Authors
Info
K. Sengupta1, M. Alam2,
S. Pailan1 and P. Saha1*
1Department of
Microbiology, Burdwan University, Burdwan-713 104, India
2Department of
Microbiology,????????? Bose Institute, Kolkata-700 054, India
*Corresponding
Author Email :
psaha@microbio.buruniv.ac.in
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Abstract
Aim: The objective of
this study was to understand the possible fate of 4-NP through the molecular
mechanism and to identify potential enzymes involved in 4-NP biodegradation
by Rhodococcus sp. strain BUPNP1
Methodology: Biodegradation of
4-NP was detected spectrophotometrically at 400 nm and also confirmed by TLC
and HPLC. Comparative study of proteomes was performed by 2-D gel
electrophoresis followed by peptide mass fingerprinting and bioinformatic
analysis to identify and/ or predict the possible functions of over-expressed
proteins in 4-NP treated cells of BUNP1.
Results: Utilization of
4-nitrophenol and its hydrolysis intermediate 4-nitrocatechol (4-NC) and
1,2,4-Benzenetriol as sole carbon source indicated the presence of genomic
information encoding the enzyme necessary for the operation of 4-nitrophenol
degradation pathway in the strain BUPNP1. It could transform 4-NP into 4-NC
by monooxygenase whose major activity was detected during initial stage of
degradation. The 4-NC further depleted in the medium to release nitrite ions.
In order to investigate the molecular changes occurring during degradation, a
comparative study of proteome profiles was carried out where; 4-nitrophenol
treated cells were compared against cells grown on glucose as control. The
comparative study indicated expression of several protein spots under
4-nitrophenol treated condition.
Interpretation: This study showed
the potential of BUPNP1 strain belonging to genus Rhodococcus towards
induced expression of some unique proteins which might have possible role in
4-NP biodegradation process.
Key words: 4-Nitrophenol, Biodegradation, Rhodococcus,
Toxicoproteome, Xenobiotic
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