Previous Article | Next Article ![]()
Applied and Environmental Microbiology, April 2000, p. 1429-1434, Vol. 66, No. 4
Institut für Mikrobiologie,
Universität Stuttgart, 70569 Stuttgart, Germany
Received 10 August 1999/Accepted 11 January 2000
A flavin reductase, which is naturally part of the ribonucleotide
reductase complex of Escherichia coli, acted in cell
extracts of recombinant E. coli strains under aerobic and
anaerobic conditions as an "azo reductase." The transfer of the
recombinant plasmid, which resulted in the constitutive expression of
high levels of activity of the flavin reductase, increased the
reduction rate for different industrially relevant sulfonated azo dyes
in vitro almost 100-fold. The flavin reductase gene (fre)
was transferred to Sphingomonas sp. strain BN6, a bacterial
strain able to degrade naphthalenesulfonates under aerobic conditions.
The flavin reductase was also synthesized in significant amounts in the
Sphingomonas strain. The reduction rates for the sulfonated
azo compound amaranth were compared for whole cells and cell extracts
from both recombinant strains, E. coli, and wild-type
Sphingomonas sp. strain BN6. The whole cells showed less
than 2% of the specific activities found with cell extracts. These
results suggested that the cytoplasmic anaerobic "azo reductases,"
which have been described repeatedly in in vitro systems, are
presumably flavin reductases and that in vivo they have insignificant
importance in the reduction of sulfonated azo compounds.
0099-2240/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
The Function of Cytoplasmic Flavin Reductases in
the Reduction of Azo Dyes by Bacteria

*
Corresponding author. Mailing address: Institut
für Mikrobiologie, Universität Stuttgart, 70569 Stuttgart,
Germany. Phone: 49-711-6855489. Fax: 49-711-6855725. E-mail:
Andreas.Stolz{at}PO.Uni-Stuttgart.DE.
Present address: Lehrbereich Biotechnologie, Universität
Kaiserslautern, 67663 Kaiserslautern, Germany.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»