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Cl
H
N
N
SO 3 H
SO 3 H
OH
OH
H
N
N
N
N
N
N
N
N
N
N
H
H
SO 3 H
SO 3 H
SO 3 H
SO 3 H
SO 3 H
RRHE7B
MW= 1480
Oxidative cleavage
Cl
H
N
N
SO 3 H
SO 3 H
OH
H
N
N
N
OH
OH
NH 2
N
N
N
N
N
+
N
H
N
H
SO 3 H
SO 3 H
SO 3 H
SO 3 H
Unknown product
Unknown product
Desulfonation
OH
OH
OH
Naphthalene-1,2,5-triol
MW= 176
Fig. 13 Proposed degradation pathway for RRHE7B by Veratryl alcohol oxidase
azoreductase. Aromatic amines are highly toxic and carcinogenic in nature. On the
other hand, decolorization of azo dyes by fungal species involves the role of oxi-
dases which don
t produce the toxic aromatic amines. Therefore, a consortium of
bacteria and fungus used for decolorization of azo dyesproduces metabolite which
was free from carcinogenic aromatic amines. Metabolites analyzed after decolor-
ization of azo dye disperse Rubine GFL by consortium of Pseudomonas sp. SUK1
and Aspergillus orchaceus NCIM 1146, showed absence of the aromatic amines.
However, Pseudomonas sp. SUK1 showed 0.14 mM concentration of aromatic
amines (Lade et al. 2012 ). At the same time, Aspergillus orchaceus NCIM 1146
showed no presence of the aromatic amines. Therefore, use of enzymatic systems
from fungal-bacterial co-cultures for decolorization of azo dyes enhances detoxi-
'
cation of azo dyes with enhanced biodegradationrate (Lade et al. 2012 ).
 
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