacter sphaeroides  (2)
  • 1
    ISSN: 1617-4623
    Keywords: DNA sequence ; recA gene induction ; Phototrophic bacterium ; Rhodobacter sphaeroides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The recA gene of Rhodobacter sphaeroides 2.4.1 has been isolated by complementation of a UV-sensitive RecA− mutant of Pseudomonas aeruginosa. Its complete nucleotide sequence consists of 1032 bp, encoding a polypeptide of 343 amino acids. The deduced amino acid sequence displayed highest identity to the RecA proteins from Rhizobium mehloti, Rhizobium phaseoli, and Agrobacterium tumefaciens. An Escherichia coli-like SOS consensus region, which functions as a binding site for the LexA repressor molecule was not present in the 215 by upstream region of the R. sphaeroides recA gene. Nevertheless, by using a recA-lacZ fusion, we have shown that expression of the recA gene of R. sphaeroides is inducible by DNA damage. A recA-defective strain of R. sphaeroides was obtained by replacement of the active recA gene by a gene copy inactived in vitro. The resulting recA mutant exhibited increased sensitivity to UV irradiation, and was impaired in its ability to perform homologous recombination as well as to trigger DNA damage-mediated expression. This is the first recA gene from a Gram-negative bacterium that lacks an E. coli-like SOS box but whose expression has been shown to be DNA damage-inducible and auto-regulated.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1617-4623
    Keywords: Carotenoid biosynthesis ; Phase transition ; Phototrophic bacterium ; Rhodobacter sphaeroides ; Spontaneous frameshifts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The synthesis of carotenoids in strain 2.4.1 of the phototrophic bacterium Rhodobacter sphaeroides is spontaneously turned on and off at a high frequency (10−5 per cell per generation) giving rise alternatively to red (wild type) and green (mutant) clones. The crtD gene is not functional in green mutants as a consequence of the spontaneous addition of a guanosine in a stretch of seven guanosines located in the 5′-terminal coding region of this gene originating a frameshift. All spontaneous wild-type revertants isolated from green mutants had recovered the crtD gene function by loss of one of these reiterated guanosines. The transition Crt+ → Crt− → Crt+, is strain-dependent, since Crt+ clones were not detected in ethyl methane sulphonate (EMS)-induced CrtD− mutants of two other strains of R. sphaeroides (WS22 and RS630) which harbour a recombinant plasmid containing the crtD gene from a spontaneous CrtD− mutant of strain 2.4.1 of R. sphaeroides.
    Type of Medium: Electronic Resource
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