Biological Chemistry Hoppe-Seyler 1991-06-01

Microbial metabolism of quinoline and related compounds. IX. Degradation of 6-hydroxyquinoline and quinoline by Pseudomonas diminuta 31/1 Fa1 and Bacillus circulans 31/2 A1.

G Bott, F Lingens

Index: Biol. Chem. Hoppe-Seyler 372(6) , 381-3, (1991)

Full Text: HTML

Abstract

Two strains, using 6-hydroxyquinoline as sole source of energy, carbon and nitrogen, have been isolated. These bacteria, designated 31/1 Fa1 and 31/2 A1, are also able to degrade quinoline. According to their physiological properties strain 31/1 Fa1 has been identified as Pseudomonas diminuta and strain 31/2 A1 as Bacillus circulans. 6-Hydroxy-2-oxo-1,2-dihydroquinoline was found as intermediate in the degradation of 6-hydroxyquinoline and quinoline. 2-Oxo-1,2-dihydroquinoline was the first metabolite in the degradation of quinoline.

Related Compounds

  • 6-Hydroxyquinoline

Related Articles:

Synthesis and antimosquito properties of 2,6-substituted benzo[d]thiazole and 2,4-substituted benzo[d]thiazole analogues against Anopheles arabiensis.

2013-07-01

[Eur. J. Med. Chem. 65 , 295-303, (2013)]

TDDFT study of the polarity controlled ion-pair separation in an excited-state proton transfer reaction.

2014-07-15

[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 128 , 280-4, (2014)]

Excited-state prototropic equilibrium dynamics of 6-hydroxyquinoline encapsulated in microporous catalytic faujasite zeolites.

2010-11-08

[Chemistry 16(42) , 12609-15, (2010)]

Excited state proton transfer in the Cinchona alkaloid cupreidine.

2010-10-21

[Phys. Chem. Chem. Phys. 12(39) , 12562-9, (2010)]

Excited-state proton transfer via hydrogen-bonded acetic acid (AcOH) wire for 6-hydroxyquinoline.

2011-01-13

[J. Phys. Chem. A 115(1) , 19-24, (2011)]

More Articles...