Literature DB >> 14102871

GREEN FLUORESCENT PIGMENT ACCUMULATED BY A MUTANT OF CELLVIBRIO GILVUS.

S H LOVE, F H HULCHER.   

Abstract

Love, Samuel H. (Bowman Gray School of Medicine, Winston-Salem, N.C.), and Frank H. Hulcher. Green fluorescent pigment accumulated by a mutant of Cellvibrio gilvus. J. Bacteriol. 87:39-45. 1964.-A mutant of Cellvibrio gilvus, designated strain 139A, liberated a green, fluorescent pigment into the surrounding culture medium. A study of the factors which affected the accumulation of this pigment led to the development of a chemically defined medium which supported maximal pigment accumulation in aerated, liquid cultures. d-Glucose, glycine or l-serine, l-phenylalanine, l-proline, and l-lysine comprised the organic components of this medium. The visible absorption spectrum of the pigment showed a maximal band at 400 mmu (pH 7.0). A difference spectrum between reduced and oxidized pigment showed loss of the band at 400 mmu upon oxidation. However, a methanol-extractable, flavinelike compound occurred in the wild strain but not in the mutant. Ferric ions added to the defined medium stimulated growth, with a concomitant reduction of pigment accumulation. Pigment was formed at a maximal rate during the stationary growth phase, and the highest yield was obtained by 18 hr. Organic solvents did not extract the pigment from water solutions. One and sometimes two, compounds absorbing at 400 mmu could be eluted by ion-exchange chromatography on Cellex-P (H(+)), which was used to separate the pigment from other components in the culture supernatants so that the radioactivity of the pigment could be measured. The mutant synthesized C(14)-labeled pigment from d-glucose-U-C(14) and from each of four amino acids (glycine-1-C(14), l-phenylalanine-U-C(14), l-proline-U-C(14), and l-lysine-U-C(14). Delta-Amino-levulenic acid-4-C(14) did not contribute C(14) to the pigment.

Entities:  

Keywords:  BACTERIA; CARBON ISOTOPES; CHROMATOGRAPHY; EXPERIMENTAL LAB STUDY; FLUORESCENCE; GLUCOSE; GLYCINE; LEVULINIC ACID; LYSINE; PHENYLALANINE; PIGMENTS; PROLINE; SERINE

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Year:  1964        PMID: 14102871      PMCID: PMC276958          DOI: 10.1128/jb.87.1.39-45.1964

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  5 in total

1.  Isolation and properties of a yellow-green fluorescent peptide from azotobacter medium.

Authors:  W A BULEN; J R LECOMTE
Journal:  Biochem Biophys Res Commun       Date:  1962-12-19       Impact factor: 3.575

2.  Azotobacter fluorescence.

Authors:  D B JOHNSTONE
Journal:  J Bacteriol       Date:  1955-04       Impact factor: 3.490

3.  Fluorescence of Azotobacter. I. A comparison of the fluorescent pigments with riboflavin.

Authors:  D B JOHNSTONE; M PFEFFER; G C BLANCHARD
Journal:  Can J Microbiol       Date:  1959-06       Impact factor: 2.419

4.  Disaccharide preference of an aerobic cellulolytic bacterium, Cellvibrio gilvus n. sp.

Authors:  F H HULCHER; K W KING
Journal:  J Bacteriol       Date:  1958-12       Impact factor: 3.490

5.  Identification of Azotobacter species by fluorescence and cell analysis.

Authors:  D B JOHNSTONE; J R FISHBEIN
Journal:  J Gen Microbiol       Date:  1956-04
  5 in total

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