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Friday, 13 October 2017

Melanoidins as major colourant in sugarcane molasses based distillery effluent and its degradation

Author
RamChandraaRam NareshBharagavaaVibhutiRaib
a
Environmental Microbiology Section, Industrial Toxicology Research Centre, Post Box No. 80, M.G. Marg, Lucknow 226001, U.P., India
b
School of Studies in Life Sciences, Pt. Ravi Shankar Shukla University, Raipur 492010, C.G., India
Received 26 May 2007, Revised 19 September 2007, Accepted 21 September 2007, Available online 7 November 2007.

Abstract

Melanoidins are natural condensation products of sugar and amino acids produced by non-enzymatic Maillard amino–carbonyl reaction taking place between the amino and carbonyl groups in organic substances. Melanoidins extensively exist in food products, drinks and wastewaters released from distilleries and fermentation industries. Melanoidins are very important from the nutritional, physiological and environmental aspects and due to their structural complexity, dark colour and offensive odor, these pose serious threat to soil and aquatic ecosystem that release of melanoidins cause increased load of recalcitrant organic material to natural water bodies. This then causes the problems, like reduction of sunlight penetration, decreased photosynthetic activity and dissolved oxygen concentration whereas on land, it causes reduction in soil alkalinity and inhibition of seed germination. Further, due to the possibility of complexation reactions of introduced melanoidins with metal ions, they could influence the biogeochemical cycle of many constituents in natural waters. This review presents an overview to dramatic progress to understand the synthesis, chemical structure and degradation pathway of melanoidins as well as microbial strategies for the degradation and decolourisation of melanoidins.

Abbreviations

MRPs
maillard reaction products
MnP
manganese dependent peroxidases
MIP
manganese independent peroxidases
H1 NMR
protonic nuclear magnetic resonance
CP-MAS
crossed polarized-magnetic angle spinning
HPLC
high performance liquid chromatography
ECD
electrochemical diode
DAD
diode array detector
GC
gas chromatography
FAB
fast atom bombardment
MS
mass spectrometry
ESI
electro spray ionization
CE
capillary electrophoresis
MALDI-TOF
matrix assisted laser desorption/ionization-time-of-flight
LC–MS
liquid chromatography–mass spectrometry
NBT
nitroblue tetrazolium
ELISA
enzyme linked immunosorbent assay
FM-AA
furoylmethyl amino acids
RP-HPLC
reverse phase-high performance liquid chromatography
CEC
cation exchange chromatography, HA, humic acid
KDa
kilo Dalton
DNA
deoxy ribose nucleic acid
LMW
low molecular weight
Dp
degree of polymerization
IR
infrared
PMDE
post-methanated distillery effluent
MWW
melanoidin wastewater
COD
chemical oxygen demand
BOD
biological oxygen demand
MSW
molasses spent wash
MDA
melanoidin degrading ability
CFU
colony forming unit
MDE
melanoidin decolourizing enzyme
p-CMB
p-chloromercuribenzoic acid
N-BSI
N-bromosuccinylimide
HTL
heat treatment liquor
SDS-PAGE
sodium dodecyl sulphate–polyacrilamide gel electrophoresis
DMP
2,6-dimethoxyphenol
ABTS
2,2′-azino-bis[3-ethyl-6-benzothiazoline sulfonate]
For further details log on website :
http://www.sciencedirect.com/science/article/pii/S0960852407008024

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